Transition from Arrhenius to non-Arrhenius temperature dependence of structural relaxation time in glass-forming liquids: continuous versus discontinuous scenario

• Published in: Physical review. E, Statistical, nonlinear, and soft matter physics Vol. 90; no. 3; p. 032308
• Main Authors: Popova, V A, Surovtsev, N V
• Format: Journal Article
• Language: English
• Published: United States 24-09-2014
• Subjects: Glass - chemistry; Light; Phase Transition; Picolines - chemistry; Salicylates - chemistry; Scattering, Radiation; Temperature; Terphenyl Compounds - chemistry
• ISSN: 1539-3755; 1550-2376
• DOI: 10.1103/physreve.90.032308

The temperature dependences of α relaxation time τ(α)(T) of three glass-forming liquids (salol, o-terphenyl, and α-picoline) were investigated by a depolarized light scattering technique. A detailed description of τ(α)(T) near T(A), the temperature of the transition from the Arrhenius law at high temperatures to a non-Arrhenius behavior of τ(α)(T) at lower temperatures, was done. It was found that this transition is quite sharp. If the transition is described as switching from the Arrhenius law to the Vogel-Fulcher-Tammann law, it occurs within the temperature range of about 15 K or less. Most of the known expressions for τ(α)(T) cannot describe this sharp transition. Our analysis revealed that this transition can be described either as a discontinuous transition in the spirit of the frustration-limited domain theory [D. Kivelson, G. Tarjus, X. Zhao, and S. A. Kivelson, Phys. Rev. E 53, 751 (1996)], implying a phase transition, or by a phenomenological expression recently suggested [B. Schmidtke, N. Petzold, R. Kahlau, M. Hofmann, and E. A. Rössler, Phys. Rev. E 86, 041507 (2012)], where the activation energy includes the term depending exponentially on temperature.