Solid polymer electrolytes in lithium metal batteries (LMBs) are susceptible to mechanical damage from lithium dendrite puncture and deformation. Although integrating self-healing functionality helps to alleviate this issue, it typically compromises either mechanical strength or ionic conductivity. To overcome this trade-off, self-healing electrolytes (AUx-BMIMy IGEs) were developed through the synergistic combination of ureido pyrimidinone (UPy)-based polymers and an imidazolium ionic liquid. The designed supramolecular networks feature quadruple hydrogen bonds from UPy units and ion-dipole interactions between imidazolium cations and polymer carbonyl groups. The mechanical strength of the electrolyte is enhanced by these dynamic reversible bonds, while the exceptional self-healing efficiency is enabled by their capacity for rapid reorganization. The ionic liquid further enhances the ionic conductivity. The optimized IGEs, named as AU7-BMIM15 IGEs, balance the tensile stress of 1.26 MPa, the ionic conductivity of 3.40 × 10-4 S cm-1, and ultrahigh self-healing efficiencies. After being cut and healed at 45 °C for merely 1 h, the Healed-AU7-BMIM15 IGEs achieved healing efficiencies of 97.6% in tensile strength and 99.1% in ionic conductivity. This efficient healing capability contributes to the remarkable stability of lithium plating/stripping. The Li||Li symmetric cell assembled with Healed-AU7-BMIM15 IGEs stably cycled for over 4500 h at 0.1 mA cm-2. Furthermore, a Li||LiFePO4 cell using Healed-AU7-BMIM15 IGEs delivered cycling for 2000 h at 0.2 C with an average Coulombic efficiency exceeding 99%, performing comparably to fresh AU7-BMIM15 IGEs. The practical viability was further underscored by multipoint puncture tests. The AU7-BMIM15 IGE with 16 puncture sites retained a critical current density of 0.30 mA cm-2 after being healed at 45 °C for 1 h. This work demonstrates a promising strategy for creating self-healing electrolytes for next-generation LMBs.
Li et al. (Thu,) studied this question.