Selective Self-Assembly of Surface-Functionalized Fullerenes in PS-PEO on Different Substrates

被引:7
|
作者
Wang, Jing
Chen, Guang-Xin [1 ]
Sun, Jianli
Li, Qifang
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2011年 / 115卷 / 12期
关键词
BLOCK-COPOLYMERS; DIBLOCK COPOLYMER; OPTICAL-PROPERTIES; THIN-FILMS; STYRENE; HOMOPOLYMER; ALIGNMENT; POLYMERS; BEHAVIOR; ORDER;
D O I
10.1021/jp111115x
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
Polystyrene-functionalized C60 (C60-PS) was synthesized by atom-transfer radical polymerization. The structure of the hybrid was characterized by gel permeation chromatography and thermal gravimetric analysis. The self-assembly of polystyrene-block-poly(ethylene oxide) (PS-PEO)/C60-PS film in annealing solvents was studied on a silicon wafer and at the air/water interface by transmission electron microscopy. The method is an easy route to produce arrays of ordered nanostructures. The addition of C60-PS has a great effect on the self-assembly of PS-PEO. Treating the film under solvent vapor can Modulate the orientation and ordering of PS-PEO microdomains. The C60-PS enhanced the formation of lamellae microstructure, and the C60-PS entered the PS phase, expanding the scale of PS domains. Nevertheless, it becomes more complex when it refers to the self-assembly at the air/water interface under solvent vapor for a long time. The selectivity of solvent to the polymer chains plays an important role as the annealing time increases.
引用
收藏
页码:2824 / 2830
页数:7
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