Time is length in self-similar logarithmic aging of physically cross-linked semiflexible polymer networks
arXiv:2510.12989 · doi:10.1103/1slf-41nm
Abstract
Physical aging in polymers is a fundamental yet poorly understood phenomenon, as diverse macromolecular systems exhibit remarkably similar slow dynamics. Through molecular dynamics simulations of physically crosslinked networks composed of semiflexible polymers, we identify a previously unexplored class of self-similar aging. The network undergoes ultra-slow coarsening characterized by a logarithmically growing mesh size, , which governs the spatial organization, cohesive and bending energies, and the aging dynamics of the system. This single time-dependent length scale defines an internal clock, giving rise to spatio- temporal self-similarity of both structure and dynamics - offering a perspective on aging in soft and disordered materials.
7 pages, 7 figures
References in corpus (7)
- Dynamics and structure of an aging binary colloidal glass
- Subdiffusion and intermittent dynamic fluctuations in the aging regime of concentrated hard spheres
- Self-assembly and cooperative dynamics of a model colloidal gel network
- Logarithmic aging via instability cascades in disordered systems
- Coarsening and Aging of Lattice Polymers: Influence of Bond Fluctuations
- On weak ergodicity breaking in mean-field spin glasses
- Aging Phenomena during Phase Separation in Fluids: Decay of autocorrelation for vapor-liquid transitions