The interplay of quantum statistics and interactions in atomic Bose–Fermi mixtures leads to a phase diagram markedly different from pure fermionic or bosonic systems. However, investigating this phase diagram remains challenging when bosons condense. Here, we observe evidence for a quantum phase transition from a polaronic to a molecular phase in a density-matched degenerate Bose–Fermi mixture. The condensate fraction, representing the order parameter of the transition, is depleted by interactions and the build-up of strong correlations results in the emergence of a molecular Fermi gas. By driving through the transition, we ultimately produce a quantum-degenerate sample of sodium-potassium molecules exhibiting a large molecule-frame dipole moment of 2.7 Debye. The observed phase transition represents a new phenomenon complementary to the paradigmatic BEC-BCS crossover observed in Fermi systems.

Scattering resonances are an essential tool for controlling the interactions of ultracold atoms and molecules. However, conventional Feshbach scattering resonances 1 , which have been extensively studied in various platforms 1 – 7 , are not expected to exist in most ultracold polar molecules because of the fast loss that occurs when two molecules approach at a close distance 8 – 10 . Here we demonstrate a new type of scattering resonance that is universal for a wide range of polar molecules. The so-called field-linked resonances 11 – 14 occur in the scattering of microwave-dressed molecules because of stable macroscopic tetramer states in the intermolecular potential. We identify two resonances between ultracold ground-state sodium–potassium molecules and use the microwave frequencies and polarizations to tune the inelastic collision rate by three orders of magnitude, from the unitary limit to well below the universal regime. The field-linked resonance provides a tuning knob to independently control the elastic contact interaction and the dipole–dipole interaction, which we observe as a modification in the thermalization rate. Our result provides a general strategy for resonant scattering between ultracold polar molecules, which paves the way for realizing dipolar superfluids 15 and molecular supersolids 16 , as well as assembling ultracold polyatomic molecules.

Ultracold fermionic Feshbach molecules are promising candidates for exploring quantum matter with strong $p$-wave interactions, however, their lifetimes were measured to be short. Here, we characterize the $p$-wave collisions of ultracold fermionic $^{23}\mathrm{Na}^{40}\mathrm{K}$ Feshbach molecules for different scattering lengths and temperatures. By increasing the binding energy of the molecules, the two-body loss coefficient reduces by three orders of magnitude leading to a second-long lifetime, 20 times longer than that of ground-state molecules. We exploit the scaling of elastic and inelastic collisions with the scattering length and temperature to identify a regime where the elastic collisions dominate over the inelastic ones allowing the molecular sample to thermalize. Our work provides a benchmark for four-body calculations of molecular collisions and is essential for producing a degenerate Fermi gas of Feshbach molecules.

We study three-body loss in an ultracold mixture of a thermal Bose gas and a degenerate Fermi gas. We find that at unitarity, where the interspecies scattering length diverges, the usual inverse-square temperature scaling of the three-body loss found in nondegenerate systems is strongly modified and reduced with the increasing degeneracy of the Fermi gas. While the reduction of loss is qualitatively explained within the few-body scattering framework, a remaining suppression provides evidence for the long-range Ruderman-Kittel-Kasuya-Yosida (RKKY) interactions mediated by fermions between bosons. Our model based on RKKY interactions quantitatively reproduces the data without free parameters, and predicts one order of magnitude reduction of the three-body loss coefficient in the deeply Fermi-degenerate regime.

Ultracold polar molecules offer strong electric dipole moments and rich internal structure, which makes them ideal building blocks to explore exotic quantum matter 1 – 9 , implement quantum information schemes 10 – 12 and test the fundamental symmetries of nature 13 . Realizing their full potential requires cooling interacting molecular gases deeply into the quantum-degenerate regime. However, the intrinsically unstable collisions between molecules at short range have so far prevented direct cooling through elastic collisions to quantum degeneracy in three dimensions. Here we demonstrate evaporative cooling of a three-dimensional gas of fermionic sodium–potassium molecules to well below the Fermi temperature using microwave shielding. The molecules are protected from reaching short range with a repulsive barrier engineered by coupling rotational states with a blue-detuned circularly polarized microwave. The microwave dressing induces strong tunable dipolar interactions between the molecules, leading to high elastic collision rates that can exceed the inelastic ones by at least a factor of 460. This large elastic-to-inelastic collision ratio allows us to cool the molecular gas to 21 nanokelvin, corresponding to 0.36 times the Fermi temperature. Such cold and dense samples of polar molecules open the path to the exploration of many-body phenomena with strong dipolar interactions.

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We demonstrate the transfer of NaK molecules from a closed-channel dominated Feshbachmolecule state to the absolute ground state. The Feshbach molecules are initially created from a gas of sodium and potassium atoms via adiabatic ramping over a Feshbach resonance at 78.3 G. The molecules are then transferred to the absolute ground state using stimulated Raman adiabatic passage with an intermediate state in the spin-orbit-coupled complex |cΣ, v = 35, J = 1〉 ∼ |BΠ, v = 12, J = 1〉. Our measurements show that the pump transition dipole moment linearly increases with the closed-channel fraction. Thus, the pump-beam intensity can be two orders of magnitude lower than is necessary with open-channel dominated Feshbach molecules. We also demonstrate that the phase noise of the Raman lasers can be reduced by filter cavities, significantly improving the transfer efficiency.

Roman Bause, 2 Andreas Schindewolf, 2 Renhao Tao, 2 Marcel Duda, 2 Xing-Yan Chen, 2 Goulven Quéméner, Tijs Karman, Arthur Christianen, 2 Immanuel Bloch, 2, 5 and Xin-Yu Luo 2, ∗ Max-Planck-Institut für Quantenoptik, 85748 Garching, Germany Munich Center for Quantum Science and Technology, 80799 München, Germany Université Paris-Saclay, CNRS, Laboratoire Aimé Cotton, 91405 Orsay, France Radboud University, Institute for Molecules and Materials, Heijendaalseweg 135, 6525 AJ Nijmegen, The Netherlands Fakultät für Physik, Ludwig-Maximilians-Universität, 80799 München, Germany (Dated: June 25, 2021)

We demonstrate a versatile, state-dependent trapping scheme for the ground and first excited rotational states of ^{23}Na^{40}K molecules. Close to the rotational manifold of a narrow electronic transition, we determine tune-out frequencies where the polarizability of one state vanishes while the other remains finite, and a magic frequency where both states experience equal polarizability. The proximity of these frequencies of only 10 GHz allows for dynamic switching between different trap configurations in a single experiment, while still maintaining sufficiently low scattering rates.