4.8 Article

Effects of alkali additives on the physicochemical characteristics and chemisorptive properties of Pt/TiO2 catalysts

Journal

JOURNAL OF CATALYSIS
Volume 260, Issue 1, Pages 141-149

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2008.09.014

Keywords

Platinum; Titanium dioxide; Promotion; Alkali; Cesium; Sodium; Hydrogen; Carbon monoxide; TPD; TPR; DRIFTS; FTIR

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The effects of alkali additives on the physicochemical and chemisorptive properties of 0.5% Pt/TiO2 have been investigated over catalysts promoted with variable amounts of Na (0-0.2 wt%) or Cs (0-0.68 wt%) with the use of diffuse reflectance infrared spectroscopy (DRIFTS) and temperature-programmed (TPD, TPR) techniques. It has been found that addition of alkalis does not affect adsorption of CO and H-2 on the surface of Pt crystallites, indicating the absence of strong electronic-type interactions between these sites and the promoters. However, the presence of alkalis results in the creation and population of new sites with increased electron density, proposed to be located at perimetric sites of Pt crystallites, which are in contact with the support. The adsorption strength of these sites toward CO increases with increasing alkali content, which is evidenced by the development of new, low-frequency IR bands in the v(CO) region. In contrast, addition of alkali results in weakening of hydrogen adsorption on sites located at the metal/support interface, which is reflected to a significant shift of the corresponding TPD peak toward lower temperatures. Results of CO-TPD experiments indicate that CO adsorbed on Pt interacts with hydroxyl associated with the support groups support to yield formate, which decomposes during TPD to CO2 and H-2. Thermal decomposition of formate is accomplished at lower temperatures in the presence of alkali. Finally, CO-TPR experiments indicate that the reducibility of TiO2 is enhanced in the presence of alkali, which can be related to the creation of the new sites at the metal/support interface. (C) 2008 Elsevier Inc. All rights reserved.

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