Kritsana Srakaew

The competition of different length scales in quantum many-body systems leads to phenomena such as correlated dynamics and nonlocal order. To investigate such effects in an itinerant lattice-based quantum simulator, it has been proposed to introduce tunable extended-range interactions using off-resonant optical coupling to Rydberg states, known as Rydberg dressing. In this work, we use this approach to realize an effective one-dimensional extended Bose-Hubbard model. Harnessing our quantum gas microscope, we probe the correlated out-of-equilibrium dynamics of extended-range repulsively bound pairs and “hard rods.” By contrast, operating near equilibrium, we observe density ordering when adiabatically turning on the extended-range interactions. Our results pave the way to realizing light-controlled extended-range interacting quantum many-body systems.

The relaxation behaviour of isolated quantum systems taken out of equilibrium is among the most intriguing questions in many-body physics¹. Quantum systems out of equilibrium typically relax to thermal equilibrium states by scrambling local information and building up entanglement entropy. However, kinetic constraints in the Hamiltonian can lead to a breakdown of this fundamental paradigm owing to a fragmentation of the underlying Hilbert space into dynamically decoupled subsectors in which thermalization can be strongly suppressed^2–5. Here we experimentally observe Hilbert space fragmentation in a two-dimensional tilted Bose–Hubbard model. Using quantum gas microscopy, we engineer a wide variety of initial states and find a rich set of manifestations of Hilbert space fragmentation involving bulk states, interfaces and defects, that is, two-, one- and zero-dimensional objects. Specifically, uniform initial states with equal particle number and energy differ strikingly in their relaxation dynamics. Inserting controlled defects on top of a global, non-thermalizing chequerboard state, we observe highly anisotropic, subdimensional dynamics, an immediate signature of their fractonic nature^6–9. An interface between localized and thermalizing states in turn shows dynamics depending on its orientation. Our results mark the observation of Hilbert space fragmentation beyond one dimension, as well as the concomitant direct observation of fractons, and pave the way for in-depth studies of microscopic transport phenomena in constrained systems.

The Mott-insulating phase of the two-dimensional (2D) Bose-Hubbard model is expected to be characterized by a nonlocal brane parity order. Parity order captures the presence of microscopic particle-hole fluctuations and entanglement, whose properties depend on the underlying lattice geometry. We realize 2D Bose-Hubbard models in dynamically tunable lattice geometries, using neutral atoms in a passively phase-stable tunable optical lattice in combination with programmable site-blocking potentials. We benchmark the performance of our system by single-particle quantum walks in the square, triangular, kagome, and Lieb lattices. In the strongly correlated regime, we microscopically characterize the geometry dependence of the quantum fluctuations and experimentally validate brane parity as a proxy for the nonlocal order parameter signaling the superfluid–to–Mott-insulating phase transition.

Enhancing light–matter coupling at the level of single quanta is essential for numerous applications in quantum science. The cooperative optical response of subwavelength atomic arrays has been found to open new pathways for such strong light–matter couplings, while simultaneously offering access to multiple spatial modes of the light field. Efficient single-mode free-space coupling to such arrays has been reported, but spatial control over the modes of outgoing light fields has remained elusive. Here, we demonstrate such spatial control over the optical response of an atomically thin mirror formed by a subwavelength array of atoms in free space using a single controlled ancilla atom excited to a Rydberg state. The switching behaviour is controlled by the admixture of a small Rydberg fraction to the atomic mirror, and consequently strong dipolar Rydberg interactions with the ancilla. Driving Rabi oscillations on the ancilla atom, we demonstrate coherent control of the transmission and reflection of the array. These results represent a step towards the realization of quantum coherent metasurfaces, the demonstration of controlled atom–photon entanglement and deterministic engineering of quantum states of light.

The Kardar-Parisi-Zhang (KPZ) universality class describes the coarse-grained behavior of a wealth of classical stochastic models. Surprisingly, KPZ universality was recently conjectured to also describe spin transport in the one-dimensional quantum Heisenberg model. We tested this conjecture by experimentally probing transport in a cold-atom quantum simulator via the relaxation of domain walls in spin chains of up to 50 spins. We found that domain-wall relaxation is indeed governed by the KPZ dynamical exponent z = 3/2 and that the occurrence of KPZ scaling requires both integrability and a nonabelian SU(2) symmetry. Finally, we leveraged the single-spin–sensitive detection enabled by the quantum gas microscope to measure an observable based on spin-transport statistics. Our results yield a clear signature of the nonlinearity that is a hallmark of KPZ universality.

Measurement-based quantum computing relies on the rapid creation of large-scale entanglement in a register of stable qubits. Atomic arrays are well suited to store quantum information, and entanglement can be created using highly-excited Rydberg states. Typically, isolating pairs during gate operation is difficult because Rydberg interactions feature long tails at large distances. Here, we engineer distance-selective interactions that are strongly peaked in distance through off-resonant laser coupling of molecular potentials between Rydberg atom pairs. Employing quantum gas microscopy, we verify the dressed interactions by observing correlated phase evolution using many-body Ramsey interferometry. We identify atom loss and coupling to continuum modes as a limitation of our present scheme and outline paths to mitigate these effects, paving the way towards the creation of large-scale entanglement.

Precise control and study of molecules is challenging due to the variety of internal degrees of freedom and local coordinates that are typically not controlled in an experiment. Employing quantum gas microscopy to position and resolve the atoms in Rydberg macrodimer states solves most of these challenges and enables unique access to the molecular frame. Here, we demonstrate this approach and present photoassociation studies in which the molecular orientation relative to an applied magnetic field, the polarization of the excitation light, and the initial atomic state are fully controlled. The observed dependencies allow for an electronic structure tomography of the molecular state. We additionally observe an orientation-dependent Zeeman shift, and we reveal a significant influence on it caused by the hyperfine interaction of the macrodimer state. Finally, we demonstrate control over the electrostatic binding potential by engineering a gap between two crossing pair potentials. Our results establish macrodimers as the most sensitive tool to benchmark Rydberg interaction potentials, and they open new perspectives for improving Rydberg dressing schemes.