L-4: Difference between revisions

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\overline{Z(x,t) } = \frac{1}{(2 \pi t T)^{d/2}}\exp\left[ -\frac{1}{2} \frac{ x^2}{t T} \right]  \exp\left[ \frac{D  t \delta_0}{2T^2}  \right]   
\overline{Z(x,t) } = \frac{1}{(2 \pi t T)^{d/2}}\exp\left[ -\frac{1}{2} \frac{ x^2}{t T} \right]  \exp\left[ \frac{D  t \delta_0}{2T^2}  \right]  = Z_{\text{free}}(x,t,T) \exp\left[ \frac{D  t \delta_0}{2T^2}
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=== The second moment ===   
=== The second moment ===   

Revision as of 18:29, 2 February 2025

Goal : final lecture on KPZ and directed polymers at finite dimension. We will show that for d>2 a "glass transition" takes place.


KPZ : from 1d to the Cayley tree

We know a lot about KPZ, but there is still much to understand:

  • In d=1, we have found θ=1/3 and a glassy regime present at all temperatures. The stationary solution of the KPZ equation describes, at long times, the fluctuations of quantities such as Emin[x]Emin[x]. However, it does not determine the actual distribution of Emin for a given x. In particular, we have no clear understanding of the origin of the Tracy-Widom distribution.
  • In d=, an exact solution exists for the Cayley tree, predicting a freezing transition to a 1RSB phase (θ=0).
  • In finite dimensions greater than one, no exact solutions are available. Numerical simulations indicate θ>0 in d=2. The case d>2 remains particularly intriguing.

Let's do replica!

To make progress in disordered systems, we need to analyze the moments of the partition function. From Valentina's lecture, recall that if

Z(x,t)2(Z(x,t))2=1

then the partition function is self-averaging, and

lnZ(x,t)=lnZ(x,t).

The condition above is sufficient but not necessary. It is enough that

Z(x,t)2(Z(x,t))2<const,

when t, to ensure the equivalence between annealed and quenched averages.

In the following, we compute this quantity, which corresponds to a two-replica calculation. For simplicity, we consider polymers starting at 0 and ending at x. We recall that:

  • V(x,τ) is a Gaussian field with
V(x,τ)=0,V(x,τ)V(x,τ)=Dδd(xx)δ(ττ)
  • From Wick's theorem, for a generic Gaussian field W, we have
exp(W)=exp[W+12(W2W2)]

The first moment

The first moment of the partition function is straightforward to compute and corresponds to a single replica:

Z(x,t)=x(0)=0x(t)=x𝒟x(τ)exp[1T0tdτ12(τx)2]exp[1TdτV(x(τ),τ)]

Note that the term T2W2=dτ1dτ2V(x,τ1)V(x,τ2)=Dtδ0 exhibits a short-distance divergence due to the delta function. Hence, we can write:

Failed to parse (syntax error): {\displaystyle \overline{Z(x,t) } = \frac{1}{(2 \pi t T)^{d/2}}\exp\left[ -\frac{1}{2} \frac{ x^2}{t T} \right] \exp\left[ \frac{D t \delta_0}{2T^2} \right] = Z_{\text{free}}(x,t,T) \exp\left[ \frac{D t \delta_0}{2T^2} }

The second moment

For the second moment, there are two replicas:

  • Step 1: The second moment is

Z(x,t)2=𝒟x1𝒟x2exp[0tdτ12T[(τx1)2+(τx2)2]]exp[1T0tdτ1V(x1(τ1),τ1)1T0tdτ2V(x2(τ2),τ2)]

  • Step 2: Using Wick's theorem, we obtain

Z(x,t)2=exp[Dtδ0T2]𝒟x1𝒟x2exp[0tdτ12T[(τx1)2+(τx2)2DT2δd[x1(τ)x2(τ)]]

and we can write:

Z(x,t)2=(Z(x,t)Zfree(x,t))2exp[Dtδ0T2]𝒟x1𝒟x2exp[0tdτ12T[(τx1)2+(τx2)2DT2δd[x1(τ)x2(τ)]]

  • Step 3: Changing coordinates X=(x1+x2)/2;u=x1x2, we get

Z(x,t)2=(Z(x,t))2u(0)=0u(t)=0𝒟uexp[0tdτ14T(τu)2DT2δd[u(τ)]]Zfree(u,t)

The two replica propagator

Hence, the quantity Z(x,t)2(Z(x,t))2 can be computed.

  • The denominator

u(0)=0u(t)=0𝒟uexp[0tdτ14T(τu)2]

is the free propagator and contributes as (4Tt)d/2.

  • Let us define the numerator:
W(0,t)=u(0)=0u(t)=0𝒟uexp[0tdτ14T(τu)2DT2δd[u(τ)]]

Using the Feynman-Kac formula, we can write the following equation:

tW(x,t)=H^W(x,t)

Here, the Hamiltonian is given by:

H^=2T2DT2δd[u]

The Spectrum of the Two-Replica Hamiltonian

The single-particle potential is time-independent and attractive. Since it is time-independent, we can use the spectral decomposition of the propagator. The long-time behavior is controlled by the low-energy part of the spectrum. In the presence of an attractive potential, we may have:

  • A discrete set of eigenvalues corresponding to bound states, followed by a continuous spectrum.
  • Only a continuous spectrum.


As a funcion of the dimension we distiguish two cases:

  • For d2:

An attractive potential always leads to the formation of a bound state.The ground state has a negative energy E0<0. At long times, the propagator behaves as:

W(x,t)e|E0|t

This implies that at all temperatures, in the limit t:

lnZ(x,t)lnZ(x,t)

  • For d>2:

The low-energy part of the spectrum is controlled by the prefactor DT2. At high temperatures, the spectrum remains continuous and positive. At low temperatures, bound states appear. Thus, in the limit t:

{lnZ(x,t)=lnZ(x,t)forT>TclnZ(x,t)lnZ(x,t)forT<Tc

This transition, in d=3, separates a high-temperature phase with θ=0 and a low-temperature phase with θ>0 and no RSB.