Wei Zhang

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Organization: Jilin University
Department: Department of Materials Science, Key Laboratory of Mobile Materials MOE, State Key Laboratory of Superhard Materials
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Co-reporter:Liang Wang;Jian Zhang;Guoxiong Wang;Chengtao Wang;Chaoqun Bian;Feng-Shou Xiao
Chemical Communications 2017 vol. 53(Issue 18) pp:2681-2684
Publication Date(Web):2017/02/28
DOI:10.1039/C6CC09599B
We reported selective hydrogenolysis of carbon–oxygen species over a CeO2-supported Au–Pt alloy catalyst (Au–Pt/CeO2) using biomass-derived formic acid as the hydrogen source. The success of this reaction is reasonably attributed to the high efficiency of Au–Pt/CeO2 in the tandem steps of formic acid dehydrogenation and carbon–oxygen species hydrodeoxygenation.
Co-reporter:Weizhen Yu, Zhiling Xin, Wei Zhang, Yanan Xie, Juan Wang, Shuo Niu, Yifei Wu, Lidong Shao
Chemical Physics Letters 2017 Volume 686(Volume 686) pp:
Publication Date(Web):16 October 2017
DOI:10.1016/j.cplett.2017.08.020
•Pd–P/OCNTs using NaH2PO2 as the P source and reducing agent was developed.•P and Pd were anchored through the electrostatic interaction and chemical bonds.•Pd NPs could be effectively incorporated with P species (P0 or PV).•P can feasibly change the outer electron structure of the Pd NPs.•Pd–P/OCNTs showed enhanced the electrocatalytic performance for FAO.In the present work, O–functionalized carbon nanotubes (OCNTs) supported Pd–P nanoparticles (Pd–P/OCNTs) were prepared by using sodium hypophosphite (NaH2PO2) as the P source and the reducing agent. The presence of O-functionalities on the carbon surface provide a microenvironment of the reaction system which favors the anchorage of P precursors and Pd salt ions through the electrostatic interaction and the formation of chemical bonds on the carbon support. Thus, Pd nanoparticles supported on the OCNTs could be efficiently incorporated with P. Pd with the modified outer electron structure enhanced the electrocatalytic performance for formic acid oxidation (FAO).Download high-res image (135KB)Download full-size image
Co-reporter:Wei Zhang;Weitao Zheng
Advanced Functional Materials 2016 Volume 26( Issue 18) pp:2988-2993
Publication Date(Web):
DOI:10.1002/adfm.201600240

The emerging single-atom field spans single-atom catalysis in chemistry and single-atom manipulation in physics up to the state-of-the-art characterization via imaging and spectroscopy. These interdisciplinary progresses have been interacted closely with the development of materials science, underscoring the principle that the single atom excels as the smallest functional material. This simple concept not only permits to reinvent our understanding of the nature of materials, but also promises unambiguously to have a great impact on other physical sciences.

Co-reporter:Wei Zhang and Wei Tao Zheng  
Physical Chemistry Chemical Physics 2015 vol. 17(Issue 22) pp:14461-14469
Publication Date(Web):06 May 2015
DOI:10.1039/C5CP01705J
The atomic features of materials' surfaces have fundamental importance for applications in numerous fields, such as heterogeneous catalysis, energy conversion and thin-film growth. Now transmission electron microscopy (TEM) and affiliated techniques have thoroughly revolutionized many disciplines of natural sciences, and are becoming some of the best solutions for surface exploration. In this Perspective, we try to summarise the important progress in surface elucidation by applying the state-of-the-art TEM, which covers (1) from the essential features of oxides to their dynamic behaviors, and the interactions between surfaces and gases; (2) the visualization of emerging materials from zero-dimensional single atoms to two-dimensional materials, and the development towards an ultimate integration of three-dimensional surfaces. Plenty of room has been made for TEM exploration of a material's surface, and the surface-integral frontiers are being pushed further.
Co-reporter:Dr. Wei Zhang;Dr. Bingsen Zhang;Dr. Weitao Zheng;Dr. Dang Sheng Su
ChemCatChem 2015 Volume 7( Issue 22) pp:3651-3654
Publication Date(Web):
DOI:10.1002/cctc.201500859

Abstract

The complex (Mo,V)-based multicomponent M1 phase with a characteristic network of pentagonal, hexagonal, and heptagonal channels is the key catalyst for the catalytic oxidation from propane to acrylic acid. Herein, the atomic-scale structural dynamics in the orthorhombic Mo-V-Te-Nb oxide were probed under electron-beam stimulation. The recorded in situ scanning transmission electron microscopy images unravel the strong bonding and correlation between the (Mo,V)O6 octahedra and the central Nb moieties in the pentagonal channels. Such dynamic electron microscopy imaging can pave the way to chemically tailoring structural units of a general catalogue of functional polyoxometalates through applying top-down electron-beam probing.

Co-reporter:HaoXiang Wang;Hong Chen;WeiTao Zheng
Science China Technological Sciences 2015 Volume 58( Issue 11) pp:1779-1798
Publication Date(Web):2015 November
DOI:10.1007/s11431-015-5930-0
Both energy density and power density are crucial for a supercapacitor device, where the trade-off must be made between the two factors towards a practical application. Herein we focus on pseudocapacitance produced from the electrode and the electrolyte of supercapacitors to simultaneously achieve high energy density and power density. On the one hand, layered transition metal hydroxides (Ni(OH)2 and Co(OH)2) are introduced as electrodes, followed with exploration of the effect of the active materials and the substrate on the electrochemical behavior. On the other hand, various redox electrolytes are utilized to improve the specific capacitance of an electrolyte. The roadmap is to select an appropriate electrode and a dedicated electrolyte in order to achieve high electrochemical performance of the supercapacitors.
Co-reporter:Liang Wang; Hong Wang; Andrew E. Rice; Wei Zhang; Xiaokun Li; Mingshu Chen; Xiangju Meng; James P. Lewis;Feng-Shou Xiao
The Journal of Physical Chemistry Letters 2015 Volume 6(Issue 12) pp:2345-2349
Publication Date(Web):June 4, 2015
DOI:10.1021/acs.jpclett.5b00655
A synergistic effect between individual components is crucial for increasing the activity of metal/metal oxide catalysts. The greatest challenge is how to control the synergistic effect to obtain enhanced catalytic performance. Through density functional theory calculations of model Au/TiO2 catalysts, it is suggested that there is strong interaction between Au nanoparticles and Ti species at the edge/corner sites of anatase, which is favorable for the formation of stable oxygen vacancies. Motivated by this theoretical analysis, we have rationally prepared Au nanoparticles attached to edge/corner sites of anatase support (Au/TiO2-EC), confirmed by their HR-TEM images. As expected, this strong interaction is well characterized by Raman, UV–visible, and XPS techniques. Very interestingly, compared with conventional Au catalysts, Au/TiO2-EC exhibits superior catalytic activity in the oxidations using O2. Our approach to controlling Au nanoparticle positioning on anatase to obtain enhanced catalytic activity offers an efficient strategy for developing more novel supported metal catalysts.
Co-reporter:Dr. Wei Zhang;Dr. Weitao Zheng
ChemCatChem 2015 Volume 7( Issue 1) pp:48-50
Publication Date(Web):
DOI:10.1002/cctc.201402757
Co-reporter:Wei Zhang and Wei Tao Zheng
Physical Chemistry Chemical Physics 2015 - vol. 17(Issue 22) pp:NaN14469-14469
Publication Date(Web):2015/05/06
DOI:10.1039/C5CP01705J
The atomic features of materials' surfaces have fundamental importance for applications in numerous fields, such as heterogeneous catalysis, energy conversion and thin-film growth. Now transmission electron microscopy (TEM) and affiliated techniques have thoroughly revolutionized many disciplines of natural sciences, and are becoming some of the best solutions for surface exploration. In this Perspective, we try to summarise the important progress in surface elucidation by applying the state-of-the-art TEM, which covers (1) from the essential features of oxides to their dynamic behaviors, and the interactions between surfaces and gases; (2) the visualization of emerging materials from zero-dimensional single atoms to two-dimensional materials, and the development towards an ultimate integration of three-dimensional surfaces. Plenty of room has been made for TEM exploration of a material's surface, and the surface-integral frontiers are being pushed further.
Co-reporter:Liang Wang, Jian Zhang, Guoxiong Wang, Wei Zhang, Chengtao Wang, Chaoqun Bian and Feng-Shou Xiao
Chemical Communications 2017 - vol. 53(Issue 18) pp:NaN2684-2684
Publication Date(Web):2017/02/07
DOI:10.1039/C6CC09599B
We reported selective hydrogenolysis of carbon–oxygen species over a CeO2-supported Au–Pt alloy catalyst (Au–Pt/CeO2) using biomass-derived formic acid as the hydrogen source. The success of this reaction is reasonably attributed to the high efficiency of Au–Pt/CeO2 in the tandem steps of formic acid dehydrogenation and carbon–oxygen species hydrodeoxygenation.
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