Complex Macrophase-Separated Nanostructure Induced by Microphase Separation in Binary Blends of Lamellar Diblock Copolymer Thin Films

被引:7
|
作者
Zhang, Jianqi [1 ]
Posselt, Dorthe [2 ]
Smilgies, Detlef-M [3 ]
Perlich, Jan [4 ]
Kyriakos, Konstantinos [1 ]
Jaksch, Sebastian [1 ]
Papadakis, Christine M. [1 ]
机构
[1] Tech Univ Munich, Dept Phys, D-85748 Garching, Germany
[2] Roskilde Univ, Dept Sci Syst & Models, IMFUFA, DK-4000 Roskilde, Denmark
[3] Cornell Univ, Wilson Lab, CHESS, Ithaca, NY 14853 USA
[4] DESY, D-22607 Hamburg, Germany
关键词
AFM; block copolymers; GISAXS; phase separation; solvent vapor annealing; SMALL-ANGLE SCATTERING; X-RAY-SCATTERING; BLOCK-COPOLYMERS; PHASE-BEHAVIOR; HOMOPOLYMER BLENDS; ORDERED STRUCTURE; PARAMETER SPACE; VAPOR; POLY(STYRENE-B-BUTADIENE); DEPENDENCE;
D O I
10.1002/marc.201400238
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The nanostructures of thin films spin-coated from binary blends of compositionally symmetric polystyrene-b-polybutadiene (PS-b-PB) diblock copolymer having different molar masses are investigated by means of atomic force microscopy (AFM) and grazing-incidence small-angle X-ray scattering (GISAXS) after spin-coating and after subsequent solvent vapor annealing (SVA). In thin films of the pure diblock copolymers having high or low molar mass, the lamellae are perpendicular or parallel to the substrate, respectively. The as-prepared binary blend thin films feature mainly perpendicular lamellae in a one-phase state, indicating that the higher molar mass diblock copolymer dominates the lamellar orientation. The lamellar thickness decreases linearly with increasing volume fraction of the low molar mass diblock copolymer. After SVA, well-defined macrophase-separated nanostructures appear, which feature parallel lamellae near the film surface and perpendicular ones in the bulk.
引用
收藏
页码:1622 / 1629
页数:8
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  • [1] Hierarchical Structures in Thin Films of Macrophase- and Microphase-Separated AB/AC Diblock Copolymer Blends
    Shi, Ling-Ying
    Zhou, Yu
    Shen, Zhihao
    Fan, Xing-He
    [J]. MACROMOLECULES, 2012, 45 (13) : 5530 - 5537
  • [2] Macrophase Separation of Blends of Diblock Copolymers in Thin Films
    Williamson, Lance D.
    Nealey, Paul F.
    [J]. MACROMOLECULES, 2015, 48 (12) : 3997 - 4003
  • [3] Hydrogen bonding induced microphase and macrophase separations in binary block copolymer blends
    Lai, Yu -Chen
    Lo, Chieh-Tsung
    [J]. POLYMER, 2022, 262
  • [4] Microphase separation induced by differential interactions in diblock copolymer/homopolymer blends
    Zhou, Jiajia
    Shi, An-Chang
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2009, 130 (23):
  • [5] Phase coherence and microphase separation transitions in diblock copolymer thin films
    Mansky, P
    Tsui, OKC
    Russell, TP
    Gallot, Y
    [J]. MACROMOLECULES, 1999, 32 (15) : 4832 - 4837
  • [6] Protonation-Induced Microphase Separation in Thin Films of a Polyelectrolyte-Hydrophilic Diblock Copolymer
    Stewart-Sloan, Charlotte R.
    Olsen, Bradley D.
    [J]. ACS MACRO LETTERS, 2014, 3 (05) : 410 - 414
  • [7] Solvent-induced microphase separation in diblock copolymer thin films with reversibly switchable morphology
    Peng, J
    Xuan, Y
    Wang, HF
    Yang, YM
    Li, BY
    Han, YC
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (23): : 11163 - 11170
  • [8] Hole nucleation and growth induced by crystallization and microphase separation of thin semicrystalline diblock copolymer films
    Fu, J
    Cong, Y
    Li, J
    Luan, B
    Pan, CY
    Yang, YM
    Li, BY
    Han, YC
    [J]. MACROMOLECULES, 2004, 37 (18) : 6918 - 6925
  • [9] MICROPHASE SEPARATION IN THIN-FILMS OF THE SYMMETRICAL DIBLOCK-COPOLYMER MELT
    KIKUCHI, M
    BINDER, K
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1994, 101 (04): : 3367 - 3377
  • [10] Electric-field-induced lamellar to hexagonally perforated lamellar transition in diblock copolymer thin films: kinetic pathways
    Mukherjee, Arnab
    Ankit, Kumar
    Reiter, Andreas
    Selzer, Michael
    Nestler, Britta
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2016, 18 (36) : 25609 - 25620