The hyperfine interaction constants, specific-mass-shift parameters, and total energies for the 3s${\mathrm{}}^2$S and 4s${\mathrm{}}^2$S states in lithium were calculated using the multiconfiguration Hartree-Fock method. The configuration expansions were obtained with the active space method, where configuration state functions are generated by excitations from the reference configuration to an active set of orbitals. The active set was increased in a systematic way, allowing the convergence of the studied parameters to be monitored. The obtained nonrelativistic energies are close to the lowest-upper-bound estimates from Hylleraas calculations. Whereas the convergence rate of the hyperfine interaction constants with respect to the increasing basis in the Hylleraas calculations degrades appreciably for higher states in the Rydberg series, no such effect could be seen for the multiconfiguration Hartree-Fock calculations. The uncertainties of the calculated hyperfine interaction constants are estimated to be less than three parts in a thousand for both of the studied states. The value for the 3s${\mathrm{}}^2$S state is in excellent agreement with results from relativistic many-body perturbation theory calculations, but is well outside the error bars from a recent precision measurement using Stark spectroscopy.

• Received 27 June 1995

DOI:https://doi.org/10.1103/PhysRevA.52.4262