文献类型：期刊文章

作　　者：乔波涛[1] 梁锦霞[2] 王爱琴[1] 刘景月[3] 张涛[1]

机构地区：[1]中国科学院大连化学物理研究所催化基础国家重点实验室,辽宁大连116023 [2]贵州师范学院贵州省纳米材料模拟与计算重点实验室,贵州贵阳550018 [3]亚利桑那州立大学物理系

出　　处：《Chinese Journal of Catalysis》

基　　金：国家自然科学基金(21303184,21503046);美国国家科学基金(CHE-1465057);中国科学院战略性先导科技专项(XDB17020100);辽宁省科技厅院士基金(2015020086-101)

年　　份：2016

卷　　号：37

期　　号：10

起止页码：1580-1587

语　　种：中文

收录情况：AJ、BDHX、BDHX2014、CAS、CSA、CSA-PROQEUST、CSCD、CSCD2015_2016、EI(收录号：20164502984020)、JST、RSC、SCI-EXPANDED(收录号：WOS:000386865300002)、SCIE、SCOPUS、WOS、ZGKJHX、核心刊

摘　　要：Low‐temperature CO oxidation is important for both fundamental studies and practical applica‐tions. Supported gold catalysts are generally regarded as the most active catalysts for low‐temperature CO oxidation. The active sites are traditionally believed to be Au nanoclusters or nanoparticles in the size range of 0.5–5 nm. Only in the last few years have single‐atom Au catalysts been proved to be active for CO oxidation. Recent advances in both experimental and theoretical studies on single‐atom Au catalysts unambiguously demonstrated that when dispersed on suitable oxide supports the Au single atoms can be extremely active for CO oxidation. In this mini‐review, recent advances in the development of Au single‐atom catalysts are discussed, with the aim of illus‐trating their unique catalytic features during CO oxidation.

关 键 词：GOLD Single atom catalyst CO oxidation  STABILITY Low temperature  

分 类 号：O643.36]