材料科学
硫代磷酸盐
电解质
拉曼光谱
阴极
离子电导率
电化学窗口
电化学
化学工程
涂层
离子键合
电导率
高压
无定形固体
化学稳定性
电压
纳米技术
离子
电极
物理化学
化学
电气工程
结晶学
有机化学
工程类
物理
光学
作者
Daxian Cao,Yubin Zhang,Adelaide M. Nolan,Xiao Sun,Chao Liu,Jinzhi Sheng,Yifei Mo,Yan Wang,Hongli Zhu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2019-09-23
卷期号:20 (3): 1483-1490
被引量:143
标识
DOI:10.1021/acs.nanolett.9b02678
摘要
All-solid-state lithium batteries (ASLBs) are promising for the next generation energy storage system with critical safety. Among various candidates, thiophosphate-based electrolytes have shown great promise because of their high ionic conductivity. However, the narrow operation voltage and poor compatibility with high voltage cathode materials impede their application in the development of high energy ASLBs. In this work, we studied the failure mechanism of Li6PS5Cl at high voltage through in situ Raman spectra and investigated the stability with high-voltage LiNi1/3Mn1/3Co1/3O2 (NMC) cathode. With a facile wet chemical approach, we coated a thin layer of amorphous Li0.35La0.5Sr0.05TiO3 (LLSTO) with 15-20 nm at the interface between NMC and Li6PS5Cl. We studied different coating parameters and optimized the coating thickness of the interface layers. Meanwhile, we studied the effect of NMC dimension to the ASLBs performance. We further conducted the first-principles thermodynamic calculations to understand the electrochemical stability between Li6PS5Cl and carbon, NMC, LLSTO, NMC/LLSTO. Attributed to the high stability of Li6PS5Cl with NMC/LLSTO and outstanding ionic conductivity of the LLSTO and Li6PS5Cl, at room temperature, the ASLBs exhibit outstanding capacity of 107 mAh g-1 and keep stable for 850 cycles with a high capacity retention of 91.5% at C/3 and voltage window 2.5-4.0 V (vs Li-In).
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