Constructing a p–n heterojunction is an efficient strategy to mitigate the charge-carrier recombination in semiconductors, thereby enhancing photocatalytic activity. This study designed and fabricated core–shell structured p–n heterojunction photocatalyst β-Ga2O3@CoGa2O4 nanorods, using an in situ self-template-etched chemical route. The experimental results revealed that CoGa2O4 nanoparticles could be intimately grown on the surface of β-Ga2O3 nanorods, and the thickness of the CoGa2O4 shells could be easily adjusted by optimizing the Co/Ga ratio. Notably, when employed as a photocatalyst for the conversion of CO2 with H2O, without requiring additional sacrificial reagents, β-Ga2O3@CoGa2O4 nanorods showed improved photocatalytic activity for CO2 reduction to CO with a yield of 21.1 μmol g–1 h–1 compared to isolated β-Ga2O3 or CoGa2O4. The presence of a p–n heterojunction in β-Ga2O3@CoGa2O4 nanorods promotes charge-carrier transportation and separation through the internal electric field caused by n-type β-Ga2O3 and p-type CoGa2O4. Consequently, this results in enhanced photocatalytic CO2 reduction activity during continuous operation. This study would offer a feasible method for achieving effective photocatalytic CO2 conversion through the rational design of p–n heterojunctions at the nanoscale.
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Liu et al. (2024) studied this question.
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