Evaluation of the restricted virtual space approximation in the algebraic-diagrammatic construction scheme for the polarization propagator to speed-up excited-state calculations

The applicability and limitations of the restricted virtual space (RVS) approximation within the algebraic-diagrammatic construction (ADC) scheme for the polarization propagator up to third order is evaluated. In RVS-ADC, not only the core but also a substantial amount of energetically high-lying vi...

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Hauptverfasser: Yang, Chong (VerfasserIn) , Dreuw, Andreas (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 27 March 2017
In: Journal of computational chemistry
Year: 2017, Jahrgang: 38, Heft: 17, Pages: 1528-1537
ISSN:1096-987X
DOI:10.1002/jcc.24794
Online-Zugang:Verlag, Volltext: http://dx.doi.org/10.1002/jcc.24794
Verlag, Volltext: http://onlinelibrary.wiley.com/doi/10.1002/jcc.24794/abstract
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Verfasserangaben:Chong Yang and Andreas Dreuw
Beschreibung
Zusammenfassung:The applicability and limitations of the restricted virtual space (RVS) approximation within the algebraic-diagrammatic construction (ADC) scheme for the polarization propagator up to third order is evaluated. In RVS-ADC, not only the core but also a substantial amount of energetically high-lying virtual orbitals is restricted in excitation energy calculations of low-lying excited electronic states. Using octatetraene, indole, and pyridine as representative examples and different standard basis sets of triple-zeta quality, RVS-ADC(2) turns out to be highly useful and to have negligible effects on ππ* excited states. However, for nπ* or πσ* states, the RVS approximation is generally less reliable but better at third-order than second-order ADC level. In addition, a unified, basis-set independent, thus normalized virtual orbital threshold (value) is introduced, making the RVS approximation more controllable and a priori applicable.
Beschreibung:Gesehen am 12.12.2017
Beschreibung:Online Resource
ISSN:1096-987X
DOI:10.1002/jcc.24794