CATALYSIS COMMUNICATIONS
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2020
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IF 3.612
Miao Ren,Fengping Fu,Qian He,Fang Liao
A novel ZSMo core-shell nanowire photocatalyst was synthesized by ion exchange and hydrothermal methods. The photocatalytic activity of ZSMo nanocomposites was evaluated via photolysis of water to produce hydrogen. The results showed that the hydrogen generation rate of ZSMo-0.1 core-shell nanowires was the highest, which was about 23 times that of pure ZnO. The improvement of photocatalytic activity was attributed to the formation of type II and ternary heterojunctions, which enable the rapid separation of photo-induced charge carriers and capture more light radiation. It was confirmed by UV–Vis diffuse reflectance spectroscopy, electrochemical impedance spectroscopy and photocurrent analysis.
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ELECTROCHIMICA ACTA
·
2019
·
IF 5.383
Shuangyue Hou,Yue Lian,Zongying Xu,Dawei Wang,Chaolei Ban,Jing Zhao,Huaihao Zhang
the ball-flower like composite (NiS 2 @MoS 2 ) was successfully synthesized by a convenient two-step hydrothermal method using Ni(NO 3 ) 2 ·6H 2 O and (NH 4 ) 6 Mo 7 O 24 ·4H 2 O as precursors. MoS 2 nano-sheets, uniformly generated on NiS 2 surface, increases the surface roughness and porosity, and accelerates the electrons and ions transfer of the composite. The synergistic effect of Mo and Ni improves the conductivity of the materials. Furthermore, by controlling the atomic ratio of Mo to Ni in precursors, the composite MN-1 (the molar ratio of MoS 2 to NiS 2 is 1:1) with the best capacity performance was obtained. The morphology and composition were characterized by a variety of means, such as TEM, SEM, XPS, XRD, BET and EDX. The electrochemical measurement results exhibited high specific capacity (848.2 C g −1 at specific current of 1 A g −1 ) and good cycling stability (83.1% specific capacity retention after 10000 GCD cycles) of MN-1 in 6 M KOH. Furthermore, an asymmetric supercapacitor was assembled with MN-1 as positive electrode and activated carbon as negative electrode. When the power density is 0.8 kW kg −1 , its energy density reaches up to 37.2 Wh kg −1 . The present work may offer new design strategy for electrode materials .
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APPLIED SURFACE SCIENCE
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2019
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IF 5.155
Wei Chen,Rui-Qiang Yan,Jian-Qun Zhu,Guo-Bo Huang,Zhong Chen
All-solid-state Z-scheme CdS/QDs/ZnIn 2 S 4 architectures with MoS 2 quantum dots as solid-state electron mediator were successfully designed and constructed by optimally combining one-dimensional CdS nanorods, zero-dimensional MoS 2 quantum dots (QDs) and two-dimensional ZnIn 2 S 4 nanosheets. The photocatalytic water splitting for hydrogen evolution demonstrated that such structural design can synergistically trigger remarkably improved visible-light-driven photocatalytic activity. Photocatalytic H 2 -evolution at 2107.5 μmol g −1 h −1 was achieved on this CdS/QDs/ZnIn 2 S 4 architectures under visible light irradiation, exceeding those of bare CdS nanorods and pure ZnIn 2 S 4 nanosheets by a factor of 26 and 62, respectively. This highly efficient photocatalytic activity arises from the effective charge separation and favourable electron mediator of MoS 2 QDs. The Z-scheme charge separation mechanism was verified by the ESR, PL-TA and organic electron acceptor test.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2019
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IF 4.084
Lei-Lei Li,Xing-Liang Yin,Dong-Hui Pang,Xin-Xin Du,Han Xue,Hua-Wei Zhou,Qing-Xia Yao,Huai-Wei Wang,Jun-Chao Qian,Jie Yang,Da-Cheng Li,Jian-Min Dou
Exploration of cost-efficient and high-performance photocatalyst for H 2 evolution by using a facile approach is of great importance. In this manuscript, a facile one-pot method was employed to fabricate MoS 2 /CdS heterostructures with MoS 2 intimately grown on the surface of CdS resulting in the formation of well-defined heterostructures. Screen experiment reveals the optimized photocatalytic H 2 evolution performance of MoS 2 /CdS is far exceeding that of pristine CdS by a factor of more than 162. The outstanding performance can be ascribed to the formation of heterostructures which accelerate charge transportation and separation, and the MoS 2 serving as a cocatalyst for the decrease of H 2 overpotential. Moreover, the photocatalytic mechanism of the MoS 2 /CdS was carefully investigated, which contributes to the deep understanding of the photocatalytic process and the designation of other low-cost and high-efficient photocatalyst.
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ACS Sustainable Chemistry & Engineering
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2019
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IF 6.97
Shan Yuan,Miaomiao Weng,Dajun Liu,Xingquan He,Li−Li Cui,Tewodros Asefa
Platinum (Pt)-based catalysts are widely used for the oxygen reduction reaction (ORR) in many energy conversion and storage devices, such as fuel cells and metal–air batteries. However, Pt is among the least earth abundant and most expensive elements; as a result, these energy devices are currently difficult to scale up. This has motivated researchers to try to develop sustainable and alternative catalysts that can replace Pt as well as other noble metal-based catalysts. Herein, novel Co nanocrystals-loaded, Zn, N, and S codoped carbon materials, dubbed (Co, Zn)/NSC, which have hollow spherical structures and which can serve as efficient ORR catalysts, are developed via a facile synthetic method involving microemulsion and pyrolysis. The key in the synthesis of these nonprecious metal-containing heteroatom-doped nanostructured carbon catalysts is the preparation of nanosized, mixed metal–organic frameworks (MOFs) in solution using microemulsion, and the exploitation of their morphology to produce hollow spherical structures via pyrolysis. Elemental mapping shows the presence of Co, Zn, N, and S atoms throughout the structures of the materials. The material obtained at pyrolysis temperature of 800 °C, denoted (Co, Zn)/NSC-800, exhibits excellent electrocatalytic activity for ORR in alkaline and acidic media, with onset potentials of 1.000 and 0.802 V vs RHE, respectively. In addition, the catalyst is stable and tolerates the methanol crossover reaction in both cases. Thus, this material has the potential to replace Pt catalysts in fuel cells. Moreover, the synthetic approach used to make it can be extended to produce other robust, nonprecious transition metal-based catalysts for ORR.
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ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY
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2019
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IF 4.527
Yunyun Li,Jiaxun Guan,Jiating Zhao,Bai Li,Yu-feng Li,Yuxi Gao
Mercury (Hg) pollution seriously threatens food safety and has attracted global attention. Phytoextraction, due to its low cost, applicability, and environmental friendliness, is considered a new technology for clean-up of heavy metal contamination in the environment. However, the low bioavailability of Hg in polluted areas greatly limits the applicability of phytoextraction. Here, we compared the effects of six common chelating ligands on the absorption and transport of Hg in maize ( Zea mays L.), which has a high biomass and short growth cycle. The results showed that the root length and biomass of maize seedlings of the groups treated with the six chelating ligands (EDTA, iodide, ammonium, thiosulfate , thiocyanate, and thiocarbamide) did not change compared with those of the non-treated groups. Co-exposure to Hg and each chelating ligand markedly alleviated the inhibitory effect induced by Hg. Iodide treatment resulted in the lowest root Hg content and highest translocation factor (TF) value, while ammonium treatment gave rise to the highest shoot Hg concentration and lowest TF. Compared with other chelating ligands, thiosulfate exhibited the maximum alleviation of Hg toxicity and achieved the highest concentration of Hg in the roots and aerial parts. Moreover, the TF and Hg accumulation in the thiosulfate and Hg co-exposed group were much higher than those in the group exposed to Hg alone. This finding suggests that, among these common chelating ligands, thiosulfate compounds have great potential for Hg phytoextraction, while the others can immobilize Hg in polluted areas.
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PubMed
高影响因子
ChemSusChem
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2019
·Vol. 13
·期 4
·756-762
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IF 7.804
Guoqiang Zhang,Xiang Ling,Guoshuai Liu,Yangsen Xu,Shuning Xiao,Qitao Zhang,Xun Yang,Chuntian Qiu,Hongwei Mi,Chenliang Su
Graphical Defective is effective : A defective Zn–Cd–S photocatalyst is prepared on a large scale and used to perform water splitting with a high apparent quantum yield (5.0 % at λ =420 nm) towards H 2 evolution in a system without a cocatalyst or sacrificial agent. Solar-driven H 2 evolution is an essential process for sustainable energy development. Currently, the greatest challenge is the development of efficient photocatalysts to drive this reaction, especially in pure water systems (without the use of a sacrificial agent). In this study, structural defects in Zn–Cd–S nanorod photocatalysts are found to increase charge separation efficiency significantly by sevenfold. Efficient H 2 evolution (352.7 μmol h −1 g −1 , 100 mg of catalyst) is achieved by using this defective Zn–Cd–S nanorod photocatalyst in the absence of sacrificial agents and precious metal cocatalysts under visible-light irradiation. Thus, this cocatalyst- and sacrificial-agent-free, visible-light-responsive system shows remarkable potential as a new artificial photosynthesis route for green H 2 production.
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ACS Applied Nano Materials
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2019
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IF 0
Le Zhou,Hongwen Zhang,Haoming Bao,Yi Wei,Hao Fu,Weiping Cai
Silver (Ag)-based Janus nanoparticles (NPs) are of broad interest for extensive applications due to their excellent photoelectric performances and special structure. However, it still remains challenging to prepare this type of Janus NP with high uniformity in a large scale. Here, we present a facile wet-chemical strategy to synthesize Ag-MoS2 Janus NPs via adding an appropriate amount of AgNO3 into the MoS2 nanosphere (200 nm in size)-contained aqueous solution. These Janus NPs represent a new type of heterogeneous nanostructure. Each Janus NP is made up of one tiny-Ag-dot-decorated MoS2 nanosphere and one polyhedral Ag single crystal (∼100 nm in size), and both of them attach together, showing a snowman-like dimer. Such Janus NPs or dimers can not be detached by the ultrasonic vibration even with a high power, showing strong adhesion between them. Further, the morphology and size of the polyhedral Ag nanocrystals attached on MoS2 nanospheres can be controlled by the AgNO3 addition amount, reaction time, and temperature. A growth model is proposed to understand the formation of these Janus NPs, which is based on the tiny Ag dots’ aggregation and oriented connection mechanism. Importantly, such Ag-MoS2 Janus NPs can be used as nanomotors, due to their asymmetric catalytic component structure, and self-propelled in H2O2 fuel solutions. They show good directional motion and significant dependence of their speed on fuel concentration. This study expands our understanding of the formation of heterogeneous Janus particles and provides a promising platform to investigate active colloids as nanomotors.
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JOURNAL OF NANOPARTICLE RESEARCH
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2020
·Vol. 22
·期 1
·1-12
·
IF 2.132
Hou Junjie,Zhou Xuemei,Yang Zhi,Nie Huagui
Oxygen evolution reaction (OER) catalysts are of central importance for electrocatalytic water oxidation and fuel generation, while it is still an urgent requirement to design and develop efficient OER catalysts with rapid kinetics and low overpotentials. Herein, we report an electrochemical deposition method to fabricate carbon nanotubes/N-doped cuprous sulfide (CNTs/N-Cu 2 S) composites using thiourea and a CuSO 4 solution as the S and Cu sources, respectively. The advantages of this strategy include low cost, simple processing and the absence of templates or surfactants that can otherwise affect the electrochemical properties of the products. The N supplied by the thiourea can be used as a doping agent as a result of the in situ formation of small N-Cu 2 S particles, which can increase larger surface area and create more active sites to enhance OER catalytic activity, compared with that obtained with materials synthesized without adding the thiourea. The synergic interface of CNTs and N-Cu 2 S can improve conductivity and efficient chemical transfer in the composites electrodes by introducing CNTs. Under the optimal experimental conditions, the CNTs/N-Cu 2 S-5cyc composites present an excellent activity with the current density of 10 mA cm −2 at a low OER overpotential of 280 mV, the Tafel slope of 63 mV dec −1 and a strong electrochemical stability in 1.0 M KOH solution.
Graphical abstract
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APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING
·
2019
·Vol. 125
·期 11
·1-7
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IF 1.784
Ge Bo,Li Fengyan,Zhao Xingchuan,Li Wenzhi,Ren Guina,Wang Min,Zhang Zhaozhu
Sewage not only contains water-soluble contaminants but water-insoluble contaminants as well. Superhydrophobic CdS–melamine foam prepared in this research satisfies the requirements of water purification. The photocatalyst CdS effectively adsorbs light energy to generate active species (⋅O 2 − ) for degrading water-soluble pollutants. At the same time, superhydrophobic/superoleophilic characteristic of the melamine sponge can be utilized to remove water-insoluble pollutants. Finally, the degradation mechanism of materials was obtained by studying the parameters such as band gap and valence band structure, as well as by analyzing the experimental data of active species.
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ELECTROCHIMICA ACTA
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2019
·
IF 5.383
Jianhui Feng,Hu Zhou,Danyang Chen,Ting Bian,Aihua Yuan
The electrocatalysts with high activity and low cost are essential for hydrogen evolution reaction (HER). Herein, we report an approach to prepare hierarchical core-shell structures Zn x Co 1-x /NC@MoS 2 . The Zn/Co ratio affects the particle sizes of Zn x Co 1-x /NC polyhedra and the distribution of Co nanoparticles , resulting in the change of the amount of exposed active sites and further afforded tunable HER activities. Notably, the hybrids exhibit significantly superior catalytic activities to pristine MoS 2 . The optimal catalyst displays an extraordinary HER performance in acid media with a low overpotential of 130 mV at 10 mA cm −2 and high durability. The remarkable HER properties mainly originate from the fantastic structural characteristics such as abundant exposure of MoS 2 edge-sites, uniform distribution of Co-N x species, as well as the porousness and high conductivity of supports. This research provides a promising strategy to develop inexpensive and highly-efficient HER electrocatalysts derived from metal-organic frameworks and MoS 2 .
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ACS Sustainable Chemistry & Engineering
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2019
·
IF 6.97
Lin Long,Erqi Yang,Xiaosi Qi,Ren Xie,Zhong-chen Bai,Shuijie Qin,Chaoyong Deng,Wei Zhong
Lots of research have focused on the core/shell structure nanocomposites owing to their synergistic effect that were considered as the most promising high-performance microwave absorbers (MAs). However, the excellent comprehensive properties of MAs are still in urgent need. Herein, positive and reverse core/shell structure CoxFe3–xO4/MoS2 (x = 1.5, 0.75 and 0.5) and MoS2/CoxFe3–xO4 (x = 0.5) nanocomposites were elaborately produced through an inexpensive two-step hydrothermal process. It was found that the CoxFe3–xO4/MoS2 samples exhibited a much smaller optimal reflection loss (RLopt) value and a broader frequency bandwidth (fb) with the lower value of matching thickness (dm) when the CoxFe3–xO4/MoS2 loadings were raised to 60 from 30 wt %. With the x value decreasing from 1.5 to 0.5, the obtained CoxFe3–xO4/MoS2 samples displayed a much smaller RLopt value with a thinner dm and a much larger fb value with the thin dm (∼2 mm). The sample consisting of 60 wt % CoxFe3–xO4/MoS2 (x = 0.5) exhibited an RLopt value of −66.83 dB with the dm of merely 1.57 mm, and its corresponding fb value could reach 6.64 GHz with the dm of 2.02 mm. Moreover, compared with the MoS2/CoxFe3–xO4 (x = 0.5) sample, the CoxFe3–xO4/MoS2 (x = 0.5) sample displayed evidently better microwave absorbing comprehensive performances in terms of low RLopt value, large fb value, and high chemical stability. Generally, the obtained results demonstrated that the designed CoxFe3–xO4/MoS2 nanocomposites could act as MAs with outstanding comprehensive properties.
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