DI-UMONS : Dépôt institutionnel de l’université de Mons

Recherche transversale
Rechercher
(titres de publication, de périodique et noms de colloque inclus)
2006-06-29 - Article/Dans un journal avec peer-review - Anglais - 1 page(s)

Engel E., Schmidt K., Beljonne David , Brédas Jean-Luc , Assa J., Fröb H., Leo K., Hoffmann M., "Transient Absorption Spectroscopy and Quantum-Chemical Studies of Matrix-Isolated Perylene Derivatives" in Physical Review. B : Condensed Matter, 73, 24, 245216

  • Edition : American Institute of Physics, New York (NY)
  • Codes CREF : Spectroscopie [électromagnétisme, optique, acoustique] (DI1255)
  • Unités de recherche UMONS : Chimie des matériaux nouveaux (S817)
  • Instituts UMONS : Institut de Recherche en Science et Ingénierie des Matériaux (Matériaux)
Texte intégral :

Abstract(s) :

(Anglais) We present a comprehensive experimental and theoretical study of the optical properties of matrix-isolated molecules of the two perylene derivatives N,N'-dimethylperylene-3,4,9,10-dicarboximide (MePTCDI) and 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA). A solid solution of the dyes in an SiO2 matrix exhibits monomer-like behavior. Transient absorption pump-probe spectroscopy in the range 1.2–2.6 eV has been performed on an ultrafast time scale. The differential transmittance reveals contributions from ground-state bleaching, stimulated emission, and excited-state absorption. Both systems exhibit broad excited-state absorption features below 2.0 eV with a clear peak around 1.8 eV. The spectra can be consistently explained by the results of quantum-chemical calculations. We have applied both the coupled cluster singles and doubles (CCSD) model and the multireference-determinant single and double configuration-interaction (MRD-CI) technique on the basis of the intermediate neglect of differential overlap (INDO) Hamiltonian. The results are insensitive to whether the geometry is optimized for the electronic ground state or first excited state. The experimental polarization anisotropies for the two major transitions are in agreement with the calculated polarizations.

Notes :
  • (Anglais) Lecture en ligne: http://www.hemica.de/HoffmannScientific/Pdf/Engel06b_web.pdf
  • (Anglais) Publié en ligne le 7 avril 2006
Identifiants :
  • DOI : 10.1103/PhysRevB.73.245216