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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.
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页数:8
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