Rational design of conjugated side chains for high-performance all-polymer solar cells. Issue 1 (3rd November 2017)
- Record Type:
- Journal Article
- Title:
- Rational design of conjugated side chains for high-performance all-polymer solar cells. Issue 1 (3rd November 2017)
- Main Title:
- Rational design of conjugated side chains for high-performance all-polymer solar cells
- Authors:
- Huang, Wei
Li, Meilin
Lin, Fengyuan
Wu, Yang
Ke, Zhifan
Zhang, Xing
Ma, Rui
Yang, Tingbin
Ma, Wei
Liang, Yongye - Abstract:
- Abstract : High-performance all-polymer solar cells were developed by employing an asymmetric benzo[1, 2- b :4, 5- b ′]dithiophene unit with one thiophene and one 4-methoxythiophene conjugated side chain in the donor polymer, which enabled fine-tuning of energy levels and phase separation. Abstract : With their rapid development in recent years, organic solar cells hold the exciting potential to be a groundbreaking form of solar harvesting technology. Among these, all-polymer solar cells (all-PSCs) stand out owing to various advantages such as complementary absorption and superior stability. However, the advance of all-PSCs has been greatly impeded by energy level mismatches and unfavorable morphology of the active layer. Here, we report a molecular engineering approach featuring asymmetrical 4-methoxythiophene/thiophene as conjugated side chains of the donor polymer to fine-tune the energy level alignment and phase separation. The corresponding polymer, namely, poly{4-[5-(2-ethylhexyl)-4-methoxythiophen-2-yl]-8-[5-(2-ethylhexyl)thiophen-2-yl]benzo[1, 2- b :4, 5- b ′]dithiophene}-alt-[bis(5-thiophene-2-yl)-5, 6-difluoro-2-(2-hexyldecyl)-2 H -benzo[ d ][1, 2, 3]triazole-4, 7-diyl] (PMOT32) exhibited a power conversion efficiency that exceeded 8.5% in all-PSCs with poly{[ N, N ′-bis(2-octyldodecyl)-1, 4, 5, 8-naphthalenedicarboximide-2, 6-diyl]-alt-5, 5′-(2, 2′-bithiophene)} (N2200) as the acceptor. PMOT32:N2200 also maintained good photovoltaic performance when processed as aAbstract : High-performance all-polymer solar cells were developed by employing an asymmetric benzo[1, 2- b :4, 5- b ′]dithiophene unit with one thiophene and one 4-methoxythiophene conjugated side chain in the donor polymer, which enabled fine-tuning of energy levels and phase separation. Abstract : With their rapid development in recent years, organic solar cells hold the exciting potential to be a groundbreaking form of solar harvesting technology. Among these, all-polymer solar cells (all-PSCs) stand out owing to various advantages such as complementary absorption and superior stability. However, the advance of all-PSCs has been greatly impeded by energy level mismatches and unfavorable morphology of the active layer. Here, we report a molecular engineering approach featuring asymmetrical 4-methoxythiophene/thiophene as conjugated side chains of the donor polymer to fine-tune the energy level alignment and phase separation. The corresponding polymer, namely, poly{4-[5-(2-ethylhexyl)-4-methoxythiophen-2-yl]-8-[5-(2-ethylhexyl)thiophen-2-yl]benzo[1, 2- b :4, 5- b ′]dithiophene}-alt-[bis(5-thiophene-2-yl)-5, 6-difluoro-2-(2-hexyldecyl)-2 H -benzo[ d ][1, 2, 3]triazole-4, 7-diyl] (PMOT32) exhibited a power conversion efficiency that exceeded 8.5% in all-PSCs with poly{[ N, N ′-bis(2-octyldodecyl)-1, 4, 5, 8-naphthalenedicarboximide-2, 6-diyl]-alt-5, 5′-(2, 2′-bithiophene)} (N2200) as the acceptor. PMOT32:N2200 also maintained good photovoltaic performance when processed as a thick film or from non-halogenated solvents. Detailed comparisons with two other polymers with pure thiophene or 4-methoxythiophene as their side chains revealed how these side chains affected the photovoltaic performance via energy level alignment and phase separation. … (more)
- Is Part Of:
- Molecular Systems Design and Engineering. Volume 3:Issue 1(2018)
- Journal:
- Molecular Systems Design and Engineering
- Issue:
- Volume 3:Issue 1(2018)
- Issue Display:
- Volume 3, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 3
- Issue:
- 1
- Issue Sort Value:
- 2018-0003-0001-0000
- Page Start:
- 103
- Page End:
- 112
- Publication Date:
- 2017-11-03
- Subjects:
- Chemistry -- Molecular aspects -- Periodicals
Chemical engineering -- Molecular aspects -- Periodicals
Nanotechnology -- Periodicals
620.5 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/me#!recentarticles&adv ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7me00088j ↗
- Languages:
- English
- ISSNs:
- 2058-9689
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.856400
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 6617.xml