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Russian Physics Journal

Two-level lasers operating on the transitions to the ground state

V. A. Gerasimov, Vladislav V. Gerasimov

Published Aug 1, 2011• 0 citations
Publisher
DOI
10.1007/s11182-011-9619-y

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A semiclassical theory of dye lasers is presented in which the relevant energy-level diagram of a dye molecule is assumed to consist of a bandlike ground state with many sublevels and an excited single state. This theory not only describes the single-frequency operation, which has a low instability threshold, but also describes the two-frequency and multifrequency steady states of operation and the transitions between the different steady states. The general solution of a multifrequency operation is given explicitly and differs essentially from the well-known Rabi oscillation. The theoretical predictions are in good agreement with recent experiments done by Hillman et al., [ Phys. Rev. Lett.52, 1605 ( 1984)], which cannot be explained by the conventional Maxwell–Bloch laser theory derived from two-level atoms.
We report on the use of depletion spectroscopy to detect ultracold ground-state KRb molecules with rotational resolution. The population of a specific ground-state vibrational level ${v}^{\ensuremath{''}}$, produced by photoassociation of ultracold atoms, is monitored by one-color two-photon pulsed-laser ionization. When a cw laser is resonant with a rovibrational transition to an excited state, the ground-state population, and hence the ion signal, is depleted. This narrow-band spectroscopic technique allows the individual rotational levels in both ground and excited states to be resolved, and thus the population of a single ground-state rovibrational level to be monitored. These resolved transitions are a necessary first step in transferring population from high vibrational levels of the ground state, such as produced by photoassociation, to the absolute molecular ground state $X\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Sigma}^{+}$ (${v}^{\ensuremath{''}}=0$, ${J}^{\ensuremath{''}}=0$). This technique can also be used to determine binding energies of high-${v}^{\ensuremath{''}}$ molecules. Combining our binding energy measurement with the results of previous spectroscopy yields an improved dissociation energy of the XXX state: ${D}_{e}=4217.822\ifmmode\pm\else\textpm\fi{}0.003\phantom{\rule{0.3em}{0ex}}{\mathrm{cm}}^{\ensuremath{-}1}$. We also report on the two-color pulsed-laser ionization used to locate the depletion transitions.