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Register a new userOptical trapping of ion Coulomb crystals
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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 which is free of driven motion and combines advantages of optical trapping, such as state-dependent confinement and nano-scale 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.
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For conventional ion traps, the trapping potential is close to independent of the electronic state, providing confinement for ions dependent primarily on their charge-to-mass ratio $Q/m$. In contrast, storing ions within an optical dipole trap results in state-dependent confinement. Here we experimentally study optical dipole potentials for $^{138}mathrm{Ba}^+$ ions stored within two distinctive traps operating at 532 nm and 1064 nm. We prepare the ions in either the $6mathrm{S}_{mathrm{1/2}}$ electronic ground or the $5mathrm{D}_{mathrm{3/2}}$/ $5mathrm{D}_{mathrm{5/2}}$ metastable excited state and probe the relative strength and polarity of the potential. On the one hand, we apply our findings to selectively remove ions from a Coulomb crystal, despite all ions sharing the same $Q/m$. On the other hand, we deterministically purify the trapping volume from parasitic ions in higher-energy orbits, resulting in reliable isolation of Coulomb crystals down to a single ion within a radio-frequency trap.
We present experiments on polarization gradient cooling of Ca$^+$ multi-ion Coulomb crystals in a linear Paul trap. Polarization gradient cooling of the collective modes of motion whose eigenvectors have overlap with the symmetry axis of the trap is achieved by two counter-propagating laser beams with mutually orthogonal linear polarizations that are blue-detuned from the S$_{1/2}$ to P$_{1/2}$ transition. We demonstrate cooling of linear chains of up to 51 ions and 2D-crystals in zig-zag configuration with 22 ions. The cooling results are compared with numerical simulations and the predictions of a simple model of cooling in a moving polarization gradient.
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 multi-dimensional 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.
Ion Coulomb crystals are currently establishing themselves as a highly controllable test-bed for mesoscopic systems of statistical mechanics. The detailed experimental interrogation of the dynamics of these crystals however remains an experimental challenge. In this work, we show how to extend the concepts of multi-dimensional nonlinear spectroscopy to the study of the dynamics of ion Coulomb crystals. The scheme we present can be realized with state-of-the-art technology and gives direct access to the dynamics, revealing nonlinear couplings even in the presence of thermal excitations. We illustrate the advantages of our proposal showing how two-dimensional spectroscopy can be used to detect signatures of a structural phase transition of the ion crystal, as well as resonant energy exchange between modes. Furthermore, we demonstrate in these examples how different decoherence mechanisms can be identified.
A magneto-optical trap (MOT) of atoms or molecules is studied when two lasers of different detunings and polarization are used. Especially for $Jrightarrow J,J-1$ transitions, a scheme using more than one frequency per transition and different polarization is required to create a significant force. Calculations have been performed with the simplest forms of the $Jrightarrow J-1$ case (i.e. $J=1 rightarrow J=0$) and $Jrightarrow J$ case (i.e. $J=1/2 rightarrow J=1/2$). A one dimensional (1D) model is presented and a complete 3D simulation using rate equations confirm the results. Even in the absence of Zeeman effect in the excited state, where no force is expected in the single laser field configuration, we show that efficient cooling and trapping forces are restored in our configuration. We study this mechanism for the C$_2^-$ molecular anion as a typical example of the interplay between the two simple transitions $J rightarrow J,J-1$.
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