The role of the ethynylene bond on the optical and electronic properties of diketopyrrolopyrrole copolymers

Pichaya Pattanasattayavong, Maria Sygletou, Emmanuel Kymakis, Emmanuel Stratakis, Feng Yan, Vasilis G. Gregoriou, Thomas Anthopoulos, Christos L. Chochos*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Scopus citations


It is presented that the introduction of an alkyne linkage could be an important tool for fine-tuning the electronic and optoelectronic properties of certain donor-acceptor (D-A) conjugated polymers. Extensive optoelectronic studies in an alternating copolymer consisting of diketopyrrolopyrrole (DPP) and ethynylene linkage (TDPPTTB) and comparison over its fully cyclic DPP analogues, such as phenyl (TDPPTP) and thiophene (TDPPTT) rings reveals the role of the ethynylene moiety when it is introduced into the polymer backbone. The ethynylene moiety decreases the donor character of the thiophenes that flank the DPP therefore the highest occupied molecular orbital (HOMO) level of TDPPTTB is situated between the HOMO levels of the TDPPTP and TDPPTT. The optical band gap (Eoptg) of TDPPTTB is fixed between the Eoptg of TDPPTT and TDPPTP with a significant blue-shift in its absorption maximum. Furthermore, detailed studies on the electronic properties of TDPPTTB have been performed in Field Effect Transistors (FETs) using various dielectric materials. Transistors based on TDPPTTB films annealed at 120 °C show ambipolar behaviour, similar to TDPPTP and TDPPTT, with carrier mobilities of 0.03 cm2 V-1 s-1 for holes and 0.02 cm2 V-1 s-1 for electrons. This journal is

Original languageEnglish (US)
Pages (from-to)58404-58411
Number of pages8
JournalRSC Advances
Issue number102
StatePublished - Oct 28 2014

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)


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