Berlin 2018 – wissenschaftliches Programm
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CPP: Fachverband Chemische Physik und Polymerphysik
CPP 10: Focus Session: Frontiers of Electronic-Structure Theory: Correlated Electron Materials I (joint session O/MM/DS/TT/CPP)
CPP 10.1: Vortrag
Montag, 12. März 2018, 10:30–10:45, HL 001
How Derivative Discontinuities in the Energy Yield Interatomic Steps in the Exact Kohn-Sham Potential of Density-Functional Theory — •Eli Kraisler1, Matthew J. P. Hodgson1, Axel Schild2, and Eberhard K.U. Gross1, 3 — 1Max-Planck-Institut für Mikrostrukturphysik, Halle (Saale), Germany — 2Laboratorium für Physikalische Chemie, ETH Zürich, Switzerland — 3Fritz Haber Center for Molecular Dynamics, Institute of Chemistry, The Hebrew University of Jerusalem, Israel
Accurate density-functional calculations hinge on reliable approximations to the unknown exchange-correlation (xc) potential. The most popular approximations usually lack features of the exact xc potential that are important for an accurate prediction of the fundamental gap and the distribution of charge in complex systems. Two principal features in this regard are the spatially uniform shift in the potential, as the number of electrons infinitesimally surpasses an integer, and the spatial steps that form, e.g., between the atoms of stretched molecules. Although both aforementioned concepts are well-known, the exact relationship between them remained unclear. In this talk, we establish this relationship and introduce a new concept: the charge-transfer derivative discontinuity, ΔCT. By numerically solving the many-electron Schrödinger equation, we extract the exact Kohn-Sham potential and directly observe its features, particularly the spatial interatomic steps. For the first time, spatial steps in the exact xc potential of a full configuration-interaction (FCI) calculation of a molecule are presented in three dimensions.