Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy
- Autores
- Hildner, Richard; Brinks, Daan; Stefani, Fernando Daniel; van Hulst, Niek F.
- Año de publicación
- 2011
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Employing femtosecond pulse-shaping techniques we investigate ultrafast, coherent and incoherent dynamics in single molecules at room temperature. In first experiments single molecules are excited into their purely electronic 0–0 transition by phase-locked double-pulse sequences with pulse durations of 75 fs and 20 nm spectral band width. Their femtosecond kinetics can then be understood in terms of a 2-level system and modelled with the optical Bloch equations. We find that we observe the coherence decay in single molecules, and the purely electronic dephasing times can be retrieved directly in the time domain. In addition, the Rabi-frequencies and thus the transition dipole moments of single molecules are determined from these data. Upon excitation of single molecules into a vibrational level of the electronically excited state also incoherent intra-molecular vibrational relaxation is recorded. Increasing the spectral band width of the excitation pulses to up to 120 nm (resulting in a transform-limited pulse width of 15 fs) coherent superpositions of excited state vibrational modes, i.e. vibrational wave packets, are excited. The wave-packet oscillations in the excited state potential energy surface are followed in time by a phase-controlled pump–probe scheme, which permits to record wave packet interference, and to determine the energies of vibrational modes and their coupling strengths to the electronic transition.
Fil: Hildner, Richard. Institut de Ciencies Fotoniques; España
Fil: Brinks, Daan. Institut de Ciencies Fotoniques; España
Fil: Stefani, Fernando Daniel. Institut de Ciencies Fotoniques; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina
Fil: van Hulst, Niek F.. Institut de Ciencies Fotoniques; España - Materia
-
single molecule
ultrafast
coherent control - 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:11336/101385
Ver los metadatos del registro completo
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Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopyHildner, RichardBrinks, DaanStefani, Fernando Danielvan Hulst, Niek F.single moleculeultrafastcoherent controlhttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1Employing femtosecond pulse-shaping techniques we investigate ultrafast, coherent and incoherent dynamics in single molecules at room temperature. In first experiments single molecules are excited into their purely electronic 0–0 transition by phase-locked double-pulse sequences with pulse durations of 75 fs and 20 nm spectral band width. Their femtosecond kinetics can then be understood in terms of a 2-level system and modelled with the optical Bloch equations. We find that we observe the coherence decay in single molecules, and the purely electronic dephasing times can be retrieved directly in the time domain. In addition, the Rabi-frequencies and thus the transition dipole moments of single molecules are determined from these data. Upon excitation of single molecules into a vibrational level of the electronically excited state also incoherent intra-molecular vibrational relaxation is recorded. Increasing the spectral band width of the excitation pulses to up to 120 nm (resulting in a transform-limited pulse width of 15 fs) coherent superpositions of excited state vibrational modes, i.e. vibrational wave packets, are excited. The wave-packet oscillations in the excited state potential energy surface are followed in time by a phase-controlled pump–probe scheme, which permits to record wave packet interference, and to determine the energies of vibrational modes and their coupling strengths to the electronic transition.Fil: Hildner, Richard. Institut de Ciencies Fotoniques; EspañaFil: Brinks, Daan. Institut de Ciencies Fotoniques; EspañaFil: Stefani, Fernando Daniel. Institut de Ciencies Fotoniques; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; ArgentinaFil: van Hulst, Niek F.. Institut de Ciencies Fotoniques; EspañaRoyal Society of Chemistry2011-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/101385Hildner, Richard; Brinks, Daan; Stefani, Fernando Daniel; van Hulst, Niek F.; Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 13; 5; 1-2011; 1888-18941463-9076CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2011/cp/c0cp02231d/unauth#!divAbstractinfo:eu-repo/semantics/altIdentifier/doi/10.1039/C0CP02231Dinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:39:12Zoai:ri.conicet.gov.ar:11336/101385instacron: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:34982025-09-29 09:39:12.999CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy |
title |
Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy |
spellingShingle |
Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy Hildner, Richard single molecule ultrafast coherent control |
title_short |
Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy |
title_full |
Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy |
title_fullStr |
Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy |
title_full_unstemmed |
Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy |
title_sort |
Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy |
dc.creator.none.fl_str_mv |
Hildner, Richard Brinks, Daan Stefani, Fernando Daniel van Hulst, Niek F. |
author |
Hildner, Richard |
author_facet |
Hildner, Richard Brinks, Daan Stefani, Fernando Daniel van Hulst, Niek F. |
author_role |
author |
author2 |
Brinks, Daan Stefani, Fernando Daniel van Hulst, Niek F. |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
single molecule ultrafast coherent control |
topic |
single molecule ultrafast coherent control |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Employing femtosecond pulse-shaping techniques we investigate ultrafast, coherent and incoherent dynamics in single molecules at room temperature. In first experiments single molecules are excited into their purely electronic 0–0 transition by phase-locked double-pulse sequences with pulse durations of 75 fs and 20 nm spectral band width. Their femtosecond kinetics can then be understood in terms of a 2-level system and modelled with the optical Bloch equations. We find that we observe the coherence decay in single molecules, and the purely electronic dephasing times can be retrieved directly in the time domain. In addition, the Rabi-frequencies and thus the transition dipole moments of single molecules are determined from these data. Upon excitation of single molecules into a vibrational level of the electronically excited state also incoherent intra-molecular vibrational relaxation is recorded. Increasing the spectral band width of the excitation pulses to up to 120 nm (resulting in a transform-limited pulse width of 15 fs) coherent superpositions of excited state vibrational modes, i.e. vibrational wave packets, are excited. The wave-packet oscillations in the excited state potential energy surface are followed in time by a phase-controlled pump–probe scheme, which permits to record wave packet interference, and to determine the energies of vibrational modes and their coupling strengths to the electronic transition. Fil: Hildner, Richard. Institut de Ciencies Fotoniques; España Fil: Brinks, Daan. Institut de Ciencies Fotoniques; España Fil: Stefani, Fernando Daniel. Institut de Ciencies Fotoniques; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: van Hulst, Niek F.. Institut de Ciencies Fotoniques; España |
description |
Employing femtosecond pulse-shaping techniques we investigate ultrafast, coherent and incoherent dynamics in single molecules at room temperature. In first experiments single molecules are excited into their purely electronic 0–0 transition by phase-locked double-pulse sequences with pulse durations of 75 fs and 20 nm spectral band width. Their femtosecond kinetics can then be understood in terms of a 2-level system and modelled with the optical Bloch equations. We find that we observe the coherence decay in single molecules, and the purely electronic dephasing times can be retrieved directly in the time domain. In addition, the Rabi-frequencies and thus the transition dipole moments of single molecules are determined from these data. Upon excitation of single molecules into a vibrational level of the electronically excited state also incoherent intra-molecular vibrational relaxation is recorded. Increasing the spectral band width of the excitation pulses to up to 120 nm (resulting in a transform-limited pulse width of 15 fs) coherent superpositions of excited state vibrational modes, i.e. vibrational wave packets, are excited. The wave-packet oscillations in the excited state potential energy surface are followed in time by a phase-controlled pump–probe scheme, which permits to record wave packet interference, and to determine the energies of vibrational modes and their coupling strengths to the electronic transition. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-01 |
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/11336/101385 Hildner, Richard; Brinks, Daan; Stefani, Fernando Daniel; van Hulst, Niek F.; Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 13; 5; 1-2011; 1888-1894 1463-9076 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/101385 |
identifier_str_mv |
Hildner, Richard; Brinks, Daan; Stefani, Fernando Daniel; van Hulst, Niek F.; Electronic coherences and vibrational wave-packets in single molecules studied with femtosecond phase-controlled spectroscopy; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 13; 5; 1-2011; 1888-1894 1463-9076 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2011/cp/c0cp02231d/unauth#!divAbstract info:eu-repo/semantics/altIdentifier/doi/10.1039/C0CP02231D |
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 |
Royal Society of Chemistry |
publisher.none.fl_str_mv |
Royal Society of Chemistry |
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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1844613239977017344 |
score |
13.070432 |