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:
-  : spatial dimension of the embedding medium
–
: spatial dimension of the embedding medium
–  : internal dimension of the manifold
–
: internal dimension of the manifold
–  : dimension of the displacement (or height) field
: dimension of the displacement (or height) field
These satisfy the relation:
 
We focus on two important cases:
Directed Polymers (d = 1)
The configuration is described by a vector function:
 ,
where
,
where  is the internal coordinate. The polymer lives in
 is the internal coordinate. The polymer lives in  dimensions.
 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:
 ,
where
,
where  is the internal coordinate and
 is the internal coordinate and  represents time.
 represents time.
Examples: domain walls and propagating fronts
Again we neglect overhangs or pinch-off:  is single-valued
 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
  
The first term  is the elastic force trying to smooth the interface, the mobility
 is the elastic force trying to smooth the interface, the mobility  is the inverse of the viscosity. The second term is the Langevin noise. It is Guassian and defined by
 is the inverse of the viscosity. The second term is the Langevin noise. It is Guassian and defined by 
  
The symbol  indicates the average over the thermal noise and the diffusion constant is fixed by the Einstein relation
 indicates the average over the thermal noise and the diffusion constant is fixed by the Einstein relation  . We set
. We set   
The potential energy of surface tension ( is the stiffness) can be expanded at the lowest order in the gradient:
 is the stiffness) can be expanded at the lowest order in the gradient: 
  
Hence, we have the Edwards Wilkinson equation:
  
Scaling Invariance
The equation enjoys of a continuous symmetry because  and
 and  cannot be distinguished. This is a condition of scale invariance:
  cannot be distinguished. This is a condition of scale invariance:
  
Here  are the dynamic and the roughness exponent respectively. From dimensional analysis
 are the dynamic and the roughness exponent respectively. From dimensional analysis
  
From which you get  in any dimension and a rough interface below
 in any dimension and a rough interface below  with
 with  .
.
Width of the interface
Consider a 1-dimensional line of size L with periodic boundary conditions.
We consider the width square of the interface 
 ![{\displaystyle w_{2}(t)=\left[\int _{0}^{L}{\frac {dr}{L}}\left(h(r,t)-\int _{0}^{L}{\frac {dr}{L}}h(r,t)\right)\right]^{2}}](https://wikimedia.org/api/rest_v1/media/math/render/svg/7e90cf86b0b1d41373e244d2b662e41a35e2f17a) 
It is useful to introduce the Fourier modes:
  
Here  and recall
 and recall  .
using de Parseval theorem for the Fourier series
.
using de Parseval theorem for the Fourier series
  
In the last step we used that  .
.
Solution in the Fourier space
show that the  EW equation writes
  
The solution of this first order linear equation writes
  
- Assume that the interface is initially flat, namely  .  Show that .  Show that
![{\displaystyle \langle {\hat {h}}_{q}(t){\hat {h}}_{-q}(t)\rangle ={\begin{cases}{\dfrac {T(1-e^{-2\nu q^{2}t})}{L\nu q^{2}}},&q\neq 0,\\[1.2em]{\frac {2T}{L}}t,&q=0.\end{cases}}}](https://wikimedia.org/api/rest_v1/media/math/render/svg/061f8784957b060f52cc90906b723171f5dab3d2) 
- The mean width square grows at short times and saturates at long times:
![{\displaystyle \langle w_{2}(t)\rangle ={\dfrac {T}{L\nu }}\sum _{q\neq 0}{\dfrac {1-e^{-2\nu q^{2}t}}{q^{2}}}={\begin{cases}T{\sqrt {\frac {2t}{\pi \nu }}},&t\ll L^{2},\\[1.2em]{\frac {T}{\nu }}{\frac {L}{12}},&t\gg L^{2}.\end{cases}}}](https://wikimedia.org/api/rest_v1/media/math/render/svg/80210d54ad41d06071b8cf376c4f26ddfe24a149) 
Directed polymers in random media
Let us consider polymers  of length
  of length   , starting in
, starting in   and ending in
  and ending in  and at thermal equlibrium at   temperature
 and at thermal equlibrium at   temperature  . The partition function of the model writes as
. The partition function of the model writes as 
 ![{\displaystyle 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]}](https://wikimedia.org/api/rest_v1/media/math/render/svg/6be96d05745484d7b16302f05367c4eb5d7e577a) 
For simplicity, we assume a white noise,  . Here, the partition function is written as a sum over all possible paths, corresponding to all possible polymer configurations that start at
. Here, the partition function is written as a sum over all possible paths, corresponding to all possible polymer configurations that start at  and end at
 and end at  , weighted by the appropriate Boltzmann factor.
, weighted by the appropriate Boltzmann factor.
Polymer partition function and propagator of a quantum particle
Let's perform the following change of variables:  . We also identifies
. We also identifies  with
 with  and
 and  as the time.
 as the time.
 ![{\displaystyle 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}}dt'{\frac {1}{2}}(\partial _{t'}x)^{2}-V(x(t'),t')\right]}](https://wikimedia.org/api/rest_v1/media/math/render/svg/fbe30988e17e8a07bb2f0ed0dc15d77bbafa04be) 
Note that ![{\displaystyle S[x]=\int _{0}^{\tilde {t}}dt'{\frac {1}{2}}(\partial _{t'}x)^{2}-V(x(t'),t')}](https://wikimedia.org/api/rest_v1/media/math/render/svg/24e6431964c1d024dccfd9c0b8060b46c6e9dc80) is the classical action of a particle with kinetic energy
 is the classical action of a particle with kinetic energy   and  time dependent potential
 and  time dependent potential  , evolving from time zero to time
, evolving from time zero to time  .
From the Feymann path integral formulation,
.
From the Feymann path integral formulation, ![{\displaystyle Z[x,{\tilde {t}}]}](https://wikimedia.org/api/rest_v1/media/math/render/svg/0b30f26c1d298b75d7c422ba277ab1565b53e8b6) is the propagator of the quantum particle.
  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:
  
Feynman-Kac formula
Let's derive the Feyman Kac formula for   in the general case:
 in the general case:
- First, focus on free paths and introduce the following probability
![{\displaystyle P[A,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}\right]\delta \left(\int _{0}^{t}d\tau V(x(\tau ),\tau )-A\right)}](https://wikimedia.org/api/rest_v1/media/math/render/svg/b0ef5c886415584cf10124c454b5606dfd73fe67)