Abstract
We propose a model for the description of the low-temperature orientational glass transition in solid molecular using the basic concepts and methods of spin-glass and multipole-glass theory. The physical origin of the frustration and the disorder is discussed. We obtain coexistence of orientational and glass orders in the glass phase and a broad maximum of the orientational specific heat in agreement with experimental data. The orientational ordering under pressure is discussed.
- Received 22 February 2007
DOI:https://doi.org/10.1103/PhysRevB.76.195408
©2007 American Physical Society