电解质
阳极
锂(药物)
电池(电)
材料科学
金属锂
化学工程
金属
离子
耐久性
纳米技术
化学
无机化学
电极
复合材料
有机化学
冶金
物理
功率(物理)
物理化学
内分泌学
医学
量子力学
工程类
作者
Yantao Zhang,Zhengyang Gou,Kaiyang Zheng,Yaying Dou,Zhen Zhou
标识
DOI:10.1021/acs.jpclett.4c01549
摘要
Despite the impressive specific capacity of Li–O2 batteries, challenges persist, particularly with lithium metal anode (LMA). These include dendritic growth and unstable solid electrolyte interface (SEI) layers, which become more pronounced in an oxygen-rich environment, a typical operation scenario for Li–O2 batteries. Herein, utilizing a hybrid dual anion electrolyte (DAE) strategy, which incorporates both inorganic LiNO3 and organic Li[(FSO2)(C2F5SO2)N] (LiFPFSI) salts, the dendritic growth is evidently inhibited by creating a "concrete-like" SEI structure. Simultaneously, it fosters the development of a fluorine-rich SEI layer. Consequently, a robust, compact, and stable barrier is formed, adeptly suppressing side reactions between LMA and the electrolyte, particularly those relevant to dissolved O2. The practicality and efficiency of this DAE strategy are validated across a variety of battery types including Li/Li, Li/Cu, and notably Li–O2 batteries, which showcased significantly improved reversibility and durability. These results underscore the important role of multifunctional salts in interphase engineering for LMA, which could lead to advancements in Li–O2 batteries.
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