催化作用
甲烷
硫黄
燃烧
甲烷厌氧氧化
氧化还原
化学工程
吸附
催化燃烧
材料科学
化学
无机化学
物理化学
有机化学
工程类
作者
Jiabin Ji,Congyun Zhang,Xianfeng Yang,Fanxin Kong,Chuanqiang Wu,Huimei Duan,Dongjiang Yang
标识
DOI:10.1016/j.cej.2023.143044
摘要
Improving the sulfur-resistance of low-temperature methane combustion catalysts is great important for industrial applications. Electronic engineering of catalyst active sites is effective in tuning the catalytic performance. Herein, IrPt0.5/TiO2 catalysts with electron-rich Ir structures modulated by Pt exhibit excellent low temperature sulfur-resistance towards methane combustion. The integrated characterization coupled with density functional theory calculations reveal that the strong electronic interaction between Ir and Pt induces the formation of electron-rich Ir structures. The electron-rich Ir structures with more defective oxygen vacancy and better redox ability greatly boost the adsorption and activation of O2 while suppress SO2 adsorption on the catalyst surface, leading to excellent sulfur tolerance towards methane combustion. This work highlights a practical electronic engineering strategy to tune the electron structure of Ir active sites for the development of practical methane oxidation catalysts.
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