电解质
聚己内酯
材料科学
阴极
阳极
锂(药物)
化学工程
限制
金属锂
聚合物
电化学
金属
能量密度
离子键合
热稳定性
聚合物电解质
电流密度
电池(电)
限制电流
无机化学
储能
热的
膜
电子设备和系统的热管理
电压
高压
阴极保护
作者
Ying Cheng Hu,ZiYi He,Qijie Yu,Yixiao Deng,Hao Yan,Tao Song,Chang Li,Jian Gu,J S Zheng,Yang Dai
出处
期刊:Small
[Wiley]
日期:2026-03-03
卷期号:22 (24): e14035-e14035
标识
DOI:10.1002/smll.202514035
摘要
ABSTRACT Integrating lithium‑rich/nickel‐rich high‑voltage cathodes with polycaprolactone‑based all‑solid‑state polymer electrolytes markedly boosts the safety and specific energy of all‐solid‑state batteries. However, interfacial incompatibility at high voltages poses a significant challenge for polycaprolactone (PCL)‐based all‐solid‐state polymer electrolytes (SPEs), therefore limiting their pairing in high‐voltage cathodes. Herein, YF 3 ‐improved PCL SPEs are designed for 4.5 V‐, and 4.8 V‐class all‐solid‐state lithium metal batteries (ASSLMBs). In modified SPEs, PCL carbonyl groups donate electron density to YF 3 , weakening Li + ‐polymer coordination and thus promoting ionic conductivity, while YF 3 with Lewis‐acid properties simultaneously improves anti‐oxidation capability. The optimized membrane delivers 5.1 V oxidative stability, high thermal robustness, and forms stable cathodic and anodic interphases. Remarkably, Ni‐rich (NCM9055) cells with the optimized electrolyte achieve 500 cycles at 4.5 V with 69.8% capacity retention, while Li‐rich cells sustain 200 cycles at 4.8 V – performance that was previously difficult to achieve. This YF 3 /PCL design validates a practical route and offers a unique dual‐interface stabilization strategy for high‐voltage ASSLMBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI