互变异构体
光催化
共价键
化学
生产(经济)
材料科学
纳米技术
催化作用
有机化学
经济
宏观经济学
作者
Yang Song,Zhu Gao,Zi Jun Hu,Chunyue Pan,Jiayin Yuan,Kam Chiu Tam,You‐Nian Liu,Guipeng Yu,Juntao Tang
标识
DOI:10.1021/acs.macromol.3c01634
摘要
The efficiency of photocatalytic production of H2O2 is constrained by the low selectivity toward oxygen reduction, and the active sites are still under debate. Herein, analogous covalent organic framework photocatalysts were synthesized from triformylphloroglucinol (Tp) and predesigned diamines, in which a molecular engineering strategy was employed to manipulate the energy barrier for the targeted proton transfers. The tautomerization of enol-imine to keto-enamine introduced abundant alkene bonds (C═C), which serve as the primary adsorption sites and have a lower energy barrier for the reduction of the O2 reduction. DHAA-Tp COF displayed a remarkable photocatalytic H2O2 production rate of 219.5 μmol h–1 g–1 without any sacrificial reagent, which stands out among the structure-related materials. A switch from a concerted one-step 2e– to a two-step single e– process in O2 reduction was observed in TCNAQ-Tp COF, which is presumably ascribed to the suppressed tautomerization mediated by the strong electron-withdrawing cyano groups. The results demonstrate a novel concept for the photocatalytic production of H2O2 using an efficient, stable, and recyclable metal-free photocatalytic system.
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