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Optics Communications

Interpretation of sub-natural linewidths in pulsed-excitation laser spectroscopy

Piers Coleman, D. Kagan, P. L. Knight

Published Jan 1, 1981• 12 citations
Publisher
DOI
10.1016/0030-4018(81)90153-x

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Quantum Interference and Subnatural Linewidths in Laser Spectroscopy

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We demonstrate polarization spectroscopy of an excited state transition in room temperature cesium vapor. An anisotropy induced by a circularly polarized pump beam on the D2 transition is observed using a weak probe on the 6P3/2 to 7S1/2 transition. When the D2 transition is saturated, a sub-natural linewidth feature is observed which theoretical modeling shows is enhanced by Doppler averaging. Polarization spectroscopy provides a simple modulation-free signal suitable for laser frequency stabilization to excited state transitions.
The exciton coherent signal decay rate in GaAs quantum wells, as measured in four-wave mixing experiments, depends on the polarization of the excitation pulses. Using polarization-dependent two-dimensional coherent spectroscopy, we show that this behavior is due to the bosonic character of excitons. Interference between two different quantum mechanical pathways results in a smaller decay rate for cocircular and colinear polarization of the optical excitation pulses. This interference does not exist for cross-linearly polarized excitation pulses resulting in a larger decay rate. Our result shows that the bosonic nature of excitons must be considered when interpreting ultrafast spectroscopic studies of exciton dephasing in semiconductors. This behavior should be considered while interpreting results of ultrafast spectroscopy experiments involving bosonlike excitations.