The relationship between the structure and activity of nanometer size gold when supported on Mg(OH)2

被引:214
作者
Cunningham, DAH
Vogel, W
Kageyama, H
Tsubota, S
Haruta, M
机构
[1] Osaka Natl Res Inst, Ikeda, Osaka 563, Japan
[2] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
关键词
D O I
10.1006/jcat.1998.2050
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 [物理化学]; 081704 [应用化学];
摘要
In the following paper catalysts of Au supported on Mg(OH)(2) were analyzed by extended X-ray absorption fine structure spectroscopy and Debye function analysis. From these studies only catalysts with Au-size distributions below 1 mm in size were found to be active for CO oxidation. Below 1 Mn in size the gold exists in two forms; icosahedral and fee cuboctahedral. Comparison of turnover frequencies for catalysts prepared with different ratios of the two symmetries suggest that the icosahedral symmetry is the more active form. Above 1 mm in size the gold takes either FCC cuboctahedral or decahedral symmetry. These results suggest that oxidation of CO over the Au/Mg(OH)(2) catalyst is structure-dependent and that care must be taken in comparing results, where no structural information is available. (C) 1998 Academic Press.
引用
收藏
页码:1 / 10
页数:10
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