Superlattices of Squishable, Self-Assembled Spheres: How does Lattice Cell Geometry Shape Thermodynamics?
ORAL
Abstract
Self-assembly of soft-molecules into spherical domains adopting Frank Kasper lattices have been observed in a variety of systems, including liquid-crystalline dendrimers, charged surfactants and block copolymers (BCPs). The formation of these complex phases has been previously attributed to optimal surface area and/or volume asymmetry (polydispersity or Voronoi partition of cells) leading to the question: What selects volume asymmetry in these assemblies and how does this impact surface area of the partitions? We will address these in the context of BCPs by drawing comparisons between Diblock Foam Model (DFM) that captures the Polyhedral Interface Limit (PIL) and SCFT for diblock melts. DFM describes thermodynamics of sphere phases in terms of competing geometric quantities: surface area and dimensionless stretching (or radius of gyration) of cellular volumes enclosing domains. DFM correctly predicts not only which of these lattices is favored in equilibrium (the sigma phase) but also their relative ranking in terms of entropy and enthalpy, and their equilibrium volume distribution among spheres. Comparison to SCFT results show that increasing conformational asymmetry between blocks drives a transition to radial-chain stretching and towards the PIL described by DFM calculations.
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Presenters
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Abhiram Reddy
- Polymer Science and Engineering, University of Massachusetts