Interaction of CO with Rh supported on stoichiometric and reduced CeO2(111) and CeO2(100) surfaces

被引:101
作者
Stubenrauch, J [1 ]
Vohs, JM [1 ]
机构
[1] UNIV PENN,RES STRUCT MATTER LAB,PHILADELPHIA,PA 19104
基金
美国国家科学基金会;
关键词
D O I
10.1006/jcat.1996.0063
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
The structure and reactivity of Rh films supported on the surface of a CeO2 single crystal were studied using Auger electron spectroscopy (AES) and temperature-programmed desorption (TPD). Rhodium films deposited from the vapor phase were found to grow via the nucleation of three-dimensional particles at a sample temperature of 300 K. Annealing of the Rh films resulted in further agglomeration of the metal layer. Carbon monoxide TPD spectra obtained from Rh supported on oxygen-annealed CeO2(111) and CeO2(100) substrates were similar to those obtained from the low-index planes of Rh single crystals, with the exception that a small fraction of the CO (ca. 2%) was oxidized to CO2. In contrast, a new high-temperature CO desorption state was observed in the TPD spectra obtained from Rh supported on partially reduced CeO2 surfaces. (C) 1996 Academic Press, Inc.
引用
收藏
页码:50 / 57
页数:8
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