The molecular frame electric dipole moment and hyperfine interactions in hafnium fluoride, HfF

13Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The (1,0) 17.92.5-X2Δ32 band of hafnium monofluoride (HfF) has been recorded using high-resolution laser-induced fluorescence spectroscopy both field-free and in the presence of a static electric field. The field-free spectra of 177HfF, 179HfF, and 180HfF were modeled to generate a set of fine and hyperfine parameter for the X2Δ32(v = 0) and 17.92.5 (v = 1) states. The observed optical Stark shifts for the 180HfF isotopologue were analyzed to produce the molecular frame electric dipole moments of 1.66(1) D and 0.419(7) D for the X2Δ32 and 17.925 state, respectively. Both the generalized effective core potential and all-electron four component approaches were used in ab initio calculations to predict the properties of ground state HfF including equilibrium distance, dipole moments, quadrupole coupling, and magnetic hyperfine constants. © 2013 American Institute of Physics.

Cite

CITATION STYLE

APA

Le, A., Steimle, T. C., Skripnikov, L., & Titov, A. V. (2013). The molecular frame electric dipole moment and hyperfine interactions in hafnium fluoride, HfF. Journal of Chemical Physics, 138(12). https://doi.org/10.1063/1.4794049

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free