Low-temperature activity of Au/CeO2 for water gas shift reaction, and characterization by ADF-STEM, temperature-programmed reaction, and pulse reaction

被引:155
作者
Sakurai, H
Akita, T
Tsubota, S
Kiuchi, M
Haruta, M
机构
[1] Natl Inst Adv Ind Sci & Technol, Ikeda, Osaka 5638577, Japan
[2] AIST, Tsukuba, Ibaraki 3058569, Japan
[3] AIST, Tsukuba, Ibaraki 3058568, Japan
关键词
gold; ceria; annular dark field scanning transmission electron microscopy; water gas shift; temperature-programmed reaction; associated mechanism;
D O I
10.1016/j.apcata.2005.02.043
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
In Au/CeO2 catalysts prepared by the deposition-precipitation method, many Au particles smaller than 3 nm in diameter were clearly observed by annular dark field scanning transmission electron microscopy (ADF-STEM). The water gas shift activity of Au/CeO2 was compared with that of Pt/CeO2, Au/TiO2, and Cu/ZnO/Al2O3 by using temperature-programmed reaction (TPRe) measurement in a stream of a reaction gas mixture composed of CO, CO2, H-2, H2O, and He. Au/CeO2 was found to be the most active at temperatures between 373 and 523 K without producing methane below 623 K. Based on transient experiments consisting of injecting CO and H2O pulses into H-2 and He streams, it is deduced that the water gas shift reaction proceeds over the perimeter interfaces of small gold particles on a reduced cerium oxide surface. The reaction proceeds by formation of a reaction intermediate (possibly a formate) from CO and OH groups, followed by decomposition of the intermediate by H2O into CO2 and H-2. Hydrogen in the reactant gas facilitates cerium oxide to form more active reduced surfaces. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:179 / 187
页数:9
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