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We report on the transport of ultracold cesium and rubidium atoms over $37.2\,$cm in under $25\,$ms using an optical conveyor belt formed by two counter-propagating beams with a controllable frequency difference that generate a movable optical lattice. By carefully selecting the waists and focus positions, we are able to use two static Gaussian beams for the transport, avoiding the need for a Bessel beam or vari-focus lenses. We characterize the transport efficiency for both species, including a comparison of different transport trajectories, gaining insight into the loss mechanisms and finding the minimum jerk trajectory to be optimum. Using the optimized parameters, we are able to transport up to $7 \times 10^6$ cesium or rubidium atoms with an efficiency up to $75\,$%. To demonstrate the viability of our transport scheme for experiments employing quantum gas microscopy, we produce Bose-Einstein condensates of either species after transport and present measurements of the simultaneous transport of both species., Comment: 15 pages, 10 figures

Ultracold polar molecules uniquely combine a rich structure of long-lived internal states with access to controllable long-range, anisotropic dipole-dipole interactions. In particular, the rotational states of polar molecules confined in optical tweezers or optical lattices may be used to encode interacting qubits for quantum computation or pseudo-spins for simulating quantum magnetism. As with all quantum platforms, the engineering of robust coherent superpositions of states is vital. However, for optically trapped molecules, the coherence time between rotational states is typically limited by inhomogeneous light shifts. Here we demonstrate a rotationally-magic optical trap for RbCs molecules that supports a Ramsey coherence time of 0.78(4) seconds in the absence of dipole-dipole interactions. This extends to >1.4 seconds at the 95% confidence level using a single spin-echo pulse. In our magic trap, dipolar interactions become the dominant mechanism by which Ramsey contrast is lost for superpositions that generate oscillating dipoles. By changing the states forming the superposition, we tune the effective dipole moment and show that the coherence time is inversely proportional to the strength of the dipolar interaction. Our work unlocks the full potential of the rotational degree of freedom in molecules for quantum computation and quantum simulation., Comment: 12 pages, 7 figures (main text and supplementary information combined)

We present a simple motorised rotation mount for a half-wave plate that can be used to rapidly change the polarization of light. We use the device to switch a high power laser beam between different optical dipole traps in an ultracold atom experiment. The device uses a stepper motor with a hollow shaft, which allows a beam to propagate along the axis of the motor shaft, minimising inertia and mechanical complexity. A simple machined adapter is used to mount the wave plate. We characterise the performance of the device, focusing on its capability to switch a beam between the output ports of a polarizing beamsplitter cube. We demonstrate a switching time of 15.9(3) ms, limited by the torque of the motor. The mount has a reaction time of 0.52(3) ms, and a rotational resolution of 0.45 degrees. The rotation is highly reproducible, with the stepper motor not missing a step in 2000 repeated tests over 11 hours., Comment: 5 pages, 4 figures, Submitted to Review of Scientific Instruments

We perform a measurement of the tune-out wavelength, $\lambda_{0}$, between the $D_{1}$, $6^2S_{1/2}\rightarrow6^2P_{1/2}$, and $D_{2}$, $6^2S_{1/2}\rightarrow6^2P_{3/2}$, transitions for $^{133}$Cs in the ground hyperfine state $(F=3, m_{F}=+3)$. At $\lambda_{0}$, the frequency-dependent scalar polarizability is zero leading to a zero scalar ac Stark shift. We measure the polarizability as a function of wavelength using Kapitza-Dirac scattering of a $^{133}$Cs Bose-Einstein condensate in a one-dimensional optical lattice, and determine the tune-out wavelength to be $\lambda_{0}=880.21790(40)_{\textrm{stat}}(8)_{\textrm{sys}}$ nm. From this measurement we determine the ratio of reduced matrix elements to be $\left|\left<{6P_{3/2}\| d\|6S_{1/2}}\right>\right|^{2}\left|\left<{6P_{1/2}\| d\|6S_{1/2}}\right>\right|^{2}=1.9808(2)$. This represents an improvement of a factor of 10 over previous results derived from excited-state lifetime measurements. We use the present measurement as a benchmark test of high-precision theory.

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., Comment: 21 pages, 9 figures

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., Comment: 19 pages, 12 figures

We explore coherent multi-photon processes in $^{87}$Rb$^{133}$Cs molecules using 3-level lambda and ladder configurations of rotational and hyperfine states, and discuss their relevance to future applications in quantum computation and quantum simulation. In the lambda configuration, we demonstrate the driving of population between two hyperfine levels of the rotational ground state via a two-photon Raman transition. Such pairs of states may be used in the future as a quantum memory, and we measure a Ramsey coherence time for a superposition of these states of 58(9) ms. In the ladder configuration, we show that we can generate and coherently populate microwave dressed states via the observation of an Autler-Townes doublet. We demonstrate that we can control the strength of this dressing by varying the intensity of the microwave coupling field. Finally, we perform spectroscopy of the rotational states of $^{87}$Rb$^{133}$Cs up to $N=6$, highlighting the potential of ultracold molecules for quantum simulation in synthetic dimensions. By fitting the measured transition frequencies we determine a new value of the centrifugal distortion coefficient $D_v=h\times207.3(2)~$Hz.

We investigate the effects of static electric and magnetic fields on the differential ac Stark shifts for microwave transitions in ultracold bosonic $^{87}$Rb$^{133}$Cs molecules, for light of wavelength $\lambda = 1064~\mathrm{nm}$. Near this wavelength we observe unexpected two-photon transitions that may cause trap loss. We measure the ac Stark effect in external magnetic and electric fields, using microwave spectroscopy of the first rotational transition. We quantify the isotropic and anisotropic parts of the molecular polarizability at this wavelength. We demonstrate that a modest electric field can decouple the nuclear spins from the rotational angular momentum, greatly simplifying the ac Stark effect. We use this simplification to control the ac Stark shift using the polarization angle of the trapping laser.

We use frequency comb-based optical two-way time-frequency transfer (O-TWTFT) to measure the optical frequency ratio of state-of-the-art ytterbium and strontium optical atomic clocks separated by a 1.5 km open-air link. Our free-space measurement is compared to a simultaneous measurement acquired via a noise-cancelled fiber link. Despite non-stationary, ps-level time-of-flight variations in the free-space link, ratio measurements obtained from the two links, averaged over 30.5 hours across six days, agree to $6\times10^{-19}$, showing that O-TWTFT can support free-space atomic clock comparisons below the $10^{-18}$ level.

Atomic clocks occupy a unique position in measurement science, exhibiting higher accuracy than any other measurement standard and underpinning six out of seven base units in the SI system. By exploiting higher resonance frequencies, optical atomic clocks now achieve greater stability and lower frequency uncertainty than existing primary standards. Here, we report frequency ratios of the $^{27}$Al$^+$, $^{171}$Yb and $^{87}$Sr optical clocks in Boulder, Colorado, measured across an optical network spanned by both fiber and free-space links. These ratios have been evaluated with measurement uncertainties between $6\times10^{-18}$ and $8\times10^{-18}$, making them the most accurate reported measurements of frequency ratios to date. This represents a critical step towards redefinition of the SI second and future applications such as relativistic geodesy and tests of fundamental physics., Comment: 51 pages, 12 figures, 6 tables

We show that the lifetime of ultracold ground-state $^{87}$Rb$^{133}$Cs molecules in an optical trap is limited by fast optical excitation of long-lived two-body collision complexes. We partially suppress this loss mechanism by applying square-wave modulation to the trap intensity, such that the molecules spend 75% of each modulation cycle in the dark. By varying the modulation frequency, we show that the lifetime of the collision complex is $0.53\pm0.06$ ms in the dark. We find that the rate of optical excitation of the collision complex is $3^{+4}_{-2}\times10^{3}$ W$^{-1}$ cm$^2$ s$^{-1}$ for $\lambda = 1550$ nm, leading to a lifetime of <100 ns for typical trap intensities. These results explain the two-body loss observed in experiments on nonreactive bialkali molecules., Comment: 6 pages, 4 figures

We report on an improved systematic evaluation of the JILA SrI optical lattice clock, achieving a nearly identical systematic uncertainty compared to the previous strontium accuracy record set by the JILA SrII optical lattice clock (OLC) at $2.1 \times 10^{-18}$. This improves upon the previous evaluation of the JILA SrI optical lattice clock in 2013, and we achieve a more than twenty-fold reduction in systematic uncertainty to $2.0 \times 10^{-18}$. A seven-fold improvement in clock stability, reaching $4.8 \times 10^{-17}/\sqrt{\tau}$ for an averaging time $\tau$ in seconds, allows the clock to average to its systematic uncertainty in under 10 minutes. We improve the systematic uncertainty budget in several important ways. This includes a novel scheme for taming blackbody radiation-induced frequency shifts through active stabilization and characterization of the thermal environment, inclusion of higher-order terms in the lattice light shift, and updated atomic coefficients. Along with careful control of other systematic effects, we achieve low temporal drift of systematic offsets and high uptime of the clock. We additionally present an improved evaluation of the second order Zeeman coefficient that is applicable to all Sr optical lattice clocks. These improvements in performance have enabled several important studies including frequency ratio measurements through the Boulder Area Clock Optical Network (BACON), a high precision comparison with the JILA 3D lattice clock, a demonstration of a new all-optical time scale combining SrI and a cryogenic silicon cavity, and a high sensitivity search for ultralight scalar dark matter., Comment: 24 pages, 9 figures

We investigate collective emission from coherently driven ultracold $ ^{88} $ Sr atoms. We perform two sets of experiments, using a strong and weak transition that are insensitive and sensitive, respectively, to atomic motion at one microKelvin. We observe highly directional forward emission with a peak intensity that is enhanced, for the strong transition, by > $ 10 ^3 $ compared to that in the transverse direction. This is accompanied by substantial broadening of spectral lines. For the weak transition, the forward enhancement is substantially reduced due to motion. Meanwhile, a density-dependent frequency shift of the weak transition (~10% of the natural linewidth) is observed. In contrast, this shift is suppressed to <1% of the natural linewidth for the strong transition. Along the transverse direction, we observe strong polarization dependences of the fluorescence intensity and line broadening for both transitions. The measurements are reproduced with a theoretical model treating the atoms as coherent, interacting, radiating dipoles., Comment: 27 pages, 4 figures

We use a phase-only spatial light modulator to generate light distributions in which the intensity decays as a power law from a central maximum, with order ranging from 2 (parabolic) to 0.5. We suggest that a sequence of these can be used as a time-dependent optical dipole trap for all-optical production of Bose-Einstein condensates in two stages: efficient evaporative cooling in a trap with adjustable strength and depth, followed by an adiabatic transformation of the trap order to cross the BEC transition in a reversible way. Realistic experimental parameters are used to verify the capability of this approach in producing larger Bose-Einstein condensates than by evaporative cooling alone., Comment: 6 pages, 6 figures, minor changes to figures, sentence added at the end of section IV