Abstract
The first Ioffe-Regel crossover for vibrational plane waves (when wavelength and mean free path are comparable) has been investigated theoretically for models of vitreous silica $(v\ensuremath{-}{\mathrm{SiO}}_{2})$ constructed by molecular dynamics. The crossover is found to be from a state of weak scattering to one of strong scattering, not vibrational localization. Three methods have been used to investigate the crossover: an analysis of the time evolution of a vibrational plane wave, a spectral-density analysis in frequency space, and an analysis of the final scattered state in momentum space. The first Ioffe-Regel crossover frequency is found by all three methods to be $\ensuremath{\sim}1$ THz for $v\ensuremath{-}{\mathrm{SiO}}_{2},$ for both longitudinal and transverse polarizations. A second Ioffe-Regel crossover occurs at $\ensuremath{\sim}6$ THz for $v\ensuremath{-}{\mathrm{SiO}}_{2},$ corresponding to the frequency at which the mean free path is minimal (comparable to the interatomic spacing), and the spectral-density width is maximal (comparable to the frequency range of the vibrational density of states).
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