Influence of Titania Synthesized by Pulsed Laser Ablation on the State of Platinum during Ammonia Oxidation

Abstract

A set of physicochemical methods, including X-ray photoelectron spectroscopy (XPS), X-ray diffraction, electron microscopy and X-ray absorption spectroscopy, was applied to study Pt/TiO2_{2} catalysts prepared by impregnation using a commercial TiO2_{2}-P25 support and a support produced by pulsed laser ablation in liquid (PLA). The Pt/TiO2_{2}-PLA catalysts showed increased thermal stability due to the localization of the highly dispersed platinum species at the intercrystalline boundaries of the support particles. In contrast, the Pt/TiO2_{2}-P25 catalysts were characterized by uniform distribution of the Pt species over the support. Analysis of Pt4f XP spectra shows that oxidized Pt2+^{2+} and Pt4+^{4+} species are formed in the Pt/TiO2_{2}-P25 catalysts, while the platinum oxidation state in the Pt/TiO2_{2}-PLA catalysts is lower due to stronger interaction of the active component with the support due to strong interaction via Pt-O-Ti bonds. The Pt4f XP spectra of the samples after reaction show Pt2+^{2+} and metallic platinum, which is the catalytically active species. The study of the catalytic properties in ammonia oxidation showed that, unlike the catalysts prepared with a commercial support, the Pt/TiO2_{2}-PLA samples show higher stability during catalysis and significantly higher selectivity to N2_{2} in a wide temperature range of 200–400 °C

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