Photocatalytic CO2 reduction presents an environmentally friendly and economically viable approach to combat the energy crisis and advance carbon neutrality. In this study, we fabricated a In(OH)3/ZnIn2S4 heterojunction photocatalyst for the photocatalytic reduction of aqueous-CO2. This innovative approach not only led to a substantial increase in the production rates of CO, CH3OH, and CH4, with the respective peak rates reaching 23.45, 29.57, and 45.25 µmol g−1h−1, but also enhanced the selectivity of premium chemical fuels (CH3OH and CH4) to an impressive 91.1 %. The remarkable outcomes can be attributed to the synergistic interplay between the constructed heterojunction and the introduced sodium bicarbonate. The formation of the heterojunction efficiently facilitated the charge separation and transfer, while the incorporation of In(OH)3 notably boosted the carbon source capture capacity. Furthermore, the direct hydrolysis of sodium bicarbonate served as a vital carbon source and acted as a proton donor, effectively boosting the production of high-value chemical fuels. These findings offer invaluable insights for the development of highly active and selective photocatalysts.
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