Abstract

We present a combined theoretical and experimental study of the effects of laser polarization on optical coherences produced in two-color, resonant four-wave mixing (TC-RFWM). A time-dependent model incorporating diagrammatic perturbation theory and spherical tensor formalism is used to interpret observations of quantum beats due to molecular hyperfine structure in time-resolved TC-RFWM in nitric oxide. Good agreement is found between the model and the observed time-resolved signals for two distinct excitation schemes and a variety of polarization configurations including both polarization and population gratings. Measured hyperfine energy intervals are reported for the $X{}^{2}{\ensuremath{\Pi}}_{1/2},$ $v=0$ ground state and the $A{}^{2}{\ensuremath{\Sigma}}^{+},$ $v=0$ excited state of NO. The experimental results demonstrate that TC-RFWM can be used to perform state-selective, quantum beat spectroscopy in three-level systems by suitably designing three experimental features: the excitation scheme for the matter-field interaction, the time ordering of the laser pulses, and the polarization of the incident laser beams.

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