We present a single solid-state laser system to cool, coherently manipulate and detect 25 Mg + ions. Coherent manipulation is accomplished by coupling two hyperfine ground state levels using a pair of far-detuned Raman laser beams. Resonant light for Doppler cooling and detection is derived from the same laser source by means of an electro-optic modulator, generating a sideband which is resonant with the atomic transition. We demonstrate ground-state cooling of one of the vibrational modes of the ion in the trap using resolved-sideband cooling. The cooling performance is studied and discussed by observing the temporal evolution of Raman-stimulated sideband transitions. The setup is a major simplification over existing state-of-the-art systems, typically involving up to three separate laser sources.
We report an experimental study of the K(2) A (1)Sigma(u) (+) state. Long-range levels up to the dissociation limit were observed in a two laser spectroscopic experiment using a highly collimated molecular beam. We derive an analytical potential energy curve for the complete A state including long-range dispersion terms. From these, we obtain radiative atomic lifetimes of 26.74(3) ns for the 4p(1/2) state and 26.39(3) ns for the 4p(3/2) state of (39)K. The dissociation energy of the X (1)Sigma(g) (+) ground state with respect to v=0, J=0 is found to be D(0)=4404.808(4) cm(-1).
Expressions for the angular distribution of tritons emitted from nuclei bombarded with deuterons have been obtained using Born's approximation and the non. perturbation method of Butler. Discussion of the effect of different forms of the triton wave function on the angular distribution is given. The theory is shown to explain the experimental angular distributions satisfactorily.
THE T H E O R Y O F (d, t) REACTIONS
X P E R I M E N T S on the emission of tritons from nuclei bombarded withdeuterons reveal angular distributions similar to those observed in (d, p) E and (d, d') reactions. This leads one to expect that this reaction also is
A diode-laser system at 467 nm is built in order to drive the 2 S 1/2 → 2 F 7/2 electric octupole transition at 467 nm in 171 Yb + . The frequency of the laser is stabilized to a reference cavity made of ultra low expansion glass and is demonstrated to have a relative instability of better than 2 × 10 −15 at 1 s and a stable linear drift rate with variations below 10 mHz/s over several hours. The system is applied for spectroscopy of a single trapped laser-cooled 171 Yb + ion. We obtain excitation spectra of the octupole transition with a resonant excitation probability of about 65% and an essentially Fourier transform-limited resolution of 13 Hz.
Optical atomic clocks are currently one of the most sensitive tools making it possible to precisely test the fundamental symmetry properties of spacetime and Einstein’s theory of relativity. At the same time, the extremely high stability and accuracy of compact transportable optical clocks open new perspectives in important fields, such as satellite navigation, relativistic geodesy, and the global time and frequency network. Our project aimed to develop a compact transportable optical clock based on a single ytterbium ion. We present the first prototype of the Yb+ clock (298 kg in 1 m3) and present several solutions aimed to improve the clock’s robustness to approach the demands of a space-qualified system. We present spectroscopic studies of a 435.5 nm quadrupole clock transition with Fourier-limited spectra of 25 Hz. The estimated instability of the output frequency at 1 GHz, which was down-converted with an optical frequency comb (OFC), is at the level of 9×10−15/τ, and the long-term instability and inaccuracy are at the level of 5×10−16. As the next steps, we present a new design for the clock laser and the OFC.
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