Inorganic Copper-Based Halide Perovskite for Efficient Photocatalytic CO Reduction.

ACS Appl Mater Interfaces

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, Lehn Institute of Functional Materials, School of Chemistry, Sun Yat-sen University, Guangzhou 510006, P. R. China.

Published: September 2022

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 CsCuCl and the corresponding Br-substituted sample (CsCuClBr) are designed and explored as the catalysts for photocatalytic CO reduction for the first time. A facile antisolvent recrystallization process with pre-prepared single crystals as the precursor is employed to controllably synthesize CsCuCl and CsCuClBr microcrystals (MCs). The electronic structure and charge transfer property analysis by theoretical and experimental investigation reveal that CsCuCl possesses a satisfying bandgap (1.92 eV) and conduction band minimum (CBM) to harvest the sunlight and drive the conversion of CO to CH 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 μmol g h is achieved for CsCuClBr MCs, which is much better than that of same-sized CsPbBr 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.

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Source
http://dx.doi.org/10.1021/acsami.2c12695DOI Listing

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