Reductive Carbon-Carbon Coupling on Metal Sites Regulates Photocatalytic CO2 Reduction in Water Using ZnSe Quantum Dots

被引:59
|
作者
Xin, Zhi-Kun [1 ,2 ]
Huang, Mao-Yong [1 ]
Wang, Yang [1 ]
Gao, Yu-Ji [1 ]
Guo, Qing [1 ]
Li, Xu-Bing [1 ,2 ]
Tung, Chen-Ho [1 ,2 ]
Wu, Li-Zhu [1 ,2 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Photochem Convers & Optoelect Mat, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Future Technol, Beijing 100049, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Artificial Photosynthesis; Carbon Dioxide Reduction; Furfural; Reaction Kinetics; ZnSe Quantum Dots; NANOPARTICLES; NANOCRYSTALS; NANOWIRES; CATALYST; IONS;
D O I
10.1002/anie.202207222
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Colloidal quantum dots (QDs) consisting of precious-metal-free elements show attractive potentials towards solar-driven CO2 reduction. However, the inhibition of hydrogen (H-2) production in aqueous solution remains a challenge. Here, we describe the first example of a carbon-carbon (C-C) coupling reaction to block the competing H-2 evolution in photocatalytic CO2 reduction in water. In a specific system taking ZnSe QDs as photocatalysts, the introduction of furfural can significantly suppress H-2 evolution leading to CO evolution with a rate of approximate to 5.3 mmol g(-1) h(-1) and a turnover number (TON) of >7500 under 24 h visible light. Meanwhile, furfural is upgraded to the self-coupling product with a yield of 99.8 % based on the consumption of furfural. Mechanistic insights show that the reductive furfural coupling reaction occurs on surface Zn-sites to consume electrons and protons originally used for H-2 production, while the CO formation pathway at surface anion vacancies from CO2 remains.
引用
收藏
页数:6
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