Increasing the applicability of density functional theory. IV. Consequences of ionization-potential improved exchange-correlation potentials
Abstract
This paper's objective is to create a “consistent” mean-field based Kohn-Sham (KS) density functional theory (DFT) meaning the functional should not only provide good total energy properties, but also the corresponding KS eigenvalues should be accurate approximations to the vertical ionization potentials (VIPs) of the molecule, as the latter condition attests to the viability of the exchange-correlation potential (V{sub XC}). None of the prominently used DFT approaches show these properties: the optimized effective potential V{sub XC} based ab initio dft does. A local, range-separated hybrid potential cam-QTP-00 is introduced as the basis for a “consistent” KS DFT approach. The computed VIPs as the negative of KS eigenvalue have a mean absolute error of 0.8 eV for an extensive set of molecule's electron ionizations, including the core. Barrier heights, equilibrium geometries, and magnetic properties obtained from the potential are in good agreement with experiment. A similar accuracy with less computational efforts can be achieved by using a non-variational global hybrid variant of the QTP-00 approach.
- Authors:
- Publication Date:
- OSTI Identifier:
- 22253049
- Resource Type:
- Journal Article
- Journal Name:
- Journal of Chemical Physics
- Additional Journal Information:
- Journal Volume: 140; Journal Issue: 18; Other Information: (c) 2014 AIP Publishing LLC; Country of input: International Atomic Energy Agency (IAEA); Journal ID: ISSN 0021-9606
- Country of Publication:
- United States
- Language:
- English
- Subject:
- 37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; ACCURACY; APPROXIMATIONS; DENSITY FUNCTIONAL METHOD; EIGENVALUES; IONIZATION; MAGNETIC PROPERTIES; MEAN-FIELD THEORY; POTENTIALS
Citation Formats
Verma, Prakash, and Bartlett, Rodney J., E-mail: bartlett@ufl.edu. Increasing the applicability of density functional theory. IV. Consequences of ionization-potential improved exchange-correlation potentials. United States: N. p., 2014.
Web. doi:10.1063/1.4871409.
Verma, Prakash, & Bartlett, Rodney J., E-mail: bartlett@ufl.edu. Increasing the applicability of density functional theory. IV. Consequences of ionization-potential improved exchange-correlation potentials. United States. https://doi.org/10.1063/1.4871409
Verma, Prakash, and Bartlett, Rodney J., E-mail: bartlett@ufl.edu. 2014.
"Increasing the applicability of density functional theory. IV. Consequences of ionization-potential improved exchange-correlation potentials". United States. https://doi.org/10.1063/1.4871409.
@article{osti_22253049,
title = {Increasing the applicability of density functional theory. IV. Consequences of ionization-potential improved exchange-correlation potentials},
author = {Verma, Prakash and Bartlett, Rodney J., E-mail: bartlett@ufl.edu},
abstractNote = {This paper's objective is to create a “consistent” mean-field based Kohn-Sham (KS) density functional theory (DFT) meaning the functional should not only provide good total energy properties, but also the corresponding KS eigenvalues should be accurate approximations to the vertical ionization potentials (VIPs) of the molecule, as the latter condition attests to the viability of the exchange-correlation potential (V{sub XC}). None of the prominently used DFT approaches show these properties: the optimized effective potential V{sub XC} based ab initio dft does. A local, range-separated hybrid potential cam-QTP-00 is introduced as the basis for a “consistent” KS DFT approach. The computed VIPs as the negative of KS eigenvalue have a mean absolute error of 0.8 eV for an extensive set of molecule's electron ionizations, including the core. Barrier heights, equilibrium geometries, and magnetic properties obtained from the potential are in good agreement with experiment. A similar accuracy with less computational efforts can be achieved by using a non-variational global hybrid variant of the QTP-00 approach.},
doi = {10.1063/1.4871409},
url = {https://www.osti.gov/biblio/22253049},
journal = {Journal of Chemical Physics},
issn = {0021-9606},
number = 18,
volume = 140,
place = {United States},
year = {Wed May 14 00:00:00 EDT 2014},
month = {Wed May 14 00:00:00 EDT 2014}
}