材料科学
锂(药物)
金属锂
电解质
快离子导体
电池(电)
离子电导率
电化学
阳极
无定形固体
化学工程
金属
电极
冶金
化学
热力学
物理化学
医学
工程类
内分泌学
功率(物理)
物理
有机化学
作者
Francisco Javier Quintero Cortes,John A. Lewis,Jared Tippens,Thomas S. Marchese,Matthew T. McDowell
摘要
The use of solid-state electrolytes (SSEs) within batteries is a promising strategy to safely access the high capacity of lithium metal anodes. However, most SSEs with practical ionic conductivity are chemically unstable in contact with lithium metal, which is detrimental to battery performance. Lithium aluminum germanium phosphate (LAGP) is an SSE with high ionic conductivity (10−4-10−3 S cm−1) and good environmental stability, but it forms an amorphous interphase region that continuously grows in contact with Li, leading to chemo-mechanical failure within solid-state batteries. Here, we find that thin (∼30 nm) chromium interlayers deposited between the lithium electrode and LAGP extend cycle life to over 1000 h at moderate current densities (0.1–0.2 mA cm−2), compared to ∼30 h without protection. This significantly improved stability occurs because the metallic interlayer alters the trajectory of interphase formation and the nature of the electrochemical reaction at the interface. This work shows the promise of interface engineering for a variety of SSE materials within solid-state batteries, while emphasizing the necessity of understanding how protection layers affect dynamic evolution of interfaces.
科研通智能强力驱动
Strongly Powered by AbleSci AI