Nano Research
·
2019
·Vol. 12
·期 6
·1375-1379
·
IF 8.515
Xu Meng,Tu Guopeng,Ji Muwei,Wan Xiaodong,Liu Jiajia,Liu Jia,Rong Hongpan,Yang Yanlian,Wang Chen,Zhang Jiatao
Utilizing vacuum-tuned-atmosphere induced dip coating method, we achieve the cross-dimensional macroscopic diverse self-assemblies by using one building block with one chemical functionality. Coordinated modulating the vacuum degree, colloid concentration and evaporation atmosphere, Au@Ag core/shell NCs can controllably assemble into diverse multi-dimensional superstructures. Under 0.08 MPa, we obtained the two-dimensional (2D) stepped superstructures with continuously tunable step width. In addition, we generated a series of tailorable nanoscale-roughened 2D Au@Ag NCs superstructures at 0.04 MPa, which exhibited the label-free ultrasensitive SERS detection for the different mutants of IAPP8-37 proteins. Under 0.01 MPa, we obtained the cross-dimensional tailorable Au@Ag NCs assemblies from random to macroscale 2D and three-dimensional (3D) densest superstructures by adjusting the capping ligand-environmental molecule interactions. This is a flexible method to generate as-prepared Au@Ag core/shell NCs into well-defined macroscopic diverse superstructures and to promote the exploitation into biological applications.
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INTERNATIONAL JOURNAL OF ENERGY RESEARCH
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2019
·Vol. 44
·期 2
·833-844
·
IF 3.343
Xiao Wang,Wei Li,Shu-ao He,Qiong Ma,Bingchang Yan,Nan Meng,Lifen Hao
Summary With the improvement of people's living standard, energy shortage is increasingly severe. Photocatalysis technology is one of the most effective means to solve this problem. Generally, poor visible-light response and fast combination of photo-induced carriers are the main limiting factors to traditional photocatalysts. Aiming at this problem, in this paper, AgBr was used as the photosensitizer to immobilize on the surface of reduced graphene oxide (rGO) for the complexation of Ag + ions and carboxyl groups of precursor graphene oxide (GO), then the two-dimensional rGO-AgBr/Ag composites (2D rGAA-α, α = 1, 2 and 3) were synthesized by solvothermal method. The structures, morphologies, chemical bonding states and photoelectrochemical properties of the samples were analyzed to study the samples, and the corresponding visible-light-driven (VLD) catalytic performances were studied by hydrogen evolution reaction (HER). Compared with pure rGO, the light absorption of rGAA-α was almost extended to full spectral range for the Z-scheme heterointerface (rGO-AgBr) construction, and the separation of photo-induced carriers can be promoted effectively. The HER results showed that the average hydrogen evolution rate ( ) of rGAA-α was significantly increased, and the rGAA-2 catalyst presented the highest (72.71 μmol h -1 g -1 ). After six recycling experiments, the very faint activity decrease and unobvious structure change suggested the high photostability. Accordingly, the enhanced catalytic activity of rGAA-α catalysts was attributed to the formation of Z-scheme heterointerface and generation of Ag plasmas, so this study will provide a simple, effective and promising method for hydrogen energy development.
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RSC Advances
·
2019
·Vol. 9
·期 71
·41561-41568
·
IF 3.049
Cuifeng Jiang,Xiaoxiu Wei,Shuai Bao,Huajian Tu,Wei Wang
Nanomaterial-based artificial peroxidase has attracted extensive interests due to their distinct advantages over natural counterpart. Cu@Au/Pt and Cu@Ag/Pt nanocomposite with rambutan-like structure were prepared and discovered to function like peroxidase, which was illustrated by catalyzing the oxidation reaction of 3,3′,5,5′-tetramethylbenzidine (TMB) accompanied with a blue color change. Steady-state investigation indicates that the catalytic kinetics of Cu@Au/Pt and Cu@Ag/Pt all followed typical Michaelis–Menten behaviors and Cu@Au/Pt showed a strong affinity for H2O2, while Cu@Ag/Pt showed strong affinity for TMB. The color change and absorbance intensity strongly depend on the concentration of H2O2, thus the direct determination of H2O2 and indirect detection of glucose were demonstrated using Cu@Au/Pt with a detection limit of 1.5 μM and 6 μM, respectively. What is more important, the method was applied for detection of glucose in 50% fetal bovine serum with a detection limit of 80 μM, which is much lower than the lowest glucose content in blood for diabetes (7 mM). Moreover, the Cu@Au/Pt nanocomposite were also successfully applied for sensing L-cysteine because of the inhibition effect. Considering the good peroxidase-like activity and novel structure, Cu@Au(Ag)/Pt is expected to have a wide range of applications in bioassays and biocatalysis.
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PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2019
·
IF 8.456
Hamidreza Abadikhah,Ehsan Naderi Kalali,Samaneh Khodi,Xin Xu,Simeon Agathopoulos
High desalination performance, dye retention, and antibacterial properties were achieved with a multifunctional thin-film nanocomposite (MTFN) membrane, fabricated by the incorporation of a novel nanocomposite structure of reduced graphene oxide@TiO2@Ag (rGO@TiO2@Ag) into the polyamide active layer. The specific characteristics of the graphene-based nanocomposite, synthesized by the microwave-assisted irradiation process, favored water channelization and provided superhydrophilicity and antibacterial properties to the MTFN membranes. In comparison with the conventional methods, such as multistep chemical process using strong agents for reduction and long-term energy-consuming hydrothermal process, microwave irradiation facilitated a green, fast, and cost-effective route for the fabrication of GO-based nanocomposites for multifunctional applications. Interfacial polymerization was performed on a polyethersulfone/Si3N4 robust hollow fiber substrate using m-phenylenediamine aqueous solution and 1,3,5-benzenetricarbonyltrichloride organic solution. The structural and chemical characteristics of the synthesized nanocomposites and the MTFN membranes were thoroughly studied by a series of characterization analyses (transmission electron microscopy, field emission scanning electron microscopy, X-ray diffraction, Fourier transform infrared, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and atomic force microscopy). The physicochemical properties and the nanofiltration performance of the MTFN membranes were investigated after the incorporation of rGO@TiO2@Ag at various concentrations. The water contact angles confirmed the superb surface hydrophilicity of the MTFN membranes. High permeability (52 L·m–2·h–1), desalination (96% for 1 g/L Na2SO4 feed solution), and dye retention (98% for 0.5 g/L rose bengal feed solution) were recorded for MTFN enriched with 0.2 wt % rGO@TiO2@Ag. A 90% reduction in the number of viable bacteria (Escherichia coli), after 3 h of contact with MTFN membranes, confirmed the superior antibacterial activity of the produced membranes.
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高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2018
·
IF 2.88
Jian Zhu,Tian-Tian Jia,Jian-Jun Li,Xin Li,Jun-Wu Zhao
In this work, we develop a simple and selective sensing method for the detection of mercury ions based on surface plasmon resonance (SPR) spectrum change of Au-Ag core-shell triangular nanoplates . When the concentration of mercury is increased, the etching-induced change of particle size and shape also leads to the decrease of the absorption peak at the fixed wavelength, until a spectrum dip takes place. This spectral change of “peak-to-dip” greatly enlarges the detection range of mercury ions, which could be fine tuned by changing the initial thickness of the Ag coating. Under optimal conditions, the decrease of the logarithmic absorption intensity has a good linear response with the concentration of mercury ions increasing from 10 to 1000 μM, and the limit of detection (LOD) is 0.88 μM. Interference studies and real samples test indicate that, this new sensing method has a good selection for mercury ions and can be practically used in lake water. This work shows the surface etching-induced SPR shift can also leads to the intensity change with “peak-to-dip” fashion, which greatly enlarge the concentration range of the detection and could be widely applied in the spectroscopy sensing based on SPR.
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高影响因子
JOURNAL OF MATERIALS SCIENCE
·
2018
·Vol. 54
·期 1
·286-301
·
IF 2.993
Fang Hongbiao,Cao Xin,Yu Jiajie,Lv Xiang,Yang Nan,Wang Tianhe,Jiang Wei
Tungsten oxide (WO 3 ) is a well-known photocatalyst, but its application is restricted due to its low conduction band and reduction power. In addition, WO 3 catalyst in powder forms has little application prospect because of difficulties in separation and regeneration. In this work, we prepared WO 3 /Ag/AgCl films on conventional glass that not only have much enhanced photocatalytic capability but also can be readily regenerated. The WO 3 film was prepared on glass substrate by calcination of spin-coated W precursor. Ag/AgCl particles were then deposited on WO 3 film by an impregnating–precipitation–photoreduction method. The photocatalytic efficiency of WO 3 /Ag/AgCl was evaluated by using methyl orange (MO) and Rhodamine B (RhB) as target pollutants. The highest photocatalytic performance was achieved with the 3-WO 3 /Ag/AgCl film, being 18 and 13 times higher than that of pure WO 3 film for degradation of MO and RhB, respectively. The degradation rate for both MO and RhB by 3-WO 3 /Ag/AgCl film catalyst decreased by less than 5% after five cycled tests. The photodegradation mechanism was discussed based on the electrochemical impedance spectroscopy Nyquist tests, photoelectrochemical analysis and reactive oxygen species scavenging experiments. A possible all-solid-state Z-scheme mechanism is proposed based on the photoelectron chemical tests and radical trapping experiments. This study provides a feasible technique to prepare a photocatalytic film with practicability and reproducibility.
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Scientific Reports
·
2014
·Vol. 4
·期 1
·1-9
·
IF 5.078
Wang Fei,Liu Pei,Sun Lin,Li Cuncheng,Petrenko Valery A.,Liu Aihua
Nanomaterials with near-infrared (NIR) absorption have been widely studied in cancer detection and photothermal therapy (PTT), while it remains a great challenge in targeting tumor efficiently with minimal side effects. Herein we report a novel multifunctional phage-mimetic nanostructure, which was prepared by layer-by-layer self-assembly of Au@Ag heterogenous nanorods (NRs) with rhodamine 6G and specific pVIII fusion proteins. Au@Ag NRs, first being applied for PTT, exhibited excellent stability, cost-effectivity, biocompatibility and tunable NIR absorption. The fusion proteins were isolated from phage DDAGNRQP specifically selected from f8/8 landscape phage library against colorectal cancer cells in a high-throughput way. Considering the definite charge distribution and low molecular weight, phage fusion proteins were assembled on the negatively charged NR core by electrostatic interactions, exposing the N-terminus fused with DDAGNRQP peptide on the surface. The fluorescent images showed that assembled phage fusion proteins can direct the nanostructure into cancer cells. The nanostructure was more efficient than gold nanorods and silver nanotriangle-based photothermal agents and was capable of specifically ablating SW620 cells after 10 min illumination with an 808 nm laser in the light intensity of 4 W/cm 2 . The prepared nanostructure would become an ideal reagent for simutaneously targeted optical imaging and PTT of tumor.
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ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2013
·
IF 5.257
Su-juan Yu,Yong-guang Yin,Jing-bo Chao,Mo-hai Shen,Jing-fu Liu
The fast growing and abundant use of silver nanoparticles (AgNPs) in commercial products alerts us to be cautious of their unknown health and environmental risks. Because of the inherent redox instability of silver, AgNPs are highly dynamic in the aquatic system, and the cycle of chemical oxidation of AgNPs to release Ag+ and reconstitution to form AgNPs is expected to occur in aquatic environments. This study investigated how inevitable environmentally relevant factors like sunlight, dissolved organic matter (DOM), pH, Ca2+/Mg2+, Cl–, and S2– individually or in combination affect the chemical transformation of AgNPs. It was demonstrated that simulated sunlight induced the aggregation of AgNPs, causing particle fusion or self-assembly to form larger structures and aggregates. Meanwhile, AgNPs were significantly stabilized by DOM, indicating that AgNPs may exist as single particles and be suspended in natural water for a long time or delivered far distances. Dissolution (ion release) kinetics of AgNPs in sunlit DOM-rich water showed that dissolved Ag concentration increased gradually first and then suddenly decreased with external light irradiation, along with the regeneration of new tiny AgNPs. pH variation and addition of Ca2+ and Mg2+ within environmental levels did not affect the tendency, showing that this phenomenon was general in real aquatic systems. Given that a great number of studies have proven the toxicity of dissolved Ag (commonly regarded as the source of AgNP toxicity) to many aquatic organisms, our finding that the effect of DOM and sunlight on AgNP dissolution can regulate AgNP toxicity under these conditions is important. The fact that the release of Ag+ and regeneration of AgNPs could both happen in sunlit DOM-rich water implies that previous results of toxicity studies gained by focusing on the original nature of AgNPs should be reconsidered and highlights the necessity to monitor the fate and toxicity of AgNPs under more environmentally relevant conditions.
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高影响因子
Journal of Materials Chemistry A
·
2013
·Vol. 2
·期 10
·3445-3451
·
IF 0
Jie-Ning Zheng,Jing-Jing Lv,Shan-Shan Li,Meng-Wei Xue,Ai-Jun Wang,Jiu-Ju Feng
In this study, a simple, facile and one-pot solvothermal method was developed for preparation of reduced graphene oxide (RGO) supported hollow Ag@Pt core–shell nanospheres (hAg@Pt), using ethylene glycol (EG) as a reducing agent and sodium dodecyl sulfate (SDS) as a soft template. Control experiments demonstrated that the molar ratios of the Pt–Ag precursors, the amount of SDS, the presence of RGO, and the reaction temperature were critical to the final nanocomposites. The as-prepared hAg@Pt–RGO showed the improved electrocatalytic activity and durability toward ethylene glycol oxidation, which can serve as a promising potential electrocatalyst in direct alcohol fuel cells.
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RSC Advances
·
2015
·Vol. 6
·期 4
·3186-3197
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IF 3.84
Zhifeng Jiang,Jimin Xie
Novel visible-light-driven Ag/Ag2O@g-C3N4 (AAC) hybrid materials were synthesized successfully via a green, facile hydrothermal treatment approach by reducing AgNO3 using carbon nanodots as reducing agent for the first time. Natural leaves were used as precursors to prepare carbon nanodots. By adjusting the feed mass ratio of AgNO3 to carbon nanodots, the average diameter of Ag/Ag2O can be modulated from 8 to 33 nm. The effects of Ag/Ag2O deposition on the optical and photocatalytic performance of AAC in the degradation of rhodamine B (RhB) under visible light irradiation were systematically investigated. It was found that the Ag/Ag2O content greatly influences the photocatalytic activity of AAC nanocomposites. A suitable amount of Ag/Ag2O in the AAC system could obtain the best photocatalytic activity. The experimental results indicated that all the AAC nanocomposites showed higher photocatalytic activities compared with that of pure g-C3N4. The remarkable visible-light photocatalytic activity of AAC heterostructures could be attributed to their absorption in the visible region and low recombination rate of the electron–hole pairs because of the heterojunction formed between Ag2O and g-C3N4. In addition, Ag nanoparticles are believed to play an essential role in affecting the photoreactivity because they are able to trap electrons, further separate the electron–hole pairs, and prolong the life of electron–hole pairs. In other words, it can be concluded that the increased photocatalytic activity of AAC was attributed to the synergic effect between g-C3N4, Ag2O and Ag. It is believed that the present work could render useful information for steering the design and application of noble nanoparticle loaded g-C3N4-based heterojunction composites with high photocatalytic activity.
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CRYSTENGCOMM
·
2017
·Vol. 19
·期 37
·5565-5575
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IF 3.474
Hui-Ze Wang,Bo Chen,Deng-Yuan Hao,Xin-Peng Miao,Dan Zhao,Ning Zhang
Pursuing a general and feasible method to construct precious metal (PM) nanostructures bounded by high-index facets (HIFs) is highly desirable for both academic and industrial interests in promising metal materials. Herein, attempts to employ modified galvanic replacement processes between MClxy− (M = Pt, Pd or Au) PM precursors and sacrificed templates of Ag nanocubic particles with deliberately introduced high [Cl−] (concentration of Cl−) were investigated to gain more acceptable HIF PM nanostructures. Typically, the Pt–Ag system was chosen as a representative system and monitored by the comprehensive characterizations of UV-vis, XRD, XPS and TEM to illuminate the evolution of the corresponding particles. It was demonstrated that the deliberately introduced Cl− at a certain concentration ([Cl−] was not lower than 1.5 M) could play dual roles in the kinetic evolution of the particles: one was dramatically lowering the etching speed to confine the reaction to the surface layers of the Ag substrates, and the other was facilitating the anisotropic etching process along the PVP-protected Ag surface through the Nernst–Einstein diffusion influence on PtCl42−, which in turn led to the formation of concave nanocubic particles with Pt-highly-dispersed [hk0] high-index surfaces (combined by the [210], [410] and [510] atomic terraces) on the Ag templates. The efficiencies of the method were further confirmed by constructing similar Pd- or Au-highly-dispersed high-index surfaces on Ag templates, suggesting that the method is a novel and general strategy to directly construct PM-based high-index surfaces with high PM dispersion in bimetallic nanostructures, which could be referenced as a solution to obtain superior precious metal materials possessing both unique HIF surface configuration and cost-saving competitiveness for advanced applications.
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JOURNAL OF POROUS MATERIALS
·
2016
·Vol. 24
·期 1
·45-54
·
IF 1.385
Ma Jing,Xu Shangyuan,Chu Jia,Xue Juanqin,Tang Jieli,Qiang Liangsheng
In this paper, a series of metal supported TiO 2 /SBA-16 photocatalysts were successfully synthesized by wet impregnation method. The synthesized samples were characterized by X-ray diffraction (XRD), Raman spectra, N 2 adsorption–desorption, transmission electron microscopy (TEM), UV–visible absorption spectra (UV-vis) and X-ray photoelectron spectroscopy (XPS). It was found that SBA-16 retained the ordered mesostructure after modification. The results shown that loading different metal elements was found to have significant influences on the crystallographic structure and physical properties. Moreover, the prepared materials were evaluated on photodegradation of Rhodamine B (RhB). Experiment results showed that the degradation of RhB by these catalysts follows the pseudo-first-order kinetic model. The effect of metal element on photocatalytic activity can be attributed that the appropriate amounts of metal concentration can enhance the photocurrent due to the reduced electron–hole recombination, which can improve the efficiency of photocatalytic reactions.
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