LBan-II: Difference between revisions

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</math></center>
</math></center>
=Directed polymers in random media=
=Directed polymers in random media=
ciao
 
Let us consider polymers <math>
x(\tau) </math>  of length  <math>
t </math>, starting in  <math>0 </math>  and ending in <math>x </math> and at thermal equlibrium at  temperature <math>T</math>. The partition function of the model writes as
<center> <math>
Z(x,t) =\int_{x(0)=0}^{x(t)=x} {\cal D} x(\tau) \exp\left[- \frac{1}{T} \int_0^t d \tau \frac{1}2(\partial_\tau x)^2 +V(x(\tau),\tau)\right]
</math></center>
For simplicity, we assume a white noise, <math> \overline{V(x,\tau) V(x',\tau')} = D \delta(x-x') \delta(\tau-\tau') </math>. Here, the partition function is written as a sum over all possible paths, corresponding to all possible polymer configurations that start at <math>0</math> and end at <math>x</math>, weighted by the appropriate Boltzmann factor.
 
=== Polymer partition function and propagator of a quantum particle===
 
Let's perform the following change of variables: <math>\tau=i t' </math>. We also identifies <math>T</math> with <math>\hbar</math> and <math> \tilde t= -i t </math> as the time.
<center> <math>
Z(x,\tilde t) =\int_{x(0)=0}^{x(\tilde t)=x} {\cal D} x(t') \exp\left[ \frac{i}{\hbar} \int_0^{\tilde t} d t' \frac{1}2(\partial_{t'} x)^2 -V(x(t'),t')\right]
</math></center>
 
Note that <math>  S[x]=  \int_0^{\tilde t} d t' \frac{1}2(\partial_{t'} x)^2 -V(x(t'),t')</math> is the classical action of a particle with kinetic energy  <math> \frac{1}2(\partial_\tau x)^2</math> and  time dependent potential <math> V(x(\tau),\tau)</math>, evolving from time zero to time <math> \tilde t</math>.
From the Feymann path integral formulation, <math> Z[x,\tilde t]</math>  is the propagator of the quantum particle.
 
In absence of disorder, one can find the propagator of the free particle, that, in the original variables, writes:
<center> <math>
Z_{\text{free}}(x,t)=\frac{e^{-x^2/(2Tt)}}{\sqrt{2 \pi Tt}}
</math></center>

Revision as of 16:25, 26 August 2025

Introduction: Interfaces and Directed Polymers

The physical properties of many materials are governed by manifolds embedded in them. Examples include: dislocations in crystals, domain walls in ferromagnets or vortex lines in superconductors. We fix the following notation: - D: spatial dimension of the embedding medium – d: internal dimension of the manifold – N: dimension of the displacement (or height) field

These satisfy the relation:

D=d+N

We focus on two important cases:

Directed Polymers (d = 1)

The configuration is described by a vector function: x→(t), where t is the internal coordinate. The polymer lives in D=1+N dimensions.

Examples: vortex lines, DNA strands, fronts.

Although polymers may form loops, we restrict to directed polymers, i.e., configurations without overhangs or backward turns.

Interfaces (N = 1)

The interface is described by a scalar height field: h(r→,t), where r→∈ℝd is the internal coordinate and t represents time.

Examples: domain walls and propagating fronts

Again we neglect overhangs or pinch-off: h(r→,t) is single-valued

Note that using our notation the 1D front is both an interface and a directed polymer

Thermal Interfaces

The dynamics is overdamped, so that we can neglect the inertial term. The Langevin equation of motion is

∂th(r,t)=−μδEpotδh(r,t)+η(r,t)

The first term −δEpot/δh(r,t) is the elastic force trying to smooth the interface, the mobility μ is the inverse of the viscosity. The second term is the Langevin noise. It is Guassian and defined by

⟨η(r,t)⟩=0,⟨η(r′,t′)η(r,t)⟩=2dDδd(r−r′)δ(t−t′)

The symbol ⟨…⟩ indicates the average over the thermal noise and the diffusion constant is fixed by the Einstein relation D=μKBT. We set μ=KB=1

The potential energy of surface tension (ν is the stiffness) can be expanded at the lowest order in the gradient:

Epot=ν∫ddr1+(∇h)2∼const.+ν2∫ddr(∇h)2

Hence, we have the Edwards Wilkinson equation:

∂th(r,t)=ν∇2h(r,t)+η(r,t)

Scaling Invariance

The equation enjoys of a continuous symmetry because h(r,t) and h(r,t)+c cannot be distinguished. This is a condition of scale invariance:

h(br,bzt)∼inlawbαh(r,t)

Here z,α are the dynamic and the roughness exponent respectively. From dimensional analysis

bα−z∂th(r,t)=bα−2∇2h(r,t)+b−d/2−z/2η(r,t)

From which you get z=2 in any dimension and a rough interface below d=2 with α=(2−d)/2.

Width of the interface

Consider a 1-dimensional line of size L with periodic boundary conditions. We consider the width square of the interface

w2(t)=[∫0LdrL(h(r,t)−∫0LdrLh(r,t))]2

It is useful to introduce the Fourier modes:

h^q(t)=1L∫0Leiqrh(r,t),h(r,t)=∑qe−iqrh^q(t)

Here q=2πn/L,n=…,−1,0,1,… and recall ∫0Ldreiqr=Lδq,0. using de Parseval theorem for the Fourier series

w2(t)=∑q≠0|h^q(t)|2=∑q≠0(h^q(t)h^−q(t))2

In the last step we used that h^q*(t)=h^−q(t).

Solution in the Fourier space

show that the EW equation writes

∂th^q(t)=−νq2h^q(t)+ηq(t),with⟨ηq1(t′)ηq2(t)⟩=2TLδq1,−q2δ(t−t′)

The solution of this first order linear equation writes

h^q(t)=h^q(0)e−νq2t+∫0tdse−νq2(t−s)ηq(s)
  • Assume that the interface is initially flat, namely h^q(0)=0. Show that
⟨h^q(t)h^−q(t)⟩={T(1−e−2νq2t)Lνq2,q≠0,2TLt,q=0.
  • The mean width square grows at short times and saturates at long times:
⟨w2(t)⟩=TLν∑q≠01−e−2νq2tq2={T2tπν,t≪L2,TνL12,t≫L2.

Directed polymers in random media

Let us consider polymers x(τ) of length t, starting in 0 and ending in x and at thermal equlibrium at temperature T. The partition function of the model writes as

Z(x,t)=∫x(0)=0x(t)=x𝒟x(τ)exp⁡[−1T∫0tdτ12(∂τx)2+V(x(τ),τ)]

For simplicity, we assume a white noise, V(x,τ)V(x′,τ′)‾=Dδ(x−x′)δ(τ−τ′). Here, the partition function is written as a sum over all possible paths, corresponding to all possible polymer configurations that start at 0 and end at x, weighted by the appropriate Boltzmann factor.

Polymer partition function and propagator of a quantum particle

Let's perform the following change of variables: τ=it′. We also identifies T with ℏ and t~=−it as the time.

Z(x,t~)=∫x(0)=0x(t~)=x𝒟x(t′)exp⁡[iℏ∫0t~dt′12(∂t′x)2−V(x(t′),t′)]

Note that S[x]=∫0t~dt′12(∂t′x)2−V(x(t′),t′) is the classical action of a particle with kinetic energy 12(∂τx)2 and time dependent potential V(x(τ),τ), evolving from time zero to time t~. From the Feymann path integral formulation, Z[x,t~] is the propagator of the quantum particle.

In absence of disorder, one can find the propagator of the free particle, that, in the original variables, writes:

Zfree(x,t)=e−x2/(2Tt)2πTt