95 research outputs found

    Raman velocity filter as a tool for collinear laser spectroscopy

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    The velocity distribution of a hot ionic beam can be filtered with a narrow stimulated Raman process to prepare a colder subensemble, as substantiated in this theoretical analysis. Using two counter-propagating, far-detuned lasers, we can define a π\pi-pulse for the resonant velocity to transfer atoms within the linewidth of the Raman resonance between the ground-states of a Λ\Lambda-system. Spontaneous emission from the two single-photon resonances, as well as the ground-state decoherence induced by laser noise, diminishes the efficiency of the filter. From a comprehensive master equation, we obtain conditions for the optimal frequency pair of the lasers and evaluate the filter performance numerically, as well as analytically. If we apply this analysis to current 40^{40}Ca+^+ ion experiments, we obtain a sensitivity for measuring high ion acceleration voltages on the ppm level or below.Comment: Corrected typos. Corrected: Missing minus in Eq. 35. Improved readability by including a few repetitions of quantity definitions and improved display of relevant quantities in Table II of the Appendi

    Trapped Ion Oscillation Frequencies as Sensors for Spectroscopy

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    The oscillation frequencies of charged particles in a Penning trap can serve as sensors for spectroscopy when additional field components are introduced to the magnetic and electric fields used for confinement. The presence of so-called “magnetic bottles” and specific electric anharmonicities creates calculable energy-dependences of the oscillation frequencies in the radiofrequency domain which may be used to detect the absorption or emission of photons both in the microwave and optical frequency domains. The precise electronic measurement of these oscillation frequencies therefore represents an optical sensor for spectroscopy. We discuss possible applications for precision laser and microwave spectroscopy and their role in the determination of magnetic moments and excited state life-times. Also, the trap-assisted measurement of radiative nuclear de-excitations in the X-ray domain is discussed. This way, the different applications range over more than 12 orders of magnitude in the detectable photon energies, from below ÎŒeV in the microwave domain to beyond MeV in the X-ray domain

    Nuclear Charge Radius of 12^{12}Be

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    The nuclear charge radius of 12^{12}Be was precisely determined using the technique of collinear laser spectroscopy on the 2s1/2→2p1/2,3/22s_{1/2}\rightarrow 2p_{1/2, 3/2} transition in the Be+^{+} ion. The mean square charge radius increases from 10^{10}Be to 12^{12}Be by \delta ^{10,12} = 0.69(5) \fm^{2} compared to \delta ^{10,11} = 0.49(5) \fm^{2} for the one-neutron halo isotope 11^{11}Be. Calculations in the fermionic molecular dynamics approach show a strong sensitivity of the charge radius to the structure of 12^{12}Be. The experimental charge radius is consistent with a breakdown of the N=8 shell closure.Comment: 5 pages, 3 figure

    Test of Time Dilation Using Stored Li+ Ions as Clocks at Relativistic Speed

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    We present the concluding result from an Ives-Stilwell-type time dilation experiment using 7Li+ ions confined at a velocity of beta = v/c = 0.338 in the storage ring ESR at Darmstadt. A Lambda-type three-level system within the hyperfine structure of the 7Li+ triplet S1-P2 line is driven by two laser beams aligned parallel and antiparallel relative to the ion beam. The lasers' Doppler shifted frequencies required for resonance are measured with an accuracy of < 4 ppb using optical-optical double resonance spectroscopy. This allows us to verify the Special Relativity relation between the time dilation factor gamma and the velocity beta to within 2.3 ppb at this velocity. The result, which is singled out by a high boost velocity beta, is also interpreted within Lorentz Invariance violating test theories

    Collinear laser spectroscopy of atomic cadmium

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    Hyperfine structure AA and BB factors of the atomic 5s\,5p\,\; ^3\rm{P}_2 \rightarrow 5s\,6s\,\; ^3\rm{S}_1 transition are determined from collinear laser spectroscopy data of 107−123^{107-123}Cd and 111m−123m^{111m-123m}Cd. Nuclear magnetic moments and electric quadrupole moments are extracted using reference dipole moments and calculated electric field gradients, respectively. The hyperfine structure anomaly for isotopes with s1/2s_{1/2} and d5/2d_{5/2} nuclear ground states and isomeric h11/2h_{11/2} states is evaluated and a linear relationship is observed for all nuclear states except s1/2s_{1/2}. This corresponds to the Moskowitz-Lombardi rule that was established in the mercury region of the nuclear chart but in the case of cadmium the slope is distinctively smaller than for mercury. In total four atomic and ionic levels were analyzed and all of them exhibit a similar behaviour. The electric field gradient for the atomic 5s\,5p\,\; ^3\mathrm{P}_2 level is derived from multi-configuration Dirac-Hartree-Fock calculations in order to evaluate the spectroscopic nuclear quadrupole moments. The results are consistent with those obtained in an ionic transition and based on a similar calculation.Comment: 12 pages, 5 figure

    Observation of the hyperfine transition in lithium-like Bismuth 209Bi80+^{209}\text{Bi}^{80+}: Towards a test of QED in strong magnetic fields

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    We performed a laser spectroscopic determination of the 2s2s hyperfine splitting (HFS) of Li-like 209Bi80+^{209}\text{Bi}^{80+} and repeated the measurement of the 1s1s HFS of H-like 209Bi82+^{209}\text{Bi}^{82+}. Both ion species were subsequently stored in the Experimental Storage Ring at the GSI Helmholtzzentrum f\"ur Schwerionenforschung Darmstadt and cooled with an electron cooler at a velocity of ≈0.71 c\approx 0.71\,c. Pulsed laser excitation of the M1M1 hyperfine-transition was performed in anticollinear and collinear geometry for Bi82+\text{Bi}^{82+} and Bi80+\text{Bi}^{80+}, respectively, and observed by fluorescence detection. We obtain ΔE(1s)=5086.3(11) meV\Delta E^{(1s)}= 5086.3(11)\,\textrm{meV} for Bi82+\text{Bi}^{82+}, different from the literature value, and ΔE(2s)=797.50(18) meV\Delta E^{(2s)}= 797.50(18)\,\textrm{meV} for Bi80+\text{Bi}^{80+}. These values provide experimental evidence that a specific difference between the two splitting energies can be used to test QED calculations in the strongest static magnetic fields available in the laboratory independent of nuclear structure effects. The experimental result is in excellent agreement with the theoretical prediction and confirms the sum of the Dirac term and the relativistic interelectronic-interaction correction at a level of 0.5% confirming the importance of accounting for the Breit interaction.Comment: 5 pages, 2 figure

    Precision Test of Many-Body QED in the Be+^+ 2p2p Fine Structure Doublet Using Short-Lived Isotopes

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    Absolute transition frequencies of the 2s\; ^2{\rm S}_{1/2} \rightarrow 2p\;^2\mathrm{P}_{1/2,3/2} transitions in Be+^+ were measured for the isotopes 7,9−12^{7,9-12}Be. The fine structure splitting of the 2p2p state and its isotope dependence are extracted and compared to results of \textit{ab initio} calculations using explicitly correlated basis functions, including relativistic and quantum electrodynamics effects at the order of mα6m \alpha^6 and mα7ln⁥αm \alpha^7 \ln \alpha. Accuracy has been improved in both the theory and experiment by 2 orders of magnitude, and good agreement is observed. This represents one of the most accurate tests of quantum electrodynamics for many-electron systems, being insensitive to nuclear uncertainties.Comment: 5 pages, 2 figure

    Commissioning of the HITRAP Cooling Trap with Offline Ions

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    Highly charged heavy ions at rest offer a wide spectrum of precision measurements. The GSI Helmholtzzentrum fĂŒr Schwerionenforschung GmbH is able to deliver ions up to U92+. As the production of these heavy, highly charged ions requires high kinetic energies, it is necessary to decelerate these ions for ultimate precision. The broad energy distribution, which results from the deceleration in the HITRAP linear decelerator, needs to be reduced to allow for further transportation and experiments. The HITRAP cooling trap is designed to cool, i.e., reduce, this energy spread by utilizing electron cooling. The commissioning of this trap is done with Ar16+-ions from a local EBIT ion source. By analyzing the signal of stored ions after ejection, properties such as ion lifetime, charge exchange, and ion motions can be observed. Here, we provide an overview of the recent results of the commissioning process and discuss future experiments
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