Electron Binding Energies of Open-Shell Species from Diagonal Electron-Propagator Self-Energies with Unrestricted Hartree-Fock Spin-Orbitals.

For closed-shell molecules, valence electron binding energies may be calculated accurately and efficiently with ab initio electron-propagator methods that have surpassed their predecessors. Advantageous combinations of accuracy and efficiency range from cubically scaling methods with mean errors of 0.2 eV to quintically scaling methods with mean errors of 0.1 eV or less. The diagonal self-energy approximation in the canonical Hartree-Fock basis is responsible for the enhanced efficiency of several methods. This work examines the predictive capabilities of diagonal self-energy approximations when they are generalized to the canonical spin-orbital basis of unrestricted Hartree-Fock (UHF) theory. Experimental data on atomic electron binding energies and high-level, correlated calculations in a fixed basis for a set of open-shell molecules constitute standards of comparison. A review of the underlying theory and analysis of numerical errors lead to several recommendations for the calculation of electron binding energies: (1) In calculations that employ the diagonal self-energy approximation, Koopmans's identity for UHF must be qualitatively correct. (2) Closed-shell reference states are preferable to open-shell reference states in calculations of molecular ionization energies and electron affinities. (3) For molecular electron binding energies between doublets and triplets, calculations of electron detachment energies are more accurate and efficient than calculations of electron attachment energies. When these recommendations are followed, mean absolute errors increase by approximately 0.05 eV with respect to their counterparts obtained with closed-shell reference orbitals.