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Giant and Tunable Anisotropy of Nanoscale Friction in Graphene
The nanoscale friction between an atomic force microscopy tip and graphene is investigated using friction force microscopy (FFM). During the tip movement, friction forces are observed to increase and then saturate in a highly anisotropic manner. As a result, the friction forces in graphene are highl...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989147/ https://www.ncbi.nlm.nih.gov/pubmed/27534691 http://dx.doi.org/10.1038/srep31569 |
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author | Almeida, Clara M. Prioli, Rodrigo Fragneaud, Benjamin Cançado, Luiz Gustavo Paupitz, Ricardo Galvão, Douglas S. De Cicco, Marcelo Menezes, Marcos G. Achete, Carlos A. Capaz, Rodrigo B. |
author_facet | Almeida, Clara M. Prioli, Rodrigo Fragneaud, Benjamin Cançado, Luiz Gustavo Paupitz, Ricardo Galvão, Douglas S. De Cicco, Marcelo Menezes, Marcos G. Achete, Carlos A. Capaz, Rodrigo B. |
author_sort | Almeida, Clara M. |
collection | PubMed |
description | The nanoscale friction between an atomic force microscopy tip and graphene is investigated using friction force microscopy (FFM). During the tip movement, friction forces are observed to increase and then saturate in a highly anisotropic manner. As a result, the friction forces in graphene are highly dependent on the scanning direction: under some conditions, the energy dissipated along the armchair direction can be 80% higher than along the zigzag direction. In comparison, for highly-oriented pyrolitic graphite (HOPG), the friction anisotropy between armchair and zigzag directions is only 15%. This giant friction anisotropy in graphene results from anisotropies in the amplitudes of flexural deformations of the graphene sheet driven by the tip movement, not present in HOPG. The effect can be seen as a novel manifestation of the classical phenomenon of Euler buckling at the nanoscale, which provides the non-linear ingredients that amplify friction anisotropy. Simulations based on a novel version of the 2D Tomlinson model (modified to include the effects of flexural deformations), as well as fully atomistic molecular dynamics simulations and first-principles density-functional theory (DFT) calculations, are able to reproduce and explain the experimental observations. |
format | Online Article Text |
id | pubmed-4989147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49891472016-08-30 Giant and Tunable Anisotropy of Nanoscale Friction in Graphene Almeida, Clara M. Prioli, Rodrigo Fragneaud, Benjamin Cançado, Luiz Gustavo Paupitz, Ricardo Galvão, Douglas S. De Cicco, Marcelo Menezes, Marcos G. Achete, Carlos A. Capaz, Rodrigo B. Sci Rep Article The nanoscale friction between an atomic force microscopy tip and graphene is investigated using friction force microscopy (FFM). During the tip movement, friction forces are observed to increase and then saturate in a highly anisotropic manner. As a result, the friction forces in graphene are highly dependent on the scanning direction: under some conditions, the energy dissipated along the armchair direction can be 80% higher than along the zigzag direction. In comparison, for highly-oriented pyrolitic graphite (HOPG), the friction anisotropy between armchair and zigzag directions is only 15%. This giant friction anisotropy in graphene results from anisotropies in the amplitudes of flexural deformations of the graphene sheet driven by the tip movement, not present in HOPG. The effect can be seen as a novel manifestation of the classical phenomenon of Euler buckling at the nanoscale, which provides the non-linear ingredients that amplify friction anisotropy. Simulations based on a novel version of the 2D Tomlinson model (modified to include the effects of flexural deformations), as well as fully atomistic molecular dynamics simulations and first-principles density-functional theory (DFT) calculations, are able to reproduce and explain the experimental observations. Nature Publishing Group 2016-08-18 /pmc/articles/PMC4989147/ /pubmed/27534691 http://dx.doi.org/10.1038/srep31569 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Almeida, Clara M. Prioli, Rodrigo Fragneaud, Benjamin Cançado, Luiz Gustavo Paupitz, Ricardo Galvão, Douglas S. De Cicco, Marcelo Menezes, Marcos G. Achete, Carlos A. Capaz, Rodrigo B. Giant and Tunable Anisotropy of Nanoscale Friction in Graphene |
title | Giant and Tunable Anisotropy of Nanoscale Friction in Graphene |
title_full | Giant and Tunable Anisotropy of Nanoscale Friction in Graphene |
title_fullStr | Giant and Tunable Anisotropy of Nanoscale Friction in Graphene |
title_full_unstemmed | Giant and Tunable Anisotropy of Nanoscale Friction in Graphene |
title_short | Giant and Tunable Anisotropy of Nanoscale Friction in Graphene |
title_sort | giant and tunable anisotropy of nanoscale friction in graphene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989147/ https://www.ncbi.nlm.nih.gov/pubmed/27534691 http://dx.doi.org/10.1038/srep31569 |
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