A comparative laboratory study of soft X-ray-induced ionization and fragmentation of five small PAH cations

Abstract: The interaction between polycyclic aromatic hydrocarbon (PAH) radical cations and X-rays predominantly leads to photofragmentation, a process that strongly depends on PAH size and geometry. In our experiments, five prototypical PAHs were exposed to monochromatic soft X-ray photons with energies in the C K-edge regime. As a function of soft X-ray photon energy, photoion yields were obtained by means of time-of-flight mass spectrometry. The resulting near-edge X-ray absorption mass spectra were interpreted using time-dependent density functional theory (TD-DFT) with a short-range corrected functional. We found that the carbon backbone of anthracene (C H ), pyrene (C H ) and coronene (C H ) can survive soft X-ray absorption, even though mostly intermediate size fragments are formed. In contrast, for hexahydropyrene (C H ) and triphenylene (C H ) molecular survival is not observed and the fragmentation pattern is dominated by small fragments. For a given excitation energy, molecular survival evidently does not simply correlate with PAH size but strongly depends on other PAH properties

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
The European physical journal. D. - 77 (2023) , 181, ISSN: 1434-6079

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2024
Urheber
Huo, Yining
Cangahuala, Mónica K. Espinoza
Zamudio-Bayer, Vicente
Goulart, Marcelo
Kubin, Markus
Timm, Martin
Lau, J. Tobias
Issendorff, Bernd von
Hoekstra, Ronnie
Faraji, Shirin
Schlathölter, Thomas

DOI
10.1140/epjd/s10053-023-00763-w
URN
urn:nbn:de:bsz:25-freidok-2543121
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:56 MESZ

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