Abstract
Ultrathin 2D/2D Ti3C2Tx/semiconductor (CdS and Bi2MoO6) dual-functional photocatalysts have been constructed for the oxidative coupling of benzylamines to imines combined with H2generation under visible light irradiation (λ≥420 nm). The optimal 2D/2D Ti3C2Tx/CdS sample exhibits high photocatalytic performance toward H2evolution (219.7 μmol g−1h−1) and imine production (155.8 μmol g−1h−1), which is 5 times and 6 times higher than that of pure CdS, respectively.In situirradiated XPS and photoelectrochemical characterizations reveal that the enhanced photoactivity over Ti3C2Tx/semiconductor heterostructures can be attributed to the facilitated charge separation from the semiconductors to the Ti3C2Txcocatalyst. A possible reaction mechanism is proposed based onin situFTIR spectroscopy of benzylamine adsorption and imine product desorption and reaction intermediate detection usingin situESR. This work provides a systematic strategy to construct ultrathin 2D/2D Ti3C2Tx/semiconductor heterojunctions for photocatalytic synthesis of high value-added products combined with H2generation.
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CITATION STYLE
Wang, H., Hu, P., Zhou, J., Roeffaers, M. B. J., Weng, B., Wang, Y., & Ji, H. (2021). Ultrathin 2D/2D Ti3C2Tx/semiconductor dual-functional photocatalysts for simultaneous imine production and H2evolution. Journal of Materials Chemistry A, 9(35), 19984–19993. https://doi.org/10.1039/d1ta03573h
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