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RSC Advances · 2016 ·Vol. 6 ·期 72 ·67827-67832 · IF 3.289

Titanate nanowire/NiO nanoflake core/shell heterostructured nanonanocomposite catalyst for methylene blue photodegradation

W. X. Chen,J. S. Yu,W. Hu,Z. L. Chen,H. Memon,G. L. Chen

A core/shell heterostructured nanonanocomposite catalyst based on NiO nanoflakes and titanate nanowires (TNWs) was fabricated. The experimental results showed that the precursor concentration and the reaction time for NiO deposition played significant roles in determining the resulting heterostructure, and an optimal precursor's concentration would result in a well-defined core/shell heterostructure. The XRD analysis demonstrated the existence of the (1 1 1), (2 0 0) and (3 1 1) lattice planes of the NiO nanoflakes. Nearly 100% of the MB pollutant (10 mg L−1) was photodegradaded by the TNWs/NiO catalyst within 50 minutes under UV light irradiation.

研究领域: 材料化学 · 环境催化 · 纳米材料科学 · 光催化降解 · 功能材料
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2011 ·Vol. 36 ·期 13 ·7374-7380 · IF 4.057

A novel silver oxides oxygen evolving catalyst for water splitting

Wei Wang,Qiang Zhao,Jinxiang Dong,Jinping Li

A novel silver oxides oxygen evolving catalyst (Ag-OEC) for hydrogen production by water splitting was formed in situ on an indium tin oxide anode, in a near-neutral potassium tetraborate (K 2 B 4 O 7 ) electrolyte. The catalyst exhibited high activity and low overpotential for O 2 evolution under mild conditions. The main functional composition of the catalyst was a redox couple of Ag 2 O/AgO. Catalytic activity during oxygen evolution was evaluated by cyclic voltammetry and Tafel plot. The effects of the concentration, temperature, and pH of K 2 B 4 O 7 solution on the catalyst, and the Faradaic efficiency of the oxygen evolving reaction were examined. The results show that the Ag-OEC exhibits excellent oxygen evolution properties, with an oxygen evolving overpotential of 318 mV at a current density of 1 mA/cm 2 .

研究领域: 电催化 · 能源化学 · 材料科学 · 物理化学 · 可持续能源
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NEW JOURNAL OF CHEMISTRY · 2019 ·Vol. 43 ·期 24 ·9628-9633 · IF 3.069

Direct fabrication of bimetallic AuPt nanobrick spherical nanoarchitectonics for the oxygen reduction reaction

Alam Venugopal Narendra Kumar,Shuli Yin,Ziqiang Wang,Xiaoqian Qian,Dandan Yang,You Xu,Xiaonian Li,Hongjing Wang,Liang Wang

The shape-controlled synthesis of bimetallic Pt-based nanoarchitectonics has attracted considerable interest due to their remarkable electrocatalytic activity for the oxygen reduction reaction (ORR). In this work, we report a direct method for the fabrication of unique bimetallic AuPt nanobrick spherical nanoarchitectonics (AuPt NSNs) in aqueous solution. Benefiting from their rugged surfaces and bimetallic compositions, AuPt NSNs exhibit excellent electrocatalytic performance for the ORR. The proposed method is very useful for the fabrication of metallic nanoarchitectonics with rugged surfaces.

研究领域: 纳米材料学 · 电化学 · 催化化学 · 材料科学 · 能源化学
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ENVIRONMENTAL RESEARCH · 2018 · IF 4.732

Photocatalytic degradation of cooking fume on a TiO2-coated carbon nanotubes composite filter

Chengwei Xu,Wenxia Xie,Xiaodong Si,Jun Zhang,Jiangang Yang

A TiO 2 /MWCNTs/Al 2 O 3 /NF (TiO 2 nanoparticles/multi-walled carbon nanotubes /Al 2 O 3 -modified nickel foams) composite filter was prepared through grown of MWCNTs upon Al 2 O 3 -modified nickel foams using chemical vapor deposition (CVD) method and then coated TiO 2 nanoparticles onto MWCNTs using dip-coating method. The MWCNTs forms a network-like structure on the surface layer of composite filter. The BET surface area of TiO 2 /MWCNTs/Al 2 O 3 /NF composite filter is more than 375 times higher than that of the pristine nickel foam. The degradation performance of oil particles was evaluated. Under optimized reaction conditions, 90% of the oleic acid on the filter was decomposed after 25 h. In addition, the effect of reaction temperature and light intensity were studied. Increased reaction temperature and light intensity were found to significantly improve the degradation rate and restrain the formation of refractory product. Furthermore, a parallel reaction kinetic model was adopted for degradation of oleic acid on the composite filter. The composite filter can reduces the accumulation of oil particles on the filter and the energy consumption of the filter. This approach proposes a new way to treat the cooking fume emission at residential building roofs.

研究领域: 环境科学 · 材料科学 · 化学工程 · 大气污染控制 · 纳米技术
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CERAMICS INTERNATIONAL · 2023 ·Vol. 49 ·期 11 ·18776-18785 · IF 5.2

Research on synthesis and nucleation mechanism of silicon nanowire by silver catalysis in molten salt

Jiaxu Cheng,Siwei Jiang,Jiahong Fan,Jun Yao,Ning Du,Xue Li,Ding Wang,Peng Dong,Zhongren Zhou,Yingjie Zhang

Molten salt electrolytic synthesis of silicon is identified as a potential industry method due to its thorough deoxidization of oxide and short-flow synthetic progress. However, figuring out a more efficient and sustainable strategy for the increase of the reduction process as well as the control of product morphology still needs endless research. In this study, benefiting from the high electrical conductivity of metallic silver and the easy separation of silver from silver-silicon alloys during the electrolysis of SiO 2 , metallic silver was introduced to electric-catalyze the production of silicon. Firstly, metallic silver was introduced into the silica matrix by a simple silver mirror reaction. Secondly, the mixed Ag\SiO 2 precursor was located at the cathode for molten salt electrolysis . Finally, silicon nanowires were herein achieved in molten NaCl–CaCl 2 . Mechanisms of metal Ag played during the electric-polarization process of silica and the electrochemical nucleation of silicon were further analyzed by X-ray diffraction (XRD), Scanning Electron Microscope (SEM), Field-Emission Scanning Electron Microscope (FESEM), Transmission Electron Microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and Raman spectra . The results demonstrate that Ag helps construct Si nanowires via a classic Ag-Si binary alloy-droplet process and provided quantitative guidance for the large-yield production of silicon nanowires via adding 0.08–0.17 g Ag versus 1 g SiO 2 , controlling the temperature at 850–900 °C and electrolysis voltage at 2.6–2.8 V (2.6V at first 1 h and 2.8V at last 5 h). The synthesized silicon nanowires present two types of linear structures based on two three-phase interlines (3PIs) models and a streamed long-straight nanowire is observed.

研究领域: 材料科学 · 纳米科技 · 电化学 · 无机化学 · 能源材料 · 半导体材料
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CHINESE JOURNAL OF CATALYSIS · 2018 ·Vol. 38 ·期 12 ·2132-2140 · IF 3.525

Nanotube array-like WO3/W photoanode fabricated by electrochemical anodization for photoelectrocatalytic overall water splitting

Lingfeng Li,Xiaolong Zhao,Donglai Pan,Guisheng Li

Photoactive WO 3 is attractive as a photocatalyst for green energy evolution through water splitting. In the present work, an electrochemical anodic oxidation method was used to fabricate a photo-responsive nanotube array-like WO 3 /W (NA-WO 3 /W) photoanode from W foil as a precursor. Compared with a reference commercial WO 3 /W electrode, the NA-WO 3 /W photoanode exhibited enhanced and stable photoelectrocatalytic (PEC) activity for visible-light-driven water splitting with a typical H 2 /O 2 stoichiometric ratio of 2:1 and quantum efficiency of approximately 5.23% under visible-light irradiation from a light-emitting diode ( λ = 420 nm, 15 mW/cm 2 ). The greatly enhanced PEC performance of the NA-WO 3 /Wphotoanode was attributed to its fast electron–hole separation rate, which resulted from the one-dimensional nanotube array-like structure, high crystallinity of monoclinic WO 3 , and strong interaction between WO 3 and W foil. This work paves the way to a facile route to prepare highly active photoelectrodes for solar light transfer to chemical energy .

研究领域: 材料科学 · 物理化学 · 能源化学 · 纳米科技 · 光催化 · 电化学 · 可再生能源
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MICROPOROUS AND MESOPOROUS MATERIALS · 2015 · IF 3.453

Synthesis and photocatalytic activity of mesoporous TiO2 nanoparticle using biological renewable resource of un-modified lignin as a template

Xiaoyun Chen,Dong-Hau Kuo,Dongfang Lu,Yongxuan Hou,Yen-Rong Kuo

Mesoporous TiO 2 was synthesized by a hydrolysis precipitation method with the utilization of the biological renewable resource of lignin as template and TiCl 4 as reactant. The photocatalytic activity of TiO 2 was investigated by the degradation of phenol under UV light irradiation. The microstructure, crystallinity , powder characteristic, and chemical bonding of the catalyst were analyzed. The 500 °C-calcined TiO 2 had average crystallite size of about 11.1 nm and a mesoporous structure with specific area of 165.8 m 2 /g and pore volume of 0.312 cm 3 /g. The results showed that TiO 2 synthesized with lignin template exhibited high photocatalytic activity, which can be attributed to the electronegativity and the network skeleton of lignin to uniformly distribute the TiO 2 precursor for forming TiO 2 mesoporous particles. The mechanism for the improved photodegradation of the lignin-assisted TiO 2 was proposed.

研究领域: 材料科学 · 环境化学 · 纳米技术 · 光催化 · 绿色化学
✓ 已验证 DOI 高影响因子
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CATALYSIS COMMUNICATIONS · 2013 · IF 2.915

CNTs/rGO spheres decorated with CuxO (x = 1 or 2) nanoparticles and its photocatalytic performance

Bin Zeng,Xiaohua Chen,Xutao Ning,Chuansheng Chen,Aiping Hu,Weina Deng

Carbon nanotubes and reduced graphene oxides (CNTs/rGO) sphere decorated with Cu 2 O, CuO nanoparticles (Cu x O–CNTs/rGO) was successfully synthesized by spray drying and post-calcinating method for the first time. Scanning electron microscopy and transmission electron microscopy observations confirmed that CNTs/rGO formed a spherical micrometer structure and Cu x O nanoparticles were decorated on their surface. The experimental results indicated that this novel architecture enhanced photocatalytic performance with 97.5% decomposition of methyl orange (MO) after 20   min in the presence of H 2 O 2 under visible light irradiation, which was much higher than that of pure Cu x O powders (31.2%).

研究领域: 材料科学 · 纳米科技 · 光催化 · 环境功能材料 · 复合材料
✓ 已验证 DOI 高影响因子
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Small · 2022 ·Vol. 18 ·期 48 ·2205163 · IF 15.153

Self-Supporting Multicomponent Hierarchical Network Aerogel as Sulfur Anchoring-Catalytic Medium for Highly Stable Lithium–Sulfur Battery

Shuhao Tian,Juanjuan Huang,Hongcen Yang,Guo Liu,Qi Zeng,Di Wang,Xiao Sun,Kun Tao,Guohan Liu,Shanglong Peng

The low utilization rate of active materials, shuttle effect of lithium polysulfides (LiPSs), and slow reaction kinetics lead to the extremely low efficiency and poor high current cycle stability of lithium sulfur batteries (Li–S batteries). In this paper, a self-supporting multicomponent hierarchical network aerogel is proposed as the modified cathode (S/GO@MX@VS 4 ). It consists of graphene (GO) and MXene nanosheets (MX) loaded with VS 4 nanoparticles. The experimental results and first-principles calculations show that the GO@MX@VS 4 aerogel has strong adsorption and reversible conversion effects on LiPSs. It can not only inhibit the shuttle effect and improve the utilization rate of active substances by keeping the chain crystal structure of VS 4 , but also promote the reversibility and kinetics of the reaction by accelerating the liquid–solid transformation in the reduction process and the decomposition of insoluble Li 2 S in the oxidation process. The GO@MX@VS 4 aerogel modified cathode with a multicomponent synergy exhibits the capacity ratios (Q 1 /Q 2 ) at different discharge stages is close to the theoretical value (1:2.8), and the capacity decay per cycle is 0.019% in 1200 cycles at 5C. Also, a high areal capacity of 6.90 mAh cm −2 is provided even at high sulfur loading (7.39 mg cm −2 ) and low electrolyte/sulfur ratio (E/S, 8.0 µL mg −1 ).

研究领域: 电化学储能 · 材料科学 · 纳米材料 · 能源化学 · 电池技术 · 表面催化
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Molecular Catalysis · 2020 · IF 3.687

Isoprene polymerizations catalyzed by TiCl4/MgCl2 type Ziegler-Natta catalysts with different titanium contents

Wei Peng,Jianmei Xie,Junying Zhang,Xia Yang,Aihua He

The isoprene polymerization kinetics by using TiCl 4 /MgCl 2 type Ziegler-Natta catalysts (TMC) with different titanium contents were studied for better understanding the possible active-specie structures of heterogeneous Ziegler-Natta (Z-N) catalysts for conjugated diene polymerizations. The catalytic features including the catalytic activity (CA), number of active centers ([C*]/[Ti]), rate constant for polymerization (k p ), stereoregularity of these TMC catalysts were studied. The low titanium content catalyst TMC-1 (Ti = 0.09 wt.%) with more isolated mononuclear titanium species showed higher CA and yielded cis-1,4-/trans-1,4- mixed microstructure polyisoprene with low molecular weight ( M w ) in the initial polymerization stage. The medium high titanium content catalyst TMC-2 (Ti = 2.38 wt.%) with more clustered mononuclear titanium species showed lower CA and yielded cis-1,4-/trans-1,4- mixed microstructure polyisoprene with high M w in the early stage of polymerization. The high titanium content catalyst TMC-3 (Ti = 3.76 wt.%) presented lowest CA and yielded high trans-1,4- polyisoprene with higher M w .

研究领域: 高分子化学 · 催化化学 · 聚合物合成 · 材料科学 · 配位聚合
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Small · 2023 ·Vol. 19 ·期 41 ·2302685 · IF 13.3

Boosting the Hydrogen Evolution Reaction Performance of P-Doped PtTe2 Nanocages via Spontaneous Defects Formation

Hancheng Ma,Xiang Huang,Luyu Li,Wei Peng,Sheng Lin,Yao Ding,Liqiang Mai

PtTe 2 , a member of the noble metal dichalcogenides (NMDs), has aroused great interest in exploring its behavior in the hydrogen evolution reaction (HER) due to the unique type-II topological semimetallic nature. In this work, a simple template-free hydrothermal method to obtain the phosphorus-doped (P-doped) PtTe 2 nanocages with abundant amorphous and crystalline interface (A/C-P-PtTe 2 ) is developed. Revealed by density functional theory calculations, the atomic Te vacancies can spontaneously form on the basal planes of PtTe 2 by the P doping, which results in the unsaturated Pt atoms exposed as the active sites in the amorphous layer for HER. Owing to the defective structure, the A/C-P-PtTe 2 catalysts have the fast Tafel step determined kinetics in HER, which contributes to an ultralow overpotential ( η = 28 mV at 10 mA cm −2 ) and a small Tafel slope of 37 mV dec −1 . More importantly, benefiting from the inner stable crystalline P-PtTe 2 nanosheets, limited decay of the performance is observed after chronopotentiometry test. This work reveals the important role of the inherent relationship between structure and activity in PtTe 2 for HER, which may bring another enlightenment for the design of efficient catalysts based on NMDs in the near future.

研究领域: 材料科学 · 电化学 · 纳米催化 · 能源材料 · 计算材料学
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Journal of Materials Chemistry A · 2020 ·Vol. 9 ·期 7 ·3985-3994 · IF 11.301

Selective hydrogen–deuterium exchange in graphitic carbon nitrides: probing the active sites for photocatalytic water splitting by solid-state NMR

Ruidi Wang,Bei-Bei Xu,Jiachen Wang,Xue Lu Wang,Ye-Feng Yao

The relationship between the structural characteristics and photocatalytic reaction mechanisms of graphitic carbon nitride (g-C3N4) still remains unclarified at the molecular level, which severely hinders the further development of this field. The present study addresses this issue by employing an innovative strategy to investigate the relationship between the H-containing structures of g-C3N4 and its water splitting properties. The exchangeable and unexchangeable protons of the H-containing groups of g-C3N4 were differentiated by selective deuteration, providing a way to distinguish the hydrophilic and relatively non-hydrophilic H-containing groups of g-C3N4. A combination of advanced solid-state NMR approaches reveals that amino group defects (CN2(NHx)) on the C–N skeleton of the photocatalyst likely serve as hydrophilic active sites for facilitating the photocatalytic hydrogen evolution reaction. Accordingly, the newly synthesized g-C3N4 sample having a high concentration of CN2(NHx) by design demonstrates an enhanced H2 yield by a factor of 17 compared to that of pure g-C3N4.

研究领域: 材料化学 · 光催化 · 固体核磁共振 · 表面科学 · 能源材料
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