Activity of CeOx and TiOx nanoparticles grown on Au(111) in the water-gas shift reaction

被引:902
作者
Rodriguez, J. A. [1 ]
Ma, S.
Liu, P.
Hrbek, J.
Evans, J.
Perez, M.
机构
[1] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[2] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[3] Cent Univ Venezuela, Fac Ciencias, Caracas 1020A, Venezuela
关键词
D O I
10.1126/science.1150038
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The high performance of Au-CeO2 and Au-TiO2 catalysts in the water- gas shift ( WGS) reaction ( H2O + CO --> H-2 + CO2) 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 TiO2-x/Au( 111) and CeO2-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.
引用
收藏
页码:1757 / 1760
页数:4
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