Multiplet-dependent wave functions from the local-spin-density approximation with self-interaction correction

Abstract
The self-interaction-corrected version of the local-spin-density (SIC-LSD) approximation for calculating the electronic structure of N-electron systems is known to give orbital energies close to the Hartree-Fock (HF) values for ground and excited states of atoms, but no similar comparison has been made of the corresponding wave functions. As a test of the wave functions, we have calculated the dipole matrix elements between the quintet and triplet ns, np, and nd excited states of the oxygen atom with n=3,4,5,6 using the SIC-LSD orbitals. The results are found to be in excellent agreement with the corresponding HF values and confirm that SIC-LSD wave functions closely approximate the HF wave functions. To distinguish the orbitals for the triplet series from those for quintets, a novel scheme has been developed for obtaining multiplet-dependent orbitals.