Ab initio calculations with a nonspherical Gaussian basis set: Excited states of the hydrogen molecule

Abstract

A basis set of generalized nonspherical Gaussian functions (GGTOs) is presented and discussed. As a first example we report on Born-Oppenheimer energies of the hydrogen molecule. Although accurate results have been obtained, we conclude that H_2 is too 'simple' to allow for a substantial gain by using nonspherical functions. We rather expect that these functions may be particularly useful in calculations on large systems. A single basis set of GGTOs was used to simultaneously calculate the potential energy curves of several states within each subspace of {1,3}Σ_{g,u} symmetry. We hereby considerd the entire region of internuclear distances 0.8 < R < 1000 a.u. In particular the results for the fourth up to sixth electronic states show a high accuracy compared to calculations which invoke explicitely correlated functions, e.g. the relative accuracy is at least of the order of magnitude of 10^{-5}a.u. Energies for the 4 ^1Σ_u^+ and 4-6 ^3Σ_u^+ were improved and accurate data for the 6 ^3Σ_g^+, 5 ^1Σ_u^+, and 6 ^1Σ_u^+ state are, to the best of the authors knowledge, presented for the first time. Energy data for the seventh up to the nineth electronic state within each subspace were obtained with an estimated error of the order of magnitude of 10^{-4}a.u. The 7 ^1Σ_g^+ and the 6 ^1Σ_u^+ state were found to exhibit a very broad deep outer well at large internuclear distances.

4 figures, subm.to J.Chem.Phys