In metastable particulate gels, it is tempting to believe that the dynamic similarities between the fluid-to-solid non-linear phase transition of rigidity percolation and the solid-to-fluid transition that occurs during yielding represent mirror images of the same continuous process. Even though these behaviors are clearly dynamically similar, their multi-scale nature makes it difficult to determine if they could also follow a unified structural pathway. We know from model monodisperse colloidal gels that both yielding and the elastic modulus seem to be heavily influenced by a small subset of topologically distinct singly-connected bridges linking mesoscale features. Here we use particle simulations to examine the participation of different classes of particle-level bonds and their contributions to the bulk mechanical response. We find that rigidity is disproportionately supported by singly connected intercluster bridges, whereas yielding localizes at bonds with high edge-betweenness centrality (EBC); strikingly, these independently identified populations substantially overlap and perform comparable mechanical roles. Bimodality exposes this correspondence by concentrating large-particle contacts in both populations, thereby providing a compositional label for the common backbone. Thus, rigidity and yielding are opposing mechanical manifestations of the same mesoscale structure: the intercluster bottlenecks that establish rigidity are also the sites at which rigidity is preferentially lost.
Colloidal gels are frequently modeled as monodisperse particle networks, although practical formulations commonly contain particles with multiple characteristic sizes. Here, we use large-scale, hydrodynamically resolved simulations of colloidal depletion gels to isolate the effects of particle size and local packing in...
Robert A. A. Campbell, Zi-Ye Zhuang, A. Mohraz et al.· 0 citations
Percolation in transient polymer networks remains poorly understood because reversible cross-links continuously reorganize the network structure. In this study, we investigated percolation in transient polymer networks by independently controlling network connectivity and polymer concentration in a well-defined Tetra...
Shota Michida, L. Jørgensen, Mitsuru Naito et al.· Macromolecules· 0 citations
Intrinsically disordered molecular systems, such as random copolymers and intrinsically disordered proteins, exhibit scale-invariant, power-law cluster distributions that cannot be explained by conventional mean-field theories. A fundamental challenge is to understand how sequence randomness, which cannot be averaged...
Chuan Tang, Yi-Fan Huang, Chun-Lai Ren et al.· Journal of the American Chem...· 0 citations
Classical contact mechanics is widely used to describe mechanical coupling in nanoparticle assemblies, yet its validity at the nanoscale remains experimentally unresolved. Here, we investigate size-dependent collective vibrational dynamics in self-assembled polystyrene nanoparticle films with particle diameters from 20...
Shaik Mohammad Imran, Nicholas Blanchard, B. Mahler et al.· Soft Matter· 0 citations
Biological materials such as the cytoskeleton and confluent cell monolayers are active, dense systems continuously subjected to internal stresses and strains, making their rheological characterization essential. While activity in soft matter can be modeled across multiple length scales, its mechanical consequences rema...
Raffaele Mendozza, Tobias Müller, P. Sollich· 0 citations
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