Controlling the ordered transition of PS-b-P4VP block copolymer ultrathin films by solvent annealing

被引:3
作者
Wang, Yang [1 ]
Narita, Chieko [2 ]
Xu, Xinhe [1 ]
Honma, Hidekazu [3 ]
Himeda, Yuki [3 ]
Yamada, Kazushi [2 ]
机构
[1] Zhejiang Sci Tech Univ, Coll Mat & Text, Key Lab Adv Text Mat & Mfg Technol, Minist Educ, Hangzhou, Zhejiang, Peoples R China
[2] Kyoto Inst Technol, Fac Fiber Sci & Engn, Sakyo Ku, Matsugasaki, Kyoto 6068585, Japan
[3] KRI Inc, Konohana Ku, Osaka 5540051, Japan
关键词
AFM; Block-copolymer; PS-b-P4VP; Sea-island structure; Network structure; Order-disorder transition; THIN-FILMS; MORPHOLOGY; POLYSTYRENE-BLOCK-POLY(2-VINYLPYRIDINE); NANOPARTICLES; MEMBRANES; ARRAYS; GOLD;
D O I
10.1016/j.matchemphys.2019.122072
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A change in morphology of ultrathin films of polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP) diblock copolymer was induced by annealing under chloroform and toluene vapor and was investigated by atomic force microscopy (AFM). The microphase separation morphology with spherical structures were formed when PS-bP-4VP was dissolved in toluene, which is a selective solvent for polystyrene (PS) segments. After chloroform annealing, a series of surface morphologies of PS-b-P4VP were observed, including spherical and network structures such as gyroid structures. During the continuous annealing treatment for the films with network structures by toluene, a reversible structure conversion from network to sea-island was observed. In addition, we have demonstrated that Au-NPs can be easily adhered to the PS-b-P4VP films with network structure on surface.
引用
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页数:8
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