This research demonstrates enhanced hydrogen peroxide production in covalent organic frameworks, indicating breakthrough photocatalytic efficiency improvements.
Covalent organic frameworks (COFs) have emerged as promising photocatalysts for the artificial photosynthesis of hydrogen peroxide (H 2 O 2 ), yet their practical application is hindered by limited photocatalytic efficiency. Herein, a bioinspired strategy is reported to enhance the photocatalytic performance of COFs by introducing an ortho ‐positioned arrangement of enol (OH) and imine (N) groups. Through rational molecular engineering, a concerted proton‐coupled electron transfer (PCET) pathway is established, which facilitates the efficient separation and transfer of photoexcited charge carriers, thereby dramatically enhancing H 2 O 2 production from water and oxygen. The TbDO COF, featuring the PCET pathway, demonstrates superior performance, achieving a remarkable H 2 O 2 production rate of 7265 μmol g −1 h −1 in a nonsacrificial system, surpassing COFs with similar structure but lacking this pathway. This study advances the design of COFs and opens new avenues for sustainable solar‐to‐chemical energy conversion.
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Wang et al. (2025) studied this question.
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