Electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse

The many-body quantum nature of molecules determines their static and dynamic properties, but remains the main obstacle in their accurate description. Here, the authors employ ultrafast spectroscopic methods to explore the dynamics of highly excited organic molecules, revealing many-body effects and...

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Autores principales:	A. Marciniak, V. Despré, V. Loriot, G. Karras, M. Hervé, L. Quintard, F. Catoire, C. Joblin, E. Constant, A. I. Kuleff, F. Lépine
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2019
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/ac2461ded8d541e4b63c4452f4b18c12
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spelling	oai:doaj.org-article:ac2461ded8d541e4b63c4452f4b18c122021-12-02T14:40:19ZElectron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse10.1038/s41467-018-08131-82041-1723https://doaj.org/article/ac2461ded8d541e4b63c4452f4b18c122019-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-08131-8https://doaj.org/toc/2041-1723The many-body quantum nature of molecules determines their static and dynamic properties, but remains the main obstacle in their accurate description. Here, the authors employ ultrafast spectroscopic methods to explore the dynamics of highly excited organic molecules, revealing many-body effects and hints of coherent vibronic dynamics which persist despite their molecular complexity.A. MarciniakV. DespréV. LoriotG. KarrasM. HervéL. QuintardF. CatoireC. JoblinE. ConstantA. I. KuleffF. LépineNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-8 (2019)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q A. Marciniak V. Despré V. Loriot G. Karras M. Hervé L. Quintard F. Catoire C. Joblin E. Constant A. I. Kuleff F. Lépine Electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse
description	The many-body quantum nature of molecules determines their static and dynamic properties, but remains the main obstacle in their accurate description. Here, the authors employ ultrafast spectroscopic methods to explore the dynamics of highly excited organic molecules, revealing many-body effects and hints of coherent vibronic dynamics which persist despite their molecular complexity.
format	article
author	A. Marciniak V. Despré V. Loriot G. Karras M. Hervé L. Quintard F. Catoire C. Joblin E. Constant A. I. Kuleff F. Lépine
author_facet	A. Marciniak V. Despré V. Loriot G. Karras M. Hervé L. Quintard F. Catoire C. Joblin E. Constant A. I. Kuleff F. Lépine
author_sort	A. Marciniak
title	Electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse
title_short	Electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse
title_full	Electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse
title_fullStr	Electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse
title_full_unstemmed	Electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse
title_sort	electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse
publisher	Nature Portfolio
publishDate	2019
url	https://doaj.org/article/ac2461ded8d541e4b63c4452f4b18c12
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Electron correlation driven non-adiabatic relaxation in molecules excited by an ultrashort extreme ultraviolet pulse

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