Co-reporter:Baojin Ma, Shan Zhang, Feng Liu, Jiazhi Duan, Shicai Wang, Jing Han, Yuanhua Sang, Xiaoqiang Yu, Dong Li, Wei Tang, Shaohua Ge, and Hong Liu
ACS Applied Materials & Interfaces October 4, 2017 Volume 9(Issue 39) pp:33717-33717
Publication Date(Web):September 14, 2017
DOI:10.1021/acsami.7b13313
It is well-accepted that most osteogenic differentiation processes do need growth factors assistance to improve efficiency. As a material cue, hydroxyapatite (HAp) can promote osteogenic differentiation of stem cells only in a way. Up to now, rare work related to the relationship between HAp nanostructures and stem cells in osteogenic differentiation process without the assistance of growth factors has been reported. In this study, one-dimensional (1D) HAp nanostructures with tunable length were synthesized by an oleic acid assisted solvothermal method by adjusting the alcohol/water ratio (η). The morphology of 1D HAp nanostructures can be changed from long nanowires into nanorods with the η value change. Different substrates constructed by 1D HAp nanostructures were prepared to investigate the effect of morphology of nanostructured HAp on stem cell fate without any growth factors or differentiation induce media. Human adipose-derived stem cells (hADSCs), a kind of promising stem cell for autologous stem cell tissue engineering, were used as the stem cell model. The experiments prove that HAp morphology can determine the performance of hADSCs cultured on different substrates. Substrate constructed by HAp nanorods (100 nm) is of little benefit to osteogenic differentiations. Substrate constructed on HAp long nanowires (50 μm) causes growth and spread inhibition of hADSCs, which even causes most cells death after 7 days of culture. However, substrate constructed by HAp short nanowires (5 μm) can destine the hADSCs differentiation to osteoblasts efficiently in normal medium (after 3 weeks) without any growth factors. It is surprise that hADSCs have changed to polyhedral morphology and exhibited the tendency to osteogenic differentiation after only 24 h culture. Hydroxyapatite nanostructures mediated stem cell osteogenic differentiation excluding growth factors provides a powerful cue to design biomaterials with special nanostructures, and helps to elucidate the interaction of stem cell and biomaterials nanostructures. The results from this study are promising for application in bone tissue engineering.Keywords: cell viability and spread; HAp nanostructures; osteogenic differentiation; tunable length; without growth factors;
Co-reporter:Yana Wang, Haidong Li, Guohui Chen, Zhou Wang, Yuanhua Sang, Hong Liu
Solar Energy Materials and Solar Cells 2017 Volume 161() pp:297-304
Publication Date(Web):March 2017
DOI:10.1016/j.solmat.2016.11.038
•Bi-phase ultrafine TiO2 nanobelts with active facet exposed have been synthesized.•The ultrafine TiO2 nanobelts have superior photocatalytic avtivity than P25.•The PdO/TiO2 heterostructures show extremely outstanding photocatalytic property.Combining the high photocatalytic activity of P25 (anatase/rutile bi-phase nanoparticle) and the good recycling property of TiO2 nanobelts is a promising approach for the preparation of high performance photocatalysts. In this work, through controlling the volume ratio of the component of organic solvent, bi-phase ultrathin TiO2 nanobelts consisting of both anatase and rutile phases have been successfully synthesized via a one-step solvothermal process by using tetrabutyl titanate as the Ti source and acetic acid/N,N-dimethylformamide (DMF) as the blended organic solvent. Compared with single phase TiO2, the bi-phase TiO2 nanobelts display a superior photocatalytic activity under ultraviolet light irradiation. Based on the refinement result of the X-ray diffraction (XRD) patterns of TiO2 nanobelts, the ratio of anatase and rutile phases in the as-synthesized TiO2 nanobelts were calculated to be 90.8 wt% and 9.2 wt%, respectively. Scanning electron microscope and high resolution transmission electron microscope images demonstrated that the thickness of the nanobelts is only 3–5 nm, and the main exposed facet is (010), a photocatalytically active facet of anatase. The bi-phase and active facet exposure characteristics endow the ultrathin TiO2 nanobelt with high photocatalytic activity, which is superior to P25. The PdO/TiO2 ultrathin nanobelt heterostructures were synthesized at ambient temperature by using ultrathin nanobelts as substrates, which exhibited outstanding photodegradation activity with methyl orange, excellent hydrogen generation, and observably enhanced photoelectrochemical activity under simulated solar irradiation. The efficient suppression of the recombination of photo-induced carriers was caused by the bi-phase characteristics of the ultrathin TiO2 nanobelts. These nanobelts will have great potential in applications for photocatalytic water treatment and hydrogen generation because of the facile synthesis process and superior photocatalytic activity.
Co-reporter:Jichuan Qiu;Kun Zhao;Linlin Li;Xin Yu;Weibo Guo;Shu Wang
Nano Research 2017 Volume 10( Issue 3) pp:776-784
Publication Date(Web):2017 March
DOI:10.1007/s12274-016-1313-5
Nanomaterials show promising opportunities to address clinical problems (such as insufficient capture of circulating tumor cells; CTCs) via the high surface area-to-volume ratio and high affinity for biological cells. However, how to apply these nanomaterials as a nano-bio interface in a microfluidic device for efficient CTC capture with high specificity remains a challenge. In the present work, we first found that a titanium dioxide (TiO2) nanorod array that can be conveniently prepared on multiple kinds of substrates has high affinity for tumor cells. Then, the TiO2 nanorod array was vertically grown on the surface of a microchannel with hexagonally patterned Si micropillars via a hydrothermal reaction, forming a new kind of a micro-nano 3D hierarchically structured microfluidic device. The vertically grown TiO2 nanorod array was used as a sensitive nano-bio interface of this 3D hierarchically structured microfluidic device, which showed high efficiency of CTC capture (76.7% ± 7.1%) in an artificial whole-blood sample.
Co-reporter:Baojin Ma, Yu Wu, Shan Zhang, Shicai Wang, Jichuan Qiu, Lili Zhao, Daidong Guo, Jiazhi Duan, Yuanhua Sang, Linlin LiHuaidong Jiang, Hong Liu
ACS Nano 2017 Volume 11(Issue 2) pp:
Publication Date(Web):February 1, 2017
DOI:10.1021/acsnano.6b08140
Terbium–aspartic acid (Tb–Asp) nanocrystals with chirality-dependent tunable fluorescent properties can be synthesized through a facile synthesis method through the coordination between Tb and Asp. Asp with different chirality (dextrorotation/d and levogyration/l) changes the stability of the coordination center following fluorescent absorption/emission ability differences. Compared with l-Asp, d-Asp can coordinate Tb to form a more stable center, following the higher quantum yield and longer fluorescence life. Fluorescence intensity of Tb–Asp linearly increases with increase ratio of d-Asp in the mixed chirality Tb–Asp system, and the fluorescent properties of Tb–Asp nanocrystals can be tuned by adjusting the chirality ratio. Tb–Asp nanocrystals possess many advantage, such as high biocompatibility, without any color in visible light irradiation, monodispersion with very small size, and long fluorescent life. Those characteristics will give them great potential in many application fields, such as low-cost antifake markers and advertisements using inkjet printers or for molds when dispersed in polydimethylsiloxane. In addition, europium can also be used to synthesize Eu–Asp nanoparticles. Importantly, the facile, low-cost, high-yield, mass-productive “green” process provides enormous advantages for synthesis and application of fluorescent nanocrystals, which will have great impact in nanomaterial technology.Keywords: chirality; print; stereo visualization; tunable fluorescence;
Co-reporter:Aixue Li, Jian Zhang, Jichuan Qiu, Zhenhuan Zhao, Cheng Wang, Chunjiang Zhao, Hong Liu
Talanta 2017 Volume 163() pp:78-84
Publication Date(Web):15 January 2017
DOI:10.1016/j.talanta.2016.10.088
•Affinity between WS2 and ssDNA was used to construct stable sensing interface.•These two sensors showed high sensitivity, selectivity and stability.•This sensing strategy can also be expanded to other analogous of WS2.•A promising approach for designing high-performance electrochemical aptasensors.It has been reported that tungsten disulfide (WS2) can bind single-stranded DNA (ssDNA) with high affinity while it has less affinity toward double stranded DNA (dsDNA). In this work, for the first time, the high affinity between WS2 and ssDNA was used to construct stable sensing interface for ATP detection. A DNA sequence with –SH at one end was first immobilized on Au electrode. WS2 nanosheets were immobilized on the SH-DNA/Au electrode surface due to the strong affinity between WS2 and ssDNA. Then the WS2 nanosheets were used to immobilize ATP binding aptamer (ABA) through the high affinity between WS2 and ssDNA, too. When ATP reacts with the ABA aptamer, duplex will be formed and dissociated from the WS2 nanosheets. On the basis of this, an electrochemical aptasensor for ATP was fabricated. This ATP sensor showed high sensitivity, selectivity and stability due to the unique WS2-ssDNA interactions and the specific aptamer–target recognition. Furthermore, this strategy was generalized to detect Hg2+ using a mercury-specific aptamer (MSO). This strategy can be expected to offer a promising approach for designing high-performance electrochemical aptasensors for a spectrum of targets.
Co-reporter:Dedong Jia;Xin Yu;Hua Tan;Xuequan Li;Feng Han;Linlin Li
Journal of Materials Chemistry A 2017 vol. 5(Issue 4) pp:1516-1525
Publication Date(Web):2017/01/24
DOI:10.1039/C6TA09229B
Hierarchical porous carbon with highly ordered straight micro-channels was prepared though a facile melt vacuum infiltration method using continuous filament glass fiber arrays as the template and glucose as the precursor. The as-prepared carbon material shows high specific surface areas up to 1880 m2 g−1 profited from the unique structure of straight micro-channels. A fine pore structure is formed in the channel wall through KOH activation after the removal of the glass fiber array. Electrochemical evaluation of the carbon material indicates that the hierarchical porous carbon exhibits a high specific capacitance of 283 F g−1 at a current density of 0.25 A g−1 with an alkaline electrolyte (6 M KOH) in a three-electrode system. It also demonstrates excellent cycling stability with a capacity retention of 88.5% over 10 000 cycles at a high current density of 6 A g−1. These exciting results demonstrate a very simple and low-cost method for large-scale preparation of electrode materials for supercapacitors.
Co-reporter:Hua Tan;Xiaoning Wang;Dedong Jia;Pin Hao;Yuanhua Sang
Journal of Materials Chemistry A 2017 vol. 5(Issue 6) pp:2580-2591
Publication Date(Web):2017/02/07
DOI:10.1039/C6TA10191G
Normally, structural details of the tissue of bio-waste affect the final properties of carbon materials. In this study, we selected two types of bio-wastes, Platanus fruit and willow catkins, to prepare hollow carbon micro-fibers, where their size and microstructure are dependent on the Platanus fruit fibers and willow catkin fibers. The electrode properties of the Platanus-derived hollow micro carbon fibers are much higher than those of the willow-derived micro carbon fibers, although carbonization and activation processes are the same for the two types of materials. It is found that the content of the organic-related elements, C, N, and S, and the content of inorganic ions, K or Na, are different. The high content of N and S induced a high doping concentration of the hollow carbon micro-fibers, which endows the Platanus-derived carbon materials with high conductivity, and the high content of inorganic elements causes a self-activation effect during the carbonization process and results in a special porous microstructure of the Platanus-derived carbon. Therefore, compared with the willow-derived hollow carbon micro-fibers, after carbonization and KOH activation, the hollow carbon micro-fibers derived from Platanus seeds possessed much higher supercapacitor electrode properties. After carbonization and activation under optimized conditions, the specific capacitance of the Platanus- and willow-derived hollow carbon micro-fibers are 304.65 F g−1 and 276.13 F g−1, respectively, at the current density of 0.5 A g−1, with a good rate capability and 88.5% and 81.05% capacity retention at 10 A g−1, respectively. The coin-type symmetric device of these two samples with 6 M KOH electrolyte exhibited a high specific capacitance of 286.5 and 267.5 F g−1, respectively, at 0.25 A g−1 (PFs 900, WFs 800), with an excellent cycling stability and 97.03% and 91.12% capacity retention after 10 000 cycles, respectively. This work not only provided two types of promising supercapacitor carbon materials but also, most importantly, offered us clues for the design and synthesis of high-performance electrode materials using the knowledge gleaned from nature.
Co-reporter:Zhihe Liu;Teng Wang;Xin Yu;Zhaoxin Geng;Yuanhua Sang
Materials Chemistry Frontiers 2017 vol. 1(Issue 10) pp:1989-1994
Publication Date(Web):2017/09/27
DOI:10.1039/C7QM00163K
Here, we report the discovery that Ti4+ in TiO2 nanostructures can be reduced in situ to Ti3+ in the presence of H2O2 to generate hydroxyl radicals for the oxidation of organic pollutants. The Ti4+ in the TiO2 nanostructure and the reduced Ti3+ driven by H2O2 can alternatively switch in situ, which endows the catalyst with a long life and excellent cyclic ability.
Co-reporter:Zhihe Liu;Teng Wang;Xin Yu;Zhaoxin Geng;Yuanhua Sang
Materials Chemistry Frontiers 2017 vol. 1(Issue 10) pp:1989-1994
Publication Date(Web):2017/09/27
DOI:10.1039/C7QM00163K
Here, we report the discovery that Ti4+ in TiO2 nanostructures can be reduced in situ to Ti3+ in the presence of H2O2 to generate hydroxyl radicals for the oxidation of organic pollutants. The Ti4+ in the TiO2 nanostructure and the reduced Ti3+ driven by H2O2 can alternatively switch in situ, which endows the catalyst with a long life and excellent cyclic ability.
Co-reporter:Lili Zhao, Yan Zhang, Fulei Wang, Shicong Hu, Xiaoning Wang, Baojin Ma, Hong Liu, Zhong Lin Wang, Yuanhua Sang
Nano Energy 2017 Volume 39(Volume 39) pp:
Publication Date(Web):1 September 2017
DOI:10.1016/j.nanoen.2017.07.037
•A micro pseudo-electrochemical polymerization reaction was proposed.•Two end-to-end BaTiO3 nanocubes can work as a micro electrochemical cell.•The electric potential is derived from the opposite spontaneous polarized charges.•Ultrasonic excitation is introduced to enhance and renew the piezoelectric charges.Conventional electrochemical polymerization is performed on electrodes driven by a direct current power source. It is impossible to realize an electrochemical polymerization reaction on the surfaces of individual nanocrystals in an aqueous system due to the difficulty of connecting all of the nanocrystals to a power source with wires or with the aid of microfabrication, especially in the environment of liquid. In this work, a micro pseudo-electrochemical polymerization reaction was proposed for in situ synthesis of polyaniline (PANI) on the surface of BaTiO3 nanocubes to form BaTiO3@PANI core-shell nanocubes. The electric potential of the micro pseudo-electrochemical polymerization originates from the opposite spontaneous polarized charges on the surface of a pair of adjacent BaTiO3 nanocubes, which form a micro-scale electrochemical cell in reaction solution. Based on the piezotronic effect of the BaTiO3 nanocubes, ultrasonic excitation was introduced to renew the piezoelectric charges on the surfaces of the BaTiO3 nanocubes, and enhance the polymerization reaction. The ferroelectric electric potential and piezotronic effect-induced micro pseudo-electrochemical reactions can also be used in other nanomaterials-based electrochemical applications, such as micro-electrochemical water splitting, micro-electrophotocatalysis, and ultrasonic therapy.Download high-res image (166KB)Download full-size image
Co-reporter:Anil Kumar;Aaron Tan;Joanna Wong;Jonathan Clayton Spagnoli;James Lam;Brianna Diane Blevins;Natasha G;Lewis Thorne;Keyoumars Ashkan;Jin Xie
Advanced Functional Materials 2017 Volume 27(Issue 39) pp:
Publication Date(Web):2017/10/01
DOI:10.1002/adfm.201700489
AbstractUnlocking the secrets of the brain is a task fraught with complexity and challenge – not least due to the intricacy of the circuits involved. With advancements in the scale and precision of scientific technologies, we are increasingly equipped to explore how these components interact to produce a vast range of outputs that constitute function and disease. Here, an insight is offered into key areas in which the marriage of neuroscience and nanotechnology has revolutionized the industry. The evolution of ever more sophisticated nanomaterials culminates in network-operant functionalized agents. In turn, these materials contribute to novel diagnostic and therapeutic strategies, including drug delivery, neuroprotection, neural regeneration, neuroimaging and neurosurgery. Further, the entrance of nanotechnology into future research arenas including optogenetics, molecular/ion sensing and monitoring, and piezoelectric effects is discussed. Finally, considerations in nanoneurotoxicity, the main barrier to clinical translation, are reviewed, and direction for future perspectives is provided.
Co-reporter:Lanchun Zhang;Chuancheng Jia;Shuren He;Youtao Zhu;Yana Wang;Zhenhuan Zhao;Xiaochun Gao;Xiaomei Zhang;Yuanhua Sang;Dongju Zhang;Xiaohong Xu
Advanced Science 2017 Volume 4(Issue 6) pp:
Publication Date(Web):2017/06/01
DOI:10.1002/advs.201600448
Hot holes in Pt-Cu alloy clusters can act as catalyst to accelerate the intrinsic aerobic oxidation reactions. It is described that under visible light irradiation the synergistic alcohol catalytic oxidation on Pt-Cu alloy clusters (≈1.1 nm)/TiO2 nanobelts could be significant promoted by interband-excitation-generated long-lifetime hot holes in the clusters.
Co-reporter:Xiaofei Zhang, Yana Wang, Baishan Liu, Yuanhua Sang, Hong Liu
Applied Catalysis B: Environmental 2017 Volume 202(Volume 202) pp:
Publication Date(Web):1 March 2017
DOI:10.1016/j.apcatb.2016.09.068
•TiO2 nanobelts heterostructured photocatalysts are summarized systematically.•The heterostructures promote charge carriers’ separation.•The second phases loaded on TiO2 nanobelt broaden the light absorption range.•Various semiconductors and optical theories are given to support the conclusions.Semiconductor photocatalysis is a promising approach to combat both environmental pollution and the global energy shortage. Advanced TiO2-based photocatalysts with novel photoelectronic properties are benchmark materials that have been pursued for their high solar energy conversion efficiency. Among the different morphological TiO2 nanostructures, TiO2 nanobelts (NBs) attract more attention due to their unique physical properties and ideal 1D ribbon-like morphology that is favorable for constructing heterostructures by assembling second-phase nanoparticles on the surface of the NBs. A large number of studies have proven that well-designed TiO2 NB heterostructures can not only broaden the photocatalytically active light band of TiO2 but also enhance the light absorption performance and the photo-induced carrier separation ability. The TiO2 NB heterostructure has become a versatile and powerful tool for building high-performance TiO2-based photocatalysts, which has stimulated intense research activities focused on the growth, properties, and applications of the 1D TiO2 NB and its heterostructures. This review attempts to cover all these aspects, including the underlying principles and key functional features of TiO2 NBs and TiO2 NB heterostructures in a comprehensive way and also discuss the prospects of this type of novel hybrid photocatalyst.Download high-res image (138KB)Download full-size image
Co-reporter:Lili Zhao, Jin Jia, Zhiyuan Yang, Jiayuan Yu, Aili Wang, Yuanhua Sang, Weijia Zhou, Hong Liu
Applied Catalysis B: Environmental 2017 Volume 210(Volume 210) pp:
Publication Date(Web):5 August 2017
DOI:10.1016/j.apcatb.2017.04.003
•A simple one-step hydrothermal method is used to synthesize CdS/MoS2/Mo.•Worm-like pores and nanosheet morphology of MoS2 improve the specific area.•Mo sheets with good conductivity facilitate fast photogenerated electrons transfer.•MoS2 co-catalyst provides active sites and inhibits charge carriers recombination.Co-catalysts for H2 production are often made from expensive noble metals, such as the most efficient Pt. The alternative non-noble metal co-catalysts with low cost and high efficiency are therefore highly desirable for economically viable H2 production. Herein, we demonstrated that a CdS/MoS2/Mo sheets system simultaneously containing photocatalysts, co-catalysts, and conductive supports, was prepared via the one-step hydrothermal process by Mo sheets as template and Mo sources. The obtained CdS/MoS2/Mo sheets possess the superior photocatalytic H2 production via water splitting under visible light irradiation, which achieved an extraordinary H2 production of 4540 μmol h−1 g−1, up to 28.6 and 3.6 times greater than that of CdS alone and Pt/CdS. The synergetic effect of MoS2 as co-catalysts and Mo sheets as conductive supports contribute to the dramatically improved photocatalytic H2 evolution activity of CdS photocatalysts, by means of facilitating charge carriers separation and providing active sites for proton reduction. These findings provide a straightforward and practical route to produce cheap and efficient co-catalysts for large-scale water splitting.Download high-res image (143KB)Download full-size image
Co-reporter:Dedong Jia, Xin Yu, Tinghan Chen, Shu Wang, Hua Tan, Hong Liu, Zhong Lin Wang, Linlin Li
Journal of Power Sources 2017 Volume 358(Volume 358) pp:
Publication Date(Web):1 August 2017
DOI:10.1016/j.jpowsour.2017.03.145
•Activated graphite fibers were synthesized after a rapid electrochemical oxidation.•The activated sample exhibits much higher capacitance compared to pristine sample.•A fiber supercapacitor based on activated graphite fibers was assembled.•The fiber supercapacitor delivers high energy density and power density.•The fiber supercapacitor with excellent flexibility could be easily weaved into cloth.Generally, carbon or graphite fibers (GFs) are used as the supporting materials for the preparation of flexible supercapacitors (SCs) by assembling various electrochemically active nanomaterials on them. A facile and rapid electrochemical oxidation method with a voltage of 3 V in a mixed H2SO4-HNO3 solution for 2–15 min is proposed to active continuous filament GFs. Detailed structural characterization, SEM, TEM, XRD, Raman and XPS demonstrate that the GFs-8 (oxidized for 8 min) possessing high specific surface area which provided numerous electrochemical sites and a large number of oxygen-containing functional groups producing pseudocapacitance. Cyclic voltammetric (CV), galvanostatic charge-discharge measurements and electrochemical impedance spectroscopy (EIS) are conducted to test the capacitive of GFs and activated GFs. The capacitance of GFs-8 reaches as high as 570 mF cm−1 at the current density of 1 mA cm−1 in LiCl electrolyte, a 1965-fold enhancement with respect to the pristine GFs (0.29 mF cm−1). The fabricated fiber solid-state supercapacitors (SSCs) provide high energy density of 0.68 mWh cm−3 at the power density 3.3 W cm−3 and have excellent durability with 90% capacitance retention after 10000 cycles. In addition, such fiber SSCs features flexibility and mechanical stability, which may have wide applications in wearable electronic devices.Download high-res image (280KB)Download full-size image
Co-reporter:Na Ren, Jianhua Li, Jichuan Qiu, Mei Yan, ... Hong Liu
Dental Materials 2017 Volume 33, Issue 5(Volume 33, Issue 5) pp:
Publication Date(Web):1 May 2017
DOI:10.1016/j.dental.2017.03.001
•Graphene oxide-coated titanate on the surface of Ti implants was prepared.•The structure was excellent vehicles for dexamethasone delivery.•The structure with dexamethasone promoted cell proliferation and osteo-differentiation.ObjectiveIn this study, the objective is to construct graphene-oxide-coated titanate on titanium foils as drug vehicle to enhance cell proliferation and osteo-differentiation of rat bone mesenchymal stem cells (rBMSCs).MethodsGraphene oxide (GO) sheets obtained using the modified Hummer’s method and characterized by AFM were coupled with bioactive titanate on Ti implants (GO-Ti) pretreated by alkali, followed by reduction (rGO-Ti). They were characterized by Raman spectroscopy, XPS, SEM, FTIR and contact angle. After dexamethasone (DEX) was loaded onto them (DEX-GO-Ti and DEX-rGO-Ti), cell proliferation of rBMSCs on them was evaluated by CCK-8 and F-actin staining, and differentiation through alkaline phosphatase activity, mRNA expression, and calcium nodules.ResultsThe obtained GO sheets were monolayers from AFM. Raman spectra exhibited two prominent peaks at D and G bands, and the I(D)/I(G) ratios increased from 0.96 to 1.68 after reduction. XPS proved the existence of oxygenated functional groups for GO-Ti and the reduction of their intensity for rGO-Ti. From SEM, GO and rGO were evenly coated on nanostructures. DEX-GO-Ti absorbed most amount of DEX and released in a sustained manner. CCK-8 results showed that DEX-GO-Ti showed excellent performance on promoting cell proliferation. RMBSCs on DEX-GO-Ti presented greatly high expression of calcium, proteins and mRNA related to osteogenic differentiation.SignificanceGO coated titanate nanostructrues on surfaces of Ti foils by a simple self-assembly method, showed excellent vechiles for DEX. The construct promoted proliferation and accelerated osteogenic differentiation of rBMSCs, and would be prosperous for their further applications.Download high-res image (297KB)Download full-size image
Co-reporter:Xiaoning Mou;Shu Wang;Xiaowang Liu;Weibo Guo;Jianhua Li;Jichuan Qiu;Xin Yu;Zhong Lin Wang;Xiaogang Liu;Zhaoxin Geng
Nanoscale (2009-Present) 2017 vol. 9(Issue 28) pp:10031-10037
Publication Date(Web):2017/07/20
DOI:10.1039/C7NR00744B
Growing experimental evidence suggests that physical cues play an important role in regulating the fate of stem cells and stimulating their differentiation behavior. We report here that static pressure enables the differentiation of rat bone marrow-derived mesenchymal stem cells (MSCs) into neural-like cells within several hours in the absence of disruptive bio-factors or chemicals. The realization of such differentiation is supported by the observation of characteristic morphology of neural-like cells with neurites, and an up-regulated expression level of neural-specific markers. Our finding also demonstrates the utility of the static pressure-based approach for in situ and specifically localized creation of neural cell systems, thereby providing profound implications for developing therapeutic application of stem cells.
Co-reporter:Baojin Ma;Shan Zhang;Ruoyu Liu;Jichuan Qiu;Lili Zhao;Shicai Wang;Jianhua Li;Yuanhua Sang;Huaidong Jiang
Nanoscale (2009-Present) 2017 vol. 9(Issue 6) pp:2162-2171
Publication Date(Web):2017/02/09
DOI:10.1039/C6NR05983J
Carbon quantum dots (CQDs) are a new type of fluorescent nanoparticle for cell imaging and tracking. However, they would easily diffuse and quench, followed by the loss of their fluorescence ability. By connecting their functional groups with other nanoparticles, the CQDs will be protected from destruction and exhibit long-time fluorescence. Here, carbon quantum dot–hydroxyapatite (CQD–HAp) hybrid nanorods were prepared by the self-assembly of CQDs on the surface of HAp nanorods through a facile one-pot process. The morphology and size of the CQD–HAp hybrid nanorods can be well controlled by using oleic acid, which meanwhile is the source of CQDs. The hydrophilic CQD–HAp hybrid nanorods have prolonged fluorescence life due to the connection between CQDs and HAp nanorods, and exhibit a higher fluorescence quantum yield than pure CQDs. In addition, when hybrid nanorods load doxorubicin (Dox) to form Dox–CQD–HAp hybrid nanorods, they can more efficiently kill human cervical cancer (HeLa) cells, rather than human prostatic cancer (PC-3) cells. Long time fluorescence for cell imaging and high efficiency in killing cancer cells as a drug-delivery medium make CQD–HAp hybrid nanorods have great potential applications in the bio-field.
Co-reporter:Xin Yu;Zhenhuan Zhao;Jian Zhang;Weibo Guo;Linlin Li;Zhong Lin Wang
CrystEngComm (1999-Present) 2017 vol. 19(Issue 1) pp:129-136
Publication Date(Web):2016/12/21
DOI:10.1039/C6CE02241C
Nanostructured TiO2 materials with a controlled morphology and structure have drawn considerable attention to both fundamental research and practical applications owing to their unique characteristics. Herein, a novel, facile, and one-step hydrothermal approach was developed to synthesize urchin-like anatase TiO2 hierarchical nanostructures assembled from ultrathin nanobelts using urea as the morphology-directing agent. The effects of the urea concentration in the preparation process were discussed intensively. Photocatalytic experiments showed that the urchin-like anatase TiO2 nanostructures possessed a much higher degradation rate of methyl orange and phenol than the most successful commercial semiconductor photocatalyst P25. The reasons for the highly efficient photocatalytic activity was ascribed to the high specific surface area (171 m2 g−1) and ultrathin 1D nanobelts of anatase TiO2 self-assembled into the urchin-like hollow spheres. The urchin-like anatase TiO2 nanostructures as photocatalysts have potential applications in environmental and energy fields for photocatalytic degradation, hydrogen production, Li-ion batteries, and dye-sensitized solar cells. In addition, new hydrothermal method can be developed for synthesis of other hierarchical nanostructures.
Co-reporter:Sujie Chang;Qiangbing Wang;Baishan Liu;Yuanhua Sang
Catalysis Science & Technology (2011-Present) 2017 vol. 7(Issue 2) pp:524-532
Publication Date(Web):2017/01/24
DOI:10.1039/C6CY02150F
Photocatalysis is an efficient approach for the degradation of organic pollutants, and continuous-flow photodegradation has advantages compared to general photocatalysis, which uses powder photocatalysts. Herein, we present a novel three-dimensional (3D) micro-nano hierarchical photocatalyst, TiO2 nanonetwork–powder metallurgical porous titanium hybrid material (TiO2/porous Ti), for continuous filtration photocatalysis/photoelectrocatalysis prepared through a hydrothermal-based chemical method. A photocatalytic layer of 3D TiO2 nanowire networks self-assembled on the surface of metallic porous Ti channels to form TiO2/porous Ti. The interconnected TiO2 thin nanowire networks with anatase–rutile bi-phases introduce a photocatalytic layer with a high photocatalytic performance. The porous structures and wire-like morphology of metallic titanium can enhance photo-induced carrier transport and separation, and it can act as a 3D electrode for photoelectrocatalysis. A novel continuous-flow photocatalytic reactor was designed by setting a group of TiO2/porous Ti sheets vertically in a quartz box equipped with ultraviolet light-emitting diodes (UV-LEDs). By applying a 0.6 V low electrical bias between the TiO2/porous Ti electrodes and a Pt wire electrode, a device with one layer of TiO2/porous Ti can result in 90% degradation of methyl orange (MO) under acidic conditions with 110 mW cm−2 of UV irradiation over 40 min; a device with three layers of TiO2/porous Ti needs just 10 min to reach the same photodegradation efficiency. The continuous degradation of other model pollutants, Rhodamine B (Rh B) and methylene blue (MB), was also demonstrated for this TiO2/porous Ti hybrid photocatalyst also with high photoelectrocatalytic efficiency. A continuous-flow photoelectrocatalytic reactor equipped with TiO2/porous Ti shows potential for the treatment of water in environmental protection applications.
Co-reporter:Pin Hao;Guanwei Cui;Xifeng Shi;Junfeng Xie;Xinyuan Xia;Yuanhua Sang;C. P. Wong;Bo Tang
Chinese Journal of Chemistry 2017 Volume 35(Issue 5) pp:699-706
Publication Date(Web):2017/05/01
DOI:10.1002/cjoc.201600722
Supercapacitor electrodes with porous structure based on renewable, eco-friendly and cost-effective materials have caused extensive concern in energy storage fields. Sliced bread, the common food ingredient, mainly containing glucose polymers, can be a promising candidate to fabricate porous supercapacitor electrodes. Highly porous carbon aerogels by using sliced bread as the raw material were synthesized through a carefully controlled aerogel carbonization-activation process. Interestingly, the specific surface area and the pore size distribution of the porous carbon were controlled by the activation temperature, which result in the varied performance of the carbon aerogel as a supercapacitor. Electrochemical investigation measurements revealed that the hierarchical porous carbon aerogel shows an excellent capacitor behavior for construction of a symmetric supercapacitor, which demonstrated a high specific capacitance of 229 F•g−1 at discharge current of 0.2 A•g−1. In addition, the fabricated supercapacitor displayed excellent capacitance retention of 95.5% over 5000 cycles.
Co-reporter:Linlin Li;Chuanfang Chen;Huiyu Liu;Changhui Fu;Longfei Tan;Shunhao Wang;Shiyan Fu;Xi Liu;Xianwei Meng
Advanced Functional Materials 2016 Volume 26( Issue 24) pp:4252-4261
Publication Date(Web):
DOI:10.1002/adfm.201600985
Carbon-based nanomaterials have been developed for photothermal cancer therapy, but it is still a great challenge to fabricate their multifunctional counterparts with facile methods, good biocompatibility and dispersity, and high efficiency for cancer theranostics. In this work, an alternative multifunctional nanoplatform is developed based on carbon–silica nanocapsules with gold nanoparticle in the cavity (Au@CSN) for cancer theranostics. The encapsulated chemodrug doxorubicin can be released from the Au@CSN with mesoporous and hollow structure in a near-infrared light and pH stimuli-responsive manner, facilitating spatiotemporal therapy to decrease off-target toxicity. The nanocapsules with efficient photothermal conversion and excellent biocompatibility achieve a synergistic effect of photothermal and chemotherapy. Furthermore, the nanocapsules can act as a multimodal imaging agent of computed tomography and photoacoustic tomography imaging for guiding the therapy. This new design platform can provide a promising strategy for precise cancer theranostics.
Co-reporter:Xiaoning Mou, Shu Wang, Weibo Guo, Shaozheng Ji, Jichuan Qiu, Deshuai Li, Xiaodi Zhang, Jin Zhou, Wei Tang, Changyong Wang and Hong Liu
Nanoscale 2016 vol. 8(Issue 27) pp:13186-13191
Publication Date(Web):14 Jun 2016
DOI:10.1039/C6NR01874B
In this study, a porous-flat TiO2 micropattern was fabricated with flat and nanoporous TiO2 ceramics for investigating the effect of topography on neural stem cell (NSC) differentiation. This finding demonstrates that localized committed differentiation could be achieved in one system by integrating materials with different topographies.
Co-reporter:Jian Zhang, Xin Yu, Weibo Guo, Jichuan Qiu, Xiaoning Mou, Aixue Li and Hong Liu
Nanoscale 2016 vol. 8(Issue 17) pp:9382-9389
Publication Date(Web):30 Mar 2016
DOI:10.1039/C6NR01360K
The demand for a highly sensitive and selective glucose biosensor which can be used for implantable or on-time monitoring is constantly increasing. In this work, TiO2 nanorods were synthesized in situ on the surface of graphite microfibers to yield TiO2 nanorod/graphite microfiber hybrid electrodes. The TiO2 nanorods not only retain the high activity of the immobilized glucose molecule, but also promote the direct electron transfer process on the electrode surface. As a working electrode in an electrochemical glucose biosensor in a flowing system, the microfiber hybrid electrodes exhibit high sensitivity, selectivity and stability. Due to its simplicity, low cost, high stability, and unique morphology, the TiO2 nanorod/graphite microfiber hybrid electrode is expected to be an excellent candidate for an implantable biosensor or for in situ flow monitoring.
Co-reporter:Jianhua Li, Jichuan Qiu, Weibo Guo, Shu Wang, Baojin Ma, Xiaoning Mou, Michael Tanes, Huaidong Jiang and Hong Liu
Nanoscale 2016 vol. 8(Issue 14) pp:7416-7422
Publication Date(Web):11 Mar 2016
DOI:10.1039/C6NR00785F
Second harmonic generation (SHG) nanocrystals have recently been reported to label cancer cells and other functional cell lines due to their unique double-frequency property. In this paper, we report for the first time the use of lithium niobate (LiNbO3, LN) nanocrystals as SHG labels for imaging stem cells. Rat mesenchymal stem cells (rMSCs) were labeled with LN nanocrystals in order to study the cellular internalization of the nanocrystals and the influence on stem cell differentiation. The results showed that LN nanocrystals were endocytosed by the rMSCs and the distribution of the internalized nanoparticles demonstrated a high consistency with the orientation of the actin filaments. Besides, LN-labeled rMSCs showed a concentration-dependent viability. Most importantly, rMSCs labeled with 50 μg per mL of LN nanocrystals retained their ability to differentiate into both osteogenic and adipogenic lineages. The results prove that LN nanocrystals can be used as a cytocompatible, near-infrared (NIR) light driven cell label for long-term imaging, without hindering stem cell differentiation. This work will promote the use of LN nanocrystals to broader applications like deep-tissue tracking, remote drug delivery and stem cell therapy.
Co-reporter:Haidong Li, Yana Wang, Guohui Chen, Yuanhua Sang, Huaidong Jiang, Jiating He, Xu Li and Hong Liu
Nanoscale 2016 vol. 8(Issue 11) pp:6101-6109
Publication Date(Web):23 Feb 2016
DOI:10.1039/C5NR08796A
Photocatalytic materials comprised of semiconductor nanostructures have attracted tremendous scientific and technological interest over the last 30 years. This is due to the fact that these photocatalytic materials have unique properties that allow for an effective direct energy transfer from light to highly reactive chemical species which are applicable in the remediation of environmental pollutants and photocatalytic hydrogen generation. Heterostructured photocatalysts are a promising type of photocatalyst which can combine the properties of different components to generate a synergic effect, resulting in a high photocatalytic activity. In this work, a heterostructured photocatalyst comprised of few-layered MoS2 nanosheets coated on a TiO2 nanobelts surface was synthesized through a simple hydrothermal treatment. The hybrid heterostructures with enhanced broad spectrum photocatalytic properties can harness UV and visible light energy to decompose organic contaminants in aqueous solutions as well as split water to hydrogen and oxygen. The mechanism of the enhancement is that the MoS2/TiO2 nanobelts heterostructure can enhance the separation of the photo-induced carriers, which results in a higher photocurrent due to the special electronic characteristics of the graphene-like layered MoS2 nanosheets. This methodology is potentially applicable to the synthesis of a range of hybrid nanostructures with promising applications in photocatalysis and other relevant areas.
Co-reporter:Weibo Guo, Shu Wang, Xin Yu, Jichuan Qiu, Jianhua Li, Wei Tang, Zhou Li, Xiaoning Mou, Hong Liu and Zhonglin Wang
Nanoscale 2016 vol. 8(Issue 4) pp:1897-1904
Publication Date(Web):28 Dec 2015
DOI:10.1039/C5NR06602F
The cell–material interface is one of the most important considerations in designing a high-performance tissue engineering scaffold because the surface of the scaffold can determine the fate of stem cells. A conductive surface is required for a scaffold to direct stem cells toward neural differentiation. However, most conductive polymers are toxic and not amenable to biological degradation, which restricts the design of neural tissue engineering scaffolds. In this study, we used a bioactive three-dimensional (3D) porcine acellular dermal matrix (PADM), which is mainly composed of type I collagen, as a basic material and successfully assembled a layer of reduced graphene oxide (rGO) nanosheets on the surface of the PADM channels to obtain a porous 3D, biodegradable, conductive and biocompatible PADM–rGO hybrid neural tissue engineering scaffold. Compared with the PADM scaffold, assembling the rGO into the scaffold did not induce a significant change in the microstructure but endowed the PADM–rGO hybrid scaffold with good conductivity. A comparison of the neural differentiation of rat bone-marrow-derived mesenchymal stem cells (MSCs) was performed by culturing the MSCs on PADM and PADM–rGO scaffolds in neuronal culture medium, followed by the determination of gene expression and immunofluorescence staining. The results of both the gene expression and protein level assessments suggest that the rGO-assembled PADM scaffold may promote the differentiation of MSCs into neuronal cells with higher protein and gene expression levels after 7 days under neural differentiation conditions. This study demonstrated that the PADM–rGO hybrid scaffold is a promising scaffold for neural tissue engineering; this scaffold can not only support the growth of MSCs at a high proliferation rate but also enhance the differentiation of MSCs into neural cells.
Co-reporter:Daidong Guo, Baojin Ma, Lili Zhao, Jichuan Qiu, Wei Liu, Yuanhua Sang, Jerome Claverie, and Hong Liu
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 19) pp:11990
Publication Date(Web):April 27, 2016
DOI:10.1021/acsami.6b01460
Cerium-doped yttrium aluminum garnet (YAG:Ce) nanorods were prepared via a partial wet chemical route followed by a calcination process by using Al2O3 nanorods as both templates and the reactant. These novel well-crystallized YAG:Ce phosphors with a 200–300 nm diameter and a 2–3 μm length have a high specific surface area while being virtually devoid of surface defects. The YAG:Ce nanorod phosphors possess good luminescent properties compared with granular YAG:Ce phosphors. Photoluminescence quantum yields of YAG:Ce nanorod phosphors are higher than those of granular ones. The YAG:Ce nanorod phosphors exhibit two luminescent decay times due to their unique morphology. The YAG:Ce nanorods exhibited good cytocompatibility with bone marrow mesenchymal stem cells and can be used as biolabel nanoparticles in bioimaging.Keywords: biolabeling; luminescent properties; nanorod phosphors; partial wet chemical route; YAG:Ce
Co-reporter:Longyue Liang;Xueliang Kang;Yuanhua Sang
Advanced Science 2016 Volume 3( Issue 7) pp:
Publication Date(Web):
DOI:10.1002/advs.201500358
One-dimensional (1D) ferroelectric nanostructures, such as nanowires, nanorods, nanotubes, nanobelts, and nanofibers, have been studied with increasing intensity in recent years. Because of their excellent ferroelectric, ferroelastic, pyroelectric, piezoelectric, inverse piezoelectric, ferroelectric-photovoltaic (FE-PV), and other unique physical properties, 1D ferroelectric nanostructures have been widely used in energy-harvesting devices, nonvolatile random access memory applications, nanoelectromechanical systems, advanced sensors, FE-PV devices, and photocatalysis mechanisms. This review summarizes the current state of 1D ferroelectric nanostructures and provides an overview of the synthesis methods, properties, and practical applications of 1D nanostructures. Finally, the prospects for future investigations are outlined.
Co-reporter:Jichuan Qiu;Deshuai Li;Xiaoning Mou;Jianhua Li;Weibo Guo;Shu Wang;Xin Yu;Baojin Ma;Shan Zhang;Wei Tang;Yuanhua Sang;Pilar Rivera Gil
Advanced Healthcare Materials 2016 Volume 5( Issue 6) pp:702-710
Publication Date(Web):
DOI:10.1002/adhm.201500770
The influence of graphene quantum dots (GQDs) on key characteristics of bone marrow derived mesenchymal stem cells (MSCs) phenotype (i.e., self-renewal, differentiation potential, and pluripotency) is systematically investigated in this work. First, the viability and impact of GQDs on the self-renewal potential of MSCs is evaluated in order to determine a threshold for the exposing dose. Second, GQDs uptake by MSCs is confirmed due to the excellent fluorescent properties of the particles. They exhibit a homogenous cytoplasmatic distribution that increases with the time and concentration. Third, the impact of GQDs on the osteogenic differentiation of MSCs is deeply characterized. An enhanced activity of alkaline phosphatase promoted by GQDs indicates early activation of osteogenesis. This is also confirmed upon GQD-induced up-regulation of phenotypically related osteogenic genes (Runx2, osteopontin, and osteocalcin) and specific biomarkers expression (osteopontin and osteocalcin). GQDs also effectively enhance the formation of calcium-rich deposits characteristics of osteoblasts. Furthermore, genes microarray results indicate that the enhanced osteogenic differentiation of MSCs by GQDs is in progress through a bone morphogenetic protein and transforming growth factor-β relative signaling pathways. Finally, intracytoplasmatic lipid detection shows that GQDs can also promote the adipogenic differentiation of MSCs, thus confirming the prevalence of their pluripotency potential.
Co-reporter:Jian Tian, Xiaolin Hu, Na Wei, Yanli Zhou, Xiaohong Xu, Hongzhi Cui, Hong Liu
Solar Energy Materials and Solar Cells 2016 Volume 151() pp:7-13
Publication Date(Web):July 2016
DOI:10.1016/j.solmat.2016.02.017
•Based on energy band matching, the RuO2/TiO2 nanobelt heterostructures are designed.•The heterostructures exhibit an improved UV and visible photocatalytic performance.•The heterostructure nanopapers present good activity for oxidation of benzyl alcohol.Based on energy band matching between RuO2 and TiO2, the RuO2/TiO2 nanobelt heterostructures are designed and fabricated. The formed heterostructures can efficiently enhance the separation of photogenerated electron-hole pairs and accelerate the transport of charges. Thanks to above-mentioned advantages, the RuO2/TiO2 nanobelt heterostructures exhibit an improved photocatalytic performance compared with P25, TiO2, and RuO2 under UV and visible light irradiation. Moreover, the nanopapers based on RuO2/TiO2 nanobelt heterostructures have been prepared via a modified paper-making process. The paper-like porous RuO2/TiO2 nanobelt heterostructures are applied in heterogeneous catalysis and present enhanced activity and selectivity for catalyzing aerobic oxidation of benzyl acohol. These results may provide a paradigm to fabricate and design the one-dimensional TiO2 nanostructured surface heterostructures with high efficiency and performance.
Co-reporter:Jian Tian, Jian Li, Na Wei, Xiaohong Xu, Hongzhi Cui, Hong Liu
Ceramics International 2016 Volume 42(Issue 1) pp:1611-1617
Publication Date(Web):January 2016
DOI:10.1016/j.ceramint.2015.09.112
One-dimensional (1D) TiO2 nanostructures can be used as the support of metal particles to form the heterostructures, which can prevent the metal agglomeration and enhance the activity of metal in various applications. Here, well-dispersed Ru nanoparticles (NPs) supported on 1D TiO2 nanobelts (NBs) are firstly synthesized by a facile photo-reduction method. The as-synthesized Ru/TiO2 NB heterostructures exhibit an improved photocatalytic performance compared with P25 and TiO2 under both UV and visible light irradiation. Our mechanistic investigation reveals that the enhanced photocatalytic activity can be attributed to the Schottky barrier effect of Ru NPs, which efficiently harvest the electrons of TiO2 and enhance the separation of photogenerated electron–hole pairs. Moreover, the Ru/TiO2 NB heterostructures are assembled into the porous nanopaper via a modified paper-making process, which can be applied in heterogeneous catalysis. The formed Ru/TiO2 NB heterostructure nanopapers exhibit enhanced activity and selectivity for catalyzing aerobic oxidation of benzyl alcohol. Ru NPs are well dispersed with the average size of about 1.5 nm on the TiO2 NBs support, which could contribute to the high catalytic activity of Ru/TiO2 catalyst.
Co-reporter:Shan Zhang, Ruibin Zhang, Baojin Ma, Jichuan Qiu, Jianhua Li, Yuanhua Sang, Wei Liu and Hong Liu
RSC Advances 2016 vol. 6(Issue 48) pp:41999-42007
Publication Date(Web):20 Apr 2016
DOI:10.1039/C6RA04046B
Potassium ion (K+) plays a central role in several fundamental physiological processes. Detection of the K+ concentration is an essential diagnostic tool for various medical diseases. However, most commercial detection methods are complex and expensive, which are not easily implemented in community hospitals or at home, in this study, we present a simple fluorescent K+ detection system based on the formation of G-quadruplex between K+ and dual-labelled thrombin aptamer oligonucleotide derivative (5′-FAM-TTTTTTAGGTTGGTGTGGTTGG-TAMRA-3′). Furthermore, based on this method, highly sensitive and selective detection of K+ in actual serum was realized by using EDTA as chelating agent to avoid the interference of Ca2+ and Mg2+ at physiological concentrations. Thus, this study paves the road toward the design and manufacture of portable potassium ions sensors based on fluorescence.
Co-reporter:Tingqiao LEOW, Hong LIU, R. HUSSIN, Z. IBRAHIM, K. DERAMAN, H.O. LINTANG, W.N.W SHAMSURI
Journal of Rare Earths 2016 Volume 34(Issue 1) pp:21-29
Publication Date(Web):January 2016
DOI:10.1016/S1002-0721(14)60573-1
AbstractA series of Eu3+ and Dy3+ doped/co-doped as well as un-doped BaB2Si2O8 phosphors were synthesized via solid state reaction method. The PL result showed typical blue and green emission from Dy3+ and red emission from Eu3+. The f-f transitions involving the lanthanide ions along with dopant site occupancy were discussed thoroughly. Phonon assisted energy transfer process was observed from Eu3+ to Dy3+, which enhanced the emissions of Dy3+. Combinations of the emissions from Eu3+ and Dy3+ showed a possible white to red tuneable emission on the CIE diagram. The white warmth emissions of the phosphor were revealed to be adjustable through designing the dopant concentration and excitation wavelengths. An unusual energy transfer that originated from Eu3+ to Dy3+ was also discovered and the energy transfer mechanism was discussed. Proposed energy transfer mechanism was investigated using luminescence decay lifetime. All the phosphor exhibited efficient excitation in the UV range which matched well with the emissions from GaN-based LED chips. This presented the BaB2Si2O8 phosphor as a promising candidate for white LED applications. The effects of doping on the structural properties and the optical band gap of BaB2Si2O8 phosphor were also discussed in this study.CIE chromaticity diagram plots of Eu3+ and Dy3+ singly doped/co-doped BaB2Si2O8 samples
Co-reporter:Weibo Guo, Xiaodi Zhang, Xin Yu, Shu Wang, Jichuan Qiu, Wei Tang, Linlin Li, Hong Liu, and Zhong Lin Wang
ACS Nano 2016 Volume 10(Issue 5) pp:5086
Publication Date(Web):May 4, 2016
DOI:10.1021/acsnano.6b00200
Engineered conductive scaffolds toward neural regeneration should have the ability to regulate mesenchymal stems cell (MSC) differentiation into neural lineage through an electrical stimulation-assisted culture process. In this work, a self-powered electrical stimulation-assisted neural differentiation system for MSCs was realized by combining a high effective triboelectric nanogenerator (TENG) to supply pulsed electric simulation signals and a poly(3,4-ethylenedioxythiophene) (PEDOT)–reduced graphene oxide (rGO) hybrid microfiber (80 μm in diameter) as a scaffold. The conductive PEDOT endows the rGO–PEDOT hybrid microfiber with an enhanced electrical conductivity and maintains a good cytocompatibility. MSCs cultured on this highly conductive rGO–PEDOT hybrid microfiber possess enhanced proliferation ability and good neural differentiation tendency. Importantly, by inducing electric pulses generated by the TENG as the electrical stimulation signal, which are triggered by human walking steps, neural differentiation of MSCs is dramatically improved. This study illustrates the customizability of the rGO–PEDOT hybrid microfiber for neural tissue engineering scaffolding applications, underlines the potential of a self-powered TENG electrical stimulation system for accelerating MSC differentiation into neural cells without bio/chemical cues, and suggests the TENG’s practical use as a wearable stimulation system to assist nerve regeneration for a walking person.Keywords: electrical stimulation; MSCs; neural differentiation; rGO−PEDOT microfiber; self-powered TENG
Co-reporter:Linlin Li, Shiyan Fu, Chuanfang Chen, Xuandong Wang, Changhui Fu, Shu Wang, Weibo Guo, Xin Yu, Xiaodi Zhang, Zhirong Liu, Jichuan Qiu, and Hong Liu
ACS Nano 2016 Volume 10(Issue 7) pp:7094
Publication Date(Web):June 16, 2016
DOI:10.1021/acsnano.6b03238
Biocompatibility and bioelimination are basic requirements for systematically administered nanomaterials for biomedical purposes. Gold-based plasmonic nanomaterials have shown potential applications in photothermal cancer therapy. However, their inability to biodegrade has impeded practical biomedical application. In this study, a kind of bioeliminable magnetoplasmonic nanoassembly (MPNA), assembled from an Fe3O4 nanocluster and gold nanoshell, was elaborately designed for computed tomography, photoacoustic tomography, and magnetic resonance trimodal imaging-guided tumor photothermal therapy. A single dose of photothermal therapy under near-infrared light induced a complete tumor regression in mice. Importantly, MPNAs could respond to the local microenvironment with acidic pH and enzymes where they accumulated including tumors, liver, spleen, etc., collapse into small molecules and discrete nanoparticles, and finally be cleared from the body. With the bioelimination ability from the body, a high dose of 400 mg kg–1 MPNAs had good biocompatibility. The MPNAs for cancer theranostics pave a way toward biodegradable bio-nanomaterials for biomedical applications.Keywords: biocompatibility; bioelimination; multimodal imaging; photothermal therapy; plasmonic nanoparticles
Co-reporter:Yuanhua Sang;Zhenhuan Zhao;Mingwen Zhao;Pin Hao;Yanhua Leng
Advanced Materials 2015 Volume 27( Issue 2) pp:363-369
Publication Date(Web):
DOI:10.1002/adma.201403264
Co-reporter:Zhenhuan Zhao;Jian Tian;Yuanhua Sang;Andreu Cabot
Advanced Materials 2015 Volume 27( Issue 16) pp:2557-2582
Publication Date(Web):
DOI:10.1002/adma.201405589
TiO2 semiconductor nanobelts have unique structural and functional properties, which lead to great potential in many fields, including photovoltaics, photocatalysis, energy storage, gas sensors, biosensors, and even biomaterials. A review of synthetic methods, properties, surface modification, and applications of TiO2 nanobelts is presented here. The structural features and basic properties of TiO2 nanobelts are systematically discussed, with the many applications of TiO2 nanobelts in the fields of photocatalysis, solar cells, gas sensors, biosensors, and lithium-ion batteries then introduced. Research efforts that aim to overcome the intrinsic drawbacks of TiO2 nanobelts are also highlighted. These efforts are focused on the rational design and modification of TiO2 nanobelts by doping with heteroatoms and/or forming surface heterostructures, to improve their desirable properties. Subsequently, the various types of surface heterostructures obtained by coupling TiO2 nanobelts with metal and metal oxide nanoparticles, chalcogenides, and conducting polymers are described. Further, the charge separation and electron transfer at the interfaces of these heterostructures are also discussed. These properties are related to improved sensitivity and selectivity for specific gases and biomolecules, as well as enhanced UV and visible light photocatalytic properties. The progress in developments of near-infrared-active photocatalysts based on TiO2 nanobelts is also highlighted. Finally, an outline of important directions of future research into the synthesis, modification, and applications of this unique material is given.
Co-reporter:Haidong Li, Yuanhua Sang, Sujie Chang, Xin Huang, Yan Zhang, Rusen Yang, Huaidong Jiang, Hong Liu, and Zhong Lin Wang
Nano Letters 2015 Volume 15(Issue 4) pp:2372-2379
Publication Date(Web):March 24, 2015
DOI:10.1021/nl504630j
An electric field built inside a crystal was proposed to enhance photoinduced carrier separation for improving photocatalytic property of semiconductor photocatalysts. However, a static built-in electric field can easily be saturated by the free carriers due to electrostatic screening, and the enhancement of photocatalysis, thus, is halted. To overcome this problem, here, we propose sonophotocatalysis based on a new hybrid photocatalyst, which combines ferroelectric nanocrystals (BaTiO3) and semiconductor nanoparticles (Ag2O) to form an Ag2O–BaTiO3 hybrid photocatalyst. Under periodic ultrasonic excitation, a spontaneous polarization potential of BaTiO3 nanocrystals in responding to ultrasonic wave can act as alternating built-in electric field to separate photoinduced carriers incessantly, which can significantly enhance the photocatalytic activity and cyclic performance of the Ag2O–BaTiO3 hybrid structure. The piezoelectric effect combined with photoelectric conversion realizes an ultrasonic-wave-driven piezophototronic process in the hybrid photocatalyst, which is the fundamental of sonophotocatalysis.
Co-reporter:Jian Tian, Pin Hao, Na Wei, Hongzhi Cui, and Hong Liu
ACS Catalysis 2015 Volume 5(Issue 8) pp:4530
Publication Date(Web):June 4, 2015
DOI:10.1021/acscatal.5b00560
We employed TiO2 nanobelts as the synthetic template and developed three-dimensional (3D) porous Bi2MoO6 nanosheet/TiO2 nanobelt heterostructures with a few-layer and uniform Bi2MoO6 nanosheets by a simple hydrothermal method. The as-prepared Bi2MoO6 nanosheet/TiO2 nanobelt heterostructure shows an excellent photodegradation performance under UV and visible light irradiation. Importantly, such a heterostructure possesses high photocatalytic oxygen production with a rate of 0.668 mmol h–1 g–1. Moreover, the Bi2MoO6 nanosheet/TiO2 nanobelt heterostructure shows an enhanced photoelectochemistry performance under irradiation of solar illumination. The current research can offer an alternative route for designing a 3D heterostructure system to effectively utilize broad-spectrum solar light.Keywords: heterostructure; oxygen production; photocatalytic; photoelectrochemistry; TiO2 nanobelt
Co-reporter:Zhenhuan Zhao, Shimeng Hao, Pin Hao, Yuanhua Sang, Ayyakkannu Manivannan, Nianqiang Wu and Hong Liu
Journal of Materials Chemistry A 2015 vol. 3(Issue 29) pp:15049-15056
Publication Date(Web):08 Jun 2015
DOI:10.1039/C5TA02770E
The notion of environmental protection and renewable sources for energy conversion and storage has become particularly important nowadays. In this research, a meso-microporous carbon was prepared by the combination of a template method and chemical activation with earth abundant cellulose and lignosulphonate as the sources. The as-synthesized meso-microporous carbon contained mesopores generated by regeneration of cellulose with the assistance of a silica template, and micropores created by chemical activation of carbon. Such a unique porous structure makes the as-synthesized meso-microporous carbon the ideal electrode active material for energy storage. The two-electrode symmetric supercapacitors built using the meso-microporous carbon electrodes show a specific capacitance of 286 F g−1 at a current density of 0.25 A g−1 in aqueous electrolyte. More importantly, the symmetric supercapacitor achieves a high energy density of 13 W h kg−1 while at a high power density of 27 kW kg−1. It is demonstrated that using renewable natural sources for the manufacturing of porous carbon with high performance for energy storage can be an effective way to lower the cost of a supercapacitor.
Co-reporter:Pin Hao, Zhenhuan Zhao, Liyi Li, Chia-Chi Tuan, Haidong Li, Yuanhua Sang, Huaidong Jiang, C. P. Wong and Hong Liu
Nanoscale 2015 vol. 7(Issue 34) pp:14401-14412
Publication Date(Web):24 Jul 2015
DOI:10.1039/C5NR04421A
Current applications of carbon-based supercapacitors are limited by their low energy density. One promising strategy to enhance the energy density is to couple metal oxides with carbon materials. In this study, a porous MnCo2O4.5 nanoneedle/carbon aerogel hybrid nanostructure was synthesized by assembling MnCo2O4.5 nanoneedle arrays on the surface of channel walls of hierarchical porous carbon aerogels derived from chitosan for the supercapacitor application. The synthetic process of the hybrid nanostructure involves two steps, i.e. the growth of Mn–Co precursors on carbon aerogel by a hydrothermal process and the conversion of the precursor into MnCo2O4.5 nanoneedles by calcination. The carbon aerogel exhibits a high electrical conductivity, high specific surface area and porous structure, ensuring high electrochemical performance of the hybrid nanostructure when coupled with the porous MnCo2O4.5 nanoneedles. The symmetric supercapacitor using the MnCo2O4.5 nanoneedle/carbon aerogel hybrid nanostructure as the active electrode material exhibits a high energy density of about 84.3 Wh kg−1 at a power density of 600 W kg−1. The voltage window is as high as 1.5 V in neutral aqueous electrolytes. Due to the unique nanostructure of the electrodes, the capacitance retention reaches 86% over 5000 cycles.
Co-reporter:Guohui Chen, Shaozheng Ji, Yuanhua Sang, Sujie Chang, Yana Wang, Pin Hao, Jerome Claverie, Hong Liu and Guangwei Yu
Nanoscale 2015 vol. 7(Issue 7) pp:3117-3125
Publication Date(Web):09 Jan 2015
DOI:10.1039/C4NR05749J
A novel scaly Sn3O4/TiO2 nanobelt heterostructured photocatalyst was fabricated via a facile hydrothermal route. The scaly Sn3O4 nanoflakes can be synthesized in situ and assembled on surface coarsened TiO2 nanobelts through a hydrothermal process. The morphology and distribution of Sn3O4 nanoflakes can be well-controlled by simply tuning the Sn/Ti molar ratio of the reactants. Compared with single phase nanostructures of Sn3O4 and TiO2, the scaly hybrid nanobelts exhibited markedly enhanced photoelectrochemical (PEC) response, which caused higher photocatalytic hydrogen evolution even without the assistance of Pt as a co-catalyst, and enhanced the degradation ability of organic pollutants under both UV and visible light irradiation. In addition to the increased exposure of active facets and broad light absorption, the outstanding performance is ascribed to the matching energy band structure between Sn3O4 and TiO2 at the two sides of the heterostructure, which efficiently reduces the recombination of photo-excited electron–hole pairs and prolongs the lifetime of charge carriers. Both photocatalytic assessment and PEC tests revealed that Sn3O4/TiO2 heterostructures with a molar ratio of Sn/Ti of 2/1 exhibited the highest photocatalytic activity. This study provides a facile and low-cost method for the large scale production of Sn3O4 based materials in various applications.
Co-reporter:Tongtong Jiang, Chuancheng Jia, Lanchun Zhang, Shuren He, Yuanhua Sang, Haidong Li, Yanqing Li, Xiaohong Xu and Hong Liu
Nanoscale 2015 vol. 7(Issue 1) pp:209-217
Publication Date(Web):03 Nov 2014
DOI:10.1039/C4NR05905K
Plasmonic photocatalysts composed of Au and bimetallic Au–Pd alloy nanoparticles (NPs) on one-dimensional TiO2 nanobelts (TiO2-NBs) were used for the aerobic oxidation of benzyl alcohol under visible light irradiation. Remarkable light-promoted activity was observed for the as-synthesized M/TiO2-NB (M = Au, Au–Pd) nanostructures based on the TiO2(B)/anatase heterostructured nanobelt. The difference in band structure and the well matched interface between the TiO2(B) and anatase phases, coupled with the one-dimensional nanostructure, enable an enhanced charge transfer within the heterostructured nanobelt. This inter-phase charge transfer greatly facilitates the flow of hot electrons from the metal NPs to TiO2 and promotes benzyl alcohol oxidation. This efficient electron transfer was identified by the much higher photocurrent response measured for the Au/TiO2-NB nanostructure with the TiO2(B)/anatase heterojunction than those with either of the single phases under visible light irradiation. Alloying Au with Pd in Au–Pd/TiO2-NB results in a significant improvement in the visible light-promoted activity compared to the monometallic Au/TiO2-NB sample. It is supposed that the plasmon-mediated charge distribution within the alloy NPs is mainly responsible for the enhanced photocatalytic activity of the bimetallic nanostructures.
Co-reporter:Guohui Chen, Shaozheng Ji, Haidong Li, Xueliang Kang, Sujie Chang, Yana Wang, Guangwei Yu, Jianren Lu, Jerome Claverie, Yuanhua Sang, and Hong Liu
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 44) pp:24950
Publication Date(Web):October 20, 2015
DOI:10.1021/acsami.5b08630
A SnO2 gas sensor was prepared by a two-step oxidation process whereby a Sn(II) precursor was partially oxidized by a hydrothermal process and the resulting Sn3O4 nanoplates were thermally oxidized to yield SnO2 nanoplates. The SnO2 sensor was selective and responsive toward ethanol at a temperature as low as 43 °C. This low sensing temperature stems from the rapid charge transport within SnO2 and from the presence of high-energy (001) facets available for oxygen chemisorption. SnO2/TiO2 nanobelt heterostructures were fabricated by a similar two-step process in which TiO2 nanobelts acted as support for the epitaxial growth of intermediate Sn3O4. At temperatures ranging from 43 to 276 °C, the response of these branched nanobelts is more than double the response of SnO2 for ethanol detection. Our observations demonstrate the potential of low-cost SnO2-based sensors with controlled morphology and reactive facets for detecting gases around room temperature.Keywords: ethanol; heterostructure; high energy facet; room temperature sensor; SnO2 nanoplates; TiO2 nanobelts
Co-reporter:Jianhua Li;Xiaoning Mou;Jichuan Qiu;Shu Wang;Dongzhou Wang;Dehui Sun;Weibo Guo;Deshuai Li;Anil Kumar;Xuebin Yang;Aixue Li
Advanced Healthcare Materials 2015 Volume 4( Issue 7) pp:998-1003
Publication Date(Web):
DOI:10.1002/adhm.201500032
Co-reporter:Haihui Jiang, Lichun Zhao, Ligang Gai, Yang Wang, Yunhua Hou, Hong Liu
Synthetic Metals 2015 Volume 207() pp:18-25
Publication Date(Web):September 2015
DOI:10.1016/j.synthmet.2015.06.006
•Fluorescent Fe3O4/PPy nanospheres with average size of 100 nm are prepared.•The Fe3O4/PPy nanospheres possess superparamagnetism and high magnetization.•Facile construction of fluorescent Fe3O4/PPy/methotrexate targeting drug is achieved.•The magnetic targeting drug exhibits controllable drug release.•The magnetic targeting drug shows specific targeting ability to HeLa cellsMagnetic composite nanospheres carrying amino groups have attracted much interest due to their potential applications in the fields of catalysis, sensor, water purification, enzyme immobilization, DNA extraction, and drug delivery. In this paper, dedoped Fe3O4/polypyrrole (PPy) nanospheres with core–shell structure, high magnetization, superparamagnetism, and size meeting the demand of biorelated applications in vivo have been achieved by an in situ polymerization approach. The amount of the surface amino groups of Fe3O4/PPy is greatly enhanced by dedoping treatment due to liberation of the amino groups ever sheltered by the dopants, a situation that is responsible for facile conjugation of fluorescein and methotrexate (MTX) onto the magnetic composite through the EDC/NHS coupling chemistry to produce the desirable fluorescent Fe3O4/PPy/MTX targeting drug with a high MTX loading of ca. 109 μg mg−1. The as-obtained magnetic targeting drug exhibits controlled drug release, enhanced intracellular drug retention, and specific targeting ability to HeLa cells, presenting a promising candidate for treatment of cancer cells overexpressing folate receptors.
Co-reporter:Dr. Yuanhua Sang;Dr. Hong Liu; Ahmad Umar
ChemCatChem 2015 Volume 7( Issue 4) pp:559-573
Publication Date(Web):
DOI:10.1002/cctc.201402812
Abstract
Owing to extensive industrial revolutions, the harvesting of sunlight for environmental remediation has attracted extensive attention and a number of potential photocatalysts have been reported. These photocatalysts were prepared according to their effectiveness under various light irradiations, that is, from UV/Vis to near-infrared (NIR) regions and finally to full solar light spectrum. This review briefly summarizes recent progress in the enhancement of photocatalytic activities of prepared photocatalysts under various light irradiations. To understand the photocatalytic process, photocatalytic mechanisms and band-structure engineering are discussed in detail in this review. Moreover, various effective photocatalysts are taken as examples of the photocatalytic process under various light irradiations. Finally, the challenges and perspectives of photocatalysis under different lights irradiations are presented.
Co-reporter:Jian Tian, Yanhua Leng, Zhenhuan Zhao, Yang Xia, Yuanhua Sang, Pin Hao, Jie Zhan, Meicheng Li, Hong Liu
Nano Energy 2015 Volume 11() pp:419-427
Publication Date(Web):January 2015
DOI:10.1016/j.nanoen.2014.10.025
•Utilize solar wide spectrum (UV, visible, and NIR) in photocatalysis for organic contaminants removal and hydrogen fuel production.•The up-converted PL properties of CQDs make the H-TiO2 nanobelts have NIR light photocatalytic activity.•A 1-D TiO2 nanostructure based heterostructure was designed: CQDs/H-TiO2 heterostructure.To make the best and highest use of solar light is the main direction and object of photocatalysis and water-splitting. Although UV and visible active photocatalysts have been extensively investigated, the use of near-infrared (NIR) wave band of solar light remains a nearly blank area. Here we report the UV–visible–NIR broad spectrum active photocatalytic property of CQDs/hydrogenated TiO2 (H-TiO2) nanobelt heterostructures. The improved UV and visible photocatalytic property can be attributed to improved optical absorption, charge carrier trapping, and hindering of the photogenerated electron–hole recombination of oxygen vacancies and Ti3+ ions in TiO2 nanobelts created by hydrogenation. The NIR photocatalytic activity is from photo-induced electron transfer, electron reservoir, and up-converted PL properties of CQDs, which can absorb NIR light and convert into visible light and transfer to visible photocatalytic active H-TiO2 nanobelts. This work offers a simple strategy for the fabrication of a wide spectrum of active heterostructured photocatalysts by assembling CQDs on the surface of UV–visible photocatalysts, which opens a door for photodegradation, photocatalytic water splitting, and enhanced solar cells using sunlight as light source.
Co-reporter:Yongjun Qiao;Zhongjun Zhai;Limei Chen
Science Bulletin 2015 Volume 60( Issue 13) pp:1193-1202
Publication Date(Web):2015 July
DOI:10.1007/s11434-015-0838-4
Bone tissue scaffolds based on bioactive polymer–hydroxyapatite composites have caused infections that seriously limit their extended application. In this study, we proposed a practical ion substitution method to synthesize in situ silver phosphate on the surface of a two-level, three-dimensional chitosan/nano-hydroxyapatite scaffold. A release test of silver ions in a phosphate buffered saline (PBS) solution was performed to demonstrate that silver ions were released continuously from the silver phosphate during the initial 6 days of the study. The antibacterial property and cytocompatibility of the scaffolds treated with different concentrations of silver nitrate solution were assessed by in vitro assays with Escherichia coli and MC3T3-E1, respectively. The ability of the silver-containing scaffolds to induce bacteriostasis was confirmed by the inhibition zone (15 mm) and high bactericidal rate (>99 %). Cell proliferation, morphology and the alkaline phosphatase activity of MC3T3-E1 cultured on the scaffold with low silver phosphate contents were comparable with those cultured on control samples.本文设计了一种具有生物相容性同时又具有抗菌功能的骨组织工程支架材料。通过离子交换,在壳聚糖/纳米羟基磷灰石三维多孔支架材料表面置换了一层磷酸银,由于银离子的缓释作用,这种支架材料具有良好的长期抗菌性能。本文构建了一种具有抗菌性和良好生物相容性的三维多孔壳聚糖/纳米羟基磷灰石骨组织工程支架材料。
Co-reporter:Pin Hao, Zhenhuan Zhao, Yanhua Leng, Jian Tian, Yuanhua Sang, Robert I. Boughton, C.P. Wong, Hong Liu, Bin Yang
Nano Energy 2015 Volume 15() pp:9-23
Publication Date(Web):July 2015
DOI:10.1016/j.nanoen.2015.02.035
•Graphene-based nitrogen self-doped hierarchical porous carbon aerogels were prepared by using renewable biopolymer chitosan as a raw material.•A formation mechanism of graphene-based carbon aerogels is proposed.•The carbonized carbon aerogel was composed of a graphene framework and amorphous carbon, and the ratio between these two components was controlled by the activation temperature.•The performance of the graphene-based carbon aerogel as a supercapacitor varied with increasing activation temperature.Graphene-based nitrogen self-doped hierarchical porous carbon aerogels were synthesized for supercapacitor electrode application by using chitosan as a raw material through a carefully controlled aerogel formation–carbonization–activation process. The as-synthesized N-doped graphene-based carbon aerogels contained both macropores and mesopores from the aerogel preparation and carbonization process, and micropores from the chemical activation, confirmed by TEM, SEM, BET, etc. Because chitosan is a nitrogen-containing renewable biopolymer, the carbon aerogel derived from chitosan in this work was N-self-doped. The carbonized carbon aerogel was composed of a graphene framework and amorphous carbon, and the ratio between these two components was controlled by the activation temperature. With an increase in activation temperature, the amorphous carbon was etched away gradually, and a stable graphene portion remained to form a framework. Accordingly, the performance of the graphene-based carbon aerogel as a supercapacitor varied with increasing activation temperature. Electrochemical investigation measurements showed that the N-doped graphene-based hierarchical porous carbon aerogel represents a good electrode candidate for construction of a solid symmetric supercapacitor, which displays a high specific capacitance of about 197 F g−1 at a current density of 0.2 A g−1. In addition, the solid state supercapacitor displayed excellent cyclability with a capacitance retention of about 92.1% over 10,000 cycles. The excellent energy storage ability of the chitosan-derived hierarchical graphene-based carbon aerogels is ascribed to the high conductivity of the graphene framework with nitrogen doping and the high storage ability of amorphous carbon with variable pore size and distribution.A facile and simple method to prepare the graphene-based nitrogen self-doped hierarchical porous carbon aerogels by using chitosan is proposed. Further the prepared hierarchical porous carbon aerogels were utilized as high performance supercapacitor electrodes which demonstrated an excellent capacitance retention (~92.1%) over 10000 cycles. The excellent energy storage ability of the chitosan-derived hierarchical graphene-based carbon aerogels is ascribed to the high conductivity of the graphene framework with nitrogen doping and the high storage ability of amorphous carbon with variable pore size and distribution.
Co-reporter:Jian Tian, Zhenhuan Zhao, Anil Kumar, Robert I. Boughton and Hong Liu
Chemical Society Reviews 2014 vol. 43(Issue 20) pp:6920-6937
Publication Date(Web):11 Jul 2014
DOI:10.1039/C4CS00180J
One-dimensional TiO2 nanostructured surface heterostructures (1D TiO2NSHs) have been comprehensively studied during the past two decades because of the possible practical applications in various fields, including photocatalysis, dye-sensitized solar cells, sensors, lithium batteries, biomedicine, catalysis, and supercapacitors. Combining extensive advancements in materials science and nanotechnology, a 1D TiO2NSH material with well-controlled size, morphology, and composition has been designed and synthesized. More importantly, its superior properties, including a high aspect ratio structure, chemical stability, large specific surface area, excellent electronic or ionic charge transfer, and a specific interface effect, have attracted a great deal of interest in improving current performance and exploring new applications. In this tutorial review, we introduce the characteristics of 1D TiO2 nanostructures, the design principles for the fabrication of 1D TiO2NSHs, and we also summarize the recent progress in developing synthesis methods and applications of 1D TiO2NSHs in different fields. The relationship between the secondary phase and the 1D TiO2 nanostructure and between the performance in applications and the excellent physical properties of 1D TiO2NSHs are also discussed.
Co-reporter:Xingqi Wang, Wenxia Liu, Jian Tian, Zhenhuan Zhao, Pin Hao, Xueliang Kang, Yuanhua Sang and Hong Liu
Journal of Materials Chemistry A 2014 vol. 2(Issue 8) pp:2599-2608
Publication Date(Web):29 Nov 2013
DOI:10.1039/C3TA14519K
Uniform well-defined nanostructured BiOBr microspheres have been fabricated via a simple hydrothermal method in the presence of cetyltrimethylammonium bromide (CTAB) and ethylene glycol (EG). The heavy metal ion adsorption on the as-synthesized nanostructured BiOBr microspheres was systematically assessed by measuring the residual concentration during the adsorption process using a colorimetric method for Cr(VI) concentration, and an extraction-colorimetric method for Cd(II) and Pb(II) concentrations. The nanostructured BiOBr microspheres showed good removal capacity for heavy metal ions (Cr, Cd, Pb), and excellent adsorption properties for low concentration heavy metal ions, indicating potential applications in water purification. Based on the quick and efficient heavy metal ion removal ability of nanostructured BiOBr microspheres, a continuous filtering-type water purification device was designed and constructed. In using this continuous filtering type water purification device, 1 g of adsorbent can purify about 4900 g of Pb(II) contaminated water, 5900 g of Cd(II) contaminated water, or 21500 g of Cr(VI) contaminated water having initial concentrations of 200 μg L−1 to successfully attain the World Health Organization standard for drinking water. The good removal capacity can be attributed to the hierarchical nanostructure, which displays a large specific surface area and strong adsorption of heavy metal ions.
Co-reporter:W. J. Zhou, Y. H. Leng, D. M. Hou, H. D. Li, L. G. Li, G. Q. Li, H. Liu and S. W. Chen
Nanoscale 2014 vol. 6(Issue 9) pp:4698-4704
Publication Date(Web):28 Jan 2014
DOI:10.1039/C3NR06565K
Ag2O/TiO2 nanobelt heterostructures have been found to possess high ultraviolet photocatalytic activity, but a poor cycling performance. After a S-doping treatment, the obtained Ag2O/Ag2S2O7/TiO2 heterostructured nanobelts exhibited an enhanced and stable photocatalytic activity under both ultraviolet and visible light irradiation, which was exemplified by photo-degradation of organic pollutants and photocurrent response measurements. Meanwhile, the crystal structure and phase transformation of Ag2O, Ag2S2O7 and Ag2S were studied by XRD and XPS measurements.
Co-reporter:Qinqin Jia, Dongfang Zhao, Bin Tang, Na Zhao, Haidong Li, Yuanhua Sang, Nan Bao, Xiaomei Zhang, Xiaohong Xu and Hong Liu
Journal of Materials Chemistry A 2014 vol. 2(Issue 38) pp:16292-16298
Publication Date(Web):2014/08/29
DOI:10.1039/C4TA01503G
Au–Cu bimetallic nanoparticles supported on a TiO2-nanobelt (TiO2-NB) have been designed and synthesized by a one-pot photodeposition-galvanic replacement method. TEM observation revealed that small-sized metal nanoparticles (less than 2 nm) were uniformly and finely dispersed on the TiO2 nanobelt. Characterization by XRD coupled with XPS demonstrated that the Au–Cu bimetallic nanoparticles are composed of an Au-rich core/CuOx shell structure. The as-synthesized one-dimensional Au–Cu/TiO2-NB nanostructure can be easily assembled into a paper-like porous monolithic catalyst and applied in heterogeneous catalysis. The formed bimetallic nanopaper catalysts presented synergistically enhanced activity and improved stability for catalyzing the aerobic oxidation of benzyl alcohol compared to their monometallic counterparts. It is likely that the Au–CuOx heterostructure is responsible for the superior catalytic properties of the bimetallic Au–Cu/TiO2-NB catalysts, and the catalytic activity can be significantly affected by the Au/Cu ratio. The uniform and high dispersion of metal nanoparticles on TiO2 nanobelts is also believed to contribute to the stability of Au–Cu/TiO2-NB catalysts, suggesting that the one-dimensional TiO2 nanobelts are a desirable support for the preparation of nanoscale metal catalysts.
Co-reporter:Jianhua Li;Bryan. A. Baker;Xiaoning Mou;Na Ren;Jichuan Qiu;Robert I. Boughton
Advanced Healthcare Materials 2014 Volume 3( Issue 4) pp:469-484
Publication Date(Web):
DOI:10.1002/adhm.201300562
With nearly 30 years of progress, tissue engineering has shown promise in developing solutions for tissue repair and regeneration. Scaffolds, together with cells and growth factors, are key components of this development. Recently, an increasing number of studies have reported on the design and fabrication of scaffolding materials. In particular, inspired by the nature of bone, polymer/ceramic composite scaffolds have been studied extensively. The purpose of this paper is to review the recent progress of the naturally derived biopolymers and the methods applied to generate biomimetic biopolymer/calcium phosphate composites as well as their biomedical applications in bone tissue engineering.
Co-reporter:Pin Hao, Zhenhuan Zhao, Jian Tian, Yuanhua Sang, Guangwei Yu, Hong Liu, Shaowei Chen, Weijia Zhou
Acta Materialia 2014 Volume 62() pp:258-266
Publication Date(Web):January 2014
DOI:10.1016/j.actamat.2013.10.006
Abstract
In this study, an effective low-temperature method was developed, for the first time, for the synthesis of bismuth titanate nanobelts by using Na2Ti3O7 nanobelts as the reactants and templates. The experimental procedure was based on ion substitution followed by a nanoscale solid-state reaction. In the first step, Na2Ti3O7 nanobelts were soaked in a bismuth nitrate solution where ion substitution at the nanobelt surfaces led to the formation of a bismuth compound overlayer. The resulting bismuth-modified nanobelts were then subject to a calcination process at controlled temperatures. At the calcination temperature of 400 °C, the top layer was converted to Bi2O3 whereas the interior was converted to TiO2(B), forming TiO2(B)@Bi2O3 core–shell nanobelts. When the calcination temperature was increased to 450 °C, a metastable interphase Bi20TiO32 was produced on the nanobelt surface whereas the interior structure remained virtually unchanged, and the nanobelts now exhibited a TiO2(B)@Bi20TiO32 core–shell structure. At calcination temperatures higher than 550 °C, the shell of the nanobelts became Bi4Ti3O12. At even higher temperatures (600–700 °C), no TiO2(B) was found and the nanobelts exhibited single-crystalline characteristics that were consistent with those of Bi4Ti3O12. Such a structural evolution was manifested in X-ray diffraction, Raman and Fourier transform infrared spectroscopic measurements, and scanning electron microscopic and transmission electron microscopic studies showed that the belt-like surface morphology was maintained without any apparent distortion or destruction. A mechanism based on nanoscale solid-state reactions was proposed to account for the structural evolution. Photoluminescence measurements showed that the core–shell nanobelts exhibited a markedly suppressed emission intensity, suggesting impeded recombination of photogenerated carriers as compared to the single-phase counterparts. Such a unique feature was found to be beneficiary to photocatalysis, as exemplified by the photodegradation of methyl orange under UV irradiation, where TiO2(B)@Bi20TiO32 core–shell nanobelts were found to exhibit the best performance among the series.
Co-reporter:Haiming Qin, Jun Jiang, Haochuan Jiang, Yuanhua Sang, Dehui Sun, Xinhai Zhang, Jiyang Wang and Hong Liu
CrystEngComm 2014 vol. 16(Issue 47) pp:10856-10862
Publication Date(Web):09 Oct 2014
DOI:10.1039/C4CE01757A
Neodymium-doped yttrium aluminum garnet (Nd:YAG) ceramics with different Al2O3/Y2O3 deviation levels were prepared using a solid-state reaction-vacuum sintering method. Transparent ceramics were obtained with their composition in between stoichiometric Nd:YAG Y2.97Nd0.03Al5O12 and 2% Y2O3 excess Nd:YAG Y2.97Nd0.03Al5O12·2%Y2O3. The stoichiometric Nd:YAG ceramic obtains a homogeneous grain microstructure and clean grain boundaries. Non-stoichiometric compositions lead to ceramic microstructures different from that of the stoichiometric Nd:YAG. Nanograins of excess Al2O3 remain inside the Nd:YAG grains in Al2O3-excess ceramics, while Y-rich compounds recrystallize at the Nd:YAG grain boundaries in Y2O3-excess ceramics. Photoluminescence spectra of the sintered ceramics around 808 and 1064 nm were also studied. Peak positions of their luminescence spectra are little affected by composition deviation, while their intensity evidently declines due to the existence of a second phase arising from the composition deviation. The results of this work can contribute toward the controllable synthesis of highly transparent YAG ceramics and further exploration of the Nd ion spectra.
Co-reporter:Shaozheng Ji, Hong Liu, Yuanhua Sang, Wei Liu, Guangwei Yu and Yanhua Leng
CrystEngComm 2014 vol. 16(Issue 32) pp:7598-7604
Publication Date(Web):23 Jun 2014
DOI:10.1039/C4CE01116C
NaNbO3 cubes and nanowires have been synthesized by a hydrothermal-based method utilizing thin Nb foil and low-concentration NaOH solution with the presence of H2O2. The Na2Nb2O6·H2O precursor can be obtained under hydrothermal conditions at 200 °C for only 4 h. Both long-time hydrothermal treatment and calcination on the precursor nanowires can realize the transition from Na2Nb2O6·H2O nanowires to NaNbO3 crystalline particles. However, the crystalline phases of the two products are different. NaNbO3 microcubes obtained by long-time hydrothermal treatment are in the antiferroelectric phase with space group Pbma, while NaNbO3 nanowires obtained by annealing Na2Nb2O6·H2O at 500 °C for 3 h are in the ferroelectric phase with space group P21ma. The experimental results from X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), high resolution electron microscopy (HRTEM) and Raman spectroscopy proved the difference between the crystalline phases of NaNbO3 microcubes and nanowires. Piezoelectric force microscopy (PFM) analysis proved that NaNbO3 nanowires exhibit piezoelectricity, while no piezoelectric response can be detected for NaNbO3 microcubes synthesized by direct hydrothermal treatment.
Co-reporter:Tao Yan, Yanhua Leng, Yonggui Yu, Dehui Sun, Jie Zhan, Wan Hairul Anuar Kamaruddin, Xiaoyong Qin, Xuxia Shi, Liuwen Chang, Mitch M. C. Chou, Jiyang Wang and Hong Liu
CrystEngComm 2014 vol. 16(Issue 29) pp:6593-6602
Publication Date(Web):17 Apr 2014
DOI:10.1039/C4CE00524D
MgO doped near stoichiometric LiNbO3 (MgOSLN) crystals have great potential for use in periodically poled structured LiNbO3 (PPLN) for doubling frequency lasers and optical parametric oscillation infrared lasers, because of their high optical damage threshold, single domain characteristics, and very low coercive field. However, few MgOSLN crystals are commercially available in the present market because of the great difficulty in growing them. This paper describes how a hanging crucible Czochralski technique with a newly-designed ship lockage type powder feeding system assisted by numerical simulation was developed for the successful growth of high quality near stoichiometric LiNbO3 (SLN) and MgOSLN (~1 mol%) crystals. The physical properties of the crystals were assessed by measuring their crystallinity, Curie temperature, optical properties, coercive field and thermal properties. These properties, including a coercive field of 1.4 kV mm−1 and a thermal conductivity of 6.61 W (m K)−1 demonstrated that the crystals meet the demands for manufacturing periodically poled crystal devices. This growth method has great potential in the mass production of SLN and other incongruently melting crystals.
Co-reporter:Jinsheng Li, Xudong Sun, Shaohong Liu, Xiaodong Li, Di Huo, Ji-Guang Li, Qi Zhu, Mu Zhang, Yuanhua Sang, Hong Liu
Journal of Alloys and Compounds 2014 Volume 585() pp:48-53
Publication Date(Web):5 February 2014
DOI:10.1016/j.jallcom.2013.09.094
•Stearate melting method can synthesize well dispersed fine YAG nanopowders.•The method ensures precise Y:Al ratio and cations mixing at atomic level.•Pure and dispersed YAG powders can be obtained at low temperature of 750 °C.•The YAG powders can be sintered into transparent ceramics at 1700 °C.Ultrafine YAG powders were synthesized by a novel stearate melting method, in which yttrium stearate and aluminum tristearate, having similar physical and chemical properties, were co-melted and then calcined to produce fine YAG nanopowders. This method has the advantages of precise control of Y:Al ratio, homogeneous mixing of cations at atomic level, fine particle size, and good particle dispersion. The formation mechanism of the precursor and the YAG nanopowder was studied by means of XRD, FT-IR, TG–DTA, BET and FE-SEM. Pure YAG nanopowder can be obtained by calcining the co-melted precursor at a relatively low temperature (750 °C), much lower than those of the traditional solid-state reaction method and various wet chemical synthesis methods. The resultant YAG powders are well dispersed and have excellent sinterability. For the YAG powder calcined at 1000 °C, the green compact has the maximum shrinkage rate at about 1450–1550 °C and a total shrinkage of ∼16.70% during constant heating rate sintering. The compact can be sintered to 99.4% of the theoretical density at 1600 °C. The prepared YAG powder can be sintered into transparent ceramics at 1700 °C for 5 h by vacuum sintering.Graphical abstract
Co-reporter:Daidong Guo, Lili Zhao, Yuanhua Sang, Hong Liu, Shaohong Liu and Xudong Sun
RSC Advances 2014 vol. 4(Issue 98) pp:55400-55406
Publication Date(Web):13 Oct 2014
DOI:10.1039/C4RA09856K
A partial wet chemical route has been developed, in which aluminium oxide (Al2O3) nanoparticles in a Y(NO3)3 solution are induced to form a core–shell-structured yttrium aluminum garnet (YAG) precursor based on a burst nucleation synthesis. By simulating the reaction conditions with urea and ammonium bicarbonate as precipitants, a two-step mechanism involving different dynamic processes is proposed to describe the core–shell structure formation. During the majority of the process, the electrostatic attraction between the opposite surface charges of Al2O3 and nanoparticles of the Y-compound is regarded as the single driving force. However, the high surface energy of Y-compound nanoparticles originating from the burst nucleation process plays a key role in completing the formation of the core–shell structure. The precursor obtained can be transformed into pure YAG nanoparticles, which retain the morphology of the Al2O3 template, and these are of sufficiently high quality for the preparation of transparent ceramics. An understanding of the mechanism makes this a novel method for the synthesis of the nanostructured core–shell binary oxide precursor.
Co-reporter:Na Ren, Guancong Wang, Hong Liu, Tadashi Ohachi
Materials Research Bulletin 2014 50() pp: 379-384
Publication Date(Web):
DOI:10.1016/j.materresbull.2013.11.002
Co-reporter:Dr. Weijia Zhou;Yu Guan;Dongzhou Wang; Xinhai Zhang; Duo Liu; Huaidong Jiang; Jiyang Wang; Xiaogang Liu; Hong Liu; Shaowei Chen
Chemistry – An Asian Journal 2014 Volume 9( Issue 6) pp:1648-1654
Publication Date(Web):
DOI:10.1002/asia.201301638
Abstract
Heterostructures play an important role not only in the manufacture of semiconductor devices, but also in the field of catalysis. Herein, we report the synthesis of PdO/TiO2 and Pd/TiO2 heterostructured nanobelts by means of a simple co-precipitation method, followed by a reduction process using surface-modified TiO2 nanobelts as templates. The as-obtained heterostructures were characterized by transmission electron microscopy, X-ray photoelectron spectroscopy, and UV/Vis diffuse reflectance spectroscopy. PdO and Pd nanoparticles with a size of about 1.3 and 1.6 nm were assembled uniformly on the surface of TiO2 nanobelts, respectively. Compared with TiO2 nanobelts, PdO/TiO2 and Pd/TiO2 hybrid nanobelts exhibit enhanced photocatalytic activity upon UV and visible-light irradiation. Photoelectrochemical technology was used to study the heterostructure effect on enhanced photocatalytic activity. Our mechanistic investigation revealed that energy-band matching is the major factor in the observed enhancement of photocatalytic activity.
Co-reporter:Jingjie Cui;Shaowei Chen;Zhen Huang
Journal of Solid State Electrochemistry 2014 Volume 18( Issue 10) pp:2693-2699
Publication Date(Web):2014 October
DOI:10.1007/s10008-014-2524-x
6-Phosphate aminopurine (6PA), a purine analog, is usually used in clinical anticancer treatment and biochemical research. Up to now, to the best of our knowledge, no literature about the electrochemical behaviors of 6PA has been reported. In this study, nano-p–n junction heterostructures based on TiO2 nanobelts were produced by the assembly of p-type semiconducting NiO nanoparticles onto the n-type surface-coarsened TiO2 nanobelts. The electrochemical behaviors of 6PA were investigated by different voltammetric techniques in a phosphate buffer solution of pH 7.4 using the heterostructures as the sensing electrode. Compared with single-phase TiO2 nanobelt electrodes, the resulting chemically modified electrodes exhibited higher surface accumulation ability and enhanced electrocatalytic activities in the oxidation for 6PA, with an irreversible oxidation peak at +0.91 V. It is proposed that the nano-p–n junction heterostructures played an important role in the enhancement of charge transport in the sensing electrodes. The results suggest that the nanoengineered TiO2 nanobelts might be a promising candidate for biosensing applications of nucleic acid drugs that will be of significance to diagnostic medicine and molecular biology research.
Co-reporter:Jian Tian;Yuanhua Sang;Guangwei Yu;Huaidong Jiang;Xiaoning Mu
Advanced Materials 2013 Volume 25( Issue 36) pp:5075-5080
Publication Date(Web):
DOI:10.1002/adma.201302014
Co-reporter:Jingjie Cui, Yakun Ge, Shaowei Chen, Hongshi Zhao, Hong Liu, Zhen Huang, Huaidong Jiang and Jing Chen
Journal of Materials Chemistry A 2013 vol. 1(Issue 15) pp:2072-2077
Publication Date(Web):11 Feb 2013
DOI:10.1039/C3TB00227F
Nano-p–n junction heterostructures based on TiO2 nanobelts with enhanced (001) facets were produced by assembling p-type semiconductor NiO nanoparticles on n-type surface-coarsened TiO2 nanobelt surfaces. The heterostructures were then used as the sensing electrode for the electrochemical detection of anticancer drugs O6-benzylguanine (O6BG) and lung cancer cells. O6BG exhibited an irreversible diffusion-controlled electrochemical process with an oxidation peak clearly identified at +0.78 V. For lung cancer cells one oxidation peak was found at +1.1 V and two reduction peaks at +0.30, and +0.90 V. These voltammetric features disappeared when O6BG was added to the lung cancer cells, which was ascribed to the structural changes of the cell membranes caused by the anticancer drug. These results suggested that nano-p–n junction heterostructures based on TiO2 nanobelts might serve as promising candidates for biosensing applications of anticancer drugs and tumor cells that will be of significance in diagnostic medicine, cancer diagnosis and molecular biology research.
Co-reporter:Xiaoyan Li, Chenguo Hu, Xueliang Kang, Qiang Len, Yi Xi, Kaiyou Zhang and Hong Liu
Journal of Materials Chemistry A 2013 vol. 1(Issue 44) pp:13721-13726
Publication Date(Web):19 Sep 2013
DOI:10.1039/C3TA12706K
Advanced thermoelectric technology offers the potential to convert waste heat into useful electricity, and a mechanism of transmission-free methods for solid state cooling. A low thermal conductivity is a prerequisite for obtaining high efficiency thermoelectric materials. It is a challenge to achieve low thermal conductivity without simultaneously destroying the electric conductivity, for which a ‘phonon glass/liquid–electron crystal’ is proposed. To realize the phonon glass–electron crystal, a host–guest cage crystal system is considered, while to realize the phonon liquid–electron crystal, superionic conductivity is needed. Here we report a novel material, a KCu7−xS4 nanowire, which exhibits enhanced thermoelectric properties compared to the traditional chalcogenide Cu7S4 nanostructure. The presence of K ions not only forms a clathrate and a superionic fluid structure, which provides the phonon glass and liquid–electron crystal, but also adjusts the product to give a nanowire-like morphology. A low thermal conductivity and large Seebeck coefficient can be achieved when the nanowires are pressed into a bulk material. Higher electrical conductivity is also obtained below 420 K. In addition, the numerous grain boundaries, Cu deficiency and the orientated nanowires further increase the thermoelectric properties. The results indicate a new strategy to obtain high efficiency thermoelectric materials by introducing kalium into copper chalcogenides to form a new crystal structure with ‘phonon glass and liquid–electron crystal’ properties.
Co-reporter:Yu Guan, Na Zhao, Bin Tang, Qinqin Jia, Xiaohong Xu, Hong Liu and Robert I. Boughton
Chemical Communications 2013 vol. 49(Issue 98) pp:11524-11526
Publication Date(Web):24 Oct 2013
DOI:10.1039/C3CC45408H
Well-dispersed small Au–Ag bimetallic nanoparticles (sub-3 nm) on one dimensional TiO2 nanobelts were synthesized by a facile successive photodeposition-galvanic replacement method. Based on these Au–Ag/TiO2-NB nanostructures, a porous paper-like monolithic catalyst was fabricated and exhibited synergistically enhanced activity and stability for catalyzing aerobic oxidation of benzyl alcohol.
Co-reporter:Jichuan Qiu, Jianhua Li, Guancong Wang, Lin Zheng, Na Ren, Hong Liu, Wei Tang, Huaidong Jiang, and Yingjun Wang
ACS Applied Materials & Interfaces 2013 Volume 5(Issue 2) pp:344
Publication Date(Web):December 17, 2012
DOI:10.1021/am302272k
As a biocompatible and bioactive natural tissue engineering scaffold, porcine acellular dermal matrix (PADM) has limitations for the application in tissue regeneration due to its low strength and rapid biodegradation. Here, purified PADM was modified by a nontoxic cross-linker (genipin) to enhance its mechanical properties and improve its resistance to enzymatic degradation. In vitro testing results demonstrated that the stiffness of the genipin cross-linked PADM was improved and biodegradation rate was decreased. Results of cell proliferation assays showed that the cross-linking reaction by genipin did not undermine the cytocompatibility of PADM. Furthermore, genipin cross-linking imparted an observable fluorescence allowing visualization of the scaffold’s three-dimensional (3D) porous structure and cell distribution by confocal laser scanning microscopy (CLSM). Immunostaining of the cell nuclei and cytoskeleton indicated that MC3T3-E1 preosteoblasts were tightly adhered to and uniformly distributed onto the cross-linked PADM scaffold. Results of this study suggest that the 3D porous genipin cross-linked PADM with intrinsic fluorescence may have broader applications for tissue engineering scaffolds where higher mechanical stiffness is needed.Keywords: biocompatibility; cross-link; fluorescence; genipin; porcine acellular dermal matrix; tissue engineering scaffold;
Co-reporter:Hao Hua, Chenguo Hu, Zhenhuan Zhao, Hong Liu, Xiao Xie, Yi Xi
Electrochimica Acta 2013 Volume 105() pp:130-136
Publication Date(Web):30 August 2013
DOI:10.1016/j.electacta.2013.05.002
•Submicrometer-sized TiO2 spheres are employed to obtain highly efficient Pt/TiO2 electrocatalyst.•This electrocatalyst used for alcohol oxidation exhibits quite outstanding property.•The enhanced catalytic activity of the Pt/TiO2 spheres is owing to the mesoporous active sites and synergistic effect of Pt and TiO2.High electrocatalytic activity for alcohol electrooxidation by Pt nanoparticles supported on submicrometer-sized TiO2 spheres is achieved. The Pt nanoparticles with a diameter of 8–20 nm are uniformly coated on the surface of the submicrometer-sized TiO2 spheres with a diameter of 370–500 nm via a simple wet chemical synthesis. The electrocatalytic performances of the Pt/TiO2 submicrometer-sized TiO2 spheres for methanol and ethanol in acidic and alkaline media are investigated systematically by electrochemical methods. Compared with the Pt catalyst supported on the commercial carbon black, the Pt/TiO2 spheres exhibit an excellent enhanced electrocatalytic activity and stability owing to the mesoporous active sites, synergistic effect of Pt/TiO2, and micro-channels for liquid diffusion and gaseous product to escape.
Co-reporter:Wanye Tan, Hongshi Zhao, Na Ren, Jianhua Li, Guohong Li, Guancong Wang, Fengcai Wei, Robert I. Boughton, Hong Liu
Ultrasonics Sonochemistry 2013 Volume 20(Issue 1) pp:216-221
Publication Date(Web):January 2013
DOI:10.1016/j.ultsonch.2012.07.020
The surface modification of titanium implants by NaOH has been widely investigated to improve their biocompatibility and bioactivity. It is very important to prepare an even network structure on titanium implants. In this work, ultrasonic irradiation (UI) is used along two different routes to obtain several modified surfaces on titanium plates: (1) the plates are first treated by a NaOH solution, and then UI is used to wash them in double distilled water; (2) the plates are modified by a NaOH solution in an ultrasonic cleaner with UI at 50 W. It is demonstrated that the UI energy can easily remove any weakly bound layers (WBL) on the titanium surface, leaving a strongly bound layer (SBL). The SBL is shown to enhance the proliferation of MC3T3-E1 preosteoblasts in comparison with the WBL. A dense and uniformly distributed nanostructure layer can be synthesized in situ on the surface of metallic titanium through a reaction between a NaOH solution and titanium under UI. The titanium plates prepared with NaOH and UI show better proliferation of preosteoblasts than titanium without UI.Highlights► UI treatment helps form an even nanostructure on titanium implants resulting from NaOH treatment. ► The titanium plates prepared with NaOH and UI promote the proliferation of MC3T3-E1 preosteoblasts. ► UI is potentially advantageous in preparing bioactive titanium implants for dental treatment.
Co-reporter:Haiming Qin, Xinhai Zhang, Hong Liu, Yuanhua Sang and Jiyang Wang
CrystEngComm 2013 vol. 15(Issue 25) pp:5076-5081
Publication Date(Web):23 Apr 2013
DOI:10.1039/C3CE40186C
In the preparation of transparent ceramics and ultrafine oxide nanopowders, ammonium sulfate ((NH4)2SO4) has been widely used as the control agent. However, the mechanism of its regulation effect has not been well studied. In the present work, precursors of yttria (Y2O3) nanopowders with controlled morphology were synthesized via a urea precipitation method using ammonium sulfate as the additive. The effect of (NH4)2SO4 is discussed throughout the preparation process. Two opposite morphology transformation modes were noticed for the precursor samples made with and without (NH4)2SO4 during the calcination process. Flocculent precursors and flowers assembled by the plate-shaped particles were obtained in the systems without and with (NH4)2SO4. By calcination, the aggregated 200–400 nm particles with massive defects and 100 nm particles with homogeneous crystalline structure were obtained, respectively. The mechanism of (NH4)2SO4 as a regulator that could mediate the nucleation and growth of the precursors as well as its decomposition behavior is verified.
Co-reporter:Haiming Qin, Xinhai Zhang, Dejun Sun, Tianzhen Zhang, Huaidong Jiang, Hong Liu, Yuanhua Sang and Jiyang Wang
CrystEngComm 2013 vol. 15(Issue 21) pp:4335-4340
Publication Date(Web):25 Mar 2013
DOI:10.1039/C3CE27026B
The mixing process of Al2O3 and Y2O3 nanopowders in aqueous suspension was studied. Charge conversion on the surface of Al2O3 particles in the Y2O3–Al2O3 colloidal system was observed. Negative charges on the surface of Al2O3 particles became positive due to the assembly of Y2O3 on the surface of Al2O3 nanoparticles in the colloidal system, as shown by zeta potential analysis of Y2O3–Al2O3 colloidal systems with different Y/Al ratios. Rheological properties of the mixed powders slurries with different Y2O3 content were also investigated. XRD peaks of Al2O3 shifted towards smaller angles with increasing amounts of Y2O3 added, implying the encapsulation of Al2O3 by Y2O3via mass transport during the mixing process, as confirmed by HRTEM measurement. A mechanism was proposed for the paragenesis of mineral in this binary colloidal system. Hydrated Y2O3 with higher Ksp attaches and migrates onto the surface of another hydrated sediment Al2O3 with smaller Ksp and opposite surface charge. The mass transfer process between Y2O3 and Al2O3 nanoparticles in this binary mixture suspension is analogous to the Ostwald ripening process. This new growth phenomenon is important for the science of crystal growth as it helps boost the exploration of new mechanisms for crystal growth in various material systems and provide clear evidence for the diffusion growth of crystalline structure in a binary colloidal system.
Co-reporter:Tao Yan, Yonggui Yu, Yongjie Guo, Yuanhua Sang, Hong Liu, Shangqian Sun, Min Xu, Jiyang Wang, Liuwen Chang, Mitch M.C. Chou
Journal of Alloys and Compounds 2013 Volume 564() pp:1-7
Publication Date(Web):5 July 2013
DOI:10.1016/j.jallcom.2013.01.177
Yb–Mg codoped LiNbO3 (LN) crystals have many applications in self-frequency doubling lasers. However, the great difficulty associated with growing this crystal is one of the obstacles for its application. In this work, Yb-, Mg-doped and Yb–Mg codoped (MgYb0.8 and MgYb1.2) single crystals were successfully grown by the Czochralski method from the congruent melt. Some basic physical properties have been measured to provide reliable reference for application of the crystals. Compared to its value in a singly doped crystal, the effective segregation coefficient of the Yb3+ ion in codoped crystals clearly decreases. When doping Yb into Mg-doped LN, the absorption edge of the crystal shifts to longer wavelengths, while the refractive index stays nearly the same. Yb3+ doping apparently decreases the Curie temperature Tc. The thermal conductivity of Yb–Mg codoped LiNbO3 was found to be identical to that of Mg-doped LN and greater than that of congruent LN (CLN), which is a benefit for laser applications. The occupation sites of the Yb3+ ions are discussed, and the distinct raised growth ridges observed are attributed to the change in the lattice structure due to Yb–Mg co-doping.Highlights► High quality Yb–Mg codoped LiNbO3 crystals in size of ∅50 × 40 mm were grown by the Czochralski method. ► Compared to that in Yb-doped crystal, the keff of Yb3+ ion in codoped crystals clearly decreases. ► The absorption edge of Yb–Mg codoped LiNbO3 shifts to longer wavelengths, compared to that of MgOCLN. ► The thermal conductivity of Yb–Mg codoped LiNbO3 was identical to MgOCLN and greater than CLN. ► The distinct raised growth ridges are attributed to the change in lattice structure due to Yb–Mg co-doping.
Co-reporter:Yuanhua Sang, Haiming Qin, Hong Liu, Lili Zhao, Yana Wang, Huaidong Jiang, Jiyang Wang
Journal of the European Ceramic Society 2013 Volume 33(13–14) pp:2617-2623
Publication Date(Web):November 2013
DOI:10.1016/j.jeurceramsoc.2013.04.009
Synthesis of Y3Al5O12 (YAG) powders respectively presents morphology control and chemical stoichiometry problems when employing the solid-state reaction or the wet-chemical route. YAG powder retaining the morphology of Al2O3 powder was designed and synthesized via a partial wet-chemical process with yttrium ions precipitating on the Al2O3 particles. The formation process of the Y-compound/Al2O3 core–shell structure is discussed on the basis of zeta-potential measurements and HRTEM results. Two stages, including direct precipitation at the surface of the Al2O3 particles and the assembly of the yttrium precipitate from explosive nucleation onto the yttrium compound-coated Al2O3 particles, are proposed. A spherical surface reaction process is illustrated. A pure YAG phase can be realized at a temperature about 300 °C lower than that of the traditional solid-state reaction process.
Co-reporter:Jie Zhang, Wenxia Liu, Xiaowei Wang, Xingqi Wang, Bin Hu, Hong Liu
Applied Surface Science 2013 Volume 282() pp:84-91
Publication Date(Web):1 October 2013
DOI:10.1016/j.apsusc.2013.05.054
Highlights
- •
Cu2O@TiO2 nanobelts were synthesized with wet chemical precipitation method. Heterostructures were formed between Cu2O particles and TiO2 nanobelts.
- •
A strong adsorption-weak photodegradation process was proposed.
- •
The strong adsorption is attributed to the exposure of the {1 1 1} facets of Cu2O.
Co-reporter:Xiaoyun Han, Ligang Gai, Haihui Jiang, Lichun Zhao, Hong Liu, Wei Zhang
Synthetic Metals 2013 Volume 171() pp:1-6
Publication Date(Web):1 May 2013
DOI:10.1016/j.synthmet.2013.02.025
Magnetic composite microspheres present a promising candidate for applications in water treatment, enzyme immobilization, drug delivery, catalysis, and sensors. In this paper, we report on the surfactant-free synthesis of well-defined Fe3O4/PANI microspheres through an interfacial polymerization approach. The as-prepared magnetic composite spheres show good dispersion, core–shell structure, and high magnetization. Also, the Fe3O4/PANI microspheres were tested as an adsorbent to remove Cr(VI) ions from water, and were found to have a strong adsorption capacity of ca. 200 mg g−1. The adsorption isotherm for Cr(VI) adsorption on Fe3O4/PANI microspheres follows the Langmuir isotherm model, and the adsorption process meets the pseudo-second-order kinetics. After reuse five times, the adsorption capacity of Fe3O4/PANI microspheres retains 90% of the initial value, indicating that the Fe3O4/PANI microspheres can serve as an excellent regenerable Cr(VI) adsorbent.Graphical abstractCore–shell structured Fe3O4/PANI microspheres were constructed by an interfacial polymerization approach without surfactant, which were found to be an excellent regenerable adsorbent to offer rapid Cr(VI) ion removal from water within 30 min.Highlights► Core–shell structured Fe3O4/PANI microspheres were constructed without surfactant. ► The composite spheres have a strong Cr(VI) ion adsorption capacity of ca. 200 mg g−1. ► The composite spheres show an excellent regenerability after reuse five times. ► The composite spheres offer rapid Cr(VI) ion removal from water within 30 min. ► The Cr(VI) adsorption isotherm follows the Langmuir isotherm model.
Co-reporter:Xiaoyan Li, Chenguo Hu, Zhenhuan Zhao, Kaiyou Zhang, Hong Liu
Sensors and Actuators B: Chemical 2013 Volume 182() pp:461-466
Publication Date(Web):June 2013
DOI:10.1016/j.snb.2013.03.029
Cubic CdS nanoparticles and hexagonal CdS nanowalls were fabricated directly on Cd foils via a modified composite hydroxide mediated approach. The phase transition of CdS nanocrystals from cubic to hexagonal phase can be controlled by varying the water content in the hydroxide melts. The metal Cd foils serves as both Cd source and substrate in the formation of the CdS nanostructures. The surface morphology and phase structure were characterized by scanning electron microscope, energy dispersive X-ray spectrometer and X-ray diffraction. The obviously enhanced photoelectrochemical performances of the hexagonal nanowalls were found under the illumination of the simulated sunlight in comparison with that of the cubic CdS nanoparticles. The surface morphology plays a vital role in its photoelectrochemical behaviors due to the different specific surface area and charge transport, indicating such three-dimensional hexagonal CdS nanostructure has prominent advantages in photoelectrochemical applications.
Co-reporter:Hulin Zhang, Dongzhou Wang, Chenguo Hu, Xueliang Kang, Hong Liu
Sensors and Actuators B: Chemical 2013 Volume 184() pp:288-294
Publication Date(Web):31 July 2013
DOI:10.1016/j.snb.2013.04.085
Sn1−xCoxO2 (x = 0, 0.01, 0.03, 0.05, 0.07) nanostructures with different morphologies are prepared by a facile hydrothermal method. The analysis from X-ray photoelectron spectroscopy indicates that the cobalt doped in SnO2 exists as Co2+. The room-temperature ferromagnetism is observed in the powder sample of Sn1−xCoxO2 with x = 0.01. The magnetic hysteresis loop is observed at room temperature with coercivity (Hc) of 120 Oe and remanent magnetization (Mr) of 3.04 × 10−2 emu/g. UV–vis spectra reveal the red shift of the band edge absorption of SnO2 after being doped with Co. The application of Sn1−xCoxO2 nanostructures in the gas sensor for detecting ethanol and acetone reveals that the as-prepared Sn1−xCoxO2 nanourchins with x = 0.03 show a high sensitivity and short response/recovery time.
Co-reporter:Zhenhuan Zhao, Jian Tian, Dongzhou Wang, Xueliang Kang, Yuanhua Sang, Hong Liu, Jiyang Wang, Shaowei Chen, Robert I. Boughton and Huaidong Jiang
Journal of Materials Chemistry A 2012 vol. 22(Issue 44) pp:23395-23403
Publication Date(Web):19 Sep 2012
DOI:10.1039/C2JM34580C
Surface engineering of TiO2 nanobelts by the controlled assembly of functional heterostructures represents an effective approach for the synthesis of high-performance photocatalysts. In this study, we prepared a novel Bi2O3/Bi4Ti3O12/TiO2 double-heterostructured nanobelt by depositing bismuth hydroxide onto the TiO2 nanobelt surface. A thermal annealing treatment led to the formation of a Bi4Ti3O12 interlayer that functioned as a bridge to link Bi2O3 and TiO2. The double-heterostructured TiO2 nanobelts exhibited better UV light photocatalytic performance than commercial P25. Importantly, the photocatalytic activity in the visible range was markedly better than that of Bi2O3 and Bi2O3/TiO2 heterostructured TiO2 nanobelts. The enhanced performance was accounted for by the material band structures where the matching was improved by the unique interlayer.
Co-reporter:Na Ren, Rui Li, Limei Chen, Guancong Wang, Duo Liu, Yingjun Wang, Lin Zheng, Wei Tang, Xiaoqiang Yu, Huaidong Jiang, Hong Liu and Nianqiang Wu
Journal of Materials Chemistry A 2012 vol. 22(Issue 36) pp:19151-19160
Publication Date(Web):25 Jul 2012
DOI:10.1039/C2JM32434B
A synthetic approach has been developed to in situ construct a new hierarchical nanostructure as an ideal biocompatible and bacteriostatic implant. A highly porous nano-network made of sodium titanate is first formed on the titanium surface by hydrothermal treatment. Silver ions are then inserted between the layered titanate lattices to form silver titanate via ion-exchange with sodium ions. Finally, silver ions are reduced by glucose, leading to the in situ growth of Ag nanoparticles that are sandwiched between layer-structured hydrogen titanate. The amount and the size of the Ag nanoparticles in the titanate–Ag nanoparticles–titanate sandwich can be adjusted by the concentrations of both the AgNO3 and the glucose solutions. The test results show that the silver ions are completely leached from silver titanate after 7 days of immersion in an aqueous solution. In contrast, the Ag ions continue to be released from the titanate–Ag nanoparticle–titanate sandwich nanostructure after 15 days. This steady and prolonged release characteristic is helpful to the long-standing antibacterial process for prevention of severe infection after surgery. A series of antimicrobial and biocompatible tests have shown that the sandwich nanostructure with a low level of silver loading exhibits a bacteriostatic rate as high as 99.99% while retaining low toxicity against cells. The titanate–Ag nanoparticle–titanate sandwich nanostructure, which is fabricated with a low-cost surface modification method, is a promising implantable material that will find applications in artificial bones, joints and dental implants.
Co-reporter:Dongzhou Wang, Weijia Zhou, Peiguang Hu, Yu Guan, Limei Chen, Jianhua Li, Guancong Wang, Hong Liu, Jiyang Wang, Guozhong Cao, Huaidong Jiang
Journal of Colloid and Interface Science 2012 Volume 388(Issue 1) pp:144-150
Publication Date(Web):15 December 2012
DOI:10.1016/j.jcis.2012.08.034
TiO2 nanobelts were prepared by the hydrothermal growth method. The surface of the nanobelts was coarsened by selective acid corrosion and functionalized with Pd catalyst particles. Three nanobelt samples (TiO2 nanobelts, surface-coarsened TiO2 nanobelts and Pd nanoparticle/TiO2 nanobelt surface heterostructures) were configured as gas sensors and their sensing ability was measured. Both the surface-coarsened nanobelts and the Pd nanoparticle-decorated TiO2 nanobelts exhibited dramatically improved sensitivity to ethanol vapor. Pd nanoparticle-decorated TiO2 nanobelts with surface heterostructures exhibited the best sensitivity, selectivity, working temperature, response/recovery time, and reproducibility. The excellent ethanol sensing performance is attributed to the large surface area and enhancement by Schottky barrier-type junctions between the Pd nanoparticles and TiO2 nanobelts.Graphical abstractHighlights► TiO2 nanobelts and Pd/TiO2 heterostructure were synthesized. ► The nanobelts were made into gas sensors. ► The sensors show good sensitivity, especially high sensitivity, good selectivity. ► The sensing mechanism was explained using a surface-depletion model.
Co-reporter:Ligang Gai, Xiuquan Duan, Haihui Jiang, Qinghu Mei, Guowei Zhou, Yan Tian and Hong Liu
CrystEngComm 2012 vol. 14(Issue 22) pp:7662-7671
Publication Date(Web):30 May 2012
DOI:10.1039/C2CE25563D
Nitrogen doping in combination with a heterostructure can not only modify the band structure of TiO2 to make it more responsive to visible light, but also suppress charge recombination and lead TiO2 to have enhanced photocatalytic activity as compared to P25. Also, one-dimensional TiO2 nanostructures can serve as electron highways for efficient charge separation and, hence, increase the lifetime of charge carriers and enhance the efficiency of interfacial charge transfer to the adsorbed substrate. In this paper, a simple one-pot synthetic strategy has been designed for preparing TiO2 nanorods with good crystallinity, nitrogen doping and anatase/brookite binary structure characters, using N2H4·H2O as an in situ nitrogen doping source. The physicochemical properties of the catalysts can be tuned by simply changing the concentration ratios of N2H4·H2O to TiO2 colloids. The synergistic effect of nitrogen doping in association with a one-dimensional and anatase/brookite binary structure is suggested to account for the higher catalytic activity of the TiO2 nanorods for decomposing methyl orange and 4-chlorophenol compared to the nanoparticle counterparts under UV and/or visible light illumination.
Co-reporter:Ligang Gai, Li Ma, Haihui Jiang, Yun Ma, Yan Tian and Hong Liu
CrystEngComm 2012 vol. 14(Issue 21) pp:7479-7486
Publication Date(Web):31 Jul 2012
DOI:10.1039/C2CE25789K
Doping indium oxide with nitrogen species is a strategy to extend its photoresponse to the visible region and to modify its band structure, enabling the material to have potential applications in photocatalysis, optoelectronics, and sensors. In this paper, we report on a simple solvothermal synthesis method for producing nitrogen-doped indium oxide nanocrystals that are composed of hierarchical structures. The samples were characterized with XRD, Raman spectroscopy, SEM, HRTEM, FTIR, XPS, UV-vis, and photoluminescence techniques, and further tested in the role of an ethanol gas sensing material. The optical properties and the gas-sensing performance of indium oxide can be tuned by controlling the nitrogen doping. Also, the nitrogen species, resulting from the nitrogen doping, function like a surface modifier to enhance the sensitivity of the sensors that were made from the nitrogen-doped indium oxides on their exposure to ethanol gas.
Co-reporter:Haiming Qin, Hong Liu, Yuanhua Sang, Yaohui Lv, Xiaolin Zhang, Yuanyuan Zhang, Tadashi Ohachi and Jiyang Wang
CrystEngComm 2012 vol. 14(Issue 5) pp:1783-1789
Publication Date(Web):06 Jan 2012
DOI:10.1039/C1CE06230A
Ammonium sulfate has been widely used as a control agent in the preparation of yttrium-aluminium-garnet (YAG) transparent ceramics, however, research of its application in the preparation in transparent ceramic yttria has not been intensively studied. Neodymium–doped yttria (Nd:Y2O3) nanopowders with controlled morphology and size were synthesized via a urea precipitation method using ammonium sulfate as the additive. The effect of ammonium sulfate was intensively studied throughout the preparation process. Morphology of precursors was found to be evidently affected by the [(NH4)2SO4]/[Nd:Y2O3] ratio (measured by weight). Uniform spheres of Nd:Y2O3 precursor were obtained without the addition of ammonium sulfate. With increasing amounts of ammonium sulfate added, the scale of the Nd:Y2O3 precursors diminished which results in the aggregation of the Nd:Y2O3 precursor. Aggregates of coral like particles after precipitation and uniform well dispersed particles after calcinations were obtained as the dosage of ammonium sulfate reached 20 wt%. It was considered to be the optimum state for the preparation of highly sinterable Nd:Y2O3 nanopowders. Ammonium sulfate was proved to be a regulator that could mediate the nucleation and growth of the precursor as well as its decomposition behaviour. Results of this paper can contribute to the controllable synthesis of transparent ceramic yttria.
Co-reporter:Yuanhua Sang, Yaohui Lv, Haiming Qin, Xiaolin Zhang, Hong Liu, Jiyang Wang, Xudong Sun, Robert I. Boughton
Ceramics International 2012 Volume 38(Issue 2) pp:1635-1641
Publication Date(Web):March 2012
DOI:10.1016/j.ceramint.2011.09.054
Abstract
The properties of YAG precursors aged at various pH levels for different aging times were examined to explore the influence of pH on the evolution of the chemical composition and the morphology of the precipitate, on the variation of phase composition during the calcination process. Precursors obtained at pH lower than 8.0 can be transformed into mono-phase YAG by calcination at low temperature, while those obtained at higher pH exhibit a variety of crystalline structures. Aging at high pH increased the impurity content of the calcined powder. Based on monitoring the pH during the precursor aging process, and the measurement of the Y/Al ratio in the precipitates, the mechanism of the chemical variation is discussed and the influence of pH and aging time on the synthesis of YAG precursor is discussed.
Co-reporter:Yaohui Lv, Wei Zhang, Hong Liu, Yuanhua Sang, Haiming Qin, Jie Tan, Liuniu Tong
Powder Technology 2012 Volume 217() pp:140-147
Publication Date(Web):February 2012
DOI:10.1016/j.powtec.2011.10.020
Neodymium-doped yttrium aluminum garnet (Nd:YAG) nanopowders were synthesized via the urea homogeneous precipitation method. The morphology and sintering property controlling effects of ammonium sulfate and urea during the synthesis process were discussed. Spawn-like and fibrillar precipitates were obtained without and with sulfate ions, respectively. Dispersive Nd:YAG nanopowder with proper sintering property was obtained with 1273 K calcination for 2 h from the precursor with 4.56 wt.% ammonium sulfate. Combined with the influence of the [urea]/[metal ions]([U]/[M]) concentration ratio, the dispersion, composition and morphology of the Nd:YAG nanopowders could be controlled via homogeneous precipitation process. A transparent Nd:YAG ceramic was achieved from the Nd:YAG powders obtained with 4.56 wt.% ammonium sulfate and a [U]/[M] concentration ratio of 40.The effects of sulfate ions on surface modification, surface charge distribution, and morphology of Nd:YAG precursor were mainly investigated. The results showed that sulfate ions played an important role in the preparation of yttrium and aluminum precursor and nanosized powders. Nd:YAG nanopowder with a uniform particle size of 80–100 nm was obtained by adding appropriate amount of sulfate ammonium.Highlights►Nd:YAG nanopowders were synthesized by the urea homogeneous precipitation method. ►SO42 − ions influence the morphology of precursor. ►SO42 − ions influence the composition of calcined powder. ►The [U]/[M] ratio influences the morphology and composition of nanopowders.
Co-reporter:Yuanhua Sang, Dehong Yu, Maxim Avdeev, Haiming Qin, Jiyang Wang, Hong Liu, Yaohui Lv
Journal of Solid State Chemistry 2012 Volume 192() pp:366-370
Publication Date(Web):August 2012
DOI:10.1016/j.jssc.2012.04.034
The presence of cation antisite defects is considered to be one of the most important factors determining the fluorescence, laser, and scintillation properties of rare earth-doped yttrium aluminum garnet (YAG) materials. However, no direct evidence or systematic investigation of antisite defect evolution as a function of cation composition variation in YAG has been reported in the previous literature. In this paper, we report a combined neutron and X-ray diffraction investigation on cation antisite defects performed on specially synthesized nonstoichiometric yttrium aluminum garnet nanoparticles to try to understand the defect chemistry in the YAG system. No evidence was found for YAl,16a, YAl,24d and AlY,24c antisite defects in these specially fabricated samples within the limit of diffraction techniques. The results suggest that YAG materials containing low level or no antisite defects can be achieved through low temperature synthesis process.Graphical AbstractThrough combined Rietveld refinement against both the NPD and XRD data, no or low level antisite defect exists in the low temperature synthesized YAG powders, bond lengths are changeless as a function of the nominal Y/Al ratio, nonstoichiometry has little influence on antisite defect formation.Highlights► Defects investigation with combined Rietveld refinement of NPD and XRD. ► No or less than 2at% for YAl,16a and YAl,24d antisite defects. ► Nonstoichiometry has little influence on antisite defect formation.
Co-reporter:Guohong Li, Hong Liu, TianDuo Li, Jiyang Wang
Materials Science and Engineering: C 2012 Volume 32(Issue 4) pp:627-636
Publication Date(Web):1 May 2012
DOI:10.1016/j.msec.2011.12.013
Silk from silkworms is composed of fibrous proteins with remarkable properties that have resulted in wide usage in the textile industry and as a biomaterial in the medical field. However, for some advanced applications, silk still has the disadvantages of wrinkling, photo-induced aging, deformation and even degradation caused by microorganism, biocompatibility problems. Based on sufficient supply of raw materials around the world and encouraged by the market demands for natural and smart materials, numerous attempts have been made in the surface modification and functionalization of silk fibroin fibers (SFFs) and silk fibroin fabric (SFF) using a wide range of functional materials and technology during last decade. Successful modification of silk may not only overcome its intrinsic shortcomings, but also enhance end-use performance. In this review, we summarize the recent progress of basic ideas, methodologies, and treatment techniques for surface modification and functionalization of SFF/SFFs with consideration of their enhanced properties and potential applications. Encouraged by achievements from experimental studies, the authors believe that such successes give silk products a promising future in both textile and biomaterial applications.Highlights► Basic treatments are reviewed, including degumming and sterilization methods. ► Three prospects of silk surface modification/functionalization are introduced. ► Biomaterials and textile application fields of modified silk are introduced.
Co-reporter:Yanmin Wang, Guojun Du, Lingbo Zhu, Hong Liu, Ching-Ping Wong, Jiyang Wang
Sensors and Actuators B: Chemical 2012 174() pp: 570-576
Publication Date(Web):
DOI:10.1016/j.snb.2012.07.076
Co-reporter:Jingjie Cui, Dehui Sun, Shaowei Chen, Weijia Zhou, Peiguang Hu, Hong Liu and Zhen Huang
Journal of Materials Chemistry A 2011 vol. 21(Issue 29) pp:10633-10636
Publication Date(Web):21 Jun 2011
DOI:10.1039/C1JM11805F
An alkaline hydrothermal and acid etching process was used to prepare surface-coarsened anatase TiO2 nanobelts (CTNs) with enhanced (001) facets. The CTNs were used for electrochemical selective determination of the perfect match and mismatch of single nucleobases at the physiological pH of 7.4. It is supposed that the structure and surface morphology of CTNs play important roles in the nature of the adsorption/bonding and packing density of single base pairs on the nanobelt surfaces. Within the present experimental context, the CTNs are considered to be promising candidates for biosensing of nucleic acids that will be of fundamental significance to diagnostic medicine and molecular biology research.
Co-reporter:Weijia Zhou, Guojun Du, Peiguang Hu, Guohong Li, Dongzhou Wang, Hong Liu, Jiyang Wang, Robert I. Boughton, Duo Liu and Huaidong Jiang
Journal of Materials Chemistry A 2011 vol. 21(Issue 22) pp:7937-7945
Publication Date(Web):27 Apr 2011
DOI:10.1039/C1JM10588D
Nanoheterostructures of TiO2 nanoparticles/TiO2 nanobelts and Ag/TiO2 nanoparticles/TiO2 nanobelts are prepared by the acid-assisted hydrothermal method followed by an in situ photo-reduction process. The experimental parameters, including acid corrosion time and calcination temperature, are investigated in detail. Compared with TiO2 nanobelts, the single nanoheterostructure TiO2 nanoparticles/TiO2 nanobelts have a better photocatalytic activity. The double nanoheterostructure Ag/TiO2 nanoparticles/TiO2 nanobelts can further dramatically enhance photocatalytic properties of TiO2 nanobelts. The mechanisms for formation of the heterostructure and the enhanced photocatalytic effect of the heterostructure are discussed. The liquid continuous-flow photocatalysis based on TiO2 nanobelt nanopaper with different heterostructures is carried out, which has an efficient photocatalytic ability. At the same time, the obtained TiO2 nanobelt heterostructures have a good gas sensitive performance for ethanol.
Co-reporter:Jianjian Lin, Jianxing Shen, Ruijun Wang, Jingjie Cui, Weijia Zhou, Peiguang Hu, Duo Liu, Hong Liu, Jiyang Wang, Robert I. Boughton and Yuanzheng Yue
Journal of Materials Chemistry A 2011 vol. 21(Issue 13) pp:5106-5113
Publication Date(Web):23 Feb 2011
DOI:10.1039/C0JM04131A
Nano-p–n junction heterostructure TiO2 nanobelts have been produced by assembling p-type semiconductor NiO nanoparticles on n-type TiO2 nanobelts for enhancement of the photocatalytic properties of TiO2 nanobelts. NiO/TiO2 nano-p–n junctions were synthesized on the surfaces of TiO2 nanobelts and surface-coarsened TiO2 nanobelts. The nanobelts were obtained using alkaline- and acid-assisted hydrothermal processes. The chemical-solution-deposition–decomposition process was used to form NiO nanoparticle/TiO2 heterostructure composite nanobelts (NiO-NP/TiO2 NBs), and NiO nanoparticle/surface-coarsened TiO2 heterostructure composite nanobelts (NiO-NP/TiO2 coarsened NBs). The uniform assembly of p-type NiO nanoparticles produces a large number of nano-p–n junction heterostructures on the surface of the TiO2 nanobelts, where NiO and TiO2 form p- and n-type semiconductors, respectively. Compared with both pure NiO nanoparticles and TiO2 nanobelts, NiO-NP/TiO2 NBs exhibit much enhanced photocatalytic activity. Interestingly, the optimized composite NiO-NP/TiO2 coarsened NBs exhibit an enhanced photocatalytic activity in the decomposition of a model dye compound, methyl orange (MO), under both ultraviolet and visible light irradiation. It is argued that the nano-p–n junctions effectively reduce the recombination of electrons and holes, thus leading to the enhancement of the photocatalytic properties of the heterostructure composites. The larger number of abundant photocatalytic-active surfaces in the surface-coarsened nanobelts increases photo-absorption and the production of charge carriers, which gives the composites an enhanced photocatalytic performance. The established approach allows for controlling the nano-p–n junction heterostructure of the nanobelts, and hence, their photocatalytic effect. The NiO/TiO2 nanobelt-based nano-p–n junction heterostructure TiO2 can provide a practical way to design and prepare nano-composites for applications as solar-cell electrodes, in solar photocatalysis, solar photolysis of water and other related fields.
Co-reporter:Guancong Wang, Lin Zheng, Hongshi Zhao, Junying Miao, Chunhui Sun, Hong Liu, Zhen Huang, Xiaoqiang Yu, Jiyang Wang, and Xutang Tao
ACS Applied Materials & Interfaces 2011 Volume 3(Issue 5) pp:1692
Publication Date(Web):April 14, 2011
DOI:10.1021/am2002185
Biomaterial surfaces and their nanostructures can significantly influence cell growth and viability. Thus, manipulating surface characteristics of scaffolds can be a potential strategy to control cell functions for stem cell tissue engineering. In this study, in order to construct a hydroxyapatite (HAp) coated genipin-chitosan conjugation scaffold (HGCCS) with a well-defined HAp nanostructured surface, we have developed a simple and controllable approach that allows construction of a two-level, three-dimensional (3D) networked structure to provide sufficient calcium source and achieve desired mechanical function and mass transport (permeability and diffusion) properties. Using a nontoxic cross-linker (genipin) and a nanocrystallon induced biomimetic mineralization method, we first assembled a layer of HAp network-like nanostructure on a 3D porous chitosan-based framework. X-ray diffraction (XRD) and high resolution transmission electron microscopy (HRTEM) analysis confirm that the continuous network-like nanostructure on the channel surface of the HGCCS is composed of crystalline HAp. Compressive testing demonstrated that the strength of the HGCCS is apparently enhanced because of the strong cross-linking of genipin and the resulting reinforcement of the HAp nanonetwork. The fluorescence properties of genipin–chitosan conjugation for convenient monitoring of the 3D porous scaffold biodegradability and cell localization in the scaffold was specifically explored using confocal laser scanning microscopy (CLSM). Furthermore, through scanning electron microscope (SEM) observation and immunofluorescence measurements of F-actin, we found that the HAp network-like nanostructure on the surface of the HGCCS can influence the morphology and integrin-mediated cytoskeleton organization of rat bone marrow-derived mesenchymal stem cells (BMSCs). Based on cell proliferation assays, rat BMSCs tend to have higher viability on HGCCS in vitro. The results of this study suggest that the fluorescent two-level 3D nanostructured chitosan-HAp scaffold will be a promising scaffold for bone tissue engineering application.Keywords: bone tissue engineering; chitosan; fluorescence; genipin; mesenchymal stem cells; nanostructure; surface characteristics
Co-reporter:Jingjie Cui, Dehui Sun, Weijia Zhou, Hong Liu, Peiguang Hu, Na Ren, Haiming Qin, Zhen Huang, Jianjian Lin and Houyi Ma
Physical Chemistry Chemical Physics 2011 vol. 13(Issue 20) pp:9232-9237
Publication Date(Web):04 Apr 2011
DOI:10.1039/C1CP20082H
Two kinds of TiO2 nanobelts were prepared from commercial P-25 powders via an alkaline hydrothermal method with and without an acid etching process. The uncauterized nanobelts (TNs) exhibited a smooth surface, and mixed phases of anatase and TiO2 (B), whereas the cauterized ones (CTNs) displayed a rough surface and a pure anatase structure. TNs and CTNs were then deposited onto a glassy carbon electrode (GCE) surface with a conductive adhesive (CA), and the resulting chemically modified electrodes exhibited electrocatalytic activities in the oxidation of nucleobases in a 0.1 M phosphate buffer solution (PBS) at pH 7.4. For guanine and adenine, well-defined oxidation peaks were observed in voltammetric measurements at about +0.62 and +0.89 V, respectively, at a potential sweep rate of 100 mV s−1, whereas for cytosine, uracil and thymine, the voltammetric features were not obvious. The average surface coverages (Γ) of guanine and adenine on the CTNs/CA/GCE electrode were estimated to be 4.75 × 10−10 and 7.44 × 10−10 mol cm−2, respectively, which were about twice those at the TNs/CA/GCE electrode. The enhanced activity of the CTN-based electrode towards purine nucleobase oxidation was ascribed to the large specific surface area and anatase structures with enhanced (001) facets of the CTN that facilitated adsorption of the analytes onto the electrode surface and charge transport through the electrode surface layer.
Co-reporter:Weijia Zhou, Ligang Gai, Peiguang Hu, Jingjie Cui, Xiaoyan Liu, Dongzhou Wang, Guohong Li, Huaidong Jiang, Duo Liu, Hong Liu and Jiyang Wang
CrystEngComm 2011 vol. 13(Issue 22) pp:6643-6649
Publication Date(Web):06 Sep 2011
DOI:10.1039/C1CE05638G
TiO2 nanobelts are very attractive due to their dimensional confinement and structurally well-defined physical and chemical properties. However, the obscure phase transformation mechanism and the low photocatalytic activity of TiO2 nanobelts limit their wide applications. Here, the phase transformations among H2Ti3O7, TiO2(B), anatase and rutile nanobelts were characterized in detail by X-ray powder diffraction, high resolution transmission electron microscopy, Raman spectroscopy and UV-Vis diffuse reflectance spectra. TiO2(B) is inevitable in the phase transformation of TiO2 nanobelts due to the shape limiting effort and the similar crystal structure between H2Ti3O7 and TiO2(B). TiO2 nanobelts have a good thermal stability for the crystal phase and nanostructures. TiO2(B)/anatase interface heterostructure nanobelts were obtained by calcining H2Ti3O7 nanobelts at 800 °C, which had an enhanced photocatalytic ability comparing with pure TiO2(B) and anatase nanobelts. The mechanisms of the phase transformation of TiO2 nanobelts and the enhanced photocatalytic activity of TiO2(B)/anatase interface heterostructure nanobelts were discussed. The self-transformed heterostructure nanobelts have good photocatalytic activity, stability and easy-recovery properties, which will have important practical applications.
Co-reporter:Weijia Zhou, Xiaoyan Liu, Jingjie Cui, Duo Liu, Jing Li, Huaidong Jiang, Jiyang Wang and Hong Liu
CrystEngComm 2011 vol. 13(Issue 14) pp:4557-4563
Publication Date(Web):12 May 2011
DOI:10.1039/C1CE05186E
Semiconductor rutileTiO2 nanostructures with a diversity of well-defined morphologies, such as microspheres, nanoflowers, nanotrees and nanobelts, are synthesized via an acid-hydrothermal process without any structure-directing agents. Their morphologies, crystal structures and orientation relationship were characterized by X-ray diffraction, scanning electron microscopy and high-resolution transmission electron microscopy. By controlling hydrochloric acid concentration, anisotropic growth of the rutile TiO2 leads to various morphologies. The synthesis mechanism of rich TiO2 nanostructures was also studied. Finally, the relationship between optical properties and the structural complexity of the rutileTiO2 nanocrystals was characterized.
Co-reporter:Guohong Li, Hong Liu, Hongshi Zhao, Yuqiang Gao, Jiyang Wang, Huaidong Jiang, R.I. Boughton
Journal of Colloid and Interface Science 2011 Volume 358(Issue 1) pp:307-315
Publication Date(Web):1 June 2011
DOI:10.1016/j.jcis.2011.02.053
A carefully designed surface modification technique for the manufacture of multifunctional silk textile nanocomposite materials is successfully developed by the functionalization of silk with TiO2 and TiO2@Ag nanoparticles (NPs). The NPs are assembled onto a silk substrate through covalent linkages, including enediol ligand–metal oxide bonding, resin dehydration and the acylation of silk. Owing to the strong chemical bonding, silk fibroin fabric (SFF) and the NPs form a stable composite system. The functionalized SFF, especially TiO2@Ag NP-functionalized SFF are endowed with remarkable UV protection properties, and an efficient anti-bacterial capability toward Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. Furthermore, the nearly total photodegradation of methylene orange (MO) under UV illumination illustrates that functionalized SFF possesses high photocatalytic and self-cleaning capability. This multifunctional silk material satisfies the market demand for natural “smart” products, and is a promising practical material for use in the textile industry, hospital sterilization and environmental cleanup.Graphical abstractSchematic illustration of the surface-modified TiO2@Ag nanoparticles covalently bonded onto the pre-modified SFF surface.Research highlights► For the first time, TiO2 and TiO2@Ag nanoparticles are chemical bonded onto silk fibroin fabric. ► The functionalized silk fibroin fabric is endowed with a high UV protection capability, excellent anti-bacterial action, a high photocatalytic and self-cleaning capability. Owing to the strong chemical bonding strength, long term durable effects are obtained. ► The biggest advantage of this simple technology is the adoption of it into the traditional anti-wrinkle finishing technology in textiles, so it is easily scaled up.
Co-reporter:Yaohui Lv, Wei Zhang, Jie Tan, Yuanhua Sang, Haiming Qin, Jinlian Hu, Liuniu Tong, Hong Liu, Jiyang Wang, Robert I Boughton
Journal of Alloys and Compounds 2011 Volume 509(Issue 6) pp:3122-3127
Publication Date(Web):10 February 2011
DOI:10.1016/j.jallcom.2010.12.016
A stable aqueous slurry using ammonium polyacrylic acid polyelectrolyte as dispersant and a neodymia–yttria–alumina mixture was prepared as the starting powder. The effect of the polyelectrolyte concentration and the pH of the slurry on the stability of the suspension is studied, and the optimal pH value and the amount of dispersant needed to obtain a stable slurry were determined. Highly consistent slurries with optimal pH and dispersant concentration were prepared by ball milling. The rheological behavior of the slip with different solid loading (48–58 wt.%) has been studied by measuring the viscosity and shear stress as a function of shear rate. Slip with solid loadings of 53 wt.% shows near-Newtonian behavior but becomes non-Newtonian with typical shear-thinning behavior above this solid loading value. The density and microstructure of the cast product bears a direct relationship to the state of the slip induced by variation of the pH and the concentration of the dispersant as well as by solid loading. Transparent Nd:YAG ceramics were obtained by sintering of compacts prepared from optimized slurries at 1750 °C in vacuum.Research highlights▶ We prepared stable aqueous slurry with ammonium polyacrylic acid as dispersant and neodymia-yttria-alumina mixture as the starting powder. ▶ A series of colloid chemistry properties of mixture was investigated. ▶ Transparent Nd:YAG ceramics were obtained from the optimized slurries.
Co-reporter:Zheng Gao, Haiming Qin, Tao Yan, Hong Liu, Jiyang Wang
Journal of Solid State Chemistry 2011 Volume 184(Issue 12) pp:3257-3261
Publication Date(Web):December 2011
DOI:10.1016/j.jssc.2011.10.010
Bismuth nanobelts in situ grown on a silicon wafer were synthesized through an ethanol-thermal method without any capping agent. The structure of the bismuth belt–silicon composite nanostructure was characterized by scanning electron microscope, energy-dispersive X-ray spectroscopy, and high resolution transmission electron microscope. The nanobelt is a multilayered structure 100–800 nm in width and over 50 μm in length. One layer has a thickness of about 50 nm. A unique sword-like nanostructure is observed as the initial structure of the nanobelts. From these observations, a possible growth mechanism of the nanobelt is proposed. Current–voltage property measurements indicate that the resistivity of the nanobelts is slightly larger than that of the bulk bismuth material.Graphical AbstractTEM images, EDS, and electron diffraction pattern of bismuth nanobelts.Highlights► Bismuth nanobelts in situ grown on silicon wafer were achieved. ► Special bismuth–silicon nanostructure. ► Potential application in sensitive magnetic sensor and other electronic devices.
Co-reporter:Jianjian Lin, Jianxing Shen, Tailin Wang, Ruijun Wang, Hong Liu, Jingjie Cui, Weijia Zhou
Materials Science and Engineering: B 2011 Volume 176(Issue 12) pp:921-925
Publication Date(Web):25 July 2011
DOI:10.1016/j.mseb.2011.05.018
In this work, heterostructures were obtained by uniformly assembling NiO nanoparticles on the surface-coarsened TiO2 nanobelts through a precipitation process. The uniform assembling of NiO nanoparticles led to a large number of nano-p–n-junction heterostructures on the surface of the TiO2 nanobelts, where NiO and TiO2 are p- and n-type semiconductors, respectively. Compared with both pure NiO nanoparticles and TiO2 nanobelts, NiO nanoparticles/TiO2 surface-coarsened nanobelt heterostructured composite exhibited a greatly enhanced photocatalytic activity in the decomposition of a model dye compound methyl orange under ultraviolet light irradiation. It was argued that the nano-p–n-junctions effectively reduce the recombination of electrons and holes, thus resulting in enhanced photocatalytic property of the heterostructured composites. The better performance of the surface-coarsened nanobelts is due to the increased photo absorption and production of charge carriers, which renders the composites with further enhanced photocatalytic performance. The established approach allows the control of the nano-p–n junction heterostructure on the nanobelts, and hence, their photocatalytic effect.Highlights► Surface-coarsening nanobelt was obtained by hydrothermal and following an acid-assisted hydrothermal approach. ► NiO NP/TiO2 SC NB was prepared through a precipitation process. ► NiO NP/TiO2 SC NB can enhance the photocatalytic performance under ultraviolet light irradiation. ► p–n-junctions effectively lead to enhancement of photocatalytic property of the composites. ► More active surfaces of SC NB render the composites with enhanced photocatalytic performance.
Co-reporter:Xin Liu;Yuming Sun;Yuanhong Zhang;Ning Zhao;Hongshi Zhao
Journal of Fluorescence 2011 Volume 21( Issue 2) pp:497-506
Publication Date(Web):2011 March
DOI:10.1007/s10895-010-0736-8
A series of carbazole cationic compounds based on donor- Π—acceptor (D-Π-A) structure were synthesized and characterized. They exhibit large two-photon absorption cross sections when excited by a 810 nm a laser beam, and their photophysical properties show that the intramolecular charge transfer (ICT) character is predominant. Moreover these compounds can easily pass though the intact cell membrane of living cells, amongst, 3-(1-hydroxyethyl -4-vinylpyridium iodine)-N-butyl carbazole (9B-HVC) has been proven to be capable of accumulating within the mitochondria possessing large membrane potential and imaging this organelle in living cells by means of two-photon fluorescence microscopy. At the same time usable fluorescent photos can be obtained at lower incident excitation power (5 mW) and low-micromolar concentrations (2 μM), which does not result in significant reduction in cell viability over a period of at least 24 h.
Co-reporter:Weijia Zhou, Hong Liu, Robert I. Boughton, Guojun Du, Jianjian Lin, Jiyang Wang and Duo Liu
Journal of Materials Chemistry A 2010 vol. 20(Issue 29) pp:5993-6008
Publication Date(Web):16 Apr 2010
DOI:10.1039/B927224K
Recent advances in the properties, synthesis, modifications and applications of one-dimensional single-crystalline Ti–O based nanostructures (including nanotubes, nanobelts, nanowires, and nanorods) are reviewed. The physical and chemical properties of one-dimensional nanostructured titanates, such as adsorption, stability, ion-exchange, optical, and proton conductivity properties, are described in connection with a particular application. The experimental parameters, morphologies, and mechanism of formation of one-dimensional nanostructured titanates produced by the alkaline hydrothermal method are critically discussed. Current progress in the modifications of one-dimensional single-crystalline Ti–O based nanostructures are discussed together with their improved performances. Examples of applications of one-dimensional nanostructured titanates in photocatalysis, lithium batteries, sensors, hydrogen production and storage, solar cells and biomedicine are presented.
Co-reporter:Weijia Zhou, Hong Liu, Jiyang Wang, Duo Liu, Guojun Du and Jingjie Cui
ACS Applied Materials & Interfaces 2010 Volume 2(Issue 8) pp:2385
Publication Date(Web):July 20, 2010
DOI:10.1021/am100394x
Ag2O/TiO2 heterostructure with high photocatalytic activity both in ultraviolet and visible-light region was synthesized via a simple and practical coprecipitation method by using surface-modified TiO2 nanobelts as substrate materials. The as-prepared heterostructure composite included Ag2O nanoparticles assembled uniformly on the rough surface of TiO2 nanobelts. Comparing with pure TiO2 nanobelts and Ag2O nanoparticles, the composite photocatalyst with a wide weight ratio between TiO2 and Ag2O exhibited enhanced photocatalytic activity under ultraviolet and visible light irradiation in the decomposition of methyl orange (MO) aqueous solution. On the basis of the characterization by X-ray diffraction, photoluminescence and UV−vis diffuse reflectance spectroscopies, two mechanisms were proposed to account for the photocatalytic activity of Ag2O/TiO2 nanobelts’ heterostructure.Keywords: Ag2O/TiO2 heterostructure; electron capture agent; photocatalytic activity; TiO2 nanobelts; visible-light photocatalysis
Co-reporter:Peiguang Hu, Guojun Du, Weijia Zhou, Jingjie Cui, Jianjian Lin, Hong Liu, Duo Liu, Jiyang Wang, and Shaowei Chen
ACS Applied Materials & Interfaces 2010 Volume 2(Issue 11) pp:3263
Publication Date(Web):October 22, 2010
DOI:10.1021/am100707h
TiO2 nanobelts were prepared by a hydrothermal process, and the structures were manipulated by surface engineering, including surface coarsening by an acid-corrosion procedure and formation of Ag−TiO2 heterostuctures on TiO2 nanobelts surface by photoreduction. Their performance in the detection of ethanol vapor was then examined and compared by electrical conductivity measurements at varied temperatures. Of the sensors based on the four nanobelt samples (TiO2 nanobelts, Ag−TiO2 nanobelts, surface-coarsened TiO2 nanobelts, and surface-coarsened Ag−TiO2 nanobelts), they all displayed improved sensitivity, selectivity, and short response times for ethanol vapor detection, in comparison with sensors based on other oxide nanostructures. Importantly, the formation of Ag−TiO2 heterostuctures on TiO2 nanobelts surface and surface coarsening of TiO2 nanobelts were found to lead to apparent further enhancement of the sensors sensitivity, as well as a decrease of the optimal working temperature. That is, within the present experimental context, the vapor sensor based on surface-coarsened Ag−TiO2 composite nanobelts exhibited the best performance. The sensing mechanism was interpreted on the basis of the surface depletion model, and the improvement by oxide surface engineering was accounted for by the chemical sensitization mechanism. This work provided a practical approach to the enhancement of gas sensing performance by one-dimensional oxide nanomaterials.Keywords: gas sensor; hydrothermal method; nanoscale Ag-TiO2 heterostructure; photoreduction; surface coarsening
Co-reporter:Yue Zhao, Hong Liu, Jin Liu, Chenguo Hu, Jiyang Wang
Applied Surface Science 2010 Volume 257(Issue 1) pp:102-108
Publication Date(Web):15 October 2010
DOI:10.1016/j.apsusc.2010.06.044
Abstract
Bismuth onion structured nanospheres with the same structure as carbon onions have been synthesized and observed. The nanospheres were synthesized through a hydrothermal method using bismuth hydroxide and silicon wafer as reactants. By controlling the heating temperature, heating time, and the pressure, nanoscale bismuth spheres can be in situ synthesized on silicon wafer, and forms a bismuth onion film on the substrate. The electronic property of the films was investigated. A formation mechanism of the formation of bismuth onions and the onion film has been proposed on the basis of experimental observations.
Co-reporter:Tao Yan, Hong Liu, Jiyang Wang, Feifei Zheng, Shuhua Yao, Zongren Xia, Jianbo Wu, Robert I. Boughton
Journal of Alloys and Compounds 2010 Volume 497(1–2) pp:412-415
Publication Date(Web):14 May 2010
DOI:10.1016/j.jallcom.2010.03.091
Reduced lithium tantalate (LiTaO3, LT) wafers were prepared by chemically reducing regular congruent LT wafers in mixed iron and lithium carbonate powders under a flowing nitrogen atmosphere. The electrical conductivity, Curie temperature, infrared spectrum, UV–vis transmittance, piezoelectric constants and dielectric properties of the LT wafers before and after reduction were measured. In comparison with regular LT wafers, it was found that both the electrical conductivity and the optical absorption in the visible region are greatly increased after reduction, which is beneficial for eliminating pyroelectric discharge and for high accuracy device processing. In addition, we also found that the piezoelectric and dielectric properties of the chemically reduced wafers remain almost the same, a prerequisite for fabricating SAW devices. The effects of mechanisms related to chemical reduction on the evolution of the physical properties of LT wafers are also discussed.
Co-reporter:Linyong Huang, Jing Liu, Zhiyuan Zuo, Hong Liu, Duo Liu, Jiyang Wang, Robert I. Boughton
Journal of Alloys and Compounds 2010 Volume 507(Issue 2) pp:429-432
Publication Date(Web):8 October 2010
DOI:10.1016/j.jallcom.2010.07.140
KCu3S2 microslabs and microbelts have been synthesized using a composite-hydroxide mediated (CHM) approach without the presence of an organic surfactant. X-ray powder diffraction results indicate that the belts possess a monoclinic KCu3S2 crystalline structure. Scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM) were used to obtain detailed characterization of the microstructure and nanostructure of this material. Measurements of the UV–vis absorption spectrum have been performed, and the results reveal that this material is semiconducting with a bandgap of 1.459 eV.Graphical abstractResearch highlights▶ One of the ternary K–Cu–S compounds, KCu3S2 microbelts and nanobelts were synthesized by using a composite-hydroxide mediated (CHM) approach with the absence of any organic surfactants. ▶ X-ray powder diffraction results indicate that the belts possess a monoclinic KCu3S2 crystalline structure. ▶ Scanning electron microscopy (SEM) and high resolution transmission electron microscopy (HRTEM) were used to obtain detailed characterization of the microstructure and nanostructure of this material. ▶ A growth mechanism of KCu3S2 microbelts was proposed. ▶ Measurements of the UV–vis absorption spectrum have been performed, and the results reveal that this material is semiconducting with a bandgap of 1.459 eV.
Co-reporter:Limei Chen, Lin Zheng, Yaohui Lv, Hong Liu, Guancong Wang, Na Ren, Duo Liu, Jiyang Wang, Robert I. Boughton
Surface and Coatings Technology 2010 204(23) pp: 3871-3875
Publication Date(Web):
DOI:10.1016/j.surfcoat.2010.05.003
Co-reporter:Chenguo Hu, Yi Xi, Hong Liu and Zhong Lin Wang
Journal of Materials Chemistry A 2009 vol. 19(Issue 7) pp:858-868
Publication Date(Web):12 Jan 2009
DOI:10.1039/B816304A
The composite-hydroxide-mediated (CHM) method is based on the use of molten composite hydroxides as a solvent in chemical reactions at ∼200 °C for the synthesis of a wide range of nanostructures. This review focuses on its recent development with an emphasis on its applications for synthesizing materials of complex oxides, hydroxides, simple oxides, sulfides, selenides, tellurides, fluorides and metals. The principle of this synthesis method is introduced, and the key factors that affect the morphology and size are studied. The advantages of its low synthesis temperature, low pressure and low cost are illustrated through the synthesis of functional wires, rods, belts and other nanostructures.
Co-reporter:Yaohui Lv, Hong Liu, Zhen Wang, Shujiang Liu, Lujiang Hao, Yuanhua Sang, Duo Liu, Jiyang Wang, R.I. Boughton
Journal of Membrane Science 2009 Volume 331(1–2) pp:50-56
Publication Date(Web):1 April 2009
DOI:10.1016/j.memsci.2009.01.007
Silver nanoparticle-decorated porous ceramic composites have been prepared by overnight exposure to a sliver nanoparticle colloid solution of a porous ceramic modified by an aminosilane coupling agent, 3-aminopropyltriethoxysilane (APTES). The connection between the nanoparticle and the ceramic relies on the coordination bonds between the –NH2 group at the top of the APTES molecule and the silver atoms on the surface of the nanoparticles. The other end of the aminosilane coupling agent attaches to silicon atoms in the ceramic through a Si–O–Si bond. There is no obvious loss of nanoparticles after immersion in an ultrasonic bath for 15 min, or after keeping the treated ceramic for several weeks in an atmospheric environment. On-line tests were conducted with a mimetic water filter. At a flow rate of 0.01 L/min, the output count of Escherichia coli was zero when the input water had a bacterial load of ∼105 colony-forming units (CFU) per millilitre. Combined with low cost and effectiveness in prohibiting the growth of E. coli, such materials should have wide application to drinking water treatment.
Co-reporter:Kegao Liu, Hong Liu, Jiyang Wang, Liming Feng
Materials Letters 2009 Volume 63(Issue 5) pp:512-514
Publication Date(Web):28 February 2009
DOI:10.1016/j.matlet.2008.10.054
Single phase SnSe2 was synthesized at 180 °C by hydrothermal co-reduction method from SnCl2·2H2O== and SeO2, its morphology and growth direction were investigated. The products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and field emission scanning electron microscope (FESEM). Experimental results show that, the SnSe2 powder almost consists of regular and homogenous hexagonal nanoflakes which grow along (0001) crystal plane, these nanoflakes are about 600–700 nm in side length and 30–40 nm in thickness.
Co-reporter:Ligang Gai, Guojun Du, Zhiyuan Zuo, Yanmin Wang, Duo Liu and Hong Liu
The Journal of Physical Chemistry C 2009 Volume 113(Issue 18) pp:7610-7615
Publication Date(Web):April 9, 2009
DOI:10.1021/jp900369y
We report here an in situ polymerization method for the controlled synthesis of core−shell structured hydrogen titanate−polyaniline composite nanowires. The microstructure and physical properties of the composite nanowires were characterized with XRD, FESEM, TEM, FT-IR, thermal analysis, and UV−vis spectroscopy. It is found that the thermal stability of polyaniline in the composite is greatly improved. A hydrogen bond-assisted formation mechanism is proposed to account for the experimental observation. In addition, the temperature dependence of electrical conductivity of an individual composite nanowire was measured as a function of temperature, which reveals improved conductivity compared with hydrogen titanate nanobelt.
Co-reporter:Yanmin Wang;Guojun Du;Duo Liu;Shubin Qin;Na Wang;Chenguo Hu;Xutang Tao;Jun Jiao;Jiyang Wang;Zhong Lin Wang
Advanced Functional Materials 2008 Volume 18( Issue 7) pp:1131-1137
Publication Date(Web):
DOI:10.1002/adfm.200701120
Abstract
Three types of TiO-compound-based nanobelts (Na2Ti3O7, H2Ti3O7, TiO2) are prepared from commercial TiO2 powders via an alkaline hydrothermal process. Nanostructured sheets based on the as-synthesized nanobelts are prepared using a paper-making process. The nanobelts are connected with hydrogen bonds or/and bridge oxygen atoms and packed together, forming a paperlike porous network structure, with an average pore size of ∼500 nm. The electrical properties and gas sensing of the nanostructured sheets are demonstrated to display sensitivity down to sub-ppb levels. H2Ti3O7 nanobelts decorated with Ag nanoparticles have also been applied as an antibacterial agent.
Co-reporter:Yaohui Lv;Zhen wang;Lujiang Hao;Jing Liu;Yangmin Wang;Guojun Du;Duo Liu;Jie Zhan;Jiyang Wang
Polymers for Advanced Technologies 2008 Volume 19( Issue 11) pp:1455-1460
Publication Date(Web):
DOI:10.1002/pat.1138
Abstract
Silver nanoparticles were covalently coated on a glass surface by overnight exposure of the glass substrate to nanoparticle solutions, using 3-aminopropyltriethoxysilane (APTES) as a coupling agent. Washing and air-drying yield a uniformly coated glass substrate, which can be used as a material capable of killing harmful microorganisms in food industry. Nanoparticles are stable on the glass surface and are not washed away by water; they even remain on the glass surface under short-term ultrasonic irradiation. The morphology of silver nanoparticles on the glass substrate was characterized by scanning electron microscope (SEM). The existence of Ag nanoparticles on the substrate was also confirmed by ultraviolet-visible (UV–Vis) spectroscopy. Fourier transform infrared (FT-IR) measurement shows that the connection is based on covalent bonds between silver nanoparticle surface/APTES molecules. Combining the effects of low cost and effectiveness in prohibiting the growth of Escherichia coli, such materials are expected to be used as antibacterial coatings, which may have large potential applications in food industry. Copyright © 2008 John Wiley & Sons, Ltd.
Co-reporter:Xudong Zhang, Hong Liu, Wen He, Jiyang Wang, Xia Li, Robert I Boughton
Journal of Alloys and Compounds 2004 Volume 372(1–2) pp:300-303
Publication Date(Web):9 June 2004
DOI:10.1016/j.jallcom.2003.10.010
Yttrium aluminum garnet (YAG) powder was synthesized by a mixed solvothermal method under milder conditions with inexpensive aluminum and yttrium nitrates as the starting materials, and the low-cost ethanol–water mixed solution as the solvent. X-ray diffraction (XRD), DTA and TEM analysis showed that the powder synthesized was single-phase YAG, with well-dispersed fine spherical grains (80 nm average) and a relatively narrow grain size distribution. Moreover, the crystallization process of YAG grains was discussed.
Co-reporter:Hongxia Li, Hong Liu, Jiyang Wang, Shushan Yao, Xiufeng Cheng, R.I. Boughton
Materials Letters 2004 Volume 58(27–28) pp:3630-3633
Publication Date(Web):November 2004
DOI:10.1016/j.matlet.2004.07.014
Zinc oxide (ZnO) films were deposited on silica glass substrates using metal–organic chemical vapor deposition (MOCVD) with diethyl zinc (DEZn) as the Zn precursor and ethanol as the oxygen source. Annealing was performed at 600°C for 1 h in air. The X-ray diffraction (XRD) patterns of the samples show sharp diffraction peaks for ZnO (0002), which indicates that the films are highly c-axis oriented. The films were also characterized by measuring the optical transmission spectrum, atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). The XPS spectra showed that the ZnO films changed from O-rich to Zn-rich after being annealed.
Co-reporter:H Liu, J.Y Wang, H.M Cui, R.J Shi, X.B Hu, Z.P Ai
Synthetic Metals 2004 Volume 145(Issue 1) pp:75-82
Publication Date(Web):27 August 2004
DOI:10.1016/j.synthmet.2004.04.013
Polyaniline (PANI)-NaFe4P12 whisker composite has been synthesized by using in situ compounding and the emulsion synthesis method. X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), high-resolution transmission electron microscope (HRTEM), infrared transmission spectra, UV-Vis spectra, thermal gravimetric analysis (TGA), and elemental analysis were used to characterize the NaFe4P12 whiskers, polyaniline, and the composite. The composite particles mainly consist of NaFe4P12 whiskers and a layer of polyaniline, which grows directionally on the surface of the whisker. In the composite powder, some particles with a “brush” structure have been found. The “hair” of the brush is polyaniline rope, consisting of several polyaniline wires about 20 nm in diameter. The directional growth of polyaniline on the surface of the NaFe4P12 whisker is assumed to be caused by the formation of coordinate linkage between the top of polyaniline molecular chains and the surface of the NaFe4P12 whisker. A growth model of plyaniline directionally on the surface of skutterudite whiskers is suggested. The conductivity of the polyaniline and the composite was measured.
Co-reporter:Xia Li, Hong Liu, Jiyang Wang, Hongmei Cui, Feng Han
Materials Research Bulletin 2004 Volume 39(Issue 12) pp:1923-1930
Publication Date(Web):4 October 2004
DOI:10.1016/j.materresbull.2004.05.013
Nano-sized Ce-doped YAG phosphor particles were synthesized by a mixed solvothermal method using the stoichiometric amounts of inorganic aluminum and yttrium salts. The formation of YAG:Ce was investigated by means of XRD and TG-DTA. The purified YAG crystalline phases was obtained under moderate synthesis condition (300 °C and 10 MPa), this indicated that ethanol replaced part of water as solvent favoring the formation of YAG. TEM images showed that YAG:Ce phosphor particles were basically spherical in shape, well dispersed and a mean grain size about 60 nm. The particle absorbed excitation energy in the range 403–510 nm, and the maximum excitation wavelength was near 470 nm. The crystalline YAG:Ce showed broad emission peaks in the range 480–650 nm and had maximum intensity at 528 nm. The excitation and emission intensity increased with increasing the synthesis temperature from 280 to 300 °C, and get the maximum brightness at 300 °C.
Co-reporter:Xia Li, Hong Liu, Ji-yang Wang, Hong-mei Cui, Feng Han, Xu-dong Zhang, R.I. Boughton
Materials Letters 2004 Volume 58(Issue 19) pp:2377-2380
Publication Date(Web):July 2004
DOI:10.1016/j.matlet.2004.02.011
Nano-sized powders of aluminum yttrium garnet (YAG) have been successfully synthesized by a mixed solvo-thermal method at low temperature (300 °C) and low pressure (10 MPa). The phase transformation, composition and micro-structural features of the crystalline samples were characterized by X-ray powder diffraction, IR and TEM techniques. It was found that type of solvent, reaction temperature and time were important factors in the YAG synthesis process. X-ray powder diffraction pattern indicated that the pure phase YAG was synthesized in mixed solvent at 300 °C. The transmission electron microscopy (TEM) revealed the averaged size of crystallite was 20 nm and well dispersed. Moreover, the mechanism for solvo-thermal crystallization of YAG is proposed based on IR results.
Co-reporter:Xia Li, Hong Liu, Jiyang Wang, Xudong Zhang, Hongmei Cui
Optical Materials 2004 Volume 25(Issue 4) pp:407-412
Publication Date(Web):May 2004
DOI:10.1016/j.optmat.2003.10.001
Yttrium aluminum garnet (YAG) nano-sized powder was prepared by co-precipitation method assisted by ultrasonic display using different precipitating agent. The precursor powder can crystallize into YAG phase after being calcined at 900 °C for 2 h, because of the uniformly distribution of Al and Y elements. DTA–TG and IR measurements on the precursor powder obtained were performed to improve the synthesis process. X-ray diffraction was conducted on the powder calcined at different temperatures to investigate the effect of reaction conditions on particle size and phase composition. The powder about 15 nm in diameter with pure YAG was obtained at lower temperature (900 °C) by controlling the pH value, precipitating agent and doping agent.
Co-reporter:Hongmei Cui, Hong Liu, Xia Li, Jiyang Wang, Feng Han, Xudong Zhang, R.I. Boughton
Journal of Solid State Chemistry 2004 Volume 177(Issue 11) pp:4001-4006
Publication Date(Web):November 2004
DOI:10.1016/j.jssc.2004.06.042
Bi2Se3 nanosheets and nanotubes were prepared by a hydrothermal co-reduction method at 150, 180, 200, and 210 °C. Bi2Se3 nanosheets, nanobelts and nanotubes were obtained. The Bi2Se3 nanoflakes are 50–500 nm in width and 2–5 nm in thickness. The Bi2Se3 nanotubes are 5–10 nm in diameter, 80–120 nm in length, and 1.3 nm in wall thickness. X-ray diffraction, transmission electron microscopy, high-resolution transmission electron microscopy, and electron diffraction were employed to characterize the products. Experimental results showed that the nanosheets and the nanotubes are hexagonal in structure with a=4.1354a=4.1354 Å and c=27.4615c=27.4615 Å. A possible formation and crystal growth mechanism of Bi2Se3 nanostructures is proposed.
Co-reporter:Xia Li, Hong Liu, Jiyang Wang, Hongmei Cui, Xudong Zhang, Feng Han
Materials Science and Engineering: A 2004 Volume 379(1–2) pp:347-350
Publication Date(Web):15 August 2004
DOI:10.1016/j.msea.2004.03.014
Nd3+ doped yttrium aluminum garnet Y3Al5O12 (YAG) nano-sized powders were prepared by a co-precipitation method using hydroxypropyl cellulose (HPC) as dispersant. The formation process and structure of the as-prepared sample were investigated by means of TG–DTA, XRD, IR, and TEM. It has been found that the YAG powders were amorphous up to 700 °C and transformed into pure phase YAG crystallite at 900 °C for 2 h, because of the uniformly distribution of Al and Y elements. The size of YAG powder is about 30 nm in diameter and mono-disperse in the presence of HPC. Optical absorption and emission spectra of nano-crystallites versus Nd3+ concentration and sintering temperature were also studied.
Co-reporter:Yaohui Lv, Hong Liu, Wei Zhang, Songlin Ran, Fangli Chi, Bin Yang, Ailin Xia
Journal of Environmental Chemical Engineering (September 2013) Volume 1(Issue 3) pp:526-533
Publication Date(Web):1 September 2013
DOI:10.1016/j.jece.2013.06.019
The nanostructured high-yield visible-light-induced photocatalyst AgI/BiOI was synthesized by a facile and ions-exchange method at room temperature with Bi(NO3)3, AgNO3, and KI. Several characterization methods, such as X-ray powder diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), the Brunauer–Emmett–Teller (BET) surface area, and UV–vis diffuse reflectance spectroscopy, were employed to study the phase structures, morphologies and optical properties of the samples. The photocatalytic properties of the as-prepared products were measured with the degradation of methyl orange (MO), rhodamine (RhB) and methyl blue (MB) at room temperature under visible light irradiation. By analyzing the zeta potential of AgI/BiOI composites, the interaction between the sample and the pollutants has been well investigated. It was found that the AgI amount in the AgI/BiOI composites played an important role in the corresponding photocatalytic properties. The photocatalytic performances of the AgI/BiOI composites were maintained for the cycling experiments.
Co-reporter:Hua Tan, Xiaoning Wang, Dedong Jia, Pin Hao, Yuanhua Sang and Hong Liu
Journal of Materials Chemistry A 2017 - vol. 5(Issue 6) pp:NaN2591-2591
Publication Date(Web):2017/01/03
DOI:10.1039/C6TA10191G
Normally, structural details of the tissue of bio-waste affect the final properties of carbon materials. In this study, we selected two types of bio-wastes, Platanus fruit and willow catkins, to prepare hollow carbon micro-fibers, where their size and microstructure are dependent on the Platanus fruit fibers and willow catkin fibers. The electrode properties of the Platanus-derived hollow micro carbon fibers are much higher than those of the willow-derived micro carbon fibers, although carbonization and activation processes are the same for the two types of materials. It is found that the content of the organic-related elements, C, N, and S, and the content of inorganic ions, K or Na, are different. The high content of N and S induced a high doping concentration of the hollow carbon micro-fibers, which endows the Platanus-derived carbon materials with high conductivity, and the high content of inorganic elements causes a self-activation effect during the carbonization process and results in a special porous microstructure of the Platanus-derived carbon. Therefore, compared with the willow-derived hollow carbon micro-fibers, after carbonization and KOH activation, the hollow carbon micro-fibers derived from Platanus seeds possessed much higher supercapacitor electrode properties. After carbonization and activation under optimized conditions, the specific capacitance of the Platanus- and willow-derived hollow carbon micro-fibers are 304.65 F g−1 and 276.13 F g−1, respectively, at the current density of 0.5 A g−1, with a good rate capability and 88.5% and 81.05% capacity retention at 10 A g−1, respectively. The coin-type symmetric device of these two samples with 6 M KOH electrolyte exhibited a high specific capacitance of 286.5 and 267.5 F g−1, respectively, at 0.25 A g−1 (PFs 900, WFs 800), with an excellent cycling stability and 97.03% and 91.12% capacity retention after 10000 cycles, respectively. This work not only provided two types of promising supercapacitor carbon materials but also, most importantly, offered us clues for the design and synthesis of high-performance electrode materials using the knowledge gleaned from nature.
Co-reporter:Dedong Jia, Xin Yu, Hua Tan, Xuequan Li, Feng Han, Linlin Li and Hong Liu
Journal of Materials Chemistry A 2017 - vol. 5(Issue 4) pp:NaN1525-1525
Publication Date(Web):2016/12/06
DOI:10.1039/C6TA09229B
Hierarchical porous carbon with highly ordered straight micro-channels was prepared though a facile melt vacuum infiltration method using continuous filament glass fiber arrays as the template and glucose as the precursor. The as-prepared carbon material shows high specific surface areas up to 1880 m2 g−1 profited from the unique structure of straight micro-channels. A fine pore structure is formed in the channel wall through KOH activation after the removal of the glass fiber array. Electrochemical evaluation of the carbon material indicates that the hierarchical porous carbon exhibits a high specific capacitance of 283 F g−1 at a current density of 0.25 A g−1 with an alkaline electrolyte (6 M KOH) in a three-electrode system. It also demonstrates excellent cycling stability with a capacity retention of 88.5% over 10000 cycles at a high current density of 6 A g−1. These exciting results demonstrate a very simple and low-cost method for large-scale preparation of electrode materials for supercapacitors.
Co-reporter:Sujie Chang, Qiangbing Wang, Baishan Liu, Yuanhua Sang and Hong Liu
Catalysis Science & Technology (2011-Present) 2017 - vol. 7(Issue 2) pp:NaN532-532
Publication Date(Web):2016/12/19
DOI:10.1039/C6CY02150F
Photocatalysis is an efficient approach for the degradation of organic pollutants, and continuous-flow photodegradation has advantages compared to general photocatalysis, which uses powder photocatalysts. Herein, we present a novel three-dimensional (3D) micro-nano hierarchical photocatalyst, TiO2 nanonetwork–powder metallurgical porous titanium hybrid material (TiO2/porous Ti), for continuous filtration photocatalysis/photoelectrocatalysis prepared through a hydrothermal-based chemical method. A photocatalytic layer of 3D TiO2 nanowire networks self-assembled on the surface of metallic porous Ti channels to form TiO2/porous Ti. The interconnected TiO2 thin nanowire networks with anatase–rutile bi-phases introduce a photocatalytic layer with a high photocatalytic performance. The porous structures and wire-like morphology of metallic titanium can enhance photo-induced carrier transport and separation, and it can act as a 3D electrode for photoelectrocatalysis. A novel continuous-flow photocatalytic reactor was designed by setting a group of TiO2/porous Ti sheets vertically in a quartz box equipped with ultraviolet light-emitting diodes (UV-LEDs). By applying a 0.6 V low electrical bias between the TiO2/porous Ti electrodes and a Pt wire electrode, a device with one layer of TiO2/porous Ti can result in 90% degradation of methyl orange (MO) under acidic conditions with 110 mW cm−2 of UV irradiation over 40 min; a device with three layers of TiO2/porous Ti needs just 10 min to reach the same photodegradation efficiency. The continuous degradation of other model pollutants, Rhodamine B (Rh B) and methylene blue (MB), was also demonstrated for this TiO2/porous Ti hybrid photocatalyst also with high photoelectrocatalytic efficiency. A continuous-flow photoelectrocatalytic reactor equipped with TiO2/porous Ti shows potential for the treatment of water in environmental protection applications.
Co-reporter:Zhenhuan Zhao, Shimeng Hao, Pin Hao, Yuanhua Sang, Ayyakkannu Manivannan, Nianqiang Wu and Hong Liu
Journal of Materials Chemistry A 2015 - vol. 3(Issue 29) pp:NaN15056-15056
Publication Date(Web):2015/06/08
DOI:10.1039/C5TA02770E
The notion of environmental protection and renewable sources for energy conversion and storage has become particularly important nowadays. In this research, a meso-microporous carbon was prepared by the combination of a template method and chemical activation with earth abundant cellulose and lignosulphonate as the sources. The as-synthesized meso-microporous carbon contained mesopores generated by regeneration of cellulose with the assistance of a silica template, and micropores created by chemical activation of carbon. Such a unique porous structure makes the as-synthesized meso-microporous carbon the ideal electrode active material for energy storage. The two-electrode symmetric supercapacitors built using the meso-microporous carbon electrodes show a specific capacitance of 286 F g−1 at a current density of 0.25 A g−1 in aqueous electrolyte. More importantly, the symmetric supercapacitor achieves a high energy density of 13 W h kg−1 while at a high power density of 27 kW kg−1. It is demonstrated that using renewable natural sources for the manufacturing of porous carbon with high performance for energy storage can be an effective way to lower the cost of a supercapacitor.
Co-reporter:Chenguo Hu, Yi Xi, Hong Liu and Zhong Lin Wang
Journal of Materials Chemistry A 2009 - vol. 19(Issue 7) pp:NaN868-868
Publication Date(Web):2009/01/12
DOI:10.1039/B816304A
The composite-hydroxide-mediated (CHM) method is based on the use of molten composite hydroxides as a solvent in chemical reactions at ∼200 °C for the synthesis of a wide range of nanostructures. This review focuses on its recent development with an emphasis on its applications for synthesizing materials of complex oxides, hydroxides, simple oxides, sulfides, selenides, tellurides, fluorides and metals. The principle of this synthesis method is introduced, and the key factors that affect the morphology and size are studied. The advantages of its low synthesis temperature, low pressure and low cost are illustrated through the synthesis of functional wires, rods, belts and other nanostructures.
Co-reporter:Jingjie Cui, Dehui Sun, Weijia Zhou, Hong Liu, Peiguang Hu, Na Ren, Haiming Qin, Zhen Huang, Jianjian Lin and Houyi Ma
Physical Chemistry Chemical Physics 2011 - vol. 13(Issue 20) pp:NaN9237-9237
Publication Date(Web):2011/04/04
DOI:10.1039/C1CP20082H
Two kinds of TiO2 nanobelts were prepared from commercial P-25 powders via an alkaline hydrothermal method with and without an acid etching process. The uncauterized nanobelts (TNs) exhibited a smooth surface, and mixed phases of anatase and TiO2 (B), whereas the cauterized ones (CTNs) displayed a rough surface and a pure anatase structure. TNs and CTNs were then deposited onto a glassy carbon electrode (GCE) surface with a conductive adhesive (CA), and the resulting chemically modified electrodes exhibited electrocatalytic activities in the oxidation of nucleobases in a 0.1 M phosphate buffer solution (PBS) at pH 7.4. For guanine and adenine, well-defined oxidation peaks were observed in voltammetric measurements at about +0.62 and +0.89 V, respectively, at a potential sweep rate of 100 mV s−1, whereas for cytosine, uracil and thymine, the voltammetric features were not obvious. The average surface coverages (Γ) of guanine and adenine on the CTNs/CA/GCE electrode were estimated to be 4.75 × 10−10 and 7.44 × 10−10 mol cm−2, respectively, which were about twice those at the TNs/CA/GCE electrode. The enhanced activity of the CTN-based electrode towards purine nucleobase oxidation was ascribed to the large specific surface area and anatase structures with enhanced (001) facets of the CTN that facilitated adsorption of the analytes onto the electrode surface and charge transport through the electrode surface layer.
Co-reporter:Weijia Zhou, Hong Liu, Robert I. Boughton, Guojun Du, Jianjian Lin, Jiyang Wang and Duo Liu
Journal of Materials Chemistry A 2010 - vol. 20(Issue 29) pp:NaN6008-6008
Publication Date(Web):2010/04/16
DOI:10.1039/B927224K
Recent advances in the properties, synthesis, modifications and applications of one-dimensional single-crystalline Ti–O based nanostructures (including nanotubes, nanobelts, nanowires, and nanorods) are reviewed. The physical and chemical properties of one-dimensional nanostructured titanates, such as adsorption, stability, ion-exchange, optical, and proton conductivity properties, are described in connection with a particular application. The experimental parameters, morphologies, and mechanism of formation of one-dimensional nanostructured titanates produced by the alkaline hydrothermal method are critically discussed. Current progress in the modifications of one-dimensional single-crystalline Ti–O based nanostructures are discussed together with their improved performances. Examples of applications of one-dimensional nanostructured titanates in photocatalysis, lithium batteries, sensors, hydrogen production and storage, solar cells and biomedicine are presented.
Co-reporter:Weijia Zhou, Guojun Du, Peiguang Hu, Guohong Li, Dongzhou Wang, Hong Liu, Jiyang Wang, Robert I. Boughton, Duo Liu and Huaidong Jiang
Journal of Materials Chemistry A 2011 - vol. 21(Issue 22) pp:NaN7945-7945
Publication Date(Web):2011/04/27
DOI:10.1039/C1JM10588D
Nanoheterostructures of TiO2 nanoparticles/TiO2 nanobelts and Ag/TiO2 nanoparticles/TiO2 nanobelts are prepared by the acid-assisted hydrothermal method followed by an in situ photo-reduction process. The experimental parameters, including acid corrosion time and calcination temperature, are investigated in detail. Compared with TiO2 nanobelts, the single nanoheterostructure TiO2 nanoparticles/TiO2 nanobelts have a better photocatalytic activity. The double nanoheterostructure Ag/TiO2 nanoparticles/TiO2 nanobelts can further dramatically enhance photocatalytic properties of TiO2 nanobelts. The mechanisms for formation of the heterostructure and the enhanced photocatalytic effect of the heterostructure are discussed. The liquid continuous-flow photocatalysis based on TiO2 nanobelt nanopaper with different heterostructures is carried out, which has an efficient photocatalytic ability. At the same time, the obtained TiO2 nanobelt heterostructures have a good gas sensitive performance for ethanol.
Co-reporter:Jingjie Cui, Dehui Sun, Shaowei Chen, Weijia Zhou, Peiguang Hu, Hong Liu and Zhen Huang
Journal of Materials Chemistry A 2011 - vol. 21(Issue 29) pp:NaN10636-10636
Publication Date(Web):2011/06/21
DOI:10.1039/C1JM11805F
An alkaline hydrothermal and acid etching process was used to prepare surface-coarsened anatase TiO2 nanobelts (CTNs) with enhanced (001) facets. The CTNs were used for electrochemical selective determination of the perfect match and mismatch of single nucleobases at the physiological pH of 7.4. It is supposed that the structure and surface morphology of CTNs play important roles in the nature of the adsorption/bonding and packing density of single base pairs on the nanobelt surfaces. Within the present experimental context, the CTNs are considered to be promising candidates for biosensing of nucleic acids that will be of fundamental significance to diagnostic medicine and molecular biology research.
Co-reporter:Zhenhuan Zhao, Jian Tian, Dongzhou Wang, Xueliang Kang, Yuanhua Sang, Hong Liu, Jiyang Wang, Shaowei Chen, Robert I. Boughton and Huaidong Jiang
Journal of Materials Chemistry A 2012 - vol. 22(Issue 44) pp:NaN23403-23403
Publication Date(Web):2012/09/19
DOI:10.1039/C2JM34580C
Surface engineering of TiO2 nanobelts by the controlled assembly of functional heterostructures represents an effective approach for the synthesis of high-performance photocatalysts. In this study, we prepared a novel Bi2O3/Bi4Ti3O12/TiO2 double-heterostructured nanobelt by depositing bismuth hydroxide onto the TiO2 nanobelt surface. A thermal annealing treatment led to the formation of a Bi4Ti3O12 interlayer that functioned as a bridge to link Bi2O3 and TiO2. The double-heterostructured TiO2 nanobelts exhibited better UV light photocatalytic performance than commercial P25. Importantly, the photocatalytic activity in the visible range was markedly better than that of Bi2O3 and Bi2O3/TiO2 heterostructured TiO2 nanobelts. The enhanced performance was accounted for by the material band structures where the matching was improved by the unique interlayer.
Co-reporter:Jianjian Lin, Jianxing Shen, Ruijun Wang, Jingjie Cui, Weijia Zhou, Peiguang Hu, Duo Liu, Hong Liu, Jiyang Wang, Robert I. Boughton and Yuanzheng Yue
Journal of Materials Chemistry A 2011 - vol. 21(Issue 13) pp:NaN5113-5113
Publication Date(Web):2011/02/23
DOI:10.1039/C0JM04131A
Nano-p–n junction heterostructure TiO2 nanobelts have been produced by assembling p-type semiconductor NiO nanoparticles on n-type TiO2 nanobelts for enhancement of the photocatalytic properties of TiO2 nanobelts. NiO/TiO2 nano-p–n junctions were synthesized on the surfaces of TiO2 nanobelts and surface-coarsened TiO2 nanobelts. The nanobelts were obtained using alkaline- and acid-assisted hydrothermal processes. The chemical-solution-deposition–decomposition process was used to form NiO nanoparticle/TiO2 heterostructure composite nanobelts (NiO-NP/TiO2 NBs), and NiO nanoparticle/surface-coarsened TiO2 heterostructure composite nanobelts (NiO-NP/TiO2 coarsened NBs). The uniform assembly of p-type NiO nanoparticles produces a large number of nano-p–n junction heterostructures on the surface of the TiO2 nanobelts, where NiO and TiO2 form p- and n-type semiconductors, respectively. Compared with both pure NiO nanoparticles and TiO2 nanobelts, NiO-NP/TiO2 NBs exhibit much enhanced photocatalytic activity. Interestingly, the optimized composite NiO-NP/TiO2 coarsened NBs exhibit an enhanced photocatalytic activity in the decomposition of a model dye compound, methyl orange (MO), under both ultraviolet and visible light irradiation. It is argued that the nano-p–n junctions effectively reduce the recombination of electrons and holes, thus leading to the enhancement of the photocatalytic properties of the heterostructure composites. The larger number of abundant photocatalytic-active surfaces in the surface-coarsened nanobelts increases photo-absorption and the production of charge carriers, which gives the composites an enhanced photocatalytic performance. The established approach allows for controlling the nano-p–n junction heterostructure of the nanobelts, and hence, their photocatalytic effect. The NiO/TiO2 nanobelt-based nano-p–n junction heterostructure TiO2 can provide a practical way to design and prepare nano-composites for applications as solar-cell electrodes, in solar photocatalysis, solar photolysis of water and other related fields.
Co-reporter:Na Ren, Rui Li, Limei Chen, Guancong Wang, Duo Liu, Yingjun Wang, Lin Zheng, Wei Tang, Xiaoqiang Yu, Huaidong Jiang, Hong Liu and Nianqiang Wu
Journal of Materials Chemistry A 2012 - vol. 22(Issue 36) pp:NaN19160-19160
Publication Date(Web):2012/07/25
DOI:10.1039/C2JM32434B
A synthetic approach has been developed to in situ construct a new hierarchical nanostructure as an ideal biocompatible and bacteriostatic implant. A highly porous nano-network made of sodium titanate is first formed on the titanium surface by hydrothermal treatment. Silver ions are then inserted between the layered titanate lattices to form silver titanate via ion-exchange with sodium ions. Finally, silver ions are reduced by glucose, leading to the in situ growth of Ag nanoparticles that are sandwiched between layer-structured hydrogen titanate. The amount and the size of the Ag nanoparticles in the titanate–Ag nanoparticles–titanate sandwich can be adjusted by the concentrations of both the AgNO3 and the glucose solutions. The test results show that the silver ions are completely leached from silver titanate after 7 days of immersion in an aqueous solution. In contrast, the Ag ions continue to be released from the titanate–Ag nanoparticle–titanate sandwich nanostructure after 15 days. This steady and prolonged release characteristic is helpful to the long-standing antibacterial process for prevention of severe infection after surgery. A series of antimicrobial and biocompatible tests have shown that the sandwich nanostructure with a low level of silver loading exhibits a bacteriostatic rate as high as 99.99% while retaining low toxicity against cells. The titanate–Ag nanoparticle–titanate sandwich nanostructure, which is fabricated with a low-cost surface modification method, is a promising implantable material that will find applications in artificial bones, joints and dental implants.
Co-reporter:Jingjie Cui, Yakun Ge, Shaowei Chen, Hongshi Zhao, Hong Liu, Zhen Huang, Huaidong Jiang and Jing Chen
Journal of Materials Chemistry A 2013 - vol. 1(Issue 15) pp:NaN2077-2077
Publication Date(Web):2013/02/11
DOI:10.1039/C3TB00227F
Nano-p–n junction heterostructures based on TiO2 nanobelts with enhanced (001) facets were produced by assembling p-type semiconductor NiO nanoparticles on n-type surface-coarsened TiO2 nanobelt surfaces. The heterostructures were then used as the sensing electrode for the electrochemical detection of anticancer drugs O6-benzylguanine (O6BG) and lung cancer cells. O6BG exhibited an irreversible diffusion-controlled electrochemical process with an oxidation peak clearly identified at +0.78 V. For lung cancer cells one oxidation peak was found at +1.1 V and two reduction peaks at +0.30, and +0.90 V. These voltammetric features disappeared when O6BG was added to the lung cancer cells, which was ascribed to the structural changes of the cell membranes caused by the anticancer drug. These results suggested that nano-p–n junction heterostructures based on TiO2 nanobelts might serve as promising candidates for biosensing applications of anticancer drugs and tumor cells that will be of significance in diagnostic medicine, cancer diagnosis and molecular biology research.
Co-reporter:Xiaoyan Li, Chenguo Hu, Xueliang Kang, Qiang Len, Yi Xi, Kaiyou Zhang and Hong Liu
Journal of Materials Chemistry A 2013 - vol. 1(Issue 44) pp:NaN13726-13726
Publication Date(Web):2013/09/19
DOI:10.1039/C3TA12706K
Advanced thermoelectric technology offers the potential to convert waste heat into useful electricity, and a mechanism of transmission-free methods for solid state cooling. A low thermal conductivity is a prerequisite for obtaining high efficiency thermoelectric materials. It is a challenge to achieve low thermal conductivity without simultaneously destroying the electric conductivity, for which a ‘phonon glass/liquid–electron crystal’ is proposed. To realize the phonon glass–electron crystal, a host–guest cage crystal system is considered, while to realize the phonon liquid–electron crystal, superionic conductivity is needed. Here we report a novel material, a KCu7−xS4 nanowire, which exhibits enhanced thermoelectric properties compared to the traditional chalcogenide Cu7S4 nanostructure. The presence of K ions not only forms a clathrate and a superionic fluid structure, which provides the phonon glass and liquid–electron crystal, but also adjusts the product to give a nanowire-like morphology. A low thermal conductivity and large Seebeck coefficient can be achieved when the nanowires are pressed into a bulk material. Higher electrical conductivity is also obtained below 420 K. In addition, the numerous grain boundaries, Cu deficiency and the orientated nanowires further increase the thermoelectric properties. The results indicate a new strategy to obtain high efficiency thermoelectric materials by introducing kalium into copper chalcogenides to form a new crystal structure with ‘phonon glass and liquid–electron crystal’ properties.
Co-reporter:Qinqin Jia, Dongfang Zhao, Bin Tang, Na Zhao, Haidong Li, Yuanhua Sang, Nan Bao, Xiaomei Zhang, Xiaohong Xu and Hong Liu
Journal of Materials Chemistry A 2014 - vol. 2(Issue 38) pp:NaN16298-16298
Publication Date(Web):2014/08/29
DOI:10.1039/C4TA01503G
Au–Cu bimetallic nanoparticles supported on a TiO2-nanobelt (TiO2-NB) have been designed and synthesized by a one-pot photodeposition-galvanic replacement method. TEM observation revealed that small-sized metal nanoparticles (less than 2 nm) were uniformly and finely dispersed on the TiO2 nanobelt. Characterization by XRD coupled with XPS demonstrated that the Au–Cu bimetallic nanoparticles are composed of an Au-rich core/CuOx shell structure. The as-synthesized one-dimensional Au–Cu/TiO2-NB nanostructure can be easily assembled into a paper-like porous monolithic catalyst and applied in heterogeneous catalysis. The formed bimetallic nanopaper catalysts presented synergistically enhanced activity and improved stability for catalyzing the aerobic oxidation of benzyl alcohol compared to their monometallic counterparts. It is likely that the Au–CuOx heterostructure is responsible for the superior catalytic properties of the bimetallic Au–Cu/TiO2-NB catalysts, and the catalytic activity can be significantly affected by the Au/Cu ratio. The uniform and high dispersion of metal nanoparticles on TiO2 nanobelts is also believed to contribute to the stability of Au–Cu/TiO2-NB catalysts, suggesting that the one-dimensional TiO2 nanobelts are a desirable support for the preparation of nanoscale metal catalysts.
Co-reporter:Xingqi Wang, Wenxia Liu, Jian Tian, Zhenhuan Zhao, Pin Hao, Xueliang Kang, Yuanhua Sang and Hong Liu
Journal of Materials Chemistry A 2014 - vol. 2(Issue 8) pp:NaN2608-2608
Publication Date(Web):2013/11/29
DOI:10.1039/C3TA14519K
Uniform well-defined nanostructured BiOBr microspheres have been fabricated via a simple hydrothermal method in the presence of cetyltrimethylammonium bromide (CTAB) and ethylene glycol (EG). The heavy metal ion adsorption on the as-synthesized nanostructured BiOBr microspheres was systematically assessed by measuring the residual concentration during the adsorption process using a colorimetric method for Cr(VI) concentration, and an extraction-colorimetric method for Cd(II) and Pb(II) concentrations. The nanostructured BiOBr microspheres showed good removal capacity for heavy metal ions (Cr, Cd, Pb), and excellent adsorption properties for low concentration heavy metal ions, indicating potential applications in water purification. Based on the quick and efficient heavy metal ion removal ability of nanostructured BiOBr microspheres, a continuous filtering-type water purification device was designed and constructed. In using this continuous filtering type water purification device, 1 g of adsorbent can purify about 4900 g of Pb(II) contaminated water, 5900 g of Cd(II) contaminated water, or 21500 g of Cr(VI) contaminated water having initial concentrations of 200 μg L−1 to successfully attain the World Health Organization standard for drinking water. The good removal capacity can be attributed to the hierarchical nanostructure, which displays a large specific surface area and strong adsorption of heavy metal ions.
Co-reporter:Yu Guan, Na Zhao, Bin Tang, Qinqin Jia, Xiaohong Xu, Hong Liu and Robert I. Boughton
Chemical Communications 2013 - vol. 49(Issue 98) pp:NaN11526-11526
Publication Date(Web):2013/10/24
DOI:10.1039/C3CC45408H
Well-dispersed small Au–Ag bimetallic nanoparticles (sub-3 nm) on one dimensional TiO2 nanobelts were synthesized by a facile successive photodeposition-galvanic replacement method. Based on these Au–Ag/TiO2-NB nanostructures, a porous paper-like monolithic catalyst was fabricated and exhibited synergistically enhanced activity and stability for catalyzing aerobic oxidation of benzyl alcohol.