Rich Oxygen Vacancies in Confined Heterostructured TiO2@In2S3 Hybrid for Boosting Solar-Driven CO2 Reduction

Solar energy driving CO2 reduction is a potential strategy that not only mitigates the greenhouse effect caused by high CO2 level in atmosphere, but also yields carbon chemicals/fuels at the same time. Herein, a facile way to design the heterogeneous TiO2@In2S3 hollow structures possessing robust light harvesting in both ultraviolet and visible regions is proposed and exhibits a higher generation rate of 25.35 and 1.24 mu mol center dot g(-1)center dot h(-1) for photocatalytic CO2 reduction to CO and CH4, respectively. The excellent photocatalytic catalytic performance comes from i) the confined heterostructured TiO2@In2S3 possesses a suitable band structure and a broadband-light absorbing capacity for CO2 photoreduction, ii) the rich interfaces between nanosized TiO2 and In2S3 on the shell can significantly reduce the diffusion length of carriers and enhance the utilization efficiency of photogenerated electron-hole pairs, and iii) enriched surface oxygen vacancies can provide more active sites for CO2 adsorption.