水煤气变换反应
催化作用
氧化物
水煤气
金属
材料科学
无机化学
纳米颗粒
过渡金属
胶体金
化学工程
化学
纳米技术
冶金
合成气
工程类
生物化学
作者
José A. Rodríguez,Suli Ma,P. Liu,Jan Hrbek,Jonathan P. Evans,Marco Pérez
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2007-12-13
卷期号:318 (5857): 1757-1760
被引量:974
标识
DOI:10.1126/science.1150038
摘要
The high performance of Au-CeO 2 and Au-TiO 2 catalysts in the water-gas shift (WGS) reaction (H 2 O + CO→H 2 + CO 2 ) relies heavily on the direct participation of the oxide in the catalytic process. Although clean Au(111) is not catalytically active for the WGS, gold surfaces that are 20 to 30% covered by ceria or titania nanoparticles have activities comparable to those of good WGS catalysts such as Cu(111) or Cu(100). In TiO 2- x /Au(111) and CeO 2- x /Au(111), water dissociates on O vacancies of the oxide nanoparticles, CO adsorbs on Au sites located nearby, and subsequent reaction steps take place at the metal-oxide interface. In these inverse catalysts, the moderate chemical activity of bulk gold is coupled to that of a more reactive oxide.
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