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dc.contributor.authorNongni, F. T.
dc.contributor.authorKalus, René
dc.contributor.authorBenhenni, Malika
dc.contributor.authorGadéa, Florent Xavier
dc.contributor.authorYousfi, Mohammed
dc.date.accessioned2024-11-13T11:40:41Z
dc.date.available2024-11-13T11:40:41Z
dc.date.issued2024
dc.identifier.citationThe Journal of Chemical Physics. 2024, vol. 160, issue 16, art. no. 161101.cs
dc.identifier.issn0021-9606
dc.identifier.issn1089-7690
dc.identifier.urihttp://hdl.handle.net/10084/155293
dc.description.abstractFor many years, the recombination of excited ions of argon, Ar+(P1/22), has been assumed negligible under ambient conditions as compared to the recombination of ground-state ions, Ar+(P3/22). This opinion was confronted with detailed experimental results that seem to clearly support it. Here, we propose a new interpretation in light of our recent calculations, which shows that the recombination efficiency is comparable for both fine-structure states. Noteworthily, in our model leading to a picture consistent with the experiment, residual dimer ions emerge from Ar+(P1/22) due to non-adiabatic dynamics effects and interplay in measured data.cs
dc.language.isoencs
dc.publisherAIP Publishingcs
dc.relation.ispartofseriesThe Journal of Chemical Physicscs
dc.relation.urihttps://doi.org/10.1063/5.0202524cs
dc.rights© 2024 Author(s). Published under an exclusive license by AIP Publishing.cs
dc.titleTernary recombination of excited Ar+(<mml:mmultiscripts>P1/2<mml:none/><mml:mprescripts/><mml:none/>2</mml:mmultiscripts>) ions, established experimental results reinterpreted with a new extended modelcs
dc.typearticlecs
dc.identifier.doi10.1063/5.0202524
dc.rights.accessopenAccesscs
dc.type.versionpublishedVersioncs
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume160cs
dc.description.issue16cs
dc.description.firstpageart. no. 161101cs
dc.identifier.wos001206881000015


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