Complex Hydride Solid Electrolytes of the Li(CB9H10)–Li(CB11H12) Quasi-Binary System: Relationship between the Solid Solution and Phase Transition, and the Electrochemical Properties

电解质 固溶体 电化学 相(物质) 锂(药物) 快离子导体 阳极 材料科学 阴极 电导率 氢化物 电池(电) 金属 无机化学 分析化学(期刊) 化学 物理化学 热力学 电极 冶金 有机化学 医学 功率(物理) 物理 内分泌学
作者
Sangryun Kim,Kazuaki Kisu,Shigeyuki Takagi,Hiroyuki Oguchi,Shin‐ichi Orimo
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:3 (5): 4831-4839 被引量:37
标识
DOI:10.1021/acsaem.0c00433
摘要

Closo-type complex hydrides have recently received much attention as promising solid electrolyte systems for all-solid-state batteries, because of the high lithium ion conductivity of their high-temperature (high-T) phases, excellent stability against a lithium metal anode, and a highly deformable nature. However, the superionic conductivity of closo-type complex hydrides is achieved in only a few materials; therefore, an understanding of the material factors involved in the formation of the high-T phase at room temperature and experimental demonstration of their battery applications are required. Here, we report the relationship between the solid solution and formation of the high-T phase of the Li(CB9H10)–Li(CB11H12) quasi-binary system, and the electrochemical properties as a solid electrolyte for all-solid-state Li–TiS2 batteries. The single-phase solid solutions, Li(CB9H10)-based phase in which [CB9H10]− is partially substituted with [CB11H12]− and Li(CB11H12)-based phase in which [CB11H12]− is partially substituted with [CB9H10]−, are obtained at compositions with low- and high-x in the (1 – x)Li(CB9H10)–xLi(CB11H12) (0.1 ≤ x ≤ 0.9) system. The effect of the solid solution on structural changes is more noticeable at low x, whereby a superionic conducting phase is formed with an identical structural framework as that of the high-T phase of Li(CB9H10) at room temperature. In addition, the 0.7Li(CB9H10)–0.3Li(CB11H12) (x = 0.3) solid electrolyte exhibits high chemical/electrochemical stability against a TiS2 cathode, which leads to superior performance in the rate capability and cycle life of all-solid-state Li–TiS2 batteries. The results presented here offer insights into strategies for the design of complex hydride lithium superionic conductors and for the development of all-solid-state batteries with these solid electrolytes.

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