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pi-Conjugated Main Chain Polymers Containing Bis(bithiophenyl dithienothiophene)-based Repeating Group and their Application to Polymer Solar Cells

Authors
Kim, Kyung HwanChung, Dae SungPark, Chan EonChoi, Dong Hoon
Issue Date
2011
Publisher
TAYLOR & FRANCIS LTD
Keywords
Absorption; conjugated polymers; dithienothiophene; mobility; organic photovoltaics; semiconductor
Citation
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, v.538, pp.187 - 192
Indexed
SCIE
SCOPUS
Journal Title
MOLECULAR CRYSTALS AND LIQUID CRYSTALS
Volume
538
Start Page
187
End Page
192
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/115063
DOI
10.1080/15421406.2011.563720
ISSN
1542-1406
Abstract
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 dodecylsubstituted 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 0.43-0.44 V, a short-circuit current density of 5.95-5.96mA/cm(2), and a fill factor of 0.34, offering an overall power conversion efficiency (PCE) of 0.9%.
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