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Real-time observation of a correlation-driven sub 3 fs charge migration in ionised adenine

Sudden ionisation of a relatively large molecule can initiate a correlation-driven process dubbed charge migration, where the electron density distribution is expected to rapidly move along the molecular backbone. Capturing this few-femtosecond or attosecond charge redistribution would represent the...

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Detalles Bibliográficos
Autores principales: Månsson, Erik P., Latini, Simone, Covito, Fabio, Wanie, Vincent, Galli, Mara, Perfetto, Enrico, Stefanucci, Gianluca, Hübener, Hannes, De Giovannini, Umberto, Castrovilli, Mattea C., Trabattoni, Andrea, Frassetto, Fabio, Poletto, Luca, Greenwood, Jason B., Légaré, François, Nisoli, Mauro, Rubio, Angel, Calegari, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814501/
https://www.ncbi.nlm.nih.gov/pubmed/36697766
http://dx.doi.org/10.1038/s42004-021-00510-5
Descripción
Sumario:Sudden ionisation of a relatively large molecule can initiate a correlation-driven process dubbed charge migration, where the electron density distribution is expected to rapidly move along the molecular backbone. Capturing this few-femtosecond or attosecond charge redistribution would represent the real-time observation of electron correlation in a molecule with the enticing prospect of following the energy flow from a single excited electron to the other coupled electrons in the system. Here, we report a time-resolved study of the correlation-driven charge migration process occurring in the nucleic-acid base adenine after ionisation with a 15–35 eV attosecond pulse. We find that the production of intact doubly charged adenine – via a shortly-delayed laser-induced second ionisation event – represents the signature of a charge inflation mechanism resulting from many-body excitation. This conclusion is supported by first-principles time-dependent simulations. These findings may contribute to the control of molecular reactivity at the electronic, few-femtosecond time scale.