Johannes Zeiher

Bosonic quantum error correction codes encode logical qubits in the Hilbert space of one or multiple harmonic oscillators. A prominent class of bosonic codes is that of Gottesman-Kitaev-Preskill (GKP) codes of which implementations have been demonstrated with trapped ions and microwave cavities. In this paper, we investigate theoretically the preparation and error correction of a GKP qubit in a vibrational mode of a neutral atom stored in an optical dipole trap. This platform has recently shown remarkable progress in simultaneously controlling the motional and electronic degrees of freedom of trapped atoms. The protocols we develop make use of motional states and, additionally, internal electronic states of the trapped atom to serve as an ancilla qubit. We compare optical tweezer arrays and optical lattices and find that the latter provide more flexible control over the confinement in the out-of-plane direction, which can be utilized to optimize the conditions for the implementation of GKP codes. Concretely, the different frequency scales that the harmonic oscillators in the axial and radial lattice directions exhibit and a small oscillator anharmonicity prove to be beneficial for robust encodings of GKP states. Finally, we underpin the experimental feasibility of the proposed protocols by numerically simulating the preparation of GKP qubits in an optical lattice with realistic parameters.

We propose a scheme to perform optical pulses that suppress the effect of photon recoil by three orders of magnitude compared to ordinary pulses in the Lamb-Dicke regime. We derive analytical insight about the fundamental limits to the fidelity of optical qubits for trapped atoms and ions. This paves the way towards applications in quantum computing for realizing $>1000$ of gates with an overall fidelity above 99\%.

Coherent many-body quantum dynamics lies at the heart of quantum simulation and quantum computation. Both require coherent evolution in the exponentially large Hilbert space of an interacting many-body system. To date, trapped ions have defined the state of the art in terms of achievable coherence times in interacting spin chains. Here, we establish an alternative platform by reporting on the observation of coherent, fully interaction-driven quantum revivals of the magnetization in Rydberg-dressed Ising spin chains of atoms trapped in an optical lattice. We identify partial many-body revivals at up to about ten times the characteristic time scale set by the interactions. At the same time, single-site-resolved correlation measurements link the magnetization dynamics with inter-spin correlations appearing at different distances during the evolution. These results mark an enabling step towards the implementation of Rydberg atom based quantum annealers, quantum simulations of higher dimensional complex magnetic Hamiltonians, and itinerant long-range interacting quantum matter.

Dominating finite-range interactions in many-body systems can lead to intriguing self-ordered phases of matter. Well known examples are crystalline solids or Coulomb crystals in ion traps. In those systems, crystallization proceeds via a classical transition, driven by thermal fluctuations. In contrast, ensembles of ultracold atoms laser-excited to Rydberg states provide a well-controlled quantum system, in which a crystalline phase transition governed by quantum fluctuations can be explored. Here we report on the experimental preparation of the crystalline states in such a Rydberg many-body system. Fast coherent control on the many-body level is achieved via numerically optimized laser excitation pulses. We observe an excitation-number staircase as a function of the system size and show directly the emergence of incompressible ordered states on its steps. Our results demonstrate the applicability of quantum optical control techniques in strongly interacting systems, paving the way towards the investigation of novel quantum phases in long-range interacting quantum systems, as well as for detailed studies of their coherence and correlation properties.