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Phys. Rev. Lett. 94, 196102 (2005) [4 pages]

Origin and Activity of Oxidized Gold in Water-Gas-Shift Catalysis

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Zhi-Pan Liu, Stephen J. Jenkins, and David A. King
Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, United Kingdom

Received 26 January 2005; published 19 May 2005

As a promising route for large-scale H2 production, the water-gas-shift reaction (WGS, CO+H2O→CO2+H2) 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 H2 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.

© 2005 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevLett.94.196102
DOI:
10.1103/PhysRevLett.94.196102
PACS:
82.65.+r, 68.35.−p, 68.43.Bc