Novel two-dimensional conjugated polymer containing fluorinated bithiophene as donor and benzoselenodiazole as acceptor units with vinyl-terthiophene pendants for polymer photovoltaic cells

Raja, R.R.RajaLuo, S.S.LuoHsiow, C.-Y.C.-Y.HsiowRwei, S.-P.S.-P.RweiWang, L.L.Wang2020-06-232020-06-23201720734360https://scholars.lib.ntu.edu.tw/handle/123456789/504207Novel two-dimensional conjugated copolymer, abbreviated as PDTBSeVTT-2TF, containing electron-deficient 4,7-di(thiophen-2-yl)benzo[c][1,2,5]selenodiazole (DTBSe) unit, conjugated vinyl-terthiophene (VTT) side chain and 3,30-difluoro-2,20-bithiophene (2TF) was designed and synthesized using microwave-assisted Stille cross-coupling polymerization. UV-visible absorption and cyclic voltammetry studies revealed that this copolymer possesses a strong and broad absorption in the range of 300-800 nm and a narrow optical bandgap (Eg) of 1.57 eV with low-lying HOMO and LUMO energy levels. Further, the bulk heterojunction polymer solar cells (PSCs) were fabricated using PDTBSeVTT-2TF as donor and [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM) as acceptor with an inverted device structure of ITO/ZnO/PDTBSeVTT-2TF:PC71BM/V2O5/Ag. The processing temperature of blend solution for preparing PDTBSeVTT-2TF:PC71BM active layer showed obvious impact on the photovoltaic performance of solar devices. The cell fabricated from the blend solution at 65 °C exhibited enhanced power conversion efficiencies (PCE) of 5.11% with a Jsc of 10.99 mA/cm-2 compared with the one at 50 °C, which had a PCE of 4.69% with a Jsc of 10.10 mA/cm-2. This enhancement is due to the dissolution of PDTBSeVTT-2TF clusters into single molecules and small aggregates, improving the miscibility between the polymer and PC71BM and thus increasing the donor/acceptor interface. © 2017 by the authors.Benzoselenodiazole; Difluoro-bithiophene; Polymer solar cell; Vinyl-terthiophene[SDGs]SDG7Butyric acid; Conjugated polymers; Cyclic voltammetry; Heterojunctions; Photoelectrochemical cells; Photovoltaic cells; Processing; Solar cells; Solar power generation; Benzoselenodiazole; Bithiophenes; Inverted device structures; Polymer photovoltaic cells; Polymer solar cell (PSCs); Power conversion efficiencies; Stille cross coupling polymerization; Terthiophenes; Polymer solar cellsNovel two-dimensional conjugated polymer containing fluorinated bithiophene as donor and benzoselenodiazole as acceptor units with vinyl-terthiophene pendants for polymer photovoltaic cellsjournal article10.3390/polym9070272