The Dynamics of Interacting Systems: Glassy Ionic Conductors and Glass-Forming Materials

1995 ◽  
Vol 411 ◽  
Author(s):  
K. L. Ngai ◽  
A. K. Rizos

ABSTRACTThe dynamics of densely packed interacting systems including glass-forming materials and glassy ionic conductors of various chemical and micro structures have been investigated experimentally by many workers, covering an immense time range from microscopic times shorter than 10−12 s to macroscopic times as long as 104 s. The short time dynamics is fundamental because it can directly reveal the microscopic mechanism of the relaxation. Several experimental investigations of structural relaxation in glass-forming substances have found that the short time dynamics shows exponential relaxation with a correlation function well described by exp(−t/τo) for t<tc where tc is temperature insensitive and has the order of magnitude of a picosecond. The correlation function then crosses over at tc to assumes the stretched exponential form, exp[−(t/τ)β], for t>tc. The relaxation times τ and τo are related by the expression τ = [tc−(1−β)τo]1/β. In this work, we focus on glassy ionic conductors and ionic glass-forming materials and experiments that employ dielectric spectroscopic and conductivity relaxation techniques, the theme of this Symposium. We show that these experimental data exhibit the same feature as described above for structural relaxation and are in accord with the predictions of the coupling model proposed by one of the authors.

2012 ◽  
Vol 1418 ◽  
Author(s):  
Kendra A. Erk ◽  
Jack F. Douglas

ABSTRACTThe shear stress relaxation of a thermally reversible, physically associating solution formed from a triblock copolymer in solvent selective for the mid-block was found to be well described over a broad temperature range by a stretched exponential function with a temperature independent ‘stretching exponent’, β ≈ 1/3. This same exponent value has been suggested to have particular significance in describing structural relaxation in a wide range of disordered viscoelastic materials ranging from associating polymer materials (‘gels’) to glass-forming liquids. We quantify the temperature dependence of the high frequency, or short time, shear modulus as function of temperature and find that this property also follows a variation often observed in gels and glass-forming materials.


2003 ◽  
Vol 118 (18) ◽  
pp. 8340-8349 ◽  
Author(s):  
A. G. Kalampounias ◽  
S. N. Yannopoulos ◽  
W. Steffen ◽  
L. I. Kirillova ◽  
S. A. Kirillov

1996 ◽  
Vol 455 ◽  
Author(s):  
J. Colmenero ◽  
A. Arbe ◽  
C. Mijangos ◽  
H. Reinecke

ABSTRACTThe so called “fast-dynamics” of glass-forming systems as observed by time of flight (TOF) neutron scattering techniques is revisited. TOF-results corresponding to several glass-forming polymers with different chemical microstructure and glass-transition temperature are presented together with the theoretical framework proposed by us to interpret these results. The main conclusion is that the TOF-data can be explained in terms of quasiharmonic vibrations and the particular short time behavior of the segmental dynamics. The segmental dynamics display in the very short time range (t ≈ 2 ps) a crossover from a simple exponential behavior towards a non-exponential regime. The first exponential decay, which is controlled by C-C rotational barriers, can be understood as a trace of the behavior of the system in absence of the effects (correlations, cooperativity, memory effects…) which characterize the dense supercooled liquid like state against the normal liquid state. The non-exponential regime at t > 2 ps corresponds to what is usually understood as α and β relaxations. Some implications of these results are also discussed.


1995 ◽  
Vol 103 (3) ◽  
pp. 1152-1159 ◽  
Author(s):  
C. M. Roland ◽  
K. L. Ngai

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