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arXiv:1809.04455 · Physical Review A

Controlling the potential landscape and normal modes of ion Coulomb crystals by a standing-wave optical potential

T. Lauprêtre, Rasmus B. Linnet, Ian D. Leroux, Haggai Landa, Aurélien Dantan, Michael Drewsen

Published Mar 7, 2019• 26 citations
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Abstract

Light-induced control of ions within small Coulomb crystals is investigated. By intense intracavity optical standing-wave fields, subwavelength localization of individual ions is achieved for one-, two-, and three-dimensional crystals. Based on these findings, we illustrate numerically how the application of such optical potentials can be used to tailor the normal-mode spectra and patterns of multidimensional Coulomb crystals. The results represent, among others, important steps towards controlling the crystalline structure of Coulomb crystals, investigating heat-transfer processes at the quantum limit, and quantum simulations of many-body systems.

DOI
10.1103/physreva.99.031401

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Light-induced control of ions within small Coulomb crystals is investigated. By intense intracavity optical standing-wave fields, subwavelength localization of individual ions is achieved for one-, two-, and three-dimensional crystals. Based on these findings, we illustrate numerically how the application of such optical potentials can be used to tailor the normal-mode spectra and patterns of multidimensional Coulomb crystals. The results represent, among others, important steps towards controlling the crystalline structure of Coulomb crystals, investigating heat-transfer processes at the quantum limit, and quantum simulations of many-body systems.
We demonstrate light-induced localization of Coulomb-interacting particles in multi-dimensional structures. Subwavelength localization of ions within small multi-dimensional Coulomb crystals by an intracavity optical standing wave field is evidenced by measuring the difference in scattering inside symmetrically red- and blue-detuned optical lattices and is observed even for ions undergoing substantial radial micromotion. These results are promising steps towards the structural control of ion Coulomb crystals by optical fields as well as for complex many-body simulations with ion crystals or for the investigation of heat transfer at the nanoscale, and have potential applications for ion-based cavity quantum electrodynamics, cavity optomechanics and ultracold ion chemistry.
Coulomb crystallisation of laser-cooled ensembles of ions in harmonic traps has been studied experimentally with many spectacular results in recent years. It is well known that for sufficiently large numbers of ions the ground state of a Coulomb crystal in such a system has a body-centred cubic (bcc) structure. However, in experiments with crystals of up to a few 104 ions, structural transitions between bcc and, for example, face centred cubic (fee) or hexagonal close packed (hep) structures are observed. For constant ion densities, the lattice spacing of the planes of highest density differs only by about 3% between bcc and fee structures and simulations predict very small energy differences, thus thermal effects even at temperatures in the mK regime are sufficient to excite these transitions. Here we study numerically the possibility of controlling and switching the crystal structure with the help of periodic potentials generated by the dipole forces of standing-wave light fields.
The electronic and motional degrees of freedom of trapped ions can be controlled and coherently coupled on the level of individual quanta.Assembling complex quantum systems ion by ion while keeping this unique level of control remains a challenging task.For many applications, linear chains of ions in conventional traps are ideally suited to address this problem.However, driven motion due to the magnetic or radio-frequency electric trapping fields sometimes limits the performance in one dimension and severely affects the extension to higher-dimensional systems.Here, we report on the trapping of multiple barium ions in a single-beam optical dipole trap without radio-frequency or additional magnetic fields.We study the persistence of order in ensembles of up to six ions within the optical trap, measure their temperature, and conclude that the ions form a linear chain, commonly called a one-dimensional Coulomb crystal.As a proof-of-concept demonstration, we access the collective motion and perform spectrometry of the normal modes in the optical trap.Our system provides a platform that is free of driven motion and combines advantages of optical trapping, such as state-dependent confinement and nanoscale potentials, with the desirable properties of crystals of trapped ions, such as long-range interactions featuring collective motion.Starting with small numbers of ions, it has been proposed that these properties would allow the experimental study of many-body physics and the onset of structural quantum phase transitions between one-and two-dimensional crystals.
We investigate numerically the structural dynamics of ion Coulomb crystals confined in a three-dimensional harmonic trap when influenced by an additional one-dimensional optically induced periodical potential. We demonstrate that transitions between thermally excited crystal structures, such as body-centered cubic and face-centered cubic, can be suppressed by a proper choice of the potential depth and periodicity. Furthermore, by varying the harmonic trap parameters and/or the optical potential in time, controlled transitions between crystal structures can be obtained with close to unit efficiency.
Leading quantum platforms are largely limited to one or two dimensions, whereas three-dimensional Coulomb crystals of trapped ions self-assemble into dense qubit arrays with no rearrangement overhead. Coherent optical control of such crystals has nonetheless been out of reach, because the optical transition couples to nearly all 3N3N3N collective modes, i.e., a thermally occupied quasi-continuum bath. Here we cool about 3,600 modes of a crystal of over 1,200 ions below single-phonon occupation, using a continuous cooling band that spans more than five octaves in vibrational spectrum, from about 50 kHz to 2.1 MHz. The crystal then serves as a register of optical qubits, allowing global initialization, coherent manipulation and collective detection. We demonstrate ensemble optical coherence of 21.6 milliseconds and reduce the optical-transition frequency uncertainty from 389 Hz for a single ion to 12 Hz for over a thousand ions, approaching the expected projection-noise scaling. Our approach could be extended to even larger crystals with phonon-mediated many-body couplings, opening a route towards entanglement-enhanced precision metrology and three-dimensional quantum simulation, particularly with spatial-shaped illumination for region-resolved collective control.
Ion Coulomb crystals are ordered structures formed by laser-cooled ions in traps that are characterized by interparticle distances of several micrometers and energy scales on the order of μμμeV. Their crystalline structure emerges from the interplay between Coulomb repulsion and the external confining potential, which can be readily tuned. Moreover, individual ions can be precisely manipulated with lasers and imaged via resonance fluorescence. These unusual and unique properties make ion crystals a powerful platform for studying phases of matter in the strongly correlated regime and at low temperatures where their dynamics is manifestly quantum mechanical. This review examines the theoretical framework and experimental characterization of ion Coulomb crystals from a condensed-matter perspective. We discuss their dynamical and thermodynamic properties in one, two, and three dimensions, and review recent investigations into their out-of-equilibrium behavior. We provide outlooks on future directions for exploring novel condensed matter phenomena with trapped ion crystals, as well as for exploiting these features for scientific and technical applications.