2002
DOI: 10.1063/1.1495078
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Direct transformation of cubic diamond to hexagonal diamond

Abstract: For a long time, hexagonal diamond has been formed only by static and shock wave compression of well-crystallized graphites. Here, we demonstrate that cubic diamond loses its structure stability and transforms to hexagonal diamond in massive. This transformation has been completed in nanoseconds under a shock wave compression of cubic diamond, in which the shock pressure and temperature are only tens of giga pascal and hundreds of kelvin, thermodynamically being within the stability of cubic diamond. The forma… Show more

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Cited by 94 publications
(54 citation statements)
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“…The spectra of the recovered sample exhibits two broad peaks centered at 1,581 and 1,355 cm Ϫ1 , respectively, which are characteristics of carbon with a very small particle size (1,11). Such spectroscopic characteristics are very similar to those of glassy carbon with a significant ratio of sp 3 ͞sp 2 bonding (13), but remarkably different from those of the starting nanotube, single-crystal graphite, or cubic and hexagonal diamond (7). The 1,355-cm Ϫ1 peak of glassy carbon is much stronger and sharper than that of the recovered hexagonal phase (1).…”
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confidence: 68%
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“…The spectra of the recovered sample exhibits two broad peaks centered at 1,581 and 1,355 cm Ϫ1 , respectively, which are characteristics of carbon with a very small particle size (1,11). Such spectroscopic characteristics are very similar to those of glassy carbon with a significant ratio of sp 3 ͞sp 2 bonding (13), but remarkably different from those of the starting nanotube, single-crystal graphite, or cubic and hexagonal diamond (7). The 1,355-cm Ϫ1 peak of glassy carbon is much stronger and sharper than that of the recovered hexagonal phase (1).…”
mentioning
confidence: 68%
“…The 1,355-cm Ϫ1 peak of glassy carbon is much stronger and sharper than that of the recovered hexagonal phase (1). It is also clear that our hexagonal form is not hexagonal diamond, since it should only have a single Raman active mode at Ϸ1,310 cm Ϫ1 , representing the occurrence of the sp 3 -hybridized bonds (6,7,12). We therefore conclude that this is an additional highpressure carbon phase.…”
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confidence: 79%
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“…However, these exceptional properties have not been proven experimentally because of the inability to synthesize lonsdaleite as a pure phase. It has been reported to form during static compression of graphite 3,9,13,[15][16][17][18] ; highpressure-high-temperature treatment of powdered diamond, graphite and amorphous carbon 19 ; explosive detonation and shock compression of graphite 11,20 and diamond 21 ; and chemical vapour deposition of hydrocarbon gases 22 ; however, in all cases the synthesis product also contained cubic diamond, graphite or both.…”
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confidence: 99%
“…Such amount of shift is also observed in hexagonal diamond with peak broadening. 37,38 At the earlier stage of the growth in our case, such hexagonal diamonds might be grown. On the other hand, the peak shift is not observed in the diamond layers grown after 5 h. More detailed analysis, e.g.…”
Section: Micro-raman Spectrum Of the Grown Particles At Various Condimentioning
confidence: 99%