Probing the microscopic origin of toughness in multiple polymer networks

Abstract

Multiple polymer networks, such as double-network elastomers comprising a sacrificial and a matrix network, exhibit exceptional mechanical resilience, commonly attributed to the formation of an extended damage zone before a crack can grow. However, the microscopic mechanisms underlying their toughness remain poorly understood. Here, we combine advanced light scattering methods and molecular dynamics simulations to explore the microscopic relaxation dynamics and stress redistribution at the polymer strand scale of single-network and double-network elastomers under uniaxial loading. Dynamic light scattering experiments show that microscopic rearrangements and bond breaking events are localized near the crack tip in single networks, readily causing the crack to advance. In contrast, double networks exhibit delocalized microscopic rearrangements well ahead of and not directly correlated with crack propagation, enabling the dissipation of energy over broader regions and timescales. Numerical simulations of the damage zone show that bond breaking in the matrix network of double networks leads to widespread stress redistribution, mitigating catastrophic damage localization. This enhanced ability to redistribute stress in a nonlocal manner allows a much larger extension before localized macroscopic failure occurs, explaining the superior toughness of double networks. Our findings identify early, delocalized bond breaking events combined with more efficient dissipation pathways through enhanced microscopic rearrangements as the key microscopic mechanisms responsible for the outstanding toughness and extensibility of multiple elastomer networks.