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Femtosecond wave-packet revivals in ozone

Authors :
Simon Holzner
Olga Razskazovskaya
Ann-Katrin Sommer
Benjamin Lasorne
Johann Riemensberger
Markus Fieß
T. Latka
Ágnes Vibók
V. Shirvanyan
Alexander Guggenmos
Clemens Jakubeit
Reinhard Kienberger
Piero Decleva
Fabien Gatti
Martin Schultze
M. Jobst
David Lauvergnat
Gábor J. Halász
Birgitta Bernhardt
Wolfram Helml
Marcus Ossiander
Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)
Max-Planck-Institut für Quantenoptik (MPQ)
Max-Planck-Gesellschaft
Ludwig-Maximilians-Universität München (LMU)
Institut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier (ICGM ICMMM)
Université Montpellier 1 (UM1)-Université Montpellier 2 - Sciences et Techniques (UM2)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
Institut des Sciences Moléculaires d'Orsay (ISMO)
Université Paris-Sud - Paris 11 (UP11)-Centre National de la Recherche Scientifique (CNRS)
Laboratoire de Chimie Physique D'Orsay (LCPO)
Université Paris-Sud - Paris 11 (UP11)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Università degli studi di Trieste
University of Debrecen
Source :
Physical Review A, Physical Review A, American Physical Society, 2019, 99 (6), pp.063405. ⟨10.1103/PhysRevA.99.063405⟩
Publication Year :
2019
Publisher :
HAL CCSD, 2019.

Abstract

Photodissociation of ozone following absorption of biologically harmful solar ultraviolet radiation is the key mechanism for the life protecting properties of the atmospheric ozone layer. Even though ozone photolysis is described successfully by post-Hartree-Fock theory, it has evaded direct experimental access so far, due to the unavailability of intense ultrashort deep ultraviolet radiation sources. The rapidity of ozone photolysis with predicted values of a few tens of femtoseconds renders both ultrashort pump and probe pulses indispensable to capture this manifestation of ultrafast chemistry. Here, we present the observation of femtosecond time-scale electronic and nuclear dynamics of ozone triggered by \ensuremath{\sim}10-fs, \ensuremath{\sim}2-\textmu{}J deep ultraviolet pulses and, in contrast to conventional attochemistry experiments, probed by extreme ultraviolet isolated pulses. An electronic wave packet is first created. We follow the splitting of the excited B-state related nuclear wave packet into a path leading to molecular fragmentation and an oscillating path, revolving around the Franck-Condon point with 22-fs wave-packet revival time. Full quantum-mechanical ab initio multiconfigurational time-dependent Hartree simulations support this interpretation.

Details

Language :
English
ISSN :
10502947 and 10941622
Database :
OpenAIRE
Journal :
Physical Review A, Physical Review A, American Physical Society, 2019, 99 (6), pp.063405. ⟨10.1103/PhysRevA.99.063405⟩
Accession number :
edsair.doi.dedup.....aaae03e8fd3b304009cdef0df5ea99c0
Full Text :
https://doi.org/10.1103/PhysRevA.99.063405⟩