电解质
材料科学
法拉第效率
锂(药物)
阳极
电化学
化学工程
聚丙烯
电池(电)
反应性(心理学)
锂离子电池
极化(电化学)
快离子导体
金属锂
电极
复合材料
化学
医学
功率(物理)
物理
替代医学
物理化学
量子力学
病理
工程类
内分泌学
作者
Dasari Bosubabu,Jeevanantham Sivaraj,S. Ramakumar,K. Ramesha
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2019-05-10
卷期号:2 (6): 4118-4125
被引量:51
标识
DOI:10.1021/acsaem.9b00301
摘要
The development of solid state batteries is constrained by imperative factors like the high reactivity of lithium with solid electrolytes, high grain boundary resistance of the solid electrolyte, and interfacial resistance between the solid electrolyte and electrodes. In the present work we exploited Li1.5Al0.5Ge1.5(PO4)3 (LAGP) as a solid electrolyte and noticed a spontaneous reactivity of lithium with LAGP. Further, we observed that introduction of a wetted polypropylene (PP) layer between LAGP and lithium successfully prevented the undesirable reaction between lithium and the surface of the solid electrolyte. Aside from that, it also considerably decreased the interfacial resistance and polarization. This strategy has been applied to both Li-ion and Li–S battery systems, and we observed considerable improvement in the electrochemical performance of these solid state devices. The lithium ion battery retained 100% capacity and Coulombic efficiency after 50 cycles with an observed capacity of 190 mAhg–1. After 200 cycles with varying C-rates, 98.5% capacity retention is observed. Similarly, in the Li–S battery, LAGP effectively restricted the polysulfide shuttle and maintained 78% of the initial capacity after 200 cycles. Such high capacity retention is the outcome of the PP layer which functions as an interlayer that protects the LAGP surface against reacting with the lithium metal anode as inferred by post-mortem analysis.
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