Levy Mel, Zahariev Federico
Department of Chemistry, Duke University, Durham, North Carolina 27708, USA and Department of Physics, North Carolina A&T State University, Greensboro, North Carolina 27411, USA and Department of Chemistry and Quantum Theory Group, Tulane University, New Orleans, Louisiana 70118, USA.
Department of Chemistry and Ames Laboratory, Iowa State University, Ames, Iowa 50011, USA.
Phys Rev Lett. 2014 Sep 12;113(11):113002. doi: 10.1103/PhysRevLett.113.113002.
It is observed that the exact interacting ground-state electronic energy of interest may be obtained directly, in principle, as a simple sum of orbital energies when a universal density-dependent term is added to w([ρ];r), the familiar Hartree plus exchange-correlation component in the Kohn-Sham effective potential. The resultant shifted potential, wover ¯, actually changes less on average than w([ρ];r) when the density changes, including the fact that wover ¯ does not undergo a discontinuity when the number of electrons increases through an integer. Thus, the approximation of wover ¯ represents an alternative direct approach for the approximation of the ground-state energy and density.