Symmetry breaking in particle-forming diblock polymer/homopolymer blends

Abstract

Compositionally asymmetric diblock copolymers provide an attractive platform for understanding the emergence of tetragonally close-packed, Frank-Kasper phases in soft matter. Block-polymer phase behavior is governed by a straightforward competition between chain stretching and interfacial tension under the constraint of filling space at uniform density. Experiments have revealed that diblock copolymers with insufficient conformational asymmetry to form Frank-Kasper phases in the neat-melt state undergo an interconversion from body-centered cubic (bcc) close-packed micelles to a succession of Frank-Kasper phases (σ to C14 to C15) upon the addition of minority-block homopolymer in the dry-brush regime, accompanied by the expected transition from bcc to hexagonally packed cylinders in the wet-brush regime. Self-consistent field theory data presented here qualitatively reproduce the salient features of the experimental phase behavior. A particle-by-particle analysis of homopolymer partitioning furnishes a basis for understanding the symmetry breaking from the high-symmetry bcc phase to the lower-symmetry Frank-Kasper phases, wherein the reconfiguration of the system into polyhedra of increasing volume asymmetry delays the onset of macroscopic phase separation.