Title | How long do regions of different dynamics persist in supercooled o-terphenyl? |
Publication Type | Journal Article |
Year of Publication | 1999 |
Authors | Wang, C. Y., and M. D. Ediger |
Journal | Journal of Physical Chemistry BJ. Phys. Chem. B |
Volume | 103 |
Pagination | 4177-4184 |
Date Published | May |
Type of Article | Article |
ISBN Number | 1089-5647 |
Accession Number | WOS:000080565100030 |
Keywords | GLASS-FORMING LIQUIDS, HETEROGENEITIES, MOLECULES, POLYMERS, POLYSTYRENE, SPECTROSCOPY, STRUCTURAL RELAXATION, TRANSITION, VISCOUS-LIQUIDS, WILLIAMS-WATTS |
Abstract | In supercooled o-terphenyl (OTP), subsets of probe molecules in more mobile environments can be selectively photobleached. The time required for the remaining slower-than-average probes to be redistributed into an equilibrium set of environments has been measured. At T-g + 4 K (T-g = 243 K), this exchange time is 6 times greater than the average probe rotational correlation time. These results are compared to previous optical measurements at T-g + 1 K (Cicerone, M. T.; Ediger, M. D. J. Chem. Phys. 1995, 103, 5684), which showed that the exchange time is more than 100 times the rotational correlation time, and to multidimensional NMR experiments on deuterated OTP at T-g + 10 K (Bohmer, R.; et al. Europhys. Lett. 1996, 36, 55), which showed that the exchange time is nearly equal to the correlation time. These results in aggregate suggest that a new relaxation process in equilibrium supercooled liquids emerges only at temperatures very near T-g. A model for selective photobleaching is proposed. The model reproduces the experimental data reasonably well and indicates that the photobleaching efficiency of a given probe is only weakly correlated with its rotational correlation time. |
Alternate Journal | J. Phys. Chem. B |