Adjustment of block copolymer nanodomain sizes at lattice defect sites

被引:53
作者
Hammond, MR
Sides, SW
Fredrickson, GH
Kramer, EJ [1 ]
Ruokolainen, J
Hahn, SF
机构
[1] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[3] Aalto Univ, Helsinki, Finland
[4] Dow Chem Co USA, Corp R&D, Midland, MI 48674 USA
关键词
D O I
10.1021/ma026001o
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Lattice defects in two-dimensional hexagonal arrays primarily take the form of dislocations, point defects that lie at the mutual terminus of two incomplete rows of material. The dislocation core is composed of one 5-fold and one 7-fold coordinated domain within the otherwise hexagonally coordinated lattice. Using scanning force microscopy to view the nanodomains of a 2D hexagonal array of vertically oriented poly(cyclohexylethylene)-poly(ethylene)-poly(cyclohexylethylene) (CEC) cylindrical triblock copolymers, we show that the domains which compose dislocation cores adjust their sizes (5-fold coordinated cylinders contract and 7-fold coordinated cylinders expand) in response to the stress field associated with the defect. Similar analysis was performed on a two-dimensional self-consistent mean-field theoretical simulation of a similar triblock copolymer system, yielding good agreement with experimental results.
引用
收藏
页码:8712 / 8716
页数:5
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