We present the results of an investigation of the different physical processes that influence the shape of the nonlinear magneto-optical signals both at small magnetic field values (~ 100 mG) and at large magnetic field values (several tens of Gauss)
. We used a theoretical model that provided an accurate description of experimental signals for a wide range of experimental parameters. By turning various effects on or off inside this model, we investigated the origin of different features of the measured signals. We confirmed that the narrowest structures, with widths on the order of 100 mG, are related mostly to coherences among ground-state magnetic sublevels. The shape of the curves at other scales could be explained by taking into account the different velocity groups of atoms that come into and out of resonance with the exciting laser field. Coherent effects in the excited state can also play a role, although they mostly affect the polarization components of the fluorescence. The results of theoretical calculations are compared with experimental measurements of laser induced fluorescence from the D2 line of atomic rubidium as a function of magnetic field.
We studied magneto-optical resonances caused by excited-state level crossings in a nonzero magnetic field. Experimental measurements were performed on the transitions of the $D_2$ line of rubidium. These measured signals were described by a theoretic
al model that takes into account all neighboring hyperfine transitions, the mixing of magnetic sublevels in an external magnetic field, the coherence properties of the exciting laser radiation, and the Doppler effect. Good agreement between the experimental measurements and the theoretical model could be achieved over a wide range of laser power densities. We further showed that the contrasts of the level-crossing peaks can be sensitive to changes in the frequency of the exciting laser radiation as small as several tens of megahertz when the hyperfine splitting of the exciting state is larger than the Doppler broadening.
Nonlinear magneto-optical resonances on the hyperfine transitions belonging to the D2 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 tempera
ture 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 lights propagation direction and magnetic field, and laser induced fluorescence (LIF) 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 Fg=2 --> Fe=3 transition of Rb-87 and near to the Fg=3 --> Fe=4 transition of Rb-85. The bright resonance became dark as the laser power density was increased above 0.6mW/cm2 or 0.8 mW/cm2, respectively. When the Fg=2 --> Fe=3 transition of Rb-87 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 50C. 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.
