电解质
违反直觉
盐(化学)
离子
化学
无机化学
化学工程
物理化学
有机化学
物理
电极
量子力学
工程类
作者
Anping Zhang,Endian Yang,Zhihong Bi,Gongrui Wang,Shihao Liao,Xiaofeng Li,Yan Yu,Qi Liu,Xinhe Bao,Zhong‐Shuai Wu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-02-14
卷期号:10 (3): 1245-1254
被引量:14
标识
DOI:10.1021/acsenergylett.4c03117
摘要
Elevating the charge cutoff voltage of LiCoO2 (LCO) from 4.4 to 4.7 V can significantly boost energy density. However, conventional electrolyte strategies encountering the viscosity and wettability obstacles for high-voltage LCO cannot tackle the issues of severe electrolyte decomposition, electrode–electrolyte interface degradation, and irreversible phase-transitions simultaneously. Herein, we achieved stable operation of commercial LCO at 4.7 V using a superwettable low-concentration fluoroborate dual-salt electrolyte (LFE). Our elaborated LFE (0.5 M) features an anion-enriched solvation structure that creates ultrathin, stable yet fast ion/electron transfer electrode/electrolyte interphases, significantly alleviating electrolyte decomposition, interface degradation, and injurious lithium dendrites. Consequently, LFE enables LCO to deliver a record capacity retention of 89.5% after 200 cycles and rate capability, far surpassing state-of-the-art 4.7 V-charged Li||LCO batteries. We assembled 1.25 Ah-class graphite||LCO pouch cells using LFE, achieving 100% capacity retention after 300 cycles and showcasing practicality. This work inaugurates an innovative pathway to maximize energy storage devices performance.
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