Koopmans's theorem in the restricted open-shell Hartree-Fock method. II. the second canonical set for orbitals and orbital energies

摘要

A treatment of the validity of Koopmans's theorem (KT) in the restricted open-shell Hartree-Fock (ROHF) method can be separated into two essentially different cases. The first of them involves the one-electron processes X→ Xj± in which the spin state of an ion Xj± having a hole or an extra electron in the closed, open or virtual orbital φ_j is correctly described by a one-determinant wave function. This case was analyzed using different methods by Plakhutin [J. Chem. Phys. 125, 204110 (2006)] and by Plakhutin and Davidson [J. Phys. Chem. A 113, 12386 (2009)]. In the present work we analyze more complex processes where the state of an ion cannot be described by a single determinant. An example of such processes is the removal of an alpha electron from the closed shell of a high-spin half-filled open-shell system X. For this case we give a slightly generalized formulation of KT in both the "frozen" orbital approximation (i.e., within the canonical ROHF method) and the limited configuration interaction approach for ionized systems. We also show that a simultaneous treatment of KT for all one-electron ionization processes possible leads to the necessity of introducing in the canonical ROHF method two different sets of orbitals and two respective sets of orbital energies. The theory developed is compared with the previous formulations of KT in the restricted (ROHF) and unrestricted Hartree-Fock methods, and in the unrestricted density functional theory. The practical applicability of the theory is verified by comparing the KT estimates of the vertical ionization potentials in molecules O_2 and NO_2 with the respective experimental data.