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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/41008

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling 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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