Promoting Photocatalytic H2 Evolution through Retarded Charge Trapping and Recombination by Continuously Distributed Defects in Methylammonium Lead Iodide Perovskite

Author:

Yao Qing1,Li Hui2,Xue Jiawei1,Jiang Shenlong3,Zhang Qun234,Bao Jun156ORCID

Affiliation:

1. National Synchrotron Radiation Laboratory University of Science and Technology of China Hefei Anhui 230029 China

2. Department of Chemical Physics School of Chemistry and Materials Science University of Science and Technology of China Hefei Anhui 230026 China

3. Hefei National Laboratory University of Science and Technology of China Hefei Anhui 230088 China

4. Hefei National Research Center for Physical Sciences at the Microscale Synergetic Innovation Center of Quantum Information and Quantum Physics University of Science and Technology of China Hefei Anhui 230026 China

5. iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) University of Science and Technology of China Hefei Anhui 230029 China

6. Key Laboratory of Precision and Intelligent Chemistry University of Science and Technology of China Hefei Anhui 230026 China

Abstract

AbstractInspired by its great success in the photovoltaic field, methylammonium lead iodide perovskite (MAPbI3) has recently been actively explored as photocatalysts in H2 evolution reactions. However, the practical application of MAPbI3 photocatalysts remains hampered by the intrinsically fast trapping and recombination of photogenerated charges. Herein, we propose a novel strategy of regulating the distribution of defective areas to promote charge‐transfer dynamics of MAPbI3 photocatalysts. By deliberately designing and synthesizing the MAPbI3 photocatalysts featuring a unique continuation of defective areas, we demonstrate that such a feature enables retardation of charge trapping and recombination via lengthening the charge‐transfer distance. As an outcome, such MAPbI3 photocatalysts turn out to achieve an impressive photocatalytic H2 evolution rate as high as 0.64 mmol ⋅ g−1 ⋅ h−1, one order of magnitude higher than that of the conventional MAPbI3 photocatalysts. This work establishes a new paradigm for controlling charge‐transfer dynamics in photocatalysis.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

General Medicine

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