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    Nonaffinity of Liquid Networks and Bicontinuous Mesophases

    Michael S. Dimitriyev1,2,*, Xueyan Feng3, Edwin L. Thomas2, and Gregory M. Grason1,†

    • 1Department of Polymer Science and Engineering, University of Massachusetts, Amherst, Massachusetts 01003, USA
    • 2Department of Materials Science and Engineering, Texas A&M University, College Station, Texas 77843, USA
    • 3Department of Macromolecular Science, State Key Laboratory of Molecular Engineering of Polymers, Fudan University, Shanghai, China 200438

    • *msdim@tamu.edu
    • †grason@umass.edu

    Phys. Rev. Lett. 132, 218201 – Published 23 May, 2024

    DOI: https://doi.org/10.1103/PhysRevLett.132.218201

    Abstract

    Amphiphiles self-assemble into a variety of bicontinuous mesophases whose equilibrium structures take the form of high-symmetry cubic networks. Here, we show that the symmetry-breaking distortions in these systems give rise to anomalously large, nonaffine collective deformations, which we argue to be a generic consequence of “mass equilibration” within deformed networks. We propose and study a minimal “liquid network” model of bicontinuous networks, in which acubic distortions are modeled by the relaxation of residually stressed mechanical networks with constant-tension bonds. We show that nonaffinity is strongly dependent on the valency of the network as well as the degree of strain-softening or strain-stiffening tension in the bonds. Taking diblock copolymer melts as a model system, liquid network theory captures quantitative features of two bicontinuous phases based on comparison with self-consistent field theory predictions and direct experimental characterization of acubic distortions, which are likely to be pronounced in soft amphiphilic systems more generally.

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