A surface interaction model for self-assembly of block copolymers under soft confinement

被引:5
|
作者
Song, Jun-Qing [1 ]
Liu, Yi-Xin [1 ]
Zhang, Hong-Dong [1 ]
机构
[1] Fudan Univ, Dept Macromol Sci, State Key Lab Mol Engn Polymers, Shanghai, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2016年 / 145卷 / 21期
基金
中国国家自然科学基金;
关键词
PATTERNED POLYMER BRUSHES; MONTE-CARLO SIMULATIONS; THIN-FILMS; DIBLOCK COPOLYMER; DENSITY MULTIPLICATION; CHEMICAL-PATTERNS; FIELD THEORY; ORIENTATION; GRAPHOEPITAXY; MICRODOMAINS;
D O I
10.1063/1.4968599
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
The surface interaction between substrates and block copolymers is one of the most important factors that control the alignment of self-assembled domains under thin film confinement. Most previous studies simply modeled substrates modified by grafting polymers as a hard wall with a specified surface energy, leading to an incomplete understanding of the role of grafted polymers. In this study, we propose a general model of surface interactions where the role of grafted polymers is decomposed into two independent contributions: the surface preference and the surface softness. Based on this model, we perform a numerical analysis of the stability competition between perpendicular and parallel lamellae of symmetric diblock copolymers on substrates modified by homopolymers using self-consistent field theory. The effects of the surface preference and the surface softness on the alignment of lamellar domains are carefully examined. A phase diagram of the alignment in the plane of the surface preference parameter and the surface softness parameter is constructed, which reveals a considerable parameter window for preparing stable perpendicular lamellae even on highly preferential substrates. Published by AIP Publishing.
引用
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页数:8
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