Complex liquid-crystal nanostructures in semiflexible ABC linear triblock copolymers: A self-consistent field theory

被引:7
|
作者
Li, Shiben [1 ]
Jiang, Ying [2 ,3 ]
Chen, Jeff Z. Y. [4 ]
机构
[1] Wenzhou Univ, Dept Phys, Wenzhou 325035, Zhejiang, Peoples R China
[2] Beihang Univ, Sch Chem & Environm, Beijing 100191, Peoples R China
[3] Beihang Univ, Ctr Soft Matter Phys & Its Applicat, Beijing 100191, Peoples R China
[4] Univ Waterloo, Dept Phys & Astron, Waterloo, ON N2L 3G1, Canada
来源
JOURNAL OF CHEMICAL PHYSICS | 2016年 / 145卷 / 18期
基金
中国国家自然科学基金;
关键词
COIL BLOCK-COPOLYMERS; POLYMER SOLAR-CELLS; ROD-COIL; DIBLOCK COPOLYMER; PHASE-DIAGRAM; MORPHOLOGY; MOLECULES; LAMELLAR; DEVICES; ORDER;
D O I
10.1063/1.4967423
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
We show that two series of ABC linear triblock copolymers possess sequences of order-to-order phase transitions between microphase-separated states, as the degree of flexibility of the semiflexible middle B-blocks varies. The spatial and orientational symmetries of these phases, some of them containing liquid-crystal ordering, are analysed in comparison with related structures previously determined experimentally and theoretically. A theoretical framework based on the self-consistent field treatment of the wormlike-chain model, which incorporates the Flory-Huggins and Maier-Saupe interactions in the free energy, is used here as a basic foundation for numerical calculations. We suggest that tuning the flexibility parameter, which reduces to the concept of degree of polymerization in the coil-like limit and characterizes the chain-persistency in the rod-like limit, provides a promising approach that can be used to design the resulting microphase-separated structures in semiflexible copolymer melts. Published by AIP Publishing.
引用
收藏
页数:18
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