Graphitization of Glassy Carbon after Compression at Room Temperature

© 2018 American Physical Society. Glassy carbon is a technologically important material with isotropic properties that is nongraphitizing up to ~3000 °C and displays complete or "superelastic" recovery from large compression. The pressure limit of these properties is not yet known. Here we...

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Main Authors: Shiell, T., McCulloch, D., McKenzie, D., Field, M., Haberl, B., Boehler, R., Cook, B., Tomas Andres, Carla de, Suarez-Martinez, Irene, Marks, Nigel, Bradby, J.
Format: Journal Article
Published: The American Physical Society 2018
Online Access:https://link.aps.org/accepted/10.1103/PhysRevLett.120.215701
http://hdl.handle.net/20.500.11937/69308
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author Shiell, T.
McCulloch, D.
McKenzie, D.
Field, M.
Haberl, B.
Boehler, R.
Cook, B.
Tomas Andres, Carla de
Suarez-Martinez, Irene
Marks, Nigel
Bradby, J.
author_facet Shiell, T.
McCulloch, D.
McKenzie, D.
Field, M.
Haberl, B.
Boehler, R.
Cook, B.
Tomas Andres, Carla de
Suarez-Martinez, Irene
Marks, Nigel
Bradby, J.
author_sort Shiell, T.
building Curtin Institutional Repository
collection Online Access
description © 2018 American Physical Society. Glassy carbon is a technologically important material with isotropic properties that is nongraphitizing up to ~3000 °C and displays complete or "superelastic" recovery from large compression. The pressure limit of these properties is not yet known. Here we use experiments and modeling to show permanent densification, and preferred orientation occurs in glassy carbon loaded to 45 GPa and above, where 45 GPa represents the limit to the superelastic and nongraphitizing properties of the material. The changes are explained by a transformation from its sp2 rich starting structure to a sp3 rich phase that reverts to fully sp2 bonded oriented graphite during pressure release.
first_indexed 2025-11-14T10:41:02Z
format Journal Article
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T10:41:02Z
publishDate 2018
publisher The American Physical Society
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spelling curtin-20.500.11937-693082023-04-26T05:10:14Z Graphitization of Glassy Carbon after Compression at Room Temperature Shiell, T. McCulloch, D. McKenzie, D. Field, M. Haberl, B. Boehler, R. Cook, B. Tomas Andres, Carla de Suarez-Martinez, Irene Marks, Nigel Bradby, J. © 2018 American Physical Society. Glassy carbon is a technologically important material with isotropic properties that is nongraphitizing up to ~3000 °C and displays complete or "superelastic" recovery from large compression. The pressure limit of these properties is not yet known. Here we use experiments and modeling to show permanent densification, and preferred orientation occurs in glassy carbon loaded to 45 GPa and above, where 45 GPa represents the limit to the superelastic and nongraphitizing properties of the material. The changes are explained by a transformation from its sp2 rich starting structure to a sp3 rich phase that reverts to fully sp2 bonded oriented graphite during pressure release. 2018 Journal Article http://hdl.handle.net/20.500.11937/69308 10.1103/PhysRevLett.120.215701 https://link.aps.org/accepted/10.1103/PhysRevLett.120.215701 http://purl.org/au-research/grants/arc/DP150103487 The American Physical Society unknown
spellingShingle Shiell, T.
McCulloch, D.
McKenzie, D.
Field, M.
Haberl, B.
Boehler, R.
Cook, B.
Tomas Andres, Carla de
Suarez-Martinez, Irene
Marks, Nigel
Bradby, J.
Graphitization of Glassy Carbon after Compression at Room Temperature
title Graphitization of Glassy Carbon after Compression at Room Temperature
title_full Graphitization of Glassy Carbon after Compression at Room Temperature
title_fullStr Graphitization of Glassy Carbon after Compression at Room Temperature
title_full_unstemmed Graphitization of Glassy Carbon after Compression at Room Temperature
title_short Graphitization of Glassy Carbon after Compression at Room Temperature
title_sort graphitization of glassy carbon after compression at room temperature
url https://link.aps.org/accepted/10.1103/PhysRevLett.120.215701
https://link.aps.org/accepted/10.1103/PhysRevLett.120.215701
http://hdl.handle.net/20.500.11937/69308