阳极
锂(药物)
化学
金属锂
电池(电)
磷酸钒锂电池
阴极
快离子导体
化学工程
金属
材料科学
纳米技术
电解质
无机化学
电极
功率(物理)
有机化学
物理
工程类
内分泌学
物理化学
医学
量子力学
作者
Thorben Krauskopf,Felix H. Richter,Wolfgang G. Zeier,Jürgen Janek
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2020-07-27
卷期号:120 (15): 7745-7794
被引量:576
标识
DOI:10.1021/acs.chemrev.0c00431
摘要
Developing reversible lithium metal anodes with high rate capability is one of the central aims of current battery research. Lithium metal anodes are not only required for the development of innovative cell concepts such as lithium-air or lithium-sulfur batteries, they can also increase the energy density of batteries with intercalation-type cathodes. The use of solid electrolyte separators is especially promising to develop well-performing lithium metal anodes, because they can act as a mechanical barrier to avoid unwanted dendritic growth of lithium through the cell. However, inhomogeneous electrodeposition and contact loss often hinder the application of a lithium metal anode in solid-state batteries. In this review, we assess the physicochemical concepts that describe the fundamental mechanisms governing lithium metal anode performance in combination with inorganic solid electrolytes. In particular, our discussion of kinetic rate limitations and morphological stability intends to stimulate further progress in the field of lithium metal anodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI