电解质
阴极
反应性(心理学)
材料科学
氧化物
锂(药物)
非阻塞I/O
化学工程
快离子导体
硫化物
碳纤维
涂层
固溶体
电极
纳米技术
化学
物理化学
催化作用
冶金
复合数
复合材料
医学
生物化学
替代医学
病理
工程类
内分泌学
作者
Hideyuki Komatsu,Swastika Banerjee,Manas Likhit Holekevi Chandrappa,Ji Qi,Balachandran Radhakrishnan,Shigemasa Kuwata,Kazuyuki Sakamoto,Shyue Ping Ong
标识
DOI:10.1021/acs.jpcc.2c05336
摘要
Among the key impediments to the practical application of all-solid-state lithium-ion batteries are the reactions occurring at the interfaces between the electrode active material, the solid electrolyte, and conductive additives such as carbon. Here, we provide in-depth insights into the relationship between composition and interfacial stability with sulfide solid electrolytes for the layered LiNixMnyCo1–x–yO2 (NMC) cathodes in widespread commercial applications today using density functional theory calculations. We show that increasing the Ni content and, to a lesser extent, increasing the Co content, has the effect of increasing reactivity with the Li6PS5Cl (LPSCl) solid electrolyte. This suggests that current efforts to reduce the Co content in cathodes may compromise potential application in all-solid-state architectures. However, we also find that common SEI phases such as Li2CO3, surface phases such as NiO, and oxide buffer layers such as LiNbO3 generally exhibit only limited reactivity with either LiMO2 or LPSCl. Hence, these phases, formed either in operando or added during synthesis, can potentially serve as effective barriers against further reaction, provided a uniform coating can be achieved.
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