Abstract
The concept of mean-field rigidity percolation at average coordination number 〈r〉=2.4 in covalently bonded inorganic glasses is shown to be relevant to the liquid-state behavior of glass-forming chalcogenide systems. In particular it correlates with remarkable variations in ‘‘fragility’’ and excess heat capacity which we observe in the model ternary system Ge-As-Se. Except near , itself depends only on 〈r〉 anywhere in the system up to 〈r〉=2.5. These findings provide an important link between key structural concepts of glass science, the relaxation phenomena, and the thermodynamic problem embodied in the Kauzmann paradox.
- Received 18 December 1989
DOI:https://doi.org/10.1103/PhysRevLett.64.1549
©1990 American Physical Society