Spatial conformation and charge recombination properties of polythiophene derivatives with thienylene-vinylene side chains investigated by static and femtosecond spectroscopy

J Phys Chem B. 2010 Mar 4;114(8):2602-6. doi: 10.1021/jp909271e.

Abstract

We report herein the photophysics of three two-dimensional polythiophene derivatives, with different lengths of thienylene-vinylene conjugated side chains, in comparison with regioregular poly(3-hexylthiophene) (P3HT). In solution, an evolution from stimulated emission to photoinduced absorption (PIA) at emission peak is discovered with increasing length of side chains, indicating larger steric hindrance by longer side chains. The exciton lifetime is reduced by a factor of five when the thienylene-vinylene side chain is prolonged to three units. In the film form, we investigate the dynamics of the two PIA bands, assigned to intrachain exciton and interchain polaron pairs, respectively. The analysis of the dynamics suggests that their intrachain exciton decays are similar to the one-dimensional P3HT. The recombination possibility of delocalized interchain polaron pairs occurring in 0.9 ps is reduced with longer thienylene-vinylene side chain samples. Compared with regioregular P3HT film, which self-organizes to form lamellae crystal morphology, the morphologies of these three two-dimensional polythiophenes are amorphous, attributed to the large steric hindrance caused by the existence of side chains. This design of polythiophene derivatives provides the reduction of recombination possibility for delocalized interchain polaron pairs generated in the polymer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Membranes, Artificial
  • Molecular Conformation
  • Spectrometry, Fluorescence
  • Spectrophotometry, Ultraviolet
  • Thiophenes / chemistry*
  • Vinyl Compounds / chemistry*
  • X-Ray Diffraction

Substances

  • Membranes, Artificial
  • Thiophenes
  • Vinyl Compounds