Composite electrolytes engineered by anion acceptors for boosted high-voltage solid-state lithium metal batteries

电解质 阳极 锂(药物) 材料科学 阴极 电化学窗口 化学工程 电池(电) 复合数 钾离子电池 无机化学 磷酸钒锂电池 电极 化学 复合材料 离子电导率 物理化学 内分泌学 功率(物理) 工程类 物理 医学 量子力学
作者
Jiahui Yu,Kangsheng Huang,Hai Xu,Chang Ming Fang,Xiaogang Zhang
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:642: 330-339 被引量:3
标识
DOI:10.1016/j.jcis.2023.03.110
摘要

Solid-state batteries (SSBs) are considered as the most promising option to replace commercial lithium-ion batteries due to their ability to address the flammability of liquid organic electrolytes and facilitate the energy density of lithium batteries. Herein, by introducing tris(trimethylsilyl) borate (TMSB) as anion acceptors, we successfully develop the light and thin electrolyte (TMSB-PVDF-HFP-LLZTO-LiTFSI, PLFB) with a wide voltage window to couple the lithium metal anode with the high-voltage cathodes. Consequently, as-prepared PLFB can greatly boost the generation of free Li+ and improve the Li+ transference numbers (tLi+=0.92) at room temperature. Moreover, combined with theoretical calculation and experimental results, the changes in the composition and properties of the composite electrolyte membrane with the addition of anionic receptors are systematically studied, which further implies the intrinsic mechanism of the stability difference. In addition, the PLFB-based SSB assembled by LiNi0.8Co0.1Mn0.1O2 cathode and lithium anode exhibits a high capacity retention of 86% after loop 400 cycles. This investigation on boosted battery performance by immobilized anions not only contributes to the directional construction of dendrite-free and lithium-ion permeable interface, but also brings new opportunities for the screening and design of the next generation of high-energy SSBs.
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