Papers › Ensemble Generalization of the Perdew-Zunger Self-Interaction Correction: a Way Out of...
Ensemble Generalization of the Perdew-Zunger Self-Interaction Correction: a Way Out of Multiple Minima and Symmetry Breaking
Sebastian Schwalbe, Wanja Timm Schulze, Kai Trepte, Susi Lehtola
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The Perdew-Zunger (PZ) self-interaction correction (SIC) is an established tool to correct unphysical behavior in density functional approximations. Yet, PZ-SIC is well-known to sometimes break molecular symmetries. An example of this is the benzene molecule, for which PZ-SIC predicts a symmetry-broken electron density and molecular geometry, since the method does not describe the two possible Kekul\'e structures on an even footing, leading to local minima [Lehtola et al, J. Chem. Theory Comput. 2016, 12, 3195]. PZ-SIC is often implemented with Fermi-L\"owdin orbitals (FLOs), yielding the FLO-SIC method, which likewise has issues with symmetry breaking and local minima [Trepte et al, J. Chem. Phys. 2021, 155, 224109]. In this work, we propose a generalization of PZ-SIC - the ensemble PZ-SIC (E-PZ-SIC) method - which shares the asymptotic computational scaling of PZ-SIC (albeit with an additional prefactor). E-PZ-SIC is straightforwardly applicable to various molecules, merely requiring one to average the self-interaction correction over all possible Kekul\'e structures, in line with chemical intuition. We showcase the implementation of E-PZ-SIC with FLOs, as the resulting E-FLO-SIC method is easy to realize on top of an existing implementation of FLO-SIC. We show that E-FLO-SIC indeed eliminates symmetry breaking, reproducing a symmetric electron density and molecular geometry for benzene. The ensemble approach suggested herein could also be employed within approximate or locally scaled variants of PZ-SIC and their FLO-SIC versions.
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