Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene

Detalhes bibliográficos
Autor(a) principal: Creutzburg, Sascha
Data de Publicação: 2021
Outros Autores: Niggas, Anna, Weichselbaum, David, Grande, Pedro Luis, Aumayr, Friedrich, Wilhelm, Richard Arthur
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/237191
Resumo: The scattering of ions in solids is accompanied with momentum transfer and electronic excitations resulting in the slowing down of the ion. The amount of energy transferred in a single scattering event depends on the particular trajectory which can be traced back through the scattering angle. Performing scattering angle dependent measurements of slow highly charged Xe ions transmitted through freestanding single-, bi-, and trilayer graphene allows us to determine the charge exchange and energy loss for different minimal interatomic distances. Interestingly, the charge exchange shows an increase with scattering angle by a factor of less than 2, while the energy loss increases by more than a factor of 10 for 3◦ compared to forward direction. Our results can be compared to a time-dependent potential model and show that determination of the stopping cross section is not straightforward even with angle-dependent data at hand.
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spelling Creutzburg, SaschaNiggas, AnnaWeichselbaum, DavidGrande, Pedro LuisAumayr, FriedrichWilhelm, Richard Arthur2022-04-13T04:52:00Z20211050-2947http://hdl.handle.net/10183/237191001139129The scattering of ions in solids is accompanied with momentum transfer and electronic excitations resulting in the slowing down of the ion. The amount of energy transferred in a single scattering event depends on the particular trajectory which can be traced back through the scattering angle. Performing scattering angle dependent measurements of slow highly charged Xe ions transmitted through freestanding single-, bi-, and trilayer graphene allows us to determine the charge exchange and energy loss for different minimal interatomic distances. Interestingly, the charge exchange shows an increase with scattering angle by a factor of less than 2, while the energy loss increases by more than a factor of 10 for 3◦ compared to forward direction. Our results can be compared to a time-dependent potential model and show that determination of the stopping cross section is not straightforward even with angle-dependent data at hand.application/pdfengPhysical review. A, Atomic, molecular, and optical physics. New York. Vol. 104, no. 4 (Oct. 2021), 042806, 8 p.Colisao de particulasPerda de energia de particulasGrafenoAngle-dependent charge exchange and energy loss of slow highly charged ions in freestanding grapheneEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001139129.pdf.txt001139129.pdf.txtExtracted Texttext/plain35557http://www.lume.ufrgs.br/bitstream/10183/237191/2/001139129.pdf.txtdda2ed5304e6b9c524a4aa285a45537bMD52ORIGINAL001139129.pdfTexto completo (inglês)application/pdf6953869http://www.lume.ufrgs.br/bitstream/10183/237191/1/001139129.pdfedfd25de1da3a7549f75042e834050dcMD5110183/2371912024-05-24 06:41:51.629589oai:www.lume.ufrgs.br:10183/237191Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-05-24T09:41:51Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
title Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
spellingShingle Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
Creutzburg, Sascha
Colisao de particulas
Perda de energia de particulas
Grafeno
title_short Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
title_full Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
title_fullStr Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
title_full_unstemmed Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
title_sort Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
author Creutzburg, Sascha
author_facet Creutzburg, Sascha
Niggas, Anna
Weichselbaum, David
Grande, Pedro Luis
Aumayr, Friedrich
Wilhelm, Richard Arthur
author_role author
author2 Niggas, Anna
Weichselbaum, David
Grande, Pedro Luis
Aumayr, Friedrich
Wilhelm, Richard Arthur
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Creutzburg, Sascha
Niggas, Anna
Weichselbaum, David
Grande, Pedro Luis
Aumayr, Friedrich
Wilhelm, Richard Arthur
dc.subject.por.fl_str_mv Colisao de particulas
Perda de energia de particulas
Grafeno
topic Colisao de particulas
Perda de energia de particulas
Grafeno
description The scattering of ions in solids is accompanied with momentum transfer and electronic excitations resulting in the slowing down of the ion. The amount of energy transferred in a single scattering event depends on the particular trajectory which can be traced back through the scattering angle. Performing scattering angle dependent measurements of slow highly charged Xe ions transmitted through freestanding single-, bi-, and trilayer graphene allows us to determine the charge exchange and energy loss for different minimal interatomic distances. Interestingly, the charge exchange shows an increase with scattering angle by a factor of less than 2, while the energy loss increases by more than a factor of 10 for 3◦ compared to forward direction. Our results can be compared to a time-dependent potential model and show that determination of the stopping cross section is not straightforward even with angle-dependent data at hand.
publishDate 2021
dc.date.issued.fl_str_mv 2021
dc.date.accessioned.fl_str_mv 2022-04-13T04:52:00Z
dc.type.driver.fl_str_mv Estrangeiro
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/237191
dc.identifier.issn.pt_BR.fl_str_mv 1050-2947
dc.identifier.nrb.pt_BR.fl_str_mv 001139129
identifier_str_mv 1050-2947
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url http://hdl.handle.net/10183/237191
dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Physical review. A, Atomic, molecular, and optical physics. New York. Vol. 104, no. 4 (Oct. 2021), 042806, 8 p.
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reponame_str Repositório Institucional da UFRGS
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