X射线光电子能谱
催化作用
氧化物
材料科学
原位
拉曼光谱
化学工程
氧化还原
相(物质)
金属
无机化学
化学
冶金
有机化学
光学
物理
工程类
作者
Mei‐Yao Wu,Beibei Wang,Weiwei Wang,Fan Yang,Chun‐Jiang Jia
出处
期刊:Chemcatchem
[Wiley]
日期:2023-08-25
卷期号:15 (22)
被引量:3
标识
DOI:10.1002/cctc.202300894
摘要
Abstract The oxides and active metals at the interface synergistically activate reactants and thus promote the reaction, but the interface structure often changes dynamically during the reaction. In the conventional supported catalysts, the metals at the interface have been extensively studied, while the structural evolution of oxides is often overlooked due to the interference of the bulk phase signal. In this work, CeO 2 −CuO inverse catalysts are designed to reveal the dynamic structure evolution of CeO 2 in the CeO 2 −CuO system during the water gas shift (WGS) reaction by in situ Raman, in situ XRD, quasi in situ XPS, and near ambient pressure XPS (NAP‐XPS). CeO 2 is partially concealed in the CuO phase in the un‐pretreated catalyst and gradually exposed to the surface, forming an inverse CeO x /Cu structure during the reducing process. This structure exhibits a high catalytic activity in the WGS reaction and remains durable under the reductive conditions. When the inverse CeO x /Cu structure is exposed to the non‐redox conditions, the reconfiguration of the reduced oxide is observed which is caused by the oxygen migration of CeO 2 . This work explores the structure evolution of CeO 2 in CeO 2 −CuO inverse catalyst under different conditions by in situ characterization technique and provides a reference for monitoring the dynamic changes of oxide structure.
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