Boundary Frustration in Double-Gyroid Thin Films.

Self-consistent field theory for thin films of AB diblock polymers in the double-gyroid phase reveals that in the absence of preferential wetting of monomer species at the film boundaries, films with the (211) plane oriented parallel to the boundaries are more stable than other orientations, consistent with experimental results. This preferred orientation is explained in the context of boundary frustration. Specifically, the angle of intersection between the A/B interface and the film boundary, the wetting angle, is thermodynamically restricted to a narrow range of values. Most termination planes in the double gyroid cannot accommodate this narrow range of wetting angles without significant local distortion relative to the bulk morphology; the (211)-oriented termination plane with the "double-wave" pattern produces relatively minimal distortion, making it the least frustrated boundary. The principle of boundary frustration provides a framework to understand the relative stability of termination planes for complex ordered block polymer phases confined between flat, nonpreferential boundaries.

The C36 Laves phase in diblock polymer melts.

The C14 and C15 Laves phases form as micelle packing structures in many types of soft matter, but the related C36 phase, which consists of alternating C14-type and C15-type layers, has not been observed in any such system. To understand this absence in the context of diblock polymers, we used self-consistent field theory to relate the morphology and energetics of C36 to other known mesophases. Two case studies were conducted: blends of AB diblock polymers with A homopolymers (where A forms the micelle core), in which C14 and C15 have stability windows, and neat AB diblock melts, in which Laves phases are metastable. Laves phases exhibit nearly identical micelle morphologies and nearly degenerate free energies, with the free energy of C36 being a near-perfect bisector of the C14 and C15 free energies in all cases, revealing an intrinsic symmetry in free energy that is attributed solely to the structural relationship between the phases in which the packing of C36 is intermediate between C14 and C15. Based on this connection between structure and free energy, C36 is thus not expected to form in flexible diblock polymers, since C14 and C15 can always form instead via facile mass transfer.