Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
62315 | Journal of Catalysis | 2009 | 10 Pages |
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.
Graphical abstractThe presence of stable oxygen on a Au/TiO2 catalyst removable by reaction with CO (‘oxygen storage capacity’) was demonstrated by TAP measurements, and for catalysts with varying Au particle size, it was shown to be correlated with the CO oxidation activity and the perimeter length of the Au/TiO2 interface.Figure optionsDownload full-size imageDownload high-quality image (88 K)Download as PowerPoint slide