Fermi‐Löwdin orbital self‐interaction corrected density functional theory: Ionization potentials and enthalpies of formation

The Fermi‐Löwdin orbital self‐interaction correction (FLO‐SIC) methodology is applied to atoms and molecules from the standard G2‐1 test set. For the first time FLO‐SIC results for the GGA‐type PBE functional are presented. In addition, examples where FLO‐SIC like any proper SIC provides qualitative improvements compared to standard DFT functionals are discussed in detail: the dissociation limit for H2+, the step‐wise linearity behavior for fractional occupation, as well as the significant reduction of the error of static polarizabilities. Further, ionization potentials and enthalpies of formation obtained by means of the FLO‐SIC DFT method are compared to other SIC variants and experimental values. The self‐interaction correction gives significant improvements if used with the LDA functional but shows worse performance in case of enthalpies of formation if the PBE‐GGA functional is used. The errors are analyzed and the importance of the overbinding of hydrogen is discussed. © 2018 Wiley Periodicals, Inc. The accuracy of the FLO‐SIC methodology is analyzed in detail for the G2‐1 benchmark set for LDA‐ and, for the first time, PBE‐FLO‐SIC. Cases where a proper self‐interaction correction delivers more accurate results than standard DFT functionals are discussed: the dissociation limit for H2+, the step‐wise linearity behavior for fractional occupation as well as the significant reduction of the error of static polarizabilities. The thermochemical performance is analyzed for the G2‐1 benchmark suite.