Stretching Bonds without Breaking Symmetries in Density Functional Theory

Kohn–Sham density functional theory (KS-DFT) stands out among electronic structure methods due to its balance of accuracy and computational efficiency. However, to achieve chemically accurate energies, standard density functional approximations in KS-DFT often need to break underlying symmetries, a long-standing “symmetry dilemma”. By employing fragment spin densities as the main variables in calculations (rather than total molecular densities, as in KS-DFT), we present an embedding framework in which this symmetry dilemma is understood and partially resolved. The spatial overlap between fragment densities is used as the main ingredient to construct a simple, physically motivated approximation to a universal functional of the fragment densities. This “overlap approximation” is shown to significantly improve semilocal KS-DFT binding energies of molecules without artificially breaking either charge or spin symmetries. The approach is shown to be applicable to covalently bonded molecules and to systems of the “strongly correlated” type.