Abstract
Self-healing materials can prolong device life, but their relatively weak mechanical strength limits their applications. Introducing tunable metal-ligand interactions into self-healing systems can improve their mechanical strength. However, applying this concept to solid elastomers is a challenge. To address this need, polyurethane-containing metal complexes were fabricated by introduction of a pyridine-containing ligand into polyurethane, and subsequent coordination with Fe2+. The strong reversible coordination bond provides mechanical strength and self-healing ability. By optimizing the monomer ratio and Fe2+ content, the resulting complex possesses a very high tensile strength of 4.6MPa at strain of around 498% and a high Young's modulus (3.2MPa). Importantly, the metal complex exhibits an extremely high self-healing efficiency of approximately 96% of tensile strength at room temperature and around 30% at 5 degrees C. The complex is notch-insensitive and the fracture energy is 76186J/m(2), which is among the highest reported values for self-healing systems.
Original language | English |
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Pages (from-to) | 432-440 |
Number of pages | 9 |
Journal | ChemPlusChem |
Volume | 84 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr-2019 |
Keywords
- Elastomers
- metal coordination
- notch-insensitivity
- polyurethane self-healing
- SUPRAMOLECULAR GELS
- MECHANICAL-PROPERTIES
- SOFT MATERIALS
- HYDROGELS
- POLYMERS
- NETWORK
- COMPLEXES
- CHEMISTRY
- BONDS