Strong Coupling of Two Individually Controlled Atoms via a Nanophotonic Cavity.

We demonstrate photon-mediated interactions between two individually trapped atoms coupled to a nanophotonic cavity. Specifically, we observe collective enhancement when the atoms are resonant with the cavity and level repulsion when the cavity is coupled to the atoms in the dispersive regime. Our approach makes use of individual control over the internal states of the atoms and their position with respect to the cavity mode, as well as the light shifts to tune atomic transitions individually, allowing us to directly observe the anticrossing of the bright and dark two-atom states. These observations open the door for realizing quantum networks and studying quantum many-body physics based on atom arrays coupled to nanophotonic devices.

Non-local propagation of correlations in quantum systems with long-range interactions.

The maximum speed with which information can propagate in a quantum many-body system directly affects how quickly disparate parts of the system can become correlated and how difficult the system will be to describe numerically. For systems with only short-range interactions, Lieb and Robinson derived a constant-velocity bound that limits correlations to within a linear effective 'light cone'. However, little is known about the propagation speed in systems with long-range interactions, because analytic solutions rarely exist and because the best long-range bound is too loose to accurately describe the relevant dynamical timescales for any known spin model. Here we apply a variable-range Ising spin chain Hamiltonian and a variable-range XY spin chain Hamiltonian to a far-from-equilibrium quantum many-body system and observe its time evolution. For several different interaction ranges, we determine the spatial and time-dependent correlations, extract the shape of the light cone and measure the velocity with which correlations propagate through the system. This work opens the possibility for studying a wide range of many-body dynamics in quantum systems that are otherwise intractable.

Microgram BaCl2 ablation targets for trapped ion experiments.

Trapped ions for quantum information processing have been an area of intense study due to the extraordinarily high fidelity operations that have been reported experimentally. Specifically, barium trapped ions have been shown to have exceptional state-preparation and measurement fidelities. The 133Ba+ (I = 1/2) isotope in particular is a promising candidate for large-scale quantum computing experiments. However, a major pitfall with this isotope is that it is radioactive and is thus generally used in microgram quantities to satisfy safety regulations. We describe a new method for creating microgram barium chloride (BaCl2) ablation targets for use in trapped ion experiments and compare our procedure to previous methods. We outline two recipes for the fabrication of ablation targets that increase the production of neutral atoms for isotope-selective loading of barium ions. We show that heat-treatment of the ablation targets greatly increases the consistency at which neutral atoms can be produced, and we characterize the uniformity of these targets using trap-independent techniques such as energy dispersive x-ray spectroscopy and neutral fluorescence collection. Our comparison between fabrication techniques and the demonstration of consistent neutral fluorescence paves a path toward reliable loading of 133Ba+ in surface traps and opens opportunities for scalable quantum computing with this isotope.

Atom-by-atom assembly of defect-free one-dimensional cold atom arrays.

The realization of large-scale fully controllable quantum systems is an exciting frontier in modern physical science. We use atom-by-atom assembly to implement a platform for the deterministic preparation of regular one-dimensional arrays of individually controlled cold atoms. In our approach, a measurement and feedback procedure eliminates the entropy associated with probabilistic trap occupation and results in defect-free arrays of more than 50 atoms in less than 400 milliseconds. The technique is based on fast, real-time control of 100 optical tweezers, which we use to arrange atoms in desired geometric patterns and to maintain these configurations by replacing lost atoms with surplus atoms from a reservoir. This bottom-up approach may enable controlled engineering of scalable many-body systems for quantum information processing, quantum simulations, and precision measurements.