Selective CO oxidation in the presence of hydrogen: fast parallel screening and mechanistic studies on ceria-based catalysts

被引:58
作者
Tibiletti, D
de Graaf, EAB
Teh, SP
Rothenberg, G
Farrusseng, D
Mirodatos, C
机构
[1] Inst Rech Catalyse, CNRS, F-69626 Villeurbanne, France
[2] Univ Amsterdam, Dept Chem Engn, NL-1080 WV Amsterdam, Netherlands
关键词
combinatorial catalysis; doped ceria; fuel cells; water-gas shift; CO selective oxidation; platinum;
D O I
10.1016/j.jcat.2004.04.031
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
An accelerated investigation of various ceria-supported platinum catalysts by means of parallel synthesis and testing reactors is reported. The aim is to discover new catalysts for purifying hydrogen for fuel cells and other applications by studying three reactions: selective CO oxidation in the absence and in the presence of hydrogen (SelOx), water-gas shift (WGS), and reverse water-gas shift (RWGS). A set of catalysts is prepared by impregnating platinum on various doped ceria supports. These catalysts display, despite their nearly identical X-ray crystal structures. diverse redox/acidic/basic properties and different selectivities in the three test reactions. The best SelOx catalysts are also the most active for WGS/RWGS equilibration. In contrast to the conventional two-stage approach of discovery screening followed by lead optimization, we demonstrate that it is possible to extract valuable mechanistic information directly from the discovery stage. Specifically, we elucidate the elementary steps coupling the SelOx and WGS processes and gain insight as to the combined effects of hydrogen presence and cation doping on the CO oxidation reaction. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:489 / 497
页数:9
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