Abstract
We present coherent-potential-approximation (CPA) calculations and first- and second-order Raman spectra for diamonds with varying concentrations of and . The calculations are based on the valence-force model of Tubino, Piseri, and Zerbi [J. Chem. Phys. 56, 1022 (1972)]. Contrary to previous claims, we find that this model does not give a sharp peak in the density of states (DOS) near the Raman mode. Alternative dispersion curves that do give such a peak are discussed. Raman results are reported for high-quality, single-crystal synthetic diamonds with isotopic compositions ranging from nearly pure to nearly pure . A measurable deviation in the Raman frequency away from a simple (‘‘virtual-crystal’’) dependence and an observable broadening of the first- and second-order spectra are qualitatively consistent with CPA predictions for the effects of isotopic disorder. Quantitative agreement between theory and experiment is achieved only if the reference DOS contains the above-mentioned peak. This supports the interpretation of the controversial second-order Raman peak in naturally abundant diamond (1.1 at. % ) at 2667 as a DOS effect. At all compositions, the effects of isotopic disorder are relatively weak because of the small mass difference between and . For 1.1 at. % , the maximum broadening predicted in the CPA is less than 1 , nearly two orders of magnitude smaller than a previous estimate. For the lowest-frequency modes most relevant to the thermal conductivity, the CPA scattering rate reduces to the usual dependence first derived by Klemens for phonon-isotope scattering. Using Callaway’s theory, we show that this term can easily account for the recently observed 50% enhancement in room-temperature thermal conductivity upon elimination of impurities, provided that sufficient normal scattering also occurs.
- Received 10 October 1991
DOI:https://doi.org/10.1103/PhysRevB.45.7171
©1992 American Physical Society
