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dc.contributor.authorShiell, T.
dc.contributor.authorMcCulloch, D.
dc.contributor.authorMcKenzie, D.
dc.contributor.authorField, M.
dc.contributor.authorHaberl, B.
dc.contributor.authorBoehler, R.
dc.contributor.authorCook, B.
dc.contributor.authorTomas Andres, Carla de
dc.contributor.authorSuarez-Martinez, Irene
dc.contributor.authorMarks, Nigel
dc.contributor.authorBradby, J.
dc.date.accessioned2018-06-29T12:29:11Z
dc.date.available2018-06-29T12:29:11Z
dc.date.created2018-06-29T12:09:04Z
dc.date.issued2018
dc.identifier.citationShiell, T. and McCulloch, D. and McKenzie, D. and Field, M. and Haberl, B. and Boehler, R. and Cook, B. et al. 2018. Graphitization of Glassy Carbon after Compression at Room Temperature. Physical Review Letters. 120 (21).
dc.identifier.urihttp://hdl.handle.net/20.500.11937/69308
dc.identifier.doi10.1103/PhysRevLett.120.215701
dc.description.abstract

© 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.

dc.publisherThe American Physical Society
dc.titleGraphitization of Glassy Carbon after Compression at Room Temperature
dc.typeJournal Article
dcterms.source.volume120
dcterms.source.number21
dcterms.source.issn0031-9007
dcterms.source.titlePhysical Review Letters
curtin.departmentSchool of Electrical Engineering, Computing and Mathematical Science (EECMS)
curtin.accessStatusFulltext not available


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