Construction of an Electron Capture and Transfer Center for Highly Efficient and Selective Solar-Light-Driven CO2 Conversion

被引:4
作者
Tang, Wangzhong [1 ,2 ]
Cao, Heng [1 ,2 ]
Ma, Peiyu [1 ,2 ]
Ding, Tao [1 ,2 ]
Huang, Sishi [1 ,2 ]
Wang, Jiajun [3 ]
Li, Qunxiang [1 ,2 ]
Xu, Xiaoliang [1 ,2 ]
Yang, Jinlong [1 ,2 ]
机构
[1] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, Natl Synchrotron Radiat Lab, Hefei 230026, Anhui, Peoples R China
[3] Tianjin Normal Univ, Coll Chem, Tianjin Key Lab Struct & Performance Funct Mol, Tianjin 300387, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
2D/2D composite; photocatalytic CO2 reduction; electron transfer; reaction mechanism; PHOTOREDUCTION;
D O I
10.1021/acs.nanolett.4c01064
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Exploring high-efficiency photocatalysts for selective CO2 reduction is still challenging because of the limited charge separation and surface reactions. In this study, a noble-metal-free metallic VSe2 nanosheet was incorporated on g-C3N4 to serve as an electron capture and transfer center, activating surface active sites for highly efficient and selective CO2 photoreduction. Quasi in situ X-ray photoelectron spectroscopy (XPS), soft X-ray absorption spectroscopy (sXAS), and femtosecond transient absorption spectroscopy (fs-TAS) unveiled that VSe2 could capture electrons, which are further transferred to the surface for activating active sites. In situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and density functional theory (DFT) calculations revealed a kinetically feasible process for the formation of a key intermediate and confirmed the favorable production of CO on the VSe2/PCN (protonated C3N4) photocatalyst. As an outcome, the optimized VSe2/PCN composite achieved 97% selectivity for solar-light-driven CO2 conversion to CO with a high rate of 16.3 mu mol<middle dot>g(-1)<middle dot>h(-1), without any sacrificial reagent or photosensitizer. This work offers new insights into the photocatalyst design toward highly efficient and selective CO2 conversion.
引用
收藏
页码:5317 / 5323
页数:7
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