Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer
- Autores
- Zheng, Fulu; Fernández Alberti, Sebastián; Tretiak, Sergei; Zhao, Yang
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Applying nonadiabatic excited-state molecular dynamics, we investigate excitation energy transfer and exciton localization dynamics in a chlorophyll a (Chla) dimer system at the interface of two monomers of light-harvesting complex II trimer. After its optical excitation at the red edge of the Soret (B) band, the Chla dimer experiences an ultrafast intra- and intermolecular nonradiative relaxation process to the lowest band (Qy). The energy relaxation is found to run faster in the Chla dimer than in the Chla monomer. Once the molecular system reaches the lowest Qy band composed of two lowest excited states S1 and S2, the concluding relaxation step involves the S2 → S1 population transfer, resulting in a relatively slower relaxation rate. The strength of thermal fluctuations exceeds intraband electronic coupling between the states belonging to a certain band (B, Qx, and Qy), producing localized states on individual chromophores. Therefore, time evolution of spatial electronic localization during internal conversion reveals transient trapping on one of the Chla monomers participating in the events of intermonomeric energy exchange. In the phase space domains where electronic states are strongly coupled, these states become nearly degenerate promoting Frenkel-exciton-like delocalization and interchromophore energy transfer. As energy relaxation occurs, redistribution of the transition density on two Chla monomers leads to nearly equal distribution of the exciton among the molecules. For a single Chla, our analysis of excitonic dynamics reveals wave function amplitude transfer from nitrogen and outer carbon atoms to inner carbon atoms during nonradiative relaxation.
Fil: Zheng, Fulu. Nanyang Technological University; Singapur
Fil: Fernández Alberti, Sebastián. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Quilmes; Argentina
Fil: Tretiak, Sergei. Los Alamos National Laboratory; Estados Unidos
Fil: Zhao, Yang. Nanyang Technological University; Singapur - Materia
-
NON-ADIABATIC MOLECULAR DYNAMICS
EXCITED STATES
CHLOROPHYLLS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/41008
Ver los metadatos del registro completo
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Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a DimerZheng, FuluFernández Alberti, SebastiánTretiak, SergeiZhao, YangNON-ADIABATIC MOLECULAR DYNAMICSEXCITED STATESCHLOROPHYLLShttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Applying nonadiabatic excited-state molecular dynamics, we investigate excitation energy transfer and exciton localization dynamics in a chlorophyll a (Chla) dimer system at the interface of two monomers of light-harvesting complex II trimer. After its optical excitation at the red edge of the Soret (B) band, the Chla dimer experiences an ultrafast intra- and intermolecular nonradiative relaxation process to the lowest band (Qy). The energy relaxation is found to run faster in the Chla dimer than in the Chla monomer. Once the molecular system reaches the lowest Qy band composed of two lowest excited states S1 and S2, the concluding relaxation step involves the S2 → S1 population transfer, resulting in a relatively slower relaxation rate. The strength of thermal fluctuations exceeds intraband electronic coupling between the states belonging to a certain band (B, Qx, and Qy), producing localized states on individual chromophores. Therefore, time evolution of spatial electronic localization during internal conversion reveals transient trapping on one of the Chla monomers participating in the events of intermonomeric energy exchange. In the phase space domains where electronic states are strongly coupled, these states become nearly degenerate promoting Frenkel-exciton-like delocalization and interchromophore energy transfer. As energy relaxation occurs, redistribution of the transition density on two Chla monomers leads to nearly equal distribution of the exciton among the molecules. For a single Chla, our analysis of excitonic dynamics reveals wave function amplitude transfer from nitrogen and outer carbon atoms to inner carbon atoms during nonradiative relaxation.Fil: Zheng, Fulu. Nanyang Technological University; SingapurFil: Fernández Alberti, Sebastián. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Quilmes; ArgentinaFil: Tretiak, Sergei. Los Alamos National Laboratory; Estados UnidosFil: Zhao, Yang. Nanyang Technological University; SingapurAmerican Chemical Society2017-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/41008Zheng, Fulu; Fernández Alberti, Sebastián; Tretiak, Sergei; Zhao, Yang; Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer; American Chemical Society; Journal of Physical Chemistry B; 121; 21; 5-2017; 5331-53391520-6106CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpcb.7b02021info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.jpcb.7b02021info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:08:41Zoai:ri.conicet.gov.ar:11336/41008instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:08:41.473CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer |
title |
Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer |
spellingShingle |
Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer Zheng, Fulu NON-ADIABATIC MOLECULAR DYNAMICS EXCITED STATES CHLOROPHYLLS |
title_short |
Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer |
title_full |
Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer |
title_fullStr |
Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer |
title_full_unstemmed |
Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer |
title_sort |
Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer |
dc.creator.none.fl_str_mv |
Zheng, Fulu Fernández Alberti, Sebastián Tretiak, Sergei Zhao, Yang |
author |
Zheng, Fulu |
author_facet |
Zheng, Fulu Fernández Alberti, Sebastián Tretiak, Sergei Zhao, Yang |
author_role |
author |
author2 |
Fernández Alberti, Sebastián Tretiak, Sergei Zhao, Yang |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
NON-ADIABATIC MOLECULAR DYNAMICS EXCITED STATES CHLOROPHYLLS |
topic |
NON-ADIABATIC MOLECULAR DYNAMICS EXCITED STATES CHLOROPHYLLS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Applying nonadiabatic excited-state molecular dynamics, we investigate excitation energy transfer and exciton localization dynamics in a chlorophyll a (Chla) dimer system at the interface of two monomers of light-harvesting complex II trimer. After its optical excitation at the red edge of the Soret (B) band, the Chla dimer experiences an ultrafast intra- and intermolecular nonradiative relaxation process to the lowest band (Qy). The energy relaxation is found to run faster in the Chla dimer than in the Chla monomer. Once the molecular system reaches the lowest Qy band composed of two lowest excited states S1 and S2, the concluding relaxation step involves the S2 → S1 population transfer, resulting in a relatively slower relaxation rate. The strength of thermal fluctuations exceeds intraband electronic coupling between the states belonging to a certain band (B, Qx, and Qy), producing localized states on individual chromophores. Therefore, time evolution of spatial electronic localization during internal conversion reveals transient trapping on one of the Chla monomers participating in the events of intermonomeric energy exchange. In the phase space domains where electronic states are strongly coupled, these states become nearly degenerate promoting Frenkel-exciton-like delocalization and interchromophore energy transfer. As energy relaxation occurs, redistribution of the transition density on two Chla monomers leads to nearly equal distribution of the exciton among the molecules. For a single Chla, our analysis of excitonic dynamics reveals wave function amplitude transfer from nitrogen and outer carbon atoms to inner carbon atoms during nonradiative relaxation. Fil: Zheng, Fulu. Nanyang Technological University; Singapur Fil: Fernández Alberti, Sebastián. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Quilmes; Argentina Fil: Tretiak, Sergei. Los Alamos National Laboratory; Estados Unidos Fil: Zhao, Yang. Nanyang Technological University; Singapur |
description |
Applying nonadiabatic excited-state molecular dynamics, we investigate excitation energy transfer and exciton localization dynamics in a chlorophyll a (Chla) dimer system at the interface of two monomers of light-harvesting complex II trimer. After its optical excitation at the red edge of the Soret (B) band, the Chla dimer experiences an ultrafast intra- and intermolecular nonradiative relaxation process to the lowest band (Qy). The energy relaxation is found to run faster in the Chla dimer than in the Chla monomer. Once the molecular system reaches the lowest Qy band composed of two lowest excited states S1 and S2, the concluding relaxation step involves the S2 → S1 population transfer, resulting in a relatively slower relaxation rate. The strength of thermal fluctuations exceeds intraband electronic coupling between the states belonging to a certain band (B, Qx, and Qy), producing localized states on individual chromophores. Therefore, time evolution of spatial electronic localization during internal conversion reveals transient trapping on one of the Chla monomers participating in the events of intermonomeric energy exchange. In the phase space domains where electronic states are strongly coupled, these states become nearly degenerate promoting Frenkel-exciton-like delocalization and interchromophore energy transfer. As energy relaxation occurs, redistribution of the transition density on two Chla monomers leads to nearly equal distribution of the exciton among the molecules. For a single Chla, our analysis of excitonic dynamics reveals wave function amplitude transfer from nitrogen and outer carbon atoms to inner carbon atoms during nonradiative relaxation. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-05 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/41008 Zheng, Fulu; Fernández Alberti, Sebastián; Tretiak, Sergei; Zhao, Yang; Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer; American Chemical Society; Journal of Physical Chemistry B; 121; 21; 5-2017; 5331-5339 1520-6106 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/41008 |
identifier_str_mv |
Zheng, Fulu; Fernández Alberti, Sebastián; Tretiak, Sergei; Zhao, Yang; Photoinduced Intra- and Intermolecular Energy Transfer in Chlorophyll a Dimer; American Chemical Society; Journal of Physical Chemistry B; 121; 21; 5-2017; 5331-5339 1520-6106 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.jpcb.7b02021 info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.jpcb.7b02021 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1846781422165032960 |
score |
12.982451 |