XPS characterization of Au/TiO2 catalysts: Binding energy assessment and irradiation effects

被引:407
作者
Kruse, Norbert [1 ]
Chenakin, Sergey [1 ,2 ]
机构
[1] ULB, B-1050 Brussels, Belgium
[2] Nat Acad Sci, Inst Met Phys, UA-03680 Kiev 142, Ukraine
关键词
Au/TiO2; catalyst; TiO2; XPS; X-ray induced damage; Valence band; RAY PHOTOELECTRON-SPECTROSCOPY; SOL-GEL METHOD; CO-OXIDATION; ELECTRONIC-STRUCTURE; GOLD CATALYSTS; ALUMINOVANADATE OXIDE; CARBON-MONOXIDE; TIO2; 110; AU; SURFACE;
D O I
10.1016/j.apcata.2010.05.039
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
X-ray photoelectron spectroscopy (XPS) was employed to study the surface composition and electronic structure of Au/TiO2 catalysts in comparison with TiO2 (anatase) and to reveal time-dependent X-ray irradiation damage of the samples. The occurrence of Au nano-sized particles on a TiO2 support was found to result in a slight shift of Ti 2p core-level spectrum and in changes of the valence band and X-ray induced Auger spectra, compared to TiO2-only. It was shown that for different means of energy referencing the charge-corrected Au 4f(7/2) binding energy in Au/TiO2 catalysts was 0.15-0.45 eV lower than that in pure bulk Au. Exposure to X-rays of Au/TiO2 catalysts and pure TiO2 caused a reduction of Ti 4+ oxidation state and desorption of oxygen from the surface. As a result, the surface chemical composition and electronic structure of the samples changed with time. The X-ray irradiation affected charge transfer processes in Au/TiO2 so that the pattern of X-ray induced damage in the Au-based catalyst turned out to be quite different from that in TiO2, with some characteristics displaying the very opposite features. Decreasing of the Au 4f(7/2) binding energy and concurrent increasing of the fraction of Ti3+ species observed in the beginning of X-ray irradiation of Au/TiO2 may be taken as direct evidence for charge transfer from oxygen vacancies created by irradiation to Au particles. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:367 / 376
页数:10
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