Origin and activity of oxidized gold in water-gas-shift catalysis

被引:310
作者
Liu, ZP [1 ]
Jenkins, SJ [1 ]
King, DA [1 ]
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
关键词
D O I
10.1103/PhysRevLett.94.196102
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
As a promising route for large-scale H-2 production, the water-gas-shift reaction (WGS, CO+H2O -> CO2+H-2) on ceria-supported Au catalysts is of enormous potential in efforts to move towards a hydrogen economy. Recent research suggests that this reaction is in fact catalyzed by Au cations instead of the conventionally regarded metallic Au particles. Here density functional theory calculations demonstrate that the presence of empty localized nonbonding f states in CeO2 permits the oxidation of Au, enabling subsequent CO adsorption. A feasible reaction pathway leading to H-2 production is identified, and it is concluded that four to six atom Au clusters at the O-vacancy sites of ceria catalyze the WGS reaction.
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页数:4
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