The strain-stiffening critical exponents in polymer networks and their universality

Disordered athermal biopolymer materials, such as collagen networks that constitute a major component in extracellular matrices and various connective tissues, are initially soft and compliant but stiffen dramatically under strain. Such network materials are topologically sub-isostatic and feature strong rigidity scale separation between the bending and stretching response of the constituent polymer fibers. Recently, a comprehensive scaling theory of the athermal strain-stiffening phase transition has been developed, providing predictions for all mean-field critical exponents characterizing the transition in terms of the distance to the critical strain and of the small rigidity scales ratio. Here, we employ large-scale computer simulations, at and away from criticality, to test the analytic predictions. We find that all numerical critical exponents are in quantitative agreement with the analytically predicted ones. Moreover, we find that all predicted mean-field exponents remain valid whether the driving strain is shear, i.e., volume-preserving, or dilation, and independent of the degree of the network's sub-isostaticity, thus establishing the universality of the strain-stiffening phase transition with respect to the symmetry of the driving strain and the network's topology.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2025-09-16
DOI
https://doi.org/10.1063/5.0280785
Primary Topic
Cellular Mechanics and Interactions
Type
article
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article

The strain-stiffening critical exponents in polymer networks and their universality

Eran Bouchbinder, Edan Lerner, Zibin Zhang
The Journal of Chemical Physics
Cellular Mechanics and Interactions
article

The strain-stiffening critical exponents in polymer networks and their universality

Eran Bouchbinder, Edan Lerner, Zibin Zhang
article en

Abstract

Disordered athermal biopolymer materials, such as collagen networks that constitute a major component in extracellular matrices and various connective tissues, are initially soft and compliant but stiffen dramatically under strain. Such network materials are topologically sub-isostatic and feature strong rigidity scale separation between the bending and stretching response of the constituent polymer fibers. Recently, a comprehensive scaling theory of the athermal strain-stiffening phase transition has been developed, providing predictions for all mean-field critical exponents characterizing the transition in terms of the distance to the critical strain and of the small rigidity scales ratio. Here, we employ large-scale computer simulations, at and away from criticality, to test the analytic predictions. We find that all numerical critical exponents are in quantitative agreement with the analytically predicted ones. Moreover, we find that all predicted mean-field exponents remain valid whether the driving strain is shear, i.e., volume-preserving, or dilation, and independent of the degree of the network's sub-isostaticity, thus establishing the universality of the strain-stiffening phase transition with respect to the symmetry of the driving strain and the network's topology.

The Journal of Chemical PhysicsVol. 163(11)
American Committee for the Weizmann Institute of Science (US), Delta Institute for Theoretical Physics (NL), Weizmann Institute of Science (IL), University of Amsterdam (NL)
Openalex Percentile: Top 73%
Cellular Mechanics and Interactions
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The strain-stiffening critical exponents in polymer networks and their universality — Eran Bouchbinder, Edan Lerner, et al. · The Journal of Chemical Physics (2025) | TGRS Research Map | TGRS