Effects of passivation on synthesis, structure and composition of molybdenum carbide supported platinum water-gas shift catalysts

被引:30
|
作者
Wyvratt, Brian M.
Gaudet, Jason R.
Thompson, Levi T. [1 ]
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
Platinum-molybdenum carbide catalysts; Water-gas shift; Surface passivation; Redox; In situ X-ray absorption spectroscopy; RAY-ABSORPTION SPECTROSCOPY; TRANSITION-METAL CARBIDES; TUNGSTEN CARBIDE; CO HYDROGENATION; IN-SITU; ALUMINA; MO2C; PERFORMANCES; ADSORPTION; REACTIVITY;
D O I
10.1016/j.jcat.2015.07.023
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
High surface area molybdenum carbides are attractive for use as catalysts and supports. Due to their pyrophoricity, carbides are typically passivated prior to use. Research described in this paper compared the synthesis, structural and compositional properties, and water gas shift activities of catalysts produced by depositing Pt onto unpassivated and passivated MO2C. Passivation had a profound effect on the character of interactions between the Pt precursor salt (H2PtCl6) and MO2C. Nanoscale Pt metal particles were deposited onto the unpassivated MO2C while very large Pt particles were deposited onto the passivated MO2C (p-MO2C). In situ X-ray absorption spectroscopy revealed reduction of Pt4+ in contact with the unpassivated MO2C with commensurate oxidation of Mo. Water gas shift activities were significantly higher for the Pt/MO2C compared to the Pt/p-MO2C catalyst. Overall, the results indicate that the passivation of MO2C prior to metal deposition had deleterious effects on the Pt loadings, structures, and activities. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:280 / 287
页数:8
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