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Heteroarene-Fused pi-Conjugated Main-Chain Polymers Containing 4,7-Bis(4-octylthiophen-2-yl)benzo[c][1,2,5]thiadiazole or 2,5-Bis(4-octylthiophen-2-yl)thiazolo[5,4-d]thiazole and Their Application to Photovoltaic Devices

Authors
Lee, Tae WanKang, Nam SuYu, Jae WoongHoang, Mai HaKim, Kyung HwanJin, Jung IlChoi, Dong Hoon
Issue Date
15-12월-2010
Publisher
WILEY-BLACKWELL
Keywords
bulk heterojunction; conjugated polymers; donor acceptor fluorescence; heteroarene fused ring; photophysics; solar cell synthesis
Citation
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, v.48, no.24, pp.5921 - 5929
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume
48
Number
24
Start Page
5921
End Page
5929
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/115113
DOI
10.1002/pola.24405
ISSN
0887-624X
Abstract
Two conjugated main chain polymers consisting of heteroarene fused pi conjuagted donor moiety alternating with 47 bis(5 bromo 4 octylthiophen 2 yl)benzo[c][1 2 5]thiadiazole (P1) or 2 5 bis(5 bromo 4 octylthiophen 2 yl) thiazolo[5 4 d]thiazole (P2) units have been synthesized They are intrinsically amor phous in nature and do not exhibit crystalline melting tempera tures during thermal analysis The effect of the fused rings on the thermal optical electrochemical charge transport and photo voltaic properties of these polymers has been investigated The polymer (P1) containing 47 bis(5 bromo 4 octylthiophen 2 yl)benzo[c][1 2 5] thiadiazole has a broad absorption extending from 300 to 600 nm with optical bandgaps as low as 2 02 eV The HOMO levels (5 42 to 5 29 eV) are more sensitive to the choice of acceptor The polymers were employed to fabricate organic photovoltaic cells with methanofullerene [6 6] phenyl C71 butyric acid methyl ester (PC71BM) As a result the poly mer solar cell device containing P1 had the best preliminary results with an open circuit voltage of 0 61 V a short circuit current density of 6 19 mA/cm(2) and a fill factor of 0 32 offer ing an overall power conversion efficiency of 1 21% (C) 2010 Wiley Periodicals Inc J Polym Sci Part A Polym Chem 48 5921-5929 2010
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