Blooming of Block Copolymer Micelles into Complex Nanostructures on a Surface

被引:10
|
作者
Zhu, Hongyan [1 ,2 ]
Wang, Xinyan [5 ]
Cui, Yan [3 ]
Cai, Jiandong [2 ,5 ]
Tian, Feng [1 ,4 ]
Wang, Jie [1 ,4 ]
Qiu, Huibin [3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[4] Chinese Acad Sci, Shanghai Adv Res Inst, Zhangjiang Lab, Shanghai 201204, Peoples R China
[5] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
基金
中国国家自然科学基金;
关键词
PATTERNS;
D O I
10.1021/acs.macromol.9b00197
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Self-assembled block copolymer (BCP) nano-structures are of important utility across a wide field. Here, we report a solution-surface sequential self-assembly approach to tailor amphiphilic BCPs in solution and subsequently on a substrate into complex nanostructures. Spherical micelles that formed in solution transform on a substrate sequentially into toroidal micelles, concentric toroidal micelles, and ring clusters upon alternating annealing in solvents that selectively swell the core but poor for the corona. This process is found in both diblock and triblock copolymer systems and appears to be independent of the nature of substrate and gravity. Thus, BCPs micelles with simple shapes can be further manipulated on a surface in a flexible fashion to constructed novel nanostructures.
引用
收藏
页码:3479 / 3485
页数:7
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