Structure and Reactivity of Surface Oxides on Pt(110) during Catalytic CO Oxidation
- ESRF, 6, rue Jules Horowitz, F-38043 Grenoble cedex (France)
- Interdisciplinary Nanoscience Center (iNANO) and Department of Physics and Astronomy, University of Aarhus, DK-8000 Aarhus C (Denmark)
- Kamerlingh Onnes Laboratory, Leiden University, P.O. Box 9504, 2300 RA Leiden (Netherlands)
- CEA-Grenoble DRFMC/SI3M/PCM17, rue des Martyrs, 38054 Grenoble cedex 9 (France)
- Departamento de Fisica, Faculdad de Ciencias, Universidad de Oviedo, Avda. Calvo Sotelo, s/n, 33007 Oviedo (Spain)
- CELLS - ALBA, Edifici Ciencies Nord. Modul C-3 centra, Campus Universitari de Bellaterra, Universita Autonoma de Barcelona, 08193 Bellaterra (Spain)
We present the first structure determination by surface x-ray diffraction during the restructuring of a model catalyst under reaction conditions, i.e., at high pressure and high temperature, and correlate the restructuring with a change in catalytic activity. We have analyzed the Pt(110) surface during CO oxidation at pressures up to 0.5 bar and temperatures up to 625 K. Depending on the O{sub 2}/CO pressure ratio, we find three well-defined structures: namely, (i) the bulk-terminated Pt(110) surface, (ii) a thin, commensurate oxide, and (iii) a thin, incommensurate oxide. The commensurate oxide only appears under reaction conditions, i.e., when both O{sub 2} and CO are present and at sufficiently high temperatures. Density functional theory calculations indicate that the commensurate oxide is stabilized by carbonate ions (CO{sub 3}{sup 2-}). Both oxides have a substantially higher catalytic activity than the bulk-terminated Pt surface.
- OSTI ID:
- 20699711
- Journal Information:
- Physical Review Letters, Vol. 95, Issue 25; Other Information: DOI: 10.1103/PhysRevLett.95.255505; (c) 2005 The American Physical Society; Country of input: International Atomic Energy Agency (IAEA); ISSN 0031-9007
- Country of Publication:
- United States
- Language:
- English
Similar Records
Adsorption and activation of CO2 on Pt/CeOx/TiO2(110): Role of the Pt-CeOx interface
A Theoretical Insight into the Catalytic Effect of a Mixed-Metal Oxide at the Nanometer Level: The Case of the Highly Active metal/CeOx/TiO2 (110) Catalysts