Relaxation in glassforming liquids and amorphous solids

被引:1924
作者
Angell, CA [1 ]
Ngai, KL
McKenna, GB
McMillan, PF
Martin, SW
机构
[1] Arizona State Univ, Dept Chem, Tempe, AZ 85287 USA
[2] USN, Res Lab, Washington, DC 20375 USA
[3] Texas Tech Univ, Dept Chem Engn, Lubbock, TX 79409 USA
[4] Iowa State Univ Sci & Technol, Dept Mat Sci & Engn, Ames, IA 50011 USA
关键词
D O I
10.1063/1.1286035
中图分类号
O59 [应用物理学];
学科分类号
摘要
The field of viscous liquid and glassy solid dynamics is reviewed by a process of posing the key questions that need to be answered, and then providing the best answers available to the authors and their advisors at this time. The subject is divided into four parts, three of them dealing with behavior in different domains of temperature with respect to the glass transition temperature, T-g, and a fourth dealing with "short time processes." The first part tackles the high temperature regime T > T-g, in which the system is ergodic and the evolution of the viscous liquid toward the condition at T-g is in focus. The second part deals with the regime T similar to T-g, where the system is nonergodic except for very long annealing times, hence has time-dependent properties (aging and annealing). The third part discusses behavior when the system is completely frozen with respect to the primary relaxation process but in which secondary processes, particularly those responsible for "superionic" conductivity, and dopart mobility in amorphous silicon, remain active. In the fourth part we focus on the behavior of the system at the crossover between the low frequency vibrational components of the molecular motion and its high frequency relaxational components, paying particular attention to very recent developments in the short time dielectric response and the high Q mechanical response. (C) 2000 American Institute of Physics. [S0021-8979(00)02213-1].
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页码:3113 / 3157
页数:45
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