Dynamics of strong and fragile glass formers: Differences and correlation with low-temperature properties
- 27 September 1993
- journal article
- research article
- Published by American Physical Society (APS) in Physical Review Letters
- Vol. 71 (13), 2062-2065
- https://doi.org/10.1103/physrevlett.71.2062
Abstract
Low-frequency Raman spectra of strong and fragile glass forming liquids were measured in a wide temperature range. From an analysis of the spectra and literature data it is found that the main difference in the dynamic structure factor is the ratio of vibrational to relaxational contributions: The stronger the glass former the higher this ratio. It is shown that this difference survives even at very low temperatures and determines the low-temperature anomalies of glasses. A possible way how the observed difference influences the fragility of a liquid is discussed.Keywords
This publication has 21 references indexed in Scilit:
- Evaluation of density of vibrational states of glasses from low-frequency Raman spectraPhysical Review B, 1993
- Secondary relaxation in the glass-transition regime ofortho-terphenyl observed by incoherent neutron scatteringPhysical Review B, 1992
- Testing mode-coupling predictions for α and β relaxation in ( near the liquid-glass transition by light scatteringPhysical Review A, 1992
- Relaxation processes in supercooled liquidsReports on Progress in Physics, 1992
- Dynamic anomaly in the glass transition region of orthoterphenylZeitschrift für Physik B Condensed Matter, 1991
- Localized Motion in Supercooled Glycerol as Measured by 2 H-NMR Spin-Lattice Relaxation and Incoherent Neutron ScatteringEurophysics Letters, 1991
- Low-temperature behavior of potassium and sodium silicate glassesPhysical Review B, 1985
- Heat Capacity and Thermodynamic Properties of o-Terphenyl Crystal, Glass, and LiquidThe Journal of Chemical Physics, 1972
- Viscosity of a vitreous potassium nitrate - calcium nitrate mixtureThe Journal of Physical Chemistry, 1969
- Inadequacies of Viscosity Theories for B2O3The Journal of Chemical Physics, 1968