Not even metastable: Cubic double-diamond in diblock copolymer melts
Micheal S. Dimitriyev, Benjamin R. Greenvall, Rejoy Matthew, Gregory M. Grason

TL;DR
This study investigates the thermodynamic stability of cubic network phases in diblock copolymer melts, revealing that the double-diamond phase is inherently unstable and can be stabilized only through specific modifications.
Contribution
The paper introduces a strong-segregation model and self-consistent field studies to analyze the stability of double-diamond and gyroid phases, highlighting the conditions that favor metastability.
Findings
Double-diamond is an unstable saddle point in symmetric diblock melts.
Homopolymer blending and elastic asymmetry can stabilize double-diamond.
Entropic free energy costs of chain packing determine phase stability.
Abstract
We study the thermodynamics of continuous transformations between two canonical, cubic network phases of block copolymer melts: double-gyroid, an equilibrium morphology for many systems; and double-diamond, often thought to be a close competitor. We use a strong-segregation approach to compute the free energy of double network morphologies as a function of two structural parameters that convert between two limiting cubic cases; a tetragonal stretch of the unit cell in combination with fusion of pairs of trihedal gyroid nodes into tetrahedral diamond nodes. For the simplest case of conformationally symmetric diblock melts, we find that cubic double-diamond sits at an unstable saddle point that is continuously deformable into the lower free energy gyroid, as well as a second metastable, tetragonal network composed by trihedral nodes. We confirm the broad instability of double-diamond at…
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Taxonomy
TopicsBlock Copolymer Self-Assembly · Material Dynamics and Properties · Advanced Physical and Chemical Molecular Interactions
