期刊
CHEM
卷 4, 期 2, 页码 308-317出版社
CELL PRESS
DOI: 10.1016/j.chempr.2017.12.011
关键词
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资金
- United States Army Research Office [W911NF-15-1-0447]
- Camille and Henry Dreyfus Foundation through a Camille Dreyfus Teacher-Scholar Award
- National Science Foundation (NSF) Materials Research Science and Engineering Center program [DMR-1719875]
- NSF
- NIH National Institute of General Medical Sciences [DMR-1332208]
- NSF [CBET-1706219]
- Department of Energy Office of Science User Facility [DE-AC02-05CH11231]
- Basic Energy Sciences program of the US Department of Energy Office of Science [DE-AC02-05CH11231]
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.
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