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Subject: Glass transition × WGL Institute: IFWD ×

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    Rejuvenation through plastic deformation of a La-based metallic glass measured by fast-scanning calorimetry
    (Amsterdam : Elsevier B.V., 2020) Meylan, C.M.; Orava, J.; Greer, A.L.
    We explore the glassy states achievable after a metallic glass is formed on liquid quenching. Samples of La55Al25Ni20 (at.%) metallic glass (rod and ribbon) are studied. The extent of structural relaxation at room temperature is characterized for this low-glass-transition temperature glass. Plastic deformation (uniaxial compression) rejuvenates the glass to states of higher enthalpy characteristic of glass formation at high cooling rate. Deformation increases the heterogeneity of the glass, widening the spectrum of relaxation times. The extent of rejuvenation in samples of low aspect ratio is compared with that under conditions of high constraint in notched samples. The deformation-induced rejuvenation is particularly susceptible to reduction on subsequent ageing. Fast-scanning calorimetry is useful in characterizing the dynamics of structural relaxation. The shadow glass transition is more evident on fast heating, and is observed in this glass for the first time. A new excess exothermic effect is observed before the glass transition.
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    A phase space approach to supercooled liquids and a universal collapse of their viscosity
    (Lausanne : Frontiers Media, 2016) Weingartner, Nicholas B.; Pueblo, Chris; Nogueira, Flavio S.; Kelton, K. F.; Nussinov, Zohar
    A broad fundamental understanding of the mechanisms underlying the phenomenology of supercooled liquids has remained elusive, despite decades of intense exploration. When supercooled beneath its characteristic melting temperature, a liquid sees a sharp rise in its viscosity over a narrow temperature range, eventually becoming frozen on laboratory timescales. Explaining this immense increase in viscosity is one of the principle goals of condensed matter physicists. To that end, numerous theoretical frameworks have been proposed, which explain and reproduce the temperature dependence of the viscosity of supercooled liquids. Each of these frameworks appears only applicable to specific classes of glassformers, and each possesses a number of variable parameters. Here, we describe a classical framework for explaining the dynamical behavior of supercooled liquids based on statistical mechanical considerations, and possessing only a single variable parameter. This parameter varies weakly from liquid to liquid. Furthermore, as predicted by this new classical theory and its earlier quantum counterpart, we find with the aid of a small dimensionless constant that varies in size from ∼0.05 to 0.12, a universal (16 decades) collapse of the viscosity data as a function of temperature. The collapse appears in all known types of glass-forming supercooled liquids (silicates, metallic alloys, organic systems, chalcogenide, sugars, and water).