Matthieu Bourguignon | Searcharxiv

arXiv2026

Amorphous Silicates -- Time-Current Superposition and the Dynamics of Plastic Flow in the Glassy State

Electron irradiation enables quantitative control over the plastic flow dynamics of silicate glasses, even far below the glass transition temperature. Through stress-relaxation experiments spanning ambient to near-glass-transition temperatures, we uncover a time-current equivalence that grants direct access to steady-state plastic flow over five decades in strain rate. This equivalence allows reconstruction of the intrinsic plastic-flow curve and quantitative assessment of the roles of network connectivity and temperature. Notably, the observed temperature dependence reveals a striking discrepancy with existing theoretical frameworks, highlighting the need for a comprehensive model of plastic flow dynamics in the glassy state.

cond-mat.soft↗

arXiv2026

Fracture initiation in silicate glasses via a universal shear localization mechanism

Shear bands lie at the root of fracture initiation in bulk metallic glasses and amorphous polymers. For silicate glasses, in contrast, studies have largely emphasized permanent volumetric strain, commonly referred to as densification. Here we systematically investigate indentation-induced fracture in two distinct families of aluminoborosilicate glasses. The results demonstrate that plastic shear flow plays a decisive role in governing fracture initiation. In addition, molecular dynamics simulations reveal a pronounced composition dependence of softening associated with plastic shear flow, closely mirroring the experimentally observed propensity for strain localization. We conclude that silicate glasses conform to a universal pattern of rupture initiation governed by localization of shear-deformation, aligning with a broad range of amorphous materials, including bulk metallic glasses and glassy polymers.

cond-mat.soft↗