Dynamics of core-excited ammonia: disentangling fragmentation pathways by complementary spectroscopic methods

dc.contributor.authorTravnikova Oksana
dc.contributor.authorHosseini Farzad
dc.contributor.authorMarchenko Tatiana
dc.contributor.authorGuillemin Renaud
dc.contributor.authorIsmail Iyas
dc.contributor.authorMoussaoui Roba
dc.contributor.authorJournel Loic
dc.contributor.authorMilosavljevic Aleksandar R.
dc.contributor.authorBozek John D.
dc.contributor.authorKukk Edwin
dc.contributor.authorPuttner Ralph
dc.contributor.authorPiancastelli Maria Novella
dc.contributor.authorSimon Marc
dc.contributor.organizationfi=materiaalitutkimuksen laboratorio|en=Materials Research Laboratory|
dc.contributor.organization-code1.2.246.10.2458963.20.15561262450
dc.converis.publication-id178035030
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/178035030
dc.date.accessioned2025-08-28T00:42:57Z
dc.date.available2025-08-28T00:42:57Z
dc.description.abstract<p>Fragmentation dynamics of core-excited isolated ammonia molecules is studied by two different and complementary experimental methods, high-resolution resonant Auger spectroscopy and electron energy-selected Auger electron–photoion coincidence spectroscopy (AEPICO). The combined use of these two techniques allows obtaining information on different dissociation patterns, in particular fragmentation before relaxation, often called ultrafast dissociation (UFD), and fragmentation after relaxation. The resonant Auger spectra contain the spectral signature of both molecular and fragment final states, and therefore can provide information on all events occurring during the core-hole lifetime, in particular fragmentation before relaxation. Coincidence measurements allow correlating Auger electrons with ionic fragments from the same molecule, and relating the ionic fragments to specific Auger final electronic states, and yield additional information on which final states are dissociative, and which ionic fragments can be produced in timescales either corresponding to the core-hole lifetime or longer. Furthermore, we show that by the combined use of two complementary experimental techniques we are able to identify more electronic states of the NH2+ fragment with respect to the single one already reported in the literature.<br></p>
dc.format.pagerange1063
dc.format.pagerange1074
dc.identifier.eissn1463-9084
dc.identifier.jour-issn1463-9076
dc.identifier.olddbid206263
dc.identifier.oldhandle10024/189290
dc.identifier.urihttps://www.utupub.fi/handle/11111/45294
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2023/CP/D2CP03488C
dc.identifier.urnURN:NBN:fi-fe202301255508
dc.language.isoen
dc.okm.affiliatedauthorKukk, Edwin
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.discipline116 Kemiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherROYAL SOC CHEMISTRY
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1039/d2cp03488c
dc.relation.ispartofjournalPhysical Chemistry Chemical Physics
dc.relation.issue2
dc.relation.volume25
dc.source.identifierhttps://www.utupub.fi/handle/10024/189290
dc.titleDynamics of core-excited ammonia: disentangling fragmentation pathways by complementary spectroscopic methods
dc.year.issued2023

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