corner
corner

Phys. Rev. B 62, R16360–R16363 (2000)

Size dependence of structural stability in nanocrystalline diamond

Download: PDF (530 kB) Buy this article Export: BibTeX or EndNote (RIS)

S. Prawer*, J. L. Peng, J. O. Orwa, J. C. McCallum, D. N. Jamieson, and L. A. Bursill
School of Physics, University of Melbourne, Parkville, Victoria, 3052, Australia

Received 21 July 2000; published in the issue dated 15 December 2000

We describe experiments which demonstrate that carbon atoms introduced into a fused-silica substrate by means of MeV ion implantation can, after suitable annealing, form nanocrystalline diamond. Unlike other methods of creating diamond, the coalescence of the carbon into diamond nanocrystals occurs when the samples are heated in a conventional furnace and does not require the application of high external pressures, or any pre-existing diamond template. Following a dose of 5×1016C/cm2 into fused quartz and after annealing in forming gas (4% hydrogen in argon), perfect cubic diamond crystallites of 5–7 nm diameter are formed. For higher doses, the same annealing treatments produce larger crystallites which are comprised of other varieties of solid carbon phases. We conclude that diamond is the stable form of carbon provided that the crystallite size is sufficiently small (less than 7 nm) and that the nanocrystallites are appropriately surface passivated.

© 2000 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevB.62.R16360
DOI:
10.1103/PhysRevB.62.R16360
PACS:
81.05.Tp, 81.15.Hi

*Email address: S.prawer@physics.unimelb.edu.au