膜
单层
化学工程
共价有机骨架
化学
羟醛反应
共价键
纳米技术
共轭体系
表面能
聚丙烯腈
材料科学
高分子化学
聚合物
有机化学
物理化学
催化作用
生物化学
工程类
作者
Li Wang,Haoyong Yang,Zhongquan Liao,Shengxu Li,Mike Hambsch,Guangen Fu,Stefan C. B. Mannsfeld,Qi Sun,Tao Zhang
摘要
sp2 carbon-conjugated covalent organic frameworks (sp2c-COFs) with superb in-plane π-conjugations, high chemical stability, and robust framework structure are expected to be ideal films/membranes for a wide range of applications including energy-related devices and optoelectronics. However, so far, sp2c-COFs have been mainly limited to microcrystalline powders, and this consequently hampered their performances in devices. Herein, we report a simple and robust methodology to fabricate large-area, free-standing, and crystalline sp2c-COF films (TFPT–TMT and TB–TMT) on various solid substrates (e.g., fluorine-doped tin oxide, aluminum sheet, polyacrylonitrile membrane) by self-assembly monolayer-assisted surface-initiated Schiff-base-mediated aldol polycondensation (namely, SI-SBMAP). The resultant sp2c-COF films show lateral sizes up to 120 cm2 and tunable thickness from tens of nanometers to a few micrometers. Owing to the robust framework and highly ordered quasi-1D channels, the sp2c-COF membrane-based osmotic power generator presents an output power density of 14.1 W m–2 under harsh conditions, outperforming most reported COF membranes as well as commercialized benchmark devices (5 W m–2). This work demonstrates a simple and robust interfacial methodology for the fabrication of sp2c-COF films/membranes for green energy applications and potential optoelectronics.
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