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arXiv:1403.7049 · Applied Physics B

Precision spectroscopy technique for dipole-allowed transitions in laser-cooled ions

Amy Gardner, Kevin Sheridan, William Groom, Nicolas Seymour-Smith, Matthias Keller

Published Jul 18, 2014• 6 citations
arXivHTMLPDF
DOI
10.1007/s00340-014-5891-1

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Atomic anions are generally not amenable to optical spectroscopy because they are loosely bound systems and rarely have bound excited states. Until recently, there was only one known negative ion with a strong bound–bound electronic transition, the osmium anion Os − . The electric-dipole transition between the 4 F e 9/2 ground and 6 D o J excited state of this ion provides unique insight into the structure of atomic anions. In addition, it may enable the preparation of ultracold ensembles of negative ions. Laser excitation of the electric-dipole transition in Os − ions could be used to laser-cool them to microkelvin temperatures. If demonstrated to be successful, the technique would allow the cooling of any species of negatively charged ions - from subatomic particles to molecular anions - to ultracold temperatures by sympathetic cooling. We have been investigating the bound-bound electric-dipole transition in Os − by high-resolution laser spectroscopy with a view to using it for the first laser cooling of negative ions. The principle of the method, its potential applications, as well as experimental results are presented.
Laser spectroscopy is a versatile tool to investigate the internal structure of atoms, molecules and nuclei.High precision spectroscopy requires laser cooling to reduce Doppler broadening and Doppler shifts.Sympathetic cooling extends these advantages to species which do not have an appropriate transition for laser cooling and allows precision spectroscopy of previously inaccessible species using the quantum logic technique.The original implementation of quantum logic spectroscopy relies on the long lifetime of the excited spectroscopy state to realize a transfer sequence.Precision spectroscopy of transitions with a short-lived excited state is typically performed using laser induced uorescence or laser absorption spectroscopy.Neither of these methods has reached the fundamental quantum projection noise limit and are rather limited by photon shot noise.For these situations, we develop the technique of photon recoil spectroscopy as an extension of quantum logic spectroscopy to broad transitions.The common motion of a sideband-cooled two-ion crystal is excited by photon recoil during photon absorption on the spectroscopically investigated ion.This motional excitation is transferred to an internal state excitation on the co-trapped ion of a dierent species and detected with high eciency.We demonstrate the technique on the 2 S 1/2 ↔ 2 P 1/2 transition of the 40 Ca + ion and resolve the line center to 1/300 of its observed linewidth.The simplicity and versatility of the technique promises applications to other previously inaccessible species.A variation of the technique is proposed for rotational state preparation of molecular ions.A moving optical lattice is employed to exert a state-dependent force on the molecule.This would allow the detection of the rotational state of the molecular ion and therefore enable precision spectroscopy of specic rovibrational transitions in the molecule.
The performance of proposed antihydrogen spectroscopy or gravity experiments will crucially depend on the temperature of the initial antihydrogen sample. Measurements by ATRAP and ATHENA have shown that antihydrogen produced with the nested-trap technique is much hotter than the temperature of the surrounding trap. Therefore, novel schemes for antihydrogen recombination as well as for the pre-cooling of antiprotons are being considered. We are investigating a possible antiproton cooling technique based on the laser cooling of negative osmium ions. If demonstrated to be successful, it will allow the sympathetic cooling of antiprotons—or any negatively charged particles—to microkelvin temperatures. As a first milestone toward the laser cooling of negative ions, we have performed collinear laser spectroscopy on negative osmium and determined the transition frequency and the cross-section of the relevant bound–bound electric-dipole transition.