Establishing intrinsic structure–property relationships in amorphous solids remains a central challenge in materials science because the absence of long-range order obscures universal structural descriptors. Here, we introduce a structural disorder function, S d ( r ), as a physically interpretable and quantitative metric for atomic-scale disorder in amorphous systems. S d ( r ) is formulated as the magnitude of the normalized vector sum from a reference atom to its neighbors within different radial shells, thereby capturing local symmetry breaking analogous in concept to the Burgers vector in crystals. Molecular dynamics simulations across diverse amorphous alloys and glasses, together with colloidal-glass experiments, demonstrate that S d ( r ) correlates meaningfully (correlation coefficient > 0.68) with key particle-scale plastic properties, including vibrational mean-square displacement, flexibility volume, atomic stiffness, and vibrational frequency. Liquid-like regions consistently exhibit higher S d ( r ) values than solid-like ones, revealing its ability to distinguish mechanical heterogeneity. When averaged over the field, S d monotonically increases with cooling rate and exhibits a universal negative linear relationship with shear strength, τ p = A – B S d , quantitatively linking structural disorder to macroscopic strength. These results establish S d ( r ) as a simple, dimensionless, and broadly applicable descriptor that unifies atomic configuration, processing history, and mechanical response in disordered materials, providing a physics-based framework for the rational design of amorphous solids.
Ding et al. (Fri,) studied this question.