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

材料科学 俘获 光催化 石墨氮化碳 氧气 光化学 兴奋剂 氮化物 碳纤维 纳米技术 光电子学 化学 催化作用 生物 有机化学 复合数 生态学 复合材料 生物化学 图层(电子)
作者
Xiaolong Zhao,Xiaoping Yi,Wending Pan,Yifei Wang,Shijing Luo,Yingguang Zhang,Ruijie Xie,Dennis Y.C. Leung
出处
期刊:Journal of Materials Science & Technology [Elsevier BV]
卷期号:133: 135-144 被引量:33
标识
DOI:10.1016/j.jmst.2022.06.022
摘要

• Oxygen (O) element is introduced in the bulk graphitic carbon nitride (CN) for the first time through a precursor pretreatment by ultraviolet (UV) light irradiation. • The doped O non-metal photocatalyst of CN increased visible light absorption and enhanced carrier density. • The optimized sample has lower charge recombination and suppressed electron deep trapping. • The optimized sample shows enhanced photoreduction activity of CO2 to CH4. While photoreduction of CO 2 to CH 4 is an effective means of producing value-added fuels, common photocatalysts have poor activity and low selectivity in photocatalytic CO 2 -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 introduced 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 electrochemical tests, photoluminescence spectroscopy, and nanosecond transient absorption. We verify that the optimized 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 robust 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 CO 2 adsorption energy and improves the CO 2 -to-CH 4 photoreduction activity; it becomes 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.
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