arXiv subjects

Xin-Yu Luo

Publications and source records attributed to Xin-Yu Luo.

At least 19 recordsLinked to original sources

arXiv2026

Controlled symmetry breaking of the Fermi surface in ultracold polar molecules

Long-range anisotropic dipole-dipole interactions between ultracold polar molecules are predicted to drive exotic quantum phases, yet direct many-body signatures of these interactions in degenerate Fermi gases have remained elusive. Here, we report the observation of an interaction-induced controlled deformation of the Fermi surface, providing a clear many-body signature in a deeply degenerate Fermi gas of $^{23}\text{Na}^{40}\text{K}$ molecules. Using double microwave (MW) shielding, we prepare $8 \times 10^3$ molecules at $0.23(1)$ times the Fermi temperature, achieving a three-fold suppression of inelastic losses compared to single MW shielding while preserving strong elastic dipolar scattering. We observe Fermi surface deformations of up to $7\,\%$, more than two times larger than those observed in magnetic atoms, despite operating at two orders of magnitude lower densities. Crucially, we demonstrate continuous tuning of the interaction potential from axial U(1) to biaxial C$_{2}$ symmetry, directly imprinting this geometry onto the Fermi surface. We find excellent agreement between our experimental results and parameter-free Hartree-Fock theory. These results establish MW-shielded polar molecules as a highly tunable platform for exploring strongly correlated dipolar Fermi matter and offer a promising path towards topological superfluidity.

cond-mat.quant-gas↗

arXiv2025

High-flux cold lithium-6 and rubidium-87 atoms from compact two-dimensional magneto-optical traps

We report a compact setup with in-series two-dimensional magneto-optical traps (2D MOTs) that provides high-flux cold lithium and rubidium atoms. Thanks to the efficient short-distance Zeeman slowing, the maximum 3D MOT loading rate of lithium atoms reaches a record value of $6.6\times 10^{9}$ atoms/s at a moderate lithium-oven temperature of 372 degrees Celsius, which is 44 times higher than that without the Zeeman slowing light. The flux of rubidium is also as high as $2.3\times10^9$ atoms/s with the rubidium oven held at room temperature. Meanwhile, the entire vacuum-chamber system, including an ultra-high-vacuum science cell, is within a small volume of $55\times65\times70~\mathrm{cm}^3$. Our work represents a substantial improvement over traditional bulky and complex dual-species cold-atom setups. It provides a good starting point for the fast production of a double-degenerate lithium-rubidium atomic mixture and large samples of ultracold lithium-rubidium ground-state molecules.

physics.atom-ph↗

arXiv2025

Generation of strong ultralow-phase-noise microwave fields with tunable ellipticity for ultracold polar molecules

Microwave(MW) fields with strong field strength, ultralow phase-noise and tunable polarization are crucial for stabilizing and manipulating ultracold polar molecules, which have emerged as a promising platform for quantum sciences. In this letter, we present the design, characterization, and performance of a robust MW setup tailored for precise control of molecular states. This setup achieves a high electric field intensity of 6.9 kV/m in the near-field from a dual-feed waveguide antenna, enabling a Rabi frequency as high as 71 MHz for the rotational transition of sodium-potassium molecules. In addition, the low noise signal source and controlled electronics provide ultralow phase-noise and dynamically tunable polarization. Narrow-band filters within the MW circuitry further reduce phase-noise by more than 20 dB at 20 MHz offset frequency, ensuring prolonged one-body molecular lifetimes up to 10 seconds. We also show practical methods to measure the MW field strength and polarization using a simple homemade dipole probe, and to characterize phase-noise down to -170 dBc/Hz with a commercial spectrum analyser and a notch filter. Those capabilities allowed us to evaporatively cool our molecular sample to deep quantum degeneracy. Furthermore, the polarization tunability enabled the observation of field-linked resonances and facilitated the creation of field-linked tetramers.These techniques advance the study of ultracold polar molecules and broaden the potential applications of MW tools in other platforms of quantum sciences.

physics.atom-ph↗

arXiv2024

Simulations of evaporation to deep Fermi degeneracy in microwave-shielded molecules

In the quest toward realizing novel quantum matter in ultracold molecular gases, we perform a numerical study of evaporative cooling in ultracold gases of microwave-shielded polar fermionic molecules. Our Monte Carlo simulations incorporate accurate two-body elastic and inelastic scattering cross sections, realistic modeling of the optical dipole trap, and the influence of Pauli blocking at low temperatures. The simulations are benchmarked against data from evaporation studies performed with ultracold NaK molecules, showing excellent agreement. We further explore the prospects for optimizing the evaporation efficiency by varying the ramp rate and duration of the evaporation trajectory. Our simulation shows that it is possible to reach $< 10\%$ of the Fermi temperature under optimal conditions even in the presence of two-body molecular losses.

cond-mat.quant-gas↗

arXiv2024

Genetics-based deperturbation analysis for the spin-orbit coupled ${\rm A}^1\Sigma^+$ and ${\rm b}^3\Pi_{0^+}$ states of LiRb

We present a deperturbation analysis of the spin-orbit coupled $\rm A^1\Sigma^+$ and $\rm b^3\Pi_{0^+}$ states of LiRb based on the rovibrational energy levels observed previously by photoassociation spectroscopy in bosonic $^7$Li$^{85}$Rb molecule. Using the genetic algorithm, we fit the potential energy curves of the $\rm A^1\Sigma^+$ state and the $\rm b^3\Pi$ state into point-wise form. We then fit these point-wise potentials along with the spin-orbit coupling into expanded Morse oscillator functional form and optimise analytical parameters based on the experimental data. From the fitted results, we calculate the transition dipole moment matrix elements for transitions from the rovibrational levels of the coupled $\rm A^1\Sigma^+$-$\rm b^3\Pi_{0^+}$ state to the Feshbach state and the absolute rovibrational ground state for fermionic $^6$Li$^{87}$Rb molecule. Based on the calculated transition dipole moment matrix elements, several levels of the coupled $\rm A^1\Sigma^+$-$\rm b^3\Pi_{0^+}$ state are predicted to be suitable as the intermediate state for stimulated Raman adiabatic passage transfer from the Feshbach state to the absolute rovibrational ground state. In addition, we also provide a similar estimation for ${\rm B}^1\Pi$-${\rm c}^3\Sigma_1^+$-${\rm b}^3\Pi_1$ state based on available $ab\ initio$ interaction potentials.

physics.atom-ph↗

arXiv2024

Formation and Dissociation of Field-Linked Tetramers

We investigate the static and dynamic properties of tetratomic molecules formed by two microwave-shielded polar molecules across field-linked resonances. In particular, we focus on two-body physics and experimental techniques unexplored in the recent experiment [X.-Y. Chen {\it et al}., Nature {\bf626}, 283 (2024)]. We show that, compared to the lowest tetramer state, higher tetramer states typically have longer lifetimes, which may facilitate a further cooling of tetramer gases towards quantum degeneracy. To detect tetramers, we identify the distinctive time-of-flight images from ramp dissociation, which can be observed by lowering the ramp rate of the microwave. Remarkably, in the modulational dissociation of tetramers, we find that multi-photon processes induce dissociation even below the threshold modulation frequency when the modulation amplitude is sufficiently high. Given the universal form of the inter-molecular potential for microwave-shielded polar molecules, our results also apply to other molecular gases widely explored in recent experiments.

quant-ph↗

arXiv2023

Ultracold field-linked tetratomic molecules

Ultracold polyatomic molecules offer intriguing new opportunities in cold chemistry, precision measurements, and quantum information processing, thanks to their rich internal structure. However, their increased complexity compared to diatomic molecules presents a formidable challenge to employ conventional cooling techniques. Here, we demonstrate a new approach to create ultracold polyatomic molecules by electroassociation in a degenerate Fermi gas of microwave-dressed polar molecules through a field-linked resonance. Starting from ground state NaK molecules, we create around $1.1\times 10^3$ tetratomic (NaK)$_2$ molecules, with a phase space density of $0.040(3)$ at a temperature of $134(3)\,\text{nK}$, more than $3000$ times colder than previously realized tetratomic molecules. We observe a maximum tetramer lifetime of $8(2)\,\text{ms}$ in free space without a notable change in the presence of an optical dipole trap, indicating these tetramers are collisionally stable. The measured binding energy and lifetime agree well with parameter-free calculations, which outlines pathways to further increase the lifetime of the tetramers. Moreover, we directly image the dissociated tetramers through microwave-field modulation to probe the anisotropy of their wave function in momentum space. Our result demonstrates a universal tool for assembling ultracold polyatomic molecules from smaller polar molecules, which is a crucial step towards Bose--Einstein condensation (BEC) of polyatomic molecules and towards a new crossover from a dipolar Bardeen-Cooper-Schrieffer (BCS) superfluid to a BEC of tetramers. Additionally, the long-lived FL state provides an ideal starting point for deterministic optical transfer to deeply bound tetramer states.

cond-mat.quant-gas↗

arXiv2023

Ultracold Sticky Collisions: Theoretical and Experimental Status

Collisional complexes, which are formed as intermediate states in molecular collisions, are typically short-lived and decay within picoseconds. However, in ultracold collisions involving bialkali molecules, complexes can live for milliseconds, completely changing the collision dynamics. This can lead to unexpected two-body loss in samples of nonreactive molecules. During the last decade, such "sticky" collisons have been a major hindrance in the preparation of dense and stable molecular samples, especially in the quantum-degenerate regime. Currently, the behavior of the complexes is not fully understood. For example, in some cases their lifetime has been measured to be many orders of magnitude longer than recent models predict. This is not only an intriguing problem in itself but also practically relevant, since understanding molecular complexes may help to mitigate their detrimental effects. Here, we review the recent experimental and theoretical progress in this field. We treat the case of molecule-molecule as well as molecule-atom collisions.

physics.chem-ph↗

arXiv2022

Field-linked resonances of polar molecules

Scattering resonances are an essential tool for controlling interactions of ultracold atoms and molecules. However, conventional Feshbach scattering resonances, which have been extensively studied in various platforms, are not expected to exist in most ultracold polar molecules due to the fast loss that occurs when two molecules approach at a close distance. Here, we demonstrate a new type of scattering resonances that is universal for a wide range of polar molecules. The so-called field-linked resonances occur in the scattering of microwave-dressed molecules due to 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 and molecular supersolids as well as assembling ultracold polyatomic molecules.

cond-mat.quant-gas↗

arXiv2022

Effective potential and superfluidity of microwave-dressed polar molecules

For microwave-dressed polar molecules, we analytically derive an intermolecular potential composed of an anisotropic van der Waals shielding core and a long-range dipolar interaction. We validate this effective potential by comparing its scattering properties with those calculated using the full multi-channel interaction potential. It is shown that scattering resonances can be induced by a sufficiently strong microwave field. We also show the power of the effective potential in the study of many-body physics by calculating the critical temperature of the Bardeen-Cooper-Schrieffer pairing in the microwave-dressed NaK gas. It turns out that the effective potential is well-behaved and extremely suitable for studying the many-body physics of the molecular gases. Our results pave the way for the studies of the many-body physics of the ultracold microwave-dressed molecular gases.

physics.atom-ph↗

arXiv2022

Suppression of Unitary Three-body Loss in a Degenerate Bose-Fermi Mixture

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 non-degenerate 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 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.

cond-mat.quant-gas↗

arXiv2022

Long-lived fermionic Feshbach molecules with tunable $p$-wave interactions

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.

cond-mat.quant-gas↗

arXiv2022

Evaporation of microwave-shielded polar molecules to quantum degeneracy

Ultracold polar molecules offer strong electric dipole moments and rich internal structure, which makes them ideal building blocks to explore exotic quantum matter, implement novel quantum information schemes, or test fundamental symmetries of nature. Realizing their full potential requires cooling interacting molecular gases deeply into the quantum degenerate regime. However, the complexity of molecules which makes their collisions intrinsically unstable at the short range, even for nonreactive molecules, has so far prevented the cooling 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 down to 21 nanokelvin, corresponding to 0.36 times the Fermi temperature. Such unprecedentedly cold and dense samples of polar molecules open the path to the exploration of novel many-body phenomena, such as the long-sought topological p-wave superfluid states of ultracold matter.

cond-mat.quant-gas↗

arXiv2021

Transition from a polaronic condensate to a degenerate Fermi gas of heteronuclear molecules

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.

cond-mat.quant-gas↗

arXiv2021

Efficient conversion of closed-channel dominated Feshbach molecules of $^{23}$Na$^{40}$K to their absolute ground state

We demonstrate the transfer of $^{23}$Na$^{40}$K molecules from a closed-channel dominated Feshbach-molecule 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 $|c^3 Σ^+, v=35, J=1 \rangle \sim |B^1Π, v=12, J=1\rangle$. 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.

cond-mat.quant-gas↗

arXiv2021

Collisions of ultracold molecules in bright and dark optical dipole traps

Understanding collisions between ultracold molecules is crucial for making stable molecular quantum gases and harnessing their rich internal degrees of freedom for quantum engineering. Transient complexes can strongly influence collisional physics, but in the ultracold regime, key aspects of their behavior have remained unknown. To explain experimentally observed loss of ground-state molecules from optical dipole traps, it was recently proposed that molecular complexes can be lost due to photo-excitation. By trapping molecules in a repulsive box potential using laser light near a narrow molecular transition, we are able to test this hypothesis with light intensities three orders of magnitude lower than what is typical in red-detuned dipole traps. This allows us to investigate light-induced collisional loss in a gas of nonreactive fermionic $^{23}$Na$^{40}$K molecules. Even for the lowest intensities available in our experiment, our results are consistent with universal loss, meaning unit loss probability inside the short-range interaction potential. Our findings disagree by at least two orders of magnitude with latest theoretical predictions, showing that crucial aspects of molecular collisions are not yet understood, and provide a benchmark for the development of new theories.

cond-mat.quant-gas↗

arXiv2020

Tune-out and magic wavelengths for ground-state $^{23}$Na$^{40}$K molecules

We demonstrate a versatile, rotational-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.

cond-mat.quant-gas↗

arXiv2018

Extending rotational coherence of interacting polar molecules in a spin-decoupled magic trap

Superpositions of rotational states in polar molecules induce strong, long-range dipolar interactions. Here we extend the rotational coherence by nearly one order of magnitude to 8.7(6) ms in a dilute gas of polar $^{23}$Na$^{40}$K molecules in an optical trap. We demonstrate spin-decoupled magic trapping, which cancels first-order and reduces second-order differential light shifts. The latter is achieved with a dc electric field that decouples nuclear spin, rotation and trapping light field. We observe density-dependent coherence times, which can be explained by dipolar interactions in the bulk gas.

cond-mat.quant-gas↗