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Auteurs principaux: Doignon, Clément Guiot du, Sinha-Roy, Rajarshi, Rabilloud, Franck, Despré, Victor
Format: Preprint
Publié: 2024
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Accès en ligne:https://arxiv.org/abs/2410.04978
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author Doignon, Clément Guiot du
Sinha-Roy, Rajarshi
Rabilloud, Franck
Despré, Victor
author_facet Doignon, Clément Guiot du
Sinha-Roy, Rajarshi
Rabilloud, Franck
Despré, Victor
contents The possibility of observing correlation-driven charge migration has been a driving force behind theoretical and experimental developments in the field of attosecond molecular science since its inception. Despite significant accomplishments, the unambiguous experimental observation of this quantum beating remains elusive. In this work, we present a method to selectively trigger such dynamics using molecules predicted to exhibit long-lived electron coherence. We show that these dynamics can be selectively triggered using infrared multi-photon ionization and probed using the spacial resolution of X-ray free-electron laser, proposing a promising experimental scheme to study these pivotal dynamics. Additionally, we demonstrate that real-time time-dependent density-functional theory can describe correlation-driven charge migration resulting from a hole mixing structure involving the HOMO of a molecule.
format Preprint
id arxiv_https___arxiv_org_abs_2410_04978
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Correlation-Driven Charge Migration Triggered by Infrared Multi-Photon Ionization
Doignon, Clément Guiot du
Sinha-Roy, Rajarshi
Rabilloud, Franck
Despré, Victor
Chemical Physics
The possibility of observing correlation-driven charge migration has been a driving force behind theoretical and experimental developments in the field of attosecond molecular science since its inception. Despite significant accomplishments, the unambiguous experimental observation of this quantum beating remains elusive. In this work, we present a method to selectively trigger such dynamics using molecules predicted to exhibit long-lived electron coherence. We show that these dynamics can be selectively triggered using infrared multi-photon ionization and probed using the spacial resolution of X-ray free-electron laser, proposing a promising experimental scheme to study these pivotal dynamics. Additionally, we demonstrate that real-time time-dependent density-functional theory can describe correlation-driven charge migration resulting from a hole mixing structure involving the HOMO of a molecule.
title Correlation-Driven Charge Migration Triggered by Infrared Multi-Photon Ionization
topic Chemical Physics
url https://arxiv.org/abs/2410.04978