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Giant activity-induced elasticity in entangled polymer solutions
Davide Breoni1,2,3, Christina Kurzthaler4,5,6, Benno Liebchen7
1Institut für Theoretische Physik II: Weiche Materie, Heinrich Heine-Universität Düsseldorf, Universitätsstraße 1, 40225, Düsseldorf, Germany.
Nature Communications
|June 12, 2025
Summary
Active polymers exhibit enhanced elasticity and fluidization due to self-propulsion. Brownian dynamics simulations reveal grip forces at entanglements, altering scaling laws for polymer length and viscosity.
Area of Science:
- Polymer Physics
- Soft Matter Physics
- Materials Science
Background:
- Equilibrium polymer physics predicts scaling laws for viscoelastic properties in natural and synthetic polymers.
- Active polymer systems, driven far from equilibrium, are gaining importance but their viscoelastic properties remain poorly understood.
Purpose of the Study:
- To investigate the viscoelastic properties of highly-entangled, flexible self-propelled polymers.
- To understand the impact of activity on polymer system dynamics and scaling laws.
Main Methods:
- Brownian dynamics simulations were employed.
- The study focused on highly-entangled, flexible self-propelled polymers.
Main Results:
- Activity significantly enhances elasticity, scaling with polymer length (∼ L) due to grip forces at entanglement points.
- Activity fluidizes the suspension, with long-time viscosity scaling as ∼ L², a change from passive systems (∼ L³).
Conclusions:
- Self-propulsion in polymers dramatically alters viscoelastic properties.
- These findings pave the way for designing novel activity-responsive polymeric materials.
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