Characterization and Reactivity in CO oxidation of Gold Nanoparticles Supported on TiO2 Prepared by Deposition-Precipitation with NaOH and Urea

Canadian Institute of Mining, Metallurgy and Petroleum
Rodolfo Zanella
Organization:
Canadian Institute of Mining, Metallurgy and Petroleum
Pages:
13
File Size:
207 KB
Publication Date:
Oct 1, 2003

Abstract

Au/TiO2 catalysts were prepared by deposition-precipitation using NaOH (DPN) (~3 wt % Au) and urea (DPU) (~8 wt % Au), and calcined at various temperatures between 100 and 400 °C. They were characterized by UV-Visible, XANES, EXAFS and TEM. Their activity were tested in the reaction of CO oxidation at 5°C. After preparation, the gold species are in the oxidic state III. They begin to transform into metallic gold under air at ~100 °C for DPN and ~150 °C for DPU. At 200 °C, all the gold is metallic for the two preparation methods. The particle size increases from 1.5 to 3.5 nm with the calcination temperature. The catalytic activity for CO oxidation increases with the percentage of metallic gold, and it is maximum at 200°C for both types of samples. The activities (per mole of Au) are the same for the two types of catalysts. At higher temperatures, the catalytic activity drops. The decrease of activity is mainly due to a change of particle shape with the calcination temperature rather than to the increase of the particle size. At a calcination temperature of 200°C, the particles present small facets with rounded parts, and their outer surface contains a large proportion of low coordinated sites (steps and corners) while at high temperature of calcination, they are truncated octahedra with smooth facets.
Citation

APA: Rodolfo Zanella  (2003)  Characterization and Reactivity in CO oxidation of Gold Nanoparticles Supported on TiO2 Prepared by Deposition-Precipitation with NaOH and Urea

MLA: Rodolfo Zanella Characterization and Reactivity in CO oxidation of Gold Nanoparticles Supported on TiO2 Prepared by Deposition-Precipitation with NaOH and Urea. Canadian Institute of Mining, Metallurgy and Petroleum, 2003.

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