化学
催化作用
反向
近程
X射线吸收精细结构
氢
工作(物理)
化学工程
无机化学
热力学
一氧化碳
有机化学
光谱学
物理
工程类
量子力学
数学
几何学
作者
Aitor Hornés,Ana B. Hungría,Parthasarathi Bera,Diego López-Cámara,Marcos Fernández‐García,A. Martínez‐Arias,Laura Barrio,Michael Estrella,Gong Zhou,José J. Fonseca,Jonathan C. Hanson,José A. Rodríguez
摘要
A novel inverse CeO(2)/CuO catalyst for preferential oxidation of CO in H(2)-rich stream (CO-PROX) has been developed on the basis of a hypothesis extracted from previous work of the group (JACS 2007, 129, 12064). Possible separation of the two competing oxidation reactions involved in the process (of CO and H(2), respectively) is the key to modulation of overall CO-PROX activity and is based on involvement of different sites as most active ones for each of the two reactions. Achievement of large size CuO particles and adequate CeO(2)-CuO interfacial configurations in the inverse catalyst apparently allows appreciable enhancement of the catalytic properties of this kind of system for CO-PROX, constituting an interesting alternative to classic direct configurations so far explored for this process. Reasons for such behavior are analyzed on the basis of operando-XRD, -XAFS, and -DRIFTS studies.
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