Phase behaviors of diblock copolymer-nanoparticle films under nanopore confinement

被引:13
|
作者
Yang, Qinghua [1 ]
Li, Ming [1 ]
Tong, Chaohui [1 ]
Zhu, Yuejin [1 ]
机构
[1] Ningbo Univ, Dept Phys, Ningbo 315211, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2009年 / 130卷 / 09期
基金
中国国家自然科学基金;
关键词
density functional theory; entropy; filled polymers; nanocomposites; nanoparticles; polymer blends; SCF calculations; solid-state phase transformations; thin films; BLOCK-COPOLYMER; CYLINDRICAL CONFINEMENT; GOLD NANOPARTICLES; THIN-FILMS; MORPHOLOGIES; SURFACTANTS; COMPOSITES; MIXTURES; NANORODS; STATE;
D O I
10.1063/1.3055601
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 employ self-consistent-field and density-functional theories to simulate the phase behaviors of diblock copolymer-nanoparticle mixtures confined in a two-dimensional circular pore. By varying the block ratio, the size of the pore, and the particle concentration, rich phase structures are discovered. It is shown that the structural frustration, the loss of conformational entropy of the polymer chains under confinement, the curvature of the pore, and the steric packing effect of the particles play important roles in determining the morphologies of the nanocomposites under circular confinement. It is found that the increase in the particle concentration can promote the transformation of concentric lamellas to the cylindrical domains. Our results suggest effective ways to stabilize the phase orderings of diblock copolymer-nanoparticle mixtures under two-dimensional circular confinement.
引用
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页数:7
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