Abstract
The peak near 1150 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ in the visible Raman spectra of poor quality chemical-vapor-deposited diamond is often used as the signature of nanocrystalline diamond. We argue that this peak should not be assigned to nanocrystalline diamond or other ${\mathrm{sp}}^{3}$-bonded phases. Its wave number disperses with excitation energy, its intensity decreases with increasing excitation energy, and it is always accompanied by another peak near 1450 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$, which acts similarly. This behavior is that expected for ${\mathrm{sp}}^{2}$-bonded configurations, with their smaller band gap. The peaks are assigned to transpolyacetylene segments at grain boundaries and surfaces.
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Publication Info
- Year
- 2001
- Type
- article
- Volume
- 63
- Issue
- 12
- Citations
- 1164
- Access
- Closed
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Identifiers
- DOI
- 10.1103/physrevb.63.121405