TY - JOUR
T1 - A fused thieno[3,2-
T2 - B] thiophene-dithiophene based donor molecule for organic photovoltaics: A structural comparative study with indacenodithiophene
AU - Abe, Yuichiro
AU - Li, Hairong
AU - Yin, Jun
AU - Soci, Cesare
AU - Grimsdale, Andrew C.
AU - Lam, Yeng Ming
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2016.
PY - 2016
Y1 - 2016
N2 - A novel donor material, di(HTh2BT)DTCTT, having a dithienocyclopenta-thieno[3,2-b]thiophene (DTCTT) core, was synthesized and used as the molecular donor in a small molecular organic photovoltaic device (sm-OPV). DTCTT has a molecular structure similar to that of indacenodithiophene (IDT) but with a central thienothiophene instead of a benzene, and the effect of the more extended conjugation of the theinothiophene on its optical, thermal and photovoltaic properties was systematically investigated. Di(HTh2BT)DTCTT showed red-shifted absorption (up to 800 nm), a higher HOMO level and greater crystallinity than its IDT analogue. The DTCTT based sm-OPV devices were fabricated by spin-coating a blend solution with PC71BM, and showed an encouraging PCE of 2.8% with Jsc of -9.3 mA cm-2, Voc of 0.73 V and FF of 0.42. This is the first report of a DTCTT-based molecular donor for sm-OPV and it can be seen that this compound has greater potential for achieving high efficiencies compared with its IDT analogue. The structural and morphological analyses indicated that further improvement may be possible by increasing the crystallinity of the blend film.
AB - A novel donor material, di(HTh2BT)DTCTT, having a dithienocyclopenta-thieno[3,2-b]thiophene (DTCTT) core, was synthesized and used as the molecular donor in a small molecular organic photovoltaic device (sm-OPV). DTCTT has a molecular structure similar to that of indacenodithiophene (IDT) but with a central thienothiophene instead of a benzene, and the effect of the more extended conjugation of the theinothiophene on its optical, thermal and photovoltaic properties was systematically investigated. Di(HTh2BT)DTCTT showed red-shifted absorption (up to 800 nm), a higher HOMO level and greater crystallinity than its IDT analogue. The DTCTT based sm-OPV devices were fabricated by spin-coating a blend solution with PC71BM, and showed an encouraging PCE of 2.8% with Jsc of -9.3 mA cm-2, Voc of 0.73 V and FF of 0.42. This is the first report of a DTCTT-based molecular donor for sm-OPV and it can be seen that this compound has greater potential for achieving high efficiencies compared with its IDT analogue. The structural and morphological analyses indicated that further improvement may be possible by increasing the crystallinity of the blend film.
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U2 - 10.1039/c6tc02089e
DO - 10.1039/c6tc02089e
M3 - Article
AN - SCOPUS:84992332939
SN - 2050-7534
VL - 4
SP - 9656
EP - 9663
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
IS - 41
ER -