Activation of Au/TiO2 catalyst for CO oxidation

被引:125
|
作者
Yang, JH
Henao, JD
Raphulu, MC
Wang, YM
Caputo, T
Groszek, AJ
Kung, MC
Scurrell, MS
Miller, JT
Kung, HH [1 ]
机构
[1] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Microscal Ltd, London W10 5AL, England
[4] Univ Witwatersrand, Sch Chem, Inst Mol Sci, Johannesburg, South Africa
[5] BP Res Ctr, Naperville, IL 60563 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2005年 / 109卷 / 20期
关键词
D O I
10.1021/jp050818c
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
Changes in a Au/TiO2 catalyst during the activation process from an as-prepared state, consisting of supported AuOx(OH)(4-2x)(-) species, were monitored with X-ray absorption spectroscopy and FTIR spectroscopy, complemented with XPS, microcalorimetry, and TEM characterization. When the catalyst was activated with H-2 pulses at 298 K, there was an induction period when little changes were detected. This was followed by a period of increasing rate of reduction of Au3+ to Au-0, before the reduction rate decreased until the sample was fully reduced. A similar trend in the activation process was observed if CO pulses at 273 K or a steady flow of CO at about 240 K was used to activate the sample. With both activation procedures, the CO oxidation activity of the catalyst at 195 K increased with the degree of reduction up to 70% reduction, and decreased slightly beyond 80% reduction. The results were consistent with metallic An being necessary for catalytic activity.
引用
收藏
页码:10319 / 10326
页数:8
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