Synthesis and photovoltaic properties of copolymers based on benzo[1,2-b:4,5-b′]dithiophene and thiazole with different conjugated side groups
Two new copolymers ( PT-Tz-DTBT and PT-Tz-DTffBT ) of benzo[1,2- b :4,5- b ′]dithiophene and thiazole ( Tz ) with different conjugated side groups 4,7-dithien-5-yl-2,1,3-benzodiathiazole ( DTBT ) and 5,6-difluoro-4,7-bis(4-hexylthiophen-2-yl)benzo[ c ][1,2,5]thiadiazole ( DTffBT ) were synthesized v...
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Published in | Polymer chemistry Vol. 4; no. 17; pp. 4737 - 4745 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
17.09.2013
|
Online Access | Get full text |
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Summary: | Two new copolymers (
PT-Tz-DTBT
and
PT-Tz-DTffBT
) of benzo[1,2-
b
:4,5-
b
′]dithiophene and thiazole (
Tz
) with different conjugated side groups 4,7-dithien-5-yl-2,1,3-benzodiathiazole (
DTBT
) and 5,6-difluoro-4,7-bis(4-hexylthiophen-2-yl)benzo[
c
][1,2,5]thiadiazole (
DTffBT
) were synthesized
via
the Stille coupling polymerization and developed for polymer solar cell applications. The thermal, photophysical, electrochemical and photovoltaic properties of the copolymers were investigated. The two copolymers exhibited relatively low HOMO energy levels of −5.58 eV for
PT-Tz-DTBT
and −5.59 eV for
PT-Tz-DTffBT
, respectively. Bulk heterojunction (BHJ) solar cells with two as-synthesized copolymers as electron donors and (6,6)-phenyl-C
61
-butyric acid methyl ester (PC
61
BM) as an electron acceptor exhibit power conversion efficiencies (PCEs) of 2.63% and 3.75% for
PT-Tz-DTBT
and
PT-Tz-DTffBT
, respectively. When PC
71
BM was used as an electron acceptor, a promising PCE of 3.65% and 4.42% for
PT-Tz-DTffBT
was achieved by using a conventional and inverted device structure, respectively.
Two copolymers with
DTBT
and
DTffBT
side chains were designed and synthesized. BHJ solar cells based on side chain polymer
PT-Tz-DTffBT
exhibited a high PCE of 4.42%. |
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ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/c3py00614j |