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Updated: Aug 18, 2025

Gyroid Nickel Nanostructures from Diblock Copolymer Supramolecules
Published on: April 28, 2014
Tuning conformational asymmetry in particle-forming diblock copolymer alloys
Logan J Case1, Frank S Bates1, Kevin D Dorfman1
1Department of Chemical Engineering and Materials Science, University of Minnesota-Twin Cities, 421 Washington Ave SE, Minneapolis, Minnesota 55455, USA. dorfman@umn.edu.
Abstract:
Self-consistent field theory is employed to compute the phase behavior of binary blends of conformationally asymmetric, micelle-forming diblock copolymers with miscible corona blocks and immiscible core blocks (a diblock copolymer "alloy"). The calculations focus on establishing conditions that promote the formation of Laves phases by tuning the relative softness of the cores of the two different Laves phase particles via independent control of their conformational asymmetries. Increasing the conformational asymmetry of the more spherical particles of the Laves structure has a stabilizing effect, consistent with the expectations of increased imprinting of the Wigner-Seitz cells on the core/corona interface as conformational asymmetry increases. The resulting phase diagram in the temperature-blend composition space features a more stable Laves phase field than that predicted for conformationally symmetric systems. The phase field closes at low temperatures in favor of macrophase separation between a hexagonally-packed cylinder (hex) phase and a body-centered cubic phase. Companion calculations, using an alloy whose components do not produce a hex phase in the neat melt state, suggest that the Laves phase field in such a blend will persist at strong segregation.
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