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arXiv:1605.05230 · Physical Review A

Raman transitions between hyperfine clock states in a magnetic trap

Julian B. Naber, Lara Torralbo-Campo, T. Hubert, R. J. C. Spreeuw

Published Jul 27, 2016• 7 citations
arXivHTMLPDF

Abstract

We present our experimental investigation of an optical Raman transition between the magnetic clock states of $^{87}\mathrm{Rb}$ in an atom chip magnetic trap. The transfer of atomic population is induced by a pair of diode lasers which couple the two clock states off-resonantly to an intermediate state manifold. This transition is subject to destructive interference of two excitation paths, which leads to a reduction of the effective two-photon Rabi frequency. Furthermore, we find that the transition frequency is highly sensitive to the intensity ratio of the diode lasers. Our results are well described in terms of light shifts in the multilevel structure of $^{87}\mathrm{Rb}$. The differential light shifts vanish at an optimal intensity ratio, which we observe as a narrowing of the transition linewidth. We also observe the temporal dynamics of the population transfer and find good agreement with a model based on the system's master equation and a Gaussian laser beam profile. Finally, we identify several sources of decoherence in our system, and discuss possible improvements.

DOI
10.1103/physreva.94.013427

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We present our experimental investigation of an optical Raman transition between the magnetic clock states of 87Rb^{87}\mathrm{Rb}87Rb in an atom chip magnetic trap. The transfer of atomic population is induced by a pair of diode lasers which couple the two clock states off-resonantly to an intermediate state manifold. This transition is subject to destructive interference of two excitation paths, which leads to a reduction of the effective two-photon Rabi frequency. Furthermore, we find that the transition frequency is highly sensitive to the intensity ratio of the diode lasers. Our results are well described in terms of light shifts in the multilevel structure of 87Rb^{87}\mathrm{Rb}87Rb. The differential light shifts vanish at an optimal intensity ratio, which we observe as a narrowing of the transition linewidth. We also observe the temporal dynamics of the population transfer and find good agreement with a model based on the system's master equation and a Gaussian laser beam profile. Finally, we identify several sources of decoherence in our system, and discuss possible improvements.
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We present recent results on the coherent control of an optical transition in a single rubidium atom, trapped in an optical tweezer. We excite the atom using resonant light pulses that are short (4 ns) compared with the lifetime of the excited state (26 ns). By varying the intensity of the laser pulses, we can observe an adjustable number of Rabi oscillations, followed by free decay once the light is switched off. To generate the pulses we have developed a novel laser system based on frequency doubling a telecoms laser diode at 1560 nm. By setting the laser intensity to make a pi-pulse, we use this coherent control to make a high quality triggered source of single photons. We obtain an average single photon rate of 9600 s-1 at the detector. Measurements of the second-order temporal correlation function show almost perfect antibunching at zero delay. In addition, we present preliminary results on the use of Raman transitions to couple the two hyperfine levels of the ground state of our trapped atom. This will allow us to prepare and control a qubit formed by two hyperfine sub-levels.
Abstract We theoretically predicted and experimentally demonstrated the sinusoidal shifts of the 87Rb atom Raman transition frequencies as the polarization vectors of the Raman lasers rotate. We also presented the vanish of the differential light shifts for the magnetic sensitive Raman transitions at some elliptically polarized configurations while no vanish for the magnetic insensitive Raman transition. These results are helpful for the evaluation and elimination of the light shifts induced systemic errors in the atomic magnetometer, atomic interferometer, atomic clock and quantum computing.
We report the results of experimental investigation of the Raman – Ramsey method of pulsed excitation of coherent population trapping (CPT) resonances in a rubidium vapour cell filled with a mixture of Ar and Ne buffer gases. For the development of compact quantum microwave frequency standards, this method is an alternative to the pulsed optical pumping method recently implemented using the same rubidium cell. Both methods have advantages over the traditional double radio-optical resonance technique, the main of which is the substantial suppression of the light shift of the clock transition frequency, since the evolution of the coherence of atomic states forming the clock transition occurs in the absence of laser radiation in the cell. The narrow (110 – 240 Hz) Raman – Ramsey resonances are obtained using the scheme of pulsed excitation of CPT resonances on the D 1 lines of the 87 Rb atom with the same linear (lin||lin) polarisations of the bichromatic laser radiation components. The process of optimising the central fringe linewidth, its contrast, and the linewidth-to-contrast ratio is described. The magnetic dependence of the Raman – Ramsey line central fringe linewidth is experimentally investigated.
We report an experimental observation of coherent population transfer in a multilevel system by adiabatic following through a trapped state. Raman transitions between ground-state sublevels are induced by two partially overlapping ${\mathrm{\ensuremath{\sigma}}}^{\ifmmode\pm\else\textpm\fi{}}$ polarized laser beams, tuned to the hyperfine transition F=4\ensuremath{\rightarrow}F'=4 of the cesium D2{\mathit{D}}_{2}D2​ line. An efficiency of more than 50% is observed for the mF{\mathit{m}}_{\mathit{F}}mF​=+4\ensuremath{\rightarrow}mF{\mathit{m}}_{\mathit{F}}mF​=-4 population transfer. The influence of other excited hyperfine levels on the transfer efficiency is pointed out. The feasibility of the technique with counterpropagating laser beams is also demonstrated.
Raman heterodyne detection of nuclear magnetic resonance is a sensitive technique for optical detection of an NMR transition, which is driven by a resonant radio-frequency field. The observed signal is linear in the transition matrix elements of the magnetic resonance transition and two optical transitions. This linearity is the reason that signal contributions from different sites or different rf transitions can interfere, in many cases destructively. In this article, we discuss such an interference effect, which appears to have been overlooked in the past. It occurs between signal contributions that originate from the same magnetic resonance transition of atoms with different positions within the inhomogeneously broadened optical resonance line. These atoms contribute to the coherent Raman scattering through different scattering paths, which involve optical transitions to different nuclear spin states of the same electronic state. We show that the interference between all possible scattering paths leads to complete signal cancellation, if the atoms that are involved in the different scattering paths are equally polarized. To study the effect and to eliminate the interference, we used a pump-and-probe technique with two laser beams. With two independent laser frequencies, it becomes possible to separate the individual scattering paths. We calculate the dependence of the signal on the frequency of both laser beams as well as on the radio frequency and compare the results to experimental data from Pr3+{\mathrm{Pr}}^{3+}Pr3+:YAlO3{\mathrm{YAlO}}_{3}YAlO3​. Our results show that the interference reduces the signal amplitude of the conventional Raman heterodyne experiment but can be eliminated in the new experiment.