Catalytic role of vacancy diffusion in ceria supported atomic gold catalyst

被引:24
|
作者
Han, Zhong-Kang [1 ,2 ,3 ]
Wang, Yang-Gang [4 ]
Gao, Yi [1 ,2 ,5 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Div Interfacial Water, Shanghai 201800, Peoples R China
[2] Chinese Acad Sci, Key Lab Interfacial Phys & Technol, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[5] Chinese Acad Sci, Shanghai Sci Res Ctr, Shanghai 201204, Peoples R China
基金
中国国家自然科学基金;
关键词
GAS SHIFT REACTION; CO OXIDATION; ACTIVE OXYGEN; AU/TIO2; STATES; AU; ACTIVATION; STABILITY; HYDROGEN; SURFACE;
D O I
10.1039/c7cc04440b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dynamics of intrinsic defects are considered fundamental in the chemistry of reducible oxides, and their effect on catalytic reactions have been rarely reported. Herein, we propose a new Ov diffusion assisted Langmuir-Hinshelwood mechanism for CO oxidation, which may largely account for the origin of high reactivity of supported atomic gold catalysts.
引用
收藏
页码:9125 / 9128
页数:4
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