Site-selective XAFS spectroscopy tuned to surface active sites of copper catalysts

被引:23
|
作者
Izumi, Y [1 ]
Kiyotaki, F [1 ]
Nagamori, H [1 ]
Minato, T [1 ]
机构
[1] Tokyo Inst Technol, Interdisciplinary Grad Sch Sci & Engn, Dept Environm Chem & Engn, Midori Ku, Yokohama, Kanagawa 2268502, Japan
关键词
XAFS; fluorescence spectrometer; energy resolution; core-hole lifetime width; chemical shift; site selection;
D O I
10.1016/S0368-2048(01)00292-4
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
To overcome the problem of X-ray absorption fine structure (XAFS) spectroscopy in which the obtained information is the average for all sites in sample, Rowland-type fluorescence spectrometer was designed to measure site-selective XAFS spectra by utilizing the chemical shift of emission peak for each site. Johansson-type cylindrically-bent Ge(111) crystal and scintillation counter were mounted on the spectrometer. The improvement of energy resolution of spectrometer was discussed when the primary beam size and two slit size in the Rowland circle were varied. The energy resolution was similar to1.1 eV, smaller than the core-hole lifetime width for Cu K alpha (1) (2.11 eV). The site selection of the Cu-0 and Cu-1 site-tune spectra was experimentally measured for the physical mixture of Cu metal+Cul and for Cu/ZnO catalyst. Obtained experimental site selection was compared to the theoretical estimations. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:193 / 199
页数:7
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