A detailed test of mode-coupling theory on all time scales: Time domain studies of structural relaxation in a supercooled liquid

被引:76
作者
Hinze, G [1 ]
Brace, DD
Gottke, SD
Fayer, MD
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] Johannes Gutenberg Univ Mainz, Inst Phys Chem, D-55099 Mainz, Germany
关键词
D O I
10.1063/1.1287595
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The dynamics of supercooled salol (phenyl salicylate) was measured in the time domain using optical Kerr effect techniques. By combining several experimental setups, data spanning more than six decades in amplitude and time (similar to 100 fs to similar to 1 mu s) were observed. The data have a complex shape, ranging from high-frequency intramolecular oscillations at short times, to nearly exponential relaxation at long times. As predicted by mode-coupling theory (MCT), the data for some ranges of time appear as power laws. The slowest power law, the von Schweidler power law, has an almost constant exponent of similar to 0.59 over the entire temperature range studied (247-340 K). Above the MCT T-c (T > similar to 1.17 T-g, where T-g is the laboratory glass transition temperature) for t > similar to 1 ps, the decays are shown to be in excellent agreement with the master curve predicted by ideal MCT when higher order terms are included. However, the data do not display the plateau predicted by ideal MCT. To discuss the data at all temperatures, the intermediate time scale portion of the data, 2 < t < 10 to 500 ps (depending on the temperature), is modeled as a power law that falls between the critical decay and the von Schweidler power law. This intermediate power law shows significant temperature dependence with an exponent that decreases to a value of similar to -1 below T-c. Calculations using extended MCT, for a full range of hopping times, demonstrate that the temperature dependence of the intermediate time scale data near and below T-c cannot be explained by extended MCT. (C) 2000 American Institute of Physics. [S0021-9606(00)50833-2].
引用
收藏
页码:3723 / 3733
页数:11
相关论文
共 70 条
[1]   PERSPECTIVE ON THE GLASS-TRANSITION [J].
ANGELL, CA .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 1988, 49 (08) :863-871
[2]   Merging of the alpha and beta relaxations in polybutadiene: A neutron spin echo and dielectric study [J].
Arbe, A ;
Richter, D ;
Colmenero, J ;
Farago, B .
PHYSICAL REVIEW E, 1996, 54 (04) :3853-3869
[3]   Depolarized light scattering spectroscopy of Ca0.4K0.6(NO3)1.4:: A reexamination of the "knee" [J].
Barshilia, HC ;
Li, G ;
Shen, GQ ;
Cummins, HZ .
PHYSICAL REVIEW E, 1999, 59 (05) :5625-5628
[4]   The glass transition dynamics of polymer micronetwork colloids. A mode coupling analysis [J].
Bartsch, E ;
Frenz, V ;
Baschnagel, J ;
Schartl, W ;
Sillescu, H .
JOURNAL OF CHEMICAL PHYSICS, 1997, 106 (09) :3743-3756
[5]  
Bartsch E., 1995, Transport Theory and Statistical Physics, V24, P1125, DOI 10.1080/00411459508203947
[6]   Dynamics around the liquid-glass transition in poly(propylene-glycol) investigated by wide-frequency-range light-scattering techniques [J].
Bergman, R ;
Borjesson, L ;
Torell, LM ;
Fontana, A .
PHYSICAL REVIEW B, 1997, 56 (18) :11619-11628
[7]  
BERNE BJ, 1990, DYNAMICAL LIGHT SCAT
[8]   NONEXPONENTIAL RELAXATIONS IN STRONG AND FRAGILE GLASS FORMERS [J].
BOHMER, R ;
NGAI, KL ;
ANGELL, CA ;
PLAZEK, DJ .
JOURNAL OF CHEMICAL PHYSICS, 1993, 99 (05) :4201-4209
[9]  
Bottcher C. J. F., 1992, THEORY ELECT POLARIZ
[10]   LOW-FREQUENCY MODES IN VITREOUS SILICA [J].
BUCHENAU, U ;
PRAGER, M ;
NUCKER, N ;
DIANOUX, AJ ;
AHMAD, N ;
PHILLIPS, WA .
PHYSICAL REVIEW B, 1986, 34 (08) :5665-5673