TY - JOUR
T1 - Synthesis and characterization of low bandgap conjugated poly[(3-alkylylthiophene-2,5-diyl)-alt-(3-cyanothiophene-2,5-diyl)] by direct heteroarylation polymerization
AU - Yoon, Ji Yeon
AU - Eo, Kyoungbok
AU - Kim, Myoeum
AU - Kwon, Yong Ku
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/2/28
Y1 - 2018/2/28
N2 - A series of novel conjugated copolymers of poly[(3-alkylthiophene-2,5-diyl)-alt- (3-cyanothiophene-2,5-diyl)]s, (PACTs), containing electron-releasing 3-alkylyl thiophene-2,5-diyl (AT) and electron-withdrawing dibromo 3-cyanothiophene- 2, 5-diyl (CT) were synthesized by the polycondensation of a direct heteroarylation reaction. The regular alteration of the electron donor and electron acceptor unit in a polymer backbone led to a decrease in the energy bandgap of conjugated poly(3-alkylylthiophene-2,5-diyl)s (P3HT). To accelerate the polycondensation reaction, microwave-assisted heating was used to reduce the reaction time and increase the molecular weight of the polymers. Owing to the strong intermolecular interactions between the neighboring 3-cyanothiophene-2,5-diyl units in the polymer backbone, the lamellar and edge-on structures of the polymer chains were induced on the substrate. The photovoltaic performance of these conjugated copolymers was also evaluated by preparing bulk heterojunction solar cell devices of ITO/PEDOT: PSS/PACT:PC71BM/Al.
AB - A series of novel conjugated copolymers of poly[(3-alkylthiophene-2,5-diyl)-alt- (3-cyanothiophene-2,5-diyl)]s, (PACTs), containing electron-releasing 3-alkylyl thiophene-2,5-diyl (AT) and electron-withdrawing dibromo 3-cyanothiophene- 2, 5-diyl (CT) were synthesized by the polycondensation of a direct heteroarylation reaction. The regular alteration of the electron donor and electron acceptor unit in a polymer backbone led to a decrease in the energy bandgap of conjugated poly(3-alkylylthiophene-2,5-diyl)s (P3HT). To accelerate the polycondensation reaction, microwave-assisted heating was used to reduce the reaction time and increase the molecular weight of the polymers. Owing to the strong intermolecular interactions between the neighboring 3-cyanothiophene-2,5-diyl units in the polymer backbone, the lamellar and edge-on structures of the polymer chains were induced on the substrate. The photovoltaic performance of these conjugated copolymers was also evaluated by preparing bulk heterojunction solar cell devices of ITO/PEDOT: PSS/PACT:PC71BM/Al.
KW - Bulk heterojunction solar cell
KW - Direct heteroarylation
KW - Energy bandgap
KW - Thiophene
UR - http://www.scopus.com/inward/record.url?scp=85041526173&partnerID=8YFLogxK
U2 - 10.1016/j.polymer.2018.01.039
DO - 10.1016/j.polymer.2018.01.039
M3 - Article
AN - SCOPUS:85041526173
SN - 0032-3861
VL - 138
SP - 33
EP - 40
JO - Polymer
JF - Polymer
ER -