Graphitization of Glassy Carbon after Compression at Room Temperature
Author(s) -
Thomas B. Shiell,
Dougal G. McCulloch,
David R. McKenzie,
Matthew R. Field,
Bianca Haberl,
R. Boehler,
Brenton A. Cook,
Carla de Tomás,
Irene SuarezMartinez,
Nigel A. Marks,
J. E. Bradby
Publication year - 2018
Publication title -
physical review letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.688
H-Index - 673
eISSN - 1079-7114
pISSN - 0031-9007
DOI - 10.1103/physrevlett.120.215701
Subject(s) - materials science , glassy carbon , isotropy , compression (physics) , carbon fibers , graphite , limit (mathematics) , composite material , phase (matter) , thermodynamics , composite number , chemistry , optics , organic chemistry , cyclic voltammetry , mathematical analysis , physics , mathematics , electrode , electrochemistry
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 sp^{2} rich starting structure to a sp^{3} rich phase that reverts to fully sp^{2} bonded oriented graphite during pressure release.
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