Co-reporter:Fang Wei;Jian Liu;Ya-Nan Zhu;Xiao-Shi Wang;Chang-Yan Cao
Science China Chemistry 2017 Volume 60( Issue 9) pp:1236-1242
Publication Date(Web):04 July 2017
DOI:10.1007/s11426-017-9042-x
Noble metal nanoparticles (Pd, Ag, Pt, Au) with small and relatively uniform sizes were loaded on polydopamine nanospheres through in situ galvanic replacement reaction in aqueous solution. No additional reductant, surfactant or organic solvent was needed. X-ray photoelectron spectroscopy results revealed that the amount of quinone increased, while the amount of phenolic hydroxyl decreased on PDA nanospheres, indicating that the galvanic displacement reaction occurred between catechol groups and noble metal ions. The as-prepared PDA/Pd exhibited high catalytic activity and excellent stability in styrene hydrogenation. Moreover, PDA spheres retains the photo-thermal effect to serve as a nano-sized heater to accelerate the catalytic reactions under near-infrared illumination.
Co-reporter:Fangfang Wei;Qiuyun Zhang;Hong Wu;Changyan Cao;Weiguo Song
Science China Chemistry 2017 Volume 60( Issue 12) pp:1588-1595
Publication Date(Web):22 November 2017
DOI:10.1007/s11426-017-9148-6
Two types of ordered mesoporous ZSM-5 zeolites with different mesopores were synthesized by a two-step method. First, carbonaceous SBA-15 was produced by in situ carbonization of SBA-15/P123 composite. Then the obtained SBA-15/C composite was transformed into crystallized mesoporous ZSM-5 by impregnation TPAOH followed by steam-assisted crystallization. The final calcined samples synthesized with typical SBA-15/P123 precursor showed a wormlike morphology with the mean mesopore size of 4.6 nm, while samples synthesized with the addition of trimethylbenzene as swelling agent in the precursor exhibited the morphology of microsphere with the mesopore size of about 9.5 nm. Both two types of mesoporous ZSM-5 zeolites exhibited large surface area and mesopore structure. The steam-assisted crystallization (SAC) was performed with lower consumption of solvents. This two-step method may also be suitable for synthesizing other ordered mesoporous zeolites used as catalysts in some catalytic processes.
Co-reporter:Sidi Zhang, Jian Liu, Peipei Huang, Hao Wang, ... Weiguo Song
Science Bulletin 2017 Volume 62, Issue 12(Volume 62, Issue 12) pp:
Publication Date(Web):30 June 2017
DOI:10.1016/j.scib.2017.05.019
Conversion of waste biomass to valuable carbonaceous material is a sustainable and environmental benign method for energy and reduction of greenhouse gas emission. Herein, a two-step hydrothermal method was developed to fabricate high performance electrode material from pomelo peels. In the first step, the pomelo peels were transformed to carbonaceous aerogel (CA), which constructed of three-dimensional, sponge-like brown monolith with hierarchical pores, low-density (0.032 g/cm3) and excellent mechanical flexibility. Then, the cobalt nickel aluminum layered double hydroxide (CoNiAl-LDH) was in situ loaded on the surface of CA to form exquisite core-shell structure (CoNiAl-LDH@CA) through the second hydrothermal step. When used as an electrode material for supercapacitor, CoNiAl-LDH@CA exhibited high specific capacitances of 1,134 F/g at 1 A/g and 902 F/g at 10 A/g, respectively. Furthermore, they displayed an excellent cycling stability without an obvious capacitance decrease after 4,000 cycles.A two-step hydrothermal method was developed to fabricate CoNiAl-LDH@carbonaceous aerogel composite from pomelo peels for high performance pseudocapacitor.Download high-res image (138KB)Download full-size image
Co-reporter:Peipei Huang;Jian Liu;Fang Wei;Yanan Zhu;Xiaoshi Wang;Changyan Cao;Weiguo Song
Materials Chemistry Frontiers 2017 vol. 1(Issue 8) pp:1550-1555
Publication Date(Web):2017/07/27
DOI:10.1039/C7QM00079K
Flower-like cobalt aluminum layered double hydroxide (CoAl-LDH) hollow microspheres were synthesized via a one-step solvothermal method without any template. An Ostwald ripening mechanism was proposed for the formation of hollow nanostructures. These flower-like CoAl-LDH hollow microspheres had a high surface area and exhibited excellent selectivity for anionic dyes. The limited space between LDH layers offered size selectivity for adsorbate molecules. For the small molecule methyl orange, the maximum adsorption capacity reached 816.0 mg g−1 under ambient conditions, while for larger molecules such as Eosin B, the adsorption capacity was only 95.1 mg g−1. All these features make the flower-like CoAl-LDH hollow microspheres an excellent adsorbent in water remediation.
Co-reporter:Yu Yu;Xiaofang Wang;Wenyu Gao;Pei Li;Wei Yan;Songmei Wu;Qiuhong Cui;Weiguo Song;Kejian Ding
Journal of Materials Chemistry A 2017 vol. 5(Issue 14) pp:6656-6663
Publication Date(Web):2017/04/04
DOI:10.1039/C6TA10415K
A sandwich-like CeO2/graphene nanocomposite (CeGS) with a uniform thin CeO2 crystalline film coating on reduced graphene oxide is presented. Large amounts of trivalent Ce and abundant oxygen vacancies (VO) were introduced onto the surface of CeGS. Due to the advantageous surficial crystal configuration, this CeGS displayed greatly enhanced catalytic activity and excellent durability for the oxygen reduction reaction (ORR). By DFT calculations, it was demonstrated that the Ce(III)-preponderant and VO-containing surface benefited the intense chemical adsorption and activation of O2 and optimized the intermediate reaction pathways.
Co-reporter:Chang Liu;Changyan Cao;Jian Liu;Xiaoshi Wang;Yanan Zhu;Weiguo Song
Journal of Materials Chemistry A 2017 vol. 5(Issue 33) pp:17464-17469
Publication Date(Web):2017/08/22
DOI:10.1039/C7TA04187J
The precise sizes of zeolites’ micropores can induce sharp shape/size-selectivity with precision of less than 1 Å in gas-phase reactions, e.g. methanol to olefin reactions (MTO). However, it is still a major challenge and an unachieved task in liquid-phase reactions. In this study, we demonstrate that shape-selectivity with one-methyl-group-precision can be realized in Knoevenagel condensation reactions on basic active sites encapsulated in zeolite crystals. Furthermore, Pd nanoparticles can also be introduced to the interior of hollow zeolite crystals, resulting in a multifunctional and shape-selective catalyst in a one-pot Knoevenagel condensation–hydrogenation cascade reaction.
Co-reporter:Yu Yu;Wei Yan;Wenyu Gao;Pei Li;Xiaofang Wang;Songmei Wu;Weiguo Song;Kejian Ding
Journal of Materials Chemistry A 2017 vol. 5(Issue 33) pp:17199-17203
Publication Date(Web):2017/08/22
DOI:10.1039/C7TA05744J
A facile strategy to fabricate modified g-C3N4 with all-carbon aromatic rings incorporated in the constitutive plane was presented. The light absorption, band structure and photo-induced carrier separation of this benzene doped g-C3N4 was extremely improved. It exhibited a 3 times higher hydrogen evolution rate (HER) and a 17 times higher HER per surface area.
Co-reporter:Zhi-Min Cui;Jing Hao;Chang-Yan Cao;Weiguo Song
Journal of Porous Materials 2017 Volume 24( Issue 1) pp:103-108
Publication Date(Web):2017 February
DOI:10.1007/s10934-016-0242-8
Mesoporous silica (meso-SiO2) was coated on the micro/nanomaterials with hierarchical structure such as flowerlike Fe2O3, flowerlike MgO, SnO2 nanospheres, Co3O4 nanosheets and nanowires from a simple solution method. The structure of the nanomaterials and the silica coating before and after stirring in solution were characterizated by SEM and TEM. The results show that meso-SiO2 coating was an ideal method to enhance the structural stability of fragile nanomaterials. The catalysis stability of flowerlike MgO was also enhanced by the meso-SiO2 coating.
Co-reporter:Yongbin Sun, Changyan Cao, Chang Liu, Jian Liu, Yanan Zhu, Xiaoshi Wang, Weiguo Song
Carbon 2017 Volume 125(Volume 125) pp:
Publication Date(Web):1 December 2017
DOI:10.1016/j.carbon.2017.09.042
Hollow carbon nanospheres have received much interest by virtue of the special shape, low density and large interior void space, allowing their many potential applications. Here we report a template-free route to produce nitrogen-doped hollow porous carbon spheres (denoted as N-HPCSs) through amination reaction of C60 with alkyl diamines and subsequent carbonization. The size of wall thickness and cavity of hollow carbon spheres could be easily regulated by the chain length of alkyl diamines. After carbonization in Ar atmosphere, the obtained N-HPCSs exhibited excellent activity and recyclability for hydrogenation of aromatic nitro compounds with hydrazine hydrate. The facile approach presented in this work provides a new way for preparation of doped hollow porous carbon spheres.Download high-res image (97KB)Download full-size image
Co-reporter:Shuliang Yang;Yanan Zhu;Changyan Cao;Li Peng;Shumu Li;Dewei Zhai;Weiguo Song
Nanoscale (2009-Present) 2017 vol. 9(Issue 36) pp:13538-13545
Publication Date(Web):2017/09/21
DOI:10.1039/C7NR05085B
The construction of core–shell structures through surface coating, and then making use of the synergistic effects between the core and shell to design and synthesize heterogeneous catalysts is a hot topic in the heterogeneous catalysis field. Developing a general coating route with functional shell materials is further highly desirable. Here we found that a poly(cyclotriphosphazene-co-4,4′-sulfonyldiphenol) (PZS) layer can be generally coated on various substrates with different components and morphologies, including metal oxides, noble metal nanoparticles, carbon materials and metal–organic frameworks (MOFs). In addition, the coating thickness could be well controlled through simply adjusting the amount of monomers. Taking advantage of the heteroatoms in the PZS layer and the synergistic effect between the core and shell, new methods for fabrication of co-doped hollow carbon shell catalysts and transition metal phosphide nanoparticles were developed. As a proof-of-concept application, the N, P, S-doped hollow carbon shells prepared by calcination of a ZnCo-ZIFs@PZS core–shell structure could act as a good carbo-catalyst for selective oxidation of C–H bonds in water.
Co-reporter:Shuliang Yang, Peipei Huang, Li Peng, Changyan Cao, Yanan Zhu, Fang Wei, Yongbin Sun and Weiguo Song
Journal of Materials Chemistry A 2016 vol. 4(Issue 2) pp:400-406
Publication Date(Web):16 Nov 2015
DOI:10.1039/C5TA08542J
Three-dimensionally hierarchical flowerlike MgO hollow spheres with an extremely high surface area of 343 m2 g−1 were prepared through a facile and environmentally friendly solvothermal route. The maximum adsorption capacity at natural pH reached 569.7 mg g−1 for the removal of arsenic in water, which is the highest among all of the reported adsorbents. In addition, flowerlike MgO hollow spheres also displayed excellent catalytic activity and stability for the Claisen–Schmidt condensation reaction as a solid base catalyst.
Co-reporter:Shuliang Yang, Changyan Cao, Li Peng, Jianling Zhang, Buxing Han and Weiguo Song
Chemical Communications 2016 vol. 52(Issue 18) pp:3627-3630
Publication Date(Web):27 Jan 2016
DOI:10.1039/C6CC00143B
A new type lead-free catalyst of a Pd–Cu2O nanocomposite was developed for highly selective semi-hydrogenation of alkynes. With unprecedented selectivity for the semi-hydrogenation of terminal alkynes to alkenes, we show for the first time that the catalyst only hydrogenated the terminal alkynes, i.e. did not hydrogenate the internal alkynes.
Co-reporter:Shuliang Yang, Changyan Cao, Li Peng, Peipei Huang, Yongbin Sun, Fang Wei and Weiguo Song
Chemical Communications 2016 vol. 52(Issue 8) pp:1575-1578
Publication Date(Web):10 Nov 2015
DOI:10.1039/C5CC09104G
A new type of spindle-shaped nanoscale yolk/shell magnetic stirring bar containing noble metal nanoparticles was prepared. The as-synthesized Pd–Fe@meso-SiO2 not only showed impressive activity and stability as a heterogeneous catalyst in a macroscopic flask system, but also acted as an efficient nanoscale magnetic stir bar in a microscopic droplet system.
Co-reporter:Zhi-Min Cui, Jing Hao, Jian Liu and Wei-Guo Song
RSC Advances 2016 vol. 6(Issue 78) pp:74545-74549
Publication Date(Web):25 Jul 2016
DOI:10.1039/C6RA15092F
Hierarchical flowerlike Fe2O3 was coated with mesoporous silica to form a Fe2O3@mesoporous silica composite with a core/shell structure through a simple solution-based method with the assistance of Fe2O3 as a precursor. When used as a catalyst for a Fenton-like reaction for the degradation of methylene blue, the Fe2O3 mesoporous silica composite was much more active than the bare flowerlike Fe2O3, which suggests that the catalytic activity of the flowerlike Fe2O3 in the Fenton-like reaction was dramatically enhanced by the mesoporous silica coating.
Co-reporter:Jing Hao, Zhi-Min Cui, Chang-Yan Cao, Weiguo Song
Chemical Physics Letters 2016 Volume 658() pp:88-91
Publication Date(Web):1 August 2016
DOI:10.1016/j.cplett.2016.06.027
Highlights
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A Pd/silica composite was produced from a simple ion-exchange via layered silicate.
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Pd nanoparticles with uniform size were dispersed well on silica lamella.
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The Pd/silica composite showed high catalytic activity to styrene hydrogenation.
Co-reporter:Yongbin Sun;Changyan Cao;Fang Wei;Peipei Huang;Shuliang Yang
Science Bulletin 2016 Volume 61( Issue 10) pp:772-777
Publication Date(Web):2016 May
DOI:10.1007/s11434-016-1070-6
Polymerized fullerene hollow spheres bonded with 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) have been successfully synthesized via amination of C60 with 4-amino-TEMPO in the presence of H2O2, and then cross-linked by 1,6-hexanediamine. The hollow spheres were analyzed by fourier transform infrared spectrometer, electron spin resonance and X-ray photoelectron spectroscopy analysis, which indicated the presence of N–O free radicals in the products. When used as a typical heterogeneous catalyst for selective oxidation of alcohols to the corresponding aldehydes or ketones, it exhibited excellent activities, selectivity and recyclability. This synthesis route is convenient and effective, and may provide a new approach to developing immobilized fullerene based heterogeneous catalysts with high activity and recyclability.在H2O2存在下,4-氨基-TEMPO加成到C60上,经1,6-己二胺交联后,得到TEMPO功能化C60聚合物(C60-TEMPO-HDA)。透射电子显微镜和扫描电子显微镜分析显示聚合物自组装成空心球结构。红外分析、电子自旋共振和X射线光电子能谱确认了氮氧自由基的存在。在醇的选择性氧化反应中,C60-TEMPO-HDA催化剂不仅表现出高的催化活性,而且具有良好的循环稳定性,使用6次后,其活性和结构都没有明显改变。此外,这种合成方法具有一定的普适性,对4-氨基-吡啶和甘氨酸等带有氨基的有机分子也是适用的,为开发其他高效多相催化剂提供了一种新思路。
Co-reporter:Yan Jiang, Bin-Bin Yu, Jie Liu, Zhi-Hua Li, Jian-Kun Sun, Xin-Hua Zhong, Jin-Song Hu, Wei-Guo Song, and Li-Jun Wan
Nano Letters 2015 Volume 15(Issue 5) pp:3088-3095
Publication Date(Web):May 1, 2015
DOI:10.1021/acs.nanolett.5b00096
The key challenges in enhancing the power conversion efficiency (PCE) of a quantum dot-sensitized solar cell (QDSSC) are efficiently achieving charge separation at the photoanode and improving the charge transfer, which is limited by the interface between the electrolyte and the counter electrode (CE). Here, hierarchically assembled ITO@Cu2S nanowire arrays with conductive single-crystalline ITO cores and Cu2S nanocrystal shells were designed as efficient QDSSCs CEs. These arrays not only provided an efficient three-dimensional charge transport network but also allowed for the effective deposition of more Cu2S nanocrystals as active sites to catalyze the electrolyte reaction. This design considerably reduced the sheet and charge transfer resistance of the CE, thus decreasing the series resistance and increasing the shunt resistance of the QDSSC. As a result, QDSSCs with this CE exhibited an unprecedentedly high Voc of 0.688 V, a fill factor of 58.39%, and a PCE of 6.12%, which is 21.2% higher than that of the conventional brass/Cu2S CE.
Co-reporter:Peipei Huang, Changyan Cao, Yongbin Sun, Shuliang Yang, Fang Wei and Weiguo Song
Journal of Materials Chemistry A 2015 vol. 3(Issue 20) pp:10858-10863
Publication Date(Web):15 Apr 2015
DOI:10.1039/C5TA02427G
Layered double hydroxide is one kind of promising material for pseudocapacitors. However, the poor conductivity limits their applications. One possible way to resolve this problem is to mix them with conductive carbon materials. In this work, we developed a one-pot strategy to synthesize sandwich-like nanocomposites with cobalt nickel aluminum layered double hydroxide growth on both sides of different amounts of reduced graphene oxide (RGO(X)@CoNiAl-LDH, X represents the amount of RGO). Such a unique structure is very beneficial for enhancing the conductivity and electrochemical performance. When used as an electrode material for supercapacitors, RGO(25)@CoNiAl-LDH exhibited the best specific capacitance of 1866 F g−1 at a current density of 1 A g−1 and 1360 F g−1 at 10 A g−1, respectively. Furthermore, they displayed excellent cycling performances without an obvious capacitance decrease after 5000 cycles. Such a simple synthesis method, high specific capacitance, rate capability and exceptional cycling stability of these composites offer great promise in energy storage device applications.
Co-reporter:Yu Yu, Wenyu Gao, Zongxu Shen, Qing Zheng, Hao Wu, Xi Wang, Weiguo Song and Kejian Ding
Journal of Materials Chemistry A 2015 vol. 3(Issue 32) pp:16633-16641
Publication Date(Web):09 Jul 2015
DOI:10.1039/C5TA03830H
A novel Ni3N/graphene nanocomposite of small Ni3N nanoparticles anchoring on the reduced graphene oxide nanosheets has been successfully synthesized. Due to the quite small size of Ni3N nanocrystals, the surface for faradic redox reaction of pseudocapacitive materials dramatically increases. The main issue of the volume change obstructing the pseudo-supercapacitor performance is concurrently resolved by the tight attachment of Ni3N nanoparticles with flexible texture. Importantly, the two-step oxidation/reduction reaction between Ni(I) and Ni(III) endows this nanocomposite with large capacitance by providing more faradic charge. The kind of electrode material behaves excellently both in three-electrode and asymmetric supercapacitors. The biggest specific capacitance reaches to 2087.5 F g−1 (at 1 A g−1), and its asymmetric supercapacitor cell with ethylene glycol modified RGO as negative electrode has a high energy density (50.5 W h kg−1 at 800 W kg−1). The cell capacitance retention exceeds 80% after 5000 cycles at different high current densities, showing its promising prospects for high-energy supercapacitors.
Co-reporter:Shuliang Yang, Changyan Cao, Peipei Huang, Li Peng, Yongbin Sun, Fang Wei and Weiguo Song
Journal of Materials Chemistry A 2015 vol. 3(Issue 16) pp:8701-8705
Publication Date(Web):16 Mar 2015
DOI:10.1039/C5TA01744K
Sandwich-like porous TiO2/reduced graphene oxide (rGO) composites were prepared through a facile solvothermal method. These composites with porous structures and high electrical conductivity showed high capacity, rate capability and cycling stability when used as an anode electrode material for lithium ion batteries. A reversible capacity of 206 mA h g−1 can be retained at a current rate of 0.1 A g−1 after 200 charge–discharge cycles. Remarkably, a high reversible capacity of ∼128 mA h g−1 at a current density of 5 A g−1 can be obtained.
Co-reporter:Yongbin Sun, Changyan Cao, Peipei Huang, Shuliang Yang and Weiguo Song
RSC Advances 2015 vol. 5(Issue 105) pp:86082-86087
Publication Date(Web):06 Oct 2015
DOI:10.1039/C5RA16011A
Four kinds of amines functionalized C60 were prepared through an amination reaction of C60 with organic amines. Their surface structures and basic properties were studied by Fourier transform infrared spectrometry (FTIR), X-ray photoelectron spectroscopy (XPS) and temperature-programmed desorption (TPD) with CO2 as the probe molecule. When used as solid base catalysts, N-aminoethylpiperazine functionalized C60 (C60-AEP) showed the best catalytic activity in the Knoevenagel condensation reaction due to the highest basic strength. In addition, the C60-AEP catalyst also showed impressive catalytic stability. All these features endowed C60-AEP with characteristics of both homogeneous and heterogeneous catalysts. More interestingly, chiral L-lysine functionalized C60 (C60-L-L) can be used for asymmetric intermolecular aldol reactions.
Co-reporter:Fang Wei, Changyan Cao, Peipei Huang and Weiguo Song
RSC Advances 2015 vol. 5(Issue 17) pp:13256-13260
Publication Date(Web):19 Jan 2015
DOI:10.1039/C4RA11018H
Excessive fluoride in water has serious effect on people's health and removal of it through adsorption is very effective and important. Developing adsorbents with high adsorption capacities and elucidating the adsorption mechanisms are the two aspects needed to be enhanced. Herein, we reported that basic aluminum carbonate (denoted as Al(OH)CO3) nanospheres with an abundance of carbonate groups exhibited excellent properties for removal of fluoride with maximum adsorption capacity of 59 mg g−1 in neutral solution. In particular, other common anions in water, such as Cl−, NO3−, PO43−, SiO32− and SO42−, had no significant effects on the adsorption properties of Al(OH)CO3 for fluoride. Based on the X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) results, a new ion exchange mechanism involving carbonate groups and fluoride ions in solution was proposed.
Co-reporter:Pei-Pei Huang, Chang-Yan Cao, Fang Wei, Yong-Bin Sun and Wei-Guo Song
RSC Advances 2015 vol. 5(Issue 14) pp:10412-10417
Publication Date(Web):06 Jan 2015
DOI:10.1039/C4RA15160G
Layered double hydroxides (LDHs) are regarded as effective adsorbents to remove arsenic and fluoride ions in water. Compared to thorough research on calcined LDHs, very few works have focused on the adsorption properties and mechanisms of LDHs themselves for these ions. In this manuscript, three-dimensional hierarchical flower-like MgAl layered double hydroxides (MgAl-LDHs) with chloride and carbonate ions as interlayer anions were synthesized via a solvothermal method without any surfactant. When tested as adsorbents for removal of As(V) and F− ions, these hierarchical MgAl-LDHs showed maximum capacities of 125.8 and 28.6 mg g−1, respectively, under neutral conditions. The adsorption mechanisms for As(V) and F− of hierarchical MgAl-LDHs were elucidated by X-ray diffraction patterns, Fourier transformed infrared spectra, X-ray photoelectron spectroscopy and energy dispersive spectra. The results suggested that ion exchange between interlayer anions in hierarchical MgAl-LDHs and As(V) or F− ions was the main adsorption mechanism. Chloride and carbonate ions intercalated in the MgAl-LDHs layers were exchanged with As(V), while only chloride ions were exchanged with F− during adsorption.
Co-reporter:Fang-Fang Wei, Zhi-Min Cui, Xiang-Ju Meng, Chang-Yan Cao, Feng-Shou Xiao, and Wei-Guo Song
ACS Catalysis 2014 Volume 4(Issue 2) pp:529
Publication Date(Web):December 22, 2013
DOI:10.1021/cs400855p
The methanol-to-olefin (MTO) reaction was studied over two one-dimensional 10-ring zeolites with similar pore structures: ZSM-22 (TON) and ZSM-23 (MTT). It was found that the initial low but detectable production of olefins over both zeolites was catalyzed by external and/or pore mouth acid sites through hydrocarbon pool mechanism. Evidence is listed as follows: The uncalcined HZSM-22 had similar MTO activity as the calcined catalyst. The HZSM-22 zeolite with smaller crystal size had higher MTO activity. Both zeolites treated by HNO3 to selectively leach the external acid sites showed significantly reduced initial MTO activity. Both zeolites coked through catalytic cracking of 1,3,5-triisopropylbenzene showed significantly lower initial MTO activity. This conclusion may also be suitable for other one-dimensional zeolites with pore size below 5.7 Å in the MTO reaction.Keywords: acid treatment; coking; external surface; MTO; pore mouth catalysis; ZSM-22 zeolite
Co-reporter:Ping Li, Yu Yu, Hua Liu, Chang-Yan Cao and Wei-Guo Song
Nanoscale 2014 vol. 6(Issue 1) pp:442-448
Publication Date(Web):22 Oct 2013
DOI:10.1039/C3NR04427K
A hierarchical core–shell–satellite structured composite system Fe3O4@MS–NH2@Pd, which was composed of Pd nanoparticles well-dispersed on an amino group functionalized mesoporous silica (MS–NH2) nanosphere, and superparamagnetic Fe3O4 nanoparticles scattered inside the silica sphere, was prepared by using a facile procedure. The composite combined the catalytic properties of amino groups and Pd nanoparticles with superparamagnetic properties of magnetite into a single platform. This integrated nanosystem acted as an efficient magnetically recyclable noble metal-base multifunctional nanocatalyst and showed excellent catalytic activity, selectivity and stability for the direct synthesis of α-alkylated nitriles under mild conditions through facile one-pot multistep cascade reaction sequences.
Co-reporter:Yu Yu, Yongbin Sun, Changyan Cao, Shuliang Yang, Hua Liu, Ping Li, Peipei Huang and Weiguo Song
Journal of Materials Chemistry A 2014 vol. 2(Issue 21) pp:7706-7710
Publication Date(Web):04 Apr 2014
DOI:10.1039/C4TA00905C
Diethylene-glycol/graphene nano-composites were produced by a simple mild solvothermal method, in which diethylene glycol was grafted onto the surfaces of reduced graphene oxides (RGO) as an inter-layer spacer to spatially separate graphene sheets, i.e. to prevent the aggregation of graphene single sheets. The presence of diethylene glycol was confirmed by several characterizations, including IR, XPS, and AFM. Because of the chain length and electrolyte affinity of the diethylene glycol spacer, most of the surface area of graphene single layer sheets could be accessed by electrolyte, leading to high capacity as supercapacitor electrodes with an impressive electrochemical capacitance (237.8 F g−1 at a charging current of 0.1 A g−1), outstanding rate performances (182.9 F g−1 at 20 A g−1), and excellent cycling stabilities (less than 5 and 10% decline after 2000 and 10000 cycles). The diethylene-glycol/graphene nano-composites are thus particularly promising for “high-power densities” and “long cycle life” supercapacitor electrodes.
Co-reporter:Hua Liu, Chang-Yan Cao, Fang-Fang Wei, Pei-Pei Huang, Yong-Bin Sun, Lei Jiang and Wei-Guo Song
Journal of Materials Chemistry A 2014 vol. 2(Issue 10) pp:3557-3562
Publication Date(Web):12 Dec 2013
DOI:10.1039/C3TA14468B
A sublimation method using terephthalic acid (PTA) as the sublimating agent was developed to generate macropores inside electrospun carbon nanofibers. During carbonization of electrospun PTA–polyacrylonitrile composite nanofibers, PTA sublimed and macropores were created within the carbon nanofiber, resulting in flexible and self-sustained carbon film. The carbon nanofiber film showed excellent oil adsorption property with maximum capacities of 62.6, 73.8, 64.0, 94.0 and 138.4 g g−1 for ethanol, pump oil, mineral oil, corn oil and silicone oil. The film exhibited excellent recyclability by rinsing with suitable organic solvent, and promising ability in cleaning up oil spills, as well as fast and efficient separation of oil in oil–water mixtures.
Co-reporter:Yu Yu, Changyan Cao, Hua Liu, Ping Li, Fangfang Wei, Yan Jiang and Weiguo Song
Journal of Materials Chemistry A 2014 vol. 2(Issue 6) pp:1677-1681
Publication Date(Web):15 Nov 2013
DOI:10.1039/C3TA14494A
Under visible light irradiation, excited electrons in heterojunction structure of Bi/BiOCl were transferred into oxygen vacancies states, and then to the Bi metal nanoparticles, resulting in effective separation of electron–hole pairs. The heterojunction photocatalyst exhibited an extraordinary high activity in photodegradation of RhB dye and persistent organic pollutants, i.e. RhB was completely degraded in 2 minutes.
Co-reporter:Ping Li, Yu Yu, Pei-Pei Huang, Hua Liu, Chang-Yan Cao and Wei-Guo Song
Journal of Materials Chemistry A 2014 vol. 2(Issue 2) pp:339-344
Publication Date(Web):17 Oct 2013
DOI:10.1039/C3TA13403B
A core–shell structured nanocomposite, with hexagonal Mg–Al mixed oxide nanoplates derived from LDHs as the inner core and Al-containing mesoporous silica as the outer shell, was prepared using an inorganic, low cost and simple route. The mesoporous silica shell was not only capable of protecting the MgAl-LDO core, but also offered a high surface area for the derivation of functional acid catalytic sites. The MgAl-LDO@Al-MS nanocomposite served as an efficient acid–base bifunctional nanoreactor for one-pot multistep cascade reaction sequences, due to the good spatial separation of antagonistic sites via the core–shell structure design, confinement and enrichment effect of the reaction species endowed by the nanoreactor features.
Co-reporter:Ping Li, Pei-Pei Huang, Fang-Fang Wei, Yong-Bin Sun, Chang-Yan Cao and Wei-Guo Song
Journal of Materials Chemistry A 2014 vol. 2(Issue 32) pp:12739-12745
Publication Date(Web):28 May 2014
DOI:10.1039/C4TA01811G
Uniform 3D flower-like hierarchical-structured CoAl–LDH spheres were prepared via a simple one-pot surfactant-free solvothermal method. Monodispersed tiny Pd nanoclusters (about 2 nm) were loaded on the CoAl–LDH support through a facile in situ reduction between the oxidative Pd precursors and the reductive Co(II) in the support. The resultant CoAl–LDH/Pd composite catalyst showed excellent activities in cross-coupling reactions. In addition, the abundant Co(II) sites in the support can efficiently capture and regenerate leached Pd species during the reaction process, leading to excellent stability of the composite. These two features are desirable in organic synthesis, and may be used on a large scale for cross-coupling reactions with lower cost and easier operation.
Co-reporter:Yan Jiang, Xing Zhang, Qian-Qing Ge, Bin-Bin Yu, Yu-Gang Zou, Wen-Jie Jiang, Jin-Song Hu, Wei-Guo Song, and Li-Jun Wan
ACS Applied Materials & Interfaces 2014 Volume 6(Issue 17) pp:15448
Publication Date(Web):August 19, 2014
DOI:10.1021/am504057y
Among the issues that restrict the power conversion efficiency (PCE) of quantum-dot-sensitized solar cells (QDSSCs), insufficient catalytic activity and stability of counter electrodes (CEs) are critical but challenging ones. The state-of-the-art Cu/Cu2S CEs still suffer from mechanical instability and uncertainty due to the reaction of copper and electrolyte. Herein, ITO@Cu2S core–shell nanowire arrays were developed to fabricate CEs for QDSSCs, which have no such issues in Cu/Cu2S CEs. These nanowire arrays exhibited small charge transfer resistance and sheet resistance, and provided more active catalytic sites and easy accessibility for electrolyte due to the three-dimensional structure upon use as CEs. More interestingly, it was found that the interface of ITO/Cu2S significantly affected the performance of ITO@Cu2S nanowire array CEs. By varying synthetic methods, a series of ITO@Cu2S nanowire arrays were prepared to investigate the influence of ITO/Cu2S interface on their performance. The results showed that ITO@Cu2S nanowire array CEs with a continuous Cu2S nanocrystal shell fabricated via an improved cation exchange route exhibited excellent and thickness-dependent performance. The PCE of corresponding QDSSCs increased by 11.6 and 16.5% compared to that with the discrete Cu2S nanocrystal and the classic Cu/Cu2S CE, respectively, indicating its promising potential as a new type of CE for QDSSCs.Keywords: counter electrodes; interface; nanowires; quantum dots; solar cells
Co-reporter:Yong-Bin Sun, Chang-Yan Cao, Shu-Liang Yang, Pei-Pei Huang, Chun-Ru Wang and Wei-Guo Song
Chemical Communications 2014 vol. 50(Issue 71) pp:10307-10310
Publication Date(Web):18 Jul 2014
DOI:10.1039/C4CC04891A
C60 fullerenol was found to be a highly active, selective and stable catalyst for cycloaddition between CO2 and epoxides to produce various cyclic carbonates with excellent yields (89–99%). A solid/liquid interfacial hydrogen-bond assisted mechanism was proposed to account for its high efficiency.
Co-reporter:Zhifeng Dou, Changyan Cao, Yong Chen and Weiguo Song
Chemical Communications 2014 vol. 50(Issue 94) pp:14889-14891
Publication Date(Web):02 Oct 2014
DOI:10.1039/C4CC05498A
The porous Co3O4 nanowires were fabricated using a fluoride anion-assisted hydrothermal and controlled annealing route. The nanowires showed superior CO gas-sensing performances, such as high selectivity against CO and optimal sensing activity at a relatively low operating temperature (Top ≤ 100 °C). Such properties were ascribed to fluoride doping and porous nanowire structure.
Co-reporter:Fang Niu, Liming Tao, Yuchao Deng, Hong Gao, Jingang Liu and Weiguo Song
New Journal of Chemistry 2014 vol. 38(Issue 12) pp:5695-5699
Publication Date(Web):06 Oct 2014
DOI:10.1039/C4NJ01534G
An amorphous covalent triazine framework, synthesized via an ion thermal method, showed excellent photocatalytic ability for the degradation of methylene blue under visible light illumination. Both the appropriate band edge positions and the good electronic conductivity play key roles in its outstanding photocatalytic performance.
Co-reporter:Fang Niu, Li-Ming Tao, Yu-Chao Deng, Qi-Hua Wang and Wei-Guo Song
New Journal of Chemistry 2014 vol. 38(Issue 6) pp:2269-2272
Publication Date(Web):26 Mar 2014
DOI:10.1039/C4NJ00162A
Phosphorus doped graphene nanosheets were prepared via high-temperature annealing of the graphene oxide and triphenylphosphine mixture. The as-prepared phosphorus doped graphene nanosheets show excellent NH3 sensing ability at room temperature with an enhanced response value compared to thermally reduced graphene.
Co-reporter:Qing Chen, Chang Xue, Wei-Ming Zhang, Wei-Guo Song, Li-Jun Wan, and Kun-Song Ma
Industrial & Engineering Chemistry Research 2014 Volume 53(Issue 34) pp:13467-13474
Publication Date(Web):2017-2-22
DOI:10.1021/ie5023546
Ultrahigh-basicity polyaluminum, an important aluminum industrial product, is manufactured by the oxidation of metallic Al with acids. The process is not economically and chemically efficient because the aluminum atoms were reduced first from alumina to aluminum metal and then oxidized again to get the polyaluminum. In this work, an integrated synthesis system has been built to produce ultrahigh-basicity polyaluminum salts, including polyaluminum chloride, sulfate, and nitrate, from aluminum hydroxide and corresponding acids directly at normal temperature and pressure. Ultrafiltration and electrodialysis with bipolar membranes work in tandem during the synthesis. Aluminum salts are produced naturally from aluminum hydroxide solids and acids in a mixing tank, which are separated as pure solutions via ultrafiltration and then basified in an electrodialysis stack with bipolar membranes to get polyaluminum and regenerate acids as byproducts. These acids are sent back to the mixing tank for reuse again. This integrated system works with maximum atomic economy and low overall cost, which makes it a green process for the production of polyaluminum salts.
Co-reporter:Shu-Liang Yang;Dr. Chang-Yan Cao;Fang-Fang Wei;Pei-Pei Huang;Yong-Bin Sun ; Wei-Guo Song
ChemCatChem 2014 Volume 6( Issue 7) pp:1868-1872
Publication Date(Web):
DOI:10.1002/cctc.201402167
Abstract
Nobel metal nanoparticle loaded carbon nanotube (CNT) composites have wide applications in heterogeneous catalysis, and the catalytic properties are largely controlled by the size, composition, and dispersion state of the noble metal nanoparticles. However, the chemically inert feature of CNTs makes it difficult to directly disperse noble metal nanoparticles in a uniform manner. In this work, by an in situ galvanic replacement reaction between Cu nanoparticles and noble metal ions, a simple and efficient strategy was developed to produce magnetic multiwalled (MW) CNTs–Fe3O4 supported noble metal nanoparticles. The MWCNTs–Fe3O4–Pd showed impressive activity in the carbonylative Sonogashira coupling reaction and in the catalytic hydrodegradation of methylene blue.
Co-reporter:Shu-Liang Yang;Dr. Chang-Yan Cao;Fang-Fang Wei;Pei-Pei Huang;Yong-Bin Sun ; Wei-Guo Song
ChemCatChem 2014 Volume 6( Issue 7) pp:
Publication Date(Web):
DOI:10.1002/cctc.201490041
Co-reporter:Wei Li;Fang Xia;Jin Qu;Ping Li;Dehong Chen;Zhe Chen;Yu Yu;Yu Lu
Nano Research 2014 Volume 7( Issue 6) pp:903-916
Publication Date(Web):2014 June
DOI:10.1007/s12274-014-0452-9
Inorganic-organic hybrid WOx-ethylenediamine (WOx-EDA) nanowires have been produced by a simple, low-cost and high-yield solvothermal method. These WOx-EDA hybrid nanowires have unique lamellar mesostructures with an alternate stacking of an interconnected [WO6] octahedral layer and a monolayer of ethylenediamine molecules. This hybrid structure integrated the functionality of ethylenediamine with the stability of the WOx frameworks. In situ synchrotronradiation X-ray diffraction is used to elucidate a possible formation mechanism of the hybrid WOx-EDA. The nanowire morphology, lamellar structure and abundant functional amino groups endow them with versatile abilities. For example, in heavy metal ion adsorption the WOx-EDA nanowires display exceptional adsorption capabilities of 925 mg·g−1 for Pb2+ and 610 mg·g−1 for UO22+. The nanowires also show outstanding stability and activity as a heterogeneous base catalyst in the Knoevenagel condensation reaction at room temperature. The catalyst can be recycled and reused for 20 cycles with nearly 100% yields. This study provides a new strategy to design inorganic-organic hybrid materials, and offers a multifunctional material that is a highly efficient adsorbent and sustainable catalyst.
Co-reporter:Ping Li, Chang-Yan Cao, Hua Liu, Yu Yu and Wei-Guo Song
Journal of Materials Chemistry A 2013 vol. 1(Issue 41) pp:12804-12810
Publication Date(Web):21 Aug 2013
DOI:10.1039/C3TA13185H
An efficient and facile method was designed to produce an acid–base bifunctional mesoporous silica nanoreactor (MS-SO3H@MS@MS-NH2) with acid sites on the inner core, unfunctionalized silica as the neutral zone shell and basic sites on the outer shell. Such acid core–neutral zone–base shell structure design resulted in excellent spatial separation of the hostile functionalities and was better than that of the core–shell structure. The spatial order of acid sites and basic sites in the mesoporous silica nanosphere offered a designated diffusion pathway that was favorable for reaction species, while the mesoporous structure endowed the material with the confinement effect. As a result, the core–shell–shell structured mesoporous silica nanosphere was an excellent bifunctional catalyst for one-pot cascade reaction sequences.
Co-reporter:Zhe Chen, Yang Yan, Sen Xin, Wei Li, Jin Qu, Yu-Guo Guo and Wei-Guo Song
Journal of Materials Chemistry A 2013 vol. 1(Issue 37) pp:11404-11409
Publication Date(Web):17 Jul 2013
DOI:10.1039/C3TA12344H
Single-crystalline copper germanate (CuGeO3) nanowires were produced and combined with reduced graphene oxide (RGO) via a one-pot hydrothermal route and were used as anode materials for Li-ion batteries (LIBs). After the initial discharge process of CuGeO3, both in situ formed CuO and Ge nanocrystals can serve as the hosts for Li ions, resulting in a large Li storage capacity and a stable cyclability of CuGeO3. The Li storage kinetics of the composite are further enhanced with the RGO conductive network. The CuGeO3@RGO composite exhibited high lithium storage capacity and remarkable cycling performance, and retained 780 mA h g−1 after 130 cycles under the current density of 100 mA g−1. The improved performance of the CuGeO3 nanowires is attributed to the synergetic Li storage effect of the in situ formed CuO and Ge, good electronic conduction of Cu nanocrystals along the length of each nanowire, short Li insertion distances, high interfacial contact area with the electrolyte and improved material durability.
Co-reporter:Fang Niu, Jin-Mei Liu, Li-Ming Tao, Wei Wang and Wei-Guo Song
Journal of Materials Chemistry A 2013 vol. 1(Issue 20) pp:6130-6133
Publication Date(Web):08 Apr 2013
DOI:10.1039/C3TA11070B
Nitrogen and silica co-doped graphene nanosheets (NSi-GNS) have been prepared via high-temperature annealing of N and Si-containing graphene oxide–ionic liquid (GO–IL) composite. As a p-type semiconductor, the as-synthesized NSi-GNS shows excellent NO2 gas sensing ability with high response value.
Co-reporter:Jin Qu, Yang Yan, Ya-Xia Yin, Yu-Guo Guo, and Wei-Guo Song
ACS Applied Materials & Interfaces 2013 Volume 5(Issue 12) pp:5777
Publication Date(Web):May 23, 2013
DOI:10.1021/am401309c
A novel layered zinc silicate/carbon composite was fabricated through carbon embedment into the interlayers of zinc silicate through a hydrothermal method. The interlayer space could be effectively tuned from 1.22 to 3.37 nm by controlling the amount of carbon precursors. Such a layered zinc silicate/carbon structure promoted the lithium ions and electron transportation within the nanostructures, while the reduced graphene oxide (RGO) network improved the conductivity between nanostructures. Such a 3-D carbon based conductive network improved zinc silicates’ lithium storage property. After 50 cycles, two composite samples with different carbon loadings showed 778 mA h/g and 704 mA h/g, respectively.Keywords: 3-D conductive network; layered; Li-ion battery; reduced graphene oxide; zinc silicate;
Co-reporter:Zhi-Min Cui, Zhe Chen, Chang-Yan Cao, Wei-Guo Song and Lei Jiang
Chemical Communications 2013 vol. 49(Issue 54) pp:6093-6095
Publication Date(Web):22 May 2013
DOI:10.1039/C3CC42504E
Flower-like MgO is a highly effective catalyst for the synthesis of dimethyl carbonate through the transesterification method, and coating the catalyst with mesoporous silica significantly enhances the stability of the MgO catalyst.
Co-reporter:Jin Qu, Ya-Xia Yin, Yong-Qing Wang, Yang Yan, Yu-Guo Guo, and Wei-Guo Song
ACS Applied Materials & Interfaces 2013 Volume 5(Issue 9) pp:3932
Publication Date(Web):April 2, 2013
DOI:10.1021/am400670d
A composited anode material with combined layered α-Fe2O3 nanodisks and reduced graphene oxide was produced by an in situ hydrothermal method for lithium-ion batteries. As thin as about 5-nm-thickness α-Fe2O3 nanosheets, open channels, and face-to-face tight contact with reduced graphene oxide via oxygen bridges made the composite have a good cyclability and rate performance, especially at high charge/discharge rates.Keywords: layered nanodisk; Li-ion battery; oxygen bridges; reduced graphene oxide; α-Fe2O3;
Co-reporter:Yu Yu, Chang Yan Cao, Zhe Chen, Hua Liu, Ping Li, Zhi Feng Dou and Wei Guo Song
Chemical Communications 2013 vol. 49(Issue 30) pp:3116-3118
Publication Date(Web):28 Feb 2013
DOI:10.1039/C3CC39212K
A new nanoreactor-type composite catalyst with Au NPs embedded into the inner wall of the mesoporous TiO2 hollow spheres resulted in an enhanced synergistic effect and superb thermal stability of highly dispersed Au NPs.
Co-reporter:Zhi-Min Cui, Zhe Chen, Chang-Yan Cao, Lei Jiang and Wei-Guo Song
Chemical Communications 2013 vol. 49(Issue 23) pp:2332-2334
Publication Date(Web):01 Feb 2013
DOI:10.1039/C3CC38649J
Through a simple polymeric carbon assisted method, a yolk–shell structured Fe2O3@mesoporous SiO2 nanoreactor was synthesized and showed excellent activity in Fenton-like reactions toward methylene blue total degradation.
Co-reporter:Jin-Xia Zhuang, Qing Chen, Shun Wang, Wei-Ming Zhang, Wei-Guo Song, Li-Jun Wan, Kun-Song Ma, Chun-Nian Zhang
Journal of Membrane Science 2013 Volume 432() pp:90-96
Publication Date(Web):1 April 2013
DOI:10.1016/j.memsci.2013.01.016
A zero discharge process was proposed to totally recover both acid and aluminum resource from the waste acid in foil industry. Diffusion dialysis (DD) was coupled with electrodialysis with bipolar membranes (EDBM) in this process, in which most of the free acid was first recovered by DD; and the resulting waste dialysate was further basified by EDBM, recovering aluminum resource and the rest of free acid. Through this process, all components in waste acid were recovered as valuable chemicals, resulting in zero discharge of dangerous effluents. This process is profitable in terms of cost analysis and significantly reduces the environmental burden of foil industry, enabling the foil industry to be more cost-effective, more environmental friendly and more sustainable.Highlights► A zero discharge process was proposed for foil industry waste acid reclamation. ► Diffusion dialysis was coupled with electrodialysis with bipolar membranes. ► Pure aluminum salts or polyaluminum, as well as free acids are recovered. ► This process is profitable in addition to environmental benefits.
Co-reporter:Zhi-Min Cui, Ahmed Mechai, Lin Guo and Wei-Guo Song
RSC Advances 2013 vol. 3(Issue 35) pp:14979-14982
Publication Date(Web):08 Jul 2013
DOI:10.1039/C3RA41941J
A Pd@SnO2 composite with the unique structure of Pd nanoparticles loaded on the inner wall of SnO2 hollow nanospheres was fabricated through a simple multi-step method. This Pd@SnO2 composite was used as a functional material for gas sensing. Compared to SnO2 hollow spheres, the Pd@SnO2 composite showed enhanced hydrogen sensing properties.
Co-reporter:Ping Li;Hua Liu;Yu Yu;Dr. Chang-Yan Cao;Dr. Wei-Guo Song
Chemistry – An Asian Journal 2013 Volume 8( Issue 10) pp:2459-2465
Publication Date(Web):
DOI:10.1002/asia.201300514
Abstract
Two kinds of multifunctional nanocomposites, SBA-15-NH2/Pd-p and SBA-15-NH2/Pd-f, with platelet-like and fiber-like morphologies, respectively, were fabricated by immobilizing Pd NPs onto amine-functionalized SBA-15. Some of the amino groups acted as anchoring sites for Pd NPs, whilst the remaining groups acted as Brønsted basic sites. As a result, the composites served as excellent multifunctional heterogeneous catalysts for one-pot multistep cascade reaction sequences. Moreover, when diffusion was the rate-determine step, SBA-15-NH2/Pd-p, with small mesopores, was superior to the fiber-like control sample, owing to its short diffusion length, a lower possibility of pore clogging, and better mass transportation for the reaction species during the catalysis.
Co-reporter:Hua Liu ; Chang-Yan Cao ; Fang-Fang Wei ; Yan Jiang ; Yong-Bin Sun ; Pei-Pei Huang
The Journal of Physical Chemistry C 2013 Volume 117(Issue 41) pp:21426-21432
Publication Date(Web):September 19, 2013
DOI:10.1021/jp4078807
The 1D hierarchical macroporous/mesoporous carbon nanofibers were prepared via electrospinning using PAN as carbon precursor and commercially available nano-CaCO3 as dual purpose template. During the carbonization process, nano-CaCO3 template decomposed and released CO2 to develop mesopores, and macropores were generated by subsequent acid removal of the as-formed CaO nanoparticles. This method is facile and low cost, allowing high-yield production of 1D hierarchical porous carbon nanofibers. The unique macro-/mesoporous structure of the nanofibers makes them a good support for anchoring palladium nanoparticles; the as-prepared catalyst shows high activity in various Suzuki cross-coupling reactions.
Co-reporter:Jin Qu;Yu Yu;Dr. Chang-Yan Cao; Wei-Guo Song
Chemistry - A European Journal 2013 Volume 19( Issue 34) pp:11172-11177
Publication Date(Web):
DOI:10.1002/chem.201301295
Co-reporter:Dr. Chang-Yan Cao;Fang Wei;Jin Qu ; Wei-Guo Song
Chemistry - A European Journal 2013 Volume 19( Issue 5) pp:1558-1562
Publication Date(Web):
DOI:10.1002/chem.201203986
Co-reporter:Wei Li, Ya-Xia Yin, Sen Xin, Wei-Guo Song and Yu-Guo Guo
Energy & Environmental Science 2012 vol. 5(Issue 7) pp:8007-8013
Publication Date(Web):22 May 2012
DOI:10.1039/C2EE21580B
A series of single-crystalline alkaline earth metal germanate nanowires, including calcium germanate (Ca2Ge7O16), strontium germanate (SrGe4O9) and barium germanate (BaGe4O9) are synthesized by a low-cost, large-scale hydrothermal route. These one-dimensional germanate nanowires represent a new class of anode material for use as Li-ion battery materials with superb lithium storage capacities, cycle performance and rate performance.
Co-reporter:Chang-Yan Cao, Ping Li, Jin Qu, Zhi-Feng Dou, Wen-Sheng Yan, Jun-Fa Zhu, Zi-Yu Wu and Wei-Guo Song
Journal of Materials Chemistry A 2012 vol. 22(Issue 37) pp:19898-19903
Publication Date(Web):01 Aug 2012
DOI:10.1039/C2JM34138G
A fast, low-cost and scalable method was developed to prepare basic aluminum carbonate (Al(OH)CO3) porous nanospheres via a microwave-assisted solvothermal process in 5 min. All chemicals used were low-cost and environmentally benign. These Al(OH)CO3 nanospheres had an extremely large surface area (484 m2 g−1), abundant carbonate groups, and showed superb adsorption properties with maximum capacities of 170 mg g−1 and 60 mg g−1 for As(V) and Cr(VI) at pH 7, respectively. These values were obviously higher than that of many other nanomaterials. In addition, for practical applications, 5 mg Al(OH)CO3 nanospheres could purify 6 kg As(V) contaminated water, reducing the As(V) concentration from 100 ppb to less than 10 ppb. A new adsorption mechanism involving ion exchange between carbonate groups and As(V) or Cr(VI) species was proposed and confirmed.
Co-reporter:Jin Qu, Wei Li, Chang-Yan Cao, Xiao-Jie Yin, Liang Zhao, Jing Bai, Zhi Qin and Wei-Guo Song
Journal of Materials Chemistry A 2012 vol. 22(Issue 33) pp:17222-17226
Publication Date(Web):25 Jun 2012
DOI:10.1039/C2JM33178K
Silica nanotubes with mesoporous walls of 30 nm thickness were used as morphology templates, as well as the silicon source, to produce various metal silicate nanotubes with nanostructured walls, including magnesium silicate, copper silicate, nickel silicate, cobalt silicate and manganese silicate. These silicate materials retained the tubular structure of the templates, which resulted in large surface areas as high as 649 m2 g−1, large total volumes as high as 1.433 cm3 g−1 and facile mass transportation on their surfaces. These features enabled them to be superb adsorbents for adsorption in water; in particular, magnesium silicates showed maximum adsorption capabilities of 929 mg g−1 for uranyl ions and 424 mg g−1 for lead ions, respectively. In practical usage, magnesium silicates could effectively adsorb uranium directly from the salt lake water, with a practical adsorption capacity of 0.23 mg g−1, and was able to enrich the uranium concentration by 8 times.
Co-reporter:Wei Li, Le-Sheng Zhang, Qiong Wang, Yu Yu, Zhe Chen, Chang-Yan Cao and Wei-Guo Song
Journal of Materials Chemistry A 2012 vol. 22(Issue 30) pp:15342-15347
Publication Date(Web):01 Jun 2012
DOI:10.1039/C2JM32031B
With greatly enhanced surface-to-volume ratios, one-dimensional (1D) carbon nanostructures are believed to be able to deliver superior performance as room temperature sensors for explosive gases. 1D carbon nanofibers composed of graphitic nanorolls were prepared using a simple electrospinning-assisted solid-phase graphitization method. This method is facile and low cost and can allow high-yield production of carbon nanofibers. The unique structure of the as-prepared graphitic carbon nanofibers is different from that of conventional 1D carbon nanostructures. It offers the optimal balance between conductivity and adsorption capacity for gas sensing and thus results in remarkable gas-sensing properties in detecting explosive gases including H2, CO, CH4 and ethanol at room temperature.
Co-reporter:Jin Qu, Chang-Yan Cao, You-Li Hong, Chao-Qiu Chen, Pei-Ping Zhu, Wei-Guo Song and Zi-Yu Wu
Journal of Materials Chemistry A 2012 vol. 22(Issue 8) pp:3562-3567
Publication Date(Web):20 Jan 2012
DOI:10.1039/C2JM15841H
A low cost and reliable hydrothermal method was developed for the tunable synthesis of flower-like and urchin-like zinc silicate nanostructures. High resolution TEM, XRD, solid state 29Si NMR spectra and X-ray nanotomography revealed new morphologies and crystal structures. Solid state NMR indicated very different silicon bonding patterns between the two materials. For urchin-like zinc silicates, a synchrotron based three dimensional X-ray nanotomography technique provided unprecedented structural details and revealed structural defects during the assembly process. For flower-like zinc silicates, HRTEM images showed that their secondary nanopetals had a clay-like layered structure, resulting in a higher BET surface area of 236 m2 g−1 as well as higher adsorption capacity for lead ions at 210 mg g−1 than reported zinc silicate samples. The adsorption isotherms and mechanism were investigated.
Co-reporter:Ping Li, Chang-Yan Cao, Zhe Chen, Hua Liu, Yu Yu and Wei-Guo Song
Chemical Communications 2012 vol. 48(Issue 85) pp:10541-10543
Publication Date(Web):31 Aug 2012
DOI:10.1039/C2CC35718F
A core–shell structured mesoporous silica nanosphere with antagonistic acid and basic sites spatially isolated and designated diffusion path was fabricated and served as an efficient acid–base bifunctional catalyst for one-pot cascade reaction sequences with excellent activity and selectivity.
Co-reporter:Zhi-Feng Dou, Chang-Yan Cao, Qiong Wang, Jin Qu, Yu Yu, and Wei-Guo Song
ACS Applied Materials & Interfaces 2012 Volume 4(Issue 10) pp:5698
Publication Date(Web):September 26, 2012
DOI:10.1021/am3016944
X-shaped goethite iron oxide crystals were synthesized by a surfactant-free mild hydrothermal synthesis method with the aid of fluorine ions. The X-shaped goethite crystals could readily self-assemble into microscopic hollow spheres through an oil–water interface induced self-assembly method. X-shaped hematite crystals were obtained by phase topotactic transformation of the goethite precursors. The gas sensor properties of X-shaped hematite iron oxide were investigated, and the mechanism for excellent sensor properties was discussed.Keywords: goethite; hematite; hydrothermal synthesis; phase transformation; self-assembly; sensor;
Co-reporter:Chang-Yan Cao, Jin Qu, Fang Wei, Hua Liu, and Wei-Guo Song
ACS Applied Materials & Interfaces 2012 Volume 4(Issue 8) pp:4283
Publication Date(Web):July 19, 2012
DOI:10.1021/am300972z
A facile method based on microwave-assisted solvothermal process has been developed to synthesize flowerlike MgO precursors, which were then transformed to MgO by simple calcinations. All the chemicals used (magnesium nitrate, urea, and ethanol) were low cost and environmentally benign. The products were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution TEM, and N2 adsorption-desorption methods. These flowerlike MgO nanostructures had high surface area and showed superb adsorption properties for Pb(II) and Cd(II), with maximum capacities of 1980 mg/g and 1500 mg/g, respectively. All these values are significantly higher than those reported on other nanomaterials. A new adsorption mechanism involving solid–liquid interfacial cation exchange between magnesium and lead or cadmium cations was proposed and confirmed.Keywords: adsorption; flowerlike; heavy metal ion; ion exchange; magnesium oxide; nanostructure;
Co-reporter:Wei-Ming Zhang, Jin-Xia Zhuang, Qing Chen, Shun Wang, Wei-Guo Song, and Li-Jun Wan
Industrial & Engineering Chemistry Research 2012 Volume 51(Issue 34) pp:11201
Publication Date(Web):August 17, 2012
DOI:10.1021/ie301048k
An integrated electrolysis system was built to synthesize polyaluminum chloride with ultra high-basicity and even pure Al13. The system converts AlCl3 solution from aluminum electrode foil industry waste to Al13 chloride directly with reasonable cost, typically $1.09 per kilogram as Al2(OH)5Cl·2H2O at 25 °C. Electrolyte temperature and current density were investigated to optimize the process. Ferron assay and 27Al NMR results indicated that the purity of Al13 is over 99% in product solutions. Ion chromatogram analysis confirmed that Cl– ions accounted for about 96.5% in all counteranions. Our integrated system is the first instance to obtain pure Al13 polycations directly. Similar high purity products are only available after tedious purification. This effective and economic synthesis procedure has potential for mass production of Al13 for water treatment and catalyst as well as cosmetic industries.
Co-reporter:Zhe Chen, Zhi-Min Cui, Chang-Yan Cao, Wei-Dong He, Lei Jiang, and Wei-Guo Song
Langmuir 2012 Volume 28(Issue 37) pp:13452-13458
Publication Date(Web):August 21, 2012
DOI:10.1021/la3022535
A nanoreactor with temperature-responsive poly(N-isopopylacrylamide) (PNIPAM) coated on the external pore mouth of mesoporous silica hollow spheres and Au nanoparticles at the internal pore mouth were fabricated. Such spatial separation allows both Au nanoparticles and PNIPAM to function without interfering with each other. Transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectra, and temperature-dependent optical transmittance curves demonstrate successful grafting of PNIPAM. This nanoreactor shows repeated on/off catalytic activity switched by temperature control. It shows excellent catalytic activity toward 4-nitrophenol (4-NP) reduction at 30 °C [below lower critical solution temperature (LCST) of PNIPAM] with a turnover frequency (TOF) of 14.8 h–1. However, when the temperature was 50 °C (above LCST), the TOF dropped to 2.4 h–1. Kinetic studies indicated that diffusion into the mesopores of the catalyst was the key factor, and the temperature-responsive behavior of PNIPAM was able to control this diffusion.
Co-reporter:Chang-Yan Cao, Jin Qu, Wen-Sheng Yan, Jun-Fa Zhu, Zi-Yu Wu, and Wei-Guo Song
Langmuir 2012 Volume 28(Issue 9) pp:4573-4579
Publication Date(Web):February 9, 2012
DOI:10.1021/la300097y
Flowerlike α-Fe2O3 nanostructures were synthesized via a template-free microwave-assisted solvothermal method. All chemicals used were low-cost compounds and environmentally benign. These flowerlike α-Fe2O3 nanostructures had high surface area and abundant hydroxyl on their surface. When tested as an adsorbent for arsenic and chromium removal, the flowerlike α-Fe2O3 nanostructures showed excellent adsorption properties. The adsorption mechanism for AsV and CrVI onto flowerlike α-Fe2O3 nanostructures was elucidated by X-ray photoelectron spectroscopy and synchrotron-based X-ray absorption near edge structure analysis. The results suggested that ion exchange between surface hydroxyl groups and AsV or CrVI species was accounted for by the adsorption. With maximum capacities of 51 and 30 mg g–1 for AsV and CrVI, respectively, these low-cost flowerlike α-Fe2O3 nanostructures are an attractive adsorbent for the removal of AsV and CrVI from water.
Co-reporter:Yu Yu;Changyan Cao;Wei Li;Ping Li;Jin Qu;Weiguo Song
Nano Research 2012 Volume 5( Issue 6) pp:434-442
Publication Date(Web):2012 June
DOI:10.1007/s12274-012-0226-1
Co-reporter:Jin Qu;Dr. Chang-Yan Cao;Zhi-Feng Dou;Hua Liu;Yu Yu;Ping Li; Wei-Guo Song
ChemSusChem 2012 Volume 5( Issue 4) pp:652-655
Publication Date(Web):
DOI:10.1002/cssc.201100839
Co-reporter:Zhe Chen ; Zhi-Min Cui ; Ping Li ; Chang-Yan Cao ; You-Li Hong ; Zi-yu Wu
The Journal of Physical Chemistry C 2012 Volume 116(Issue 28) pp:14986-14991
Publication Date(Web):June 22, 2012
DOI:10.1021/jp303992g
Shape selectivity is one of the crown jewels of catalysis. It is frequently reported on microporous materials, mostly zeolite materials in gas phase reactions, but is rarely reported on mesoporous catalysts in liquid solution. Here we report reactant shape selectivity inside the mesoporous pores of Pd@meso-SiO2 nanoreactor, which is a hollow composite with mesoporous silica walls and Pd nanoparticles residing at the inside pore mouths. The composite has structural features that resemble a nanoreactor and shows extremely high activity for Suzuki cross-coupling reaction between phenylboronic acid and iodobenzene. We observed sharp shape selectivity on phenylboronic acid. N-Butyl phenylboronic acid resulted in an 86% product yield, while tert-butyl phenylboronic acid resulted in a 0% product yield. We propose that nanoreactor feature of the catalyst and collective diffusion barrier induced by the preferential adsorption of bulky phenylboronic acid molecules account for these observations.
Co-reporter:Fang Niu, Jingyi Wu, Lesheng Zhang, Ping Li, Junfa Zhu, Ziyu Wu, Chunru Wang, and Weiguo Song
ACS Catalysis 2011 Volume 1(Issue 10) pp:1158
Publication Date(Web):August 15, 2011
DOI:10.1021/cs200317d
Fullerenol is a superb hydrogen bond catalyst with high catalytic activity, selectivity, and stability in several organic reactions. It exhibits favorable features from both homogeneous and heterogeneous catalysis.Keywords: Aldol reaction; Fullerenol; Henry reaction; heterogeneous catalysis; hydrogen bond catalysis;
Co-reporter:Chaoqiu Chen, Yu Yu, Wei Li, Changyan Cao, Ping Li, Zhifeng Dou and Weiguo Song
Journal of Materials Chemistry A 2011 vol. 21(Issue 34) pp:12836-12841
Publication Date(Web):21 Jul 2011
DOI:10.1039/C1JM11685A
Macroporous networks assembled by interconnected mesoporous Ce1−xZrxO2 solid solution nanofibers were prepared using an electrospinning technique followed by a self-sustaining combustion procedure. This hierarchical porosity helped the mass transfer and resulted in a much higher catalytic activity and stability for the catalytic combustion of volatile organic compounds than bulk and ordered mesoporous Ce1−xZrxO2 materials.
Co-reporter:Chaoqiu Chen, Jin Qu, Changyan Cao, Fang Niu and Weiguo Song
Journal of Materials Chemistry A 2011 vol. 21(Issue 15) pp:5774-5779
Publication Date(Web):10 Mar 2011
DOI:10.1039/C0JM04568C
A one-pot solvothermal synthetic method to prepare uniform CuO colloidal nanocrystal clusters (CNCs) with sizes of approximately 60 nm was developed. To enhance their stabilities, the CuO CNCs were coated with mesoporous SiO2 shells to form CuO CNCs@meso-SiO2 nanocomposites. The CuO CNCs as well as the CuO CNCs@meso-SiO2 composite catalyst were characterized by transmission electron microscopy, small-angle X-ray diffraction and N2adsorption-desorption methods. These results indicate that the SiO2 shells have winding mesoporous channels with an average size of 3.7 nm, which are very favorable for mass transfer and catalytic reactions. This nanocomposite catalyst exhibited excellent activity and stability in olefin epoxidation reactions. The structure of the composite catalyst remained intact after eight consecutive runs, while pure CuO CNCs severely aggregated after only 1 run.
Co-reporter:Chang-Yan Cao, Wei Guo, Zhi-Min Cui, Wei-Guo Song and Wei Cai
Journal of Materials Chemistry A 2011 vol. 21(Issue 9) pp:3204-3209
Publication Date(Web):25 Jan 2011
DOI:10.1039/C0JM03749D
A rapid method based on an efficient gas/liquid interfacial microwave-assisted process has been developed to synthesize flowerlike NiO hollow nanosphere precursors, which were then transformed to NiO by simple calcinations. The wall of the sphere is composed of twisted NiO nanosheets that intercalated with each other. Such hollow structure is different from widely reported flowerlike nanostructures with solid cores. An Ostwald ripening mechanism was proposed for the formation of the hollow nanostructures. The products were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution TEM, energy-dispersive X-ray analysis, and N2adsorption-desorption methods. These flowerlike NiO hollow nanospheres have high surface area of 176 m2 g−1. Electrochemical properties show a high specific capacitance of 585 F g−1 at a discharge current of 5 A g−1 and excellent cycling stability, suggesting its promising potentials in supercapacitors.
Co-reporter:Wei Li, Chang-Yan Cao, Chao-Qiu Chen, Yong Zhao, Wei-Guo Song and Lei Jiang
Chemical Communications 2011 vol. 47(Issue 12) pp:3619-3621
Publication Date(Web):03 Feb 2011
DOI:10.1039/C0CC05485B
Unprecedented multi-channel TiN micro/nanotubes as well as various metal nitride nanofibers, including TiN, VN, NbN and ternary metal nitride nanofibers, were fabricated by a template free electrospinning method combined with post-nitridation.
Co-reporter:Zhi-Min Cui, Zhe Chen, Ling-Yan Jiang, Wei-Guo Song, Lei Jiang
Materials Letters 2011 Volume 65(Issue 1) pp:82-84
Publication Date(Web):15 January 2011
DOI:10.1016/j.matlet.2010.09.032
An Au/Fe3O4 nanocomposite catalyst was fabricated through a simple deposition–precipitation method. The Au/Fe3O4 nanocomposite is a true nanocomposite that has single crystalline Au nanoparticles supported on single crystalline Fe3O4 nanoparticles. Lattice fringes from both Au and Fe3O4 single nanoparticles were simultaneously observed by transmission electron microscope (TEM). This nanocomposite catalyst showed much high activity in low temperature CO oxidation reaction. The Au/Fe3O4 nanocomposite catalyst reaches 100% CO conversion at 40 °C. In comparison, Au/commercial Fe3O4 catalyst needs 375 °C to convert CO. This Au/Fe3O4 nanocomposite is an ideal sample to study synergetic effect between the catalyst and the support at nanoscale.
Co-reporter:Qiong Wang ; Zhi-Min Cui ; Chang-Yan Cao
The Journal of Physical Chemistry C 2011 Volume 115(Issue 50) pp:24987-24992
Publication Date(Web):November 16, 2011
DOI:10.1021/jp209182u
Two one-dimensional zeolite catalysts with similar pore structures and 0.3 Å difference in pore sizes (5.6 Å × 6.0 Å for H-ZSM-12 and 4.6 Å × 5.7 Å for H-ZSM-22) were exploited to gauge the critical sizes of the key intermediate species formed during the methanol conversion to olefins. Both zeolite catalysts are characterized by powder X-ray diffraction, scanning electron microscopy, 27Al solid-state NMR spectroscopy, NH3 temperature-programmed desorption, and N2 adsorption/desorption analysis. In the methanol-to-olefin (MTO) process, the hydrocarbon-pool mechanism worked on the H-ZSM-12 zeolite with the 6.0 Å pore size, while the catalytic cycle could not be completed inside the H-ZSM-22 zeolite with the smaller 5.7 Å pore size. This finding strongly confirms that the hydrocarbon-pool mechanism is a space-demanding process and suggests that the size of key reactive hydrocarbon-pool intermediates for the MTO process is between 5.7 and 6.0 Å. These results will provide a strong experimental base for both theoretical and experimental studies in the MTO process.
Co-reporter:Le-Sheng Zhang, Ling-Yan Jiang, Chao-Qiu Chen, Wei Li, Wei-Guo Song and Yu-Guo Guo
Chemistry of Materials 2010 Volume 22(Issue 2) pp:414
Publication Date(Web):December 2, 2009
DOI:10.1021/cm902973e
Multiwalled carbon nanotubes (MWCNTs) and metal oxide composites, including MWCNTs@SnO2, MWCNTs@ZrO2, MWCNTs@Fe2O3, as well as corresponding metal oxides (MO) hollow structure consisted of SnO2, ZrO2, or CeO2 metal oxide single crystals, respectively, are produced using porous carbonaceous coating and multiwalled carbon nanotube core as dual templates. The synthesis procedure involves programmed steps in which the templates are removed in a controlled sequence. The carbonaceous layer coated on MWCNTs provides porous surface for the adsorption of metal oxide precursors and a buffer zone to help the dispersion of metal oxide nanocrystals. The MWCNTs provide mechanical supports during the whole process before they are removed. MWCNTs@MO nanocomposite are obtained by the removal of the porous carbonaceous layer, and metal oxides hollow structure is produced after the removal of the MWCNTs. MWCNTs@SnO2 nanocomposite shows excellent lithium storage property as anode material for lithium-ion batteries, and SnO2 hollow structure shows high sensitivity and response rate as gas sensor material.
Co-reporter:Fang Niu, Le-Sheng Zhang, Chao-Qiu Chen, Wei Li, Lin Li, Wei-Guo Song and Lei Jiang
Nanoscale 2010 vol. 2(Issue 8) pp:1480-1484
Publication Date(Web):08 Jun 2010
DOI:10.1039/C0NR00182A
TiO2 porous nanospheres on polypropylene (PP) films (TiO2/PP composite) are produced at ambient temperature. Particle/pore size match up is the key anchoring point to overcome the low affinity between hydrophilic materials and hydrophobic materials. With the hydrophilic TiO2 catalyst evenly dispersed on a hydrophobic surface, the aqueous solution will selectively skip the substrate and wet the catalysts. Such a wettability-induced smart system maximizes the degrading activity of the TiO2 catalyst. In photodegrading reactions, the resulting TiO2/PP composite film exhibits a 10 times higher activity in flow-type setup than the same TiO2 catalyst in a traditional batch-type setup.
Co-reporter:Chao-Qiu Chen, Wei Li, Chang-Yan Cao and Wei-Guo Song
Journal of Materials Chemistry A 2010 vol. 20(Issue 33) pp:6968-6974
Publication Date(Web):09 Jul 2010
DOI:10.1039/C0JM01320J
Methane in coal mine ventilation air is a major source of green house gases. The best way to abate its environmental impact is to combust it at moderate temperature. In this work, several oxide nanofibers with perovskite crystal structures, including LaCoO3, LaMnO3, LaFeO3, La0.8Sr0.2CoO3 and La0.9Ce0.1CoO3, were fabricated by an electrospinning method followed by moderate temperature treatment. The as-prepared nanofibers were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, thermal gravimetric and differential thermal analysis, Fourier transform infrared spectroscopy, and a N2 adsorption–desorption method. The results indicated that the pure perovskite oxide nanofibers with high surface areas were formed after 350 °C treatment for 1 h. The perovskite oxide nanofibers exhibited high catalytic activities for the combustion of methane in coal mine ventilation air. 100% methane conversion was reached at a moderate temperature of 470 °C due to the large surface area and porous structure of the La0.8Sr0.2CoO3 perovskite nanofibers.
Co-reporter:Le-Sheng Zhang, Ling-Yan Jiang, Hui-Juan Yan, Wei D. Wang, Wei Wang, Wei-Guo Song, Yu-Guo Guo and Li-Jun Wan
Journal of Materials Chemistry A 2010 vol. 20(Issue 26) pp:5462-5467
Publication Date(Web):03 Jun 2010
DOI:10.1039/C0JM00672F
A two step programmed method is developed to load mono dispersed SnO2 nanoparticles onto single layer graphene sheets. The SnO2-G composite has near mono dispersion of the SnO2 nanocrystals as well as a high SnO2 content of over 60 wt%. These outstanding features are desirable and enable the composite material to be an excellent anode material for Li-ion batteries.
Co-reporter:Zhe Chen, Zhi-Min Cui, Fang Niu, Lei Jiang and Wei-Guo Song
Chemical Communications 2010 vol. 46(Issue 35) pp:6524-6526
Publication Date(Web):10 Aug 2010
DOI:10.1039/C0CC01786H
A true nanoreactor composed of mesoporous silica hollow spheres and Pd nanoparticles residing inside the spheres shows superior activity in Suzuki coupling reactions with 99.5% yield in 3 min.
Co-reporter:Fang Niu, Long Zhang, San-Zhong Luo and Wei-Guo Song
Chemical Communications 2010 vol. 46(Issue 7) pp:1109-1111
Publication Date(Web):23 Dec 2009
DOI:10.1039/B920009F
Fe3O4@Fe(OH)3 composite microspheres are highly active, environmentally friendly and easy to recycle catalysts for aldol reactions, which are catalyzed by a solid–liquid interfacial hydrogen bond catalyst at room temperature.
Co-reporter:Le-Sheng Zhang, Xian-Qing Liang, Wei-Guo Song and Zi-Yu Wu
Physical Chemistry Chemical Physics 2010 vol. 12(Issue 38) pp:12055-12059
Publication Date(Web):19 Aug 2010
DOI:10.1039/C0CP00789G
Heat treatment of graphene oxide (GO) with ammonia flow at various temperatures resulted in different distribution of nitrogen species. Synchrotron based X-ray absorption near-edge structure (XANES) spectroscopy provides unambiguous evidence for the presence of three nitrogen species. The Pt/NG-800 composite exhibits outstanding electrocatalytic activity for methanol oxidation.
Co-reporter:Shao-Wei Bian, Yu-Liang Zhang, Hui-Ling Li, Yu Yu, Yan-Lin Song, Wei-Guo Song
Microporous and Mesoporous Materials 2010 Volume 131(1–3) pp:289-293
Publication Date(Web):June 2010
DOI:10.1016/j.micromeso.2010.01.004
In this paper, we report a procedure using soft/hard dual templates to produce γ-alumina with hierarchically ordered mesopores and macropores (HOMA). Polystyrene spheres colloidal crystals and block co-polymer are sequentially used as templates for ordered macropores and mesopores, respectively. Both macropores and mesopores are ordered pores. The wall of cage-like 500 nm macropores is composed of ordered mesopores of 3.6 nm, and the walls of mesopores are composed of γ-alumina. When loaded with Pt nanoparticles for CO oxidation, Pt/HOMA catalyst shows excellent catalytic properties.
Co-reporter:Chang-Yan Cao;Chao-Qiu Chen;Wei Li; Wei-Guo Song; Wei Cai
ChemSusChem 2010 Volume 3( Issue 11) pp:1241-1244
Publication Date(Web):
DOI:10.1002/cssc.201000229
Co-reporter:Chang-Yan Cao, Zhi-Min Cui, Chao-Qiu Chen, Wei-Guo Song and Wei Cai
The Journal of Physical Chemistry C 2010 Volume 114(Issue 21) pp:9865-9870
Publication Date(Web):May 13, 2010
DOI:10.1021/jp101553x
Ceria hollow nanospheres composed of CeO2 nanocrystals were synthesized via a template-free and microwave-assisted aqueous hydrothermal method. This is a low-cost and environmentally benign method. The chemicals used are all environmentally benign materials (cerium nitrate, urea, and water). An Ostwald ripening mechanism coupled with a self-templated, self-assembly process, in which amorphous solid spheres are converted to crystalline nanocrystals and the latter self-assemble into hollow structures, was proposed for the formation of the hollow structures. The products were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution TEM, energy-dispersive X-ray analysis, X-ray photoelectron spectroscopy, and N2 adsorption−desorption methods. These ceria hollow nanospheres show an excellent adsorption capacity for heavy metal ions, for example, 22.4 mg g−1 for As(V) and 15.4 mg g−1 for Cr(VI). These values are significantly higher than reported data from other ceria nanostructures. These ceria hollow nanospheres are also excellent supports for gold nanoparticles, forming a Au/CeO2 composite catalyst. In CO oxidation, a 100% CO conversion was achieved at room temperature.
Co-reporter:Fang Niu;Yan Jiang;Weiguo Song
Nano Research 2010 Volume 3( Issue 11) pp:757-763
Publication Date(Web):2010 November
DOI:10.1007/s12274-010-0043-3
An in situ method has been used to load Cu2O nanoparticles on the surface of a hydroxyl group rich TiO2 precursor. Cu2O nanoparticles are formed by in situ reduction of Cu(OH)2 with Sn2+ ions linked to the surface of the TiO2 precursor. The initial Cu2O nanoparticles serve as seeds for subsequent particle growth. The resulting Cu2O nanoparticles are evenly dispersed on the surface of the TiO2 precursor, and are heat and air stable. The as-prepared composite is an excellent catalyst for Ullmann type cross coupling reactions of aryl halides with phenol. The composite catalyst also showed good stability, remaining highly active after five consecutive runs.
Co-reporter:Qiong Wang ; Le-Sheng Zhang ; Jian-Feng Wu ; Wei David Wang ; Wei-Guo Song ;Wei Wang
The Journal of Physical Chemistry C 2010 Volume 114(Issue 51) pp:22671-22676
Publication Date(Web):December 9, 2010
DOI:10.1021/jp1098156
Hierarchical three-dimensional flower-like nanostructured SnO2 spheres have been used for a parallel gas sensing and solid-state NMR study. The SnO2 spheres exhibited a good response and reversibility for carbon monoxide, methane, methanol, and ethanol. In a parallel solid-state NMR study, surface carbonate species were observed on SnO2 samples after exposed to all sensing gases (CO, CH4, CH3OH, and CH3CH2OH) at different temperatures. After the SnO2 samples were exposed to CO, CH3OH, and CH3CH2OH, the important intermediate species, e.g., surface formate species and acetate species, were also observed, which could be transformed into carbonate species at higher temperatures. The surface carbonate species would be further decomposed on the SnO2 surface and transformed into the final product CO2. This combined sensing and solid-state NMR study provides crucial information for the surface chemistry during the sensing process.
Co-reporter:Zhi-Min Cui, Ling-Yan Jiang, Wei-Guo Song and Yu-Guo Guo
Chemistry of Materials 2009 Volume 21(Issue 6) pp:1162
Publication Date(Web):February 16, 2009
DOI:10.1021/cm8033609
A beaker-in-autoclave setup is designed for interfacial synthesis of Fe3O4 nanoparticles with precise size control. They exhibit superparamagnetic properties and can be homogeneously incorporated into a carbon matrix to form Fe3O4@C composite, in which Fe3O4 remains highly dispersed in the solid state. The Fe3O4@C composites exhibit excellent cycling and rate performances as anode material for lithium-ion batteries.
Co-reporter:Fang Niu, Jin Zhai, Lei Jiang and Wei-Guo Song
Chemical Communications 2009 (Issue 31) pp:4738-4740
Publication Date(Web):29 Jun 2009
DOI:10.1039/B908834B
UV light switches on the catalytic activities of several metal oxides in hydrogen bond catalyzed reactions because of the changes in the concentration of the surface hydroxyl groups.
Co-reporter:Shao-Wei Bian, Zhuo Ma, Le-Sheng Zhang, Fang Niu and Wei-Guo Song
Chemical Communications 2009 (Issue 10) pp:1261-1263
Publication Date(Web):16 Jan 2009
DOI:10.1039/B821196E
Silica nanotubes with mesoporous walls of 30 nm thickness and various internal morphologies are produced using hard/soft dual templates; this hierarchical pore structure shows faster mass transportation in catalysis.
Co-reporter:Wei-Ming Zhang, Jin-Song Hu, Hai-Tao Ding, Li-Jun Wan and Wei-Guo Song
Analytical Chemistry 2009 Volume 81(Issue 7) pp:2815
Publication Date(Web):February 25, 2009
DOI:10.1021/ac802670q
Nanobarcodes with Morse code patterns are fabricated by a programmed electrochemical deposition process. These bimetallic nanobarcodes are stable and easy to decode using optical or electrical devices. Their discretionally patterned codes offer mass memory capacity for information carriers. They show promising features as probe molecules’ carriers in multiplexing bioanalysis.
Co-reporter:Xing-Long Wu, Qiang Liu, Yu-Guo Guo, Wei-Guo Song
Electrochemistry Communications 2009 Volume 11(Issue 7) pp:1468-1471
Publication Date(Web):July 2009
DOI:10.1016/j.elecom.2009.05.033
Carbon nanosprings (CNSs) with spring diameter of ∼140 nm, carbon ring diameter of ∼100 nm and pitch distance of ∼150 nm, synthesized by using a catalytic chemical vapor deposition technology, have been investigated for potential applicability in lithium batteries as anode materials. The electrochemical results demonstrate that the present CNSs are superior anode materials for rechargeable lithium-ion batteries with high-rate capabilities, as well as long-term cycling life. At a current density as high as 3 A g−1, CNSs can still deliver a reversible capacity of 160 mA h g−1, which is about six times larger than that of graphite and three times larger than that of multi-wall carbon nanotubes under the same current density. After hundreds of cycles, there is no significant capacity loss for CNSs at both low and high current densities. The much improved electrochemical performances could be attributed to the nanometer-sized building blocks as well as the unusual spring-like morphology.
Co-reporter:Le-Sheng Zhang, Wei Li, Zhi-Min Cui and Wei-Guo Song
The Journal of Physical Chemistry C 2009 Volume 113(Issue 48) pp:20594-20598
Publication Date(Web):November 10, 2009
DOI:10.1021/jp907989j
An effective solid-state approach for producing porous and graphitic carbon materials using Fe3O4 nanoparticles embedded into the carbonaceous matrix as catalyst was presented. High dispersion of Fe3O4 nanoparticles enables the solid-state graphitization to be limited at the local region around the Fe3O4 nanoparticles, resulting in porous and graphitic materials. This porous and graphitic material possesses a large specific surface area and a high degree of crystallinity. The materials are characterized by transmission electron microscopy, scanning electron microscopy, Raman spectra, X-ray powder diffraction patterns, and N2 sorption isotherms. High sensitivity and quick response properties were exhibited when this material was used in electrochemical detection of trinitrotoluene due to the porous and graphitic structure.
Co-reporter:Shao-Wei Bian, Zhuo Ma and Wei-Guo Song
The Journal of Physical Chemistry C 2009 Volume 113(Issue 20) pp:8668-8672
Publication Date(Web):April 22, 2009
DOI:10.1021/jp810630k
Carbon nitride nanotubes were produced by using porous anodic aluminum oxide membranes as the template through a polymerization reaction between ethylenediamine and carbon tetrachloride. The synthesized nanotubes were systematically studied by scan electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), Fourier transform IR, X-ray photoelectron spectroscopy (XPS), elemental analysis, and thermogravimetric analysis (TGA). The so-called carbon nitride materials obtained from this method were in fact carbon materials doped with nitrogen, and were partially oxidized. The carbon nitride nanotubes were then loaded with Pt nanoparticles, which are mostly loaded at the outside wall of the nanotubes and show excellent catalytic ability in cyclohexene hydrogenation.
Co-reporter:Jin-Song Hu;Liang-Shu Zhong;Li-Jun Wan
Advanced Materials 2008 Volume 20( Issue 15) pp:2977-2982
Publication Date(Web):
DOI:10.1002/adma.200800623
Abstract
Hierarchically structured metal oxides have two or more levels of structure. Their nanometer-sized building blocks provide a high surface area, a high surface-to-bulk ratio, and surface functional groups that can interact with, e.g., heavy metal ions. Their overall micrometer-sized structure provides desirable mechanical properties, such as robustness, facile species transportation, easy recovery, and regeneration. In combination these features are suitable for the removal of heavy metal ions from water. Several general synthesis routes for the fabrication of metal oxides with various morphologies and hierarchical structures are discussed including soft and hard template-assisted routes. These routes are general, reliable, and environmentally friendly methods to prepare transition and rare earth metal oxides, including cobalt oxide, iron oxide, and ceria. As-prepared hierarchically structured metal oxides show excellent adsorption capacities for AsV and CrVI ions in water.
Co-reporter:Fang Niu, Chang-Chang Liu, Zhi-Min Cui, Jin Zhai, Lei Jiang and Wei-Guo Song
Chemical Communications 2008 (Issue 24) pp:2803-2805
Publication Date(Web):11 Apr 2008
DOI:10.1039/B801361F
Surface hydroxyl group rich nano-structured solids dramatically increase the rate of several organic reactions; such effect is attributed to the formation of interfacial hydrogen bonds between the surface hydroxyl groups and the reactants; this catalytic effect is versatile and applicable for a broad range of reaction conditions.
Co-reporter:Liang-Shu Zhong, Jin-Song Hu, Li-Jun Wan and Wei-Guo Song
Chemical Communications 2008 (Issue 10) pp:1184-1186
Publication Date(Web):11 Jan 2008
DOI:10.1039/B718300C
Highly nanoporous TiO2 (anatase) spheres with an excellent ability in environmental applications have been successfully prepared viain situhydrolysis of titanium glycolate precursor spheres.
Co-reporter:Zhuo Ma ; Qiang Liu ; Zhi-Min Cui ; Shao-Wei Bian
The Journal of Physical Chemistry C 2008 Volume 112(Issue 24) pp:8875-8880
Publication Date(Web):May 22, 2008
DOI:10.1021/jp800703w
A nanotubular catalytic reactor composed of an parallel array of Pt-loaded polyoxometalates/polyelectrolyte nanotubes is presented. Pt/POM composite nanotubes with precisely controlled wall thickness as well as tube inside diameters are prepared by a layer by layer method. Negative-charged polyoxometalates (POMs) and positive-charged polyelectrolytes were alternatively coated onto the inside walls of the porous polycarbonate template. The wall thicknesses as well as the inside diameters of the tubes are precisely controlled by the number of coating bilayers, with a stepwise tailoring at 2.2 nm per step and up to at least 40 steps. Scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, UV, fluorescence spectroscopy, and solid-state NMR characterization of the POM/polyelectrolyte tubes were carried out. The Pt/POM nanotubular reactor with smaller inside diameters shows higher catalytic activities for cyclohexene hydrogenation, indicating promising potential in designing reactors with specific sizes for specific reactions.
Co-reporter:Fang Niu, An-Min Cao, Wei-Guo Song and Li-Jun Wan
The Journal of Physical Chemistry C 2008 Volume 112(Issue 46) pp:17988-17993
Publication Date(Web):2017-2-22
DOI:10.1021/jp807779j
A highly symmetric trapezohedron of lanthanum glycolate precursor is converted to hollow La(OH)3 with the same morphology via a simple hydrothermal treatment of the lanthanum glycolate precursor in an alkaline solution. The formation process of the hollow structure is the result of the Kirkendall effect, in which a new diffusion couple, water and lanthanum glycolate, is proposed. This expands the scope of the Kirkendall effect in material fabrication. The hollow La(OH)3 trapezohedron can be further converted into hollow La2O3 material by calcinations. The as-prepared La(OH)3 hollow trapezohedron shows excellent ability to remove certain organic pollutants in wastewater.
Co-reporter:Shao-Wei Bain, Zhuo Ma, Zhi-Min Cui, Le-Sheng Zhang, Fang Niu and Wei-Guo Song
The Journal of Physical Chemistry C 2008 Volume 112(Issue 30) pp:11340-11344
Publication Date(Web):July 8, 2008
DOI:10.1021/jp802863j
Micrometer-sized nanostructured flowerlike MgO nanostructures were synthesized by an ethylene-glycol-mediated self-assembly process. The synthesized samples were studied systematically by X-ray powder diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, Fourier-transform IR, and energy-dispersive X-ray analysis. The results show that the flowerlike MgO have uniform morphologies with an average diameter of 600 nm for micrometer-sized spheres and 16 nm for the ribbonlike nano building blocks. Compared to hierarchical structured cobalt oxide, a new morphology evolution process is observed for the MgO precursor, indicating a new kinetic control mechanism for morphology evolution. Because of its micrometer-sized nanostructure, the as-obtained MgO shows high catalytic activity, high stability, and easy recovery for the Claisen−Schmidt condensation between benzaldehyde and acetophenone.
Co-reporter:Zhi-Min Cui;Qiang Liu ;Li-Jun Wan
Angewandte Chemie International Edition 2006 Volume 45(Issue 39) pp:
Publication Date(Web):13 SEP 2006
DOI:10.1002/anie.200602488
Com-paring mechanisms: The so-called hydrocarbon pool mechanism does not operate with zeolite ZSM-22 in the methanol-to-olefin (MTO) conversion process as a result of the narrow channels (0.57 nm) in its framework structure. However, this provided a condition free of secondary reactions for detailed mechanistic studies, with H/D exchange patterns of toluene suggesting a paring mechanism.
Co-reporter:Zhi-Min Cui;Qiang Liu ;Li-Jun Wan
Angewandte Chemie 2006 Volume 118(Issue 39) pp:
Publication Date(Web):13 SEP 2006
DOI:10.1002/ange.200602488
Genauer Blick: Der so genannte Kohlenwasserstoffpool-Mechanismus funktioniert bei der Umwandlung von Methanol in Olefine (MTO-Prozess) am Zeolith ZSM-22 wegen der engen Gerüstkanäle (0.57 nm) nicht. Dafür bot dieses System die Möglichkeit zu genauen mechanistischen Studien ohne Störung durch Sekundärreaktionen. Die dabei erhaltenen H/D-Austauschmuster von Toluol sprechen für einen Schälmechanismus (paring mechanism).
Co-reporter:Yongbin Sun, Changyan Cao, Fang Wei, Peipei Huang, ... Weiguo Song
Science Bulletin (May 2016) Volume 61(Issue 10) pp:772-777
Publication Date(Web):1 May 2016
DOI:10.1007/s11434-016-1070-6
Polymerized fullerene hollow spheres bonded with 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) have been successfully synthesized via amination of C60 with 4-amino-TEMPO in the presence of H2O2, and then cross-linked by 1,6-hexanediamine. The hollow spheres were analyzed by fourier transform infrared spectrometer, electron spin resonance and X-ray photoelectron spec troscopy analysis, which indicated the presence of N–O free radicals in the products. When used as a typical heterogeneous catalyst for selective oxidation of alcohols to the corresponding aldehydes or ketones, it exhibited excellent activities, selectivity and recyclability. This synthesis route is convenient and effective, and may provide a new approach to developing immobilized fullerene based heterogeneous catalysts with high activity and recyclability.
Co-reporter:Hua Liu, Changyan Cao, Ping Li, Yu Yu, Weiguo Song
Journal of Energy Chemistry (January 2014) Volume 23(Issue 1) pp:50-56
Publication Date(Web):1 January 2014
DOI:10.1016/S2095-4956(14)60117-0
Core-shell structured nanospheres with mesoporous silica shell and Ni core (denoted as Ni@meso-SiO2) are prepared through a three-step process. Monodispersed Ni precursors are first prepared, and then coated with mesoporous SiO2. Final Ni@meso-SiO2 spheres are obtained after calcination. The products are characterized by X-ray powder diffraction, transmission electron microscopy and N2 adsorption-desorption methods. These spheres have a high surface area and are well dispersed in water, showing a high catalytic activity with a TOF value of 18.5, and outstanding stability in hydrolytic dehydrogenation of ammonia borane at room temperature.Core-shell structured nanospheres with Ni core and mesoporous silica shell are prepared, and they show high catalytic activity with a TOF value of 18.5 molH2 /(molcat·min) and outstanding stability in hydrolytic dehydrogenation of ammonia borane at room temperature.Download full-size image
Co-reporter:Zhi-Min Cui, Qiang Liu, Zhuo Ma, Shao-Wei Bian, Wei-Guo Song
Journal of Catalysis (15 August 2008) Volume 258(Issue 1) pp:83-86
Publication Date(Web):15 August 2008
DOI:10.1016/j.jcat.2008.05.029
In this paper, we studied olefin homologation reactions on zeolite ZSM-22, whose one dimensional pore structure inhibited the hydrocarbon pool mechanism and secondary reactions of the methanol to olefin (MTO) conversion. Homologation of ethylene, propylene and styrene were directly observed between 13C labeled methanol and olefins. Isotopic tracking shows high selectivity for homologation reaction, e.g. from ethylene, propene has one 13C atom, butene has two 13C atoms, and pentene has three 13C atoms. Homologation of styrene's side chain also showed very specific isotopic pattern. The role of olefin homologation is speculated as a key reaction during the induction time of MTO process.
Co-reporter:Le-Sheng Zhang, Xian-Qing Liang, Wei-Guo Song and Zi-Yu Wu
Physical Chemistry Chemical Physics 2010 - vol. 12(Issue 38) pp:NaN12059-12059
Publication Date(Web):2010/08/19
DOI:10.1039/C0CP00789G
Heat treatment of graphene oxide (GO) with ammonia flow at various temperatures resulted in different distribution of nitrogen species. Synchrotron based X-ray absorption near-edge structure (XANES) spectroscopy provides unambiguous evidence for the presence of three nitrogen species. The Pt/NG-800 composite exhibits outstanding electrocatalytic activity for methanol oxidation.
Co-reporter:Le-Sheng Zhang, Ling-Yan Jiang, Hui-Juan Yan, Wei D. Wang, Wei Wang, Wei-Guo Song, Yu-Guo Guo and Li-Jun Wan
Journal of Materials Chemistry A 2010 - vol. 20(Issue 26) pp:NaN5467-5467
Publication Date(Web):2010/06/03
DOI:10.1039/C0JM00672F
A two step programmed method is developed to load mono dispersed SnO2 nanoparticles onto single layer graphene sheets. The SnO2-G composite has near mono dispersion of the SnO2 nanocrystals as well as a high SnO2 content of over 60 wt%. These outstanding features are desirable and enable the composite material to be an excellent anode material for Li-ion batteries.
Co-reporter:Chao-Qiu Chen, Wei Li, Chang-Yan Cao and Wei-Guo Song
Journal of Materials Chemistry A 2010 - vol. 20(Issue 33) pp:NaN6974-6974
Publication Date(Web):2010/07/09
DOI:10.1039/C0JM01320J
Methane in coal mine ventilation air is a major source of green house gases. The best way to abate its environmental impact is to combust it at moderate temperature. In this work, several oxide nanofibers with perovskite crystal structures, including LaCoO3, LaMnO3, LaFeO3, La0.8Sr0.2CoO3 and La0.9Ce0.1CoO3, were fabricated by an electrospinning method followed by moderate temperature treatment. The as-prepared nanofibers were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, thermal gravimetric and differential thermal analysis, Fourier transform infrared spectroscopy, and a N2 adsorption–desorption method. The results indicated that the pure perovskite oxide nanofibers with high surface areas were formed after 350 °C treatment for 1 h. The perovskite oxide nanofibers exhibited high catalytic activities for the combustion of methane in coal mine ventilation air. 100% methane conversion was reached at a moderate temperature of 470 °C due to the large surface area and porous structure of the La0.8Sr0.2CoO3 perovskite nanofibers.
Co-reporter:Chaoqiu Chen, Jin Qu, Changyan Cao, Fang Niu and Weiguo Song
Journal of Materials Chemistry A 2011 - vol. 21(Issue 15) pp:NaN5779-5779
Publication Date(Web):2011/03/10
DOI:10.1039/C0JM04568C
A one-pot solvothermal synthetic method to prepare uniform CuO colloidal nanocrystal clusters (CNCs) with sizes of approximately 60 nm was developed. To enhance their stabilities, the CuO CNCs were coated with mesoporous SiO2 shells to form CuO CNCs@meso-SiO2 nanocomposites. The CuO CNCs as well as the CuO CNCs@meso-SiO2 composite catalyst were characterized by transmission electron microscopy, small-angle X-ray diffraction and N2adsorption-desorption methods. These results indicate that the SiO2 shells have winding mesoporous channels with an average size of 3.7 nm, which are very favorable for mass transfer and catalytic reactions. This nanocomposite catalyst exhibited excellent activity and stability in olefin epoxidation reactions. The structure of the composite catalyst remained intact after eight consecutive runs, while pure CuO CNCs severely aggregated after only 1 run.
Co-reporter:Chaoqiu Chen, Yu Yu, Wei Li, Changyan Cao, Ping Li, Zhifeng Dou and Weiguo Song
Journal of Materials Chemistry A 2011 - vol. 21(Issue 34) pp:NaN12841-12841
Publication Date(Web):2011/07/21
DOI:10.1039/C1JM11685A
Macroporous networks assembled by interconnected mesoporous Ce1−xZrxO2 solid solution nanofibers were prepared using an electrospinning technique followed by a self-sustaining combustion procedure. This hierarchical porosity helped the mass transfer and resulted in a much higher catalytic activity and stability for the catalytic combustion of volatile organic compounds than bulk and ordered mesoporous Ce1−xZrxO2 materials.
Co-reporter:Chang-Yan Cao, Ping Li, Jin Qu, Zhi-Feng Dou, Wen-Sheng Yan, Jun-Fa Zhu, Zi-Yu Wu and Wei-Guo Song
Journal of Materials Chemistry A 2012 - vol. 22(Issue 37) pp:NaN19903-19903
Publication Date(Web):2012/08/01
DOI:10.1039/C2JM34138G
A fast, low-cost and scalable method was developed to prepare basic aluminum carbonate (Al(OH)CO3) porous nanospheres via a microwave-assisted solvothermal process in 5 min. All chemicals used were low-cost and environmentally benign. These Al(OH)CO3 nanospheres had an extremely large surface area (484 m2 g−1), abundant carbonate groups, and showed superb adsorption properties with maximum capacities of 170 mg g−1 and 60 mg g−1 for As(V) and Cr(VI) at pH 7, respectively. These values were obviously higher than that of many other nanomaterials. In addition, for practical applications, 5 mg Al(OH)CO3 nanospheres could purify 6 kg As(V) contaminated water, reducing the As(V) concentration from 100 ppb to less than 10 ppb. A new adsorption mechanism involving ion exchange between carbonate groups and As(V) or Cr(VI) species was proposed and confirmed.
Co-reporter:Jin Qu, Wei Li, Chang-Yan Cao, Xiao-Jie Yin, Liang Zhao, Jing Bai, Zhi Qin and Wei-Guo Song
Journal of Materials Chemistry A 2012 - vol. 22(Issue 33) pp:NaN17226-17226
Publication Date(Web):2012/06/25
DOI:10.1039/C2JM33178K
Silica nanotubes with mesoporous walls of 30 nm thickness were used as morphology templates, as well as the silicon source, to produce various metal silicate nanotubes with nanostructured walls, including magnesium silicate, copper silicate, nickel silicate, cobalt silicate and manganese silicate. These silicate materials retained the tubular structure of the templates, which resulted in large surface areas as high as 649 m2 g−1, large total volumes as high as 1.433 cm3 g−1 and facile mass transportation on their surfaces. These features enabled them to be superb adsorbents for adsorption in water; in particular, magnesium silicates showed maximum adsorption capabilities of 929 mg g−1 for uranyl ions and 424 mg g−1 for lead ions, respectively. In practical usage, magnesium silicates could effectively adsorb uranium directly from the salt lake water, with a practical adsorption capacity of 0.23 mg g−1, and was able to enrich the uranium concentration by 8 times.
Co-reporter:Wei Li, Le-Sheng Zhang, Qiong Wang, Yu Yu, Zhe Chen, Chang-Yan Cao and Wei-Guo Song
Journal of Materials Chemistry A 2012 - vol. 22(Issue 30) pp:NaN15347-15347
Publication Date(Web):2012/06/01
DOI:10.1039/C2JM32031B
With greatly enhanced surface-to-volume ratios, one-dimensional (1D) carbon nanostructures are believed to be able to deliver superior performance as room temperature sensors for explosive gases. 1D carbon nanofibers composed of graphitic nanorolls were prepared using a simple electrospinning-assisted solid-phase graphitization method. This method is facile and low cost and can allow high-yield production of carbon nanofibers. The unique structure of the as-prepared graphitic carbon nanofibers is different from that of conventional 1D carbon nanostructures. It offers the optimal balance between conductivity and adsorption capacity for gas sensing and thus results in remarkable gas-sensing properties in detecting explosive gases including H2, CO, CH4 and ethanol at room temperature.
Co-reporter:Jin Qu, Chang-Yan Cao, You-Li Hong, Chao-Qiu Chen, Pei-Ping Zhu, Wei-Guo Song and Zi-Yu Wu
Journal of Materials Chemistry A 2012 - vol. 22(Issue 8) pp:
Publication Date(Web):
DOI:10.1039/C2JM15841H
Co-reporter:Fang Niu, Jin-Mei Liu, Li-Ming Tao, Wei Wang and Wei-Guo Song
Journal of Materials Chemistry A 2013 - vol. 1(Issue 20) pp:NaN6133-6133
Publication Date(Web):2013/04/08
DOI:10.1039/C3TA11070B
Nitrogen and silica co-doped graphene nanosheets (NSi-GNS) have been prepared via high-temperature annealing of N and Si-containing graphene oxide–ionic liquid (GO–IL) composite. As a p-type semiconductor, the as-synthesized NSi-GNS shows excellent NO2 gas sensing ability with high response value.
Co-reporter:Zhe Chen, Yang Yan, Sen Xin, Wei Li, Jin Qu, Yu-Guo Guo and Wei-Guo Song
Journal of Materials Chemistry A 2013 - vol. 1(Issue 37) pp:NaN11409-11409
Publication Date(Web):2013/07/17
DOI:10.1039/C3TA12344H
Single-crystalline copper germanate (CuGeO3) nanowires were produced and combined with reduced graphene oxide (RGO) via a one-pot hydrothermal route and were used as anode materials for Li-ion batteries (LIBs). After the initial discharge process of CuGeO3, both in situ formed CuO and Ge nanocrystals can serve as the hosts for Li ions, resulting in a large Li storage capacity and a stable cyclability of CuGeO3. The Li storage kinetics of the composite are further enhanced with the RGO conductive network. The CuGeO3@RGO composite exhibited high lithium storage capacity and remarkable cycling performance, and retained 780 mA h g−1 after 130 cycles under the current density of 100 mA g−1. The improved performance of the CuGeO3 nanowires is attributed to the synergetic Li storage effect of the in situ formed CuO and Ge, good electronic conduction of Cu nanocrystals along the length of each nanowire, short Li insertion distances, high interfacial contact area with the electrolyte and improved material durability.
Co-reporter:Yu Yu, Yongbin Sun, Changyan Cao, Shuliang Yang, Hua Liu, Ping Li, Peipei Huang and Weiguo Song
Journal of Materials Chemistry A 2014 - vol. 2(Issue 21) pp:NaN7710-7710
Publication Date(Web):2014/04/04
DOI:10.1039/C4TA00905C
Diethylene-glycol/graphene nano-composites were produced by a simple mild solvothermal method, in which diethylene glycol was grafted onto the surfaces of reduced graphene oxides (RGO) as an inter-layer spacer to spatially separate graphene sheets, i.e. to prevent the aggregation of graphene single sheets. The presence of diethylene glycol was confirmed by several characterizations, including IR, XPS, and AFM. Because of the chain length and electrolyte affinity of the diethylene glycol spacer, most of the surface area of graphene single layer sheets could be accessed by electrolyte, leading to high capacity as supercapacitor electrodes with an impressive electrochemical capacitance (237.8 F g−1 at a charging current of 0.1 A g−1), outstanding rate performances (182.9 F g−1 at 20 A g−1), and excellent cycling stabilities (less than 5 and 10% decline after 2000 and 10000 cycles). The diethylene-glycol/graphene nano-composites are thus particularly promising for “high-power densities” and “long cycle life” supercapacitor electrodes.
Co-reporter:Hua Liu, Chang-Yan Cao, Fang-Fang Wei, Pei-Pei Huang, Yong-Bin Sun, Lei Jiang and Wei-Guo Song
Journal of Materials Chemistry A 2014 - vol. 2(Issue 10) pp:NaN3562-3562
Publication Date(Web):2013/12/12
DOI:10.1039/C3TA14468B
A sublimation method using terephthalic acid (PTA) as the sublimating agent was developed to generate macropores inside electrospun carbon nanofibers. During carbonization of electrospun PTA–polyacrylonitrile composite nanofibers, PTA sublimed and macropores were created within the carbon nanofiber, resulting in flexible and self-sustained carbon film. The carbon nanofiber film showed excellent oil adsorption property with maximum capacities of 62.6, 73.8, 64.0, 94.0 and 138.4 g g−1 for ethanol, pump oil, mineral oil, corn oil and silicone oil. The film exhibited excellent recyclability by rinsing with suitable organic solvent, and promising ability in cleaning up oil spills, as well as fast and efficient separation of oil in oil–water mixtures.
Co-reporter:Ping Li, Yu Yu, Pei-Pei Huang, Hua Liu, Chang-Yan Cao and Wei-Guo Song
Journal of Materials Chemistry A 2014 - vol. 2(Issue 2) pp:NaN344-344
Publication Date(Web):2013/10/17
DOI:10.1039/C3TA13403B
A core–shell structured nanocomposite, with hexagonal Mg–Al mixed oxide nanoplates derived from LDHs as the inner core and Al-containing mesoporous silica as the outer shell, was prepared using an inorganic, low cost and simple route. The mesoporous silica shell was not only capable of protecting the MgAl-LDO core, but also offered a high surface area for the derivation of functional acid catalytic sites. The MgAl-LDO@Al-MS nanocomposite served as an efficient acid–base bifunctional nanoreactor for one-pot multistep cascade reaction sequences, due to the good spatial separation of antagonistic sites via the core–shell structure design, confinement and enrichment effect of the reaction species endowed by the nanoreactor features.
Co-reporter:Peipei Huang, Changyan Cao, Yongbin Sun, Shuliang Yang, Fang Wei and Weiguo Song
Journal of Materials Chemistry A 2015 - vol. 3(Issue 20) pp:NaN10863-10863
Publication Date(Web):2015/04/15
DOI:10.1039/C5TA02427G
Layered double hydroxide is one kind of promising material for pseudocapacitors. However, the poor conductivity limits their applications. One possible way to resolve this problem is to mix them with conductive carbon materials. In this work, we developed a one-pot strategy to synthesize sandwich-like nanocomposites with cobalt nickel aluminum layered double hydroxide growth on both sides of different amounts of reduced graphene oxide (RGO(X)@CoNiAl-LDH, X represents the amount of RGO). Such a unique structure is very beneficial for enhancing the conductivity and electrochemical performance. When used as an electrode material for supercapacitors, RGO(25)@CoNiAl-LDH exhibited the best specific capacitance of 1866 F g−1 at a current density of 1 A g−1 and 1360 F g−1 at 10 A g−1, respectively. Furthermore, they displayed excellent cycling performances without an obvious capacitance decrease after 5000 cycles. Such a simple synthesis method, high specific capacitance, rate capability and exceptional cycling stability of these composites offer great promise in energy storage device applications.
Co-reporter:Yu Yu, Wenyu Gao, Zongxu Shen, Qing Zheng, Hao Wu, Xi Wang, Weiguo Song and Kejian Ding
Journal of Materials Chemistry A 2015 - vol. 3(Issue 32) pp:NaN16641-16641
Publication Date(Web):2015/07/09
DOI:10.1039/C5TA03830H
A novel Ni3N/graphene nanocomposite of small Ni3N nanoparticles anchoring on the reduced graphene oxide nanosheets has been successfully synthesized. Due to the quite small size of Ni3N nanocrystals, the surface for faradic redox reaction of pseudocapacitive materials dramatically increases. The main issue of the volume change obstructing the pseudo-supercapacitor performance is concurrently resolved by the tight attachment of Ni3N nanoparticles with flexible texture. Importantly, the two-step oxidation/reduction reaction between Ni(I) and Ni(III) endows this nanocomposite with large capacitance by providing more faradic charge. The kind of electrode material behaves excellently both in three-electrode and asymmetric supercapacitors. The biggest specific capacitance reaches to 2087.5 F g−1 (at 1 A g−1), and its asymmetric supercapacitor cell with ethylene glycol modified RGO as negative electrode has a high energy density (50.5 W h kg−1 at 800 W kg−1). The cell capacitance retention exceeds 80% after 5000 cycles at different high current densities, showing its promising prospects for high-energy supercapacitors.
Co-reporter:Shuliang Yang, Changyan Cao, Peipei Huang, Li Peng, Yongbin Sun, Fang Wei and Weiguo Song
Journal of Materials Chemistry A 2015 - vol. 3(Issue 16) pp:NaN8705-8705
Publication Date(Web):2015/03/16
DOI:10.1039/C5TA01744K
Sandwich-like porous TiO2/reduced graphene oxide (rGO) composites were prepared through a facile solvothermal method. These composites with porous structures and high electrical conductivity showed high capacity, rate capability and cycling stability when used as an anode electrode material for lithium ion batteries. A reversible capacity of 206 mA h g−1 can be retained at a current rate of 0.1 A g−1 after 200 charge–discharge cycles. Remarkably, a high reversible capacity of ∼128 mA h g−1 at a current density of 5 A g−1 can be obtained.
Co-reporter:Shuliang Yang, Peipei Huang, Li Peng, Changyan Cao, Yanan Zhu, Fang Wei, Yongbin Sun and Weiguo Song
Journal of Materials Chemistry A 2016 - vol. 4(Issue 2) pp:NaN406-406
Publication Date(Web):2015/11/16
DOI:10.1039/C5TA08542J
Three-dimensionally hierarchical flowerlike MgO hollow spheres with an extremely high surface area of 343 m2 g−1 were prepared through a facile and environmentally friendly solvothermal route. The maximum adsorption capacity at natural pH reached 569.7 mg g−1 for the removal of arsenic in water, which is the highest among all of the reported adsorbents. In addition, flowerlike MgO hollow spheres also displayed excellent catalytic activity and stability for the Claisen–Schmidt condensation reaction as a solid base catalyst.
Co-reporter:Zhe Chen, Zhi-Min Cui, Fang Niu, Lei Jiang and Wei-Guo Song
Chemical Communications 2010 - vol. 46(Issue 35) pp:NaN6526-6526
Publication Date(Web):2010/08/10
DOI:10.1039/C0CC01786H
A true nanoreactor composed of mesoporous silica hollow spheres and Pd nanoparticles residing inside the spheres shows superior activity in Suzuki coupling reactions with 99.5% yield in 3 min.
Co-reporter:Wei Li, Chang-Yan Cao, Chao-Qiu Chen, Yong Zhao, Wei-Guo Song and Lei Jiang
Chemical Communications 2011 - vol. 47(Issue 12) pp:NaN3621-3621
Publication Date(Web):2011/02/03
DOI:10.1039/C0CC05485B
Unprecedented multi-channel TiN micro/nanotubes as well as various metal nitride nanofibers, including TiN, VN, NbN and ternary metal nitride nanofibers, were fabricated by a template free electrospinning method combined with post-nitridation.
Co-reporter:Zhi-Min Cui, Zhe Chen, Chang-Yan Cao, Lei Jiang and Wei-Guo Song
Chemical Communications 2013 - vol. 49(Issue 23) pp:NaN2334-2334
Publication Date(Web):2013/02/01
DOI:10.1039/C3CC38649J
Through a simple polymeric carbon assisted method, a yolk–shell structured Fe2O3@mesoporous SiO2 nanoreactor was synthesized and showed excellent activity in Fenton-like reactions toward methylene blue total degradation.
Co-reporter:Ping Li, Chang-Yan Cao, Zhe Chen, Hua Liu, Yu Yu and Wei-Guo Song
Chemical Communications 2012 - vol. 48(Issue 85) pp:NaN10543-10543
Publication Date(Web):2012/08/31
DOI:10.1039/C2CC35718F
A core–shell structured mesoporous silica nanosphere with antagonistic acid and basic sites spatially isolated and designated diffusion path was fabricated and served as an efficient acid–base bifunctional catalyst for one-pot cascade reaction sequences with excellent activity and selectivity.
Co-reporter:Shuliang Yang, Changyan Cao, Li Peng, Peipei Huang, Yongbin Sun, Fang Wei and Weiguo Song
Chemical Communications 2016 - vol. 52(Issue 8) pp:NaN1578-1578
Publication Date(Web):2015/11/10
DOI:10.1039/C5CC09104G
A new type of spindle-shaped nanoscale yolk/shell magnetic stirring bar containing noble metal nanoparticles was prepared. The as-synthesized Pd–Fe@meso-SiO2 not only showed impressive activity and stability as a heterogeneous catalyst in a macroscopic flask system, but also acted as an efficient nanoscale magnetic stir bar in a microscopic droplet system.
Co-reporter:Yu Yu, Xiaofang Wang, Wenyu Gao, Pei Li, Wei Yan, Songmei Wu, Qiuhong Cui, Weiguo Song and Kejian Ding
Journal of Materials Chemistry A 2017 - vol. 5(Issue 14) pp:NaN6663-6663
Publication Date(Web):2017/02/23
DOI:10.1039/C6TA10415K
A sandwich-like CeO2/graphene nanocomposite (CeGS) with a uniform thin CeO2 crystalline film coating on reduced graphene oxide is presented. Large amounts of trivalent Ce and abundant oxygen vacancies (VO) were introduced onto the surface of CeGS. Due to the advantageous surficial crystal configuration, this CeGS displayed greatly enhanced catalytic activity and excellent durability for the oxygen reduction reaction (ORR). By DFT calculations, it was demonstrated that the Ce(III)-preponderant and VO-containing surface benefited the intense chemical adsorption and activation of O2 and optimized the intermediate reaction pathways.
Co-reporter:Peipei Huang, Jian Liu, Fang Wei, Yanan Zhu, Xiaoshi Wang, Changyan Cao and Weiguo Song
Inorganic Chemistry Frontiers 2017 - vol. 1(Issue 8) pp:NaN1555-1555
Publication Date(Web):2017/03/22
DOI:10.1039/C7QM00079K
Flower-like cobalt aluminum layered double hydroxide (CoAl-LDH) hollow microspheres were synthesized via a one-step solvothermal method without any template. An Ostwald ripening mechanism was proposed for the formation of hollow nanostructures. These flower-like CoAl-LDH hollow microspheres had a high surface area and exhibited excellent selectivity for anionic dyes. The limited space between LDH layers offered size selectivity for adsorbate molecules. For the small molecule methyl orange, the maximum adsorption capacity reached 816.0 mg g−1 under ambient conditions, while for larger molecules such as Eosin B, the adsorption capacity was only 95.1 mg g−1. All these features make the flower-like CoAl-LDH hollow microspheres an excellent adsorbent in water remediation.
Co-reporter:Shuliang Yang, Changyan Cao, Li Peng, Jianling Zhang, Buxing Han and Weiguo Song
Chemical Communications 2016 - vol. 52(Issue 18) pp:NaN3630-3630
Publication Date(Web):2016/01/27
DOI:10.1039/C6CC00143B
A new type lead-free catalyst of a Pd–Cu2O nanocomposite was developed for highly selective semi-hydrogenation of alkynes. With unprecedented selectivity for the semi-hydrogenation of terminal alkynes to alkenes, we show for the first time that the catalyst only hydrogenated the terminal alkynes, i.e. did not hydrogenate the internal alkynes.
Co-reporter:Yu Yu, Chang Yan Cao, Zhe Chen, Hua Liu, Ping Li, Zhi Feng Dou and Wei Guo Song
Chemical Communications 2013 - vol. 49(Issue 30) pp:NaN3118-3118
Publication Date(Web):2013/02/28
DOI:10.1039/C3CC39212K
A new nanoreactor-type composite catalyst with Au NPs embedded into the inner wall of the mesoporous TiO2 hollow spheres resulted in an enhanced synergistic effect and superb thermal stability of highly dispersed Au NPs.
Co-reporter:Yong-Bin Sun, Chang-Yan Cao, Shu-Liang Yang, Pei-Pei Huang, Chun-Ru Wang and Wei-Guo Song
Chemical Communications 2014 - vol. 50(Issue 71) pp:NaN10310-10310
Publication Date(Web):2014/07/18
DOI:10.1039/C4CC04891A
C60 fullerenol was found to be a highly active, selective and stable catalyst for cycloaddition between CO2 and epoxides to produce various cyclic carbonates with excellent yields (89–99%). A solid/liquid interfacial hydrogen-bond assisted mechanism was proposed to account for its high efficiency.
Co-reporter:Zhifeng Dou, Changyan Cao, Yong Chen and Weiguo Song
Chemical Communications 2014 - vol. 50(Issue 94) pp:NaN14891-14891
Publication Date(Web):2014/10/02
DOI:10.1039/C4CC05498A
The porous Co3O4 nanowires were fabricated using a fluoride anion-assisted hydrothermal and controlled annealing route. The nanowires showed superior CO gas-sensing performances, such as high selectivity against CO and optimal sensing activity at a relatively low operating temperature (Top ≤ 100 °C). Such properties were ascribed to fluoride doping and porous nanowire structure.
Co-reporter:Zhi-Min Cui, Zhe Chen, Chang-Yan Cao, Wei-Guo Song and Lei Jiang
Chemical Communications 2013 - vol. 49(Issue 54) pp:NaN6095-6095
Publication Date(Web):2013/05/22
DOI:10.1039/C3CC42504E
Flower-like MgO is a highly effective catalyst for the synthesis of dimethyl carbonate through the transesterification method, and coating the catalyst with mesoporous silica significantly enhances the stability of the MgO catalyst.
Co-reporter:Fang Niu, Jin Zhai, Lei Jiang and Wei-Guo Song
Chemical Communications 2009(Issue 31) pp:NaN4740-4740
Publication Date(Web):2009/06/29
DOI:10.1039/B908834B
UV light switches on the catalytic activities of several metal oxides in hydrogen bond catalyzed reactions because of the changes in the concentration of the surface hydroxyl groups.
Co-reporter:Fang Niu, Long Zhang, San-Zhong Luo and Wei-Guo Song
Chemical Communications 2010 - vol. 46(Issue 7) pp:NaN1111-1111
Publication Date(Web):2009/12/23
DOI:10.1039/B920009F
Fe3O4@Fe(OH)3 composite microspheres are highly active, environmentally friendly and easy to recycle catalysts for aldol reactions, which are catalyzed by a solid–liquid interfacial hydrogen bond catalyst at room temperature.
Co-reporter:Shao-Wei Bian, Zhuo Ma, Le-Sheng Zhang, Fang Niu and Wei-Guo Song
Chemical Communications 2009(Issue 10) pp:NaN1263-1263
Publication Date(Web):2009/01/16
DOI:10.1039/B821196E
Silica nanotubes with mesoporous walls of 30 nm thickness and various internal morphologies are produced using hard/soft dual templates; this hierarchical pore structure shows faster mass transportation in catalysis.
Co-reporter:Liang-Shu Zhong, Jin-Song Hu, Li-Jun Wan and Wei-Guo Song
Chemical Communications 2008(Issue 10) pp:NaN1186-1186
Publication Date(Web):2008/01/11
DOI:10.1039/B718300C
Highly nanoporous TiO2 (anatase) spheres with an excellent ability in environmental applications have been successfully prepared viain situhydrolysis of titanium glycolate precursor spheres.
Co-reporter:Fang Niu, Chang-Chang Liu, Zhi-Min Cui, Jin Zhai, Lei Jiang and Wei-Guo Song
Chemical Communications 2008(Issue 24) pp:NaN2805-2805
Publication Date(Web):2008/04/11
DOI:10.1039/B801361F
Surface hydroxyl group rich nano-structured solids dramatically increase the rate of several organic reactions; such effect is attributed to the formation of interfacial hydrogen bonds between the surface hydroxyl groups and the reactants; this catalytic effect is versatile and applicable for a broad range of reaction conditions.
Co-reporter:Yu Yu, Changyan Cao, Hua Liu, Ping Li, Fangfang Wei, Yan Jiang and Weiguo Song
Journal of Materials Chemistry A 2014 - vol. 2(Issue 6) pp:NaN1681-1681
Publication Date(Web):2013/11/15
DOI:10.1039/C3TA14494A
Under visible light irradiation, excited electrons in heterojunction structure of Bi/BiOCl were transferred into oxygen vacancies states, and then to the Bi metal nanoparticles, resulting in effective separation of electron–hole pairs. The heterojunction photocatalyst exhibited an extraordinary high activity in photodegradation of RhB dye and persistent organic pollutants, i.e. RhB was completely degraded in 2 minutes.
Co-reporter:Ping Li, Pei-Pei Huang, Fang-Fang Wei, Yong-Bin Sun, Chang-Yan Cao and Wei-Guo Song
Journal of Materials Chemistry A 2014 - vol. 2(Issue 32) pp:NaN12745-12745
Publication Date(Web):2014/05/28
DOI:10.1039/C4TA01811G
Uniform 3D flower-like hierarchical-structured CoAl–LDH spheres were prepared via a simple one-pot surfactant-free solvothermal method. Monodispersed tiny Pd nanoclusters (about 2 nm) were loaded on the CoAl–LDH support through a facile in situ reduction between the oxidative Pd precursors and the reductive Co(II) in the support. The resultant CoAl–LDH/Pd composite catalyst showed excellent activities in cross-coupling reactions. In addition, the abundant Co(II) sites in the support can efficiently capture and regenerate leached Pd species during the reaction process, leading to excellent stability of the composite. These two features are desirable in organic synthesis, and may be used on a large scale for cross-coupling reactions with lower cost and easier operation.
Co-reporter:Ping Li, Chang-Yan Cao, Hua Liu, Yu Yu and Wei-Guo Song
Journal of Materials Chemistry A 2013 - vol. 1(Issue 41) pp:NaN12810-12810
Publication Date(Web):2013/08/21
DOI:10.1039/C3TA13185H
An efficient and facile method was designed to produce an acid–base bifunctional mesoporous silica nanoreactor (MS-SO3H@MS@MS-NH2) with acid sites on the inner core, unfunctionalized silica as the neutral zone shell and basic sites on the outer shell. Such acid core–neutral zone–base shell structure design resulted in excellent spatial separation of the hostile functionalities and was better than that of the core–shell structure. The spatial order of acid sites and basic sites in the mesoporous silica nanosphere offered a designated diffusion pathway that was favorable for reaction species, while the mesoporous structure endowed the material with the confinement effect. As a result, the core–shell–shell structured mesoporous silica nanosphere was an excellent bifunctional catalyst for one-pot cascade reaction sequences.
Co-reporter:Chang-Yan Cao, Wei Guo, Zhi-Min Cui, Wei-Guo Song and Wei Cai
Journal of Materials Chemistry A 2011 - vol. 21(Issue 9) pp:NaN3209-3209
Publication Date(Web):2011/01/25
DOI:10.1039/C0JM03749D
A rapid method based on an efficient gas/liquid interfacial microwave-assisted process has been developed to synthesize flowerlike NiO hollow nanosphere precursors, which were then transformed to NiO by simple calcinations. The wall of the sphere is composed of twisted NiO nanosheets that intercalated with each other. Such hollow structure is different from widely reported flowerlike nanostructures with solid cores. An Ostwald ripening mechanism was proposed for the formation of the hollow nanostructures. The products were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, high-resolution TEM, energy-dispersive X-ray analysis, and N2adsorption-desorption methods. These flowerlike NiO hollow nanospheres have high surface area of 176 m2 g−1. Electrochemical properties show a high specific capacitance of 585 F g−1 at a discharge current of 5 A g−1 and excellent cycling stability, suggesting its promising potentials in supercapacitors.