Thierry Lahaye

An atom-by-atom assembler of defect-free arbitrary two-dimensional atomic arrays

Making perfect atomic arrays Arrays of atoms can be a useful resource for quantum information. However, loading atoms into arrays is typically a stochastic process, which leads to imperfections. Two groups have now performed defect-free assembly of atoms into arrays (see the Perspective by Regal). The researchers first loaded the atoms stochastically and imaged the system. They then shuttled the atoms around to form perfect arrays. Barredo et al. worked with two-dimensional arrays, creating a variety of spatial configurations. Endres et al. manipulated atoms along a line. By further cooling down the atoms and generating interactions among them, the techniques may also find use in quantum simulation. Science, this issue p. 972, p. 1021; see also p. 1024 Two-dimensional arrays of arbitrary geometries are deterministically loaded with around 50 atoms. Large arrays of individually controlled atoms trapped in optical tweezers are a very promising platform for quantum engineering applications. However, deterministic loading of the traps is experimentally challenging. We demonstrate the preparation of fully loaded two-dimensional arrays of up to ~50 microtraps, each containing a single atom and arranged in arbitrary geometries. Starting from initially larger, half-filled matrices of randomly loaded traps, we obtain user-defined target arrays at unit filling. This is achieved with a real-time control system and a moving optical tweezers, which together enable a sequence of rapid atom moves depending on the initial distribution of the atoms in the arrays. These results open exciting prospects for quantum engineering with neutral atoms in tunable two-dimensional geometries.

Facilitation Dynamics and Localization Phenomena in Rydberg Lattice Gases with Position Disorder

We explore the dynamics of Rydberg excitations in an optical tweezer array under antiblockade (or facilitation) conditions. Because of the finite temperature the atomic positions are randomly spread, an effect that leads to quenched correlated disorder in the interatomic interaction strengths. This drastically affects the facilitation dynamics as we demonstrate experimentally on the elementary example of two atoms. To shed light on the role of disorder in a many-body setting we show that here the dynamics is governed by an Anderson-Fock model, i.e., an Anderson model formulated on a lattice with sites corresponding to many-body Fock states. We first consider a one-dimensional atom chain in a limit that is described by a one-dimensional Anderson-Fock model with disorder on every other site, featuring both localized and delocalized states. We then illustrate the effect of disorder experimentally in a situation in which the system maps on a two-dimensional Anderson-Fock model on a trimmed square lattice. We observe a clear suppression of excitation propagation, which we ascribe to the localization of the many-body wave functions in Hilbert space.Disordered systems provide paradigmatic instances of ergodicity breaking and localization phenomena. Here we explore the dynamics of excitations in a system of Rydberg atoms held in optical tweezers. The finite temperature produces an intrinsic uncertainty in the atomic positions, which translates into quenched correlated disorder in the interatomic interaction strengths. In a simple approach, the dynamics in the many-body Hilbert space can be understood in terms of a one-dimensional Anderson-like model with disorder on every other site, featuring both localized and delocalized states. We conduct an experiment on an eight-atom chain and observe a clear suppression of excitation transfer. Our experiment accesses a regime which is described by a twodimensional Anderson model on a “trimmed” square lattice. Our results thus provide a concrete example in which the absence of excitation propagation in a many-body system is directly related to Anderson-like localization in the Hilbert space, which is believed to be the mechanism underlying many-body localization.

Synthetic three-dimensional atomic structures assembled atom by atom

A great challenge in current quantum science and technology research is to realize artificial systems of a large number of individually controlled quantum bits for applications in quantum computing and quantum simulation. Many experimental platforms are being explored, including solid-state systems, such as superconducting circuits1 or quantum dots2, and atomic, molecular and optical systems, such as photons, trapped ions or neutral atoms3–7. The latter offer inherently identical qubits that are well decoupled from the environment and could provide synthetic structures scalable to hundreds of qubits or more8. Quantum-gas microscopes9 allow the realization of two-dimensional regular lattices of hundreds of atoms, and large, fully loaded arrays of about 50 microtraps (or ‘optical tweezers’) with individual control are already available in one10 and two11 dimensions. Ultimately, however, accessing the third dimension while keeping single-atom control will be required, both for scaling to large numbers and for extending the range of models amenable to quantum simulation. Here we report the assembly of defect-free, arbitrarily shaped three-dimensional arrays, containing up to 72 single atoms. We use holographic methods and fast, programmable moving tweezers to arrange—atom by atom and plane by plane—initially disordered arrays into target structures of almost any geometry. These results present the prospect of quantum simulation with tens of qubits arbitrarily arranged in space and show that realizing systems of hundreds of individually controlled qubits is within reach using current technology.Arbitrarily shaped, defect-free three-dimensional synthetic structures with up to 72 individually controlled atoms are assembled using holographic methods and moving tweezers.

Two-dimensional arrays of individual Rydberg atoms for quantum simulation of spin Hamiltonians

In our experiments, we generate arrays of up to 50 optical tweezers arranged in arbitrary two-dimensional geometries, each containing a single cold atom, and separated by distances of a few micrometers (Fig. 1). This is achieved by active sorting of atoms in larger arrays that are initially loaded stochastically [1]. By exciting the atoms to Rydberg states (with principal quantum numbers in the range 50–100), we can induce strong, tunable dipolar interactions between the atoms [2].