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Physical Review A

Decay of trapped ultracold alkali atoms by recombination

A. J. Moerdijk, H. M. J. M. Boesten, BOUDEWIJN J. VERHAAR

Published Feb 1, 1996• 110 citations
Publisher

Abstract

Using the knowledge of two-body collision properties that has recently become available, we estimate the three-body recombination rate for doubly-spin-polarized ultracold gas samples of $^{7}\mathrm{Li}$, $^{23}\mathrm{Na}$ and $^{87}\mathrm{Rb}$ on the basis of the Jastrow approximation. We find that only recombination leading to the formation of the highest two-body bound states is important. The rate for the highest bound level with zero angular momentum is found to increase strongly with the absolute value of the two-body scattering length. \textcopyright{} 1996 The American Physical Society.

DOI
10.1103/physreva.53.916

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Using the knowledge of two-body collision properties that has recently become available, we estimate the three-body recombination rate for doubly-spin-polarized ultracold gas samples of 7Li^{7}\mathrm{Li}7Li, 23Na^{23}\mathrm{Na}23Na and 87Rb^{87}\mathrm{Rb}87Rb on the basis of the Jastrow approximation. We find that only recombination leading to the formation of the highest two-body bound states is important. The rate for the highest bound level with zero angular momentum is found to increase strongly with the absolute value of the two-body scattering length. \textcopyright{} 1996 The American Physical Society.
We discuss three-body recombination of ultracold atoms to a weakly bound sss level. In this case, characterized by large and positive scattering length aaa for pair interaction, we find a repulsive effective potential for three-body collisions, which strongly reduces the recombination probability. In the zero temperature limit we obtain a universal relation, independent of the detailed shape of the interaction potential, for the (event) rate constant of three-body recombination: ${\ensuremath{\alpha}}_{\mathrm{rec}}\phantom{\rule{0ex}{0ex}}=\phantom{\rule{0ex}{0ex}}3.9\ensuremath{\Elzxh}{a}^{4}/m$, where mmm is the atom mass.
We identify two qualitatively different mechanisms that control three-body recombination in a spin-polarized gas near zero temperature. A universal curve describes the recombination rate versus the two-body scattering length aaa. It grows as a4{a}^{4}a4 for large ∣a∣,|a|,∣a∣, with different mechanisms for a<0a<0a<0 and a>0a>0a>0. Our calculations document a previously established mechanism that causes K3{K}_{3}K3​ to grow rapidly as the two-body scattering length aaa increases toward $+\ensuremath{\infty}$, and a new tunneling mechanism that produces an even stronger enhancement of K3{K}_{3}K3​ as $a\ensuremath{\rightarrow}\ensuremath{-}\ensuremath{\infty}$. The expectations based on these two mechanisms can be modified by quantum mechanical interference or resonance effects.
This work treats resonant collisions between five identical ultracold bosons in the framework of the adiabatic hyperspherical representation. The five-body recombination rate coefficient is quantified using a semiclassical description in conjunction with an analysis of the lowest five-body hyperspherical adiabatic potential curves in a scattering length regime with no universal weakly bound tetramers, trimers, or dimers. A comparison is made between these results and the only existing experimental measurement of five-body loss in an ultracold gas of bosonic cesium atoms and with the lone theoretical estimation of the loss rate. The recombination rate for the process B + B + B + B + B → B 4 + B is also computed in a different regime of scattering lengths where there is one universal bound tetramer by implementing a few-channel quantum scattering calculation based on five-body hyperspherical potential curves and nonadiabatic couplings. Our calculations predict regions where five-body recombination can cause decay of the atom cloud in an ultracold gas that is even faster than 3-body and 4-body recombination, which can ideally be tested by using the current generation of box traps having nearly uniform density.
We have studied hydrogen-hydrogen-alkali three-body systems in the adiabatic hyperspherical representation. For the spin-stretched case, there exists a single XXXH molecular state when XXX is one of the bosonic alkali atoms: 7Li^{7}\mathrm{Li}7Li, 23Na^{23}\mathrm{Na}23Na, 39K^{39}\mathrm{K}39K, 87Rb^{87}\mathrm{Rb}87Rb, or 133Cs^{133}\mathrm{Cs}133Cs. As a result, the only recombination process is the one that leads to formation of XXXH molecules, $\text{H}+\text{H}+X\ensuremath{\rightarrow}X\text{H}+\text{H}$, and such molecules will be stable against vibrational relaxation. We have calculated the collision rates for recombination and collision-induced dissociation as well as the elastic cross sections for H+XH\text{H}+X\text{H}H+XH collisions up to a temperature of 0.5 K, including the partial wave contributions from ${J}^{\ensuremath{\Pi}}={0}^{+}$ to ${5}^{\ensuremath{-}}$. We have also found that there is just one three-body bound state for such systems for ${J}^{\ensuremath{\Pi}}={0}^{+}$ and no bound states for higher angular momenta.
Three-body recombination in helium-helium--alkali-metal collisions at cold temperatures is studied using the adiabatic hyperspherical representation. The rates for the three-body recombination processes $^{4}\text{H}\text{e}+^{4}\text{H}\text{e}+X\ensuremath{\rightarrow}^{4}\text{H}\text{e}+^{4}\text{H}\text{e}X$ and $^{4}\text{H}\text{e}+^{4}\text{H}\text{e}+X\ensuremath{\rightarrow}{^{4}\text{H}\text{e}}_{2}+X$, with X=7LiX=^{7}\text{L}\text{i}X=7Li, 23Na^{23}\text{N}\text{a}23Na, 39K^{39}\text{K}39K, 85Rb^{85}\text{R}\text{b}85Rb, and 133Cs^{133}\text{C}\text{s}133Cs, are calculated at nonzero collision energies by including not only zero total angular momentum, J=0J=0J=0, states but also J>0J>0J>0 states. The three-body recombination rates show a relatively weak dependence on the alkali-metal species, differing from each other only by about one order of magnitude, except for the 4He-4He-23Na^{4}\text{H}\text{e-}^{4}\text{H}\text{e-}^{23}\text{N}\text{a}4He-4He-23Na system.