Abstract
The reduction of CO2 achieved by photocatalysis can simultaneously alleviate the energy crisis and solve environmental issues. Nevertheless, it remains challenging for the rational design of photocatalysts with high-efficiency carrier migration ability. Herein, the Z-scheme g-C3N4/In2O3 (CN/INO) heterostructure was fabricated via metal–organic frameworks (MOFs) assisted thermal deposition which could form a fully encapsulated hollow tubular structure. The unique structure was based on the MOFs-derived hollow hexagonal In2O3 tubular integrated with ultrathin g-C3N4. The Z-scheme CN/INO heterojunction exhibited a larger specific surface area and excellent charge separation efficiency. Benefiting from the above features, the Z-scheme CN/INO heterojunction demonstrated superior performance on photocatalytic CO2 reduction. The formation of CO and CH3OH over the optimized CN/INO-2 catalyst was 7.94 and 1.44 µmol⋅g−1⋅h−1, respectively. Moreover, the density functional theory (DFT) calculations and Kelvin probe force microscopy (KPFM) was carried out to further investigate the situation of charge transfer on the interface of CN/INO. The in-situ Fourier transform infrared spectroscopy (FTIR) was measured to confirm the immediate products and the possible mechanism of photocatalytic CO2 reduction was proposed. This work provided a MOFs-assisted strategy to construct a Z-scheme system for photocatalytic CO2 reduction.
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