电解质
材料科学
锂(药物)
共晶体系
电化学
电池(电)
阳极
硝酸锂
溶剂化
钝化
化学工程
成核
氧气
无机化学
纳米技术
电极
合金
化学
离子
热力学
冶金
物理化学
离子键合
医学
功率(物理)
物理
有机化学
工程类
内分泌学
图层(电子)
作者
Jiaxian Wang,Tiansheng Bai,Yihong Liang,Lin Xie,Hongqiang Zhang,Zhen Zeng,Siyu Fang,Dandan Gao,Wanbao Wu,Zhenglin Hu,Jingyu Lu,Jiaheng Zhang,Lijie Ci,Deping Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-03-15
标识
DOI:10.1021/acsnano.4c18523
摘要
Lithium–oxygen batteries (LOBs), with an extremely high theoretical energy density (3500 Wh kg–1), have been regarded as potential candidates for future large-scale energy storage facilities. However, the unique semiopen system puts a hurdle on the long-lasting operation of LOBs with critical issues like the severe volatilization of the aprotic electrolyte, surface passivation or dendrite growth of the lithium metal anode, and the sluggish oxygen redox reactions. Herein, we propose a strategy to tackle the above issues with a solvation structure regulated deep eutectic electrolyte (DEE) for LOBs. With modulated content of LiNO3 as the interface stabilizer, the Li/NMA-2.0/Li symmetric cell achieves a prolonged cycling stability of over 700 h under a semiopen O2 atmosphere. It can also operate in real air, while the good high temperature conductivity of the electrolyte enables the battery to cycle for more than 100 times at 60 °C. Besides, the solvation structure of the DEE electrolyte alters the discharge/charge reaction kinetics via lowering the nucleation energy of Li2O2, achieving the formation of nanoscale discharge products and realizing a superlong cyclability of 779 cycles at a high current density of 500 mA g–1. Moreover, the underlying mechanisms are well revealed through systematically designed experiments and theoretical simulations. This work will provide guidance in designing electrolytes for alkali-metal batteries and semiopen electrochemical systems.
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