Self-assembly of grafted Y-shaped ABC triblock copolymers in solutions

被引:19
|
作者
Yin, Yuhua [1 ]
Jiang, Run [1 ]
Li, Baohui [1 ]
Jin, Qinghua [1 ]
Ding, Datong [1 ]
Shi, An-Chang [2 ]
机构
[1] Nankai Univ, Coll Phys, Key Lab Funct Polymer Mat, Minist Educ, Tianjin 300071, Peoples R China
[2] McMaster Univ, Dept Phys & Astron, Hamilton, ON L8S 4M1, Canada
来源
JOURNAL OF CHEMICAL PHYSICS | 2008年 / 129卷 / 15期
基金
加拿大自然科学与工程研究理事会; 中国国家自然科学基金;
关键词
D O I
10.1063/1.2992079
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
Self-assembled morphologies of grafted Y-shaped ABC triblock copolymers are investigated using a simulated annealing method. The block copolymers are composed of two incompatible arms (A and B) and a short stem (C), with the C-stems grafted onto a flat surface. A rich array of novel morphologies is discovered. The formation of these morphologies is controlled by polymer grafting density, the incompatibility between the A-B-blocks, as well as the quality and selectivity of the solvents. In particular, it is observed that solvent selectivity drives lateral and/or perpendicular microphase separation. A phase diagram for systems with low grafting density is constructed. It is predicted that multiple morphological transitions, such as these from mixed or core-shell micelles to internally segregated micelles, to hamburger-like micelles, to segmented wormlike micelles, to connected micelles, and to split micelles, can be induced by varying either the incompatibility between the two arms or the quality of the solvents. These results are consistent with previous experiments and theories. (c) 2008 American Institute of Physics. [DOI: 10.1063/1.2992079]
引用
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页数:11
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