CO oxidation performance of Au/Co3O4 catalyst on the micro gas sensor device

被引:24
|
作者
Nishibori, M. [1 ,2 ]
Shin, W. [2 ]
Izu, N. [2 ]
Itoh, T. [2 ]
Matsubara, I. [2 ]
机构
[1] Kyushu Univ, Res Ctr Synchrotron Light Applicat, Kasuga, Fukuoka 8168580, Japan
[2] Natl Inst Adv Ind Sci & Technol, Moriyama Ku, Nagoya, Aichi 4638560, Japan
基金
日本科学技术振兴机构;
关键词
CO oxidation; Au/Co3O4; catalyst; Micro gas sensor; XAFS; XPS; SUPPORTED GOLD CATALYSTS; LOW-TEMPERATURE OXIDATION; PREFERENTIAL OXIDATION; PARTICLE-SIZE; AU; TIO2; XPS; SELECTIVITY; REACTIVITY; HYDROGEN;
D O I
10.1016/j.cattod.2012.04.037
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The CO oxidation performance of the Au/Co3O4 catalyst on the micro gas sensor device with different treatment conditions has been investigated. The CO oxidation performance of the Au/Co3O4 catalyst on the micro device has been improved by the H-2 combustion treatment under the flow of H-2 in air and the reduction treatment under the flow of H-2 in N-2. The H-2 combustion treatment of the Au/Co3O4 catalyst on the micro device prevented the degradation of the CO oxidation performance. To investigate the chemical states and microstructures of Au and Co in the Au/Co3O4 catalysts after the reduction and H-2 combustion treatments, transmission X-ray absorption fine structure (XAFS) measurement and Xray photoelectron spectroscopy (XPS) have been performed. Au particles of Au/Co3O4 were found to be metallic Au regardless of the treatment conditions. However, a hydroxyl group bonded to the transition metal Co as a form of Co(OH)(2) was found on the catalyst surface after the H-2 combustion treatment. The H-2 combustion treatment of Au/Co3O4 results in the formation of OH-in the metal-support interface, which is considered to be an origin of the improvement of the CO oxidation performance of the Au/Co3O4 catalyst. (C) 2012 Elsevier B. V. All rights reserved.
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页码:85 / 91
页数:7
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