Selective Photocatalytic Reduction of CO2 to Syngas Over Tunable Metal-Perovskite Interface

被引:9
|
作者
Zhang, Li [1 ,2 ]
Yang, Yanling [1 ,2 ]
Tian, Jinshu [3 ]
Li, Jianhui [4 ]
Chen, Gui [1 ]
Zhou, Liujiang [5 ]
Sun, Yifei [2 ]
Qiu, Yongfu [1 ]
机构
[1] Dongguan Univ Technol, Sch Environm & Civil Engn, Dongguan 523808, Guangdong, Peoples R China
[2] Xiamen Univ, Coll Energy, Xiamen 361005, Peoples R China
[3] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Peoples R China
[4] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
[5] Univ Elect Sci & Technol China, Sch Phys, Chengdu 610054, Peoples R China
基金
中国国家自然科学基金;
关键词
Ag; carbon dioxide fixation; CO2; reduction; exsolution; photocatalysis; AG NANOPARTICLES; LAFEO3; CONVERSION; WATER; H2O; HYDROGENATION; EVOLUTION; DESIGN; GROWTH;
D O I
10.1002/cssc.202102729
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The extensive emission of CO2 results in critical environmental issues, such as global warming. Photocatalytic CO2 conversion is a meaningful route to convert CO2 into useful chemicals. However, the highly selective reduction of CO2 with the avoidance of hydrogen evolution is still challenging. Herein, the photocatalytic reduction CO2 to synthesis gas (syngas) was achieved on a metal Ag socketed perovskite LaFeO3 (LFO) catalytic interface prepared by an in-situ exsolution method. The conduction band of Ag-exsolved LFO is more negative than LFO, benefiting efficient CO2 reduction. By tuning the dopant Ag cation in the lattice to nanoparticles pinned on the surface, the CO formation rate was improved around five-fold from 0.51 to 2.41 mu mol g(-1) h(-1). Meanwhile, the H-2/CO molar ratio also showed strong dependence on the modality of Ag at the metal-perovskite interface. The design offers a promising pathway for transforming CO2 to valuable chemicals based on efficient photocatalysts design.
引用
收藏
页数:10
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