材料科学
光催化
结晶
成核
钙钛矿(结构)
制氢
压电
铁电性
煅烧
化学工程
化学物理
表面电荷
氢
极化(电化学)
分解水
纳米技术
压电响应力显微镜
光电子学
载流子
Boosting(机器学习)
催化作用
工作(物理)
电荷(物理)
光催化分解水
作者
Weiyu Cheng,L H Li,Changyi Xu,Hengyu Cao,Ruonan Wang,Chao‐Ran Huang,Chen Wang,Zhicheng Zhou,Jiating Li,Wei-Qiang Liao,Fan Liao,Xiong Yan,Xiawei Zhang,Shan Cong,Zhenhui Kang,Ren‐Gen Xiong,Guifu Zou
出处
期刊:Small
[Wiley]
日期:2026-02-11
卷期号:22 (18): e14679-e14679
被引量:2
标识
DOI:10.1002/smll.202514679
摘要
ABSTRACT Using sunlight and water to get hydrogen (H 2 ) offers a promising pathway toward a sustainable future. Severe recombination of photogenerated electron–hole pairs directly impedes photocatalytic H 2 production, while the strong polarized field from ferroelectric materials has been demonstrated to effectively promote charge separation. However, several drawbacks still remain, such as low piezoelectric coefficient, difficulty in forming a polarized field, and complex calcination preparation process. Herein, we present an in situ heterogeneous nucleation crystallization strategy for organic‐inorganic hybrid perovskite ferroelectrics, involving heterogeneous crystallization on the surface of solid photocatalyst, the emanation of a polarized field, and the enhancement of photocatalytic H 2 production. Under the mechanical stimulus, a polarized field is generated with deformation of the molecular ferroelectrics, which reinforces the charge separation efficiency. Thus, photocatalytic H 2 production increases to 6.725 mmol g −1 h −1 , almost 26‐fold compared to the control C 3 N 4 catalyst (0.255 mmol g −1 h −1 ). Our work demonstrates the extensive application of molecular ferroelectrics for high performance photocatalyst design with enhanced photocharge separation.
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