Self-assembled liquid-crystalline gels designed from the bottom up

被引:70
|
作者
Kempe, MD
Scruggs, NR
Verduzco, R
Lal, J
Kornfield, JA
机构
[1] CALTECH, Pasadena, CA 91125 USA
[2] Argonne Natl Lab, Argonne, IL 60439 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/nmat1074
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Liquid crystals are often combined with polymers to influence the liquid crystals' orientation and mechanical properties, but at the expense of reorientation speed or uniformity of alignment. We introduce a new method to create self-assembled nematic liquid-crystal gels using an ABA triblock copolymer with a side-group liquid-crystalline midblock and liquid-crystal-phobic endblocks. In contrast to in situ polymerized networks, these physical gels are homogeneous systems with a solubilized polymer network giving them exceptional optical uniformity and well-defined crosslink density. Furthermore, the unusually high-molecular-weight polymers used allow gels to form at lower concentrations than previously accessible. This enables these gels to be aligned by surface anchoring, shear, or magnetic fields. The high content of small-molecule liquid crystal (greater than or equal to95%) allows access to a regime of fast reorientation dynamics.
引用
收藏
页码:177 / 182
页数:6
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