We developed a facile ultrasonic vibration route is developed to synthesize BMGs and metallic glass-glass composites.

Glasses have markedly different stability around their glass transition temperature ( T _g ), and metallic glasses (MGs) are conventionally regarded as metastable compared to other glasses such as silicate glass or amber. Here, we show an aging experiment on a Ce-based MG around its T _g (~0.85 T _g ) for more than 17 years. We find that the MG with strong fragility could transform into kinetic and thermodynamic hyperstable state after the long-term room temperature aging and exhibits strong resistance against crystallization. The achieved hyperstable state is closer to the ideal glass state compared with that of other MGs and similar to that of the million-year-aged amber, which is attributed to its strong fragility and strong resistance against nucleation. It is also observed through the asymmetrical approaching experiment that the hyperaged Ce-based MG can reach equilibrium liquid state below T _g without crystallization, which supports the idea that nucleation only occurs after the completion of enthalpy relaxation.

Mechanical deformation of amorphous solids can be described as consisting of an elastic part in which the stress increases linearly with strain, up to a yield point at which the solid either fractures or starts deforming plastically. It is well established, however, that the apparent linearity of stress with strain is actually a proxy for a much more complex behavior, with a microscopic plasticity that is reflected in diverging nonlinear elastic coefficients. Very generally, the complex structure of the energy landscape is expected to induce a singular response to small perturbations. In the athermal quasistatic regime, this response manifests itself in the form of a scale-free plastic activity. The distribution of the corresponding avalanches should reflect, according to theoretical mean-field calculations [S. Franz and S. Spigler, Phys. Rev. E 95, 022139 (2017)], the geometry of phase space in the vicinity of a typical local minimum. In this work, we characterize this distribution for simple models of glass-forming systems, and we find that its scaling is compatible with the mean-field predictions for systems above the jamming transition. These systems exhibit marginal stability, and scaling relations that hold in the stationary state are examined and confirmed in the elastic regime. By studying the respective influence of system size and age, we suggest that marginal stability is systematic in the thermodynamic limit.

Amorphous materials have a rich relaxation spectrum, which is usually described in terms of a hierarchy of relaxation mechanisms. In this work, we investigate the local dynamic modulus spectra in a model glass just above the glass transition temperature by performing a mechanical spectroscopy analysis with molecular dynamics simulations. We find that the spectra, at the local as well as on the global scale, can be well described by the Cole-Davidson formula in the frequency range explored with simulations. Surprisingly, the Cole-Davidson stretching exponent does not change with the size of the local region that is probed. The local relaxation time displays a broad distribution, as expected based on dynamic heterogeneity concepts, but the stretching is obtained independently of this distribution. We find that the size dependence of the local relaxation time and moduli can be well explained by the elastic shoving model.