Modulating electronic Metal-Support interactions of Pt-CuO/CeO2 catalyst via quenching to optimize catalytic activity

被引:2
|
作者
Zhao, Shuaiqi [1 ,2 ]
Lin, Jiajin [3 ]
Gong, Wenqiang [1 ]
Xu, Aihua [1 ,2 ]
Li, Xiaoxia [1 ]
Qiu, Yongcai [3 ]
机构
[1] Wuhan Text Univ, Sch Chem & Chem Engn, Wuhan 430200, Peoples R China
[2] Wuhan Text Univ, Hubei Key Lab Biomass Fibers & Ecodyeing & Finishi, Wuhan 430200, Peoples R China
[3] South China Univ Technol, Sch Environm & Energy, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Atmospher Environm & Pollut, Guangzhou 510000, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Quenching; EMSI; CO oxidation; Pt-based catalysts; Electron redistribution; IN-SITU RAMAN; CO OXIDATION; SINGLE ATOMS; NANOPARTICLES; CERIA; DISPERSION; CLUSTERS; CEO2;
D O I
10.1016/j.seppur.2023.125864
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Pt-based catalysts are one of the most extensively used heterogeneous catalysts for the degradation of pollutants, and regulating electron-metal-support interaction (EMSI) is an efficient strategy to enhance the performance of Pt-based catalysts. Herein, we introduced a quenching technique for regulating the EMSI of Pt-CuO/CeO2 catalysts to significantly boost its CO catalytic activity. The EMSI optimized by quenching was determined to promote the electron redistribution between Pt and CuO/CeO2 via Cu-O-Pt structure, thus forming more electron-rich Pt species and enhancing the surface oxygen species activity. From comprehensive characterization investigations, we confirmed that the superior activity arouse from the moderate Pt0/Pt2+ ratio, in which CO molecules were preferentially adsorbed on the electron-rich Pt sites and reacted with active oxygen species from PtOx or CuO/CeO2, accelerating the whole CO catalytic process. Our finding provided a new inspiration to control EMSI of Pt-based catalysts and widened the application of quenching chemistry in heterogeneous catalysis.
引用
收藏
页数:10
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