Synthesis and characterization of poly(dialkylterthiophene-bithiophene) and poly(dialkylterthiophene-thienothiophene) for organic thin film transistors and organic photovoltaic cells

Chan Woo Jeon, So Hee Kang, Hui Jun Yun, Tae Kyu An, Hyojung Cha, Chan Eon Park, Yun Hi Kim

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

We designed new polymers composed of dialkylated terthiophene and thieno[3,2-b]thiophene, 2,2′-bithiophene for the fabrication of organic thin film transistors and polymer solar cells. Poly[5-(thieno[3,2-b]thiophene-2- yl)3′,4′-dioctyl-2,2′:5′,2″-terthiophene] (PTTOT), and poly[5-((2,2′-bithiophene)-5-yl)3′,4′-dioctyl-2,2′: 5′,2″-terthiophene] (PBTOT) were synthesized via Stille coupling and Suzuki coupling reaction. The obtained polymers were confirmed by 1H NMR and FT-IR spectra. The weight average molecular, the thermal, optical and electronic properties of the polymers were investigated by gel permeation chromatography (GPC), differential scanning calorimetry (DSC), ultraviolet-visible (UV-vis) absorption and photoluminescence (PL) spectroscopies and cyclic voltammetry (CV). The crystallinity of polymer films was investigated by X-ray diffraction (XRD). Field-effect hole mobilities of PTTOT and PBTOT based solution-processed OTFTs were 3.54 × 10-3 cm2 V-1 S-1 and 1.73 × 10-2 cm2 V-1 S-1, respectively. And, each of the polymers was investigated as an electron donor material with PC71BM as an electron acceptor in bulk hetero junction solar cells. The polymers of PTTOT and PBTOT showed the power conversion efficiency (PCE) of 0.096% (J sc = 0.1 mA/cm-2, FF = 83.49%) and 3.2% (JSC = 8.9 mA/cm-2, FF = 51.9%), respectively.

Original languageEnglish
Pages (from-to)159-166
Number of pages8
JournalSynthetic Metals
Volume185-186
DOIs
StatePublished - 2013

Keywords

  • Dialkylterthiophene
  • Organic thin film transistor
  • Solar cell

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