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The Nature of Singlet Exciton Fission in Carotenoid Aggregates
[Image: see text] Singlet exciton fission allows the fast and efficient generation of two spin triplet states from one photoexcited singlet. It has the potential to improve organic photovoltaics, enabling efficient coupling to the blue to ultraviolet region of the solar spectrum to capture the energ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440407/ https://www.ncbi.nlm.nih.gov/pubmed/25825939 http://dx.doi.org/10.1021/jacs.5b01130 |
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author | Musser, Andrew J. Maiuri, Margherita Brida, Daniele Cerullo, Giulio Friend, Richard H. Clark, Jenny |
author_facet | Musser, Andrew J. Maiuri, Margherita Brida, Daniele Cerullo, Giulio Friend, Richard H. Clark, Jenny |
author_sort | Musser, Andrew J. |
collection | PubMed |
description | [Image: see text] Singlet exciton fission allows the fast and efficient generation of two spin triplet states from one photoexcited singlet. It has the potential to improve organic photovoltaics, enabling efficient coupling to the blue to ultraviolet region of the solar spectrum to capture the energy generally lost as waste heat. However, many questions remain about the underlying fission mechanism. The relation between intermolecular geometry and singlet fission rate and yield is poorly understood and remains one of the most significant barriers to the design of new singlet fission sensitizers. Here we explore the structure–property relationship and examine the mechanism of singlet fission in aggregates of astaxanthin, a small polyene. We isolate five distinct supramolecular structures of astaxanthin generated through self-assembly in solution. Each is capable of undergoing intermolecular singlet fission, with rates of triplet generation and annihilation that can be correlated with intermolecular coupling strength. In contrast with the conventional model of singlet fission in linear molecules, we demonstrate that no intermediate states are involved in the triplet formation: instead, singlet fission occurs directly from the initial 1B(u) photoexcited state on ultrafast time scales. This result demands a re-evaluation of current theories of polyene photophysics and highlights the robustness of carotenoid singlet fission. |
format | Online Article Text |
id | pubmed-4440407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-44404072015-05-23 The Nature of Singlet Exciton Fission in Carotenoid Aggregates Musser, Andrew J. Maiuri, Margherita Brida, Daniele Cerullo, Giulio Friend, Richard H. Clark, Jenny J Am Chem Soc [Image: see text] Singlet exciton fission allows the fast and efficient generation of two spin triplet states from one photoexcited singlet. It has the potential to improve organic photovoltaics, enabling efficient coupling to the blue to ultraviolet region of the solar spectrum to capture the energy generally lost as waste heat. However, many questions remain about the underlying fission mechanism. The relation between intermolecular geometry and singlet fission rate and yield is poorly understood and remains one of the most significant barriers to the design of new singlet fission sensitizers. Here we explore the structure–property relationship and examine the mechanism of singlet fission in aggregates of astaxanthin, a small polyene. We isolate five distinct supramolecular structures of astaxanthin generated through self-assembly in solution. Each is capable of undergoing intermolecular singlet fission, with rates of triplet generation and annihilation that can be correlated with intermolecular coupling strength. In contrast with the conventional model of singlet fission in linear molecules, we demonstrate that no intermediate states are involved in the triplet formation: instead, singlet fission occurs directly from the initial 1B(u) photoexcited state on ultrafast time scales. This result demands a re-evaluation of current theories of polyene photophysics and highlights the robustness of carotenoid singlet fission. American Chemical Society 2015-03-31 2015-04-22 /pmc/articles/PMC4440407/ /pubmed/25825939 http://dx.doi.org/10.1021/jacs.5b01130 Text en Copyright © 2015 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Musser, Andrew J. Maiuri, Margherita Brida, Daniele Cerullo, Giulio Friend, Richard H. Clark, Jenny The Nature of Singlet Exciton Fission in Carotenoid Aggregates |
title | The
Nature of Singlet Exciton Fission in Carotenoid
Aggregates |
title_full | The
Nature of Singlet Exciton Fission in Carotenoid
Aggregates |
title_fullStr | The
Nature of Singlet Exciton Fission in Carotenoid
Aggregates |
title_full_unstemmed | The
Nature of Singlet Exciton Fission in Carotenoid
Aggregates |
title_short | The
Nature of Singlet Exciton Fission in Carotenoid
Aggregates |
title_sort | the
nature of singlet exciton fission in carotenoid
aggregates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440407/ https://www.ncbi.nlm.nih.gov/pubmed/25825939 http://dx.doi.org/10.1021/jacs.5b01130 |
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