Journal
JOURNAL OF CATALYSIS
Volume 264, Issue 1, Pages 67-76Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2009.03.013
Keywords
Au/TiO2; CO oxidation; Oxygen storage capacity (OSC); Temporal analysis of products (TAP)
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Funding
- Deutsche Forschungsgemeinschaft [SPP1181, Be 1201/13-2]
- Alexander von Humboldt Foundation
- German Academic Exchange Service (DAAD)
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We investigated the oxygen storage capacity (OSC) of Au/TiO2 catalysts as well as its correlation with the activity for CO oxidation and in particular the influence of the Au particle size on these properties in kinetic measurements and in temporal analysis of products (TAP) reactor measurements. Catalysts with identical Au loading but different Au particle sizes were prepared by calcination of the same raw catalyst in air at different temperatures; the Au particle sizes were characterized by transmission electron microscopy and X-ray diffraction. TAP multi-pulse data indicate that oxygen stored on the catalyst surface reacts with CO; both the OSC and the activity for CO oxidation increase with decreasing Au particle size. From the small amount of removable oxygen, between 0.4 and 1.0% of the total surface oxygen of the support material, and its almost linear relation with the perimeter sites of the interface between the gold particles and the support, we suggest that the removable oxygen species are located at these interfacial perimeter sites. Furthermore, these oxygen species are shown to represent the active oxygen in the CO oxidation reaction under the present reaction conditions. (C) 2009 Elsevier Inc. All rights reserved.
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