TY - JOUR
T1 - Synthesis and characterization of poly(dialkylterthiophene-bithiophene) and poly(dialkylterthiophene-thienothiophene) for organic thin film transistors and organic photovoltaic cells
AU - Jeon, Chan Woo
AU - Kang, So Hee
AU - Yun, Hui Jun
AU - An, Tae Kyu
AU - Cha, Hyojung
AU - Park, Chan Eon
AU - Kim, Yun Hi
PY - 2013
Y1 - 2013
N2 - 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.
AB - 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.
KW - Dialkylterthiophene
KW - Organic thin film transistor
KW - Solar cell
UR - http://www.scopus.com/inward/record.url?scp=84888157769&partnerID=8YFLogxK
U2 - 10.1016/j.synthmet.2013.10.007
DO - 10.1016/j.synthmet.2013.10.007
M3 - Article
AN - SCOPUS:84888157769
SN - 0379-6779
VL - 185-186
SP - 159
EP - 166
JO - Synthetic Metals
JF - Synthetic Metals
ER -