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arXiv:2402.08054 · Physical Review A

Probing the interaction energy of two Rb85 atoms in an optical tweezer via spin-motion coupling

Jun Zhuang, Kunpeng Wang, Pengxiang Wang, Ming-Rui Wei, Bahtiyar Mamat, Cheng Sheng, Peng Xu, Min Liu, Jin Wang, Xiaodong He, Mingsheng Zhan

Published Apr 23, 2024• 3 citations
arXivHTMLPDF

Abstract

The inherent polarization gradients in tight optical tweezers can be used to couple the atomic spins to the two-body motion under the action of a microwave spin-flip transition, so that such a spin-motion coupling offers an important control knob on the motional states of optically trapped two colliding atoms. Here, after preparing two elastically scattering $^{85}\mathrm{Rb}$ atoms in the three-dimensional ground-state in the optical tweezer, we employed this control in order to probe the colliding energies of elastic and inelastic channels. The combination of microwave spectra and corresponding s-wave pseudopotential model allows us to infer the effect of the state-dependent trapping potentials on the elastic colliding energies, as well as to reveal how the presence of inelastic interactions affects elastic part of the relative potential. Our work shows that the spin-motion coupling in a tight optical tweezer expand the experimental toolbox for fundamental studies of ultracold collisions in the two body systems with reactive collisions, and potentially for that of more complex interactions, such as optically trapped atom-molecule and molecule-molecule interactions.

DOI
10.1103/physreva.109.043320

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The inherent polarization gradients in tight optical tweezers can be used to couple the atomic spins to the two-body motion under the action of a microwave spin-flip transition, so that such a spin-motion coupling offers an important control knob on the motional states of optically trapped two colliding atoms. Here, after preparing two elastically scattering 85Rb^{85}\mathrm{Rb}85Rb atoms in the three-dimensional ground-state in the optical tweezer, we employed this control in order to probe the colliding energies of elastic and inelastic channels. The combination of microwave spectra and corresponding s-wave pseudopotential model allows us to infer the effect of the state-dependent trapping potentials on the elastic colliding energies, as well as to reveal how the presence of inelastic interactions affects elastic part of the relative potential. Our work shows that the spin-motion coupling in a tight optical tweezer expand the experimental toolbox for fundamental studies of ultracold collisions in the two body systems with reactive collisions, and potentially for that of more complex interactions, such as optically trapped atom-molecule and molecule-molecule interactions.
We report on experiments investigating the collisional properties of atoms at ultralow collision energies using an all-optical atom collider. By using a pair of optical tweezers, we can manipulate two ultracold atom clouds and collide them together at energies up to three orders of magnitude larger than their thermal energy. Our experiments measure the scattering of 87 Rb, 40 K, and 40 K- 87 Rb collisions. The versatility of our collider allows us to probe both shape resonances and Feshbach resonances in any partial wave. As examples, we present experiments demonstrating p-wave scattering with indistinguishable fermions, inelastic scattering at non-zero energies near a homonuclear Feshbach resonance, and partial wave interference in heteronuclear collisions.
Abstract We prepare pairs of 133Cs atoms in a single optical tweezer and perform Feshbach spectroscopy for collisions of atoms in the states (f = 3, m f = ±3). We detect enhancements in pair loss using a detection scheme where the optical tweezers are repeatedly subdivided. For atoms in the state (3, −3), we identify resonant features by performing inelastic loss spectroscopy. We carry out coupled-channel scattering calculations and show that at typical experimental temperatures the loss features are mostly centred on zeroes in the scattering length, rather than resonance centres. We measure the number of atoms remaining after a collision, elucidating how the different loss processes are influenced by the tweezer depth. These measurements probe the energy released during an inelastic collision, and thus give information on the states of the collision products. We also identify resonances with atom pairs prepared in the absolute ground state (f = 3, m f = 3), where two-body radiative loss is engineered by an excitation laser blue-detuned from the Cs D2 line. These results demonstrate optical tweezers to be a versatile tool to study two-body collisions with number-resolved detection sensitivity.
Abstract We report the preparation of exactly one 87Rb atom and one 133Cs atom in the same optical tweezer as the essential first step towards the construction of a tweezer array of individually trapped 87Rb133Cs molecules. Through careful selection of the tweezer wavelengths, we show how to engineer species-selective trapping potentials suitable for high-fidelity preparation of Rb + Cs atom pairs. Using a wavelength of 814 nm to trap Rb and 938 nm to trap Cs, we achieve loading probabilities of 0.508(6) for Rb and 0.547(6) for Cs using standard red-detuned molasses cooling. Loading the traps sequentially yields exactly one Rb and one Cs atom in 28.4(6)% of experimental runs. Using a combination of an acousto-optic deflector and a piezo-controlled mirror to control the relative position of the tweezers, we merge the two tweezers, retaining the atom pair with a probability of 0.9 9 ( − 0.02 ) ( + 0.01 ) . We use this capability to study hyperfine-state-dependent collisions of Rb and Cs in the combined tweezer and compare the measured two-body loss rates with coupled-channel quantum scattering calculations.
Abstract Optical tweezers are used to facilitate cold collisions between two Rydberg rubidium atoms (87Rb) by controlling the impact parameter and collision energy. One atom is held stationary while the other is propelled to a constant velocity. After the tweezers are deactivated, both atoms are excited to a Rydberg state using a π-pulse. Following the collision, a second π-pulse is applied. If the stationary atom undergoes minimal momentum transfer and returns to its ground state, it can be recaptured when the tweezer is reactivated. The collision probability as a function of the impact parameter is extracted from the atom loss in the tweezer and used to determine the collisional cross section between Rydberg atoms. Numerical simulations of elastic two-body collisions agree well with the experimental data, providing valuable insights into the parameter regime where quantum effects will become important.
We theoretically investigate the collisions between ultracold polar molecules in the presence of two lasers ensuring a Raman resonant transition on individual molecules to suppress photon scattering, taking the example of bosonic Na 23 K 39 molecules. By varying laser detunings and intensities, we enable a repulsive long-range interaction potential between molecules. After solving a set of coupled Schrödinger equations with the Hamiltonian written in the basis of laser-dressed states of the molecule pair at infinite distance, we identify quasiresonant conditions under which elastic collisions are favored over inelastic and reactive ones, by a factor of about 2, thus demonstrating a promising pathway for efficient two-photon optical shielding of ultracold molecular collisions. The results are analyzed in terms of scattering length of the colliding laser-dressed molecules, which exhibit prominent resonances assigned to the interaction of the entrance channel with other specific channels, consistent with the existence of a quasibound level of the long-range molecular pair induced by the lasers.
Abstract Understanding ultracold collisions involving molecules is of fundamental importance for current experiments, where inelastic collisions typically limit the lifetime of molecular ensembles in optical traps. Here we present a broad study of optically trapped ultracold RbCs molecules in collisions with one another, in reactive collisions with Rb atoms, and in nonreactive collisions with Cs atoms. For experiments with RbCs alone, we show that by modulating the intensity of the optical trap, such that the molecules spend 75% of each modulation cycle in the dark, we partially suppress collisional loss of the molecules. This is evidence for optical excitation of molecule pairs mediated via sticky collisions. We find that the suppression is less effective for molecules not prepared in the spin-stretched hyperfine ground state. This may be due either to longer lifetimes for complexes in the dark or to laser-free decay pathways. For atom–molecule mixtures, RbCs + Rb and RbCs + Cs, we demonstrate that the rate of collisional loss of molecules scales linearly with the density of atoms. This indicates that, in both cases, the loss of molecules is rate-limited by two-body atom–molecule processes. For both mixtures, we measure loss rates that are below the thermally averaged universal limit.