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Effect of an Ionic Liquid Solvent on the Phase Behavior of Block Copolymers
被引:54
|作者:
Virgili, Justin M.
[1
,2
]
Hoarfrost, Megan L.
[1
,3
]
Segalman, Rachel A.
[1
,2
]
机构:
[1] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Mat Sci, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Energy & Environm Technol Div, Berkeley, CA 94720 USA
关键词:
BRONSTED ACID-BASE;
THIN-FILM TRANSISTORS;
DIBLOCK COPOLYMERS;
SELECTIVE SOLVENTS;
FUEL-CELLS;
POLYMER;
ELECTROLYTES;
MICELLES;
MEMBRANES;
BLENDS;
D O I:
10.1021/ma902804e
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
The phase behavior of concentrated mixtures of block copolymers with an ionic liquid has been studied using a large series of block copolymers with varying molecular weight and volume traction to gain a thorough understanding of the thermodynamics of self-assembly. The lyotropic phase behavior of mixtures of poly(styrene-block-2-vinylpyridine) (S2VP) copolymers with the ionic liquid imidazolium bis(trifluoromethane)sulfonimide ([Im][TFSI]) is reminiscent of block copolymer/selective molecular solvent mixtures, and ordered microstructures corresponding to lamellae, hexagonally close-packed cylinders, body-centered cubic, and face-centered cubic oriented micelles are observed. Scaling analysis reveals that, in contrast to observations of block copolymer/molecular solvent mixtures, the interfacial area occupied by each S2VP chain decreases upon the addition of [Im][TFSI], indicating a considerable increase in the effective segregation strength of the S2VP copolymer with ionic liquid addition.
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页码:5417 / 5423
页数:7
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