溶剂
共价键
材料科学
膜
氧化物
石墨烯
化学工程
纳米材料
光催化
三嗪
多孔性
分子
纳米技术
化学
高分子化学
有机化学
复合材料
生物化学
工程类
催化作用
作者
J. Paul Chen,Guiliang Li,Haibo Lin,Fu Liu
标识
DOI:10.1016/j.cej.2021.132401
摘要
Covalent triazine frameworks (CTFs) are drawing substantial interest as porous crystalline two-dimensional (2D) or three-dimensional (3D) nanomaterials. Fabrication of CTFs nanoribbon is challenging but appealing to separation and photocatalysis. Here we for the first time report the synthesis of crystalline CTF-1 nanoribbons (CTF-1-NR) comprising 2–3 covalent triazine framework units in width through a polar solvent-induced fragmentation strategy. The width of 1D nanoribbons can be facilely tuned by varying the solvent (e.g. ethanol) volume in trifluoromethanesulfonic acid layer after trimerization of aromatic nitriles. The CTF-1-NR are intercalated with Graphene oxide (GO) membranes to extend 1H NMR transverse relaxation time (T2) and enlarge the confined interspacing (∼8.8 Å), providing ultrafast water transport (∼60 L m-2h−1 bar−1) and high dye molecules rejection (98%). More significantly, the bridging CTF-1-NR enhances charge-carrier separation and gains superior solar-cleaning recoverable permeability (∼7 folds higher than GO). This study provides novel insight into the synthesis of crystalline COF nanoribbons and membrane separation.
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