2017
DOI: 10.1002/pola.28941
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Synthesis and characterization of highly conjugated side‐group‐substituted benzo[1,2‐b:4,5‐b′]dithiophene‐based copolymer for use in organic solar cells

Abstract: A new donor-acceptor (D-A) conjugated copolymer based on benzo [1,2-b:4,5-b 0 ]dithiophene (BDT) and thieno [3,4c]pyrrole-4,6-dione (TPD) was synthesized via a Stille crosscoupling reaction. A highly conjugated thiophene-based side group, tris(thienylenevinylene) (TTV), was incorporated into each BDT unit to generate the two-dimensional D-A copolymer (PBDT-TTV). An alkoxy-substituted BDT-based TPD copolymer (PBDT-OR) was synthesized using the same polymerization method for comparison. PBDT-TTV thin films produ… Show more

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Cited by 5 publications
(1 citation statement)
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“…Afterward, to further enhancing the electronegative of TT unit, by creating two active sites and introducing the functional group carbonyl, 4H , 6H -5λ 2 -thieno [3, 4-c ] pyrrole-4,6-dione (TPD) unit with a strong electron-withdrawing was successfully constructed. Subsequently, based on the polymer backbone BDT-T-TPD-T, PBDT-TPD (2014) andPBDTT-TPD (2014) were designed by Kim et al [138] ; P1 (2016) , PBDT-Th-TPD (2017) , PBDT-TTV (2018) and PTPD (2020) were prepared by Kranthiraja et al [139] , Kotturappa et al [140] , Kim et al [141] , and Zhao et al [142] in turn; a series of polymer donors TPD-1 (2020) , TPD-2 (2020) , TPD-3 (2020) and TPD-3F (2020) were also synthesized by Liao et al [143] After applying for OSC devices, the introduction of thiophene-based and benzene-based side chains further extend the π-π conjugated plane of polymer donors, thereby these polymer donor: acceptor based OSC achieved a promisingV oc , especially for P1 (2016): PC 71 BM based OSC (0.99 V). Furthermore, based on the main chain of BDT-T-TPD-T, due to the substitution of alkyl-thiophene side chain extend the original π-π conjugated plane of polymer backbone as well as enhance the electron-donating of BDT unit, meanwhile, the introduction of long alkyl chain also optimized the miscibility and blend film morphology of active layer.…”
Section: δ-π-α-π τψπε πολψμερ δονορςmentioning
confidence: 99%
“…Afterward, to further enhancing the electronegative of TT unit, by creating two active sites and introducing the functional group carbonyl, 4H , 6H -5λ 2 -thieno [3, 4-c ] pyrrole-4,6-dione (TPD) unit with a strong electron-withdrawing was successfully constructed. Subsequently, based on the polymer backbone BDT-T-TPD-T, PBDT-TPD (2014) andPBDTT-TPD (2014) were designed by Kim et al [138] ; P1 (2016) , PBDT-Th-TPD (2017) , PBDT-TTV (2018) and PTPD (2020) were prepared by Kranthiraja et al [139] , Kotturappa et al [140] , Kim et al [141] , and Zhao et al [142] in turn; a series of polymer donors TPD-1 (2020) , TPD-2 (2020) , TPD-3 (2020) and TPD-3F (2020) were also synthesized by Liao et al [143] After applying for OSC devices, the introduction of thiophene-based and benzene-based side chains further extend the π-π conjugated plane of polymer donors, thereby these polymer donor: acceptor based OSC achieved a promisingV oc , especially for P1 (2016): PC 71 BM based OSC (0.99 V). Furthermore, based on the main chain of BDT-T-TPD-T, due to the substitution of alkyl-thiophene side chain extend the original π-π conjugated plane of polymer backbone as well as enhance the electron-donating of BDT unit, meanwhile, the introduction of long alkyl chain also optimized the miscibility and blend film morphology of active layer.…”
Section: δ-π-α-π τψπε πολψμερ δονορςmentioning
confidence: 99%