Thermal Fluctuations Lead to Cumulative Disorder and Enhance Charge Transport in Conjugated Polymers

Wenlin Zhang, Joel H. Bombile, Albree R. Weisen, Renxuan Xie, Ralph H. Colby, Michael J. Janik, Scott T. Milner, Enrique D. Gomez

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

All conjugated polymers examined to date exhibit significant cumulative lattice disorder, although the origin of this disorder remains unclear. Using atomistic molecular dynamics (MD) simulations, the detailed structures for single crystals of a commonly studied conjugated polymer, poly(3-hexylthiophene-2,5-diyl) (P3HT) are obtained. It is shown that thermal fluctuations of thiophene rings lead to cumulative disorder of the lattice with an effective paracrystallinity of about 0.05 in the π–π stacking direction. The thermal-fluctuation-induced lattice disorder can in turn limit the apparent coherence length that can be observed in diffraction experiments. Calculating mobilities from simulated crystal structures demonstrates that thermal-fluctuation-induced lattice disorder even enhances charge transport in P3HT. The mean inter-chain charge transfer integral is enhanced with increasing cumulative lattice disorder, which in turn leads to pathways for fast charge transport through crystals.

Original languageEnglish (US)
Article number1900134
JournalMacromolecular Rapid Communications
Volume40
Issue number15
DOIs
StatePublished - 2019
Externally publishedYes

Keywords

  • charge transport
  • conjugated polymers
  • disorder
  • simulations

ASJC Scopus subject areas

  • Organic Chemistry
  • Polymers and Plastics
  • Materials Chemistry

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