催化作用
氧化还原
氧化物
碳氢化合物
过渡金属
无机化学
金属
化学
铂金
电子转移
贵金属
材料科学
化学工程
光化学
有机化学
工程类
作者
Baoju Wang,Jingpeng Zhang,Yu Han,Yi-Kai Gao,Guolei Xiang,Guang‐Wen Chu,Yong Luo
出处
期刊:ACS Engineering Au
[American Chemical Society]
日期:2022-06-10
卷期号:2 (6): 486-495
被引量:3
标识
DOI:10.1021/acsengineeringau.2c00017
摘要
CuOx/CeO2 is emerging as an effective catalyst for CO oxidation due to its unique redox properties; however, its activity and stability still need to be enhanced compared with supported platinum group metals. Here, an approach is demonstrated to increase the CO oxidation performance and resistance to hydrocarbon inhibition through the K+ modification of the CuOx/CeO2 catalyst. The K+ can improve the electron transfer at the metal–oxide interface, shifting the redox equilibrium (Cu2+ + Ce3+ ↔ Cu+ + Ce4+) to be right to accelerate the formation of highly active Cu+ species. The reaction activity of the K+-modified CuOx/CeO2 catalyst was in the same order of magnitude as the noble metal of Pt and Pd catalysts. In addition, the K+-modified catalyst showed significantly improved resistance to hydrocarbon inhibition. This work demonstrates a facile way to tune the redox properties of binary transition metal oxides.
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