过氧化氢
光催化
共价键
光化学
共价有机骨架
接受者
催化作用
化学
化学工程
砜
材料科学
有机化学
高分子化学
物理
工程类
凝聚态物理
作者
C. Shu,Xiaoju Yang,Lunjie Liu,Xunliang Hu,Ruixue Sun,Xuan Yang,Andrew I. Cooper,Bien Tan,Xiaoyan Wang
标识
DOI:10.1002/anie.202403926
摘要
Abstract The solar‐driven photocatalytic production of hydrogen peroxide (H 2 O 2 ) from water and oxygen using semiconductor catalysts offers a promising approach for converting solar energy into storable chemical energy. However, the efficiency of photocatalytic H 2 O 2 production is often restricted by the low photo‐generated charge separation, slow surface reactions and inadequate stability. Here, we developed a mixed‐linker strategy to build a donor‐acceptor‐acceptor (D–A–A) type covalent organic framework (COF) photocatalyst, FS‐OHOMe‐COF. The FS‐OHOMe‐COF structure features extended π–π conjugation that improves charge mobility, while the introduction of sulfone units not only as active sites facilitates surface reactions with water but also bolsters stability through increased interlayer forces. The resulting FS‐OHOMe‐COF has a low exciton binding energy, long excited‐state lifetime and high photo‐stability that leads to high performance for photocatalytic H 2 O 2 production (up to 1.0 mM h −1 ) with an H 2 O 2 output of 19 mM after 72 hours of irradiation. Furthermore, the catalyst demonstrates high stability, which sustained activity over 192 hours of photocatalytic experiment.
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