The directed self-assembly of amphiphilic diblock copolymers in selective solvents

被引:2
|
作者
Zhang, Jun [1 ]
Kong, Weixin [1 ]
Duan, Haiming [1 ]
机构
[1] Xinjiang Univ, Coll Phys Sci & Technol, Urumqi 830046, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Aggregate; diblock copolymer; inducer; the directed self-assembly; BLOCK CO-MICELLES; CYLINDRICAL MICELLES; ENABLING NANOTECHNOLOGY; TRIBLOCK COPOLYMERS; NANOPARTICLES; POLYMERS; GOLD; NANOSTRUCTURES; SURFACE; ARCHITECTURES;
D O I
10.1080/01932691.2017.1305907
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 directed self-assembly of diblock copolymers in solvents is studied systematically using a simulated annealing method. Effects of the shape, scale, and adsorption capacity of the induced surface on the morphology of the aggregates are examined. A variety of morphologies are predicted. By increasing the scale of induced surface, the micellar shape transforms from cylinder to sheet with a tail and finally to thin sheet without tail. The shape of induced surface determines the sheet's shape, such as rounded and square. Configurations of hydrophobic blocks and interfacial energies are investigated by calculating the mean square end-to-end distances and the contact numbers between hydrophobic monomer and other species, respectively. [GRAPHICS] .
引用
收藏
页码:326 / 332
页数:7
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