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Influence of titania synthesized by pulsed laser ablation on the state of platinum during ammonia oxidation A. I. Stadnichenko, D. Svintsitskiy, L. S. Kibis [et al.]

Contributor(s): Svintsitskiy, Dmitry A | Kibis, Lidiya S | Fedorova, Elizaveta A | Stonkus, Olga A | Slavinskaya, Elena M | Lapin, Ivan N | Fakhrutdinova, Elena D | Romanenko, Anatoly V | Stadnichenko, Andrey I | Doronkin, Dmitry E | Marchuk, Vasyl | Grunwaldt, Jan-Dierk | Boronin, Andrei I | Svetlichnyi, Valerii AMaterial type: ArticleArticleContent type: Текст Media type: электронный Subject(s): импульсная лазерная абляция | рентгеновская фотоэлектронная спектроскопия | катализаторы | диоксид титана | платинаGenre/Form: статьи в журналах Online resources: Click here to access online In: Applied sciences Vol. 10, № 14. P. 4699 (1-25)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 catalysts prepared by impregnation using a commercial TiO2-P25 support and a support produced by pulsed laser ablation in liquid (PLA). The Pt/TiO2-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-P25 catalysts were characterized by uniform distribution of the Pt species over the support. Analysis of Pt4f XP spectra shows that oxidized Pt2+ and Pt4+ species are formed in the Pt/TiO2-P25 catalysts, while the platinum oxidation state in the Pt/TiO2-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+ 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-PLA samples show higher stability during catalysis and significantly higher selectivity to N2 in a wide temperature range of 200–400 °C.
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Библиогр.: 51 назв.

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 catalysts prepared by impregnation using a commercial TiO2-P25 support and a support produced by pulsed laser ablation in liquid (PLA). The Pt/TiO2-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-P25 catalysts were characterized by uniform distribution of the Pt species over the support. Analysis of Pt4f XP spectra shows that oxidized Pt2+ and Pt4+ species are formed in the Pt/TiO2-P25 catalysts, while the platinum oxidation state in the Pt/TiO2-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+ 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-PLA samples show higher stability during catalysis and significantly higher selectivity to N2 in a wide temperature range of 200–400 °C.

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