材料科学
卤化物
氟化锂
电化学窗口
电化学
电负性
氟
X射线光电子能谱
电解质
金属
兴奋剂
锂(药物)
氟化物
化学工程
快离子导体
无机化学
离子电导率
电极
物理化学
化学
有机化学
冶金
内分泌学
工程类
医学
光电子学
作者
Tianwei Yu,Jianwen Liang,Liang Luo,Limin Wang,Feipeng Zhao,Guofeng Xu,Xiangtao Bai,Rong Yang,Shangqian Zhao,Jiantao Wang,Jinqiu Yu,Xueliang Sun
标识
DOI:10.1002/aenm.202101915
摘要
Abstract The halide solid‐state electrolytes (SSEs) have received significant attention due to their high ionic conductivity and desirable compatibility with cathode materials. However, the reduction potential of the halide is still >0.6 V (versus Li/Li + ). Reduction stability is still one of the challenges that need to be addressed. The fluorides have a wide electrochemical stability window due to the large electronegativity of F – . In contrast, Li 3 YBr 6 (LYB) bromides have a narrower electrochemical window, although they have high lithium ion conductivity (>10 –3 S cm –1 ). Herein, a fluorine doping strategy is employed. The interfacial stability between fluoride‐doped bromides and lithium metal is researched by cycling of lithium symmetric cells. Li plating/stripping can maintain over 1000 h at 0.75 mA cm –2 . Interfacial protection mechanisms investigated by X‐ray photoelectron spectroscopy. A fluoride‐rich interfacial layer is formed in situ during the cycle, which achieves inhibition of the reduction. The Li metal treated fluorine doping of LYB exhibits significant potential in full cells. In fact, the induction of a stable in situ interfacial layer by fluorine doping can effectively improve the interfacial stability of bromides to lithium metal. Fluorine‐doped modification offers a new attempt to realize lithium metal applications in all‐solid‐state lithium batteries.
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