arXiv subjects

Eliane Luc-Koenig

Publications and source records attributed to Eliane Luc-Koenig.

14 recordsLinked to original sources

arXiv2026

Quantum study of ultracold atom-ion excitation exchange

The quantum dynamics of ultracold collisions between rubidium atoms and excited metastable strontium ions is treated in the laboratory frame, enlightening the importance of the coupling between internal angular momenta of the particles and their mutual rotation. The study reveals a subtle competition between electronic excitation exchange and fine structure quenching, with no charge exchange, which is found to be very sensitive to the details of ion-atom interactions. The rate constant for electronic excitation exchange is found in agreement with the experimental results of Ben-Shlomi \textit{et al.} (Phys. Rev. A \textbf{102}, 031301(R) (2020)), while the rate for fine structure quenching is predicted to strongly depend on the initial polarization of the reactants.

physics.atom-ph↗

arXiv2024

Competing excitation quenching and charge exchange in ultracold Li-Ba$^+$ collisions

Hybrid atom-ion systems are a rich and powerful platform for studying chemical reactions, as they feature both excellent control over the electronic state preparation and readout as well as a versatile tunability over the scattering energy, ranging from the few-partial wave regime to the quantum regime. In this work, we make use of these excellent control knobs, and present a joint experimental and theoretical study of the collisions of a single $^{138}$Ba$^+$ ion prepared in the $5d\,^2D_{3/2,5/2}$ metastable states with a ground state $^6$Li gas near quantum degeneracy. We show that in contrast to previously reported atom-ion mixtures, several non-radiative processes, including charge exchange, excitation exchange and quenching, compete with each other due to the inherent complexity of the ion-atom molecular structure. We present a full quantum model based on high-level electronic structure calculations involving spin-orbit couplings. Results are in excellent agreement with observations, highlighting the strong coupling between the internal angular momenta and the mechanical rotation of the colliding pair, which is relevant in any other hybrid system composed of an alkali-metal atom and an alkaline-earth ion.

quant-ph↗

arXiv2020

Laser control of ultracold molecule formation: The case of RbSr

We have studied the formation of ultracold RbSr molecules with laser pulses. After discussing the advantages of the Mott insulator phase for the control with pulses, we present two classes of strategies. The first class involves two electronic states. Two extensions of stimulated Raman adiabatic passage (STIRAP) for multi-level transitions are used : alternating STIRAP (A-STIRAP) and straddle STIRAP (S-STIRAP). Both transfer dynamics are modeled and compared. The second class of strategies involves only the electronic ground state and uses infrared (IR)/TeraHertz (THz) pulses. The chemical bond is first created by the application of a THz chirped pulse or $π$-pulse. Subsequently, the molecules are transferred to their ro-vibrational ground state using IR pulses. For this last step, different optimized pulse sequences through optimal control techniques, have been studied. The relative merits of these strategies in terms of efficiency and robustness are discussed within the experimental feasibility criteria of present laser technology.

physics.atom-ph↗

arXiv2018

Defining the $p$-wave scattering volume in the presence of dipolar interactions

The definition of the scattering volume for $p$-wave collisions needs to be generalized in the presence of dipolar interactions for which the potential decreases with the interparticle separation as $1/R^3$. Here, we propose a generalized definition of the scattering volume characterizing the short-range interactions in odd-parity waves, obtained from an analysis of the $p$-wave component of the two-body threshold wave function. Our approach uses an asymptotic model and introduces explicitly the anisotropic dipole-dipole interaction, which governs the ultracold collision dynamics at long-range. The short-range interactions, which are essential to describe threshold resonances, are taken into account by a single parameter which is determined by the field-free $s$-wave scattering length.

quant-ph↗

arXiv2018

Controlling ultracold $p$-wave collisions with non-resonant light: Predictions of an asymptotic model for the generalized scattering volume

Interactions in a spin-polarized ultracold Fermi gas are governed by $p$-wave collisions and can be characterized by the $p$-wave scattering volume. Control of these collisions by Feshbach resonances is hampered by huge inelastic losses. Here, we suggest non-resonant light control of $p$-wave collisions, exploiting the anisotropic coupling of non-resonant light to the polarizability of the atoms. The $p$-wave scattering volume can be controlled by strong non-resonant light, in close analogy to the $s$-wave scattering length. For collision partners that are tightly trapped, the non-resonant light induces an energy shift directly related to the generalized scattering volume. This effect could be used to climb the ladder of the trap. We also show that controlling the generalized scattering volume implies control, at least roughly, over the orientation of the interparticle axis relative to the polarization direction of the light at short interatomic distances. Our proposal is based on an asymptotic model that explicitly accounts for the anisotropic dipole-dipole interaction which governs the ultracold collision dynamics at long-range.

quant-ph↗

arXiv2018

Proposal for the formation of ultracold deeply-bound RbSr dipolar molecules by all-optical methods

Ultracold paramagnetic and polar diatomic molecules are among the promising systems for quantum simulation of lattice-spin models. Unfortunately, their experimental observation is still challenging. Based on our recent \textit{ab-initio} calculations, we analyze the feasibility of all-optical schemes for the formation of ultracold $^{87}$Rb$^{84}$Sr bosonic molecules. First, we have studied the formation by photoassociation followed by spontaneous emission. The photoassociation rates to levels belonging to electronic states converging to the $^{87}$Rb$(5s\,^2S)$+$^{84}$Sr($5s5p\,^3P_{0,1,2}$) asymptotes are particularly small close to the asymptote. The creation of molecules would be more interesting by using deeply levels that preferentially relaxes to the $v''=0$ level of the ground state. On the other hands, the photoassociation rates to levels belonging to electronic states converging to the Rb$(5p\,^2P_{1/2,3/2})$+Sr($5s^2\,^1S$) asymptotes have high value close to the asymptote. The relaxation from the levels close to the asymptotes creates weakly-bound molecules in mosty only one vibrational level. Second, stimulated Raman adiabatic passage (STIRAP) achieved in a tight optical trap efficiently creates weakly-bound ground-state molecules in a well-defined level, thus providing an alternative to magnetic Feshbach resonances to implement several schemes for an adiabatic population transfer toward the lowest ground-state level of RbSr. Finally, we have studied STIRAP process for transferring the weakly-bound molecules into the $v''=0$ level of the RbSr ground state.

physics.atom-ph↗

arXiv2016

Controlling the s-wave scattering length with non-resonant light: Predictions of an asymptotic model

A pair of atoms interacts with non-resonant light via its anisotropic polarizability. This effect can be used to tune the scattering properties of the atoms. Although the light-atom interaction varies with interatomic separation as $1/R^{3}$, the effective s-wave potential decreases more rapidly, as $1/R^{4}$ such that the field-dressed scattering length can be determined without any formal difficulty. The scattering dynamics are essentially governed by the long-range part of the interatomic interaction and can thus be accurately described by an asymptotic model [Crubellier et al., New J. Phys. 17, 045020 (2015)]. Here we use the asymptotic model to determine the field-dressed scattering length from the s-wave radial component of a particular threshold wave function. Applying our theory to the scattering of two strontium isotopes, we calculate the variation of the scattering length with the intensity of the non-resonant light. Moreover, we predict the intensities at which the scattering length becomes infinite for any pair of atoms.

physics.atom-ph↗

arXiv2015

Four-body long-range interactions between ultracold weakly-bound diatomic molecules

Using the multipolar expansion of electrostatic and magnetostatic potential energies, we characterize the long-range interactions between two weakly-bound diatomic molecules, taking as an example the paramagnetic Er$_2$ Feshbach molecules which were produced recently. Since inside each molecule, individual atoms conserve their identity, the intermolecular potential energy can be expanded as the sum of pairwise atomic potential energies. In the case of Er$_2$ Feshbach molecules, we show that the interaction between atomic magnetic dipoles gives rise to the usual $R^{-3}$ term of the multipolar expansion, with $R$ the intermolecular distance, but also to additional terms scaling as $R^{-5}$, $R^{-7}$, and so on. Those terms are due to the interaction between effective molecular multipole moments, and are strongly anisotropic with respect to the orientation of the molecules. Similarly the atomic pairwise van der Waals interaction results in $R^{-6}$, $R^{-8}$, ... terms in the intermolecular potential energy. By calculating the reduced electric-quadrupole moment of erbium ground level $\langle J=6||\hat{Q}_2||J=6\rangle = -1.305$ a.u., we also demonstrate that the electric-quadrupole interaction energy is negligible with respect to the magnetic-dipole and van der Waals interaction energies. The general formalism presented in this article can be applied to calculate the long-range potential energy between arbitrary charge distributions composed of almost free subsystems.

physics.atom-ph↗

arXiv2014

Asymptotic model for shape resonance control of diatomics by intense non-resonant light: Universality in the single-channel approximation

Non-resonant light interacting with diatomics via the polarizability anisotropy couples different rotational states and may lead to strong hybridization of the motion. The modification of shape resonances and low-energy scattering states due to this interaction can be fully captured by an asymptotic model, based on the long-range properties of the scattering [Crubellier et al. arXiv:1412.0569]. Remarkably, the properties of the field-dressed shape resonances in this asymptotic multi-channel description are found to be approximately linear in the field intensity up to fairly large intensity. This suggests a perturbative single-channel approach to be sufficient to study the control of such resonances by the non-resonant field. The multi-channel results furthermore indicate the dependence on field intensity to present, at least approximately, universal characteristics. Here we combine the nodal line technique to solve the asymptotic Schrödinger equation with perturbation theory. Comparing our single channel results to those obtained with the full interaction potential, we find nodal lines depending only on the field-free scattering length of the diatom to yield an approximate but universal description of the field-dressed molecule, confirming universal behavior.

physics.atom-ph↗

arXiv2014

Asymptotic model for shape resonance control of diatomics by intense non-resonant light

We derive a universal model for atom pairs interacting with non-resonant light via the polarizability anisotropy, based on the long range properties of the scattering. The corresponding dynamics can be obtained using a nodal line technique to solve the asymptotic Schrödinger equation. It consists in imposing physical boundary conditions at long range and vanishing of the wavefunction at a position separating inner zone and asymptotic region. We show that nodal lines which depend on the intensity of the non-resonant light can satisfactorily account for the effect of the polarizability at short range. The approach allows to determine the resonance structure, energy, width, channel mixing and hybridization even for narrow resonances.

physics.atom-ph↗

arXiv2007

The dynamical hole in ultrafast photoassociation: analysis of the compression effect

Photoassociation of a pair of cooled atoms by excitation with a short chirped laser pulse creates a dynamical hole in the initial continuum wavefunction. This hole is manifested by a void in the pair wavefunction and a momentum kick. Photoassociation into loosely bound levels of the external well in Cs_2 0$_g^-$(6S + 6P$_{3/2}$ is considered as a case study. After the pulse, the free evolution of the ground triplet state wavepacket is analyzed. Due to a negative momentum kick, motion to small distances is manifested and a compression effect is pointed out, markedly increasing the density of atom pairs at short distance. A consequence of the hole is the redistribution of the vibrational population in the ground triplet state, with population of the last bound level and creation of pairs of hot atoms. The physical interpretation makes use of the time dependence of the probability current and population on each channel to understand the role of the parameters of the photoassociation pulse. By varying such parameters, optimization of the compression effect in the ground state wavepacket is demonstrated. Due to an increase of the short range density probability by more than two orders of magnitude, we predict important photoassociation rates into deeply bound levels of the excited state by a second pulse, red-detuned relative to the first one and conveniently delayed.

quant-ph↗

arXiv2007

Dynamical interferences to probe short-pulse photoassociation of Rb atoms and stabilization of Rb_2 dimers

We analyze the formation of Rb_2 molecules with short photoassociation pulses applied to a cold Rb-85 sample. A pump laser pulse couples a continuum level of the ground electronic state X ^1Σ_{g}^+ with bound levels in the 0_{u}^+ (5S+5P_{1/2}) and 0_{u}^+ (5S+5P_{3/2}) vibrational series. The nonadiabatic coupling between the two excited channels induces time-dependent beatings in the populations. We propose to take advantage of these oscillations to design further laser pulses that probe the photoassociation process via photoionization or that optimize the stabilization in deep levels of the ground state.

physics.atom-ph↗

arXiv2005

Making ultracold molecules in a two color pump-dump photoassociation scheme using chirped pulses

This theoretical paper investigates the formation of ground state molecules from ultracold cesium atoms in a two-color scheme. Following previous work on photoassociation with chirped picosecond pulses [Luc-Koenig et al., Phys. Rev. A {\bf 70}, 033414 (2004)], we investigate stabilization by a second (dump) pulse. By appropriately choosing the dump pulse parameters and time delay with respect to the photoassociation pulse, we show that a large number of deeply bound molecules are created in the ground triplet state. We discuss (i) broad-bandwidth dump pulses which maximize the probability to form molecules while creating a broad vibrational distribution as well as (ii) narrow-bandwidth pulses populating a single vibrational ground state level, bound by 113 cm$^{-1}$. The use of chirped pulses makes the two-color scheme robust, simple and efficient.

physics.atom-ph↗

arXiv2004

Optimizing the photoassociation of cold atoms by use of chirped laser pulses

Photoassociation of ultracold atoms induced by chirped picosecond pulses is analyzed in a non-perturbative treatment by following the wavepackets dynamics on the ground and excited surfaces. The initial state is described by a Boltzmann distribution of continuum scattering states. The chosen example is photoassociation of cesium atoms at temperature T=54 $μK$ from the $a^3 Σ_u^+(6s,6s)$ continuum to bound levels in the external well of the $0_g^-(6s+6p_{3/2})$ potential. We study how the modification of the pulse characteristics (carrier frequency, duration, linear chirp rate and intensity) can enhance the number of photoassociated molecules and suggest ways of optimizing the production of stable molecules.

physics.atm-clus↗