Angle-dependent charge exchange and energy loss of slow highly charged ions in freestanding graphene
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , |
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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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 info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
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 001139129 |
url |
http://hdl.handle.net/10183/237191 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
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. |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFRGS instname:Universidade Federal do Rio Grande do Sul (UFRGS) instacron:UFRGS |
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Universidade Federal do Rio Grande do Sul (UFRGS) |
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UFRGS |
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Repositório Institucional da UFRGS |
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Repositório Institucional da UFRGS |
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