Time-resolved Auger–Meitner spectroscopy of the photodissociation dynamics of CS<sub>2</sub>

Abstract The photodissociation dynamics of UV excited CS 2 are investigated using time-resolved Auger–Meitner (AM) spectroscopy. AM decay is initiated by inner-shell ionisation with a femtosecond duration x-ray (179.9 eV) probe generated by the FERMI free electron laser. The time-delayed x-ray probe removes an electron from the S(2p) orbital leading to secondary emission of a high energy electron through AM decay. We monitor the electron kinetic energy of the AM emission as a function of pump-probe delay and observe time-dependent changes in the spectrum that correlate with the formation of bound, excited-state CS 2 molecules at early times, and CS + S fragments on the picosecond timescale. The results are analysed based on a simplified kinetic scheme that provides a time constant for dissociation of approximately 1.2 ps, in agreement with previous time-resolved x-ray photoelectron spectroscopy measurements (Gabalski, et al 2023 J. Phys. Chem. Lett. 14 7126–7133).

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Publication Details

Journal
Journal of Physics B Atomic Molecular and Optical Physics
Published
2024-09-23
DOI
https://doi.org/10.1088/1361-6455/ad7e89
Citations
3
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
1.01

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article

Time-resolved Auger–Meitner spectroscopy of the photodissociation dynamics of CS2

Daniel Rolles, Oksana Plekan, Felix Allum, Cesare Grazioli et al.
3 citations
Journal of Physics B Atomic Molecular and Optical Physics
Advanced Chemical Physics Studies
1.01
article

Time-resolved Auger–Meitner spectroscopy of the photodissociation dynamics of CS2

Daniel Rolles, Oksana Plekan, Felix Allum, Cesare Grazioli, Michele Di Fraia, Marcello Coreno, Marco Zangrando, Piero Decleva, Nitish Pal, M. Danailov, Michele Devetta, Michael S. Schuurman, Richard J. Squibb, C. Vozzi, Ruaridh Forbes, Russell S. Minns, P. Piseri, D.M.P. Holland, Kevin C. Prince, Davide Faccialà, Bruno Nunes Cabral Tenorio, Sonia Coriani, R. Feifel, Alberto Simoncig, Alexander Demidovich, Carlo Callegari, Alexander Darius Brynes, Matteo Bonanomi, Henry J. Thompson
article en
3 citations

Abstract

Abstract The photodissociation dynamics of UV excited CS 2 are investigated using time-resolved Auger–Meitner (AM) spectroscopy. AM decay is initiated by inner-shell ionisation with a femtosecond duration x-ray (179.9 eV) probe generated by the FERMI free electron laser. The time-delayed x-ray probe removes an electron from the S(2p) orbital leading to secondary emission of a high energy electron through AM decay. We monitor the electron kinetic energy of the AM emission as a function of pump-probe delay and observe time-dependent changes in the spectrum that correlate with the formation of bound, excited-state CS 2 molecules at early times, and CS + S fragments on the picosecond timescale. The results are analysed based on a simplified kinetic scheme that provides a time constant for dissociation of approximately 1.2 ps, in agreement with previous time-resolved x-ray photoelectron spectroscopy measurements (Gabalski, et al 2023 J. Phys. Chem. Lett. 14 7126–7133).

Journal of Physics B Atomic Molecular and Optical PhysicsVol. 57(21)
Quantum Technologies (Sweden) (SE), Technical University of Denmark (DK)
U.S. Department of Energy, Leverhulme Trust, University of Southampton, European Commission, Ministero dell’Istruzione, dell’Università e della Ricerca, Knut och Alice Wallenbergs Stiftelse, Vetenskapsrådet, Office of Science, Engineering and Physical Sciences Research Council, Science and Technology Facilities Council, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division, EPSRC Centre for Doctoral Training in Technology Enhanced Chemical Synthesis, SLAC National Accelerator Laboratory
Affordable and clean energy
Openalex Percentile: Top 24%
Advanced Chemical Physics Studies
1.01
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