In situ construction of two-dimensional (2D)/2D pg-C 3 N 4 /Ti 3 AlC 2 MAX heterojunction was achieved using a protonated assisted sonication approach, while TiO 2 nanoparticles were embedded over the layered heterostructure using a sol–gel method. This multiheterojunction system exhibits proficient charge transfer and superior activity toward photocatalytic reduction of CO 2 through dry reforming of methanol (DRM). Using pg-C 3 N 4 /Ti 3 AlC 2 /TiO 2 composite, H 2 and CO production rates at 91.9 and 4.97 mmol (g of cat.) −1 h –1 were achieved, which are 18- and 6-fold higher than using pristine pg-C 3 N 4, respectively. The enhancement in photocatalytic activity is mainly attributed to intimate interfacial contact due to the formation of a multiheterojunction for better light absorption, boosted electron separation, and stronger photoreductive potential. More importantly, CO 2 reduction with H 2 O produces CO-rich syngas; however, the methanol/water mixture promoted hydrogen-rich syngas production. Higher quantum yield and prolonged stability are further achieved over the composite catalyst, attributed to the exfoliated 2D Ti 3 AlC 2 MAX structure with strong metal/support interaction. This work demonstrates DRM as a potential approach to get hydrogen-rich syngas and provides a new pathway for the construction of highly stable 2D MAX based structured composite for water splitting and CO 2 reforming applications.
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Muhammad Daniyal Tahir (2020) studied this question.
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