Enhanced Photocatalytic Activity of Lead‐Free Cs2TeBr6/g‐C3N4 Heterojunction Photocatalyst and Its Mechanism

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Abstract
In this study, a new type of lead‐free double perovskite Cs2TeBr6 combined with metal‐free semiconductor g‐C3N4 heterojunction is constructed and used for photocatalytic CO2 reduction for the first time. The S‐scheme charge transfer mechanism between Cs2TeBr6 and g‐C3N4 is systematically verified by X‐ray photoelectron spectroscopy (XPS), electron spin resonance (ESR) and in situ Fourier infrared spectroscopy(FT‐IR). The formation of S‐type heterojunction makes the photocatalyst have higher charge separation ability and highest redox ability. The results show that 5%‐CTB/CN heterojunction material has the best photocatalytic reduction effect on CO2 under visible light irradiation. After 3 h of illumination, the yield of CO and CH4 are 468.9 µmol g−1 and 61.31 µmol g−1, respectively. The yield of CO is 1.5 times and 32 times that of pure Cs2TeBr6 and g‐C3N4, and the yield of CH4 is doubled compared with pure Cs2TeBr6. However, g‐C3N4 almost does not produce CH4, which indicates that the construction of heterojunction helps to further improve the photocatalytic performance of the material. This study provides a new idea for the preparation of Cs2TeBr6/g‐C3N4 heterojunction and its effective interfacial charge separation.
Funding Information
  • National Natural Science Foundation of China (61975023,51775070,22072010,61875211,62271089,62375032)
  • Natural Science Foundation of Chongqing Municipality (Grant No. cstc2021ycjh‐bgzxm0181)

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