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The Journal of Chemical Physics

Communication: Classical threshold law for ion-neutral-neutral three-body recombination

Jesús Pérez‐Ríos, Chris H. Greene

Published Jul 28, 2015• 52 citations
Publisher

Abstract

A very recently method for classical trajectory calculations for three-body collision [Pérez-Ríos et al., J. Chem. Phys. 140, 044307 (2014)] has been applied to describe ion-neutral-neutral ternary processes for low energy collisions: 0.1 mK-10 mK. As a result, a threshold law for the three-body recombination cross section is obtained and corroborated numerically. The derived threshold law predicts the formation of weakly bound dimers, with binding energies comparable to the collision energy of the collisional partners. In this low energy range, this analysis predicts that molecular ions should dominate over molecular neutrals as the most products formed.

DOI
10.1063/1.4927702

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•Jan 1, 2013•0 citations
A very recently method for classical trajectory calculations for three-body collision [Pérez-Ríos et al., J. Chem. Phys. 140, 044307 (2014)] has been applied to describe ion-neutral-neutral ternary processes for low energy collisions: 0.1 mK-10 mK. As a result, a threshold law for the three-body recombination cross section is obtained and corroborated numerically. The derived threshold law predicts the formation of weakly bound dimers, with binding energies comparable to the collision energy of the collisional partners. In this low energy range, this analysis predicts that molecular ions should dominate over molecular neutrals as the most products formed.
A very recently method for classical trajectory calculations for three-body collision [J. Pérez-Ríos, S. Ragole, J. Wang and C. H. Greene, J. Chem. Phys. {\bf 140}, 044307 (2014)] has been applied to describe ion-neutral-neutral ternary processes for low energy collisions: 0.1 mK - 10 mK. As a result, a threshold law for the three-body recombination cross section is obtained and corroborated both, experimentally and numerically. The derived threshold law predicts the formation of weakly bound dimers, with binding energies comparable to the collision energy of the collisional partners. In this low energy range, this analysis predicts that molecular ions should dominate over molecular neutrals as the most products formed.
The recent development of hybrid traps technology has revolutionized the field of cold chemistry. Recently, new trap configurations have been built in order to explore more involve chemical processes, among them is the three-body recombination involving ions and neutrals. Different ion-neutral-neutral reactions at low collision energies: 0.1 mK - 10 mK, are studied by means of a very recent method for classical trajectory calculations in hyperspherical coordinates for treating three-body collisions [J. Pérez-Ríos, S. Ragole, J. Wang and C. H. Greene, J. Chem. Phys. 140, 044307 (2014)]. On the other hand a classically derived threshold law is obtained and numerically confirmed. The derived threshold law predicts molecular ions should dominate over molecular neutrals as the most products formed.
We study the role of pairwise long-range interactions in the formation of van der Waals molecules through direct three-body recombination processes A + B + B → AB + B, based on a classical trajectory method in hyperspherical coordinates developed in our earlier works [J. Pérez-Ríos et al., J. Chem. Phys. 140, 044307 (2014); M. Mirahmadi and J. Pérez-Ríos, J. Chem. Phys. 154, 034305 (2021)]. In particular, we find the effective long-range potential in hyperspherical coordinates with an exact expression in terms of dispersion coefficients of pairwise potentials. Exploiting this relation, we derive a classical threshold law for the total cross section and the three-body recombination rate yielding an analytical expression for the three-body recombination rate as a function of the pairwise long-range coefficients of the involved partners.
We study three-body recombination of Ba^{+}+Rb+Rb in the mK regime where a single ^{138}Ba^{+} ion in a Paul trap is immersed into a cloud of ultracold ^{87}Rb atoms. We measure the energy dependence of the three-body rate coefficient k_{3} and compare the results to the theoretical prediction, k_{3}∝E_{col}^{-3/4}, where E_{col} is the collision energy. We find agreement if we assume that the nonthermal ion energy distribution is determined by at least two different micromotion induced energy scales. Furthermore, using classical trajectory calculations we predict how the median binding energy of the formed molecules scales with the collision energy. Our studies give new insights into the kinetics of an ion immersed in an ultracold atom cloud and yield important prospects for atom-ion experiments targeting the s-wave regime.
Three-body recombination is a chemical reaction where the collision of three atoms leads to the formation of a diatomic molecule. In the ultracold regime it is expected that the production rate of a molecule generally decreases with its binding energy Eb{E}_{b}Eb​, however, its precise dependence and the physics governing it have been left unclear so far. Here we present a comprehensive experimental and theoretical study of the energy dependency for three-body recombination of ultracold Rb. For this, we determine production rates for molecules in a state-to-state resolved manner, with the binding energies Eb{E}_{b}Eb​ ranging from 0.02 to 77 $\mathrm{GHz}\ifmmode\times\else\texttimes\fi{}h$. We find that the formation rate approximately scales as ${E}_{b}^{\ensuremath{-}\ensuremath{\alpha}}$, where $\ensuremath{\alpha}$ is in the vicinity of 1. The formation rate typically varies only within a factor of two for different rotational angular momenta of the molecular product, apart from a possible centrifugal barrier suppression for low binding energies. In addition to numerical three-body calculations we present a perturbative model which reveals the physical origin of the energy scaling of the formation rate. Furthermore, we show that the scaling law potentially holds universally for a broad range of interaction potentials.
During the last few decades, the two fields of ultracold neutral atoms and of single trapped ions have undergone an amazing development. The incorporation of these systems into a single experiment exploits the complementary physical properties of the subsystems and opens up novel lines of research. I present experimental results obtained in one of the first hybrid atom-ion setups accessing the cold regime. Single ions interact with ultracold samples of 87Rb atoms. The collision energies are set by heating mechanisms in the Paul trap and are on the order of mK·kB. Interactions are generally strong and long-ranged. We observe elastic atom-ion scattering in the semi-classical energy regime in which the cross section depends on the collision energy and favors scattering at small angles. We were able to obtain a general good understanding of atom-ion two-body collisions. We observed sympathetic cooling of the ion over four orders of magnitude in energy through collisions with the ultracold atoms. Further, we utilized atom-ion scattering events to develop a novel method to compensate excess ion micromotion, the primary source of ion heating. Three-body collisions between two atoms and the ion play an important role. We identified these processes through the large amounts of energy that they release. This makes them detectable despite their suppression with respect to two-body collisions. We also showed that atom-ion three-body collisions become more prominent as the collision energy decreases. Finally, we employed our atom-ion apparatus to gain novel insights into three-body recombination between ultracold atoms. In these experiments the ion trap acts as an extremely sensitive ion detector. Through three-body recombination a Rb2 molecule is formed and can undergo ionization by absorbing photons from a strong laser. By scanning the frequency of the ionization laser we obtained a molecular spectrum and identified a relatively broad distribution over final molecular states.