Quan Yuan

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Name: 袁荃; Quan Yuan
Organization: Wuhan University , China
Department: College of Chemistry and Molecular Sciences
Title: Professor(PhD)

TOPICS

Co-reporter:Yanbing Yang, Xiangdong Yang, Shasha Chen, Mingchu Zou, Zhihao Li, Anyuan Cao, and Quan Yuan
ACS Applied Materials & Interfaces July 12, 2017 Volume 9(Issue 27) pp:22819-22819
Publication Date(Web):June 22, 2017
DOI:10.1021/acsami.7b05032
Nanostructuring silicon (Si) and combining Si with carbon shells have been studied in recent Li-ion battery electrodes, yet it remains a grand challenge to overcome the low electrical conductivity and associated volume change of Si. Here, by first coating a mesoporous SiO2 (meso-SiO2) onto carbon nanotube (CNT) networks and then converting it into a meso-Si layer covered by carbon, we obtained a freestanding, highly porous composite sponge electrode consisting of three-dimensionally interconnected sandwiched carbon-Si-CNT skeletons. In this hierarchical structure, the macropores among the sponge connect to mesopores in the meso-Si layer so that Li+ diffusion is facilitated, whereas the underlying CNT networks serve as conductive paths for electrons transport. Meanwhile, the outer carbon coating on meso-Si could buffer the volume expansion and prevent material shedding. As a result, our sandwiched carbon-Si-CNT electrodes exhibit large specific capacity, high rate capability and long cycle life. The combination of carbon-wrapped meso-Si and CNT sponges might be a potential strategy for developing efficient electrodes in various energy storage systems.Keywords: CNT; flexible; hierarchical; lithium-ion battery; mesoporous Si;
Co-reporter:Jie Wang, Qinqin Ma, Xiao-Xiao Hu, Haoyang Liu, Wei Zheng, Xueyuan Chen, Quan Yuan, and Weihong Tan
ACS Nano August 22, 2017 Volume 11(Issue 8) pp:8010-8010
Publication Date(Web):August 3, 2017
DOI:10.1021/acsnano.7b02643
Optical bioimaging is an indispensable tool in modern biology and medicine, but the technique is susceptible to autofluorescence interference. Persistent nanophosphors provide an easy-to-perform and highly efficient means to eliminate tissue autofluorescence. However, direct synthesis of persistent nanophosphors with tunable properties to meet different bioimaging requirements remains largely unexplored. In this work, zinc gallogermanate (Zn1+xGa2–2xGexO4:Cr, 0 ≤ x ≤ 0.5, ZGGO:Cr) persistent luminescence nanoparticles with composition-dependent size and persistent luminescence are reported. The size of the ZGGO:Cr nanoparticles gradually increases with the increase of x in the chemical formula. Moreover, the intensity and decay time of persistent luminescence in ZGGO:Cr nanoparticles can also be fine-tuned by simply changing x in the formula. In vivo bioimaging tests demonstrate that ZGGO:Cr nanoparticles can efficiently eliminate tissue autofluorescence, and the nanoparticles also show good promise in long-term bioimaging as they can be easily reactivated in vivo. Furthermore, an aptamer-guided ZGGO:Cr bioprobe is constructed, and it displays excellent tumor-specific accumulation. The ZGGO:Cr nanoparticles are ideal for autofluorescence-free targeted bioimaging, indicating their great potential in monitoring cellular networks and construction of guiding systems for surgery.Keywords: aptamer; autofluorescence; bioimaging; nanoparticle; near-infrared light; persistent luminescence;
Co-reporter:Jie Wang, Qinqin Ma, Wei Zheng, Haoyang Liu, Changqing Yin, Fubing Wang, Xueyuan Chen, Quan Yuan, and Weihong Tan
ACS Nano August 22, 2017 Volume 11(Issue 8) pp:8185-8185
Publication Date(Web):June 30, 2017
DOI:10.1021/acsnano.7b03128
Persistent luminescence nanoparticles (PLNPs), which can remain luminescent after cessation of excitation, have emerged as important materials in biomedicine due to their special ability to eliminate tissue autofluorescence. Even though significant advances have been made in bioimaging, studies on controlled synthesis of PLNPs with tunable properties are lacking. Until now, only a few studies have reported the synthesis of quasi-spherical ZnGa2O4:Cr PLNPs, and direct synthesis of PLNPs with other shapes and chemical compositions has not been reported. Herein, we report the direct synthesis of Zn2GeO4:Mn (ZGO:Mn) persistent luminescence nanorods (NRs). The length and persistent luminescence of ZGO:Mn NRs can be fine-tuned by simply changing the pH of the hydrothermal reaction system. Moreover, ZGO:Mn NRs exhibit rapid growth rate, and NRs with strong persistent luminescence can be obtained within 30 min of hydrothermal treatment. Aptamer-guided ZGO:Mn bioprobes were further constructed and applied to serum lysozyme analysis. Serum samples from patients with lung cancer, gastric cancer, and colorectal cancer were collected, and the concentrations of lysozyme in these samples were determined. Since the bioprobes displayed long persistent luminescence, serum autofluorescence interference was completely eliminated. The lysozyme quantification results were in good agreement with those obtained using a clinical method, suggesting the good potential of the bioprobes in the analysis of clinical samples. The developed ZGO:Mn NRs possess tunable length and persistent luminescence, and they are ideal for eliminating autofluorescence interference in biosensing, making them valuable in research areas such as studying the functions of biomolecules and monitoring of molecular/cellular networks in their native contexts.Keywords: aptamer; autofluorescence; biosensing; lysozyme; persistent luminescence; serum;
Co-reporter:Jie Wang;Qinqin Ma;Yingqian Wang;Haijing Shen
Nanoscale (2009-Present) 2017 vol. 9(Issue 19) pp:6204-6218
Publication Date(Web):2017/05/18
DOI:10.1039/C7NR01488K
Persistent luminescence nanoparticles (PLNPs) are an emerging group of promising luminescent materials that can remain luminescent after the excitation ceases. In the past decade, PLNPs with intriguing optical properties have been developed and their applications in biomedicine have been widely studied. Due to the ultra-long decay time of persistent luminescence, autofluorescence interference in biosensing and bioimaging can be efficiently eliminated. Moreover, PLNPs can remain luminescent for hours, making them valuable in bio-tracing. Also, persistent luminescence imaging can guide cancer therapy with a high signal-to-noise ratio (SNR) and superior sensitivity. Briefly, PLNPs are demonstrated to be a newly-emerging class of functional materials with unprecedented advantages in biomedicine. In this review, we summarized recent advances in the preparation of PLNPs and the applications of PLNPs in biosensing, bioimaging and cancer therapy.
Co-reporter:Yulan Wang;Xiaoxia Hu;Jing Dai;Jie Wang;Yaning Tan;Xiangdong Yang;Shuang Yang;Yufeng Zhang
Journal of Materials Chemistry B 2017 vol. 5(Issue 33) pp:6794-6800
Publication Date(Web):2017/08/23
DOI:10.1039/C7TB01515A
Development of a cell-free scaffold with excellent mechanical properties and osteoconductivity is of significant need for bone regeneration. Herein, a reduced graphene oxide (rGO) functionalized hierarchical macro–mesoporous bioactive glass scaffold integrated with an osteoblast-specific aptamer is rationally designed to recruit and induce the rapid differentiation of osteoblasts for bone regeneration. This scaffold exhibits a macroporous structure with fully interconnected open pores and shows excellent mechanical properties with a Young's modulus of ∼80 kPa, which provides a strong scaffold to support the growth of osteoblasts and bone tissue regeneration. Furthermore, the scaffold displays good performance in accelerating osteoblast differentiation and promoting new bone formation. The osteoblast recruitment is achieved since the osteoblast-specific aptamer can specifically target osteoblasts with strong binding affinity. Micro-computed tomography and histological tests confirmed that the large bone defects fully heal with new plate-like-pattern bone appearing both peripherally and centrally, suggesting the outstanding bone regeneration performance of this cell-free and graphene functionalized scaffold. Considering the promising bioapplications of the graphene functionalized bioactive glass scaffold with osteoblast recruitment capacity, our strategy paves a way for the design of new bioactive functional materials for tissue regeneration and shows attractive prospects in targeted therapy.
Co-reporter:Qinqin Ma;Jie Wang;Zhiheng Li;Dong Wang;Xiaoxia Hu;Yisheng Xu
Inorganic Chemistry Frontiers 2017 vol. 4(Issue 7) pp:1166-1172
Publication Date(Web):2017/07/11
DOI:10.1039/C7QI00194K
Information security has attracted broad attention in today's information age, and information encryption on paper has been widely studied since paper is still the most important information carrier. Fluorescent inks are commonly used in information encryption on paper, but they suffer from background fluorescence interference. Herein, we develop a background-free and easy-to-perform method for information encryption based on the inkjet printing of upconversion nanoparticles (UCNPs). The UCNPs can efficiently eliminate background fluorescence interference since phosphors in paper cannot be activated by near-infrared (NIR) light. Moreover, owing to their small size, excellent dispersibility and good stability, UCNP inks can be directly applied to commercial inkjet printers for convenient and high-throughput information encryption on paper. Information was easily printed on different kinds of paper substrates and the information can only be visualized under NIR light excitation. Furthermore, a novel information encryption strategy was designed by utilizing UCNPs with different excitation wavelengths. Only excitation at the defined wavelength can obtain the correct information. This proposed information encryption strategy can completely avoid background fluorescence interference, and it also features easy operation, high throughput as well as low costs, indicating its good promise to serve as a household encryption method in our daily life.
Co-reporter:Xiaoxia Hu;Yingqian Wang;Haoyang Liu;Jie Wang;Yaning Tan;Fubing Wang;Weihong Tan
Chemical Science (2010-Present) 2017 vol. 8(Issue 1) pp:466-472
Publication Date(Web):2016/12/19
DOI:10.1039/C6SC03401B
Development of a portable device for the detection of multiple mRNAs is a significant need in the early diagnosis of cancer. We have designed a biochip-based mRNA detection device by combining a hydrophilic–hydrophobic micropattern with upconversion luminescence (UCL) probes. The device achieves highly sensitive detection, using the naked eye, of multiple mRNAs among patient samples. The high sensitivity is attributed to enrichment of the target concentration and a fluorescence enhancement effect. In addition, since the photonic crystal (PC) dot biochip is functionalized with dual-wavelength excitation UCL probes, two kinds of mRNAs in the heterogeneous biological samples are detected simultaneously, and the corresponding luminescence signals are captured using an unmodified camera phone. The biochip-based mRNA detection device reported here demonstrates that multiple mRNAs extracted from patient samples can be simultaneously and sensitively detected in a visual way without sophisticated instrumentation. Therefore, this device is promising for real-time detection of multiple biomarkers in patient samples, and it is anticipated that it will provide a powerful tool for convenient early diagnosis of cancer.
Co-reporter:Yanbing Yang;Xiangdong Yang;Xuming Zou;Shiting Wu;Da Wan;Anyuan Cao;Lei Liao;Xiangfeng Duan
Advanced Functional Materials 2017 Volume 27(Issue 19) pp:
Publication Date(Web):2017/05/01
DOI:10.1002/adfm.201604096
Graphene is an attractive material for flexible electronics and biosensors, yet its zero bandgap nature has limited the on/off ratio of field-effect transistors (FETs) and the sensitivity of biosensors based on graphene. Graphene nanomesh (GNM), a continuous 2D graphene nanostructure with a high density of holes punched in the basal plane, has been created to introduce lateral confinement and enable improved on/off ratio. However, the GNMs produced to date typically have a relatively large dimension (constriction neck width >5 nm) and low on/off ratio (≈100) limited by the resolution of the lithography process used. Here, the exploration of a directly grown mesoporous silica template is reported for the preparation of ultrafine GNMs with considerably narrower neck width (<3 nm) and strong quantum confinement to enable flexible FETs with greatly improved on/off ratio (up to 1000). With excellent electronic properties and high surface area for the functionalization of specific receptors, it is further shown that the GNM FETs can be readily used to construct highly sensitive biosensors for selective detection of human epidermal growth factor receptor 2, which is further demonstrated for real-time detection of breast cancer cells overexpressed with receptor 2 down to single-cell level. The studies provide a simple and scalable method to GNMs with potential applications for flexible nanoelectronics and biosensors.
Co-reporter:Jie Wang;Haijing Shen;Chi Huang;Qinqin Ma;Yaning Tan;Fenglei Jiang
Nano Research 2017 Volume 10( Issue 1) pp:145-156
Publication Date(Web):2017 January
DOI:10.1007/s12274-016-1273-9
Adsorbents are widely employed in both fundamental and applied research areas such as separation technology, biotechnology, and environmental science. Selectivity and reusability are two most important requirements for adsorbents. Aptamers exhibit perfect selectivity and easy regeneration, which make them uniquely effective adsorption materials. Herein, we have rationally designed novel aptamer-based adsorbents and investigated their performance in extraction/separation of targets from an aqueous solution. These adsorbents can selectively extract targets from complicated sample matrices containing background compounds. Moreover, they can also be easily recycled without a significant loss of adsorption capacity. Notably, the adsorbents did not affect the activity of isolated biological samples, revealing their potential for the purification/separation of biomolecules. Composite adsorbents were constructed using aptamer-based adsorbents and a porous polymer, displaying highly efficient target separation from aqueous solution. Finally, separation columns were constructed, and targets in the aqueous solution were efficiently separated by these columns. The aptamerbased adsorbents described here exhibit great promise for potential applications in separation technology, biotechnology, and environment-related areas.
Co-reporter:Haijing Shen, Jie Wang, Haoyang Liu, Zhihao Li, Fenglei Jiang, Fu-Bing Wang, and Quan Yuan
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 30) pp:19371
Publication Date(Web):July 14, 2016
DOI:10.1021/acsami.6b06671
Sepsis and bacteremia are life-threatening clinical syndromes associated with significant patient morbidity and mortality. Rapid and sensitive detection of pathogenic bacteria is the key to improve patient survival rates. Herein, we have rationally constructed a simple aptamer-based capture platform to shorten the time needed for confirmation of bacterial bloodstream infection in clinical blood samples. This capture platform is made of a mesoporous TiO2-coated magnetic nanoparticle and is modified with target aptamer. It features excellent bacterial enrichment efficiency of about 80% even at low bacterial concentrations (10–2000 CFU mL–1). More importantly, the bacteria can be enriched within 2 h, and the time for bacterial identification is effectively shortened in comparison to the “gold standard” in clinical diagnosis of bloodstream infection. The aptamer-based capture platform may pave a way for the detection of biomarkers and find potential applications in disease diagnosis.Keywords: aptamer; bacteria; bloodstream infection; magnetic nanoparticle; sepsis
Co-reporter:Dong Wang, Jie Wang, Zi-en Liu, Xiangdong Yang, Xiaoxia Hu, Jinqi Deng, Nianjun Yang, Qijin Wan, and Quan Yuan
ACS Applied Materials & Interfaces 2016 Volume 8(Issue 42) pp:28265
Publication Date(Web):October 6, 2015
DOI:10.1021/acsami.5b08294
The electrochemical applications of traditional carbon nanomaterials such as carbon nanotubes (CNTs) and graphene (G) powders are significantly impeded by their poor three-dimensional (3D) conductivity and lack of hierarchical porous structure. Here, we have constructed a 3D highly conductive CNTs networks and further combined it with mesoporous carbon (mC) for the creation of a core–shell structured (CNT@mC) composite sponge that featured 3D conductivity and hierarchical porous structure. In the composite sponge, interconnected CNTs efficiently eliminates the contact resistance and the hierarchical pores significantly facilitate the mass transport. The electron transfer rates, electroactive surface area and catalytic activity of the CNT@mC composite sponge based catalysts were tested in the direct methanol fuel cells (DMFCs) and electrochemical sensors. In DMFCs, the Pd nanoparticles deposited CNT@mC showed significantly improved catalytic activity and methanol oxidization current. As for amperometric sensing of endocrine disrupting compounds (EDCs), CNT@mC-based catalyst gave a liner range from 10 nM to 1 mM for bisphenol A (BPA) detection and showed great promise for simultaneous detection of multiple EDCs. BPA recovery from environmental water further indicated the potential practical applications of the sensor for BPA detection. Finally, the electrochemical performance of CNT@mC were also investigated in impedimetric sensors. Good selectivity was obtained in impedimetric sensing of BPA and the detection limit was measured to be 0.3 nM. This study highlighted the exceptional electrochemical properties of the CNT@mC composite sponge enabled by its 3D conductivity and hierarchical porous structure. The strategy described may further pave a way for the creation of novel functional materials through integrating multiple superior properties into a single nanostructure for future clean energy technologies and environmental monitoring systems.Keywords: aptamer; carbon nanotube; electroanalysis; graphene; mesoporous carbon
Co-reporter:Jie Wang;Haijing Shen;Xiaoxia Hu;Yan Li;Zhihao Li;Jinfan Xu;Xiufeng Song;Haibo Zeng
Advanced Science 2016 Volume 3( Issue 3) pp:
Publication Date(Web):
DOI:10.1002/advs.201500289

For the water remediation techniques based on adsorption, the long-standing contradictories between selectivity and multiple adsorbability, as well as between affinity and recyclability, have put it on weak defense amid more and more severe environment crisis. Here, a pollutant-targeting hydrogel scavenger is reported for water remediation with both high selectivity and multiple adsorbability for several pollutants, and with strong affinity and good recyclability through rationally integrating the advantages of multiple functional materials. In the scavenger, aptamers fold into binding pockets to accommodate the molecular structure of pollutants to afford perfect selectivity, and Janus nanoparticles with antibacterial function as well as anisotropic surfaces to immobilize multiple aptamers allow for simultaneously handling different kinds of pollutants. The scavenger exhibits high efficiencies in removing pollutants from water and it can be easily recycled for many times without significant loss of loading capacities. Moreover, the residual concentrations of each contaminant are well below the drinking water standards. Thermodynamic behavior of the adsorption process is investigated and the rate-controlling process is determined. Furthermore, a point of use device is constructed and it displays high efficiency in removing pollutants from environmental water. The scavenger exhibits great promise to be applied in the next generation of water purification systems.

Co-reporter:Yu Zheng, Yanbing Yang, Shasha Chen and Quan Yuan  
CrystEngComm 2016 vol. 18(Issue 23) pp:4218-4235
Publication Date(Web):05 Feb 2016
DOI:10.1039/C5CE02510A
Among the various energy storage systems, supercapacitors are considered to be the most promising alternative to batteries due to their high power density, long cycle life and fast charge–discharge process. Especially, flexible electrochemical supercapacitors with their unique advantages such as flexibility, shape-conformability, and light weight are attracting ever-increasing attention to meet the current requirements for portable and wearable electric devices in modern energy storage markets. In this perspective, we summarize the most recent progress in flexible all-solid supercapacitors from the point of view of flexible electrode materials. Various flexible electrode materials like carbon nanotubes, graphene, and pseudo capacitive materials are discussed and their performance is comprehensively analyzed. In addition, an overview of the latest progress in strategies to improve the energy and power density is discussed. Further research targets in multifunctional integrated systems and challenges in realizing idealized flexible energy storage systems are also proposed.
Co-reporter:Yurou Ma;Xiangdong Yang;Yurong Wei
Chinese Journal of Chemistry 2016 Volume 34( Issue 3) pp:291-298
Publication Date(Web):
DOI:10.1002/cjoc.201500835

Abstract

In addition to its inherited genetic function, DNA is one of the smartest and most flexible self-assembling nanomaterials with programmable and predictable features, for which, more and more scientists combine DNA with nanomaterials and put them into designing, synthesizing and assembling. In this review, four modes of action of DNA molecules are introduced in a figurative and intuitive way, based on the four different roles it plays in synthesis and assembly of nanomaterials: (a) smart linkers to guide nanoparticle assembly, (b) 2D or 3D scaffold with well-designed binding sites, (c) nucleation sites to directly facilitate Au/Pd/Ag/Cu nanowires, nanoparticles, nano- arrays and (d) serving as capping agents to prevent crystal growth, and control size and morphology. To be sure, this state-of-the-art combination of functional DNA molecules and inorganic nanomaterials greatly encouraged step towards the development of analytical science, life science, environmental science, and other promising field they can address. DNA-guided nanofabrication will eventually exceed expectations far beyond our scope in the near future.

Co-reporter:Yurong Wei;Xiangdong Yang;Yurou Ma;Shengfu Wang
Chinese Journal of Chemistry 2016 Volume 34( Issue 6) pp:558-569
Publication Date(Web):
DOI:10.1002/cjoc.201500755

Abstract

Lanthanide (Ln, or rare-earth) doped nanoparticles are well-known for their prominent optical properties and have been widely used for biological applications, especially in biological assays and medical imaging. Recently, the extensive attention of near infrared (NIR) wavelength range has dramatically increased for its fast feedback, high spatial resolution and deep tissue penetration. Tissues have minimal absorbance in this region. While a lot of excellent reviews cover various aspects of biomedical imaging based on lanthanide doped nanoparticles, there has not been a review that systematically summarizes NIR-to-NIR imaging with lanthanide doped nanoparticles. In this review, we focus on the recent development of NIR-to-NIR imaging based on lanthanide doped nanoparticles, and discuss challenges and opportunities in it.

Co-reporter:Yanbing Yang, Wei Yin, Shiting Wu, Xiangdong Yang, Wei Xia, Yue Shen, Yunhui Huang, Anyuan Cao, and Quan Yuan
ACS Nano 2016 Volume 10(Issue 1) pp:1240
Publication Date(Web):December 17, 2015
DOI:10.1021/acsnano.5b06592
Perovskite is an excellent candidate as low cost catalyst for Li–O2 cells. However, the limited porosity, which impedes molecular transport, and the inherent low electronic conductivity are the main barriers toward production of high-performance electrodes. Here, we designed a hierarchical porous flexible architecture by coating thin mesoporous yet crystalline LaSrMnO layers throughout a graphene foam to form graphene/meso-LaSrMnO sandwich-like nanosheets. In this well-designed system, the macropore between nanosheets facilitates O2 and Li+ diffusion, the mesopore provides large surface area for electrolyte immersion and discharge products deposition, the perovskite phase catalyst decreases reactive overpotential, and the graphene serves as conductive network for electrons transport. When used as a freestanding electrode of Li–O2 cell, it shows high specific capacity, superior rate capability, and cyclic stability. Combination of mesoporous perovskites with conductive graphene networks represents an effective strategy for developing efficient electrodes in various energy storage systems.Keywords: graphene; LaSrMnO; LiO2 cell; mesoporous; perovskite;
Co-reporter:Jie Wang; Yurong Wei; Xiaoxia Hu; Yu-Yan Fang; Xinyang Li; Jian Liu; Shengfu Wang
Journal of the American Chemical Society 2015 Volume 137(Issue 33) pp:10576-10584
Publication Date(Web):August 10, 2015
DOI:10.1021/jacs.5b04894
Regulation of protein activity is vital for understanding the molecular mechanism of biological activities. In this work, protein activity is suppressed by proximity-dependent surface hybridization and subsequently restored by near-infrared (NIR) light stimulation. Specifically, by constructing closed-loop structures with two aptamer-based affinity ligands, significantly enhanced inhibition of thrombin activity is achieved compared to traditional single affinity ligand based inhibitors. Furthermore, the activity of inhibited thrombin is efficiently recovered under NIR light stimulation by using gold nanorods (AuNRs) as photothermal agents to disrupt the closed-loop structures. Real-time and in situ monitoring of the conversion of fibrinogen into fibrin catalyzed by both inhibited and recovered thrombin was performed with light scattering spectroscopy and laser scanning confocal microscopy (LSCM). Thrombin trapped in the closed-loop structures shows slow reaction kinetics, while the photothermally liberated thrombin displays largely recovered catalytic activity. Human plasma was further employed to demonstrate that both the inhibited and restored thrombin can be applied to clotting reaction in reality. This strategy provides protein activity regulation for studying the molecular basis of biological activities and can be further applied to potential areas such as metabolic pathway regulation and the development of protein-inhibitor pharmaceuticals.
Co-reporter:Zi-en Liu, Jie Wang, Yan Li, Xiaoxia Hu, Junwen Yin, Yeqing Peng, Zhihao Li, Yawen Li, Baomin Li, and Quan Yuan
ACS Applied Materials & Interfaces 2015 Volume 7(Issue 34) pp:19416
Publication Date(Web):August 13, 2015
DOI:10.1021/acsami.5b05633
Core–satellite is one of the most powerful superstructures since it leads to enhanced or completely new properties through compatible combination of each component. Here we create a novel ceria-based core–shell–satellite supersandwich structure with near-infrared (NIR) light manipulated catalytic activity by integrating the upconversion luminescent and catalytic functionality of CeO2 nanoparticles. Specifically, lanthanide-doped octahedral CeO2 nanoparticles (o-CeO2) are coated with silica layer (o-CeO2@SiO2) to enhance their luminescence intensity. The pH-dependent catalytic active cubic CeO2 nanoparticles (c-CeO2) are then assembled on the surface of o-CeO2@SiO2 to form the supersandwich structure (o-CeO2@SiO2@c-CeO2) following a classic chemical reaction. The upconversion quantum yield of o-CeO2 in this nanostructure can be nearly doubled. Furthermore, under NIR light irradiation, the o-CeO2@SiO2@c-CeO2 supersandwich structure based composite catalyst displays superior catalytic activity in selective reduction of aromatic nitro compounds to corresponding azo compounds, and the composite photocatalyst can be easily recycled for several times without significant loss of catalytic activity. This strategy may serve as a universal method for the construction of multifunctional nanostructures and shed light on the green chemistry for chemical synthesis.Keywords: cerium oxide; green chemistry; near-infrared light; photocatalysis; upconversion
Co-reporter:Xueying Ge, Zhenxing Li, Quan Yuan
Journal of Materials Science & Technology 2015 Volume 31(Issue 6) pp:645-654
Publication Date(Web):June 2015
DOI:10.1016/j.jmst.2015.01.008
Ceria has emerged as a fascinating and lucrative material in bio-application, for instance, disease treatment, bioimaging and drug delivery due to its abilities of transforming oxidation states between Ce4+ and Ce3+ and scavenging free radicals, which can produce biological effect, such as being potentially antioxidant towards reactive oxygen species. Recently, many studies about one dimension (1D) CeO2 nanomaterials have received much attention because of the unique properties of their length and aspect ratio. We highlight here current research activities focused on the bio-application of 1D ceria nanomaterials. The synthesis methods of 1D cerium oxide nanomaterials were introduced. Several synthesis routes, including template, hydrothermal, sonochemical and other methods, were then discussed with examples developed by recent research. The differences among these methods were also analyzed. This review provides a comprehensive introduction to the synthesis of 1D ceria, its potential applications in biological fields and perspectives on this exciting realm.
Co-reporter:Lin Cheng;Xuefeng Xu;Yuyan Fang;Yan Li;Jiaxi Wang
Science China Chemistry 2015 Volume 58( Issue 5) pp:850-857
Publication Date(Web):2015 May
DOI:10.1007/s11426-014-5237-1
Rare-earth doped titania single-crystalline hollow nanoparticles of 20 nm are constructed via a simple sol-gel process. Amphiphilic ABA tri-block copolymers played a key role in assisting the formation of hollow structure, for which a hollow nanostructure growth mechanism is proposed. By introducing rare earth into the synthesis process, the as-prepared nanoparticles exhibit near-infrared light absorption properties. Photo-decomposition efficiency of Orange II azo dye can be successfully evaluated when using Yb3+-doped TiO2 hollow nanoparticles as photocatalysts; it is more than two times higher than the pure TiO2 hollow nanoparticles. The hollow nanostructured Yb3+-doped TiO2 samples are exploited as photoanodes in N719-sensitized solar cells and prove able to improve the photoelectric conversion efficiency by measuring the solar cell parameters of dye-sensitized solar cells (DSSCs) under simulative sunlight.
Co-reporter:Yanbing Yang, Enzheng Shi, Peixu Li, Dehai Wu, Shiting Wu, Yuanyuan Shang, Wenjing Xu, Anyuan Cao and Quan Yuan  
Nanoscale 2014 vol. 6(Issue 7) pp:3585-3592
Publication Date(Web):08 Jan 2014
DOI:10.1039/C3NR05931F
Applications of mesoporous silica (m-SiO2) have suffered from its fragility (monolithic m-SiO2 easily collapses under compression) and limited internal molecular exchange through small channels. Previously reported hierarchical porous m-SiO2 structures containing interconnected macropores could improve adsorption properties, but they were still intrinsically fragile without sufficient mechanical strength to sustain deformation. Here, we embed a three-dimensional carbon nanotube (CNT) skeleton into m-SiO2 to fabricate bulk, robust sponges that can be compressed to large strains (60% volume reduction) repeatedly in both air and water. This is done by directly casting a uniform m-SiO2 layer with tunable thickness onto the surface of CNTs while maintaining the original network and open porous structure, resulting in a core–shell CNT@m-SiO2 hybrid sponge. By pumping fluid through the CNT@m-SiO2 sponges under cyclic compression, the adsorption rate and efficiency of dye molecules can be significantly enhanced due to the mesoporous coating on CNTs and enhanced fluid exchange throughout internal pores. The CNT@m-SiO2 sponges may be used as robust and flexible adsorption media, and chemical and biological sensors with high performance.
Co-reporter:Xiaoxia Hu, Ting Wei, Jie Wang, Zi-En Liu, Xinyang Li, Binhao Zhang, Zhihao Li, Lele Li, and Quan Yuan
Analytical Chemistry 2014 Volume 86(Issue 20) pp:10484
Publication Date(Web):September 22, 2014
DOI:10.1021/ac5032308
The development of a portable and easy-to-use device for the detection of explosives with high sensitivity and selectivity is in high demand for homeland security and public safety. In this study, we demonstrate miniaturized devices depending on the upconversion ratiometric luminescent probe for point-of-care (POC) assay of explosives with the naked-eye. When the PEI-coated upconversion nanoparticles (UCNPs) selectively bonded to 2,4,6-trinitrotoluene (TNT) explosives by the formation of Meisenheimer complex, the formed of UCNP–Meisenheimer complexes show turned visible multicolor upconversion luminescence (UCL) on account of TNT-modulating Förster resonance energy transfer process under near-infrared excitation. With UCL emission at 808 nm as internal standard and ratiometric UCL at 477 nm to that at 808 nm (I477/I808) as output signal, the probe can simultaneously meet the accuracy for TNT explosives quantitative analysis. In addition, this easy-to-use visual technique provides a powerful tool for convenient POC assay of rapid explosives identification.
Co-reporter:Jie Wang;Ting Wei;Xinyang Li;Binhao Zhang;Jiaxi Wang;Chi Huang ;Dr. Quan Yuan
Angewandte Chemie International Edition 2014 Volume 53( Issue 6) pp:1616-1620
Publication Date(Web):
DOI:10.1002/anie.201308843

Abstract

Photoluminescence is one of the most sensitive techniques for fingerprint detection, but it also suffers from background fluorescence and selectivity at the expense of generality. The method described herein integrates the advantages of near-infrared-light-mediated imaging and molecular recognition. In principle, upconversion nanoparticles (UCNPs) functionalized with a lysozyme-binding aptamer were used to detect fingerprints through recognizing lysozyme in the fingerprint ridges. UCNPs possess the ability to suppress background fluorescence and make it possible for fingerprint imaging on problematic surfaces. Lysozyme, a universal compound in fingerprints, was chosen as the target, thus simultaneously meeting the selectivity and generality criteria in photoluminescence approaches. Fingerprints on different surfaces and from different people were detected successfully. This strategy was used to detect fingerprints with cocaine powder by using UCNPs functionalized with a cocaine-binding aptamer.

Co-reporter:Jie Wang;Ting Wei;Xinyang Li;Binhao Zhang;Jiaxi Wang;Chi Huang ;Dr. Quan Yuan
Angewandte Chemie International Edition 2014 Volume 53( Issue 6) pp:
Publication Date(Web):
DOI:10.1002/anie.201400193
Co-reporter:Jie Wang;Ting Wei;Xinyang Li;Binhao Zhang;Jiaxi Wang;Chi Huang ;Dr. Quan Yuan
Angewandte Chemie 2014 Volume 126( Issue 6) pp:1642-1646
Publication Date(Web):
DOI:10.1002/ange.201308843

Abstract

Photoluminescence is one of the most sensitive techniques for fingerprint detection, but it also suffers from background fluorescence and selectivity at the expense of generality. The method described herein integrates the advantages of near-infrared-light-mediated imaging and molecular recognition. In principle, upconversion nanoparticles (UCNPs) functionalized with a lysozyme-binding aptamer were used to detect fingerprints through recognizing lysozyme in the fingerprint ridges. UCNPs possess the ability to suppress background fluorescence and make it possible for fingerprint imaging on problematic surfaces. Lysozyme, a universal compound in fingerprints, was chosen as the target, thus simultaneously meeting the selectivity and generality criteria in photoluminescence approaches. Fingerprints on different surfaces and from different people were detected successfully. This strategy was used to detect fingerprints with cocaine powder by using UCNPs functionalized with a cocaine-binding aptamer.

Co-reporter:Jie Wang;Ting Wei;Xinyang Li;Binhao Zhang;Jiaxi Wang;Chi Huang ;Dr. Quan Yuan
Angewandte Chemie 2014 Volume 126( Issue 6) pp:
Publication Date(Web):
DOI:10.1002/ange.201400193
Co-reporter:Qinqin Ma, Jie Wang, Zhiheng Li, Dong Wang, Xiaoxia Hu, Yisheng Xu and Quan Yuan
Inorganic Chemistry Frontiers 2017 - vol. 4(Issue 7) pp:NaN1172-1172
Publication Date(Web):2017/05/08
DOI:10.1039/C7QI00194K
Information security has attracted broad attention in today's information age, and information encryption on paper has been widely studied since paper is still the most important information carrier. Fluorescent inks are commonly used in information encryption on paper, but they suffer from background fluorescence interference. Herein, we develop a background-free and easy-to-perform method for information encryption based on the inkjet printing of upconversion nanoparticles (UCNPs). The UCNPs can efficiently eliminate background fluorescence interference since phosphors in paper cannot be activated by near-infrared (NIR) light. Moreover, owing to their small size, excellent dispersibility and good stability, UCNP inks can be directly applied to commercial inkjet printers for convenient and high-throughput information encryption on paper. Information was easily printed on different kinds of paper substrates and the information can only be visualized under NIR light excitation. Furthermore, a novel information encryption strategy was designed by utilizing UCNPs with different excitation wavelengths. Only excitation at the defined wavelength can obtain the correct information. This proposed information encryption strategy can completely avoid background fluorescence interference, and it also features easy operation, high throughput as well as low costs, indicating its good promise to serve as a household encryption method in our daily life.
Co-reporter:Xiaoxia Hu, Yingqian Wang, Haoyang Liu, Jie Wang, Yaning Tan, Fubing Wang, Quan Yuan and Weihong Tan
Chemical Science (2010-Present) 2017 - vol. 8(Issue 1) pp:NaN472-472
Publication Date(Web):2016/08/19
DOI:10.1039/C6SC03401B
Development of a portable device for the detection of multiple mRNAs is a significant need in the early diagnosis of cancer. We have designed a biochip-based mRNA detection device by combining a hydrophilic–hydrophobic micropattern with upconversion luminescence (UCL) probes. The device achieves highly sensitive detection, using the naked eye, of multiple mRNAs among patient samples. The high sensitivity is attributed to enrichment of the target concentration and a fluorescence enhancement effect. In addition, since the photonic crystal (PC) dot biochip is functionalized with dual-wavelength excitation UCL probes, two kinds of mRNAs in the heterogeneous biological samples are detected simultaneously, and the corresponding luminescence signals are captured using an unmodified camera phone. The biochip-based mRNA detection device reported here demonstrates that multiple mRNAs extracted from patient samples can be simultaneously and sensitively detected in a visual way without sophisticated instrumentation. Therefore, this device is promising for real-time detection of multiple biomarkers in patient samples, and it is anticipated that it will provide a powerful tool for convenient early diagnosis of cancer.
5-CARBOXYFLUORESCEIN
Lanthanum manganese strontium oxide
YTTERBIUM TRIFLUOROACETATE
ERBIUM(3+);2,2,2-TRIFLUOROACETATE
Sodium yttrium fluoride
6-Benzothiazolesulfonicacid, 2,2'-(1,2-hydrazinediylidene)bis[3-ethyl-2,3-dihydro-