材料科学
光催化
亚胺
苯
共价键
乙炔
催化作用
光化学
化学工程
相(物质)
结晶度
有机化学
化学
复合材料
工程类
作者
Tao Yang,Yue Chen,Yingchu Wang,Xueqing Peng,Aiguo Kong
标识
DOI:10.1021/acsami.2c20506
摘要
Conversing oxygen (O2) to hydrogen peroxide (H2O2) driven by solar energy is a promising H2O2 onsite production route but often short of efficient and durable photocatalysts. Herein, strong π–π conjugate polycyclic aromatic benzene and acetylene units have been constructed into new covalent organic frameworks (COFs) linked by imine C═N bonding. These COFs demonstrated two-dimensional hexagonal crystalline frameworks with higher crystallinity and larger surface area (>600 m2 g–1). Covalent benzene–acetylene frameworks possessed appropriate visible light-responsive band structure and the suppressed charge recombination rate. The −OH groups on their frameworks enable them to be weakly hydrophilic. As a result, it served as high-performance but durable photocatalysts for H2O2 production in the water–benzyl alcohol (BA) two-phase system. It delivered a H2O2 production rate of 1240 μmol h–1 gcat–1 and durable catalytic efficiency within 60 h, comparable to the best COF-based catalysts. This study provides an efficient two-phase photocatalytic system for H2O2 production based on weakly hydrophilic imine-linked benzene–acetylene organic photocatalysts.
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