A copolymer near a selective interface: variational characterization of the free energy
E. Bolthausen, F. den Hollander, A.A. Opoku

TL;DR
This paper models a two-dimensional copolymer near an interface, deriving a variational formula for its quenched free energy and analyzing phase transitions between localized and delocalized states.
Contribution
It provides a variational characterization of the quenched free energy for copolymers near an interface, extending the analysis to general disorder distributions and paths.
Findings
Derived a variational expression for the quenched free energy.
Compared quenched and annealed free energies and phase transition curves.
Showed the quenched free energy is strictly less than the annealed free energy in the localized phase.
Abstract
In this paper we consider a two-dimensional copolymer consisting of a random concatenation of hydrophobic and hydrophilic monomers near a linear interface separating oil and water acting as solvents. The configurations of the copolymer are directed paths that can move above and below the interface. The interaction Hamiltonian, which rewards matches and penalizes mismatches of the monomers and the solvents, depends on two parameters: the interaction strength and the interaction bias . The quenched excess free energy per monomer has a phase transition along a quenched critical curve separating a localized phase, where the copolymer stays close to the interface, from a delocalized phase, where the copolymer wanders away from the interface. We derive a variational expression for…
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Taxonomy
TopicsStochastic processes and statistical mechanics · Theoretical and Computational Physics · Diffusion and Search Dynamics
