Applications of the spontaneous light force

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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

An optical molasses is formed by laser cooling of atoms using the spontaneous light force. We study this first by reviewing the spontaneous light force, then investigating a one-dimensional molasses. This provides an excellent scenario to establish an important limit to laser cooling, the Doppler limit, beyond which laser Doppler cooling fails due to the balance established between momentum loss and diffusion of momentum due to the randomness of the classical light field. We then describe the three-dimensional molasses, and conclude with a discussion of laser cooling as an illustration of the fluctuation-dissipation theorem of statistical physics.

The spontaneous light force

Consider a two-level atom with energy spacing $\omega _{0}$, interacting with a single mode laser beam:

Let the laser intensity be $I$, and the interaction matrix element between atom and light be $\hbar \omega _{R}={\vec {E}}\cdot |\langle 1|e{\vec {r}}|2{\rangle }|$, where $\omega _{R}$ is known as the Rabi frequency, ${\vec {E}}$ is the electric field strength, and $e{\vec {r}}$ is the dipole moment of the atom.

It is useful to define a quantity known as the saturation intensity $I_{0}$ as the intensity of light at which the rabi frequency becomes $\omega _{R}=\Gamma /{\sqrt {2}}$, where $\Gamma$ is the spontaneous emission rate (the natural decay rate of the atom from $|2{\rangle }$ to $|1{\rangle }$, excited to ground state). This gives

${\frac {I}{I_{0}}}={\frac {2\omega _{R}^{2}}{\Gamma ^{2}}}\,.$

The rate at which photons are scattered from the atom is known to be

$\gamma _{s}={\frac {\Gamma }{2}}{\frac {I/I_{0}}{1+{\frac {I}{I_{0}}}+(2\delta /\Gamma )^{2}}}\,,$

where $\delta$ is the frequency detuning of the laser from the center of resonance of the atom. Two useful limits of this scattering rate are

${\begin{array}{rcl}\lim _{I\rightarrow \infty }\gamma _{s}&=&{\frac {\Gamma }{2}}={\frac {1}{2\tau }}\\\lim _{I\rightarrow I_{0}}\gamma _{s}&=&{\frac {\Gamma }{4}}\,,\end{array}}$

where we have assumed $\delta =0$ (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 $\Gamma /2$ 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

$F=\hbar k\gamma _{s}\,,$

where $\hbar k$ 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 $\hbar k/mk\ll \Gamma$, meaning that the jump in the Doppler shift is less than the natural linewidth.

Typically, for alkali atoms, this force is $F\leq 10^{5}g$ times the mass of an atom ($g$ being the acceleration due to gravity). This means that light can stop a sodium atom going at $1000$ 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

$F=\hbar k{\frac {\Gamma }{2}}{\frac {I/I_{0}}{1+{\frac {I}{I_{0}}}+\left[{\frac {2(\delta +kv)}{\Gamma }}\right]^{2}}}\,,$

where $v$ 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:

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, $I\ll I_{0}$. 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:

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 $v=0$ can be expanded linearly, giving

$F(v)=\alpha v\,,$

where $\alpha$ 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 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 $\alpha$ can be calculated to be

$\alpha =2\hbar k^{2}{\frac {(2I/I_{0})(2\delta /\Gamma )}{\left(1+\left({\frac {2\delta }{\Gamma }}\right)^{2}\right)^{2}}}\,.$

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

${\dot {E}}_{\rm {cool}}=Fv=-\alpha v^{2}=-{\frac {2\alpha }{M}}E\,,$

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

$p_{\rm {final}}^{RMS}=\hbar k{\sqrt {N}}\,,$

on average, due to the random walk. Note that the momentum spread is

${\begin{array}{rcl}\langle p^{2}\rangle &=&(\hbar k)^{2}N\\{\frac {d\langle p^{2}{\rangle }}{dt}}&=&(\hbar k)^{2}\gamma _{s}\,.\end{array}}$

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 fewer photons, due to the Poissonian statistics of absorption.

Time variation of kinetic energy

The time variation of the kinetic energy due to the spontaneous emission is forces is

${\dot {E}}_{\rm {heat}}^{\rm {em}}={\frac {\hbar ^{2}k^{2}\gamma _{s}}{2M}}={\frac {D^{\rm {em}}}{M}}\,,$

where $D$ is the momentum diffusion coefficient

$D={\frac {1}{2}}{\frac {\mathrm {d} }{\mathrm {d} t}}\left(\langle p^{2}\rangle -\langle p\rangle ^{2}\right)\,,$

And $D^{\rm {em}}$ is $D$ in the special case that we only consider the heating due to spontaneous emission. Later we'll see that $D$ is a correlation function of the force fluctuations.

Accounting for the Poissonian variance in number of absorbed photons adds a factor of two to the heating rate, which yields

${\dot {E}}_{\rm {heat}}={\frac {2\hbar ^{2}k^{2}\gamma _{s}}{2M}}={\frac {D}{M}}\,,$

Balance of heating and cooling

Let us now derive the Doppler limit for cooling. In equilibrium, ${\dot {E}}_{heat}={\dot {E}}_{cool}$. This means

${\frac {D}{M}}={\frac {2\alpha }{M}}E\,.$

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:

$2E_{final}=kT_{\rm {doppler}}={\frac {D}{\alpha }}$

$\alpha$ is a viscosity parameter: it reflects transport. $D$ 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,

$kT_{\rm {doppler}}={\frac {\hbar \Gamma }{2}}\,.$

This optimal temperature is achieved for $I\ll I_{0}$, and detuning of $\delta =-\Gamma /2$ (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 $240$ $\mu$K, corresponding to a velocity of $30$ 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 $1$ mK, for the first time (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 $F=-\alpha v$ and $\alpha >0$. Assume we have a detuning of about one linewith, $\delta =-\Gamma$. Now plot the friction coefficient $\alpha$ as a function of intensity:

Initially, at small intensities, $\alpha$ 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. $\alpha$ increases with $I/I_{0}$ at first, and peaks around $0.5$, but above the saturation limit $\alpha$ actually changes sign and starts heating. When $\alpha <0$ 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 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 two Lorentzians, as we have seen; this fails at higher intensities, however. In particular, the optical Bloch equation component $u$ combines with the usual steady state term a new a velocity dependent term:

$u=u_{st}+v()\,.$

One can approximate that $u({\vec {r}})\approx u_{st}({\vec {r}}-{\vec {v}}\Delta t)$ 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,

${\vec {F}}=-\alpha {\vec {v}}$

At weak intensities, $\alpha _{sw}=2\alpha _{tw}$, but at high intensities $\alpha$ 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

${\begin{array}{rcl}2D^{p}={\frac {d}{dt}}\langle (p-\langle p{\rangle })^{2}{\rangle }\,.\end{array}}$

This can be directly calculated if we have a fluctuating force, using the fact that $d{\vec {p}}/dt={\vec {f}}$ is a force:

${\begin{array}{rcl}2D^{p}&=&{\frac {d}{dt}}\left[{\langle }{\vec {p}}\cdot {\vec {p}}{\rangle }-{\langle }{\vec {p}}{\rangle }{\langle }{\vec {p}}\rangle \right]\\&=&2\left[{\langle }{\vec {p}}\cdot {\vec {f}}{\rangle }-{\langle }{\vec {p}}{\rangle }{\langle }{\vec {f}}\rangle \right]\\&=&2\int _{-\infty }^{0}{\langle }{\vec {f}}(0)\cdot {\vec {f}}(t)\rangle -\langle {\vec {f}}(0){\rangle }{\langle }{\vec {f}}(t)\rangle \,dt\,,\end{array}}$

showing that the diffusion is given by the integral of the force-force correlation function. Essentially:

${\begin{array}{rcl}2D^{p}&=&2\int _{-\infty }^{0}\langle {\vec {f}}(t)\cdot {\vec {f}}(0)\rangle \,dt\,.\end{array}}$

This results due to the fluctuation-dissipation theorem.

Spatial diffusion

Spatial diffusion 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 $\alpha$, 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

${\frac {1}{\gamma }}={\frac {M}{\alpha }}\,.$

Spatial diffusion can be described by a random walk (in space), with a step size $\ell$ given by the RMS velocity of the atoms and the damping time,

$\ell ={\frac {v_{rms}}{\gamma }}\,,$

Thus, starting from a point distribution, by the standard random walk result, after time $t_{d}$, we obtain

$\langle r^{2}\rangle =2\ell ^{2}t_{d}\gamma \,,$

where the number of steps is $t_{d}\gamma$ and the extra factor of $2$ comes from a more rigorous treatment.. This is

${\begin{array}{rcl}\langle r^{2}\rangle &=&2{\frac {v_{rms}^{2}}{\gamma }}t_{d}\\=2{\frac {D^{p}t_{d}}{\alpha ^{2}}}\,.\end{array}}$

Now recall the definition

$\langle r^{2}\rangle =2D^{x}t_{d}\,,$

where $D^{x}$ is the spatial diffusion coefficient. This gives a relation between the spatial and momentum diffusion coefficients,

$D^{x}={\frac {D^{p}}{\alpha ^{2}}}={\frac {kT}{\alpha }}\,.$

Note the similarity of this expression with the Einstein relation for carriers in semiconductors, $D/\mu =kT/q$.

Example: laser cooling of sodium atoms

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 $0.5$ cm at the Doppler temperature? Using the formulas above, we get $t_{d}=1$ second. This is very accessible in the laboratory, and is one of the reasons why optical molasses are so useful in practice.

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 molasses. 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 chirped slowing} and {\em Zeeman slowing}, the techniques of choice in modern 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

$F=-\hbar k{\frac {\Gamma }{2}}{\frac {I/I_{0}}{1+I/I_{0}+\left[{\frac {2(\delta +kv)}{\Gamma }}\right]^{2}}}$

Let $a$ denote the atom's acceleration. Let us assume a frame of reference and experimental setup such that $a<0$, $v>0$, $k>0$, $a_{max}>0$. We can call $\hbar k\Gamma /2=Ma_{max}$, where $M$ is the atom's mass.

Step 2

The scheme begins by selecting the deceleration desired, some $a<0$. Then set $F=-Ma$, and look for a $\delta '=\delta +kv$ to obtain this desired force. This will exist if

$|a|<{\frac {I/I_{0}}{1+I/I_{0}}}a_{max}\,.$

Step 3

Next, select an initial velocity $v_{0}$ such that $v(t)=v_{0}+at$. $\delta '$ is the detuning for this "targeted" velocity group, so we must provide a laser with frequency in the lab frame of $\delta (t)=\delta '-kv(t)$. The atom's velocity will differ from the desired target group by $v'=v-v(t)$.

Step 4

With these definitions, we now have

$F=-\hbar k{\frac {\Gamma }{2}}{\frac {I/I_{0}}{1+I/I_{0}+\left[{\frac {2(\delta '+kv')}{\Gamma }}\right]^{2}}}\,,$

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 $F_{fict}=-Ma$, and

$F'(v')=Ma_{max}\left[{\frac {I/I_{0}}{1+I/I_{0}+\left[{\frac {2(\delta '+kv')}{\Gamma }}\right]^{2}}}+{\frac {I/I_{0}}{1+I/I_{0}+\left[{\frac {2(\delta ')}{\Gamma }}\right]^{2}}}\right]$

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

Note that for small $v'$, this force is linear in velocity, $F'(v')=-\alpha v'$.

Decelerating Frame

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

Therefore, there is now a stable "lock" point, where $F'=0$ as a function of $v'$. In other words, when the atoms have a negative velocity $v'$, the atoms all accelerate towards zero velocity (in the decelerating frame). And when atoms have a small positive velocity, they also move towards $v'=0$. In contrast the point where the Lorentzian has $F'(v')=0$ at $v'>0$, is unstable.

Thus, we may write, as we did with the molasses, an expression for the linearized force around this point, $F'(v')=-\alpha v'$, in which $\alpha _{beam}=\alpha _{molasses}/2$. There is also randomness, as there was in the optical molasses case, for which we may calculate a momentum diffusion coefficient, and we find that $D_{beam}=D_{molasses}/2$. Thus, the final temperature limit of the beam is actually the same as that achievable with a molasses: $kT_{beam}=kT_{molasses}$.

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:

Initially, our zero force point is at the targeted velocity $v_{0}$. All atoms at larger velocity experience a constant positive force, accelerating them. After a later time $t$, 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 $v'$ back to $v$. This means that we just shift all the distributions down in velocity. We start with a broad distribution at $t=0$. There is a velocity group at $t=0$ 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:

All the atoms at lower velocities are pushed up in velocity until they stack up at $v_{0}$, producing a narrow distribution around $v_{0}$.

The width of this narrow velocity distribution is given by $k_{B}T=D/\alpha$, which is proportional to ${\sqrt {kT_{beam}}}/M$.

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 $\omega _{0}$, but can be absorbed when the photon is just slightly less than $\omega _{0}$. The emission is isotropic, whereas the incident light is directed and Doppler shift dependent.

Doppler cooling can be explained in this picture. Incident laser light is detuned below $\omega _{0}$ ("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:

How hard is it to cool liquids and solids? Consider a system at $T=1$K; that gives the phonon energy. Then $\hbar \omega =25,000$ 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 $1-1/25000$, 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.

Magneto-Optical Traps

The Magneto-Optical Trap (MOT) is a configuration of atoms in laser cooling beams and coils producing static magnetic fields, which is astonishingly effective in cooling atoms from room temperature to microkelvin scale temperatures. Today, the MOT is a workhorse of atomic physics, and the starting point for many atomic physics experiments, such as with Bose-Einstein condensates.

We begin our study of the MOT with an explanation of how it was originally thought to be impossible, due to the optical Earnshaw theorem. We then present the physics of two-level atoms in a one-dimensional MOT, from which generalization to 3D MOT's trapping real multi-level atoms is straightforward.

Optical Earnshaw Theorem

Some history helps place the MOT in context. In the 1970's and 1980's, many people discussed prospects for, and limitations of the stimulated and spontaneous force. In 1983, Gordon and Ashkin derived the optical Earnshaw theorem. The (standard, electromagnetic) Earnshaw theorem states that a charged particle will never be in a stable equilibrium in a static, 3D configuration of electric fields. This holds because for a particle to be stable, all field lines must point inwards, but we know that the divergence of the electric field in vacuum is zero.

The optical Earnshaw theorem states, in a similar way, that a 3D sponteneous light force trap is not possible. This was not a very positive start for atom trapping. The proof goes as follows. Recall that the sponeaneous light force is related to the Poynting vector as

${\vec {F}}_{S}=c{\vec {S}}\,,$

where ${\vec {S}}$ is the Poynting vector. From electromagnetism, however, we know that

${\frac {\partial U}{\partial t}}+{\vec {\nabla }}\cdot {\vec {S}}=0\,,$

but we know that ${\vec {\nabla }}\cdot {\vec {F}}_{S}=0$ if there is zero local energy density $U$. This contradicts the requirement that ${\vec {\nabla }}\cdot {\vec {F}}_{S}<0$.

Where is the flaw in this reasoning? In 1986, David Pritchard realized there were many ways to circumvent the optical Earnshaw theorem. What is ignored here is the {\em internal structure of the atom}. After all, the spontaneous light force is actually not just proportional to the incident light flux. The assumption that every atom which is exposed to the same Poynting vector experiences the same force, is just wrong. Namely,

$\nabla (c({\vec {r}}){\vec {S}}({\vec {v}}))\neq 0\,.$

The force can thus be spatially dependent. First, $c({\vec {r}})$ can experience saturation. Second, optical pumping can be used, taking advantage of internal structure of the atoms. Third, there can be line shifts due to external static fields, as when hyperfine states are used which are magnetic field sensitive.

The perfect solution was demonstrated in 1987, in a collaboration between MIT (paper by Raab et al) and Steve Chu's group at Bell Labs.

1-dimensional MOT

Consider two counterpropagating laser beams with opposite circular polarizations, incident on some atoms, in the presence of a static magnetic field gradient:

The energy levels of three hyperfine levels, with $m=0$ and $m=\pm 1$, become a function of space due to the magnetic field, so that the $\sigma _{-}$ and $\sigma _{+}$ polarized light beams interact with spatially localized classes of atoms:

This scenario is similar to an optical molasses, but the frequency shifts $\pm Bz$ are due to a magnetic field gradient $\beta =\mu B'/\hbar$. Just as in the molasses analysis, we must add the effects of the left and right laser beams. Assume we have low intensity, so we find that

$F=F_{R}+F_{L}={\frac {\hbar k\Gamma }{2}}\left[{\frac {I/I_{0}}{1+4\left({\frac {\delta -kv-\beta z}{\Gamma }}\right)^{2}}}-\cdots \right]$

For small $v$, $z$,

$F(v,z)={\frac {\hbar k\Gamma }{2}}\left[-kv-\beta z\right]$

The equation of motion for the atom is thus that of a harmonic oscillator, because the force is linear with displacement:

${\ddot {z}}+v{\dot {z}}+\omega _{\rm {trap}}^{2}z=0\,,$

where the trap frequency is given by the ratio of the light momentum $k$ and the field gradient strenght $\beta$,

$\omega _{\rm {trap}}\propto {\frac {\beta }{k}}\,.$

Typically, experimental parameters lead this to be an overdamped harmonic oscillator, with $\omega _{\rm {trap}}\sim 2\pi \times 1$ kHz, and a damping time of about $50$ $\mu$s. The static well depth is usually around a few Kelvin, but the dynamic depth is even larger. The dynamic depth refers to how much kinetic energy an atom can get before it is recaptured by the trap, because it is cooled by optical molasses effects even after it leaves the local potential well.

3D MOT trapping with real atoms

Real atoms have a multilevel structure, with complicated hyperfine structure. If you have a complicated ground state structure, you need to include optical pumping effects between all the levels, but the combination of these effects and the simple Zeeman shift model discussed above works very well.

Recall that optical molasses works better than originally anticipated, in which it was found that the damping due to polarization gradients was much much larger than the damping due to doppler cooling, $\gamma _{pg}\gg \gamma _{\rm {doppler}}$ The same turns out to be true for the restoring force in magneto-optical traps.

We have discussed only the 1D scheme above. You may not appreciate it, but a lot of spontaneous light forces which were discussed to circumvent the optical Earnshaw theorem worked in 1D, but were very difficult to generalize to 3D. The MOT scheme, on the other hand, generalizes very well to 3D. By using three pairs of anti-Helmholtz coils to create the field gradients, and six laser beams, you get the generalizeation to 3D and it works as well as in one dimension.

Example: vapor cell MOT

Consider a cesium vapor cell MOT. The atoms, initially at 300K, can be cooled to $3$ $\mu$K. The density starts at $10^{8}$ cm$^{-3}$, which is increased to $10^{11}$ cm$^{-3}$. This means that the phase space density, which is $n/T^{3/2}$, has been increased by $15$ order of magnitude. Initially, the phase space density before cooling is $20$ orders magnitide away from Bose-Einstein condensation; after MOT trapping, the system is much closer - only $5$ orders of magnitude closer, but not yet there.

References

• References:
  • Molasses, beam slowing and MOT:
  • Nice summary on both dipole traps and radiation pressure traps
    • W.D. Phillips, Laser cooling and trapping of neutral atoms, in Laser Manipulation of Atoms and Ions, edited by E. Arimondo, W.D. Phillips, and F. Strumia, Proceedings of the International School of Physics “Enrico Fermi”, Course CXVIII (North-Holland, Amsterdam, 1992) Download
  • Original paper on optical molasses, Chu et al.
  • Original paper on MOT, Raab et al.
  • Original papers on optical Earnshaw theorem
    • Ashkin and Gordon
    • Pritchard et al.