Singlet Fission in a New Series of Systematically Designed Through‐space Coupled Tetracene Oligomers

Singlet fission (SF) holds great promise for current photovoltaic technologies, where tetracenes, with their relatively high triplet energies, play a major role for application in silicon‐based solar cells. However, the SF efficiencies in tetracene dimers are low due to the unfavorable energetics of...

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Published inAngewandte Chemie International Edition Vol. 63; no. 16; pp. e202401103 - n/a
Main Authors Majdecki, Maciej, Hsu, Chao‐Hsien, Wang, Chih‐Hsing, Shi, Emily Hsue‐Chi, Zakrocka, Magdalena, Wei, Yu‐Chen, Chen, Bo‐Han, Lu, Chih‐Hsuan, Yang, Shang‐Da, Chou, Pi‐Tai, Gaweł, Przemysław
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 15.04.2024
Wiley Subscription Services, Inc
EditionInternational ed. in English
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Online AccessGet full text
ISSN1433-7851
1521-3773
1521-3773
DOI10.1002/anie.202401103

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Abstract Singlet fission (SF) holds great promise for current photovoltaic technologies, where tetracenes, with their relatively high triplet energies, play a major role for application in silicon‐based solar cells. However, the SF efficiencies in tetracene dimers are low due to the unfavorable energetics of their singlet and triplet energy levels. In the solid state, tetracene exhibits high yields of triplet formation through SF, raising great interest about the underlying mechanisms. To address this discrepancy, we designed and prepared a novel molecular system based on a hexaphenylbenzene core decorated with 2 to 6 tetracene chromophores. The spatial arrangement of tetracene units, induced by steric hindrance in the central part, dictates through‐space coupling, making it a relevant model for solid‐state chromophore organization. We then revealed a remarkable increase in SF quantum yield with the number of tetracenes, reaching quantitative (196 %) triplet pair formation in hexamer. We observed a short‐lived correlated triplet pair and limited magnetic effects, indicating ineffective triplet dissociation in these through‐space coupled systems. These findings emphasize the crucial role of the number of chromophores involved and the interchromophore arrangement for the SF efficiency. The insights gained from this study will aid designing more efficient and technology‐compatible SF systems for applications in photovoltaics. A collection of through‐space tetracene oligomers demonstrates sub‐picosecond singlet fission, as revealed by femtosecond‐resolved transient absorption spectroscopy. These oligomers exhibit a remarkably high yield of the triplet pair state, a characteristic seldom observed in tetracene derivatives owing to the unfavorable energetics associated with their singlet and triplet energy levels.
AbstractList Singlet fission (SF) holds great promise for current photovoltaic technologies, where tetracenes, with their relatively high triplet energies, play a major role for application in silicon-based solar cells. However, the SF efficiencies in tetracene dimers are low due to the unfavorable energetics of their singlet and triplet energy levels. In the solid state, tetracene exhibits high yields of triplet formation through SF, raising great interest about the underlying mechanisms. To address this discrepancy, we designed and prepared a novel molecular system based on a hexaphenylbenzene core decorated with 2 to 6 tetracene chromophores. The spatial arrangement of tetracene units, induced by steric hindrance in the central part, dictates through-space coupling, making it a relevant model for solid-state chromophore organization. We then revealed a remarkable increase in SF quantum yield with the number of tetracenes, reaching quantitative (196 %) triplet pair formation in hexamer. We observed a short-lived correlated triplet pair and limited magnetic effects, indicating ineffective triplet dissociation in these through-space coupled systems. These findings emphasize the crucial role of the number of chromophores involved and the interchromophore arrangement for the SF efficiency. The insights gained from this study will aid designing more efficient and technology-compatible SF systems for applications in photovoltaics.Singlet fission (SF) holds great promise for current photovoltaic technologies, where tetracenes, with their relatively high triplet energies, play a major role for application in silicon-based solar cells. However, the SF efficiencies in tetracene dimers are low due to the unfavorable energetics of their singlet and triplet energy levels. In the solid state, tetracene exhibits high yields of triplet formation through SF, raising great interest about the underlying mechanisms. To address this discrepancy, we designed and prepared a novel molecular system based on a hexaphenylbenzene core decorated with 2 to 6 tetracene chromophores. The spatial arrangement of tetracene units, induced by steric hindrance in the central part, dictates through-space coupling, making it a relevant model for solid-state chromophore organization. We then revealed a remarkable increase in SF quantum yield with the number of tetracenes, reaching quantitative (196 %) triplet pair formation in hexamer. We observed a short-lived correlated triplet pair and limited magnetic effects, indicating ineffective triplet dissociation in these through-space coupled systems. These findings emphasize the crucial role of the number of chromophores involved and the interchromophore arrangement for the SF efficiency. The insights gained from this study will aid designing more efficient and technology-compatible SF systems for applications in photovoltaics.
Singlet fission (SF) holds great promise for current photovoltaic technologies, where tetracenes, with their relatively high triplet energies, play a major role for application in silicon-based solar cells. However, the SF efficiencies in tetracene dimers are low due to the unfavorable energetics of their singlet and triplet energy levels. In the solid state, tetracene exhibits high yields of triplet formation through SF, raising great interest about the underlying mechanisms. To address this discrepancy, we designed and prepared a novel molecular system based on a hexaphenylbenzene core decorated with 2 to 6 tetracene chromophores. The spatial arrangement of tetracene units, induced by steric hindrance in the central part, dictates through-space coupling, making it a relevant model for solid-state chromophore organization. We then revealed a remarkable increase in SF quantum yield with the number of tetracenes, reaching quantitative (196 %) triplet pair formation in hexamer. We observed a short-lived correlated triplet pair and limited magnetic effects, indicating ineffective triplet dissociation in these through-space coupled systems. These findings emphasize the crucial role of the number of chromophores involved and the interchromophore arrangement for the SF efficiency. The insights gained from this study will aid designing more efficient and technology-compatible SF systems for applications in photovoltaics.
Singlet fission (SF) holds great promise for current photovoltaic technologies, where tetracenes, with their relatively high triplet energies, play a major role for application in silicon‐based solar cells. However, the SF efficiencies in tetracene dimers are low due to the unfavorable energetics of their singlet and triplet energy levels. In the solid state, tetracene exhibits high yields of triplet formation through SF, raising great interest about the underlying mechanisms. To address this discrepancy, we designed and prepared a novel molecular system based on a hexaphenylbenzene core decorated with 2 to 6 tetracene chromophores. The spatial arrangement of tetracene units, induced by steric hindrance in the central part, dictates through‐space coupling, making it a relevant model for solid‐state chromophore organization. We then revealed a remarkable increase in SF quantum yield with the number of tetracenes, reaching quantitative (196 %) triplet pair formation in hexamer. We observed a short‐lived correlated triplet pair and limited magnetic effects, indicating ineffective triplet dissociation in these through‐space coupled systems. These findings emphasize the crucial role of the number of chromophores involved and the interchromophore arrangement for the SF efficiency. The insights gained from this study will aid designing more efficient and technology‐compatible SF systems for applications in photovoltaics. A collection of through‐space tetracene oligomers demonstrates sub‐picosecond singlet fission, as revealed by femtosecond‐resolved transient absorption spectroscopy. These oligomers exhibit a remarkably high yield of the triplet pair state, a characteristic seldom observed in tetracene derivatives owing to the unfavorable energetics associated with their singlet and triplet energy levels.
Singlet fission (SF) holds great promise for current photovoltaic technologies, where tetracenes, with their relatively high triplet energies, play a major role for application in silicon-based solar cells. However, the SF efficiencies in tetracene dimers are low due to the unfavorable energetics of their singlet and triplet energy levels. In the solid state, tetracene exhibits high yields of triplet formation through SF, raising great interest about the underlying mechanisms. To address this discrepancy, we designed and prepared a novel molecular system based on a hexaphenylbenzene core decorated with 2 to 6 tetracene chromophores. The spatial arrangement of tetracene units, induced by steric hindrance in the central part, dictates through-space coupling, making it a relevant model for solid-state chromophore organization. We then revealed a remarkable increase in SF quantum yield with the number of tetracenes, reaching quantitative (196 %) triplet pair formation in hexamer. We observed a short-lived correlated triplet pair and limited magnetic effects, indicating ineffective triplet dissociation in these through-space coupled systems. These findings emphasize the crucial role of the number of chromophores involved and the interchromophore arrangement for the SF efficiency. The insights gained from this study will aid designing more efficient and technology-compatible SF systems for applications in photovoltaics. A collection of through-space tetracene oligomers demonstrates sub-picosecond singlet fission, as revealed by femtosecond-resolved transient absorption spectroscopy. These oligomers exhibit a remarkably high yield of the triplet pair state, a characteristic seldom observed in tetracene derivatives owing to the unfavorable energetics associated with their singlet and triplet energy levels.+ image
Author Zakrocka, Magdalena
Chou, Pi‐Tai
Wei, Yu‐Chen
Yang, Shang‐Da
Chen, Bo‐Han
Lu, Chih‐Hsuan
Hsu, Chao‐Hsien
Majdecki, Maciej
Wang, Chih‐Hsing
Gaweł, Przemysław
Shi, Emily Hsue‐Chi
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Issue 16
Keywords FUSION
DELOCALIZATION
singlet fission
MOLECULES
global analysis
FLUORESCENCE
triplet pair state
ENHANCEMENT
DYNAMICS
EXCITON FISSION
sensitization
through-space, tetracene
CHARGE
Language English
License Attribution
2024 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.
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Notes These authors contributed equally to this work.
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2023; 62
2014; 2
2015; 137
2013; 117
2013; 52
2010; 110
2016; 116
2005; 70
2013; 110
2017; 121
2001; 11
2006; 128
2003; 42
2021; 6
2007; 129
2015; 6
2023; 14
2018; 140
2015; 18
2013; 46
2023; 15
2020; 142
2015; 54
2008; 10
2021; 143
2007; 10
2019; 141
2018; 20
1999; 5
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2011; 9
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2021; 13
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SSID ssj0028806
Score 2.488683
Snippet Singlet fission (SF) holds great promise for current photovoltaic technologies, where tetracenes, with their relatively high triplet energies, play a major...
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StartPage e202401103
SubjectTerms Chemistry
Chemistry, Multidisciplinary
Chromophores
Energy levels
Fission
global analysis
Magnetic effects
Pair bond
Photovoltaic cells
Photovoltaics
Physical Sciences
Science & Technology
sensitization
singlet fission
Solar cells
Steric hindrance
through-space, tetracene
triplet pair state
Title Singlet Fission in a New Series of Systematically Designed Through‐space Coupled Tetracene Oligomers
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https://www.ncbi.nlm.nih.gov/pubmed/38412017
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https://www.proquest.com/docview/2932436006
Volume 63
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