An additive long-range potential to correct for the charge-transfer failure of time-dependent density functional theory
Time-dependent density functional theory is one of the most widely used methods for the calculation of excited states of large molecules. However, it exhibits substantial problems with charge-transfer excited states when conventional exchange-correlation functionals are employed. Here, we introduce...
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| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
10. Mai 2010
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| In: |
Zeitschrift für physikalische Chemie
Year: 2010, Jahrgang: 224, Heft: 3/4, Pages: 311-324 |
| ISSN: | 2196-7156 |
| DOI: | 10.1524/zpch.2010.6107 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1524/zpch.2010.6107 Verlag, lizenzpflichtig, Volltext: https://www.degruyterbrill.com/document/doi/10.1524/zpch.2010.6107/html 
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| Verfasserangaben: | Andreas Dreuw, Jürgen Plötner, Michael Wormit, Martin Head-Gordon, Anthony Dean Dutoi |
| Zusammenfassung: | Time-dependent density functional theory is one of the most widely used methods for the calculation of excited states of large molecules. However, it exhibits substantial problems with charge-transfer excited states when conventional exchange-correlation functionals are employed. Here, we introduce an additive long-range potential that can, in principle, be directly employed with any existing local, GGA or hybrid-functional, without re-fitting of the original functionals. The additive potential shifts the excitation energies to higher values and corrects for the wrong asymptotic behavior of their potential energy surfaces with respect to charge-separating coordinates. First examples of its successful application are shown. |
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| Beschreibung: | Gesehen am 16.02.2023 |
| Beschreibung: | Online Resource |
| ISSN: | 2196-7156 |
| DOI: | 10.1524/zpch.2010.6107 |