All‐Inorganic Perovskite NiTiO3/Cs3Sb2I9 Heterostructure for Photocatalytic CO2 Reduction to CH4 with High Selectivity

Author:

Fan Shuhan1,Yang Qu1,Yin Guilin1,Qi Xiaosi1,Feng Yuyu1,Ding Junfei1,Peng Qiong1,Qu Yunpeng1,Wang Qinglong2,Shen Yan3,Wang Mingkui3,Gong Xiu1ORCID

Affiliation:

1. College of Physics, & Guizhou Province Key Laboratory for Photoelectrics Technology and Application Guizhou University Guiyang 550025 China

2. State Key Laboratory of Catalysis Dalian National Laboratory for Clean Energy Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

3. Wuhan National Laboratory for Optoelectronics School of Optical and Electronic Information Huazhong University of Science and Technology Wuhan Hubei 430074 China

Abstract

AbstractDeveloping efficient and stable halide perovskite‐based photocatalysts for highly selectivity reduction CO2 to valuable fuels remains a significant challenge due to their intrinsic instability. Herein, a novel heterostructure featuring 2D Cs3Sb2I9 nanosheets on a 3D flower‐like mesoporous NiTiO3 framework using a top‐down stepwise membrane fabrication technique is constructed. The unique bilayer heterostructure formed on the 3D mesoporous framework endowed NiTiO3/Cs3Sb2I9 with sufficient and close interface contact, minimizing charge transport distance, and effectively promoting the charge transfer at the interface, thus improving the reaction efficiency of the catalyst surface. As revealed by characterization and calculation, the coupling of Cs3Sb2I9 with NiTiO3 facilitates the hydrogenation process during catalytic, directing reaction intermediates toward highly selective CH4 production. Furthermore, the van der Waals forces inherent in the 3D/2D heterostructure with face‐to‐face contact provide superior stability, ensuring the efficient realization of photocatalytic CO2 reduction to CH4. Consequently, the optimized 3D/2D NiTiO3/Cs3Sb2I9 heterostructure demonstrates an impressive CH4 yield of 43.4 µmol g−1 h−1 with a selectivity of up to 88.6%, surpassing most reported perovskite‐based photocatalysts to date. This investigation contributes to overcoming the challenges of commercializing perovskite‐based photocatalysts and paves the way for the development of sustainable and efficient CO2 conversion technologies.

Funder

National Natural Science Foundation of China

Science and Technology Program of Guizhou Province

Publisher

Wiley

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