杰纳斯
共价有机骨架
材料科学
膜
共价键
Knoevenagel冷凝
选择性
聚丙烯腈
化学工程
光催化
人工光合作用
纳米技术
基质(水族馆)
莲花效应
共轭体系
能量转换效率
表面改性
光化学
光合作用
亚胺
纳米复合材料
作者
雷玉荷,Shihuan Gao,Y H Bai,K. Yang,Shuang Li,Mao Wang,Chong Cheng,Changsheng Zhao
摘要
ABSTRACT Covalent organic framework (COF)‐based photocatalysts hold considerable promise for solar‐driven chemical transformations, yet their practical performance in conventional powder or membrane systems is often constrained by poor dispersibility, inefficient interfacial mass transport, and suboptimal charge utilization. Here, we report COF‐based Janus membrane photocatalysts with an extended π‐conjugation for continuous photosynthesis of H 2 O 2 and value‐added chemicals, in which COF structures bearing expanded conjugated side chains are uniformly immobilized on the polyacrylonitrile (PAN) substrate to create a Janus‐like interfacial architecture. This design integrates the efficient light‐harvesting and charge‐transport capabilities of the COF framework with a PAN‐induced planar interface and tunable surface hydrophobicity. As a result, the Janus COF‐membrane exhibits enhanced hydrophobicity, achieving an H 2 O 2 production rate of 7888 µmol·g −1 h −1 under visible‐light irradiation, which is 2.23 times that of the control group, alongside excellent recyclability and long‐term operational stability. Furthermore, this straightforward approach can be extended to a range of COF‐derived photocatalysts for the photosynthesis of value‐added chemicals, which demonstrate superior activity in benzylamine coupling (99% conversion and selectivity within 3 h) and Knoevenagel condensation reactions (90%–99% conversion and selectivity within an average of 6 h). Together, our findings underscore the effectiveness of interfacial microenvironment engineering in designing COF membrane‐based photocatalytic systems.
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