Free-volume microstructure of glycerol and its supercooled liquid-state dynamics

被引:59
作者
Bartos, J
Sausa, O
Kristiak, J
Blochowicz, T
Rössler, E
机构
[1] Univ Bayreuth, Inst Phys, D-95440 Bayreuth, Germany
[2] Slovak Acad Sci, Inst Phys, Bratislava 84228, Slovakia
关键词
D O I
10.1088/0953-8984/13/50/307
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
A positron annihilation lifetime spectroscopic (PALS) study was carried out on a typical representative of simple hydrogen-bonded glass formers-glycerol-over a wide temperature region from 100 K up to room temperature. Several crossover temperatures, T-bi, were identified in the temperature dependences of the ortho-positronium (o-Ps) lifetime and the relative o-Ps intensity. The onset temperature of free-volume change, 137 K, was compared with the value of 135 +/- 13 K obtained from extrapolating thermodynamic data and with the temperatures from relaxation data. In order to determine the influence of the free-volume evolution on the relaxation dynamics above the glass transition temperature T-g, the free-volume fraction from the PALS data was related to the behaviour of the dielectric loss of glycerol. A new relationship between the temperature parameters of the onset of free-volume change and of the high-frequency wing of the dielectric loss is presented. Taking the PALS free-volume data as input for a free-volume model (Doolittle ansatz), it was found that the relaxation times tau(alpha) can be reproduced above the bend temperature T-b2 = 241 K; the latter lies in the vicinity of crossover temperatures reported from mode coupling theory analyses of dynamic data. In the lower-temperature region T-b2 > T > T-bl congruent to T-g, a contribution from thermally activated mobility has to be included to reproduce the dielectric relaxation time data.
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页码:11473 / 11484
页数:12
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