The slow energy relaxation in quenched glasses is a ubiquitous yet poorly understood phenomenon. Despite extensive study, the microscopic origin of the observed power-law decay remains debated, with proposed mechanisms ranging from saddle-point slowdown and marginal stability to coarsening of localized excitations and phonon dynamics. Here, by simulating gradient descent in archetypal structural glass formers, we show that none of these scenarios can account for our data. Instead, the power-law behavior emerges from a remarkably simple caging effect: each particle experiences an effective stiffening potential that arises from many-body confinement and diverges at a characteristic cage size. This mechanism analytically yields the observed power-law decay and is quantitatively reproduced by a minimal single-particle cage model with fixed neighbours, demonstrating that collective relaxation modes are not essential. The dynamics is punctuated by fluctuations as the system rolls through inflection points on the energy landscape, which act as `speed bumps'but do not affect the overall power-law behaviour. In contrast to mean-field spin glass theory, we find no characteristic temperature that separates distinct dynamical regimes; state following within a given glass basin occurs universally for all initial temperatures whenever the system is sufficiently close to the inherent structure. Our results establish a complete physical picture of gradient descent dynamics in typical structural glasses.
Soft materials store, dissipate and release mechanical stresses through relaxation processes that often span many orders of magnitude in time. Such relaxation spectra are widely used to infer internal material dynamics and are usually regarded as fingerprints of microscopic complexity, disorder, or heterogeneity. Here...
Niloyendu Roy, Rupayan Saha, Debankur Das et al.· 0 citations
We investigate the slowing down of dynamics in a glass-forming mixture interacting via an inverse-power-law (IPL) potential using a combination of theory and large-scale molecular dynamics simulations. We measure the static pair-correlation function, configurational entropy, inherent-structure energy, and structural re...
Ankit Singh, Vinay Vaibhav, S. L. Singh et al.· 0 citations
On cooling liquids towards their glass-transition temperature, the dramatic increase of their relaxation times is accompanied by changes in particle dynamics at two distinct temperatures: A high-T crossover, where particles become temporarily caged by their neighbors, and a low-T crossover, where the cage escape mechan...
Kamlesh B. Mishra, R. Ganapathy, Walter Kob· 0 citations
The dramatic slowing down of structural relaxation in supercooled liquids is accompanied by the emergence of dynamic heterogeneity. A monotonically increasing dynamical correlation length, measured at the $\alpha$-timescale, is one of the remarkable features of this phenomenon. Here we show that this picture is incompl...
Corentin C. L. Laudicina, Ilian Pihlajamaa, Liesbeth M. C. Janssen et al.· 0 citations
Microscopic nonequilibrium statistical mechanical theory is employed to construct a unified framework for the prototypical soft matter system of dense Brownian colloidal suspensions with short-range attractive interactions under continuous step-rate shear deformation and the subsequent re-equilibration dynamics after s...
Anoop Mutneja, Kenneth S. Schweizer· Soft Matter· 0 citations
Diffusion in rugged energy landscapes is central to chemical physics, with relevance to glasses, disordered solids, and biomolecular motion. Most theories assume quenched disorder, but in many condensed-phase and biological systems, local energies fluctuate because of solvent reorganization, structural relaxation, or c...
Biman Bagchi· Journal of Chemical Physics· 0 citations
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