电解质
锂(药物)
相间
材料科学
形态学(生物学)
电极
固态
金属锂
化学工程
纳米技术
化学
工程类
细胞生物学
生物
医学
内科学
物理化学
遗传学
作者
John A. Lewis,Francisco Javier Quintero Cortes,Matthew G. Boebinger,Jared Tippens,Thomas S. Marchese,Neha Kondekar,Xiaoming Liu,Miaofang Chi,Matthew T. McDowell
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-01-28
卷期号:4 (2): 591-599
被引量:222
标识
DOI:10.1021/acsenergylett.9b00093
摘要
The interfaces between many solid-state electrolytes (SSEs) and lithium metal are (electro)chemically unstable, and improved understanding of how interfacial transformations influence electrochemical degradation is necessary to stabilize these interfaces and therefore enable a wider range of viable SSEs for batteries. Here, the (electro)chemical reaction processes that occur at the interface between Li1.4Al0.4Ge1.6(PO4)3 (LAGP) electrolyte and lithium are studied using in situ transmission electron microscopy and ex situ techniques. The reaction of lithium with LAGP causes amorphization and volume expansion, which induce mechanical stress and fracture of the SSE along with a massive increase in impedance. The evolved interphase has a nonuniform morphology at high currents, which causes accelerated chemo-mechanical failure. This work demonstrates that the current-dependent nature of the reaction at the SSE/Li interface plays a crucial role in determining chemo-mechanical degradation mechanisms, with implications for understanding and controlling degradation in a wide variety of SSE materials with unstable interfaces.
科研通智能强力驱动
Strongly Powered by AbleSci AI