Self-Stabilized LiNi0.8Mn0.1Co0.1O2 in thiophosphate-based all-solid-state batteries through extra LiOH

硫代磷酸盐 材料科学 电解质 电化学 涂层 化学工程 阴极 储能 快离子导体 纳米技术 锂(药物) 电极 化学 电气工程 工程类 物理化学 有机化学 内分泌学 医学 功率(物理) 量子力学 物理
作者
Yubin Zhang,Xiao Sun,Daxian Cao,Guanhui Gao,Zhenzhen Yang,Hongli Zhu,Yan Wang
出处
期刊:Energy Storage Materials [Elsevier BV]
卷期号:41: 505-514 被引量:63
标识
DOI:10.1016/j.ensm.2021.06.024
摘要

Nickle-rich LiNi0.8Co0.1Mn0.1O2 (NMC 811) cathode material exhibits engaging properties in high energy density and low cost, making it great potential for the next generation high-energy all-solid-state lithium batteries (ASSLBs). However, NMC 811 suffers from severe surface electrochemical, chemical, and voltage incompatibility towards solid-state electrolytes (SSE), especially thiophosphate-based electrolytes like Li6PS5Cl. Although diverse coating methods have been made to overcome this issue, they are typically cumbersome and expensive. A coating strategy that satisfied all the requirements of cost-efficiency, stability, uniformity, scalability, and easy-achieving is still challenging. In this work, we developed a LiOH-based surface stabilization strategy that provides a ~10 nm stable permeable layer on NMC 811. After one-step sintering of NMC 811 precursor mixed with LiOH, which is commonly used for NMC 811 lithiation process, excessive LiOH simultaneously distributes on NMC 811 particles. Unlike other reported methods, this coating method can be easily controlled and fabricated without additional complicated processes. By simply controlling the thickness of LiOH layer, which protects the Li6PS5Cl solid electrolyte materials from being oxidized, optimized cycling stability can be obtained for 600 cycles with capacity of 130 mAh g − 1 on average at a wide electrochemical window of 2.50−4.20 V (vs. Li-In).
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