Thermodynamic behavior of glass-forming metallic supercooled liquids

2013 ◽  
Vol 426 ◽  
pp. 1-5 ◽  
Author(s):  
M.B. Tang ◽  
J.T. Zhao
2008 ◽  
Vol 607 ◽  
pp. 48-52 ◽  
Author(s):  
Josef Bartoš

A phenomenological description of the ortho-positronium (o-Ps) response from positron annihilation spectroscopy (PALS) and the dynamics from viscosity studies on two typical glass-forming compounds within the framework of the two-order parameter (TOP) model is presented. The dynamical data are accounted for by the modified Vogel – Fulcher – Tamman - Hesse (M-VFTH) equation. Subsequently, the quasi-sigmoidal course of the o-Ps lifetime, τ3, with or without the high-temperature plateau region as a function of the temperature over a wide temperature range can be described by an effective free volume version of the TOP model. This simultaneous description suggests a close relationship between the PALS response and the dynamics of supercooled liquids and seems to support the liquid - like and solid - like domain physical picture of all the three physical states of the disordered phase of the condensed systems.


2016 ◽  
Vol 18 (10) ◽  
pp. 7169-7183 ◽  
Author(s):  
M. H. Yang ◽  
Y. Li ◽  
J. H. Li ◽  
B. X. Liu

Molecular dynamics simulation with well-developed EAM potentials was carried out to investigate the transport properties and local atomic structure of Cu–Zr and Ni–Zr metallic glasses and supercooled liquids.


2007 ◽  
Vol 19 (11) ◽  
pp. 116103 ◽  
Author(s):  
Jing Guo ◽  
Xiufang Bian ◽  
Yan Zhao ◽  
Shijiao Zhang ◽  
Taibao Li ◽  
...  

1996 ◽  
Vol 464 ◽  
Author(s):  
X. Yan ◽  
C. Streck ◽  
R. Richert

ABSTRACTThe orientational dynamics of organic supercooled liquids of low molecular weight confined to the geometry of porous glasses are studied by two highly related techniques, the optical method of probing the dynamics of solvation regarding a chromophoric host molecule and dielectric relaxation spectroscopy. The dielectric results display marked effects of the confinement to mesopores in terms of altered structural dynamics which appear to separate into a raster and slower responses relative to the bulk liquid. We also demonstrate that there is no trivial relation between the ε*(ω) data and the liquid dynamics in these heterogeneous samples. These effects are partially paralleled by the solvation dynamics results, but with the spatial range inherent in the optical technique being inconsistent with associating the fast and slow dynamical components to spatially distinct regimes. We conclude on the slow component being a signature of non-ergodicity which arises from the competition between the length scale of cooperativity and the pore size.


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