B. Bastian, J. D. Asmussen, L. Ben Ltaief, H. B. Pedersen, K. Sishodia, S. De, S. R. Krishnan, C. Medina, N. Pal, R. Richter, N. Sisourat, M. Mudrich
{"title":"Observation of interatomic Coulombic decay induced by double excitation of helium in nanodroplets","authors":"B. Bastian, J. D. Asmussen, L. Ben Ltaief, H. B. Pedersen, K. Sishodia, S. De, S. R. Krishnan, C. Medina, N. Pal, R. Richter, N. Sisourat, M. Mudrich","doi":"arxiv-2310.15835","DOIUrl":null,"url":null,"abstract":"Interatomic Coulombic decay (ICD) plays a crucial role in weakly bound\ncomplexes exposed to intense or high-energy radiation. So far, neutral or ionic\natoms or molecules have been prepared in singly excited electron or hole states\nwhich can transfer energy to neighboring centers and cause ionization and\nradiation damage. Here we demonstrate that a doubly excited atom, despite its\nextremely short lifetime, can decay by ICD; evidenced by high-resolution\nphotoelectron spectra of He nanodroplets excited to the 2s2p+ state. We find\nthat ICD proceeds by relaxation into excited He$^*$He$^+$ atom-pair states, in\nagreement with calculations. The ability of inducing ICD by resonant excitation\nfar above the single-ionization threshold opens opportunities for controlling\nradiation damage to a high degree of element specificity and spectral\nselectivity.","PeriodicalId":501259,"journal":{"name":"arXiv - PHYS - Atomic and Molecular Clusters","volume":"15 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - PHYS - Atomic and Molecular Clusters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2310.15835","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Interatomic Coulombic decay (ICD) plays a crucial role in weakly bound
complexes exposed to intense or high-energy radiation. So far, neutral or ionic
atoms or molecules have been prepared in singly excited electron or hole states
which can transfer energy to neighboring centers and cause ionization and
radiation damage. Here we demonstrate that a doubly excited atom, despite its
extremely short lifetime, can decay by ICD; evidenced by high-resolution
photoelectron spectra of He nanodroplets excited to the 2s2p+ state. We find
that ICD proceeds by relaxation into excited He$^*$He$^+$ atom-pair states, in
agreement with calculations. The ability of inducing ICD by resonant excitation
far above the single-ionization threshold opens opportunities for controlling
radiation damage to a high degree of element specificity and spectral
selectivity.