Porous C3N4 nanosheet supported Au single atoms as an efficient catalyst for enhanced photoreduction of CO2 to CO

被引:7
作者
Hu, Shan [1 ,2 ]
Qiao, Panzhe [4 ]
Liu, Zixin [1 ,2 ]
Zhang, Xueli [1 ,2 ]
Zhang, Fangyuan [1 ,2 ]
Ye, Jinhua [1 ,2 ,3 ]
Wang, Defa [1 ,2 ]
机构
[1] Tianjin Univ, TJU NIMS Int Collaborat Lab, Key Lab Adv Ceram & Machining Technol, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Mat Sci & Engn, Tianjin Key Lab Composite & Funct Mat, Tianjin 300072, Peoples R China
[3] Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton WPI MANA, Tsukuba, Ibaraki 3050044, Japan
[4] Chinese Acad Sci, Shanghai Synchrotron Radiat Facil, Shanghai Adv Res Inst, Shanghai 201210, Peoples R China
基金
中国国家自然科学基金;
关键词
Au single atom; M-N(4 )coordination; CO2; photoreduction; CO selectivity; C3N4; REDUCTION; STRATEGIES; CONVERSION; LIQUID; G-C3N4; WATER;
D O I
10.1016/j.jcat.2024.115405
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Artificial photosynthesis utilizing solar energy to convert carbon dioxide (CO2) and water (H2O) into fuels and high-value chemicals offers a promising technology for mitigating energy consumption and environmental pollution. However, the development of efficient photocatalysts with high product selectivity remains a big challenge due to the sluggish dynamic transfer of photogenerated charge carriers. Herein, porous C3N4 nanosheet supported Au single atoms photocatalyst (Au1@CN) with Au-N4 coordination is fabricated via a facile "impregnation + freeze-drying" process. The as-synthesized Au1@CN exhibits efficient and stable CO2 photoreduction activity with a CO evolution rate of 0.58 mu mol h-1 (amount of catalyst: 10 mg), CO selectivity of 94 %, and a turnover frequency (TOF) of 10.0 h-1 using H2O as the reductant, which exceed most previous works on C3N4-based single-atom photocatalysts for CO2 reduction. Experimental studies and density functional theory (DFT) calculations reveal that the unique Au-N4 coordination promotes the dynamic transfer of photogenerated charge carriers, facilitates the adsorption/activation of CO2 molecules and generation of *COOH intermediate, thereby significantly enhancing the CO2 photoreduction activity with high CO selectivity. This study demonstrates an effective strategy for the design of M-N4 coordinated single-atom catalyst toward efficient and selective photoreduction of CO2 to CO.
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页数:9
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