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2009-01-22 - Article/Dans un journal avec peer-review - Anglais - 12 page(s)

Dykstra T.E., Hennebicq E., Beljonne David , Gierschner J., Claudio G., Bittner E.R., Knoester J., Scholes G.D., "Conformational Disorder and Ultrafast Exciton Relaxation in PPV-family Conjugated Polymers" in Journal of Physical Chemistry B, 113, 38, 656-667

  • Edition : American Chemical Society, Washington (DC)
  • 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 report combined experimental and theoretical studies of excitation relaxation in poly[2-methoxy,5-(2'-ethyl-hexoxy)-1,4-phenylenevinylene] (MEH-PPV), oligophenylenevinylene (OPV) molecules of varying length, and model PPV chains. We build on the paradigm that the basic characteristics of conjugated polymers are decided by conformational subunits defined by conjugation breaks caused by torsional disorder along the chain. The calculations reported here indicate that for conjugated polymers like those in the PPV family, these conformational subunits electronically couple to neighboring subunits, forming subtly delocalized collective states of nanoscale excitons that determine the polymer optical properties. We find that relaxation among these exciton states can lead to a decay of anisotropy on ultrafast time scales. Unlike in Frster energy transfer, the exciton does not necessarily translate over a large distance. Nonetheless, the disorder in the polymer chain means that even small changes in the exciton size or location has a significant effect on the relaxation pathway and therefore the anisotropy decay.

Notes :
  • (Anglais) Publié en ligne le 23 décembre 2008
Identifiants :
  • DOI : 10.1021/jp807249b