亚胺
异构化
光催化
共价键
光化学
化学
单体
共价有机骨架
吸附
氢键
析氧
氧气
过氧化氢
分子
催化作用
有机化学
物理化学
电化学
聚合物
电极
作者
Wei Wang,Shouxin Zhang,Hongqi Chu,Zhen Zhan,Qi Huang,Zhenzi Li,Xuepeng Wang,Fu‐Quan Bai,Wei Zhou
出处
期刊:Small
[Wiley]
日期:2024-09-27
标识
DOI:10.1002/smll.202406527
摘要
Abstract Constitutional‐isomerized covalent organic frameworks (COFs), constructed by swapping monomers around imine bonds, have attracted attention for their distinct optoelectronic properties, which significantly impact photocatalytic performance. However, limited research has delved into the inherent relationship between isomerization and the enhancement of H 2 O 2 photosynthesis. Herein, a pair of isomeric COFs linked by imine bonds (PB‐PT‐COF and PT‐PB‐COF) is synthesized, and it is proved that isomeric COFs exhibit different rate‐determining steps in the generation process of H 2 O 2 , resulting in a twofold increase in photocatalytic efficiency. Specifically, PT‐PB‐COF demonstrates effective adsorption and activation of molecular oxygen (O 2 + e − → •O 2 − + e − → H 2 O 2 ), leading to a significant improvement in H 2 O 2 photocatalytic efficiency. In contrast, PB‐PT‐COF exhibits robust interaction with H 2 O, enabling direct oxidation of H 2 O (H 2 O + h + → H 2 O 2 ). This study provides a thorough understanding of the intrinsic mechanism underlying the constitutional‐isomerized COFs in the photocatalytic H 2 O 2 generation, offering insights for further optimizing building units.
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