On the localized phase of a copolymer in an emulsion: supercritical percolation regime
Frank den Hollander, Nicolas P\'etr\'elis

TL;DR
This paper analyzes a directed copolymer model in a random emulsion, establishing the nature of phase transitions and the smoothness of free energy in the supercritical percolation regime, extending previous results.
Contribution
It proves the critical curve is strictly increasing, the phase transition is second order, and the free energy is infinitely differentiable within the localized phase.
Findings
Critical curve is strictly increasing.
Phase transition is second order.
Free energy is infinitely differentiable in the localized phase.
Abstract
In this paper we study a two-dimensional directed self-avoiding walk model of a random copolymer in a random emulsion. The copolymer is a random concatenation of monomers of two types, and , each occurring with density 1/2. The emulsion is a random mixture of liquids of two types, and , organised in large square blocks occurring with density and , respectively, where . The copolymer in the emulsion has an energy that is minus times the number of -matches minus times the number of -matches, where without loss of generality the interaction parameters can be taken from the cone . To make the model mathematically tractable, we assume that the copolymer is directed and can only enter and exit a pair of neighbouring blocks at diagonally opposite corners. In \cite{dHW06}, it was…
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