Freezing transition of the directed polymer in a random medium : location of the critical temperature and unusual critical properties
arXiv:cond-mat/0603041 · doi:10.1103/PhysRevE.74.011101
Abstract
In dimension , the directed polymer in a random medium undergoes a phase transition between a free phase and a disorder dominated phase. For the latter, Fisher and Huse have proposed a droplet theory based on the scaling of the free energy fluctuations . On the other hand, in related growth models belonging to the KPZ universality class, Forrest and Tang have found that the height-height correlation function is logarithmic at the transition. For the directed polymer model at criticality, this translates into logarithmic free energy fluctuations with . In this paper, we propose a droplet scaling analysis exactly at criticality based on this logarithmic scaling. Our main conclusion is that the typical correlation length of the low temperature phase, diverges as . Furthermore, the logarithmic dependence of leads to the conclusion that the critical temperature actually coincides with the explicit upper bound derived by Derrida and coworkers, where corresponds to the temperature below which the ratio diverges exponentially in . Finally, since the Fisher-Huse droplet theory was initially introduced for the spin-glass phase, we briefly mention the similarities and differences with the directed polymer model. If one speculates that the free energy of droplet excitations for spin-glasses is also logarithmic at , one obtains a logarithmic decay for the mean square correlation function at criticality .
final version, 16 pages, Appendix added
References in corpus (2)
Cited by in corpus (4)
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