arXiv subjects

Jun-Ru Li

Publications and source records attributed to Jun-Ru Li.

11 recordsLinked to original sources

arXiv2022

Tunable itinerant spin dynamics with polar molecules

Strongly interacting spins underlie many intriguing phenomena and applications ranging from magnetism to quantum information processing. Interacting spins combined with motion display exotic spin transport phenomena, such as superfluidity arising from pairing of spins induced by spin attraction. To understand these complex phenomena, an interacting spin system with high controllability is desired. Quantum spin dynamics have been studied on different platforms with varying capabilities. Here we demonstrate tunable itinerant spin dynamics enabled by dipolar interactions using a gas of potassium-rubidium molecules confined to two-dimensional planes, where a spin-1/2 system is encoded into the molecular rotational levels. The dipolar interaction gives rise to a shift of the rotational transition frequency and a collision-limited Ramsey contrast decay that emerges from the coupled spin and motion. Both the Ising and spin exchange interactions are precisely tuned by varying the strength and orientation of an electric field, as well as the internal molecular state. This full tunability enables both static and dynamical control of the spin Hamiltonian, allowing reversal of the coherent spin dynamics. Our work establishes an interacting spin platform that allows for exploration of many-body spin dynamics and spin-motion physics utilizing the strong, tunable dipolar interaction.

cond-mat.quant-gas↗

arXiv2022

Dynamical generation of spin squeezing in ultra-cold dipolar molecules

We study a bulk fermionic dipolar molecular gas in the quantum degenerate regime confined in a two-dimensional geometry. We consider two rotational states that encode a spin 1/2 degree of freedom. We derive a long-range interacting XXZ model describing the many-body spin dynamics of the molecules valid in the regime where motional degrees of freedom are frozen. Due to the spatially extended nature of the harmonic oscillator modes, the interactions in the spin model are very long-ranged and the system behaves close to the collective limit, resulting in robust dynamics and generation of entanglement in the form of spin squeezing even at finite temperature and in presence of dephasing and chemical reactions. We demonstrate how the internal state structure can be exploited to realise time-reversal and enhanced metrological sensing protocols.

quant-ph↗

arXiv2021

Reactions Between Layer-Resolved Molecules Mediated by Dipolar Exchange

Microscopic control over polar molecules with tunable interactions would enable realization of novel quantum phenomena. Using an applied electric field gradient, we demonstrate layer-resolved state preparation and imaging of ultracold potassium-rubidium molecules confined to two-dimensional planes in an optical lattice. The coherence time of rotational superpositions in individual layers is maximized by rotating the electric field relative to the optical trap polarization to achieve state-insensitive trapping. Molecules in adjacent layers interact via dipolar exchange of rotational angular momentum; by adjusting the interaction strength between spatially separated ensembles of molecules, we regulate the local chemical reaction rate. The observed resonance width of the exchange process vastly exceeds the dipolar interaction energy, an effect we attribute to the thermal energy. This work realizes precise control of interacting molecules, enabling electric field microscopy on subwavelength length scales and allowing access to unexplored physics in two-dimensional systems.

cond-mat.quant-gas↗

arXiv2021

Tuning of dipolar interactions and evaporative cooling in a three-dimensional molecular quantum gas

Ultracold polar molecules possess long-range, anisotropic, and tunable dipolar interactions, providing the opportunities to probe quantum phenomena inaccessible with existing cold gas platforms. However, experimental progress has been hindered by the dominance of two-body loss over elastic interactions, which prevents efficient evaporative cooling. Though recent work has demonstrated controlled interactions by confining molecules to a two-dimensional geometry, a general approach for tuning molecular interactions in a three-dimensional (3D), stable system has been lacking. Here, we demonstrate tunable elastic dipolar interactions in a bulk gas of ultracold 40K87Rb molecules in 3D, facilitated by an electric field-induced shielding resonance which suppresses the reactive loss by a factor of thirty. This improvement in the ratio of elastic to inelastic collisions enables direct thermalization. The thermalization rate depends on the angle between the collisional axis and the dipole orientation controlled by an external electric field, a direct manifestation of the anisotropic dipolar interaction. We achieve evaporative cooling mediated by the dipolar interactions in three dimensions. This work demonstrates full control of a long-lived bulk quantum gas system with tunable long-range interactions, paving the way for the study of collective quantum many-body physics.

cond-mat.quant-gas↗

arXiv2020

Resonant collisional shielding of reactive molecules using electric fields

Full control of molecular interactions, including reactive losses, would open new frontiers in quantum science. Here, we demonstrate extreme tunability of chemical reaction rates by using an external electric field to shift excited collision channels of ultracold molecules into degeneracy with the initial collision channel. In this situation, resonant dipolar interactions mix the channels at long range, dramatically altering the intermolecular potential. We prepare fermionic potassium-rubidium (KRb) molecules in their first excited rotational state and observe a three orders-of-magnitude modulation of the chemical reaction rate as we tune the electric field strength by a few percent across resonance. In a quasi-two-dimensional geometry, we accurately determine the contributions from the three lowest angular momentum projections of the collisions. Using the resonant features, we shield the molecules from loss and suppress the reaction rate by up to an order of magnitude below the background value, realizing a long-lived sample of polar molecules in large electric fields.

cond-mat.quant-gas↗

arXiv2020

Dipolar evaporation of reactive molecules to below the Fermi temperature

Molecules are the building blocks of matter and their control is key to the investigation of new quantum phases, where rich degrees of freedom can be used to encode information and strong interactions can be precisely tuned. Inelastic losses in molecular collisions, however, have greatly hampered the engineering of low-entropy molecular systems. So far, the only quantum degenerate gas of molecules has been created via association of two highly degenerate atomic gases. Here, we use an external electric field along with optical lattice confinement to create a two-dimensional (2D) Fermi gas of spin-polarized potassium-rubidium (KRb) polar molecules, where elastic, tunable dipolar interactions dominate over all inelastic processes. Direct thermalization among the molecules in the trap leads to efficient dipolar evaporative cooling, yielding a rapid increase in phase-space density. At the onset of quantum degeneracy, we observe the effects of Fermi statistics on the thermodynamics of the molecular gas. These results demonstrate a general strategy for achieving quantum degeneracy in dipolar molecular gases to explore strongly interacting many-body phases.

cond-mat.quant-gas↗

arXiv2020

Quantum Many-Body Physics with Ultracold Polar Molecules: Nanostructured Potential Barriers and Interactions

We design dipolar quantum many-body Hamiltonians that will facilitate the realization of exotic quantum phases under current experimental conditions achieved for polar molecules. The main idea is to modulate both single-body potential barriers and two-body dipolar interactions on a spatial scale of tens of nanometers to strongly enhance energy scales and, therefore, relax temperature requirements for observing new quantum phases of engineered many-body systems. We consider and compare two approaches. In the first, nanoscale barriers are generated with standing wave optical light fields exploiting optical nonlinearities. In the second, static electric field gradients in combination with microwave dressing are used to write nanostructured spatial patterns on the induced electric dipole moments, and thus dipolar interactions. We study the formation of inter-layer and interface bound states of molecules in these configurations, and provide detailed estimates for binding energies and expected losses for present experimental setups.

cond-mat.quant-gas↗

arXiv2019

Thermalization and Sub-Poissonian Density Fluctuations in a Degenerate Molecular Fermi Gas

We observe thermalization in the production of a degenerate Fermi gas of polar ${}^{40}\text{K}{}^{87}\text{Rb}$ molecules. By measuring the atom--dimer elastic scattering cross section near the Feshbach resonance, we show that Feshbach molecules rapidly reach thermal equilibrium with both parent atomic species. Equilibrium is essentially maintained through coherent transfer to the ground state. Sub-Poissonian density fluctuations in Feshbach and ground-state molecules are measured, giving an independent characterization of degeneracy and directly probing the molecular Fermi--Dirac distribution.

cond-mat.quant-gas↗

arXiv2019

Floquet Heating in Interacting Atomic Gases with an Oscillating Force

We theoretically investigate the collisional heating of a cold atom system subjected to time-periodic forces. We show within the Floquet framework that this heating rate due to two-body collisions has a general semiclassical expression $\mathcal{P}\propto ρσv_{\rm col} E_0$, depending on the kinetic energy $E_0$ associated with the shaking, particle number density $ρ$, elastic collision cross section $σ$, and an effective collisional velocity $v_{\rm col}$ determined by the dominant energy scale in the system. We further show that the collisional heating is suppressed by Pauli blocking in cold fermionic systems, and by the modified density of states in systems in lower dimensions. Our results provide an exactly solvable example and reveal some general features of Floquet heating in interacting systems.

physics.atom-ph↗

arXiv2018

How to dress radio-frequency photons with tunable momentum

We demonstrate how the combination of oscillating magnetic forces and radio-frequency (RF) pulses endows RF photons with tunable momentum. We observe velocity-selective spinflip transitions and the associated Doppler shift. This realizes the key component of purely magnetic spin-orbit coupling schemes for ultracold atoms, which does not involve optical transitions and therefore avoids the problem of heating due to spontaneous emission.

physics.atom-ph↗

arXiv2017

Observation of the supersolid stripe phase in spin-orbit coupled Bose-Einstein condensates

Supersolidity is an intriguing concept. It combines the property of superfluid flow with the long-range spatial periodicity of solids, two properties which are often mutually exclusive. The original discussion of quantum crystals and supersolidity focuses on solid Helium-4 where it was predicted that vacancies could form dilute weakly interacting Bose-Einstein condensates. In this system, direct observation of supersolidity has been elusive. The concept of supersolidity was then generalized to include other superfluid systems which break the translational symmetry of space. One of such systems is a Bose-Einstein condensate with spin-orbit coupling which has a supersolid stripe phase. Despite several recent studies of this system, the stripe phase has not been observed. Here we report the direct observation of the predicted density modulation of the stripe phase using Bragg reflection. Our work establishes a system with unique symmetry breaking properties. Of future interest is further spatial symmetry breaking through the introduction of vortices, solitons, impurities or disorder.

cond-mat.quant-gas↗