LBan-II: Difference between revisions

From Disordered Systems Wiki
Jump to navigation Jump to search
Line 174: Line 174:
This hamiltonian is time dependent because of the multiplicative noise <math>V(x,\tau)/T</math>. For a <Strong> time independent </Strong> hamiltonian, we can use the spectrum of the operator. In general we will have to parts:
This hamiltonian is time dependent because of the multiplicative noise <math>V(x,\tau)/T</math>. For a <Strong> time independent </Strong> hamiltonian, we can use the spectrum of the operator. In general we will have to parts:
* A discrete set of eigenvalues <math>E_n</math> with the eigenstates <math>\psi_n(x)</math>  
* A discrete set of eigenvalues <math>E_n</math> with the eigenstates <math>\psi_n(x)</math>  
* A continuum part where the states <math>\psi_E(x)</math> have energy <math>E</math>. We define the density of states  <math>\rho(E)</math>, such that the number of states with energy in <math>E, E + dE</math> is <math>\rho(E) dE </math>.
* A continuum part where the states <math>\psi_E(x)</math> have energy <math>E</math>. We define the density of states  <math>\rho(E)</math>, such that the number of states with energy in (<math>E, E + dE</math>) is <math>\rho(E) dE </math>.


In this case <math> Z[x,t] </math> can be written has the sum of two contributions:
In this case <math> Z[x,t] </math> can be written has the sum of two contributions:

Revision as of 17:37, 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 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(rr)δ(tt)

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=νddr1+(h)2const.+ν2ddr(h)2

Hence, we have the Edwards Wilkinson equation:

th(r,t)=ν2h(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

bαzth(r,t)=bα22h(r,t)+bd/2z/2η(r,t)

From which you get z=2 in any dimension and a rough interface below d=2 with α=(2d)/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)=1L0Leiqrh(r,t),h(r,t)=qeiqrh^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)=q0|h^q(t)|2=q0(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),withηq1(t)ηq2(t)=2TLδq1,q2δ(tt)

The solution of this first order linear equation writes

h^q(t)=h^q(0)eνq2t+0tdseνq2(ts)ηq(s)
  • Assume that the interface is initially flat, namely h^q(0)=0. Show that
h^q(t)h^q(t)={T(1e2νq2t)Lνq2,q0,2TLt,q=0.
  • The mean width square grows at short times and saturates at long times:
w2(t)=TLνq01e2νq2tq2={T2tπν,tL2,TνL12,tL2.

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[1T0tdτ12(τx)2+V(x(τ),τ)]

For simplicity, we assume a white noise, V(x,τ)V(x,τ)=Dδ(xx)δ(ττ). 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 and t~=it as the time.

Z(x,t~)=x(0)=0x(t~)=x𝒟x(t)exp[i0t~dt12(tx)2V(x(t),t)]

Note that S[x]=0t~dt12(tx)2V(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)=ex2/(2Tt)2πTt

Feynman-Kac formula

Let's derive the Feyman Kac formula for Z(x,t) in the general case:

  • First, focus on free paths and introduce the following probability
P[A,x,t]=x(0)=0x(t)=x𝒟x(τ)exp[1T0tdτ12(τx)2]δ(0tdτV(x(τ),τ)A)
  • Second, the moments generating function
Zp(x,t)=dAepAP[A,x,t]=x(0)=0x(t)=x𝒟x(τ)e1T0tdτ12(τx)2p0tdτV(x(τ),τ)
  • Third, the backward approach. Consider free paths evolving up to t+dt and reaching x :
Zp(x,t+dt)=ep0t+dtdτV(x(τ),τ)=ep0tdτV(x(τ),τ)epV(x,t)dt=[1pV(x,t)dt+]Zp(xΔx,t)Δx

Here is the average over all free paths, while Δx is the average over the last jump, namely Δx=0 and Δx2=Tdt.

  • At the lowest order we have
Zp(x,t+dt)=Zp(x,t)+dt[T2x2ZppV(x,t)Zp]+O(dt2)

Replacing p=1/T we obtain the partition function is the solution of the Schrodinger-like equation:

tZ(x,t)=H^Z=[T2d2dx2+V(x,τ)T]Z(x,t)

Z[x,t=0]=δ(x)

Remarks

Remark 1:

This equation is a diffusive equation with multiplicative noise. Edwards Wilkinson is instead a diffusive equation with additive noise. The Cole Hopf transformation allows to map the diffusive equation with multiplicative noise in a non-linear equation with additive noise. We will apply this tranformation and have a surprise.

Remark 2: This hamiltonian is time dependent because of the multiplicative noise V(x,τ)/T. For a time independent hamiltonian, we can use the spectrum of the operator. In general we will have to parts:

  • A discrete set of eigenvalues En with the eigenstates ψn(x)
  • A continuum part where the states ψE(x) have energy E. We define the density of states ρ(E), such that the number of states with energy in (E,E+dE) is ρ(E)dE.

In this case Z[x,t] can be written has the sum of two contributions:

Z[x,t]=(eH^t)0x=nψn(0)ψn*(x)eEnt+0dEρ(E)ψE(0)ψE*(x)eEt.