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Physical Chemistry Chemical Physics

Scattering length scaling rules for atom–atom–anion three-body recombination of zero-energy 4 He 4 He 6 Li − system

Binbin Wang

Published Jan 1, 2021• 5 citations
Publisher

Abstract

The scattering length scaling rules for three-body recombination (TBR) of the 4He4He6Li- system in the zero-energy limit (E → 0) are investigated by considering various post-Born-Oppenheimer (post-BO) contributions to the standard BO potential of He-He interaction. It is found that these post-BO effects on the TBR rates that lead to different dimer products could be well fitted by the scattering length scalings Cab with a being the scattering length of the He-He interaction, and b and C the constants. It is interesting to find that the powers b about both the weakly and deeply bound dimer products are quite different from the well-known powers given by the scattering length scaling laws in the fields of ultracold neutral atomic gases. Such difference and the distinct powers associated with various dimer products are qualitatively accounted for by the properties of the major effective potentials and relatively long-range nonadiabatic couplings. Particularly, from these properties, the scaling powers are expected to be dependent on systems, but the power scattering length scaling behaviors to be universal, which has also been checked to apply to a wide range of a by tuning the He-He interaction.

DOI
10.1039/d1cp01347e

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The scattering length scaling rules for three-body recombination (TBR) of the 4He4He6Li- system in the zero-energy limit (E → 0) are investigated by considering various post-Born-Oppenheimer (post-BO) contributions to the standard BO potential of He-He interaction. It is found that these post-BO effects on the TBR rates that lead to different dimer products could be well fitted by the scattering length scalings Cab with a being the scattering length of the He-He interaction, and b and C the constants. It is interesting to find that the powers b about both the weakly and deeply bound dimer products are quite different from the well-known powers given by the scattering length scaling laws in the fields of ultracold neutral atomic gases. Such difference and the distinct powers associated with various dimer products are qualitatively accounted for by the properties of the major effective potentials and relatively long-range nonadiabatic couplings. Particularly, from these properties, the scaling powers are expected to be dependent on systems, but the power scattering length scaling behaviors to be universal, which has also been checked to apply to a wide range of a by tuning the He-He interaction.
Generally, the three-body recombination (TBR) of the ultracold helium atoms in the zero-collision-energy limit could be described by the original zero-range (Efimov) universal function [E. Braaten, D. Kang, and L. Platter, Phys. Rev. A 75, 052714 (2007)] using the scattering length aaa of the He-He interaction and a three-body parameter a∗{a}_{*}a∗​ as input, where a∗{a}_{*}a∗​ is associated with the positive scattering length at which an interference minimum in the TBR rate occurs at the threshold. This universal property has been reinvestigated by considering various post-Born-Oppenheimer (post-BO) effects on the relevant scattering process. It is found that a linear correction to 1/a∗1/{a}_{*}1/a∗​ versus 1/a1/a1/a should be introduced to give a better description of these considered TBR cases because of the finite-range effects. Particularly, such a correction may be ascribed not only to the general scattering properties associated with the Efimov channel at the short hyperradial distance, but also to the tunneling probability in the lowest incident channel. In addition, a successful fit of the modified universal function that includes correctly the finite-range effects [E. Garrido, M. Gattobigio, and A. Kievsky, Phys. Rev. A 88, 032701 (2013)] or the zero-range universal function with a linearly variational 1/a∗1/{a}_{*}1/a∗​ versus 1/a1/a1/a to numerically accurate data also indicates a clear manifestation of the van der Waals universality. Finally, the post-BO effects on the TBR process for the partial wave with the total angular momentum J>0J>0J>0 are also discussed.
Atom-atom-anion three-body recombination (TBR) in mixed 4He and xLi− (x = 6 or 7) is investigated in the adiabatic hyperspherical representation by quantum mechanically solving the Schrödinger equation. The distributions of product states following these TBR processes are found to be relatively different for the two systems when the collision energy is less than roughly 0.6 mK × kB or 0.3 mK × kB for 4He4He6Li− and 4He4He7Li− systems, respectively, with kB being the Boltzmann constant. For 4He4He6Li− systems, the rate of recombination into (v=0) l = 04He6Li− molecular anions is the largest with v and l denoting the rovibrational quantum numbers, while the TBR rate that leads to the formation of l = 14He6Li− molecular anions is a little smaller than that of neutral 4He2 molecules. For 4He4He7Li− systems, neutral 4He2 molecules tend to be the most products, following the yields of l = 0 and 1 4He7Li− molecular anions. However, in spite of these distinctly different distributions, the products of molecular anions, the sum of l = 0 and 1 4HexLi− products, are relatively larger than that of neutral 4He2 molecules for both the two systems.
Few-body systems with large scattering length aaa have universal properties that do not depend on the details of their interactions at short distances. The rate constant for three-body recombination of bosonic atoms of mass mmm into a shallow dimer scales as $\ensuremath{\hbar}{a}^{4}∕m$ times a log-periodic function of the scattering length. We calculate the leading and subleading corrections to the rate constant, which are due to the effective range of the atoms, and study the correlation between the rate constant and the atom-dimer scattering length. Our results are applied to 4He^{4}\mathrm{He}4He atoms as a test case.
The atom-atom-anion three-body recombination (TBR) and collision induced dissociation (CID) processes of the 3He–3He–T− system at ultracold temperatures are investigated by solving the Schrödinger equation in the adiabatic hyperspherical representation. The variations of the TBR and CID rates with the collision energies in the ultracold temperatures are obtained. It is found that the JΠ = 1− symmetry dominates the TBR and CID processes in most of the considered collision energy range. The rate of TBR (CID) into (from) the l = 1 anion is larger than those for the l = 0 and l = 2 anions, with the l representing the rotational quantum number of 3HeT−. This can be understood via the nonadiabatic couplings among the different channels.
We use universality in two-body dipolar physics to study three-body recombination. We present results for the universal structure of weakly bound two-dipole states that depend only on the s-wave scattering length (a). We study threshold three-body recombination rates into weakly bound dimer states as a function of the scattering length. A Fermi golden rule analysis is used to estimate rates for different events mediated by the dipole-dipole interaction and a phenomenological contact interaction. The three-body recombination rate in the limit where a≫D contains terms which scale as a{4}, a{2}D{2}, and D4, where D is the dipolar length. When a≪D, the three-body recombination rate scales as D4.
The ultracold state-to-state chemistry for three-body recombination (TBR) in realistic systems has recently been experimentally investigated with full quantum state resolution. However, many detected phenomena remain challenging to be explored and explained from the theoretical viewpoints because this generally requires computational powers beyond state of the art. Here, the product-state distributions after TBR of 3He2–alkaline-earth-metal systems, i.e., after the processes of 3He + 3He + X → 3HeX + 3He with X being 9Be, 24Mg, 40Ca, 88Sr, or 138Ba, in the zero-collision-energy limit are theoretically studied. Two propensity rules for the distribution of the products found in current experiments have been checked, and the mechanism underlying these product-state distributions is explored. Particularly, two main intriguing transition pathways are identified, which may be responsible for the nonlinear distribution of the products vs their respective rotational quantum number. In addition, the TBR rates of these systems are also influenced by details of the interaction potential and relevant nonadiabatic couplings.