Ultimately deformed double-network gels possess positive energetic elasticity

TL;DR

This paper reveals that highly deformed double-network gels transition from entropy-driven to energy-driven elasticity, emphasizing the role of chemical bond deformation in their mechanical behavior.

Contribution

It introduces a thermodynamic analysis and a simple mechanical model showing the energetic contribution dominates elasticity in highly deformed double-network gels.

Findings

Elasticity transitions from entropy to energy dominance with deformation

Developed a model reproduces temperature-dependent stress-strain behavior

Highlights chemical bond deformation's importance in rubbery networks

Abstract

The elasticity of rubbery polymer networks has been considered to be entropy-driven. On the other hand, studies on single polymer chain mechanics have revealed that the elasticity of ultimately stretched polymer chains is dominated by the energetic contribution mainly originating from chemical bond deformation. Here, we experimentally found that the elasticity of the double-network gel transits from the entropy-dominated one to the internal energy-driven one with its uniaxial deformation through the thermodynamic analysis. Based on this finding, we developed a simple mechanical model that takes into account the energetic contribution and found that this model approximately reproduces the temperature dependence of the stress-strain curve of the double-network gel. This study demonstrates the importance of the chemical perspective in the mechanical analysis of highly deformed rubbery polymer networks.