One-Dimensional Ceria as Catalyst for the Low-Temperature Water-Gas Shift Reaction

被引:57
|
作者
Han, Wei-Qiang [1 ]
Wen, Wen [1 ]
Hanson, Jonathan C. [2 ]
Teng, Xiaowei [1 ]
Marinkovic, Nebojsa [3 ]
Rodriguez, Jose A. [2 ]
机构
[1] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
[2] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[3] Univ Delaware, Dept Chem Engn, Newark, DE 19716 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2009年 / 113卷 / 52期
关键词
OXYGEN STORAGE CAPACITY; OXIDE NANOPARTICLES; HYDROGEN-PRODUCTION; CEO2; GOLD; SPECTROSCOPY; REDUCTION; NANOTUBES; BEHAVIOR; HYDRIDE;
D O I
10.1021/jp9066444
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
Synchrotron-based in Situ time-resolved X-ray diffraction and X-ray absorption spectroscopy were used to study pure ceria and Pd-loaded ceria nanotubes and nanorods (1D-ceria) as catalysts for the water-gas shift (WGS) reaction. While bulk ceria is very poor as WGS catalysts, pure I D-ceria displayed catalytic activity at a temperature as low as 300 degrees C. The reduction of the pure ID-ceria in pure hydrogen started at 150 degrees C, which is a much lower temperature than those previously reported for the reduction of 3D ceria nanoparticles. This low reduction temperature reflects the novel morphology of the oxide systems and may be responsible for the low-temperature WGS catalytic activity seen for the 1D-ceria. Pd-loaded 1D ceria displayed significant WGS activity starting at 200 degrees C. During pretreatment in H(2), the ceria lattice parameter increased significantly around 60 degrees C, which indicates that Pd-oxygen interactions may facilitate the reduction of Pd-loaded 1D-ceria. Pd and ceria both participate in the formation of the active sites for the catalytic reactions. The low-temperature hydrogen pretreatment results in higher WGS activity for Pd-loaded 1D-ceria.
引用
收藏
页码:21949 / 21955
页数:7
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