Adsorption and reaction of methanol on thin-film cerium oxide

被引:138
作者
Mullins, DR [1 ]
Robbins, MD [1 ]
Zhou, J [1 ]
机构
[1] Oak Ridge Natl Lab, Oak Ridge, TN 37831 USA
关键词
cerium; alcohols; thermal desorption spectroscopy; soft X-ray photoelectron spectroscopy; near-edge extended x-ray absorption fine structure (NEXAFS); catalysis;
D O I
10.1016/j.susc.2006.02.011
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
Methanol adsorption and reaction has been studied on cerium oxide thin films that were vapor deposited on Ru(0 0 0 1). The methanol behavior was examined as a function of temperature and Ce oxidation state. Methanol reacts at low temperatures with fully oxidized CeO2 to produce water at 200 K while formaldehyde and methanol desorb near 560 K. This leads to the reduction of the ceria. On reduced ceria, more methanol can be adsorbed and it undergoes more extensive decomposition producing CO and H-2 near 640 K in addition to formaldehyde and water. As the degree of ceria reduction increases, more H-2 and less H2O are produced. TPD experiments using isotopically labeled CH3OD show that deuterated water is produced from the oxidized surface at low temperatures, whereas the deuterium is stabilized on the reduced surface and is incorporated into the dihydrogen that desorbs near 600 K. High resolution C Is and O 1s XPS and C k-edge NEXAFS measurements were performed to quantify the amount of methanol adsorbed and to identify the adsorbed species. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1547 / 1558
页数:12
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