Correlated excitations and Raman scattering in glasses

Abstract
The dominant Raman line in AX2 tetrahedral glasses is demonstrated to be caused by correlated symmetric stretch motions of the bridging X atoms. Using a bond-polarizability model and the central-force model of Sen and Thorpe, we derive simple analytic forms for Raman spectra. We show that correlations may cause qualitative changes in the polarized spectrum leading to a peak at the edge of a band of vibrational states, whereas the depolarized spectrum is less affected and mimics the density of states. Both features are clearly observed in GeO2 and explain features in many other glasses. The same reasoning leads to a prediction of unusual spectral features in electronic spectra of disordered solids which may be observable in angular-dependent photoemission.