Absorption spectrum and solvatochromism of the [Ru(4,4′-COOH-2,2′-bpy)2(NCS)2] molecular dye by time dependent density functional theory

Simona Fantacci, Filippo De Angelis, Annabella Selloni

Research output: Contribution to journalArticle

282 Scopus citations

Abstract

We present a combined Density Functional/Time Dependent Density Functional study of the molecular structure, electronic states, and optical absorption spectrum of [Ru(4,4′-COOH-2,2′-bpy)2(NCS)2], a widely used charge-transfer sensitizer in nanocrystalline TiO2 solar cells. Calculations have been performed both for the complex in vacuo and in ethanol and water solvents, using a continuum model to account for solute-solvent interactions. Inclusion of the solvent leads to important changes of the energies and composition of the molecular orbitals of the complex; as a consequence, whereas the computed spectrum for the Ru-complex in vacuo deviates from the experimental one in both energy and shape, the spectra calculated in the presence of the solvent are in good agreement with the experiment. The first two absorption bands are found to originate from mixed ruthenium-NCS to bipyridine-π* transitions rather than to pure metal-to-ligand-charge-transfer (MLCT) transitions, whereas the third band arises from intraligand π → π * transitions. The experimentally observed blue-shift of the spectrum in water with respect to ethanol is well reproduced by our calculations and appears to be related to a decreased dipole moment in the excited state.

Original languageEnglish (US)
Pages (from-to)4381-4387
Number of pages7
JournalJournal of the American Chemical Society
Volume125
Issue number14
DOIs
StatePublished - Apr 9 2003

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

Fingerprint Dive into the research topics of 'Absorption spectrum and solvatochromism of the [Ru(4,4′-COOH-2,2′-bpy)<sub>2</sub>(NCS)<sub>2</sub>] molecular dye by time dependent density functional theory'. Together they form a unique fingerprint.

  • Cite this