Configuration interaction calculations with terms linear in the interelectronic coordinate for the ground state of H+3. A benchmark study

Publisher Website
Google Scholar
Abstract
The CISD‐R12 method is applied to the ground states of H2 and H+ 3 at their equilibrium configurations, with both bare nuclear Hamiltonian (BNH) and self‐consistent field (SCF) references with eight basis sets that range from 10 s (i.e., ten contracted s‐type Gaussians) to 30s20p12d9f. With the largest basis set, the energy of H2 is obtained with an error of 2μE h , while for H+ 3, the error is probably smaller and the best calculated energy of −1.343 835E h is supposed to be accurate to all indicated figures. The BNH reference is always superior to the SCF reference. The relativistic corrections are evaluated at the SCF level by means of ‘‘direct perturbation theory’’ both for H2 and H+ 3. The Hylleraas‐SCF methods and related concepts for the construction of an optimum reference function are discussed in the Appendix.