Linking Equilibrium and Nonequilibrium Dynamics in Glass-Forming Systems

被引:24
|
作者
Guo, Xiaoju [1 ]
Smedskjaer, Morten M. [1 ,2 ]
Mauro, John C. [1 ]
机构
[1] Corning Inc, Sci & Technol Div, Corning, NY 14831 USA
[2] Aalborg Univ, Dept Chem & Biosci, DK-9220 Aalborg, Denmark
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2016年 / 120卷 / 12期
关键词
STRETCHED EXPONENTIAL RELAXATION; TOPOLOGICAL CONSTRAINT THEORY; ION-EXCHANGED GLASS; ENERGY LANDSCAPE; SUPERCOOLED LIQUIDS; STRUCTURAL RELAXATION; VISCOSITY; MODEL; TEMPERATURE; TRANSITION;
D O I
10.1021/acs.jpcb.6b00141
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
Understanding nonequilibrium glassy dynamics is of great scientific and technological importance. However, prediction of the temperature, thermal history, and composition dependence of nonequilibrium viscosity is challenging due to the noncrystalline and nonergodic nature of the glassy state. Here, we show that the nonequilibrium glassy dynamics are intimately connected with the equilibrium liquid dynamics. This is accomplished by deriving a new functional form for the thermal history dependence of nonequilibrium viscosity, which is validated against experimental measurements of industrial silicate glasses and computed viscosities for selenium over a wide range of conditions. Since the temperature and composition dependence of liquid viscosity can be predicted using temperature-dependent constraint theory, our work also opens the possibility to improve understanding of the physics of nonequilibrium viscosity.
引用
收藏
页码:3226 / 3231
页数:6
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