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Conversion of bright magneto-optical resonances into dark resonances at fixed laser frequency for D2 excitation of atomic rubidium

  • University of Latvia

Research output: Contribution to journal › Article › peer-review

18 Citations (Scopus)

Abstract

Nonlinear magneto-optical resonances on the hyperfine transitions belonging to the D 2 line of rubidium were changed from bright to dark resonances by changing the laser power density of the single exciting laser field or by changing the vapor temperature in the cell. In one set of experiments atoms were excited by linearly polarized light from an extended cavity diode laser with polarization vector perpendicular to the light's propagation direction and magnetic field, and laser-induced fluorescence was observed along the direction of the magnetic field, which was scanned. A low-contrast bright resonance was observed at low laser power densities when the laser was tuned to the F g=2→F e=3 transition of 87Rb and near to the F g=3→F e=4 transition of 85Rb. The bright resonance became dark as the laser power density was increased above 0.6 mW/cm2 or 0.8 mW/cm2, respectively. When the F g=2→F e=3 transition of 87Rb was excited with circularly polarized light in a second set of experiments, a bright resonance was observed, which became dark when the temperature was increased to around 50 -C. The experimental observations at room temperature could be reproduced with good agreement by calculations based on a theoretical model, although the theoretical model was not able to describe measurements at elevated temperatures, where reabsorption was thought to play a decisive role. The model was derived from the optical Bloch equations and included all nearby hyperfine components, averaging over the Doppler profile, mixing of magnetic sublevels in the external magnetic field, and a treatment of the coherence properties of the exciting radiation field.

Original languageEnglish
Article number033418
JournalPhysical Review A: Atomic, Molecular, and Optical Physics
Volume85
Issue number3
DOIs
Publication statusPublished - 16 Mar 2012

OECD Field of Science

  • 1.3 Physical Sciences

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