TY - JOUR
T1 - π-Conjugated main chain polymers containing bis(bithiophenyl dithienothiophene)-based repeating group and their application to polymer solar cells
AU - Kim, Kyung Hwan
AU - Chung, Dae Sung
AU - Park, Chan Eon
AU - Choi, Dong Hoon
N1 - Funding Information:
This research was supported by Priority Research Centers Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (NRF20100020209)
PY - 2011
Y1 - 2011
N2 - New dithienothiophene (DTT)-containing conjugated polymers, such as poly(2,6-bis(2-thiophenyl-3-dodecylthiophene-2-yl)dithieno[3,2-b;2',3'-d] thiophene, 1 and poly(2,6-bis(2-thiophenyl-4-dodecylthiophene-2-yl)dithieno[3,2- b;2',3'-d]thiophene, 2 have been successfully synthesized via Stille coupling reactions using dodecyl-substituted thiophene-based monomer, bistributyltin dithienothiophene, and bistributyltin bithiophene. The main difference between two polymers is the substitution position of dodecyl side chains in a repeating group. The semiconducting properties of the two polymers have been evaluated in organic photovoltaics (OPVs). Two conjugated polymers are also well mixed with methanofullerene [6,6]-phenyl C61-butyric acid methyl ester (PCBM) for fabricating bulk heterojunction PV devices. As a result, the polymer solar cell devices made of polymers 1 and 2 had the best preliminary results with an open-circuit voltage of 0.43-0.44V, a short-circuit current density of 5.95-5.96mA/cm2, and a fill factor of 0.34, offering an overall power conversion efficiency (PCE) of 0.9%.
AB - New dithienothiophene (DTT)-containing conjugated polymers, such as poly(2,6-bis(2-thiophenyl-3-dodecylthiophene-2-yl)dithieno[3,2-b;2',3'-d] thiophene, 1 and poly(2,6-bis(2-thiophenyl-4-dodecylthiophene-2-yl)dithieno[3,2- b;2',3'-d]thiophene, 2 have been successfully synthesized via Stille coupling reactions using dodecyl-substituted thiophene-based monomer, bistributyltin dithienothiophene, and bistributyltin bithiophene. The main difference between two polymers is the substitution position of dodecyl side chains in a repeating group. The semiconducting properties of the two polymers have been evaluated in organic photovoltaics (OPVs). Two conjugated polymers are also well mixed with methanofullerene [6,6]-phenyl C61-butyric acid methyl ester (PCBM) for fabricating bulk heterojunction PV devices. As a result, the polymer solar cell devices made of polymers 1 and 2 had the best preliminary results with an open-circuit voltage of 0.43-0.44V, a short-circuit current density of 5.95-5.96mA/cm2, and a fill factor of 0.34, offering an overall power conversion efficiency (PCE) of 0.9%.
KW - Absorption
KW - conjugated polymers
KW - dithienothiophene
KW - mobility
KW - organic photovoltaics
KW - semiconductor
UR - http://www.scopus.com/inward/record.url?scp=79957602961&partnerID=8YFLogxK
U2 - 10.1080/15421406.2011.563720
DO - 10.1080/15421406.2011.563720
M3 - Article
AN - SCOPUS:79957602961
SN - 1542-1406
VL - 538
SP - 187
EP - 192
JO - Molecular Crystals and Liquid Crystals
JF - Molecular Crystals and Liquid Crystals
ER -