Surface-dependent oxidation of H2 on CeO2 surfaces

被引:106
作者
Desaunay, T. [1 ]
Bonura, G. [2 ]
Chiodo, V. [2 ]
Freni, S. [2 ]
Couzinie, J. -P. [3 ]
Bourgon, J. [3 ]
Ringuede, A. [1 ]
Labat, F. [1 ]
Adamo, C. [1 ]
Cassir, M. [1 ]
机构
[1] Chimie ParisTech, Ecole Natl Super Chim Paris, UMR CNRS 7575, Lab Electrochim Chim Interfaces & Modelisat Energ, F-75231 Paris 05, France
[2] CNR ITAE Nicola Giordano, I-98126 Messina, Italy
[3] MCMC, ICMPE CNRS UPEC UMR7182, F-94320 Thiais, France
关键词
CeO2; Hydrogen; Surface dependence; TPR; SOFC; CO OXIDATION; ELECTRONIC-STRUCTURE; CERIA; NANOCRYSTALS; ADSORPTION; REDUCTION; NANORODS; MECHANISMS; HYDROGEN;
D O I
10.1016/j.jcat.2012.10.011
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 this study, ceria nanoparticles with well-defined surface states were synthesized in order to enable the study of different ceria surfaces, independently. Ceria nanocubes were shown to expose only (1 0 0) surfaces, ceria nanooctahedra only (1 1 1) surfaces, and ceria nanorods are more complex, with at least 50% of (1 1 0) surfaces, as shown by high-resolution transmission electron microscopy. Temperature-programmed reduction (TPR) by hydrogen performed on these powders shows the following order of reaction temperatures: cubes < rods < octahedra. Moreover, activation energies associated with the first surface reduction in each sample show a similar trend. Ceria (1 0 0) surface is the most reactive toward hydrogen oxidation, while (1 1 1) surface is the less reactive, and (1 1 0) surface has likely an intermediate behavior. These results confirm that hydrogen oxidation is highly surface-dependent and that a strong attention must be paid to the surface state of the catalyst in these devices. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:193 / 201
页数:9
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