光催化
钙钛矿(结构)
碘化物
重组
电荷(物理)
化学物理
俘获
纳米技术
化学
材料科学
光化学
催化作用
无机化学
物理
结晶学
生态学
生物化学
量子力学
生物
基因
作者
Qing Yao,Hui Li,Jiawei Xue,Shenlong Jiang,Qun Zhang,Jun Bao
标识
DOI:10.1002/ange.202308140
摘要
Abstract Inspired by its great success in the photovoltaic field, methylammonium lead iodide perovskite (MAPbI 3 ) has recently been actively explored as photocatalysts in H 2 evolution reactions. However, the practical application of MAPbI 3 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 MAPbI 3 photocatalysts. By deliberately designing and synthesizing the MAPbI 3 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 MAPbI 3 photocatalysts turn out to achieve an impressive photocatalytic H 2 evolution rate as high as 0.64 mmol ⋅ g −1 ⋅ h −1 , one order of magnitude higher than that of the conventional MAPbI 3 photocatalysts. This work establishes a new paradigm for controlling charge‐transfer dynamics in photocatalysis.
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