Insights into capacity loss mechanisms of all-solid-state Li-ion batteries with Al anodes

被引:43
作者
Leite, Marina S. [1 ,2 ,3 ]
Ruzmetov, Dmitry [2 ,3 ]
Li, Zhipeng [4 ]
Bendersky, Leonid A. [4 ]
Bartelt, Norman C. [5 ]
Kolmakov, Andrei [2 ]
Talin, A. Alec [2 ,5 ]
机构
[1] Inst Res Elect & Appl Phys, Dept Mat Sci & Engn, College Pk, MD 20742 USA
[2] NIST, Ctr Nanoscale Sci & Technol, Gaithersburg, MD 20899 USA
[3] Univ Maryland, Maryland NanoCtr, College Pk, MD 20899 USA
[4] NIST, Mat Measurement Lab, Gaithersburg, MD 20899 USA
[5] Sandia Natl Labs, Livermore, CA USA
关键词
ELECTROCHEMICAL LITHIATION; LITHIUM; ALUMINUM; DIFFUSION; DELITHIATION; SILICON;
D O I
10.1039/c4ta03716b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The atomistic mechanism for lithiation/delithiation in all-solid-state batteries is still an open question, and the 'holy grail' to engineer devices with extended lifetime. Here, by combining real-time scanning electron microscopy in ultra-high vacuum with electrochemical cycling, we quantify the dynamic degradation of Al anodes in Li-ion all-solid-state batteries, a promising alternative for ultra lightweight devices. We find that AlLi alloy mounds are formed on the top surface of the Al anode and that degradation of battery capacity occurs because of Li trapped in them. Our approach establishes a new platform for probing the real-time degradation of electrodes, and can be expanded to other complex systems, allowing for high throughput characterization of batteries with nanoscale resolution.
引用
收藏
页码:20552 / 20559
页数:8
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