arXiv subjects

Juliana J. Park

Publications and source records attributed to Juliana J. Park.

9 recordsLinked to original sources

arXiv2024

Collisional Cooling of Ultracold Molecules

Since the original work on Bose-Einstein condensation, quantum degenerate gases of atoms have allowed the quantum emulation of important systems from condensed matter and nuclear physics, as well as the study of novel many-body states with no analog in other fields of physics. Ultracold molecules in the micro- and nano-Kelvin regimes promise to bring powerful new capabilities to quantum emulation and quantum computing, thanks to their rich internal degrees of freedom compared to atoms. They also open new possibilities for precision measurement and the study of quantum chemistry. Quantum gases of atoms were made possible by collision-based cooling schemes, such as evaporative cooling. For ultracold molecules, thermalization and collisional cooling have not been realized. With other techniques such as supersonic jets and cryogenic buffer gases, studies have been limited to temperatures above 10 mK. Here we show cooling of NaLi molecules at micro- and nano-Kelvin temperatures through collisions with ultracold Na atoms, both prepared in their stretched hyperfine spin states. We find a lower bound on the elastic to inelastic collision ratio between molecules and atoms greater than 50 -- large enough to support sustained collisional cooling. By employing two stages of evaporation, we increase the phase-space density (PSD) of the molecules by a factor of 20, achieving temperatures as low as 220 nK. The favorable collisional properties of a Na and NaLi mixture show great promise for making deeply quantum degenerate dipolar molecules and suggest the potential for such cooling in other systems.

cond-mat.quant-gas↗

arXiv2023

Ab initio calculation of the spectrum of Feshbach resonances in NaLi + Na collisions

We present a combined experimental and theoretical study of the spectrum of magnetically tunable Feshbach resonances in NaLi $(a^3Σ^+)$ $+$ Na collisions. In the accompanying paper, we observe experimentally 8 and 17 resonances occur between $B=0$ and $1400$~G in upper and lower spin-stretched states, respectively. Here, we perform ab initio calculations of the NaLi $+$ Na interaction potential and describe in detail the coupled-channel scattering calculations of the Feshbach resonance spectrum. The positions of the resonances cannot be predicted with realistic uncertainty in the state-of-the-art ab initio potential, but our calculations yield a typical number of resonances that is in near-quantitative agreement with experiment. We show that the main coupling mechanism results from spin-rotation and spin-spin couplings in combination with the anisotropic atom-molecule interaction. The calculations furthermore explain the qualitative difference between the numbers of resonances in either spin state.

physics.atom-ph↗

arXiv2023

Spectrum of Feshbach resonances in NaLi $+$ Na collisions

Collisional resonances of molecules can offer a deeper understanding of interaction potentials and collision complexes, and allow control of chemical reactions. Here, we experimentally map out the spectrum of Feshbach resonances in collisions between ultracold triplet ro-vibrational ground-state NaLi molecules and Na atoms over a range of 1400 G. Preparation of the spin-stretched state puts the system initially into the non-reactive quartet potential. A total of 25 resonances are observed, in agreement with quantum-chemistry calculations using a coupled-channels approach. Although the theory cannot predict the positions of resonances, it can account for several experimental findings and provide unprecedented insight into the nature and couplings of ultracold, strongly interacting complexes. Previous work has addressed only weakly bound complexes. We show that the main coupling mechanism results from spin-rotation and spin-spin couplings in combination with the anisotropic atom-molecule interaction, and that the collisional complexes which support the resonances have a size of 30-40 $a_0$. This study illustrates the potential of a combined experimental and theoretical approach.

physics.atom-ph↗

arXiv2022

Magnetic trapping of ultracold molecules at high density

Trapping ultracold molecules in conservative traps is essential for applications -- such as quantum state-controlled chemistry, quantum simulations, and quantum information processing. These applications require high densities or phase-space densities. We report magnetic trapping of NaLi molecules in the triplet ground state at high density ($\approx 10^{11} \; \rm{cm}^{-3}$) and ultralow temperature ($\approx 1\;{\rm μK}$). Magnetic trapping at these densities allows studies on both atom-molecule and molecule-molecule collisions in the ultracold regime in the absence of trapping light, which has often lead to undesired photo-chemistry. We measure the inelastic loss rates in a single spin sample and spin-mixtures of fermionic NaLi as well as spin-stretched NaLi$+$Na mixtures. We demonstrate sympathetic cooling of NaLi molecules in the magnetic trap by radio frequency evaporation of co-trapped Na atoms and observe an increase in the molecules' phase-space density by a factor of $\approx 16$.

physics.atom-ph↗

arXiv2022

A Feshbach resonance in collisions between ultracold ground state molecules

Collisional resonances are an important tool which has been used to modify interactions in ultracold gases, for realizing novel Hamiltonians in quantum simulations, for creating molecules from atomic gases and for controlling chemical reactions. So far, such resonances have been observed for atom-atom collisions, atom-molecule collisions and collisions between Feshbach molecules which are very weakly bound. Whether such resonances exist for ultracold ground state molecules has been debated due to the possibly high density of states and/or rapid decay of the resonant complex. Here we report a very pronounced and narrow (25 mG) Feshbach resonance in collisions between two ground state NaLi molecules. This molecular Feshbach resonance has two special characteristics. First, the collisional loss rate is enhanced by more than two orders of magnitude above the background loss rate which is saturated at the $p$-wave universal value, due to strong chemical reactivity. Second, the resonance is located at a magnetic field where two open channels become nearly degenerate. This implies the intermediate complex predominantly decays to the second open channel. We describe the resonant loss feature using a model with coupled modes which is analogous to a Fabry-Pérot cavity. Our observations prove the existence of long-lived coherent intermediate complexes even in systems without reaction barriers and open up the possibility of coherent control of chemical reactions.

cond-mat.quant-gas↗

arXiv2022

Control of reactive collisions by quantum interference

In this study, we achieved magnetic control of reactive scattering in an ultracold mixture of $^{23}$Na atoms and $^{23}$Na$^{6}$Li molecules. In most molecular collisions, particles react or are lost near short range with unity probability, leading to the so-called universal rate. By contrast, the Na{+}NaLi system was shown to have only $\sim4\%$ loss probability in a fully spin-polarized state. By controlling the phase of the scattering wave function via a Feshbach resonance, we modified the loss rate by more than a factor of $100$, from far below to far above the universal limit. The results are explained in analogy with an optical Fabry-Perot resonator by interference of reflections at short and long range. Our work demonstrates quantum control of chemistry by magnetic fields with the full dynamic range predicted by our models.

physics.atom-ph↗

arXiv2018

Photoassociation of Ultracold NaLi

We perform photoassociation spectroscopy in an ultracold $^{23}$Na-$^6$Li mixture to study the $c^3Σ^+$ excited triplet molecular potential. We observe 50 vibrational states and their substructure to an accuracy of 20 MHz, and provide line strength data from photoassociation loss measurements. An analysis of the vibrational line positions using near-dissociation expansions and a full potential fit is presented. This is the first observation of the $c^3Σ^+$ potential, as well as photoassociation in the NaLi system.

physics.atom-ph↗

arXiv2018

Two-Photon Spectroscopy of the NaLi Triplet Ground State

We employ two-photon spectroscopy to study the vibrational states of the triplet ground state potential ($a^3Σ^+$) of the $^{23}$Na$^{6}$Li molecule. Pairs of Na and Li atoms in an ultracold mixture are photoassociated into an excited triplet molecular state, which in turn is coupled to vibrational states of the triplet ground potential. Vibrational state binding energies, line strengths, and potential fitting parameters for the triplet ground $a^3Σ^+$ potential are reported. We also observe rotational splitting in the lowest vibrational state.

physics.atom-ph↗

arXiv2018

Long-Lived Ultracold Molecules with Electric and Magnetic Dipole Moments

We create fermionic dipolar $^{23}$Na$^6$Li molecules in their triplet ground state from an ultracold mixture of $^{23}$Na and $^6$Li. Using magneto-association across a narrow Feshbach resonance followed by a two-photon STIRAP transfer to the triplet ground state, we produce $3\,{\times}\,10^4$ ground state molecules in a spin-polarized state. We observe a lifetime of $4.6\,\text{s}$ in an isolated molecular sample, approaching the $p$-wave universal rate limit. Electron spin resonance spectroscopy of the triplet state was used to determine the hyperfine structure of this previously unobserved molecular state.

cond-mat.quant-gas↗