Relaxation processes in aqueous systems upon X-ray ionization: entanglement of electronic and nuclear dynamics

The knowledge of primary processes following the interaction of high-energy radiation with molecules in liquid phase is rather limited. In the present Perspective, we report on a newly discovered type of relaxation process involving simultaneous autoionization and proton transfer between adjacent mo...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Slavíček, Petr (VerfasserIn) , Kryzhevoi, Nikolai V. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2016
In: The journal of physical chemistry letters
Year: 2015, Jahrgang: 7, Heft: 2, Pages: 234-243
ISSN:1948-7185
DOI:10.1021/acs.jpclett.5b02665
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.jpclett.5b02665
Volltext
Verfasserangaben:Petr Slavíček, Nikolai V. Kryzhevoi, Emad F. Aziz, and Bernd Winter
Beschreibung
Zusammenfassung:The knowledge of primary processes following the interaction of high-energy radiation with molecules in liquid phase is rather limited. In the present Perspective, we report on a newly discovered type of relaxation process involving simultaneous autoionization and proton transfer between adjacent molecules, so-called proton transfer mediated charge separation (PTM-CS) process. Within PTM-CS, transients with a half-transferred proton are formed within a few femtoseconds after the core-level ionization event. Subsequent nonradiative decay of the highly nonequilibrium transients leads to a series of reactive species, which have not been considered in any high-energy radiation process in water. Nonlocal electronic decay processes are surprisingly accelerated upon proton dynamics. Such strong coupling of electronic and nuclear dynamics is a general phenomenon for hydrogen-bonded systems, however, its probability correlates strongly with hydration geometry. We suggest that the newly observed processes will impact future high-energy radiation-chemistry-relevant modeling, and we envision application of autoionization spectroscopy for identification of solution structure details.
Beschreibung:Published: December 29, 2015
Gesehen am 08.05.2020
Beschreibung:Online Resource
ISSN:1948-7185
DOI:10.1021/acs.jpclett.5b02665