光催化
钙钛矿(结构)
碘化物
重组
俘获
化学物理
电荷(物理)
材料科学
纳米技术
载流子
化学
光化学
光电子学
催化作用
物理
无机化学
结晶学
生态学
基因
生物
量子力学
生物化学
作者
Qing Yao,Hui Li,Jiawei Xue,Shenlong Jiang,Qun Zhang,Jun Bao
标识
DOI:10.1002/anie.202308140
摘要
Inspired 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.
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