相间
电解质
锂(药物)
电池(电)
电化学
自行车
金属锂
断裂(地质)
材料科学
化学
复合材料
纳米技术
物理
热力学
电极
物理化学
生物
历史
内分泌学
功率(物理)
考古
医学
遗传学
作者
Jared Tippens,John Miers,Arman Afshar,John A. Lewis,Francisco Javier Quintero Cortes,Haipeng Qiao,Thomas S. Marchese,Claudio V. Di Leo,Christopher Saldaña,Matthew T. McDowell
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-06-04
卷期号:4 (6): 1475-1483
被引量:264
标识
DOI:10.1021/acsenergylett.9b00816
摘要
Transformations at interfaces between solid-state electrolytes (SSEs) and lithium metal electrodes can lead to high impedance and capacity decay during cycling of solid-state batteries, but the links between structural/chemical/mechanical evolution of interfaces and electrochemistry are not well understood. Here, we use in situ X-ray computed tomography to reveal the evolution of mechanical damage within a Li1+xAlxGe2–x(PO4)3 (LAGP) SSE caused by interphase growth during electrochemical cycling. The growth of an interphase with expanded volume drives fracture in this material, and the extent of fracture during cycling is found to be the primary factor causing the impedance increase, as opposed to the resistance of the interphase itself. Cracks are observed to initiate near the edge of the lithium/LAGP interface, which agrees with simulations. The chemomechanical effects of interphase growth studied here are expected to play a role in a variety of SSE materials, and this work is a step toward designing durable interfaces.
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