The D1∑+ state of Li7 H: Comparison of observations with vibronic theory

Abstract

The excited D +1 electronic state of Li7 H has been observed up to near its dissociation limit by a pulsed optical-optical double resonance fluorescence depletion spectroscopic technique. An extensive vibronic calculation has been performed with a diabatic approach with purely potential couplings involving a set of eight diabatic states of +1 symmetry, corresponding to seven neutral states and one ionic state. Twenty-six new vibrational levels have been observed. Both the derived vibrational energy spacings and the vibronic ones are similarly irregular. The observed spectral linewidths and vibronic resonance widths are found to vary similarly with increasing energy. Observed asymmetric spectral lineshapes may be attributed to the strong radial couplings between the discrete levels of the D +1 electronic state and the continuum states of the C +1 electronic state. The mutual agreement between the spectral results and the vibronic results demonstrates that the D +1 electronic state of Li7 H is better characterized by the vibronic approach. © 2008 American Institute of Physics.