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Bulletin of the American Physical Society

Fine structure changing collisions between ultra-cold lithium atoms

Brian P. Anderson, Nicholas W. M. Ritchie, Yinan Xiao

Published Dec 1, 1992• 0 citations
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Abstract

The authors have designed and assembled an experiment to determine the rate of fine structure changing collisions between ultra-cold ({approximately} 1 mK) laser cooled Li atoms. The atoms are confined by a magneto-optical trap which consists of six polarized orthogonal laser beams tuned slightly below the 2S{sub 1/2}-2P{sub 3/2} resonance frequency of lithium. Measurements show that about 2 x 10{sup 7} atoms are confined to a roughly spherical region of about 1 mm in diameter. Fine structure changing collisions occur when an atom in the 2S{sub 1/2} state and an atom in the 2P{sub 3/2} state collide, and yield an atom in the 2S{sub 1/2} state and an atom in the 2P{sub 1/2} state, with an energy release corresponding to about 10 GHz. This energy adds kinetic energy to the atoms in the trap, and knocks atoms out of the trap. The authors have devised a method to measure the rate of this collisional loss mechanism. The method uses a laser diode and a dye laser to selectively photo-ionize the 2P{sub 1/2} atoms, and a channeltron particle multipiler measures the rate of ion formation. We will report the progress of this experiment.

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•Aug 1, 1997•0 citations
The authors have designed and assembled an experiment to determine the rate of fine structure changing collisions between ultra-cold ({approximately} 1 mK) laser cooled Li atoms. The atoms are confined by a magneto-optical trap which consists of six polarized orthogonal laser beams tuned slightly below the 2S{sub 1/2}-2P{sub 3/2} resonance frequency of lithium. Measurements show that about 2 x 10{sup 7} atoms are confined to a roughly spherical region of about 1 mm in diameter. Fine structure changing collisions occur when an atom in the 2S{sub 1/2} state and an atom in the 2P{sub 3/2} state collide, and yield an atom in the 2S{sub 1/2} state and an atom in the 2P{sub 1/2} state, with an energy release corresponding to about 10 GHz. This energy adds kinetic energy to the atoms in the trap, and knocks atoms out of the trap. The authors have devised a method to measure the rate of this collisional loss mechanism. The method uses a laser diode and a dye laser to selectively photo-ionize the 2P{sub 1/2} atoms, and a channeltron particle multipiler measures the rate of ion formation. We will report the progress of this experiment.
Measurements of the trap loss rate in ultra-cold magneto-optically trapped sp6\\sp6sp6Li and sp7\\sp7sp7Li are presented and compared. Clear evidence is presented for two different trap loss mechanisms involving inelastic collisions between one ground state atom and one excited state atom. The fine-structure changing (FSC) mechanism, in which the excited state atom changes fine-structure level during a collision, is seen to dominate the rate at low trap laser intensities. However, as the intensity is increased, the trap becomes sufficiently deep to be able to contain the products of FSC collisions and this mechanism no longer contributes to trap loss. It is a unique aspect of Li that the energy imparted to an atom in a FSC collision is in a range that may be recaptured with experimentally attainable trap parameters. When the products of all FSC collisions remain trapped, only the radiative escape (RE) trap loss mechanism, due to the emission of a less energetic photon than the initial excitation photon, contributes to the trap loss rate. At small detunings, the rate of the RE trap loss mechanism is seen to be over two orders-of-magnitude smaller than the FSC rate. The FSC trap loss rate for sp6\\sp6sp6Li and sp7\\sp7sp7Li were found to be largest at smaller detunings and of comparable magnitude in sp6\\sp6sp6Li and sp7\\sp7sp7Li. The RE trap loss rate in sp6\\sp6sp6Li was seen to be roughly four times the RE trap loss rate in sp7\\sp7sp7Li. To understand better the dynamics of trap loss and magneto-optical traps in general, a sophisticated model of magneto-optical trap kinetics has been developed. This model has demonstrated that most critical factor determining the maximum velocity an atom may have and yet remained trapped is the initial atom's frame detuning, Delta\\DeltaDelta - k v, where Delta\\DeltaDelta is the trap laser detuning, k is the propagation vector of the trap beam most nearly anti-parallel to v, the atom's velocity. All else being equal, minimizing the magnitude of this quantity maximizes the velocity that a trap will retain. More detailed results of this model are also presented.
We have successfully trapped sp7\\sp7sp7Li in a vapor cell magneto-optical trap (MOT). The trap is studied in detail and the parameters are measured from the experiment. The trapping mechanism has been understood in terms of the radiation force and a simple one dimensional model is used in interpreting and predicting the experimental results. The cold-cold atom collision rate coefficient is measured in a beam MOT. The two collision mechanisms, fine structure changing and radiative escape, are discussed in a molecular picture. One of the channels, the fine structure changing channel, can be turned on and off by the experimental conditions, namely the laser intensity in this experiment. The rate coefficient for each mechanism has been determined from the experiment.
Collisions between ultra-cold (T << 1K) atoms confined in a magneto- optical trap (MOT) may result in the ejection of atoms from the trap. These collisional loss processes, which involve ground state/excited state collisions, fundamentally limit the density attainable in MOT traps. Although accurate calculations of collision rates between ultra-cold atoms require precise knowledge of the molecular potentials over a long range, the loss rate for Li was recently predicted to be significantly less than for the other alkali metals. Motivated by this result, we are measuring the collisional loss rate of Li in a vapor-cell MOT using a red-detuned laser beam to catalyze the collisions, similar to recent experiments using Rb and Cs. We will report our progress to measure the trap loss rate for {sup 6}Li and {sup 7}Li, which will be compared to investigate an isotopic dependence, as was recently observed for Rb.
Storing and cooling simultaneously lithium and sodium atoms in a two-species magneto-optical trap, rate coefficients for collisions between these two atomic species were determined. The experiments were performed at different trap depths, thus for Li atoms the trap losses due to finestructure changing collisions could be distinguished from losses due to radiative escape. The rate coefficient for collisions between sodium and lithium atoms shows also a step when increasing the trap depth. The formation of cold heteronuclear molecules is claimed.
Collisions between ultracold neutral atoms have for some time been the subject of investigation, initially with hydrogen and more recently with laser cooled alkali atoms. Advances in laser cooling and trapping of neutral atoms in a Magneto-Optic Trap (MOT) have made cold atoms available as the starting point for many laser cooled atomic physics investigations. The most spectacularly successful of these, the observation of Bose-Einstein Condensation (BEC) in a dilute ultra-cold spin polarized atomic vapor, has accelerated the study of cold collisions. Experimental and theoretical studies of BEC and the long range interaction between cold alkali atoms is at the boundary of atomic and low temperature physics. Such studies have been difficult and would not have been possible without the development and advancement of laser cooling and trapping of neutral atoms. By contrast, ion-atom interactions at low temperature, also very difficult to study prior to modern day laser cooling, have remained largely unexplored. But now, many laboratories worldwide have almost routine access to cold neutral atoms. The combined technologies of ion trapping, together with laser cooling of neutrals has made these studies experimentally feasible and several very important, novel applications might come out of such investigations . This paper is an investigation of ion-atom interactions in the cold and ultra-cold temperature regime. Some of the collisional ion-atom interactions present at room temperature are very much reduced in the low temperature regime. Reaction rates for charge transfer between unlike atoms, A + B(+) approaches A(+) + B, are expected to fall rapidly with temperature, approximately as T(sup 5/2). Thus, cold mixtures of atoms and ions are expected to coexist for very long times, unlike room temperature mixtures of the same ion-atom combination. Thus, it seems feasible to cool ions via collisions with laser cooled atoms. Many of the conventional collisional interactions, exploited as a useful tool at room temperature and higher, are greatly enhanced at low energy. For example, collisional spin transfer from one species of polarized atoms to another has long been a useful method for polarizing a sample of atoms where no other means was available. Because optical pumping cannot be used to polarize the nuclear spin of Xe-129 or He-3 (for use in nmr imaging of the lungs), the nuclear spins are polarized via collisions with an optically pumped Rb vapor in a cell containing both gases. In another case, a spin polarized thermal Cs beam was used to polarize the hyperfine states of trapped He(+)-3 ions in order to measure their hyperfine clock transition frequency. The absence of an x-ray light source to optically pump the ground state of the He(+)-3 ion necessitated this alternative state preparation. Similarly, Cd(+) and Sr(+) ions were spin-oriented via collisions in a cell with optically pumped Rb vapor. Resonant RF spin changing transitions in the ground state of the ions were detected by changes in the Rb resonance light absorption. Because cold collision spin exchange rates scale with temperature as T(sup -1/2) this technique is expected to be a far more powerful tool than the room temperature counterpart. This factor of 100 or more enhancement in spin exchange reaction rates at low temperatures is the basis for a novel trapped ion clock where laser cooled neutrals will cool, state select and monitor the ion clock transition. The advantage over conventional direct laser cooling of trapped ions is that the very expensive and cumbersome UV laser light sources, required to excite the ionic cooling transition, are effectively replaced by simple diode lasers.