Metal-support and preparation influence on the structural and electronic properties of gold catalysts

被引:88
作者
Casaletto, MP
Longo, A
Venezia, AM
Martorana, A
Prestianni, A
机构
[1] CNR, Ist Studio Mat Nanostrutt, I-90146 Palermo, Italy
[2] Univ Palermo, Dipartimento Chim Inorgan & Anal S Cannizzaro, I-90128 Palermo, Italy
关键词
CO oxidation; XPS; XANES; oxidation state of gold; particle size effect; Au/CeO2; Au/SiO2;
D O I
10.1016/j.apcata.2006.02.005
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanostructured gold catalysts supported on CeO2 and SiO2 were prepared by the deposition-precipitation (DP) and the solvated metal atom dispersion (SMAD) techniques. The structural and electronic properties of the catalysts were investigated by X-ray diffraction (XRD), X-ray absorption spectroscopy (XAS) and X-ray photoelectron spectroscopy (XPS). Gold was found as small metal nanoparticles (cluster size similar to 2 nm) in the SMAD-prepared samples and in ionic state in the DP catalysts. The catalytic activity of the samples was tested in the reaction of low temperature CO oxidation. Gold nanosized particles in a pure metallic state exhibited a worse catalytic performance, both on ceria and silica. The presence of non-metallic Au species seems to be the main requisite for the achievement of the highest CO conversion at the lowest temperature. The higher activity of the Au/CeO2 (DP) sample with respect to the Au/SiO2 (DP) catalyst can be ascribed to a better stabilization of the Au+1 ions, probably as AuO- species, by the cerium oxide. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:309 / 316
页数:8
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