Dimensional reduction occurs when the critical behavior of one system can be related to that of another system in a lower dimension. We show that this occurs for directed branched polymers (DBP) by giving an exact relationship between DBP models in D+1 dimensions and repulsive gases at negative activity in D dimensions. This implies relations between exponents of the two models: $γ(D+1)=α(D)$ (the exponent describing the singularity of the pressure), and $ν_{\perp}(D+1)=ν(D)$ (the correlation length exponent of the repulsive gas). It also leads to the relation $θ(D+1)=1+σ(D)$, where $σ(D)$ is the Yang-Lee edge exponent. We derive exact expressions for the number of DBP of size N in two dimensions.
In [math-ph/0107005] we have proven that the generating function for self-avoiding branched polymers in D+2 continuum dimensions is proportional to the pressure of the hard-core continuum gas at negative activity in D dimensions. This result explains why the critical behavior of branched polymers should be the same as that of the $i ϕ^3$ (or Yang-Lee edge) field theory in two fewer dimensions (as proposed by Parisi and Sourlas in 1981). - In this article we review and generalize the results of [math-ph/0107005]. We show that the generating functions for several branched polymers are proportion…
This article will review recent results on dimensional reduction for branched polymers, and discuss implications for critical phenomena. Parisi and Sourlas argued in 1981 that branched polymers fall into the universality class of the Yang-Lee edge in two fewer dimensions. Brydges and I have proven in [math-ph/0107005] that the generating function for self-avoiding branched polymers in D+2 continuum dimensions is proportional to the pressure of the hard-core continuum gas at negative activity in D dimensions (which is in the Yang-Lee or $i ϕ^3$ class). I will describe how this equivalence arise…
We establish an exact relation between self-avoiding branched polymers in D+2 continuum dimensions and the hard-core continuum gas at negative activity in D dimensions. We review conjectures and results on critical exponents for D+2 = 2,3,4 and show that they are corollaries of our result. We explain the connection (first proposed by Parisi and Sourlas) between branched polymers in D+2 dimensions and the Yang-Lee edge singularity in D dimensions.
Building on and from the work of Brydges and Imbrie, we give an elementary calculation of the volume of the space of branched polymers of order $n$ in the plane and in 3-space. Our development reveals some more general identities, and allows exact random sampling. In particular we show that a random 3-dimensional branched polymer of order $n$ has diameter of order $\sqrt{n}$.
Melonic graphs constitute the family of graphs arising at leading order in the 1/N expansion of tensor models. They were shown to lead to a continuum phase, reminiscent of branched polymers. We show here that they are in fact precisely branched polymers, that is, they possess Hausdorff dimension 2 and spectral dimension 4/3.
It is shown that a recently conjectured form for the critical scaling function for planar self-avoiding polygons weighted by their perimeter and area also follows from an exact renormalization group flow into the branched polymer problem, combined with the dimensional reduction arguments of Parisi and Sourlas. The result is generalized to higher-order multicritical points, yielding exact values for all their critical exponents and exact forms for the associated scaling functions.
The determinant method in the conformal bootstrap is applied for the critical phenomena of a single polymer in arbitrary $D$ dimensions. The scale dimensions (critical exponents) of the polymer ($2< D \le 4$) and the branched polymer ($3 < D \le 8$) are obtained from the small determinants. It is known that the dimensional reduction of the branched polymer in $D$ dimensions to Yang-Lee edge singularity in $D$-$2$ dimensions holds exactly. We examine this equivalence by the small determinant method.
In this brief technical communication it is demonstrated how using Bethe ansatz technique the explicit expression for the two-point free energy distribution function in (1+1) directed polymers can be derived in rather simple way. Obtained result is equivalent to the one derived earlier by Prolhac and Spohn.
The explicit expression for the the probability distribution function of the endpoint fluctuations of one-dimensional directed polymers in random potential is derived in terms of the Bethe ansatz replica technique by mapping the replicated problem to the N-particle quantum boson system with attractive interactions.
The distribution function of the free energy fluctuations in one-dimensional directed polymers with free boundary conditions is derived by mapping the replicated problem to the N-particle quantum boson system with attractive interactions. It is shown that in the thermodynamic limit this function is described by the universal Tracy-Widom distribution of the Gaussian orthogonal ensemble.
We study the recently introduced Inverse-Beta polymer, an exactly solvable, anisotropic finite temperature model of directed polymer on the square lattice, and obtain its stationary measure. In parallel we introduce an anisotropic zero temperature model of directed polymer on the square lattice, the Bernoulli-Geometric polymer, and obtain its stationary measure. This new exactly solvable model is dual to the Inverse-Beta polymer and interpolates between models of first and last passage percolation on the square lattice. Both stationary measures are shown to satisfy detailed balance. We also ob…
We study the directed polymer with fixed endpoints near an absorbing wall, in the continuum and in presence of disorder, equivalent to the KPZ equation on the half space with droplet initial conditions. From a Bethe Ansatz solution of the equivalent attractive boson model we obtain the exact expression for the free energy distribution at all times. It converges at large time to the Tracy Widom distribution $F_4$ of the Gaussian Symplectic Ensemble (GSE). We compare our results with numerical simulations of the lattice directed polymer, both at zero and high temperature.
We prove a central limit theorem for the winding number of a directed polymer on a cylinder, which is equivalent with proving the Gaussian fluctuations of the endpoint of the directed polymer in a spatial periodic environment.
We study the semi-discrete directed polymer model introduced by O'Connell-Yor in its stationary regime, based on our previous work on the stationary $q$-totally asymmetric simple exclusion process ($q$-TASEP) using a two-sided $q$-Whittaker process. We give a formula for the free energy distribution of the polymer model in terms of Fredholm determinant and show that the universal KPZ stationary distribution appears in the long time limit. We also consider the limit to the stationary KPZ equation and discuss the connections with previously found formulas.
We consider two models for directed polymers in space-time independent random media (the O'Connell-Yor semi-discrete directed polymer and the continuum directed random polymer) at positive temperature and prove their KPZ universality via asymptotic analysis of exact Fredholm determinant formulas for the Laplace transform of their partition functions. In particular, we show that for large time tau, the probability distributions for the free energy fluctuations, when rescaled by tau^{1/3}, converges to the GUE Tracy-Widom distribution. We also consider the effect of boundary perturbations to the…
The Brydges-Imbrie dimensional reduction formula relates the pressure of a $d$-dimensional gas of hard spheres to a model of $(d+2)$-dimensional branched polymers. Brydges and Imbrie's proof was non-constructive and relied on a supersymmetric localization lemma. The main result of this article is a constructive proof of a more general dimensional reduction formula that contains the Brydges--Imbrie formula as a special case. Central to the proof are invariance lemmas, which were first introduced by Kenyon and Winkler for branched polymers. The new dimensional reduction formulas rely on invarian…
It is a well-known open problem in the literature on random polymers to show that a directed polymer in random environment localizes around a favorite path at low temperature. A precise statement of this conjecture is formulated and proved in this article.
We study the semi-discrete directed random polymer model introduced by O'Connell and Yor. We obtain a representation for the moment generating function of the polymer partition function in terms of a determinantal measure. This measure is an extension of the probability measure of the eigenvalues for the Gaussian Unitary Ensemble (GUE) in random matrix theory. To establish the relation, we introduce another determinantal measure on larger degrees of freedom and consider its few properties, from which the representation above follows immediately.
Very recently, Junk [11] showed that for directed polymers in bounded random environments, the weak disorder (uniform integrable) phase implies that the polymer martingale is bounded in $L^p$ for some $p>1$ and also in $L^q$ for some $q<0$. Here, we establish this characterization of the weak disorder phase without requiring the boundedness assumption on the environments.
We consider the fluctuations of the free energy of positive temperature directed polymers in thin rectangles (N,N^α), α< 3/14. For general weight distributions with finite fourth moment we prove that the distribution of these fluctuations converges as N goes to infinity to the GUE Tracy-Widom distribution.
We prove a formula conjectured in O'Connell and Yor (2001) for the free energy density of a directed polymer in a Brownian environment in 1+1 dimensions.
We give an explicit formula for the joint density of the max and argmax of the Airy$_2$ process minus a parabola. The argmax has a universal distribution which governs the rescaled endpoint for large time or temperature of directed polymers in 1+1 dimensions.
We consider $(1+1)$-dimensional directed polymers in a random potential and provide sufficient conditions guaranteeing joint localization. Joint localization means that for typical realizations of the environment, and for polymers started at different starting points, all the associated endpoint distributions localize in a common random region that does not grow with the length of the polymer. In particular, we prove that joint localization holds when the reference random walk of the polymer model is either a simple symmetric lattice walk or a Gaussian random walk. We also prove that the very …
Explicit expression for the $N$-point free energy distribution function in one dimensional directed polymers in a random potential is derived in terms of the Bethe ansatz replica technique. The obtained result is equivalent to the one derived earlier by Prolhac and Spohn [J. Stat. Mech., 2011, P03020].
In this short note, we prove a central limit theorem for a type of replica overlap of the Brownian directed polymer in a Gaussian random environment, in the low temperature regime and in all dimensions. The proof relies on a superconcentration result for the KPZ equation driven by a spatially mollified noise, which is inspired by the recent work of Chatterjee \cite{C1}.
We prove that the random variable $\ct=\argmax_{t\in\rr}\{\aip(t)-t^2\}$ has tails which decay like $e^{-ct^3}$. The distribution of $\ct$ is a universal distribution which governs the rescaled endpoint of directed polymers in 1+1 dimensions for large time or temperature.
We compute the fluctuation exponents for a solvable model of one-dimensional directed polymers in random environment in the intermediate regime. This regime corresponds to taking the inverse temperature to zero with the size of the system. The exponents satisfy the KPZ scaling relation and coincide with physical predictions. In the critical case, we recover the fluctuation exponents of the Cole-Hopf solution of the KPZ equation in equilibrium and close to equilibrium.
We study a (1+1)-dimensional directed polymer in a random environment on the integer lattice with log-gamma distributed weights. Among directed polymers, this model is special in the same way as the last-passage percolation model with exponential or geometric weights is special among growth models, namely, both permit explicit calculations. With appropriate boundary conditions, the polymer with log-gamma weights satisfies an analogue of Burke's theorem for queues. Building on this, we prove the conjectured values for the fluctuation exponents of the free energy and the polymer path, in the cas…
We consider a stochastic model of N evolving particles studied by Brunet and Derrida. This model can be seen as a directed polymer in random medium with N sites in the transverse direction. Cook and Derrida, use heuristic arguments to obtain a formula for the ground state energy of the polymer. In this paper, we formalize their argument and show that there is an additional term in the formula in the critical case. We also consider a generalization of the model, and show that in the noncritical case the behavior is basically the same, whereas in the critical case a new correction appears.
We consider the Brownian directed polymer in Poissonian environment in dimension 1+1, under the so-called intermediate disorder regime, which is a crossover regime between the strong and weak disorder regions. We show that, under a diffusive scaling involving different parameters of the system, the renormalized point-to-point partition function of the polymer converges in law to the solution of the stochastic heat equation with Gaussian multiplicative noise. The Poissonian environment provides a natural setting and strong tools, such as the Wiener-Ito chaos expansion, which, applied to the par…
We study the free energy of the directed polymer in random environment in dimension 1+1 and 1+2. For dimension 1, we improve the statement of Comets and Vargas concerning very strong disorder by giving sharp estimates on the free energy at high temperature. In dimension 2, we prove that very strong disorder holds at all temperatures, thus solving a long standing conjecture in the field.
We study the scaling exponents of a 1+1-dimensional directed polymer in a Brownian random environment introduced by O'Connell and Yor. For a version of the model with boundary conditions that are stationary in a space-time sense we identify the exact values of the exponents. For the version without the boundary conditions we get the conjectured upper bounds on the exponents.
It is shown that when $d\ge 3$, the growing random surface generated by the $(d+1)$-dimensional directed polymer model at sufficiently high temperature, after being smoothed by taking microscopic local averages, converges to a solution of the deterministic KPZ equation in a suitable scaling limit.
We investigate the high-temperature behavior of the directed polymer model in dimension $1+2$. More precisely we study the difference $Δ\mathtt{F}(β)$ between the quenched and annealed free energies for small values of the inverse temperature $β$. This quantity is associated to localization properties of the polymer trajectories, and is related to the overlap fraction of two replicas. Adapting recent techniques developed by the authors in the context of the disordered pinning model (Berger and Lacoin, arXiv:1503.07315 [math-ph]), we identify the sharp asymptotic high temperature behavior \[\li…
We show that the partition function of the multi-layer semi-discrete directed polymer converges in the intermediate disorder regime to the partition function for the multi-layer continuum polymer introduced by O'Connell and Warren. This verifies, modulo a previously hidden constant, an outstanding conjecture proposed by Corwin and Hammond. A consequence is the identification of the KPZ line ensemble as logarithms of ratios of consecutive layers of the continuum partition function. Other properties of the continuum partition function, such as continuity, strict positivity and contour integral f…
