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Novel Two-Dimensional Conjugated Polymer Containing Fluorinated Bithiophene as Donor and Benzoselenodiazole as Acceptor Units with Vinyl-Terthiophene Pendants for Polymer Photovoltaic Cells

Novel 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 3,3′-difluoro-2,2′-bithiophene (2TF) was designed and synthesized using microwave...

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Autores principales: Raja, Rathinam, Luo, Shengkai, Hsiow, Chuen-Yo, Rwei, Syang-Peng, Wang, Leeyih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431906/
https://www.ncbi.nlm.nih.gov/pubmed/30970950
http://dx.doi.org/10.3390/polym9070272
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author Raja, Rathinam
Luo, Shengkai
Hsiow, Chuen-Yo
Rwei, Syang-Peng
Wang, Leeyih
author_facet Raja, Rathinam
Luo, Shengkai
Hsiow, Chuen-Yo
Rwei, Syang-Peng
Wang, Leeyih
author_sort Raja, Rathinam
collection PubMed
description Novel 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 3,3′-difluoro-2,2′-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 (E(g)) 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-C(71)-butyric acid methyl ester (PC(71)BM) as acceptor with an inverted device structure of ITO/ZnO/PDTBSeVTT-2TF:PC(71)BM/V(2)O(5)/Ag. The processing temperature of blend solution for preparing PDTBSeVTT-2TF:PC(71)BM 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 J(sc) of 10.99 mA/cm(−2) compared with the one at 50 °C, which had a PCE of 4.69% with a J(sc) 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 PC(71)BM and thus increasing the donor/acceptor interface.
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spelling pubmed-64319062019-04-02 Novel Two-Dimensional Conjugated Polymer Containing Fluorinated Bithiophene as Donor and Benzoselenodiazole as Acceptor Units with Vinyl-Terthiophene Pendants for Polymer Photovoltaic Cells Raja, Rathinam Luo, Shengkai Hsiow, Chuen-Yo Rwei, Syang-Peng Wang, Leeyih Polymers (Basel) Article Novel 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 3,3′-difluoro-2,2′-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 (E(g)) 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-C(71)-butyric acid methyl ester (PC(71)BM) as acceptor with an inverted device structure of ITO/ZnO/PDTBSeVTT-2TF:PC(71)BM/V(2)O(5)/Ag. The processing temperature of blend solution for preparing PDTBSeVTT-2TF:PC(71)BM 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 J(sc) of 10.99 mA/cm(−2) compared with the one at 50 °C, which had a PCE of 4.69% with a J(sc) 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 PC(71)BM and thus increasing the donor/acceptor interface. MDPI 2017-07-07 /pmc/articles/PMC6431906/ /pubmed/30970950 http://dx.doi.org/10.3390/polym9070272 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Raja, Rathinam
Luo, Shengkai
Hsiow, Chuen-Yo
Rwei, Syang-Peng
Wang, Leeyih
Novel Two-Dimensional Conjugated Polymer Containing Fluorinated Bithiophene as Donor and Benzoselenodiazole as Acceptor Units with Vinyl-Terthiophene Pendants for Polymer Photovoltaic Cells
title Novel Two-Dimensional Conjugated Polymer Containing Fluorinated Bithiophene as Donor and Benzoselenodiazole as Acceptor Units with Vinyl-Terthiophene Pendants for Polymer Photovoltaic Cells
title_full Novel Two-Dimensional Conjugated Polymer Containing Fluorinated Bithiophene as Donor and Benzoselenodiazole as Acceptor Units with Vinyl-Terthiophene Pendants for Polymer Photovoltaic Cells
title_fullStr Novel Two-Dimensional Conjugated Polymer Containing Fluorinated Bithiophene as Donor and Benzoselenodiazole as Acceptor Units with Vinyl-Terthiophene Pendants for Polymer Photovoltaic Cells
title_full_unstemmed Novel Two-Dimensional Conjugated Polymer Containing Fluorinated Bithiophene as Donor and Benzoselenodiazole as Acceptor Units with Vinyl-Terthiophene Pendants for Polymer Photovoltaic Cells
title_short Novel Two-Dimensional Conjugated Polymer Containing Fluorinated Bithiophene as Donor and Benzoselenodiazole as Acceptor Units with Vinyl-Terthiophene Pendants for Polymer Photovoltaic Cells
title_sort novel two-dimensional conjugated polymer containing fluorinated bithiophene as donor and benzoselenodiazole as acceptor units with vinyl-terthiophene pendants for polymer photovoltaic cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431906/
https://www.ncbi.nlm.nih.gov/pubmed/30970950
http://dx.doi.org/10.3390/polym9070272
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