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Lewis Acid and Hydroxyl Enabled PEO Electrolytes for Solid-State Lithium Metal Batteries

Authors: WANG Rui-Qing; QIU Zhao-Dong; WANG Lin-Dong; FAN Yi-Qi; HU Zhi-Yi; ZHANG Xi-Kun; DENG Zhao; CHEN Li-Hua; LI Yu; SU Bao-Lian

DOI: 10.1007/s40843-026-4321-xStatus: Verified Translated Edition
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Key Findings in This Report

• • Ionic conductivity of 8.3 × 10-4 S cm-1 at 60 ℃ exceeds conventional PEO-LiTFSI electrolytes by roughly an order of magnitude, directly enabling higher current densities and faster charging in solid-state cells. • • Li+ transference number of 0.57 (vs. ~0.2 for pristine PEO) reduces concentration polarization, mitigating lithium dendrite nucleation and extending cycle life under practical areal capacities. • • Electrochemical stability window of 5.2 V supports high-voltage cathodes (e.g., NMC622, NMC811) without oxidative decomposition, broadening the accessible energy density beyond 4 V-class systems. • • Li||Li symmetric cells sustain over 1200 h at 0.1 mA cm-2, and LFP||Li full cells retain 80% capacity after 400 cycles at 0.5 C, demonstrating industrial-grade cycling durability for stationary and EV applications.
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