Understanding and controlling collisions is crucial to the burgeoning field of ultracold molecules. All experiments so far have observed fast loss of molecules from the trap. However, the dominant mechanism for collisional loss is not well understood when there are no allowed 2-body loss processes. Here we experimentally investigate collisional losses of nonreactive ultracold 87 Rb 133 Cs molecules, and compare our findings with the sticky collision hypothesis that pairs of molecules form long-lived collision complexes. We demonstrate that loss of molecules occupying their rotational and hyperfine ground state is best described by second-order rate equations, consistent with the expectation for complex-mediated collisions, but that the rate is lower than the limit of universal loss. The loss is insensitive to magnetic field but increases for excited rotational states. We demonstrate that dipolar effects lead to significantly faster loss for an incoherent mixture of rotational states.

Polar molecules are an emerging platform for quantum technologies based on their long-range electric dipole-dipole interactions, which open new possibilities for quantum information processing and the quantum simulation of strongly correlated systems. Here, we use magnetic and microwave fields to design a fast entangling gate with >0.999 fidelity and which is robust with respect to fluctuations in the trapping and control fields and to small thermal excitations. These results establish the feasibility to build a scalable quantum processor with a broad range of molecular species in optical-lattice and optical-tweezers setups.

We model sympathetic cooling of ground-state CaF molecules by ultracold Li and Rb atoms. The molecules are moving in a microwave trap, while the atoms are trapped magnetically. We calculate the differential elastic cross sections for CaF-Li and CaF-Rb collisions, using model Lennard-Jones potentials adjusted to give typical values for the s-wave scattering length. Together with trajectory calculations, these differential cross sections are used to simulate the cooling of the molecules, the heating of the atoms, and the loss of atoms from the trap. We show that a hard-sphere collision model based on an energy-dependent momentum transport cross section accurately predicts the molecule cooling rate but underestimates the rates of atom heating and loss. Our simulations suggest that Rb is a more effective coolant than Li for ground-state molecules, and that the cooling dynamics are less sensitive to the exact value of the s-wave scattering length when Rb is used. Using realistic experimental parameters, we find that molecules can be sympathetically cooled to 100$\mu$K in about 10s. By applying evaporative cooling to the atoms, the cooling rate can be increased and the final temperature of the molecules can be reduced to 1$\mu$K within 30s.Comment: 16 pages, 14 figures. Minor corrections picked up at proof stag

We investigate the behaviour of single-channel theoretical models of cold and ultracold collisions that take account of inelastic and reactive processes using a single parameter to represent shortrange loss. We present plots of the resulting energy-dependence of elastic and inelastic or reactive cross-sections over the full parameter space of loss parameters and short-range phase shifts. We then test the single-channel model by comparing it with the results of coupled-channel calculations of rotationally inelastic collisions between LiH molecules and Li atoms. We find that the range of cross-sections predicted by the single-channel model becomes increasingly accurate as the initial LiH rotational quantum number increases, with a corresponding increase in the number of open loss channels. The results suggest that coupled-channel calculations at very low energy (in the s-wave regime) could in some cases be used to estimate a loss parameter and then to predict the range of possible loss rates at higher energy, without the need for explicit coupled-channel calculations for higher partial waves., the long-range wavefunction may be expressed in terms of the analytical solutions for the long-range potential [11,12]. The model of Idziaszek and Julienne [6] successfully explained the temperature dependence of reactive KRb+KRb collisions at temperatures below 1 μK, and was later extended [13] to handle the additional − r 3 dipole-dipole potential that exists when the KRb molecules are oriented with an external electric field. More recently, Jachymski et al [14,15] have extended similar models up to the high-temperature limit, and used them to interpret merged-beam experiments on Penning ionization in collisions of metastable He with Ar [4].

We perform two-photon photoassociation spectroscopy of the heteronuclear CsYb molecule to measure the binding energies of near-threshold vibrational levels of the X 2 Σ + 1/2 molecular ground state. We report results for 133 Cs 170 Yb, 133 Cs 173 Yb and 133 Cs 174 Yb, in each case determining the energy of several vibrational levels including the least-bound state. We fit an interaction potential based on electronic structure calculations to the binding energies for all three isotopologs and find that the ground-state potential supports 77 vibrational levels. We use the fitted potential to predict the interspecies s-wave scattering lengths for all seven Cs+Yb isotopic mixtures.