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Abstract Flat bands in condensed matter systems can host emergent states of matter, from insulating states in twisted bilayer graphene to fractionalized excitations in frustrated magnets and quantum Hall materials. A key phenomenon in certain flat-band systems is Aharonov–Bohm caging, where particles become localized due to destructive interference caused by gauge fields. Here we report on the experimental realization of highly tunable flat-band models populated by strongly interacting Rydberg atoms. By employing synthetic dimensions, we engineer a flat-band rhombic lattice with twisted boundaries and explore the control of Aharonov–Bohm caging during non-equilibrium dynamics through a tunable gauge field. Microscopic measurements of Rydberg pairs reveal the interaction-driven breakdown of Aharonov–Bohm caging in the limit of strong dipolar interactions, where lattice bands mix. In the limit of weak interactions, where caging persists, we observe effective magnetism arising from the interaction-driven mixing of degenerate flat-band states. These observations offer insights into emergent phenomena in synthetic quantum materials and expand our understanding of quantum many-body physics in engineered lattice systems. 

Abstract Molecules have vibrational, rotational, spin-orbit and hyperfine degrees of freedom or quantum states, each of which responds in a unique fashion to external electromagnetic radiation. The control over superpositions of these quantum states is key to coherent manipulation of molecules. For example, the better the coherence time the longer quantum simulations can last. The important quantity for controlling an ultracold molecule with laser light is its complex-valued molecular dynamic polarizability. Its real part determines the tweezer or trapping potential as felt by the molecule, while its imaginary part limits the coherence time. Here, our study shows that efficient trapping of a molecule in its vibrational ground state can be achieved by selecting a laser frequency with a detuning on the order of tens of GHz relative to an electric-dipole-forbidden molecular transition. Close proximity to this nearly forbidden transition allows to create a sufficiently deep trapping potential for multiple rotational states without sacrificing coherence times among these states from Raman and Rayleigh scattering. In fact, we demonstrate that magic trapping conditions for multiple rotational states of the ultracold²³Na⁸⁷Rb polar molecule can be created. 

Abstract Synthetic dimensions, wherein dynamics occurs in a set of internal states, have found great success in recent years in exploring topological effects in cold atoms and photonics. However, the phenomena thus far explored have largely been restricted to the non-interacting or weakly interacting regimes. Here, we extend the synthetic dimensions playbook to strongly interacting systems of Rydberg atoms prepared in optical tweezer arrays. We use precise control over driving microwave fields to introduce a tunableU(1) flux in a four-site lattice of coupled Rydberg levels. We find highly coherent dynamics, in good agreement with theory. Single atoms show oscillatory dynamics controllable by the gauge field. Small arrays of interacting atoms exhibit behavior suggestive of the emergence of ergodic and arrested dynamics in the regimes of intermediate and strong interactions, respectively. These demonstrations pave the way for future explorations of strongly interacting dynamics and many-body phases in Rydberg synthetic lattices. 

Novel geometries can be created using microwaves to couple the internal states of atoms or molecules and mimic movement in real space. 

The geometrical Berry phase is key to understanding the behavior of quantum states under cyclic adiabatic evolution. When generalized to non-Hermitian systems with gain and loss, the Berry phase can become complex and should modify not only the phase but also the amplitude of the state. Here, we perform the first experimental measurements of the adiabatic non-Hermitian Berry phase, exploring a minimal two-site PT-symmetric Hamiltonian that is inspired by the Hatano-Nelson model. We realize this non-Hermitian model experimentally by mapping its dynamics to that of a pair of classical oscillators coupled by real-time measurement-based feedback. As we verify experimentally, the adiabatic non-Hermitian Berry phase is a purely geometrical effect that leads to significant amplification and damping of the amplitude also for noncyclical paths within the parameter space even when all eigenenergies are real. We further observe a non-Hermitian analog of the Aharonov-Bohm solenoid effect, observing amplification and attenuation when encircling a region of broken PT symmetry that serves as a source of imaginary flux. This experiment demonstrates the importance of geometrical effects that are unique to non-Hermitian systems and paves the way towards further studies of non-Hermitian and topological physics in synthetic metamaterials. 

Non-Hermitian two-site dimers serve as minimal models in which to explore the interplay of gain and loss in dynamical systems. In this paper, we experimentally and theoretically investigate the dynamics of non-Hermitian dimer models with nonreciprocal hoppings between the two sites. We investigate two types of non-Hermitian couplings; one is when asymmetric hoppings are externally introduced, and the other is when the nonreciprocal hoppings depend on the population imbalance between the two sites, thus introducing the non-Hermiticity in a dynamical manner. We engineer the models in our synthetic mechanical setup comprised of two classical harmonic oscillators coupled by measurement-based feedback. For fixed nonreciprocal hoppings, we observe that, when the strength of these hoppings is increased, there is an expected transition from a PT-symmetric regime, where oscillations in the population are stable and bounded, to a PT-broken regime, where the oscillations are unstable and the population grows/decays exponentially. However, when the non-Hermiticity is dynamically introduced, we also find a third intermediate regime in which these two behaviors coexist, meaning that we can tune from stable to unstable population dynamics by simply changing the initial phase difference between the two sites. As we explain, this behavior can be understood by theoretically exploring the emergent fixed points of a related dimer model in which the nonreciprocal hoppings depend on the normalized population imbalance. Our study opens the way for the future exploration of non-Hermitian dynamics and exotic lattice models in synthetic mechanical networks. 

Metamaterials based on mechanical elements have been developed over the past decade as a powerful platform for exploring analogs of electron transport in exotic regimes that are hard to produce in real materials. In addition to enabling new physics explorations, such developments promise to advance the control over acoustic and mechanical metamaterials, and consequently to enable new capabilities for controlling the transport of sound and energy. Here, we demonstrate the building blocks of highly tunable mechanical metamaterials based on real-time measurement and feedback of modular mechanical elements. We experimentally engineer synthetic lattice Hamiltonians describing the transport of mechanical energy (phonons) in our mechanical system, with control over local site energies and loss and gain as well as over the complex hopping between oscillators, including a natural extension to nonreciprocal hopping. Beyond linear terms, we experimentally demonstrate how this measurement-based feedback approach makes it possible to independently introduce nonlinear interaction terms. Looking forward, synthetic mechanical lattices open the door to exploring phenomena related to topology, non-Hermiticity, and nonlinear dynamics in nonstandard geometries, higher dimensions, and with novel multibody interactions.