材料科学
快离子导体
锂(药物)
反应性(心理学)
X射线光电子能谱
电解质
锂电池
金属
化学工程
离子
分析化学(期刊)
无机化学
电极
物理化学
离子键合
冶金
病理
内分泌学
工程类
化学
物理
替代医学
医学
量子力学
色谱法
作者
Andrea Paolella,Wen Zhu,Gui‐Liang Xu,Andrea La Monaca,S. Savoie,Gabriel Girard,Ashok K. Vijh,Hendrix Demers,Alexis Péréa,Nicolas Delaporte,Abdelbast Guerfi,Xiang Liu,Yang Ren,Chengjun Sun,Jun Lü,Khalil Amine,Karim Zaghib
标识
DOI:10.1002/aenm.202001497
摘要
Abstract The thickness of solid‐state electrolytes (SSEs) significantly affects the energy density and safety performance of all‐solid‐state lithium batteries. However, a sufficient understanding of the reactivity toward lithium metal of ultrathin SSEs (<100 µm) based on NASICON remains lacking. Herein, for the first time, a self‐standing and ultrathin (70 µm) NASICON‐type Li 1.5 Al 0.5 Ge 1.5 (PO 4 ) 3 (LAGP) electrolyte via a scalable solution process is developed, and X‐ray photoelectron spectroscopy reveals that changes in LAGP at the metastable Li–LAGP interface during battery operation is temperature dependent. Severe germanium reduction and decrease in LAGP particle size are detected at the Li–LAGP interface at elevated temperature. Oriented plating of lithium metal on its preferred (110) face occurs during in situ X‐ray diffraction cycling.
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