Directed Polymer in finite dimension
State of the Art
The directed polymer in random media belongs to the KPZ universality class. The behavior of this system is well understood in one dimension and in the mean-field case, more precisely for the directed polymer on the Cayley tree. In particular:
- In
, we have
and a glassy regime present at all temperatures. The model is integrable through a non-standard Bethe Ansatz, and the distribution of
for a given boundary condition is of the Tracy–Widom type.
- In
, for the Cayley tree, an exact solution exists, predicting a freezing transition to a 1RSB phase (
).
In finite dimensions greater than one, no exact solutions are available. Numerical simulations indicate
in
and a glassy regime present at all temperatures. The case
remains particularly intriguing.
Let's do replica!
To make progress in disordered systems, we need to analyze the moments of the partition function. The first moment provide the annealed average and the second moment tell us about the fluctuantions. In particular, the partition function is self-averaging if
In this case annealed and the quenched average coincides in the thermodynamic limit. This strict condition is sufficient, but not necessary. What is necessary is to show that for large t
,
In the following, we compute these moments via a replica calculation, considering polymers starting at
and ending at
.
To proceed, we only need two ingredients:
- The random potential
is a Gaussian field characterized by
- Since the disorder is Gaussian, averages of exponentials can be computed using Wick’s theorem:
for any Gaussian random variable
.
These two properties are all we need to carry out the replica calculation below.
First Moment
Due to the short-distance divergence of
,
Hence,
Second Moment
For the second moment we need two replicas:
- Step 3: Change of Coordinates
Let
and
. Then:
Here,
Two-Replica Propagator
Define the propagator:
By the Feynman-Kac formula:
The single-particle potential is time-independent and attractive. Long-time behavior is governed by the low-energy eigenstates.
For
, the attractive potential always produces a bound state with energy
. Hence, at long times:
This explosion means that the quenched free energy is smaller than the annealed one at all temperatures.
For
, The low-energy behavior depends on
:
- High temperature: the spectrum is positive and continuous. Annealed and quenched coincide, the exponent
.
- Low temperature: bound states appear. No replica-symmetry breaking (RSB), but the quenched free energy is smaller than the annealed one. Numerical simulations show
.
Back to REM: condensation of the Gibbs measure
Thanks to the computation of
, we can identify an important fingerprint of the glassy phase. Let's compare the weight of the ground state against the weight of all other states:
Behavior in Different Phases:
- High-Temperature Phase (
):
- In this regime, the total weight of the excited states dominates over the weight of the ground state. The ground state is therefore not deep enough to overcome the finite entropy contribution. As a result, the probability of sampling the same configuration twice from the Gibbs measure is exponentially small in 'N'.
- Low-Temperature Phase (
):
- In this regime, the integral is finite:
In this regime, the total weight of the excited states is of the same order as the weight of the ground state. Consequently, the ground state is occupied with finite probability, reminiscent of Bose–Einstein condensation. However, unlike the directed polymer in finite dimension, this condensation involves not only the ground state but also the first excited states.
Overlap Distribution and Replica Symmetry Breaking:
The structure of states can be further characterized through the overlap between two configurations
and
, defined as
which takes values in the interval
. The distribution
of the overlap between two configurations sampled from the Gibbs measure distinguishes the two phases:
At high temperature (
), the system is replica symmetric and the overlap distribution is concentrated at zero:
At low temperature (
), the system exhibits one-step replica symmetry breaking, and the overlap distribution becomes
More general REM and systems in Finite dimensions
In random energy models with i.i.d. random variables, the distribution
determines the dependence of
and
on M, and consequently their scaling with N, the number of degrees of freedom. It is insightful to consider a more general case where an exponent
describes the fluctuations of the ground state energy:
Three distinct scenarios emerge depending on the sign of
:
- For
: The freezing temperature vanishes with increasing system size, leading to the absence of a freezing transition. This scenario occurs in many low-dimensional systems, such as the Edwards-Anderson model in two dimensions.
- For
: A freezing transition is guaranteed. For the Random Energy Model discussed earlier,
. An important feature of this transition, as will be explored in the next section, is that condensation does not occur solely in the ground state but also involves a large (albeit not extensive) number of low-energy excitations.
- For
: The freezing temperature grows with the system size, resulting in only the glassy phase. The system condenses entirely into the ground state since the excited states are characterized by prohibitively high energies. This scenario, while less intricate than the
case, corresponds to a glassy phase with a single deep ground state.
The extent to which these scenarios persist in real systems in finite dimensions remains an open question. In these systems, such as the directed polymers, the fluctuations of the ground state energy are characterized by an exponent
:
where
is the linear size of the system and
is the number of degrees of freedom.
At finite temperatures, an analogous exponent is defined by studying the fluctuations of the free energy,
. For the directed polymer in low dimwnsion the fluctuations of the ground state exhibit a positive and temperature-independent
. In such cases, only the glassy phase exists, aligning with the
scenario in REMs.
On the other hand, for the directed polymer in high dimension,
is positive at low temperatures but vanishes at high temperatures. This behavior defines a glass transition mechanism entirely distinct from those observed in mean-field models.