Abstract
Generalizing the mode-coupling theory for ideal liquid-glass transitions, equations of motion are derived for the correlation functions describing the glassy dynamics of a diatomic probe molecule immersed in a simple glass-forming system. The molecule is described in the interaction-site representation and the equations are solved for a dumbbell molecule consisting of two fused hard spheres in a hard-sphere system. The results for the molecule's arrested position in the glass state and the reoricntational correlators for angular-momentum index / = 1 and / = 2 near the glass transition are compared with those obtained previously within a theory based on a tensor-density description of the molecule in order to demonstrate that the two approaches yield equivalent results. For strongly hindered reorientational motion, the dipole-relaxation spectra for the a process can be mapped on the dielectric-loss spectra of glycerol if a rescaling is performed according to a suggestion by Dixon et al. [Phys. Rev. Lett. 65, 1138 (1990)]. It is demonstrated that the glassy dynamics is inoependent of the molecule's inertia parameters.
Original language | English |
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Article number | 011206 |
Pages (from-to) | 112061-1120616 |
Number of pages | 1008556 |
Journal | Physical Review E - Statistical Physics, Plasmas, Fluids, and Related Interdisciplinary Topics |
Volume | 63 |
Issue number | 1 I |
DOIs | |
State | Published - 2001 |