Inorganic Copper-Based Halide Perovskite for Efficient Photocatalytic CO2 Reduction

In view of the toxicity of the Pb element, exploring eco-friendly Pb-free halide perovskites with excellent photoelectric properties is of great research and practical application significance. Herein, copper-based halide perovskite CsCuCl3 and the corresponding Br--substituted sample (CsCuCl2 Br) are designed and explored as the catalysts for photocatalytic CO2 reduction for the first time. A facile antisolvent recrystallization process with pre-prepared single crystals as the precursor is employed to controllably synthesize CsCuCl3 and CsCuCll2Br microcrystals (MCs). The electronic structure and charge transfer property analysis by theoretical and experimental investigation reveal that CsCuCl3 possesses a satisfying bandgap (1.92 eV) and conduction band minimum (CBM) to harvest the sunlight and drive the conversion of CO2 to CH4 and CO. The Br- substitution can not only narrow the bandgap but also facilitate the transportation of charge carriers. Thus, a total electron consumption rate of 44.71 mu mol g(-1) h(-1) is achieved for CsCuCl2Br MCs, which is much better than that of same-sized CsPbBr3 microcrystals or even better than many perovskite nanocrystal photocatalysts. This study suggests that Cu-based perovskites can serve as promising candidates for artificial photosynthesis or other photocatalytic applications, which may propose a new thought to construct lead-free, low-cost photocatalysts.

Automated summary

This study explores copper-based halide perovskite CsCuCl3 and CsCuCl2Br as catalysts for photocatalytic CO2 reduction. The results show that these perovskites have excellent photoelectric properties and can efficiently consume electrons in the process of CO2 reduction.