arXiv subjects

Jeremy M. Hutson

Publications and source records attributed to Jeremy M. Hutson.

At least 37 records · Page 2Linked to original sources

arXiv2023

Shielding collisions of ultracold CaF molecules with static electric fields

We study collisions of ultracold CaF molecules in strong static electric fields. These fields allow the creation of long-range barriers in the interaction potential, effectively preventing the molecules from reaching the short-range region where inelastic and other loss processes are likely to occur. We carry out coupled-channel calculations of rate coefficients for elastic scattering and loss. We develop an efficient procedure for including energetically well-separated rotor functions in the basis set via a Van Vleck transformation. We show that shielding is particularly efficient for CaF and allows the rate of two-body loss processes to be reduced by a factor of $10^7$ or more at a field of 23 kV/cm. The loss rates remain low over a substantial range of fields. Electron and nuclear spins cause strong additional loss in some small ranges of field, but have little effect elsewhere. These results pave the way for evaporative cooling of CaF towards quantum degeneracy.

quant-ph↗

arXiv2023

Tunable Feshbach resonances in collisions of ultracold molecules in $^2Σ$ states with alkali-metal atoms

We consider the magnetically tunable Feshbach resonances that may exist in ultracold mixtures of molecules in $^2Σ$ states and alkali-metal atoms. We focus on Rb+CaF as a prototype system. There are likely to be Feshbach resonances analogous to those between pairs of alkali-metal atoms. We investigate the patterns of near-threshold states and the resonances that they cause, using coupled-channel calculations of the bound states and low-energy scattering on model interaction potentials. We explore the dependence of the properties on as-yet-unknown potential parameters. There is a high probability that resonances will exist at magnetic fields below 1000 G, and that these will be broad enough to control collisions and form triatomic molecules by magnetoassociation. We consider the effect of CaF rotation and potential anisotropy, and conclude that they may produce additional resonances but should not affect the existence of rotation-free resonances.

physics.atom-ph↗

arXiv2023

Long-range states and Feshbach resonances in collisions between ultracold alkali-metal diatomic molecules and atoms

We consider the long-range states expected for complexes formed from an alkali-metal diatomic molecule in a singlet state and an alkali-metal atom. We explore the structure of the Hamiltonian for such systems, and the couplings between the six angular momenta that are present. We consider the patterns and densities of the long-range states, and the terms in the Hamiltonian that can cause Feshbach resonances when the states cross threshold as a function of magnetic field. We present a case study of $^{40}$K$^{87}$Rb+$^{87}$Rb. We show multiple types of resonance due to long-range states with rotational and/or hyperfine excitation, and consider the likelihood of them existing at low to moderate magnetic fields.

physics.atom-ph↗

arXiv2023

Formation of ultracold molecules by merging optical tweezers

We demonstrate the formation of a single RbCs molecule during the merging of two optical tweezers, one containing a single Rb atom and the other a single Cs atom. Both atoms are initially predominantly in the motional ground states of their respective tweezers. We confirm molecule formation and establish the state of the molecule formed by measuring its binding energy. We find that the probability of molecule formation can be controlled by tuning the confinement of the traps during the merging process, in good agreement with coupled-channel calculations. We show that the conversion efficiency from atoms to molecules using this technique is comparable to magnetoassociation.

physics.atom-ph↗

arXiv2023

Magnetic Feshbach resonances between atoms in $^2$S and $^3$P$_0$ states: mechanisms and dependence on atomic properties

Magnetically tunable Feshbach resonances exist in ultracold collisions between atoms in $^2$S and $^3$P$_0$ states, such as an alkali-metal atom colliding with Yb or Sr in a clock state. We investigate the mechanisms of these resonances and identify the terms in the collision Hamiltonian responsible for them. They involve indirect coupling between the open and closed channels, via intermediate channels involving atoms in $^3$P$_1$ states. The resonance widths are generally proportional to the square of the magnetic field and are strongly enhanced when the magnitude of the background scattering length is large. For any given pair of atoms, the scattering length can be tuned discretely by choosing different isotopes of the $^3$P$_0$ atom. For each combination of an alkali-metal atom and either Yb or Sr, we consider the prospects of finding an isotopic combination that has both a large background scattering length and resonances at high but experimentally accessible field. We conclude that $^{87}$Rb+Yb, Cs+Yb and $^{85}$Rb+Sr are particularly promising combinations.

physics.atom-ph↗

arXiv2022

Diatomic-py: A python module for calculating the rotational and hyperfine structure of $^1Σ$ molecules

We present a computer program to calculate the quantised rotational and hyperfine energy levels of $^{1}Σ$ diatomic molecules in the presence of dc electric, dc magnetic, and off-resonant optical fields. Our program is applicable to the bialkali molecules used in ongoing state-of-the-art experiments with ultracold molecular gases. We include functions for the calculation of space-fixed electric dipole moments, magnetic moments and transition dipole moments.

physics.comp-ph↗

arXiv2022

Pinpointing Feshbach Resonances and Testing Efimov Universalities in $^{39}$K

Using a combination of bound-state spectroscopy and loss spectroscopy, we pinpoint eight intrastate Feshbach resonances in $^{39}$K, as well as six previously unexplored interstate ones. We also perform a detailed characterization of four of the intrastate resonances and two of the interstate ones. We carry out coupled-channel scattering calculations and find good agreement with experiment. The combination of experiment and theory provides a faithful map of the scattering length $a$ and permits precision measurements of the signatures of Efimov physics across four intermediate-strength resonances. We measure the modulation of the $a^4$ scaling of the three-body loss coefficient for both $a<0$ and $a>0$, as well as the many-body loss dynamics at unitarity (where $a$ diverges). The absolute positions of the observed Efimov features confirm a ubiquitous breakdown of Efimov--van-der-Waals universality in $^{39}$K, while their relative positions are in agreement with the universal Efimov ratios. The loss dynamics at the three broadest Feshbach resonances are universal within experimental uncertainties, consistent with observing little variation in the Efimov width parameters.

cond-mat.quant-gas↗

arXiv2022

Observation of magnetic Feshbach resonances between Cs and ${}^{173}$Yb

We report the first observation of magnetic Feshbach resonances between ${}^{173}$Yb and $^{133}$Cs. In a mixture of Cs atoms prepared in the $(f=3, m_f=3)$ state and unpolarized fermionic ${}^{173}$Yb we observe resonant atom loss due to two sets of magnetic Feshbach resonances around 622~G and 702~G. Resonances for individual Yb nuclear spin components $m_{i,\mathrm{Yb}}$ are split by its interaction with the Cs electronic spin, which also provides the main coupling mechanism for the observed resonances. The observed splittings and relative resonance strengths are in good agreement with theoretical predictions from coupled-channel calculations.

physics.atom-ph↗

arXiv2022

Interaction potential for NaCs for ultracold scattering and spectroscopy

We obtain the interaction potential for NaCs by fitting to experiments on ultracold scattering and spectroscopy in optical tweezers. The central region of the potential has been accurately determined from Fourier-Transform spectroscopy at higher temperatures, so we focus on adjusting the long-range and short-range parts. We use coupled-channel calculations of binding energies and wave functions to understand the nature of the molecular states observed in ultracold spectroscopy, and of the state that causes the Feshbach resonance used to create ultracold NaCs molecules. We elucidate the relationships between the experimental quantities and features of the interaction potential. We establish the combinations of experimental quantities that determine particular features of the potential. We find that the long-range dispersion coefficient $C_6$ must be increased by about 0.9% to 3256(1) $E_\textrm{h} a_0^6$ to fit the experimental results. We use coupled-channel calculations on the final potential to predict bound-state energies and resonance positions.

physics.atom-ph↗

arXiv2022

Feshbach resonances and molecule formation in ultracold mixtures of Rb and Yb($^3$P) atoms

We have investigated magnetically tunable Feshbach resonances in ultracold collisions of Rb with Yb in its metastable $^3$P$_2$ and $^3$P$_0$ states, using coupled-channel scattering and bound-state calculations. For the $^3$P$_2$ state, we find sharp resonances when both atoms are in their lowest Zeeman sublevels. However, these resonances are decayed by inelastic processes that produce Yb atoms in $^3$P$_1$ and $^3$P$_0$ states. The molecules that might be produced by magnetoassociation at the $^3$P$_2$ thresholds can decay by similar pathways and would have lifetimes no more than a few microseconds. For the $^3$P$_0$ state, by contrast, there are resonances that are promising for magnetoassociation. There are resonances due to both rotating and non-rotating molecular states that are significantly stronger than the analogous resonances for Yb($^1$S). The ones due to rotating states are denser in magnetic field; in contrast to Yb($^1$S), they exist even for bosonic isotopes of Yb($^3$P$_0$).

physics.atom-ph↗

arXiv2022

Improved characterization of Feshbach resonances and interaction potentials between $^{23}$Na and $^{87}$Rb atoms

The ultracold mixture of \Na and \Rb atoms has become an important system for investigating physics in Bose-Bose atomic mixtures and for forming ultracold ground-state polar molecules. In this work, we provide an improved characterization of the most commonly used Feshbach resonance near 347.64 G between \Na and \Rb in their absolute ground states. We form Feshbach molecules using this resonance and measure their binding energies by dissociating them via magnetic field modulation. We use the binding energies to refine the singlet and triplet potential energy curves, using coupled-channel bound-state calculations. We then use coupled-channel scattering calculations on the resulting potentials to produce a high-precision mapping between magnetic field and scattering length. We also observe 10 additional $s$-wave Feshbach resonances for \Na and \Rb in different combinations of Zeeman sublevels of the $F = 1$ hyperfine states. Some of the resonances show 2-body inelastic decay due to spin exchange. We compare the resonance properties with coupled-channel scattering calculations that full take account of inelastic properties.

cond-mat.quant-gas↗

arXiv2022

Lee-Huang-Yang effects in the ultracold mixture of $^{23}$Na and $^{87}$Rb with attractive interspecies interactions

The beyond-mean-field Lee-Huang-Yang (LHY) correction is ubiquitous in dilute ultracold quantum gases. However, its effects are often elusive due to the typically much larger influence of the mean-field energy. In this work, we study an ultracold mixture of $^{23}$Na and $^{87}$Rb with tunable attractive interspecies interactions. The LHY effects manifest in the formation of self-bound quantum liquid droplets and the expansion dynamics of the gas-phase sample. A liquid-to-gas phase diagram is obtained by measuring the critical atom numbers below which the self-bound behavior disappears. In stark contrast to trapped gas-phase condensates, the gas-phase mixture formed following the liquid-to-gas phase transition shows an anomalous expansion featuring a larger release energy for increasing mean-field attractions.

cond-mat.quant-gas↗

arXiv2021

Magnetic Feshbach resonances in collisions of $^{23}$Na$^{40}$K with $^{40}$K

We present measurements of more than 80 magnetic Feshbach resonances in collisions of ultracold $^{23}$Na$^{40}$K with $^{40}$K. We assign quantum numbers to a group of low-field resonances and show that they are due to long-range states of the triatomic complex in which the quantum numbers of the separated atom and molecule are approximately preserved. The resonant states are not members of chaotic bath of short-range states. Similar resonances are expected to be a common feature of alkali-metal diatom + atom systems.

physics.atom-ph↗

arXiv2021

Complexes formed in collisions between ultracold alkali-metal diatomic molecules and atoms

We explore the properties of 3-atom complexes of alkali-metal diatomic molecules with alkali-metal atoms, which may be formed in ultracold collisions. We estimate the densities of vibrational states at the energy of atom-diatom collisions, and find values ranging from 2.2 to 350~K$^{-1}$. However, this density does not account for electronic near-degeneracy or electron and nuclear spins. We consider the fine and hyperfine structure expected for such complexes. The Fermi contact interaction between electron and nuclear spins can cause spin exchange between atomic and molecular spins. It can drive inelastic collisions, with resonances of three distinct types, each with a characteristic width and peak height in the inelastic rate coefficient. Some of these resonances are broad enough to overlap and produce a background loss rate that is approximately proportional to the number of outgoing inelastic channels. Spin exchange can increase the density of states from which laser-induced loss may occur.

physics.atom-ph↗

arXiv2021

Molecule-molecule and atom-molecule collisions with ultracold RbCs molecules

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 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.

physics.atom-ph↗

arXiv2021

Collisions in a dual-species magneto-optical trap of molecules and atoms

We study inelastic collisions between CaF molecules and $^{87}$Rb atoms in a dual-species magneto-optical trap. The presence of atoms increases the loss rate of molecules from the trap. By measuring the loss rates and density distributions, we determine a collisional loss rate coefficient $k_{2} = (1.43 \pm 0.29) \times 10^{-10}$ cm$^{3}$/s at a temperature of 2.4 mK. We show that this is not substantially changed by light-induced collisions or by varying the populations of excited-state atoms and molecules. The observed loss rate is close to the universal rate expected in the presence of fast loss at short range, and can be explained by rotation-changing collisions in the ground electronic state.

physics.atom-ph↗

arXiv2021

Collisions Between Ultracold Molecules and Atoms in a Magnetic Trap

We prepare mixtures of ultracold CaF molecules and Rb atoms in a magnetic trap and study their inelastic collisions. When the atoms are prepared in the spin-stretched state and the molecules in the spin-stretched component of the first rotationally excited state, they collide inelastically with a rate coefficient of $k_2 = (6.6 \pm 1.5) \times 10^{-11}$ cm$^{3}$/s at temperatures near 100~$μ$K. We attribute this to rotation-changing collisions. When the molecules are in the ground rotational state we see no inelastic loss and set an upper bound on the spin relaxation rate coefficient of $k_2 < 5.8 \times 10^{-12}$ cm$^{3}$/s with 95% confidence. We compare these measurements to the results of a single-channel loss model based on quantum defect theory. The comparison suggests a short-range loss parameter close to unity for rotationally excited molecules, but below 0.04 for molecules in the rotational ground state.

physics.atom-ph↗

arXiv2021

Robust storage qubits in ultracold polar molecules

Quantum states with long-lived coherence are essential for quantum computation, simulation and metrology. The nuclear spin states of ultracold molecules prepared in the singlet rovibrational ground state are an excellent candidate for encoding and storing quantum information. However, it is important to understand all sources of decoherence for these qubits, and then eliminate them, in order to reach the longest possible coherence times. Here, we fully characterise the dominant mechanisms for decoherence of a storage qubit in an optically trapped ultracold gas of RbCs molecules using high-resolution Ramsey spectroscopy. Guided by a detailed understanding of the hyperfine structure of the molecule, we tune the magnetic field to where a pair of hyperfine states have the same magnetic moment. These states form a qubit, which is insensitive to variations in magnetic field. Our experiments reveal an unexpected differential tensor light shift between the states, caused by weak mixing of rotational states. We demonstrate how this light shift can be eliminated by setting the angle between the linearly polarised trap light and the applied magnetic field to a magic angle of $\arccos{(1/\sqrt{3})}\approx55^{\circ}$. This leads to a coherence time exceeding 6.9 s (90% confidence level). Our results unlock the potential of ultracold molecules as a platform for quantum computation.

cond-mat.quant-gas↗