Static correlation and electron localization in molecular dimers from the self-consistent RPA and GW approximation

M. Hellgren, F. Caruso, D.R. Rohr, X. Ren, A. Rubio, M. Scheffler, P. Rinke

Tutkimustuotos: LehtiartikkeliArticleScientificvertaisarvioitu

37 Sitaatiot (Scopus)
161 Lataukset (Pure)

Abstrakti

We investigate static correlation and delocalization errors in the self-consistent GW and random-phase approximation (RPA) by studying molecular dissociation of the H2 and LiH molecules. Although both approximations contain topologically identical diagrams, the nonlocality and frequency dependence of the GW self-energy crucially influence the different energy contributions to the total energy as compared to the use of a static local potential in the RPA. The latter leads to significantly larger correlation energies, which allow for a better description of static correlation at intermediate bond distances. The substantial error found in GW is further analyzed by comparing spin-restricted and spin-unrestricted calculations. At large but finite nuclear separation, their difference gives an estimate of the so-called fractional spin error normally determined only in the dissociation limit. Furthermore, a calculation of the dipole moment of the LiH molecule at dissociation reveals a large delocalization error in GW making the fractional charge error comparable to the RPA. The analyses are supplemented by explicit formulas for the GW Green's function and total energy of a simplified two-level model providing additional insights into the dissociation limit.
AlkuperäiskieliEnglanti
Artikkeli165110
Sivut1-12
JulkaisuPhysical Review B
Vuosikerta91
Numero16
DOI - pysyväislinkit
TilaJulkaistu - 2015
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

Tutkimusalat

  • GW
  • Hydrogen
  • RPA
  • static correlation

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