Describing static correlation in bond dissociation by Kohn-Sham density functional theory

M. Fuchs, Y. M. Niquet, X. Gonze, K. Burke

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170 Citations (Scopus)


We show that density functional theory within the RPA (random phase approximation for the exchange-correlation energy) provides a correct description of bond dissociation in H 2 in a spin-restricted Kohn-Sham formalism, i.e., without artificial symmetry breaking. We present accurate adiabatic connection curves both at equilibrium and beyond the Coulson-Fisher point. The strong curvature at large bond length implies important static (left-right) correlation, justifying modern hybrid functional constructions but also demonstrating their limitations. Although exact at infinite separation and accurate near the equilibrium bond length, the RPA dissociation curve displays unphysical repulsion at larger but finite bond lengths. Going beyond the RPA by including the exact exchange kernel (RPA+X), we find a similar repulsion. We argue that this deficiency is due to the absence of double excitations in adiabatic linear response theory. Further analyzing the H 2 dissociation limit we show that the RPA+X is not size consistent, in contrast to the RPA.

Original languageEnglish
Article number094116
JournalJournal of Chemical Physics
Issue number9
Publication statusPublished - 2005
Externally publishedYes


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