Lewis-Acid-Catalyzed Interfacial Polymerization of Covalent Organic Framework Films

被引:426
作者
Matsumoto, Michio [1 ]
Valentino, Lauren [2 ]
Stiehl, Gregory M. [3 ]
Balch, Halleh B. [4 ]
Corcos, Amanda R. [1 ]
Wang, Feng [4 ]
Ralph, Daniel C. [3 ]
Marinas, Benito J. [2 ]
Dichtel, William R. [1 ]
机构
[1] Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA
[2] Univ Illinois, Dept Civil & Environm Engn, Safe Global Water Inst, Urbana, IL 61801 USA
[3] Cornell Univ, Dept Phys, Ithaca, NY 14853 USA
[4] Univ Calif Berkeley, Dept Phys, Berkeley, CA 94720 USA
来源
CHEM | 2018年 / 4卷 / 02期
基金
美国国家科学基金会;
关键词
CHANNEL-WALL FUNCTIONALIZATION; THIN-FILMS; ENERGY-STORAGE; NANOFILTRATION MEMBRANES; PROTON CONDUCTION; REVERSE-OSMOSIS; ACTIVE LAYERS; GAS-STORAGE; SEPARATION; POLYMERS;
D O I
10.1016/j.chempr.2017.12.011
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Covalent organic frameworks (COFs) are crystalline polymers with covalent bonds in two or three dimensions, providing pores 1-5 nm in diameter. COFs are typically isolated as microcrystalline powders, which are unsuitable for many applications that would leverage their tunable structures, such as opto-electronic devices and nanofiltration membranes. Here, we report the interfacial polymerization of polyfunctional amine and aldehyde monomers with a Lewis acid catalyst, Sc(OTf)(3). Immiscible solutions segregate the catalyst from the monomers, confining polymerization to the solution interface. This method provides large-area, continuous COF films (several cm(2)) with a thickness tuned from 100 mu m to 2.5 nm. Relatively thick films were crystalline, whereas the films that are a few nanometers thick were presumably amorphous. The COF films were transferred onto polyethersulfone supports, and the resulting membranes showed enhanced rejection of Rhodamine WT, a model water contaminant. The large area, tunable pore size, and tailored molecular composition show promise for nanofiltration applications.
引用
收藏
页码:308 / 317
页数:10
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