Cold Matter Assembled Atom-by-Atom

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 novel platform for the deterministic preparation of regular 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 over 50 atoms in less than 400 ms. 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 enables controlled engineering of scalable many-body systems for quantum information processing, quantum simulations, and precision measurements.Comment: 12 pages, 9 figures, 3 movies as ancillary file

Continuous Cold-atom Inertial Sensor with 1 nrad.s−11\ \text{nrad.s}^{-1} Rotation Stability

We report the operation of a cold-atom inertial sensor which continuously captures the rotation signal. Using a joint interrogation scheme, where we simultaneously prepare a cold-atom source and operate an atom interferometer (AI) enables us to eliminate the dead times. We show that such continuous operation improves the short-term sensitivity of AIs, and demonstrate a rotation sensitivity of $100\ \text{nrad.s}^{-1}.\text{Hz}^{-1/2}$ in a cold-atom gyroscope of $11 \ \text{cm}^2$ Sagnac area. We also demonstrate a rotation stability of $1 \ \text{nrad.s}^{-1}$ at $10^4$ s of integration time, which establishes the record for atomic gyroscopes. The continuous operation of cold-atom inertial sensors will enable to benefit from the full sensitivity potential of large area AIs, determined by the quantum noise limit.Comment: 4 pages, 3 figure

Structure of the Alkali-metal-atom-Strontium molecular ions: towards photoassociation and formation of cold molecular ions

The potential energy curves, permanent and transition dipole moments, and the static dipolar polarizability, of molecular ions composed of one alkali-metal atom and a Strontium ion are determined with a quantum chemistry approach. The molecular ions are treated as effective two-electron systems and are treated using effective core potentials including core polarization, large gaussian basis sets, and full configuration interaction. In the perspective of upcoming experiments aiming at merging cold atom and cold ion traps, possible paths for radiative charge exchange, photoassociation of a cold Lithium or Rubidium atom and a Strontium ion are discussed, as well as the formation of stable molecular ions

Quantum-gas microscopes - A new tool for cold-atom quantum simulators

This "Perspectives" paper gives a brief overview of the recent developments with quantum-gas microscopes and how they can be used to build the next generation of cold-atom quantum simulators.Comment: "Perspectives" paper for Special Issue "Cold Atom Physics" of Natl. Sci. Rev; published online April 19, 201

The cold atom Hubbard toolbox

We review recent theoretical advances in cold atom physics concentrating on strongly correlated cold atoms in optical lattices. We discuss recently developed quantum optical tools for manipulating atoms and show how they can be used to realize a wide range of many body Hamiltonians. Then we describe connections and differences to condensed matter physics and present applications in the fields of quantum computing and quantum simulations. Finally we explain how defects and atomic quantum dots can be introduced in a controlled way in optical lattice systems.Comment: Review article, 31 pages, 14 figures, to be published in Annals of Physic

Cold heteronuclear atom-ion collisions

We study cold heteronuclear atom ion collisions by immersing a trapped single ion into an ultracold atomic cloud. Using ultracold atoms as reaction targets, our measurement is sensitive to elastic collisions with extremely small energy transfer. The observed energy-dependent elastic atom-ion scattering rate deviates significantly from the prediction of Langevin but is in full agreement with the quantum mechanical cross section. Additionally, we characterize inelastic collisions leading to chemical reactions at the single particle level and measure the energy-dependent reaction rate constants. The reaction products are identified by in-trap mass spectrometry, revealing the branching ratio between radiative and non-radiative charge exchange processes