Determination of dispersion of precious metals on CeO2-containing supports

被引:144
|
作者
Takeguchi, T
Manabe, S
Kikuchi, R
Eguchi, K
Kanazawa, T
Matsumoto, S
Ueda, W
机构
[1] Hokkaido Univ, Catalysis Res Ctr, Kita Ku, Sapporo, Hokkaido 0010021, Japan
[2] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
[3] Toyota Motor Co Ltd, Toyota, Aichi 4718572, Japan
关键词
Pt/CeO2; Pt/CeO2-ZrO2; CO adsorption; CO2; treatment;
D O I
10.1016/j.apcata.2005.07.013
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
Precious metal (PM) dispersions on CeO2-containing supports were examined. When dispersions were evaluated by the H-2-O-2 titration method, the CeO2-containing supports hide the true redox of PM because of the large oxygen storage-reduction capacity of the oxide, resulting in higher apparent dispersions than the exact values. When Pt dispersions on the CeO2 support were evaluated by the ordinary CO pulse method, CO was adsorbed on the CeO2 Support as carbonate species accompanying the oxidation with lattice oxygen. Therefore, the dispersions estimated from the CO uptake were also higher than the exact value. Infrared spectra also clearly evidenced the presence of carbonate species after CO adsorption. To prevent the CO adsorption on CeO2 as the carbonate species, we treated Pt/CeO2 with CO2 before CO adsorption. The strong bands arising from carbonate species on CeO2 were observed in the infrared spectra. When CO was adsorbed on CO2-terated Pt/CeO2, CO was selectively adsorbed on the surface atoms of Pt particles. By the O-2-CO2-H-2-CO pulse method, the amount of CO adsorbed on surface atoms of the Pt particles could be separated, and a precise dispersion was determined. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:91 / 96
页数:6
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