共 71 条
Soft Confinement-Induced Morphologies of Diblock Copolymers
被引:111
作者:
Chi, Peng
[1
,2
]
Wang, Zheng
[1
,2
]
Li, Baohui
[1
,2
]
Shi, An-Chang
[3
]
机构:
[1] Nankai Univ, Sch Phys, Minist Educ, Tianjin 300071, Peoples R China
[2] Nankai Univ, Key Lab Funct Polymer Mat, Minist Educ, Tianjin 300071, Peoples R China
[3] McMaster Univ, Dept Phys & Astron, Hamilton, ON L8S 4M1, Canada
来源:
基金:
中国国家自然科学基金;
加拿大自然科学与工程研究理事会;
关键词:
DISSIPATIVE PARTICLE DYNAMICS;
MONTE-CARLO SIMULATIONS;
2 HOMOGENEOUS SURFACES;
BLOCK-COPOLYMERS;
MICROPHASE SEPARATION;
THIN-FILMS;
CYLINDRICAL CONFINEMENT;
METHACRYLATE) PARTICLES;
NANOPARTICLES;
TRANSITIONS;
D O I:
10.1021/la202448c
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The self-assembly of diblock copolymers under soft confinement is studied systematically using a simulated annealing method applied to a lattice model of polymers. The soft confinement is realized by the formation of polymer droplets in a poor solvent environment. Multiple sequences of soft confinement-induced copolymer aggregates with different shapes and self-assembled internal morphologies are predicted as functions of solvent-polymer interaction and the monomer concentration. It is discovered that the self-assembled internal morphology of the aggregates is largely controlled by a competition between the bulk morphology of the copolymer and the solvent-polymer interaction, and the shape of the aggregates can be non-spherical when the internal morphology is anisotropic and the solvent-polymer interaction is weak. These results demonstrate that droplets of diblock copolymers formed in poor solvents can be used as a model system to study the self-assembly of copolymers under soft confinement.
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页码:11683 / 11689
页数:7
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