Difference between revisions of "Applications of the spontaneous light force"

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== Optical Molasses ==
 
== Optical Molasses ==
  
=== The spontaneous light force ===
+
{{:Optical Molasses}
Consider a two-level atom with energy spacing <math>\omega_0</math>,
 
interacting with a single mode laser beam:
 
::[[Image:chapter1-intro-to-cooling-Lec1-twolevel.png|thumb|408px|none|]]
 
Let the laser intensity be <math>I</math>, and the interaction matrix element
 
between atom and light be <math>\hbar\omega_R = \vec{E}\cdot
 
| \langle 1|e\vec{r}|2{\rangle}|</math>, where <math>\omega_R</math> is known as the Rabi frequency,
 
<math>\vec{E}</math> is the electric field strength, and <math>e\vec{r}</math> is the dipole
 
moment of the atom.
 
 
 
It is useful to define a quantity known as the saturation intensity
 
<math>I_0</math> as the intensity of light at which the rabi frequency becomes
 
<math>\omega_R = \Gamma/\sqrt{2}</math>, where <math>\Gamma</math> is the spontaneous
 
emission rate (the natural decay rate of the atom from <math>|2{\rangle}</math> to
 
<math>|1{\rangle}</math>, excited to ground state).  This gives
 
:<math>
 
\frac{I}{I_0} = \frac{2\omega_R^2}{\Gamma^2}
 
\,.
 
</math>
 
The rate at which photons are scattered from the atom is known to be
 
:<math>
 
\gamma_s = \frac{\Gamma}{2} \frac{I/I_0}{1+\frac{I}{I_0} +
 
(2\delta/\Gamma)^2}
 
\,,
 
 
</math>
 
where <math>\delta</math> is the frequency detuning of the laser from the center
 
of resonance of the atom.  Two useful limits of this scattering rate
 
are
 
:<math>\begin{array}{rcl} 
 
\lim_{I\rightarrow\infty} \gamma_s &=& \frac{\Gamma}{2}
 
= \frac{1}{2\tau}
 
\\
 
\lim_{I\rightarrow I_0} \gamma_s &=& \frac{\Gamma}{4}
 
\,,
 
\end{array}</math>
 
where we have assumed <math>\delta=0</math> (resonant light).  These expressions
 
have a natural physical interpretation: in the limit of infinite
 
intensity, the atomic levels become equally populated between the
 
excited and ground state, and thus only half the atoms (the excited
 
ones) can scatter light.  Thus, the scattering rate is <math>\Gamma/2</math> in
 
that limit.
 
 
 
Suppose the force imparted by light on the atom is given by the recoil
 
of photons spontaneously emitted from the atom.  This force would then
 
be
 
:<math>
 
F = \hbar k \gamma_s
 
\,,
 
</math>
 
where <math>\hbar k</math> is the momentum of each photon.  This expression makes
 
several assumptions: that is is the net momentum transfer in absorption,
 
that there is no "stimulated" force, and that <math>\hbar k/m k \ll
 
\Gamma</math>, meaning that the jump in the Doppler shift is less than the
 
natural linewidth.
 
 
 
Typically, for alkali atoms, this force is <math>F\leq 10^5 g</math> times the
 
mass of an atom (<math>g</math> being the acceleration due to gravity). This
 
means that light can stop a sodium atom going at <math>1000</math> m/s in one
 
millisecond, or about half a meter.  In comparison to electrostatic
 
forces on ions, this is very small, however: it is comparable to the
 
force exerted by an electric field of 1 millivolt/cm on an ionized
 
sodium atom.
 
 
 
Moving atoms experience a Doppler shift, which we can model as a
 
frequency dependent force, based on Eq.(\ref{eq:ci:lorentzian}), as
 
:<math>
 
F = \hbar k \frac{\Gamma}{2} \frac{I/I_0}{1+\frac{I}{I_0} +
 
2\left[\frac{(2\delta+kv)}{\Gamma}\right]^2}
 
\,,
 
 
</math>
 
where <math>v</math> is the velocity of the atom.  The effect of a fixed laser
 
frequency on an ensemble of atoms is to modify their Maxwell-Boltzmann
 
thermal velocity distribution:
 
::[[Image:chapter1-intro-to-cooling-l1fig2.png|thumb|408px|none|]]
 
Note how the initial distribution changes to one with atoms piling up
 
below the velocity group resonant with the laser.  The atoms bunch.
 
Historically, this is the first method that was done to cool atoms to
 
Kelvin temperatures.
 
 
 
=== One-dimensional optical molasses ===
 
Let us now turn to a method which allows cooling of atoms to zero
 
velocity.  Consider two laser beams incident on an atom from opposite
 
directions.  We assume that the total force is the sum of the two
 
forces, ignore standing wave effects, and take the laser intensity to
 
be low compared with the saturation intensity, <math>I\ll I_0</math>.  Taking the
 
force to be the sum of two forces described by Eq.(\ref{eq:ci:vdf}),
 
we find that the two lorentzians sum to give the following force as a
 
function of velocity:
 
 
 
::[[Image:20090410-094308_light-force-fig2.png|thumb|500px|none|]]
 
The velocity dependent force is positive from one light beam, and
 
negative from the other.  With a detuning chosen such that force is
 
zero at zero velocity, the force around <math>v=0</math> can be expanded
 
linearly, giving
 
:<math>
 
F(v) = -\alpha v
 
\,,
 
</math>
 
where <math>\alpha</math> describes the viscosity imparted by the light
 
force to the atom, reflecting the restoring force applied when the
 
atom is not at zero velocity.  This configuration is known as an {\em
 
optical molasses}, because of this restoring force, which makes the
 
light behave like a thick, viscous medium for the atoms in it.
 
The damping coefficient <math>\alpha</math> can be calculated to be
 
:<math>
 
\alpha = 2\hbar k^2
 
\frac{(2I/I_0)(2\delta/\Gamma)}{\left(1+\left(\frac{2\delta}{\Gamma}\right)^2\right)^2}
 
\,.
 
</math>
 
 
 
=== The Doppler cooling limit ===
 
 
 
We have seen that the spontaneous light force, characterized by the
 
Lorentzian response of an atom to light, together with the Doppler
 
shift due to movement of the atom, gives a velocity dependent force,
 
which can be zero at zero velocity.  Does this mean that the atoms can
 
be cooled to zero temperature?
 
 
 
If the rate of energy loss due to cooling is
 
:<math>
 
\dot{E}_{\rm cool} = F v = -\alpha v^2 = -\frac{2\alpha}{M} E
 
\,,
 
</math>
 
then we should reach zero velocity, and zero temperature.  Indeed, the
 
kinetic energy decays exponentially.  However, the spontaneous force
 
has a random character, and thus has fluctuations which limit the
 
minimum temperature achievable.
 
 
 
==== Momentum diffusion limit ====
 
 
 
This limit is determined by momentum diffusion.  The force imparted
 
can be described by a random walk.  The final momentum is
 
:<math>
 
p_{\rm final}^{RMS} = \hbar k \sqrt{N}
 
\,,
 
</math>
 
on average, due to the random walk.  Note that the momentum spread is
 
:<math>\begin{array}{rcl} 
 
\langle p^2 \rangle  &=& (\hbar k)^2 v
 
\\
 
\frac{d \langle p^2{\rangle}}{dt} &=& (\hbar k)^2 \gamma_s
 
\,.
 
\end{array}</math>
 
This describes heating which arises due to photons randomly scattering
 
in all directions, such that the net momentum almost adds up to zero,
 
but not quite.  There is also a similar term due to absorption: some
 
atoms will absorb more or less photons, due to the Poissonian
 
statistics of absorption.
 
 
 
==== Time variation of kinetic energy ====
 
 
 
Thus, the time variation of the kinetic energy due to the fluctuating
 
forces is
 
:<math>
 
\dot{E}_{\rm heat} = \frac{2\hbar^2 k^2\gamma_s}{2M} = \frac{D}{M}
 
\,,
 
</math>
 
where <math>D</math> is the momentum diffusion coefficient
 
:<math>
 
D = \frac{ \langle p^2{\rangle}}{2}
 
\,,
 
</math>
 
which we'll later see is a correlation function of the fluctuation
 
forces.
 
 
 
==== Balance of heating and cooling ====
 
 
 
Let us now derive the Doppler limit for cooling.  In equilibrium,
 
<math>\dot{E}_{heat} = \dot{E}_{cool}</math>.  This means
 
:<math>
 
\frac{D}{M} = \frac{2\alpha}{M}E
 
\,.
 
</math>
 
The heating rate is independent of kinetic energy, whereas the cooling
 
rate is a function of kinetic energy.  So as the atoms cool down, the
 
cooling rate slows down, resulting in a final temperature equilibrium
 
being reached:
 
:<math>
 
2E_{final} = kT_{\rm doppler} = \frac{D}{\alpha}
 
</math>
 
<math>\alpha</math> is a viscosity parameter: it reflects transport.  <math>D</math>
 
reflects mobility.  Thus, this is an Einstein relation, a universal
 
expression in statistical mechanics resulting from the fundamental
 
theorem which relates dissipation to fluctuations.
 
 
 
==== The Doppler limit temperature ====
 
 
 
We've now obtained an expression for the Doppler limit temperature, a
 
limit on the temperature an ideal two-level atom can be cooled to by
 
laser beams,
 
:<math>
 
k T_{\rm doppler} = \frac{\hbar\Gamma}{2}
 
\,.
 
</math>
 
This optimal temperature is achieved for <math>I\ll I_0</math>, and detuning of
 
<math>\delta = -\Gamma/2</math> (half a linewidth).  Physically, at low
 
temperatures, the atom cannot determine whether the photon comes from
 
left or right; at higher temperatures, the atom can discriminate
 
whether photons come from left or right, thus cooling.  For sodium,
 
this temperature is <math>240</math> <math>\mu</math>K, corresponding to a velocity of <math>30</math>
 
cm/s.
 
 
 
 
 
=== 3D molasses, high intensities ===
 
 
 
To cool atoms along not just one axis, but along three axes, use six
 
counter-propagating laser beams.  This configuration is called a 3D
 
molasses.  Everything we've discussed in one dimension can be applied;
 
just sum up the forces.  Some care must be taken, however, if
 
interference patterns are created between the beams.  As long as the
 
atoms move a distance greater than the wavelength, interference may be
 
neglected.  But large field gradients can add extra forces and
 
heating.
 
 
 
One can also alternate between the six beams, but having simultaneous
 
beams actually turns out to be better, due to the interference between the beams.  In particular, it gives polarization gradients
 
and other subtle effects which provide extra cooling.  This wasn't initially forseen, but when implemented it was rapidly recognized that 3D cooling with six simultaneous beams was much more powerful than originally thought.
 
A significant landmark was achieved when, in 1985, Steve Chu used chirped slowing and a 3D molasses
 
configuration to obtain atoms colder than <math>1</math> mK, for the first time ([https://cua-admin.mit.edu:8443/wiki/images/4/47/Chu85_molasses.pdf  Original paper on optical molasses, Chu et al.]).
 
 
 
=== Cooling at high intensities ===
 
 
 
Let us consider an example, of laser cooling at high laser intensities.  Keep in mind that laser cooling works because <math>F=-\alpha v</math> and
 
<math>\alpha>0</math>.  Assume we have a detuning of about one linewith,
 
<math>\delta=-\Gamma</math>.  Now plot the friction coefficient <math>\alpha</math> as a function of intensity:
 
 
 
::[[Image:chapter1-intro-to-cooling-Lec1-high-inten.png|thumb|408px|none|]]
 
Initially, at small intensities, <math>\alpha</math> increases as a function of intensity.  Don't be
 
confused by the fact that the Doppler limit is achieved at low
 
intensities.  The diffusion coefficient is also linear in intensity at
 
low intensity.  <math>\alpha</math> increases with <math>I/I_0</math> at first, and peaks
 
around <math>0.5</math>, but above the saturation limit <math>\alpha</math> actually changes
 
sign and starts heating.  When <math>\alpha<0</math> then, counter-intuitively,
 
blue detuned light can be used to cool atoms. 
 
 
 
==== Cooling with blue detuned light ====
 
 
 
This is a
 
non-trivial result (where does the energy go?), which can be undersood in the
 
context of the optical Bloch equation and the dressed atom model (see [https://cua-admin.mit.edu:8443/wiki/images/a/af/Ashk83_Earnshaw.pdf Gordon and Ashkin]).
 
Specifically, the underlying physical reason which allows blue detuned light to cool is that
 
at low intensities, the force seen by an atom comes from adding to
 
Lorentzians, as we have seen; this fails at higher intensities, however.
 
In particular, the optical Bloch equation component <math>u</math> combines with the usual steady state term a new a
 
velocity dependent term:
 
:<math>
 
u = u_{st} + v()
 
\,.
 
</math>
 
One can approximate that <math>u(\vec{r}) \approx
 
u_{st}(\vec{r}-\vec{v}\Delta t</math>
 
When you average the light force in the standing wave over an optical
 
wavelength, then you find an average force which is a friction force,
 
:<math>
 
        \vec{F} = -\alpha \vec{v}
 
</math>
 
At weak intensities, <math>\alpha_{sw} = 2\alpha_{tw}</math>, but at high
 
intensities <math>\alpha</math> changes sign.
 
 
 
=== Momentum and spatial diffusion ===
 
 
 
Let us return to the physics of the randomness of spontaneous light force induced cooling, and revisit the behavior of the diffusion of the cooled atom's momentum and spatial position.  We shall see that the physical balance involved is an excellent example of the important fluctuation-dissipation theorem of statistical mechanics.
 
 
 
==== Momentum diffusion ====
 
First, consider diffusion of the momentum of an atom being cooled.
 
The momentum diffusion coefficient is defined as
 
:<math>\begin{array}{rcl} 
 
2D^p = \frac{d}{dt}  \langle (p- \langle p{\rangle}^2)^2{\rangle}
 
\,.
 
\end{array}</math>
 
This can be directly calculated if we have a fluctuating force, using
 
the fact that <math>d\vec{p}/dt = \vec{f}</math> is a force:
 
:<math>\begin{array}{rcl} 
 
2D^p &=& \frac{d}{dt} \left[
 
  {\langle}\vec{p}\cdot\vec{p}{\rangle}-{\langle}\vec{p}{\rangle}{\langle}\vec{p} \rangle  \right]
 
\\
 
&=& 2 \left[
 
  {\langle}\vec{p}\cdot\vec{f}{\rangle}-{\langle}\vec{p}{\rangle}{\langle}\vec{f} \rangle  \right]
 
\\ &=& 2 \int^0_{-\infty}
 
  {\langle}\vec{f}(0) \cdot \vec{f}(t)  \rangle  - \langle  \vec{f}(0) {\rangle}{\langle}
 
  \vec{f}(t) \rangle  \, dt
 
\,,
 
\end{array}</math>
 
showing that the diffusion is given by the integral of the force-force
 
correlation function.  Essentially:
 
:<math>\begin{array}{rcl} 
 
2D^p
 
&=& 2 \int^0_{-\infty}  \langle  \vec{f}(t) \cdot \vec{f}(0)  \rangle  \, dt
 
\,.
 
\end{array}</math>
 
This results due to the fluctuation-dissipation theorem.
 
 
 
=== Spatial diffusion ===
 
This is less frequently discussed in the literature compared with
 
momentum diffusion, but it is of practical importance in
 
experiments. Suppose the atoms start in a single point, embedded in a
 
3D optical molasses.  How does the point distribution expand?  On the
 
time scale determined by <math>\alpha</math>, the atoms loose their memory of
 
their original velocities.  The molasses has a nearly perfect thermal
 
distribution, despite atoms in the cloud never interacting with each
 
other, because they thermalize to the laser beam.
 
 
 
The damping time is
 
:<math>
 
\frac{1}{\gamma} = \frac{M}{\alpha}
 
\,.
 
</math>
 
Spatial diffusion can be described by a random walk (in space), with a
 
step size <math>L</math> given by the RMS velocity of the atoms and the damping
 
time,
 
:<math>
 
\ell = 2 \frac{v_{rms}}{\gamma}
 
\,,
 
</math>
 
where the extra factor of <math>2</math> comes from a more rigorous treatment.
 
Thus, starting from a point distribution, by the standard random walk
 
result, after time <math>t_d</math>, we obtain
 
:<math>
 
\langle r^2 \rangle  = 2 \ell^2 t_d \gamma
 
\,,
 
</math>
 
where the number of steps is <math>t_d\gamma</math>.  This is
 
:<math>\begin{array}{rcl} 
 
\langle r^2 \rangle  &=& 2 \frac{v_{rms}^2}{\gamma} t_d
 
\\
 
\frac{D^p t_d}{\alpha^2}
 
\,.
 
\end{array}</math>
 
Now recall the definition
 
:<math>
 
\langle r^2 \rangle  = 2 D^x t_d
 
\,,
 
</math>
 
where <math>D^x</math> is the spatial diffusion coefficient.
 
This gives a relation between the spatial and momentum diffusion
 
coefficients,
 
:<math>
 
D^x = \frac{D^p}{\alpha^2} = \frac{KT}{\alpha}
 
\,.
 
</math>
 
Note the similarity of this expression with the Einstein relation for
 
carriers in semiconductors, <math>D/\mu = kT/q</math>.
 
 
 
These expressions are useful in the laboratory context, as an example
 
illustrates.  How long does a typical trapped alkali atom (eg cesium
 
or sodium) take to diffuse out by <math>0.5</math> cm at the Doppler temperature?
 
Using the formulas above, we get <math>t_d = 1</math> second.  This is very
 
accessible in the laboratory, and is one of the reasons why optical
 
molasses are so useful in practice.
 
  
 
== Beam slowing ==
 
== Beam slowing ==

Revision as of 20:02, 15 April 2009

Spontaneous emission leads to a redistribution of momentum of an atom, absorbed from incident photons. Here, we discuss three applications of this spontaneous light force:

  • Optical Molasses
  • Beam Slowing
  • Magneto-Optical Traps

Optical Molasses

{{:Optical Molasses}

Beam slowing

We have previously looked at cooling with two laser beams, focusing on the idea that if you want to cool, you need a force which is linear with velocity. Now, let us see how you can cool with a single laser beam. That is what you do when you have a single atomic beam. With a single laser beam, you can not only slow them down, but also bunch them up, obtaining the same velocity distribution you get with a molassas. This is the only example of laser cooling I know of which has a very simple, closed form solution, which is possible because there is only one laser beam.

Imagine, if you have a single Lorentzian, how can you cool? Generically, you need a ``lock point, which is stable and has atoms moving to that point in phase space from either velocity direction. With a single beam you don't apparently have such, but as we shall see there is something else interesting that can be done.

Consider a single beam of atoms, with this velocity distribution. Using a laser, you can push some of the atoms to become cooler (red line below), bunching them up in a lower velocity regime, and leaving atoms faster than some velocity unchanged. What do you have to do if you want to bunch all the atoms at zero velocity? It becomes clear that you want more than one laser frequency, for example. By applying a broad range of frequencies which cover the whole velocity distribution, you can slow down all the atoms. There are several techniques using such an approach, known as white light slowing, or diffuse light slowing. But none of those are as powerful as {\em chirpedd slowing} and {\em Zeeman slowing}, the techniques of choice in modener laser cooling.


Chirped slowing

The idea behind chirped slowing is to get the atoms to "ride the surf". In other words, the frequency chirp of the laser beam and the deceleration of the atoms should be synchronized.

Balance of equations

Step 1

The force on an atom in the beam due to the light is

Let denote the atom's acceleration. Let us assume a frame of reference and experimental setup such that , , , . We can call , where is the atom's mass.

Step 2

The scheme begins by selecting the deceleration desired, some . Then set , and look for a to obtain this desired force. This will exist if

Step 3

Next, select an initial velocity such that . is the detuning for this "targeted" velocity group, so we must provide a laser with frequency in the lab frame of . The atom's velocity will differ from the desired target group by .

Step 4

With these definitions, we now have

in the frame of reference of the atoms in the target velocity group.

Step 5

Transforming into this decelerating frame, we get a fictitious force with is , and

This second term has the same structure as the first, but it is velocity independent. Note that this is exact, and valid for arbitrary . All we've done is to substitute definitions, so far, but they provide useful intuition.

Note that for small , this force is linear in velocity, .

Decelerating Frame

In the lab frame, we have a force which is a positive Lorentzian. In the decelerating frame, we had to add (the inertial force), so this Lorentzian shifts down, when we plot the total force as a function of the velocity in the decelerating frame :

Chapter1-intro-to-cooling-Lec1-beam-slowing-lock.png

Therefore, there is now a stable "lock" point, where as a function of . In other words, when the atoms have a negative velocity , the atoms all accelerate towards zero velocity (in the decelerating frame). And when atoms have a small positive velocity, they also move towards . In contrast the point where the Lorentzian has at , is unstable.

Thus, we may write, as we did with the molasses, an expression for the linearized force around this point, , in which . There is also randomness, as there was in the optical molassas case, for which we may calculate a momentum diffusion coefficient, and we find that . Thus, the final temperature limit of the beam is actually the same as that achievable with a molasses: .


We've seen that one laser can bunch up atoms from a beam at a single velocity. Physically, what happens is that if the atoms fall behind, the light does not interact with them, but if the atoms are too fast, the laser cools them, much like in the molasses case.

Graphical summary

Here is a graphical summary of what we've learned about beam slowing. In the decelerating frame, this is the situation. Change sign, so that in the frame the decelerating force is positive, for this graph:

Chapter1-intro-to-cooling-Lec1-bs-velocity.png

Initially, our zero force point is at the targeted velocity . All atoms at larger velocity experience a constant positive force, accelerating them. After a later time , the tail of the maxwell-Boltzmann distribution is pushed to higher velocities. The peak of distribution of atoms grows higher and higher with time, while the positive tail moves to higher velocities.

This is the description in the decelerating frame.

In the lab frame, we shift from back to . This means that we just shift all the distributions down in velocity. We start with a broad distribution at . There is a velocity group at which is on resonance with the laser beam. As time goes on, the laser beam chirps, causing more and more atoms to come into resonance, piling them up in a lower velocity class. What happens is that after the laser beam is switched off, you may still have a low velocity tail which is not reached by the laser, but you have a huge peak of atoms that have been cooled:

Chapter1-intro-to-cooling-Lec1-bs-lab-frame.png

All the atoms at lower velocities are pushed up in velocity until they stack up at , producing a narrow distribution around .

The width of this narrow velocity distribution is given by , which is proportional to .

Beam cooling is actually the simplest and cleanest example of laser cooling. It has the same physics as the molasses case, with the second beam being replaced in a sense by a ficticious force. Note that in the two-beam molasses case, there are more complications, since one should really consider interference effects.

Energy conservation in laser cooling

Kinetic energy conservation

Where does the lost kinetic energy go, in cooling the atoms? In the beam cooling scenario, for example, you have moved a large number of atoms from high velocities to low velocities. How can this be reconciled with energy conservation? Well, there are only several possibilities for where the energy can go. In particular, there is light scattered by the atoms, and the energy is radiated away by spontaneous emission, as we shall now see.

Absorption is responsible for momentum change, and emission is responsible for energy conservation. Light emitted by the atom is at the resonant energy , but can be absorbed when the photon is just slightly less than . The emission is isotropic, whereas the incident light is directed and Doppler shift dependent.

Chapter1-intro-to-cooling-Lec1-energy.png

Doppler cooling can be explained in this picture. Incident laser light is detuned below ("red detuned"), whereas emitted photons are, on average, at a higher frequency, so more energy is emitted than is absorbed, when an atom is cooled.

Energy conservation in general cooling schemes

The same intuition can be applied to all cooling schemes, including those used to cool solids and liquids. Phonon assisted absorption is balanced against emission, resulting in cooling:

Chapter1-intro-to-cooling-Lec1-cooling-solid.png

How hard is it to cool liquids and solids? Consider a system at K; that gives the phonon energy. Then Kelvin. In practice, there is a lower than unity fluorescence quantum yield, because there are non-radiative ways to exit the excited state. The cooling will be efficient, however, only when the quantum yield is higher than , which is typically unrealistic. Cooling with laser light is therefore not typically practical, for systems other than atoms, which have a unity fluorescence quantum yield. Molecules are hard, because they have non-radiative de-excitation pathways.


References