We have measured the hyperfine structure of mutually perturbing rovibrational levels of the 1(b) 3Pi0 and 2(A) 1Sigma+ states of the NaK molecule, using the perturbation-facilitated optical-optical double resonance method with copropagating lasers. The unperturbed 1(b) 3Pi0 levels are split into four hyperfine components by the Fermi contact interaction bFIS. Mixing between the 1(b) 3Pi0 and 2(A) 1Sigma+ levels imparts hyperfine structure to the nominally singlet component of the perturbed levels and reduces the hyperfine splitting of the nominally triplet component. Theoretical analysis relates these observations to the hyperfine splitting that each 1(b) 3Pi0 level would have if it were not perturbed by a 2(A) 1Sigma+ level. Using this analysis, we demonstrate that significant hyperfine splitting arises because the 1(b) 3Pi0 state cannot be described as pure Hund's case (a). We determine bF for the 1(b) 3Pi0 levels and also a more accurate value for the magnitude of the singlet-triplet spin-orbit coupling HSO=[1(b) 3Pi0(vb,J)(H(SO))2(A) 1Sigma+(vA,J). Using the known spectroscopic constants of the 1(b) 3Pi state, we obtain bF=0.009 89+/-0.000 27 cm(-1). The values of (H(SO)) are found to be between 2 and 3 cm(-1), depending on vb, vA, and J. Dividing (H(SO)) by calculated vibrational overlap integrals, and taking account of the 1(b) 3Pi(Omega) rotational mixing, we can determine the magnitude of the electronic part H(el) of H(SO). Our results yield (H(el))=(16.33+/-0.15) cm(-1), consistent with our previous determinations using different techniques.

We report experimental observation of electromagnetically induced transparency (EIT) in an inhomogeneously broadened V-type Na 2 molecular system. The experiment is performed with both co-and counter-propagating arrangements for the propagation direction of the coupling and probe laser beams. In our theoretical model we employ the density matrix formalism, as well as perturbative methods for obtaining the probe field absorption profile for both open and closed systems. Simulations of the experimental data show excellent agreement with the predictions derived from the basic theory. Our fluorescent intensity measurements show that in the copropagating configuration the EIT plus saturation window depth is about 95%, while under similar conditions in the counter-propagating geometry we observed 40-45% reduction in the fluorescence signal around line center. To separate the two simultaneously occurring mechanisms in a V-type system, namely EIT and saturation, that are induced by the coupling field, we have carried out theoretical calculations, which show that in the co-propagating case a significant fraction of the depth of the dip is due to the coherent effect of EIT. When the

The intensity dependent absorption was measured on the D 1 line (6S 1/2 → 6P 1/2 transition) in atomic cesium. The magnetic field applied to the vapour and the spatial cross section of the laser beam were controlled and varied during data collection. A three-level rate equation model is presented in an attempt to explain the results. We show that this well known approach does not sucessfully model the data obtained in the absence of a magnetic field. Hence, a more complex and complete model that explicitly includes all of the hyperfine magnetic sublevels (a multilevel model) is presented. This approach accurately models all of the data collected. The good agreement betweeen this model and the data allows the determination of the transit relaxation rate (due to atomic time of flight through the laser beam), t = (1.13 ± 0.20)v rms /D, where v rms is the two-dimensional root-mean-squared speed of the atom and D is the FWHM of the Gaussian laser beam spatial profile.

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