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

Panagiotopoulou Paraskevi, Dimitris I. Kondarides

Πλήρης Εγγραφή


URI: http://purl.tuc.gr/dl/dias/5536B115-0F94-417F-A13D-0035A2FB356F
Έτος 2008
Τύπος Δημοσίευση σε Περιοδικό με Κριτές
Άδεια Χρήσης
Λεπτομέρειες
Βιβλιογραφική Αναφορά . P. Panagiotopoulou, D.I. Kondarides, “Effects of alkali additives on the physicochemical characteristics and chemisorptive properties of Pt/TiO2 catalysts”, Journal of Catalysis, Vol. 260, no.1, pp. 141-149, Nov. 2008. doi:10.1016/j.jcat.2008.09.014. https://doi.org/10.1016/j.jcat.2008.09.014
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Περίληψη

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 H2 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 ν(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 groups associated with the support to yield formate, which decomposes during TPD to CO2 and H2. 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.

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