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Near coalescent submicron polycrystalline diamond films deposited on silicon: hydrogen bonding and thermal enhanced carbide formation

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journal contribution
posted on 2009-12-16, 00:00 authored by A Stacey, S Michaelson, Julius Orwa, S Rubanov, S Prawer, B C C Cowie, A Hoffman
The influence of high temperature annealing up to 1200 °C in vacuum on ∼100 nm nearly continuous thick diamond films consisting of 30-50 nm crystallites, deposited onto silicon substrates is reported. The hydrogen bonding and phase composition of the films were studied with Raman spectroscopy, while the surface microstructure and composition were studied with high resolution scanning electron microscopy (SEM), transmission electron microscopy (TEM), and x-ray photoelectron spectroscopy (XPS), respectively. Annealing to 800-900 °C of ∼100 nm thick films results in a decrease in the intensities of the peaks associated with hydrogen bonding (Raman), as well as changes to the morphological microstructure at the film surface. Heating the films to 1000 °C resulted in the complete disappearance of the Raman peaks associated with hydrogen bonding at grain boundaries, and an increase in the relative intensity of the diamond peak relative to the graphite-related D and G Raman peaks, concomitant with changes to the microstructure (SEM and TEM). Ex situ XP analysis of the films annealed to 800 and 1000 °C provides clear evidence for the formation of SiC on the films surface and near surface region. However a sharp SiC Raman peak at 796 cm-1 appears only after annealing to 1200 °C and it is concomitant with a decrease in the Raman peaks associated with sp2 bonded carbon. Our results suggest that formation of SiC phase preferentially consumes sp2/sp hybridized carbon matrix, produced by thermal desorption of hydrogen atoms at diamond grain boundary and at the diamond film-silicon substrate interface.



Journal of applied physics





Article number



1 - 8


American Institute of Physics


Melville, N.Y.





Publication classification

C Journal article; C1.1 Refereed article in a scholarly journal

Copyright notice

2009, American Institute of Physics