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Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants
Aiswarya Abhisek Mohapatra,
Yifan Dong,
Puttaraju Boregowda,
Ashutosh Mohanty,
Aditya Sadhanala,
Xuechen Jiao,
Awadhesh Narayan,
Christopher R. McNeill,
James Durrant
The Journal of Physical Chemistry C, Volume: 125, Issue: 12, Pages: 6886 - 6896
Swansea University Author: James Durrant
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DOI (Published version): 10.1021/acs.jpcc.1c00340
Abstract
The low dielectric constant of organic semiconductors limits the efficiency of organic solar cells (OSCs). In an attempt to improve the dielectric constant of conjugated polymers, we report the synthesis of three semiconducting copolymers by combining the thiophene-substituted diketopyrrolopyrrole (...
Published in: | The Journal of Physical Chemistry C |
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ISSN: | 1932-7447 1932-7455 |
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American Chemical Society (ACS)
2021
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URI: | https://cronfa.swan.ac.uk/Record/cronfa56837 |
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2025-01-02T10:18:21.1138448 v2 56837 2021-05-10 Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants f3dd64bc260e5c07adfa916c27dbd58a 0000-0001-8353-7345 James Durrant James Durrant true false 2021-05-10 EAAS The low dielectric constant of organic semiconductors limits the efficiency of organic solar cells (OSCs). In an attempt to improve the dielectric constant of conjugated polymers, we report the synthesis of three semiconducting copolymers by combining the thiophene-substituted diketopyrrolopyrrole (TDPP) monomer with three different monomeric units with varying electron donating/accepting strengths: benzodithiophene (BBT-3TEG-TDPP), TDPP (TDPP-3TEG-TDPP), and naphthalene diimide (P(gNDI-TDPP)). Among the series, BBT-3TEG-TDPP and P(gNDI-TDPP) exhibited the highest dielectric constants (∼5) at 1 MHz frequency, signifying the contribution of dipolar polarization from TEG side-chains. Furthermore, transient absorption spectroscopic studies performed on these polymers indicated low exciton diffusion length as observed in common organic semiconducting polymers. Our findings suggest that utilizing the polar side-chains enhances the dielectric constant in a frequency regime of megahertz. However, it is not sufficient to reduce the Coulombic interaction between hole and electron in excitonic solar cells. Journal Article The Journal of Physical Chemistry C 125 12 6886 6896 American Chemical Society (ACS) 1932-7447 1932-7455 Dielectric constant, triethyleneglycol sidechains, diketopyrrolopyrrole, Naphthalene diimide 1 4 2021 2021-04-01 10.1021/acs.jpcc.1c00340 COLLEGE NANME Engineering and Applied Sciences School COLLEGE CODE EAAS Swansea University 2025-01-02T10:18:21.1138448 2021-05-10T10:09:50.4368285 Faculty of Science and Engineering School of Engineering and Applied Sciences - Materials Science and Engineering Aiswarya Abhisek Mohapatra 1 Yifan Dong 2 Puttaraju Boregowda 3 Ashutosh Mohanty 4 Aditya Sadhanala 5 Xuechen Jiao 6 Awadhesh Narayan 7 Christopher R. McNeill 8 James Durrant 0000-0001-8353-7345 9 56837__20200__34039b41f1514f018f0e0e7134aa0e50.pdf 56837.pdf 2021-06-18T17:56:59.5657754 Output 3926847 application/pdf Accepted Manuscript true 2022-03-23T00:00:00.0000000 true eng |
title |
Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants |
spellingShingle |
Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants James Durrant |
title_short |
Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants |
title_full |
Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants |
title_fullStr |
Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants |
title_full_unstemmed |
Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants |
title_sort |
Rational Design of Donor–Acceptor Based Semiconducting Copolymers with High Dielectric Constants |
author_id_str_mv |
f3dd64bc260e5c07adfa916c27dbd58a |
author_id_fullname_str_mv |
f3dd64bc260e5c07adfa916c27dbd58a_***_James Durrant |
author |
James Durrant |
author2 |
Aiswarya Abhisek Mohapatra Yifan Dong Puttaraju Boregowda Ashutosh Mohanty Aditya Sadhanala Xuechen Jiao Awadhesh Narayan Christopher R. McNeill James Durrant |
format |
Journal article |
container_title |
The Journal of Physical Chemistry C |
container_volume |
125 |
container_issue |
12 |
container_start_page |
6886 |
publishDate |
2021 |
institution |
Swansea University |
issn |
1932-7447 1932-7455 |
doi_str_mv |
10.1021/acs.jpcc.1c00340 |
publisher |
American Chemical Society (ACS) |
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Faculty of Science and Engineering |
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Faculty of Science and Engineering |
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School of Engineering and Applied Sciences - Materials Science and Engineering{{{_:::_}}}Faculty of Science and Engineering{{{_:::_}}}School of Engineering and Applied Sciences - Materials Science and Engineering |
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description |
The low dielectric constant of organic semiconductors limits the efficiency of organic solar cells (OSCs). In an attempt to improve the dielectric constant of conjugated polymers, we report the synthesis of three semiconducting copolymers by combining the thiophene-substituted diketopyrrolopyrrole (TDPP) monomer with three different monomeric units with varying electron donating/accepting strengths: benzodithiophene (BBT-3TEG-TDPP), TDPP (TDPP-3TEG-TDPP), and naphthalene diimide (P(gNDI-TDPP)). Among the series, BBT-3TEG-TDPP and P(gNDI-TDPP) exhibited the highest dielectric constants (∼5) at 1 MHz frequency, signifying the contribution of dipolar polarization from TEG side-chains. Furthermore, transient absorption spectroscopic studies performed on these polymers indicated low exciton diffusion length as observed in common organic semiconducting polymers. Our findings suggest that utilizing the polar side-chains enhances the dielectric constant in a frequency regime of megahertz. However, it is not sufficient to reduce the Coulombic interaction between hole and electron in excitonic solar cells. |
published_date |
2021-04-01T20:07:39Z |
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1821527988303298560 |
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11.047674 |