Highly Selective Vertically Aligned Nanopores in Sustainably Derived Polymer Membranes by Molecular Templating

被引:90
作者
Feng, Xunda [1 ]
Kawabata, Kohsuke [1 ]
Kaufman, Gilad [1 ]
Elimelech, Menachem [1 ]
Osuji, Chinedum O. [1 ]
机构
[1] Yale Univ, Dept Chem & Environm Engn, New Haven, CT 06511 USA
基金
美国国家科学基金会;
关键词
polymer membranes; vertically aligned nanopores; directed self-assembly; liquid crystals; sustainable polymers; LIQUID-CRYSTAL ASSEMBLIES; 1 NM PORES; THERMOPLASTIC ELASTOMERS; BLOCK-COPOLYMER; RENEWABLE RESOURCES; IONIC-CONDUCTIVITY; NEXT-GENERATION; METHYLENE-BLUE; ALIGNMENT; FILMS;
D O I
10.1021/acsnano.7b00304
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe a combination of molecular templating and directed self-assembly to realize highly selective vertically aligned nanopores in polymer membranes using sustainably derived materials. The approach exploits a structure-directing molecule to template the assembly of plant-derived fatty acids into highly ordered columnar mesophases. Directed self-assembly using physical confinement and magnetic fields provides vertical alignment of the columnar nanostructures in large area (several cm(2)) thin films. Chemically cross-linking the mesophase with added conventional vinyl comonomers and removing the molecular template results in a mechanically robust polymer film with vertically aligned 1.2-1.5 nm diameter nanopores with a large specific surface area of similar to 670 m(2)/g. The nanoporous polymer films display exceptional size and charge selectivity as demonstrated by adsorption experiments using model penetrant molecules. These materials have significant potential to function as high-performance nanofiltration membranes and as nanoporous thin films for high-density lithographic pattern transfer. The scalability of the fabrication process suggests that practical applications can be reasonably anticipated.
引用
收藏
页码:3911 / 3921
页数:11
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