RESUMEN
Polarization labeling spectroscopy technique was used to measure excitation spectra of LiCs molecule in the spectral range of 16,000-18,500 cm(-1). Four band systems were observed and assigned to transitions from the ground X(1)Σ(+) state to excited states (4)Ω = 0(+), (5)Ω = 0(+), (5)Ω = 1, and (6)Ω = 1 (in Hund's case (c) notation proper here), the latter three states being fine structure components of the states d(3)Π and e(3)Σ(+), nominally of triplet symmetry. The observed states are characterized spectroscopically and the experimental results are compared with predictions of theoretical calculations, showing accuracy of the theoretical electronic term values better than 100 cm(-1) and of the ω(e) and R(e) constants within 5%.
RESUMEN
We present an accurate potential energy curve of the B (1)Pi state in the LiCs molecule for which vibrational levels between v(') = 0 and v(') = 35 (bound by 11.4 GHz) were measured by photoassociation spectroscopy in an ultracold ensemble of (7)Li and (133)Cs atoms. By the combination of conventional spectroscopic data of the B-X system and the new photoassociation measurements a very precise value of the dissociation energy of the ground state X (1)Sigma(+) of LiCs was determined to be D(0) = 5783.495(5) cm(-1).
RESUMEN
Two previously unknown (1)Pi states and one (1)Sigma(+) state of NaLi are experimentally investigated in the energy region of 34,000-36,000 cm(-1) above the bottom of the molecular ground state potential well by using polarization labeling spectroscopy technique. Potential energy curves are deduced for all three states from the observed rovibrational levels. The identity of the observed states is discussed in relation with the recently published theoretical calculations on electronic structure of NaLi by Petsalakis et al. [J. Chem. Phys. 129, 054306 (2008)] and Mabrouk and Berriche [J. Phys. B41, 155101 (2008)].
RESUMEN
We recently reported the formation of ultracold LiCs molecules in the rovibrational ground state X1sigma+, v" = 0,J" = 0 (J. Deiglmayr et al., Phys. Rev. Lett., 2008, 101, 133004). Here we discuss details of the experimental setup and present a thorough analysis of the photoassociation step including the photoassociation line shape. We predict the distribution of produced ground state molecules using accurate potential energy curves combined with an ab initio dipole transition moment and compare this prediction with experimental ionization spectra. Additionally we improve the value of the dissociation energy for the X1sigma+ state by high resolution spectroscopy of the vibrational ground state.
RESUMEN
Ultracold LiCs molecules in the absolute ground state X1Sigma+, v'' = 0, J'' = 0 are formed via a single photoassociation step starting from laser-cooled atoms. The selective production of v'' = 0, J'' = 2 molecules with a 50-fold higher rate is also demonstrated. The rotational and vibrational state of the ground state molecules is determined in a setup combining depletion spectroscopy with resonant-enhanced multiphoton ionization time-of-flight spectroscopy. Using the determined production rate of up to 5 x 10(3) molecules/s, we describe a simple scheme which can provide large samples of externally and internally cold dipolar molecules.
RESUMEN
We describe a modification of the inverted perturbation approach method allowing to construct physically sensible potential energy curves for electronic states of diatomic molecules even when some parts of the potential are not adequately characterized by the experimental data. The method is based on a simple regularization procedure, imposing an additional constraint on the constructed potential curve. In the present work it is applied to the double minimum 4 (1)Sigma(u) (+) state of Na(2), observed experimentally by polarization labeling spectroscopy technique.
