Block copolymer microstructures in the intermediate-segregation regime

被引:431
作者
Matsen, MW [1 ]
Bates, FS [1 ]
机构
[1] UNIV MINNESOTA, DEPT CHEM ENGN & MAT SCI, MINNEAPOLIS, MN 55455 USA
关键词
D O I
10.1063/1.473153
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
A detailed examination of the intermediate-segregation regime of diblock copolymer melts is presented using the incompressible Gaussian chain model and self-consistent field theory (SCFT). We find that the competition between interfacial tension and chain stretching used to describe behavior in the strong-segregation regime also explains behavior in this regime. Phase transitions from lamellae (L) to cylinders (C) to spheres (S) occur due to the spontaneous curvature produced as the asymmetry in the diblock composition increases. Complex phases, gyroid (G), perforated lamellar (PL), and double diamond (D), have curvatures between those of L and C, and therefore they compete for stability along the L/C boundary. Nevertheless, only C exhibits a region of stability. To explain why, we recognize that interfacial tension prefers the formation of constant mean curvature (CMC) surfaces to reduce interfacial area, and chain stretching favors domains of uniform thickness so as to avoid packing frustration. While the classical structures, L, C, and S, are successful at doing both simultaneously, the complex phases are not. Of the complex phases, C is the least frustrated and consequently is stable at intermediate decrees of segregation. However, G becomes unstable in the strong-segregation regime because;he relative penalty for packing frustration increases with segregation. The PL and D structures are simply too frustrated, and therefore are never stable. (C) 1997 American Institute of Physics.
引用
收藏
页码:2436 / 2448
页数:13
相关论文
共 44 条
[1]   MICRODOMAIN MORPHOLOGY OF STAR COPOLYMERS IN THE STRONG-SEGREGATION LIMIT [J].
ANDERSON, DM ;
THOMAS, EL .
MACROMOLECULES, 1988, 21 (11) :3221-3230
[2]  
Anderson DM., 1990, ADV CHEM PHYS, V77, P337
[3]   POLYMERS GRAFTED TO A CONVEX SURFACE [J].
BALL, RC ;
MARKO, JF ;
MILNER, ST ;
WITTEN, TA .
MACROMOLECULES, 1991, 24 (03) :693-703
[4]   FLUCTUATIONS, CONFORMATIONAL ASYMMETRY AND BLOCK-COPOLYMER PHASE-BEHAVIOR [J].
BATES, FS ;
SCHULZ, MF ;
KHANDPUR, AK ;
FORSTER, S ;
ROSEDALE, JH ;
ALMDAL, K ;
MORTENSEN, K .
FARADAY DISCUSSIONS, 1994, 98 :7-18
[5]   BLOCK COPOLYMER THERMODYNAMICS - THEORY AND EXPERIMENT [J].
BATES, FS ;
FREDRICKSON, GH .
ANNUAL REVIEW OF PHYSICAL CHEMISTRY, 1990, 41 (01) :525-557
[6]   FLUCTUATION EFFECTS IN THE THEORY OF MICROPHASE SEPARATION IN BLOCK COPOLYMERS [J].
FREDRICKSON, GH ;
HELFAND, E .
JOURNAL OF CHEMICAL PHYSICS, 1987, 87 (01) :697-705
[7]   STABILITY OF A CATENOID-LAMELLAR PHASE FOR STRONGLY STRETCHED BLOCK COPOLYMERS [J].
FREDRICKSON, GH .
MACROMOLECULES, 1991, 24 (11) :3456-3458
[8]  
GROSSEBRAUCKMAN.K, 1995, FAMILY CONSTANT MEAN
[9]   STABILITY OF LYOTROPIC PHASES WITH CURVED INTERFACES [J].
GRUNER, SM .
JOURNAL OF PHYSICAL CHEMISTRY, 1989, 93 (22) :7562-7570
[10]   THE GYROID - A NEW EQUILIBRIUM MORPHOLOGY IN WEAKLY SEGREGATED DIBLOCK COPOLYMERS [J].
HAJDUK, DA ;
HARPER, PE ;
GRUNER, SM ;
HONEKER, CC ;
KIM, G ;
THOMAS, EL ;
FETTERS, LJ .
MACROMOLECULES, 1994, 27 (15) :4063-4075