UV light-induced oxygen doping in graphitic carbon nitride with suppressed deep trapping for enhancement in CO2 photoreduction activity

被引:21
|
作者
Zhao, Xiaolong [1 ]
Yi, Xiaoping [2 ]
Pan, Wending [1 ]
Wang, Yifei [1 ,3 ]
Luo, Shijing [1 ]
Zhang, Yingguang [1 ]
Xie, Ruijie [1 ]
Leung, Dennis Y. C. [1 ]
机构
[1] Univ Hong Kong, Dept Mech Engn, Pokfulam Rd, Hong Kong, Peoples R China
[2] Univ Sci & Technol Beijing, Sch Energy & Environm Engn, Beijing 100083, Peoples R China
[3] Harbin Inst Technol, Sch Mech Engn & Automat, Shenzhen 518055, Peoples R China
关键词
UV light; Oxygen doping; Charge transfer; Graphitic carbon nitride; CO2; reduction; G-C3N4; NANOSTRUCTURES; PERFORMANCE; REDUCTION; MECHANISM; SURFACE; PHOTOANODE; OXIDATION; EPOXY;
D O I
10.1016/j.jmst.2022.06.022
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
While photoreduction of CO2 to CH4 is an effective means of producing value-added fuels, common pho-tocatalysts have poor activity and low selectivity in photocatalytic CO2-reduction processes. Even though creating defects is an effective photocatalyst fabrication route to improve photocatalytic activity, there are some challenges with the facile photocatalyst synthesis method. In this work, an O element is in-troduced into a graphitic carbon nitride (CN) skeleton through a precursory ultraviolet light irradiation pretreatment to increase the visible light absorption and enhance the carrier density of this modified non-metal CN photocatalyst; the charge transfer dynamics thereof are also studied through electrochem-ical tests, photoluminescence spectroscopy, and nanosecond transient absorption. We verify that the op-timized sample exhibits lower charge recombination and a suppressed 84 ns electron-trapping lifetime, compared to the 103 ns electron-trapping lifetime of the CN counterpart, and thereby contributes to ro-bust detrapping and a fast transfer of active electrons. Through density functional theory calculations, we find that the improved light absorption and increased electron density are ascribed to O-element doping, which enhances the CO2 adsorption energy and improves the CO2-to-CH4 photoreduction activity; it be-comes 17 times higher than that of the bare CN, and the selectivity is 3.8 times higher than that of CN. Moreover, the optimized sample demonstrates excellent cyclic stability in a 24-hour cycle test. (C) 2022 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
引用
收藏
页码:135 / 144
页数:10
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