期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 41, 期 9, 页码 4993-5002出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2016.01.099
关键词
COPrOx; Cobalt; In situ Raman
资金
- UNL
- ANPCyT
- CONICET
The in situ Raman spectroscopy constitutes a powerful procedure to characterize catalytic surfaces under reaction conditions. In this work, we studied the species present in Co/CeO2 and Co/ZrO2 catalysts during the COPrOx reaction carried out between room temperature and 500 degrees C. For both catalysts, TPR and Raman results suggest that a redox mechanism proceeds in which the reduction step with either hydrogen or CO is the rate-limiting step. The CeO2 support is better than the ZrO2 one because the former accelerates the surface exchange between reduced and oxidized species due to the high mobility of surface lattice oxygen and the presence of oxygen vacancies. The Ce4+ + Co2+ <-> Ce3+ + Co3+ process acts as a buffer effect by which Co3+, which is the active species in this reaction, is always present even in a reducing atmosphere, as shown by in situ Raman characterization. Copyright (C) 2016, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据