Finite-temperature and finite-time scaling of the directed polymer free energy with respect to its geometrical fluctuations

Elisabeth Agoritsas, Sebastian Bustingorry, Vivien Lecomte, Grégory Schehr, and Thierry Giamarchi
Phys. Rev. E 86, 031144 – Published 27 September 2012

Abstract

We study the fluctuations of the directed polymer in 1+1 dimensions in a Gaussian random environment with a finite correlation length ξ and at finite temperature. We address the correspondence between the geometrical transverse fluctuations of the directed polymer, described by its roughness, and the fluctuations of its free energy, characterized by its two-point correlator. Analytical arguments are provided in favor of a generic scaling law between those quantities, at finite time, nonvanishing ξ, and explicit temperature dependence. Numerical results are in good agreement both for simulations on the discrete directed polymer and on a continuous directed polymer (with short-range correlated disorder). Applications to recent experiments on liquid crystals are discussed.

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  • Received 28 June 2012

DOI:https://doi.org/10.1103/PhysRevE.86.031144

©2012 American Physical Society

Authors & Affiliations

Elisabeth Agoritsas1, Sebastian Bustingorry2, Vivien Lecomte3, Grégory Schehr4, and Thierry Giamarchi1

  • 1DPMC-MaNEP, Université de Genève, 24 quai Ernest Ansermet, 1211 Genève, Switzerland
  • 2CONICET, Centro Atómico Bariloche, 8400 San Carlos de Bariloche, Río Negro, Argentina
  • 3Laboratoire de Probabilités et Modèles Aléatoires (CNRS UMR 7599), Universités Paris VI & Paris VII, site Chevaleret, 175 rue du Chevaleret, 75013 Paris, France
  • 4Laboratoire de Physique Théorique et Modèles Statistiques (UMR du CNRS 8626), Université Paris Sud, 91405 Orsay Cedex, France

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Issue

Vol. 86, Iss. 3 — September 2012

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