阳极
电解质
锂(药物)
材料科学
储能
快离子导体
阴极
工程物理
纳米技术
金属锂
电流密度
能量密度
电极
电气工程
工程类
化学
物理
功率(物理)
医学
物理化学
量子力学
内分泌学
作者
Subhajit Sarkar,Venkataraman Thangadurai
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-03-29
卷期号:7 (4): 1492-1527
被引量:99
标识
DOI:10.1021/acsenergylett.2c00003
摘要
All-solid-state lithium batteries (ASSLBs) are considered promising next-generation energy storage devices due to their safety and high volumetric energy densities. However, achieving the key U.S. DOE milestone of a power density of 33 kW L–1 appears to be a significant hurdle in current ASSLBs. One of the main reasons is that advancements in solid electrolyte (SE) conductivity have been prioritized over the critical current density (CCD) when employing an elemental Li anode. Several aspects of Li electrode- and SE interface-based difficulties must be resolved before commercialization. Here, we very deeply analyze some crucial parameters that effectively restrict Li dendrite formation while achieving high CCD. Mechanistic explanations are provided to comprehend the critical relationship between a cell failure and development of Li dendrites. The latest progress is discussed in achieving higher CCD in emerging SE structures, including Li-stuffed garnets, Na superionic conductors (NASICONs), Li sulfides, and lithium phosphorus oxynitride (LiPON). Furthermore, primary strategies for improving CCDs by tailoring SE design and stabilizing interfaces are proposed for advanced ASSLBs.
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