Understanding the ordering mechanisms of self-assembled nanostructures of block copolymers during zone annealing

被引:25
作者
Cong, Zhinan [1 ]
Zhang, Liangshun [1 ]
Wang, Liquan [1 ]
Lin, Jiaping [1 ]
机构
[1] E China Univ Sci & Technol, Shanghai Key Lab Adv Polymer Mat, State Key Lab Bioreactor Engn, Key Lab Ultrafine Mat,Minist Educ,Sch Mat Sci & E, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
MOVING TEMPERATURE-GRADIENT; THIN-FILMS; CYLINDRICAL DOMAINS; DIBLOCK COPOLYMER; MICROPHASE SEPARATION; MESOSCOPIC DYNAMICS; DISORDER TRANSITION; PHASE-SEPARATION; POLYMER BLENDS; MEAN-FIELD;
D O I
10.1063/1.4943864
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
A theoretical method based on dynamic version of self-consistent field theory is extended to investigate directed self-assembly behaviors of block copolymers subjected to zone annealing. The ordering mechanisms and orientation modulation of microphase-separated nanostructures of block copolymers are discussed in terms of sweep velocity, wall preference, and Flory-Huggins interaction parameter. The simulated results demonstrate that the long-range ordered nanopatterns are achieved by lowering the sweep velocity of zone annealing due to the incorporation of templated ordering of block copolymers. The surface enrichment by one of the two polymer species induces the orientation modulation of defect-free nanostructures through finely tuning the composition of block copolymers and the preference of walls. Additionally, the Flory-Huggins interaction parameters of block copolymers in the distinct regions are main factors to design the zone annealing process for creating the highly ordered nanostructures with single orientation. (C) 2016 AIP Publishing LLC.
引用
收藏
页数:11
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