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Created page with "<Strong> Goal </Strong>: This is the first lecture about the localization. Localization is a <Strong> wave phenomenon induced by disorder.</Strong> == The Gaussian packet of free particles: the ballistic behaviour == == The conductance and the diffusive behaviour == Ohm's laws characterize electric transport of (good or bad) conductors: * First law: <center><math> \frac{V}{I}= R, \quad \text{or} \quad \frac{I}{V}= G </math></center> Here <math>R </math> is the res..."
 
 
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<Strong> Goal </Strong>: This is the first lecture about the localization. Localization is a <Strong> wave phenomenon induced by disorder.</Strong>
'''Goal.''' This lecture introduces the phenomenon of localization. Localization is a '''wave phenomenon induced by disorder''' that suppresses transport in a system.


== The Gaussian packet of free particles: the ballistic behaviour ==
== Short recap: wavefunctions and eigenstates ==


Before discussing localization we briefly recall a few basic notions of quantum mechanics.


A quantum particle in one dimension is described by a '''wavefunction''' <math>\psi(x,t)</math>. 
The quantity <math>|\psi(x,t)|^2</math> is the probability density of finding the particle at position <math>x</math> at time <math>t</math>.  The wavefunction therefore satisfies the normalization condition


== The conductance and the diffusive behaviour  ==
<math display="block">
\int_{-\infty}^{\infty} dx\, |\psi(x,t)|^2 = 1 .
</math>


Ohm's laws characterize electric transport of (good or bad) conductors:
The time evolution of the wavefunction is governed by the Schrödinger equation
* First law:
 
<center><math> \frac{V}{I}= R, \quad \text{or} \quad \frac{I}{V}= G </math></center>
<math display="block">
Here <math>R </math> is the resistence of the sample and <math> G </math> is its conductance.\
i\hbar \partial_t \psi(x,t) = H\psi(x,t),
* Second law
</math>
<center><math> R =\rho \frac{L}{S}\sim \rho L^{2-d} , \quad \text{or} \quad  G = \sigma \frac{S}{L}\sim \sigma L^{d-2} </math></center>
 
Here <math> \rho, \sigma</math> are the resistivity and the conductivity. These are material properties, independent of the geometry of the sample 
where <math>H</math> is the Hamiltonian of the system. For a particle moving in one dimension in a potential <math>V(x)</math>, the Hamiltonian reads
These phenomenological laws are a macroscpic manifestation of the diffusive motion of the electrons.  
 
From the Drude model we know that disorder is the crucial ingredient to justify the presence of diffusion.
<math display="block">
]
H = -\frac{\hbar^2}{2m}\partial_x^2 + V(x).
</math>
 
=== Eigenstates ===
 
A particularly important class of solutions are the '''eigenstates''' of the Hamiltonian
 
<math display="block">
H\psi_n(x) = E_n \psi_n(x).
</math>
 
If the particle is in an eigenstate the full solution reads
 
<math display="block">
\psi_n(x,t)=\psi_n(x)e^{-iE_n t/\hbar}.
</math>
 
The probability density <math>|\psi_n(x,t)|^2</math> is therefore independent of time: eigenstates are stationary states.
Two qualitatively different situations may occur depending on the form of the potential.
 
=== Discrete and continuous spectra ===
 
 
* '''Discrete spectrum (bound states)'''
 
The energies take isolated values <math>E_n</math>. 
This typically happens when the particle is confined in a finite region
(for instance in a potential well).
 
The corresponding eigenfunctions are normalizable,
 
<math display="block">
\int dx\, |\psi_n(x)|^2 = 1,
</math>
 
and the particle remains localized in space. These states are called
bound states.
 
* '''Continuous spectrum (continuum states)'''
 
The energy can take any value in a continuous interval.
This occurs for instance for a free particle or for a particle with
energy above the confining potential.
 
A simple example is provided by plane waves
 
<math display="block">
\psi_k(x)=\frac{1}{\sqrt{2\pi}} e^{ikx},
\qquad
E=\frac{\hbar^2 k^2}{2m}.
</math>
These states are not normalizable in the usual sense. They are instead
normalized using Dirac delta functions,
 
<math display="block">
\int dx\, \psi_k^*(x)\psi_{k'}(x)=\delta(k-k').
</math>
 
They form a continuous basis that can be used to construct physical
wave packets.
 
=== Superposition principle ===
 
The Schrödinger equation is linear. As a consequence, any linear combination
of solutions is again a solution. This property is known as the
superposition principle.
 
If the spectrum is discrete, an arbitrary wavefunction can be expanded
in the basis of eigenstates
 
<math display="block">
\psi(x,t)=\sum_n c_n e^{-iE_n t/\hbar}\psi_n(x).
</math>
 
If the spectrum is continuous the expansion becomes an integral
 
<math display="block">
\psi(x,t)=\int dk\, c(k)\psi_k(x,t),
\qquad
\int dk\, |c(k)|^2=1.
</math>
 
By choosing the coefficients <math>c(k)</math> appropriately one can construct
a localized '''wave packet''' describing a particle initially confined in space.
 
 
In many physical situations the Hamiltonian has a mixed spectrum, containing both discrete bound states and continuum states. In this case a general wavefunction can be expressed as a superposition involving contributions from both sets of eigenstates.
A simple example is a finite potential well: it supports a finite number of bound states with discrete energies, while particles with higher energies belong to the continuum and correspond to scattering states.
 
=== Probability current ===
 
Besides the probability density one can define a '''probability current'''
 
<math display="block">
J(x,t)=\frac{\hbar}{2mi}
\left(
\psi^* \frac{d\psi}{dx}
-
\psi \frac{d\psi^*}{dx}
\right).
</math>
 
This quantity measures the '''flow of probability''' across a point in space.
 
Its expression follows from combining the Schrödinger equation with the
conservation of probability. Indeed the probability density
 
<math>
\rho(x,t)=|\psi(x,t)|^2
</math>
 
satisfies the continuity equation
 
<math display="block">
\partial_t \rho(x,t) + \partial_x J(x,t)=0,
</math>
 
which has the same structure as a conservation law in hydrodynamics.
 
For a plane wave
 
<math display="block">
\psi(x)=e^{ikx}
</math>
 
one finds
 
<math display="block">
J=\frac{\hbar k}{m}.
</math>
 
Thus plane waves describe particles propagating through space and carrying
a non–zero probability current.
 
If the wavefunction is real the probability current vanishes, since the two
terms in the expression of <math>J</math> cancel. This is the case for bound
states in one dimension: for a real potential the eigenfunctions can be
chosen real, and bound states in 1D are non–degenerate. Physically this
corresponds to a '''standing wave''' rather than a propagating wave.
 
=== Scattering states ===
 
Transport problems often involve a localized potential (for instance a sample
or a potential barrier) surrounded by free space. Outside this region the
solutions of the Schrödinger equation are plane waves.
 
When a particle interacts with the sample, the wavefunction generally contains
three contributions:
 
* an incoming wave,
* a reflected wave,
* a transmitted wave.
 
The corresponding solutions are called '''scattering states'''.
 
For example, a particle incoming from the left is described asymptotically by
 
<math display="block">
\psi_{k,L}(x)=
\begin{cases}
e^{ikx}+r\, e^{-ikx} & x\to -\infty \\
t\, e^{ikx} & x\to +\infty
\end{cases}
</math>
 
The first term represents the incoming wave, the second the reflected wave,
while the transmitted wave propagates to the right with amplitude <math>t</math>.
 
Using the expression of the probability current, one finds that a plane wave
<math>e^{ikx}</math> carries a current
 
<math display="block">
J=\frac{\hbar k}{m}.
</math>
 
Thus the incoming, reflected and transmitted waves correspond to incoming,
reflected and transmitted probability currents.
 
Since probability is conserved, the current must be the same on both sides
of the sample. This implies the relation
 
<math display="block">
R + T = 1,
</math>
 
where
 
<math display="block">
R = |r|^2, \qquad T = |t|^2
</math>
 
are the reflection and transmission probabilities.
 
== Free particles and ballistic behaviour ==
 
We now illustrate how a localized quantum particle evolves in the absence of disorder.
 
For a free particle the Hamiltonian reads
 
<math display="block">
H=-\frac{\hbar^2}{2m}\frac{d^2}{dx^2}.
</math>
 
As discussed above, the eigenstates of this Hamiltonian are plane waves with a continuous spectrum
 
<math display="block">
\psi_k(x,t)=\frac{1}{\sqrt{2\pi}}e^{ikx}e^{-iE_k t/\hbar},
\qquad
E_k=\frac{\hbar^2k^2}{2m}.
</math>
 
Since plane waves are completely delocalized, a physical particle must be described by a superposition of eigenstates, forming a '''wave packet'''
 
<math display="block">
\psi(x,t)=\int_{-\infty}^{\infty}dk\,c(k)\psi_k(x,t),
\qquad
\int_{-\infty}^{\infty}dk\,|c(k)|^2=1.
</math>
 
=== Evolution of a Gaussian wave packet ===
 
* '''Initial state'''
 
At time <math>t=0</math> consider a Gaussian wave packet
 
<math display="block">
\psi(x,0)=\frac{e^{-x^2/(4a^2)}}{(2\pi a^2)^{1/4}},
\qquad
|\psi(x,0)|^2=\frac{e^{-x^2/(2a^2)}}{\sqrt{2\pi a^2}}.
</math>
 
Show that the coefficients of the plane-wave decomposition are
 
<math display="block">
c(k)=\left(\frac{2a^2}{\pi}\right)^{1/4}e^{-a^2k^2}.
</math>
 
* '''Time evolution'''
 
Define the spreading velocity
 
<math display="block">
v_s=\frac{\hbar}{2ma}.
</math>
 
Show that the time evolution of the packet is
 
<math display="block">
\psi(x,t)=
\frac{e^{-x^2/(4a^2(1+i (v_s/a) t))}}
{[2\pi a^2(1+i (v_s/a) t)]^{1/4}}.
</math>
 
* '''Ballistic spreading'''
 
The probability density becomes
 
<math display="block">
|\psi(x,t)|^2=
\frac{e^{-x^2/(2a^2(1+(v_s/a)^2 t^2))}}
{\sqrt{2\pi a^2(1+(v_s/a)^2 t^2)}}.
</math>
 
Hence
 
<math display="block">
\sqrt{\langle x^2\rangle}
=
\left(\int dx\,x^2|\psi(x,t)|^2\right)^{1/2}
=
a\sqrt{1+(v_s/a)^2 t^2}.
</math>
 
At long times
 
<math display="block">
\sqrt{\langle x^2\rangle}\sim v_s t.
</math>
 
This linear growth is called '''ballistic spreading'''.
 
It should be contrasted with two other possible transport regimes:
 
* '''Diffusive motion'''  
<math>\sqrt{\langle x^2\rangle}\sim \sqrt{t}</math>
 
* '''Localized regime''' 
<math>\sqrt{\langle x^2\rangle}</math> saturates at long times.
 
Understanding how disorder modifies ballistic motion and eventually suppresses transport is the main goal of the following sections.
 
== Localization of the packet: general idea and experiment ==
 
[[File:Localization1DB.png|thumb|left|x240px|BEC condensate expanding in a 1D disordered potential. Billy et al., Nature (2008).]]
 
In 1958, P. Anderson proposed that disorder can suppress transport in quantum systems. This phenomenon, known as '''Anderson localization''', has since been observed both numerically and experimentally.
 
In the experiment shown here, a Gaussian packet of a Bose–Einstein condensate is prepared in a harmonic trap. When the trap is removed the cloud initially expands but quickly stops spreading and remains localized.
 
To understand this behaviour we must solve the eigenstate problem of the Hamiltonian in the presence of disorder.
 
[[File:Localization1dB.png|thumb|left|x140px|Semilog plot of the particle density. Billy et al., Nature (2008).]]
 
In a disordered potential an eigenstate of energy <math>E_k</math> has the form
 
<math display="block">
\psi_k(x,t)=\psi_k(x)e^{-iE_k t/\hbar}.
</math>
 
The spatial part of the wavefunction is localized around some position <math>\bar{x}</math> and decays exponentially
 
<math display="block">
\psi_k(x)\sim
e^{-|x-\bar{x}|/\xi_{\text{loc}}}.
</math>
 
Here <math>\xi_{\text{loc}}</math> is the localization length.
 
Because the eigenstates are localized, the wave packet is built from states localized near its initial position. Eigenstates far from the packet contribute exponentially little, and states composing the packet decay exponentially away from their center.
 
As a consequence transport far from the initial position of the particle is '''exponentially suppressed'''.
== Diffusive transport ==
In most materials weak disorder does not lead to localization but to diffusive transport. A simple microscopic description is provided by the Drude model.
 
Electrons in a metal do not start from rest. Even in the absence of an electric field they move with a typical velocity of order the Fermi velocity
 
<math display="block">
v_F=\frac{\hbar k_F}{m}.
</math>
 
Their motion is interrupted by scattering events with impurities, defects, or phonons. These collisions occur on average after a characteristic time <math>\tau</math>, called the '''mean free time'''.
 
Between two collisions electrons move essentially freely. The typical distance traveled during this time is the mean free path:
 
<math display="block">
\ell = v_F \tau .
</math>
 
The motion therefore has two distinct regimes:
 
* On length scales smaller than <math>\ell</math>, electrons propagate ballistically.
* On length scales much larger than <math>\ell</math>, repeated random scattering events lead to diffusion.
 
We now introduce an external electric field <math>E</math>. An electron of charge <math>-e</math> obeys the equation of motion
 
<math display="block">
m\frac{dv}{dt}=-eE.
</math>
 
Between two collisions the electron accelerates under the electric field. After each collision its velocity is randomized again. Averaging over many such scattering events leads to a small systematic drift velocity
 
<math display="block">
v_d=-\frac{eE\tau}{m}.
</math>
 
Note that this drift velocity is extremely small compared with the typical electron velocity, <math>
v_d \ll v_F </math>. Thus electrons move very rapidly with random directions, while the electric field only produces a tiny bias in this motion. If the electron density is <math>n</math>, the electric current density is
 
<math display="block">
j=-ne\,v_d.
</math>
 
Substituting the drift velocity gives
 
<math display="block">
j=\frac{ne^2\tau}{m}E.
</math>
 
This provides the microscopic origin of Ohm's law
 
<math display="block">
j=\sigma E,
\qquad
\sigma=\frac{ne^2\tau}{m}.
</math>
 
It is important to stress that the Drude model is purely '''classical'''. It ignores the wave nature of electrons and quantum interference effects. A fully quantum derivation of Ohm's law is much more subtle and typically relies on Green functions and diagrammatic methods.
 
In the following we will focus on the regime where quantum interference becomes important and can eventually suppress diffusion altogether, leading to localization.
 
== Conductance ==
 
The conductance <math>G</math> is the inverse of the resistance. Understanding how it depends on the system size will be the starting point for the scaling theory of localization.
 
=== Diffusive transport ===
 
Consider a wire of length <math>L</math> and cross section <math>S</math>. The total current is
 
<math display="block">
I=jS,
</math>
 
while the voltage drop is
 
<math display="block">
V=EL.
</math>
 
Using Ohm's law <math>j=\sigma E</math> we obtain
 
<math display="block">
I=\sigma \frac{S}{L} V.
</math>
 
Therefore
 
<math display="block">
G=\frac{I}{V}=\sigma \frac{S}{L}.
</math>
 
For a sample of linear size <math>L</math> in spatial dimension <math>d</math>, the cross section scales as
 
<math display="block">
S\sim L^{d-1}.
</math>
 
Hence
 
<math display="block">
G(L)\sim \sigma L^{d-2}.
</math>
 
This power-law scaling is the characteristic signature of diffusive transport.
 
=== Localized regime ===
 
When disorder is strong diffusion is suppressed and the system becomes insulating.
 
In Exercise 15 we studied transport using the Landauer picture. In this approach the conductance is proportional to the transmission probability through the sample:
 
<math display="block">
G=\frac{e^2}{\hbar}|t(E_F)|^2.
</math>
 
The factor <math>e^2/\hbar</math> sets the natural quantum scale of conductance for a single transport channel.
 
In a localized system the transmission probability typically decays exponentially with the system size
 
<math display="block">
|t(E_F)|^2 \sim e^{-2L/\xi_{\text{loc}}},
</math>
 
where <math>\xi_{\text{loc}}</math> is the localization length.
 
This leads to
 
<math display="block">
G(L)\sim e^{-2L/\xi_{\text{loc}}}.
</math>
 
Thus in the localized phase the conductance decreases exponentially with the system size.
 
== The “Gang of Four” scaling theory ==
 
The two behaviors discussed above raise a natural question: how does the conductance of a disordered system evolve when the system size is increased?
 
In a famous PRL (1979), Abrahams, Anderson, Licciardello and Ramakrishnan proposed a scaling theory of localization that addresses this question.
 
The key quantity is the '''dimensionless conductance'''
 
<math display="block">
g=\frac{G\hbar}{e^2}.
</math>
 
The factor <math>e^2/\hbar</math> is the natural quantum unit of conductance (see the Landauer formula). The quantity <math>g</math> therefore measures the effective number of conducting channels.
 
Instead of computing the conductance microscopically, the scaling theory studies how <math>g</math> evolves when the system size <math>L</math> is increased.
 
This evolution is described by the scaling equation
 
<math display="block">
\frac{d\ln g}{d\ln L}=\beta(g).
</math>
 
The function <math>\beta(g)</math> depends only on <math>g</math> and on the spatial dimension.
 
Two limiting regimes are known.
 
* '''Metallic regime''' (<math>g\gg1</math>)
 
Transport is diffusive. From the Drude result
 
<math display="block">
G(L)\sim L^{d-2},
</math>
 
we obtain
 
<math display="block">
\beta(g)\to d-2.
</math>
 
* '''Localized regime''' (<math>g\ll1</math>)
 
The conductance decreases exponentially
 
<math display="block">
g(L)\sim e^{-L/\xi_{\text{loc}}},
</math>
 
which implies
 
<math display="block">
\beta(g)\sim \ln g.
</math>
 
The simplest scenario is that the beta function is monotonic.
 
This leads to a striking dimensional prediction:
 
* for <math>d>2</math> the beta function changes sign and a '''metal–insulator transition''' exists
* for <math>d\le2</math> the beta function remains negative and '''all states are localized'''.
 
The scaling theory therefore predicts that in low dimension disorder inevitably destroys diffusion.
 
To understand how localization emerges microscopically, we must now study the spectrum and eigenstates of quantum particles moving in a random potential.

Latest revision as of 11:50, 9 March 2026

Goal. This lecture introduces the phenomenon of localization. Localization is a wave phenomenon induced by disorder that suppresses transport in a system.

Short recap: wavefunctions and eigenstates

Before discussing localization we briefly recall a few basic notions of quantum mechanics.

A quantum particle in one dimension is described by a wavefunction ψ(x,t). The quantity |ψ(x,t)|2 is the probability density of finding the particle at position x at time t. The wavefunction therefore satisfies the normalization condition

dx|ψ(x,t)|2=1.

The time evolution of the wavefunction is governed by the Schrödinger equation

itψ(x,t)=Hψ(x,t),

where H is the Hamiltonian of the system. For a particle moving in one dimension in a potential V(x), the Hamiltonian reads

H=22mx2+V(x).

Eigenstates

A particularly important class of solutions are the eigenstates of the Hamiltonian

Hψn(x)=Enψn(x).

If the particle is in an eigenstate the full solution reads

ψn(x,t)=ψn(x)eiEnt/.

The probability density |ψn(x,t)|2 is therefore independent of time: eigenstates are stationary states. Two qualitatively different situations may occur depending on the form of the potential.

Discrete and continuous spectra

  • Discrete spectrum (bound states)

The energies take isolated values En. This typically happens when the particle is confined in a finite region (for instance in a potential well).

The corresponding eigenfunctions are normalizable,

dx|ψn(x)|2=1,

and the particle remains localized in space. These states are called bound states.

  • Continuous spectrum (continuum states)

The energy can take any value in a continuous interval. This occurs for instance for a free particle or for a particle with energy above the confining potential.

A simple example is provided by plane waves

ψk(x)=12πeikx,E=2k22m. These states are not normalizable in the usual sense. They are instead normalized using Dirac delta functions,

dxψk*(x)ψk(x)=δ(kk).

They form a continuous basis that can be used to construct physical wave packets.

Superposition principle

The Schrödinger equation is linear. As a consequence, any linear combination of solutions is again a solution. This property is known as the superposition principle.

If the spectrum is discrete, an arbitrary wavefunction can be expanded in the basis of eigenstates

ψ(x,t)=ncneiEnt/ψn(x).

If the spectrum is continuous the expansion becomes an integral

ψ(x,t)=dkc(k)ψk(x,t),dk|c(k)|2=1.

By choosing the coefficients c(k) appropriately one can construct a localized wave packet describing a particle initially confined in space.


In many physical situations the Hamiltonian has a mixed spectrum, containing both discrete bound states and continuum states. In this case a general wavefunction can be expressed as a superposition involving contributions from both sets of eigenstates. A simple example is a finite potential well: it supports a finite number of bound states with discrete energies, while particles with higher energies belong to the continuum and correspond to scattering states.

Probability current

Besides the probability density one can define a probability current

J(x,t)=2mi(ψ*dψdxψdψ*dx).

This quantity measures the flow of probability across a point in space.

Its expression follows from combining the Schrödinger equation with the conservation of probability. Indeed the probability density

ρ(x,t)=|ψ(x,t)|2

satisfies the continuity equation

tρ(x,t)+xJ(x,t)=0,

which has the same structure as a conservation law in hydrodynamics.

For a plane wave

ψ(x)=eikx

one finds

J=km.

Thus plane waves describe particles propagating through space and carrying a non–zero probability current.

If the wavefunction is real the probability current vanishes, since the two terms in the expression of J cancel. This is the case for bound states in one dimension: for a real potential the eigenfunctions can be chosen real, and bound states in 1D are non–degenerate. Physically this corresponds to a standing wave rather than a propagating wave.

Scattering states

Transport problems often involve a localized potential (for instance a sample or a potential barrier) surrounded by free space. Outside this region the solutions of the Schrödinger equation are plane waves.

When a particle interacts with the sample, the wavefunction generally contains three contributions:

  • an incoming wave,
  • a reflected wave,
  • a transmitted wave.

The corresponding solutions are called scattering states.

For example, a particle incoming from the left is described asymptotically by

ψk,L(x)={eikx+reikxxteikxx+

The first term represents the incoming wave, the second the reflected wave, while the transmitted wave propagates to the right with amplitude t.

Using the expression of the probability current, one finds that a plane wave eikx carries a current

J=km.

Thus the incoming, reflected and transmitted waves correspond to incoming, reflected and transmitted probability currents.

Since probability is conserved, the current must be the same on both sides of the sample. This implies the relation

R+T=1,

where

R=|r|2,T=|t|2

are the reflection and transmission probabilities.

Free particles and ballistic behaviour

We now illustrate how a localized quantum particle evolves in the absence of disorder.

For a free particle the Hamiltonian reads

H=22md2dx2.

As discussed above, the eigenstates of this Hamiltonian are plane waves with a continuous spectrum

ψk(x,t)=12πeikxeiEkt/,Ek=2k22m.

Since plane waves are completely delocalized, a physical particle must be described by a superposition of eigenstates, forming a wave packet

ψ(x,t)=dkc(k)ψk(x,t),dk|c(k)|2=1.

Evolution of a Gaussian wave packet

  • Initial state

At time t=0 consider a Gaussian wave packet

ψ(x,0)=ex2/(4a2)(2πa2)1/4,|ψ(x,0)|2=ex2/(2a2)2πa2.

Show that the coefficients of the plane-wave decomposition are

c(k)=(2a2π)1/4ea2k2.

  • Time evolution

Define the spreading velocity

vs=2ma.

Show that the time evolution of the packet is

ψ(x,t)=ex2/(4a2(1+i(vs/a)t))[2πa2(1+i(vs/a)t)]1/4.

  • Ballistic spreading

The probability density becomes

|ψ(x,t)|2=ex2/(2a2(1+(vs/a)2t2))2πa2(1+(vs/a)2t2).

Hence

x2=(dxx2|ψ(x,t)|2)1/2=a1+(vs/a)2t2.

At long times

x2vst.

This linear growth is called ballistic spreading.

It should be contrasted with two other possible transport regimes:

  • Diffusive motion

x2t

  • Localized regime

x2 saturates at long times.

Understanding how disorder modifies ballistic motion and eventually suppresses transport is the main goal of the following sections.

Localization of the packet: general idea and experiment

BEC condensate expanding in a 1D disordered potential. Billy et al., Nature (2008).

In 1958, P. Anderson proposed that disorder can suppress transport in quantum systems. This phenomenon, known as Anderson localization, has since been observed both numerically and experimentally.

In the experiment shown here, a Gaussian packet of a Bose–Einstein condensate is prepared in a harmonic trap. When the trap is removed the cloud initially expands but quickly stops spreading and remains localized.

To understand this behaviour we must solve the eigenstate problem of the Hamiltonian in the presence of disorder.

Semilog plot of the particle density. Billy et al., Nature (2008).

In a disordered potential an eigenstate of energy Ek has the form

ψk(x,t)=ψk(x)eiEkt/.

The spatial part of the wavefunction is localized around some position x¯ and decays exponentially

ψk(x)e|xx¯|/ξloc.

Here ξloc is the localization length.

Because the eigenstates are localized, the wave packet is built from states localized near its initial position. Eigenstates far from the packet contribute exponentially little, and states composing the packet decay exponentially away from their center.

As a consequence transport far from the initial position of the particle is exponentially suppressed.

Diffusive transport

In most materials weak disorder does not lead to localization but to diffusive transport. A simple microscopic description is provided by the Drude model.

Electrons in a metal do not start from rest. Even in the absence of an electric field they move with a typical velocity of order the Fermi velocity

vF=kFm.

Their motion is interrupted by scattering events with impurities, defects, or phonons. These collisions occur on average after a characteristic time τ, called the mean free time.

Between two collisions electrons move essentially freely. The typical distance traveled during this time is the mean free path:

=vFτ.

The motion therefore has two distinct regimes:

  • On length scales smaller than , electrons propagate ballistically.
  • On length scales much larger than , repeated random scattering events lead to diffusion.

We now introduce an external electric field E. An electron of charge e obeys the equation of motion

mdvdt=eE.

Between two collisions the electron accelerates under the electric field. After each collision its velocity is randomized again. Averaging over many such scattering events leads to a small systematic drift velocity

vd=eEτm.

Note that this drift velocity is extremely small compared with the typical electron velocity, vdvF. Thus electrons move very rapidly with random directions, while the electric field only produces a tiny bias in this motion. If the electron density is n, the electric current density is

j=nevd.

Substituting the drift velocity gives

j=ne2τmE.

This provides the microscopic origin of Ohm's law

j=σE,σ=ne2τm.

It is important to stress that the Drude model is purely classical. It ignores the wave nature of electrons and quantum interference effects. A fully quantum derivation of Ohm's law is much more subtle and typically relies on Green functions and diagrammatic methods.

In the following we will focus on the regime where quantum interference becomes important and can eventually suppress diffusion altogether, leading to localization.

Conductance

The conductance G is the inverse of the resistance. Understanding how it depends on the system size will be the starting point for the scaling theory of localization.

Diffusive transport

Consider a wire of length L and cross section S. The total current is

I=jS,

while the voltage drop is

V=EL.

Using Ohm's law j=σE we obtain

I=σSLV.

Therefore

G=IV=σSL.

For a sample of linear size L in spatial dimension d, the cross section scales as

SLd1.

Hence

G(L)σLd2.

This power-law scaling is the characteristic signature of diffusive transport.

Localized regime

When disorder is strong diffusion is suppressed and the system becomes insulating.

In Exercise 15 we studied transport using the Landauer picture. In this approach the conductance is proportional to the transmission probability through the sample:

G=e2|t(EF)|2.

The factor e2/ sets the natural quantum scale of conductance for a single transport channel.

In a localized system the transmission probability typically decays exponentially with the system size

|t(EF)|2e2L/ξloc,

where ξloc is the localization length.

This leads to

G(L)e2L/ξloc.

Thus in the localized phase the conductance decreases exponentially with the system size.

The “Gang of Four” scaling theory

The two behaviors discussed above raise a natural question: how does the conductance of a disordered system evolve when the system size is increased?

In a famous PRL (1979), Abrahams, Anderson, Licciardello and Ramakrishnan proposed a scaling theory of localization that addresses this question.

The key quantity is the dimensionless conductance

g=Ge2.

The factor e2/ is the natural quantum unit of conductance (see the Landauer formula). The quantity g therefore measures the effective number of conducting channels.

Instead of computing the conductance microscopically, the scaling theory studies how g evolves when the system size L is increased.

This evolution is described by the scaling equation

dlngdlnL=β(g).

The function β(g) depends only on g and on the spatial dimension.

Two limiting regimes are known.

  • Metallic regime (g1)

Transport is diffusive. From the Drude result

G(L)Ld2,

we obtain

β(g)d2.

  • Localized regime (g1)

The conductance decreases exponentially

g(L)eL/ξloc,

which implies

β(g)lng.

The simplest scenario is that the beta function is monotonic.

This leads to a striking dimensional prediction:

  • for d>2 the beta function changes sign and a metal–insulator transition exists
  • for d2 the beta function remains negative and all states are localized.

The scaling theory therefore predicts that in low dimension disorder inevitably destroys diffusion.

To understand how localization emerges microscopically, we must now study the spectrum and eigenstates of quantum particles moving in a random potential.