Gyroid versus double-diamond in ABC triblock copolymer melts

被引:190
|
作者
Matsen, MW [1 ]
机构
[1] Univ Reading, Ctr Polymer Sci, Reading RG6 6AF, Berks, England
来源
JOURNAL OF CHEMICAL PHYSICS | 1998年 / 108卷 / 02期
关键词
D O I
10.1063/1.475439
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
Monodisperse melts of ABC linear triblock copolymer are examined using self-consistent field theory (SCFT). Our study is restricted to symmetric triblocks, where the A and C blocks are equal in size and the A/B and B/C interactions are identical. Furthermore, we focus on the regime where B forms the majority domain. This system has been studied earlier using density functional theory (DFT), strong-segregation theory (SST), and Monte Carlo (MC), and it corresponds closely to a series of isoprene-styrene-vinylpyridine triblocks examined by Mogi and co-workers. In agreement with these previous studies, we find stable lamellar, complex, cylindrical, and spherical phases. In the spherical phase, the minority A and C domains alternate on a body-centered cubic lattice. In order to produce alternating A and C domains in the cylinder phase, the melt chooses a tetragonal packing rather than the usual hexagonal one. This amplifies the packing frustration in the cylinder phase, which results in a large complex phase region. Contrary to the previous evidence that the complex phase is double-diamond, we predict the gyroid morphology. The earlier theoretical results are easily rationalized and the experimental data are, in fact, more consistent with gyroid. (C) 1998 American Institute of Physics.
引用
收藏
页码:785 / 796
页数:12
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