Abstract This present study illustrates the synthesis and preparation of polyoxanorbornene‐based bottlebrush polymers with poly(ethylene oxide) (PEO) side chains by ring‐opening metathesis polymerization for solid polymer electrolytes (SPE). In addition to the conductive PEO side chains, the polyoxanorbornene backbones may act as another ion conductor to further promote Li‐ion movement within the SPE matrix. These results suggest that these bottlebrush polymer electrolytes provide impressively high ionic conductivity of 7.12 × 10−4S cm−1at room temperature and excellent electrochemical performance, including high‐rate capabilities and cycling stability when paired with a Li metal anode and a LiFePO4cathode. The new design paradigm, which has dual ionic conductive pathways, provides an unexplored avenue for inventing new SPEs and emphasizes the importance of molecular engineering to develop highly stable and conductive polymer electrolytes for lithium‐metal batteries (LMB).
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Novel Zwitterionic Polyurethane‐in‐Salt Electrolytes with High Ion Conductivity, Elasticity, and Adhesion for High‐Performance Solid‐State Lithium Metal Batteries
Abstract This study presents a novel polymer‐in‐salt (PIS) zwitterionic polyurethane‐based solid polymer electrolyte (zPU‐SPE) that offers high ionic conductivity, strong interaction with electrodes, and excellent mechanical and electrochemical stabilities, making it promising for high‐performance all solid‐state lithium batteries (ASSLBs). The zPU‐SPE exhibits remarkable lithium‐ion (Li+) conductivity (3.7 × 10⁻⁴ S cm−1at 25 °C), enabled by exceptionally high salt loading of up to 90 wt.% (12.6 molar ratio of Li salt to polymer unit) without phase separation. It addresses the limitations of conventional SPEs by combining high ionic conductivity with a Li+transference number of 0.44, achieved through the incorporation of zwitterionic groups that enhance ion dissociation and transport. The high surface energy (338.4 J m−2) and elasticity ensure excellent adhesion to Li anodes, reducing interfacial resistance and ensuring uniform Li+flux. When tested in Li||zPU||LiFePO₄ and Li||zPU||S/C cells, the zPU‐SPE demonstrated remarkable cycling stability, retaining 76% capacity after 2000 cycles with the LiFePO4cathode, and achieving 84% capacity retention after 300 cycles with the S/C cathode. Molecular simulations and a range of experimental characterizations confirm the superior structural organization of the zPU matrix, contributing to its outstanding electrochemical performance. The findings strongly suggest that zPU‐SPE is a promising candidate for next‐generation ASSLBs.
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- PAR ID:
- 10638245
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Energy Materials
- Volume:
- 15
- Issue:
- 30
- ISSN:
- 1614-6832
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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