TY - JOUR
T1 - Network Evolution Controlling Strain-Induced Damage and Self-Healing of Elastomers with Dynamic Bonds
AU - Yin, Yikai
AU - Mohanty, Shaswat
AU - Cooper, Christopher B.
AU - Bao, Zhenan
AU - Cai, Wei
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/7/9
Y1 - 2024/7/9
N2 - Highly stretchable and self-healable supramolecular elastomers are promising materials for future soft electronics, biomimetic systems, and smart textiles, due to their dynamic cross-linking bonds. The dynamic or reversible nature of the cross-links gives rise to interesting macroscopic responses in these materials such as self-healing and rapid stress-relaxation. However, the relationship between bond activity and macroscopic mechanical response, and the self-healing properties of these dynamic polymer networks (DPNs) remains poorly understood. Using coarse-grained molecular dynamics (CGMD) simulations, we reveal a fundamental connection between the macroscopic behaviors of DPNs and the shortest paths between distant nodes in the polymer network. Notably, the trajectories of the material on the shortest path-strain map provide key insights into understanding the stress-strain hysteresis, anisotropy, stress relaxation, and self-healing of DPNs. Based on CGMD simulations under various loading histories, we formulate a set of empirical rules that dictate how the shortest path interacts with stress and strain. This lays the foundation for the development of a physics-based theory centered around the nonlocal microstructural feature of shortest paths to predict the mechanical behavior of DPNs.
AB - Highly stretchable and self-healable supramolecular elastomers are promising materials for future soft electronics, biomimetic systems, and smart textiles, due to their dynamic cross-linking bonds. The dynamic or reversible nature of the cross-links gives rise to interesting macroscopic responses in these materials such as self-healing and rapid stress-relaxation. However, the relationship between bond activity and macroscopic mechanical response, and the self-healing properties of these dynamic polymer networks (DPNs) remains poorly understood. Using coarse-grained molecular dynamics (CGMD) simulations, we reveal a fundamental connection between the macroscopic behaviors of DPNs and the shortest paths between distant nodes in the polymer network. Notably, the trajectories of the material on the shortest path-strain map provide key insights into understanding the stress-strain hysteresis, anisotropy, stress relaxation, and self-healing of DPNs. Based on CGMD simulations under various loading histories, we formulate a set of empirical rules that dictate how the shortest path interacts with stress and strain. This lays the foundation for the development of a physics-based theory centered around the nonlocal microstructural feature of shortest paths to predict the mechanical behavior of DPNs.
UR - https://www.scopus.com/pages/publications/85196643639
U2 - 10.1021/acs.macromol.4c00409
DO - 10.1021/acs.macromol.4c00409
M3 - Article
AN - SCOPUS:85196643639
SN - 0024-9297
VL - 57
SP - 6410
EP - 6418
JO - Macromolecules
JF - Macromolecules
IS - 13
ER -