Please use this identifier to cite or link to this item:
標題: The D (1)Sigma(+) state of (7)LiH: Comparison of observations with vibronic theory
作者: Wu, C.Y.
Luh, W.T.
Gadea, F.X.
Stwalley, W.C.
關鍵字: isotopic lithium hydrides;potential-energy curves;adiabatic;corrections;radiative lifetimes;laser-fluorescence;diatomic-molecules;lih molecule;c state;dissociation;system
Project: Journal of Chemical Physics
期刊/報告no:: Journal of Chemical Physics, Volume 128, Issue 6.
The excited D (1)Sigma(+) electronic state of (7)LiH 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)Sigma(+) 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)Sigma(+) electronic state and the continuum states of the C (1)Sigma(+) electronic state. The mutual agreement between the spectral results and the vibronic results demonstrates that the D (1)Sigma(+) electronic state of (7)LiH is better characterized by the vibronic approach. (C) 2008 American Institute of Physics.
ISSN: 0021-9606
DOI: 10.1063/1.2827132
Appears in Collections:期刊論文

Show full item record

Google ScholarTM




Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.