材料科学
离子电导率
电解质
相容性(地球化学)
电导率
化学工程
锂(药物)
离子键合
热传导
离子
快离子导体
相(物质)
离子液体
不稳定性
纳米技术
化学物理
电阻率和电导率
工作(物理)
电化学窗口
残余物
电化学
导电体
相变
复合材料
作者
Linnan Bi,Tianrui Sun,Jiajun Li,Ying Lin,Xiongbang Wei,Jiaxuan Liao
标识
DOI:10.1021/acsami.5c15546
摘要
Interfacial instability and low ionic conductivity impede the utilization of PVDF-based electrolytes in solid-state lithium batteries. Herein, a molecular self-sacrificing strategy using bis(catecholato)diboron (B 2 cat 2 ) to stabilize the LLZTO/P(VDF-CTFE) interface was proposed. B 2 cat 2 effectively suppresses dehydrofluorination and regulates residual DMF at the molecular level, improving both the bulk phase and interfacial stability. Spectroscopic analyses (UV–vis, XPS, and NMR) confirm strong interactions between B 2 cat 2 and LLZTO, leading to enhanced ion transport and lithium interfacial compatibility. The optimized eutectogel hybrid electrolytes (EHEs) achieve high lithium conductivity (0.59 mS cm –1 ) and lithium-ion transference number (0.66), long-term cycling (1000 h at 0.3 mA cm – 2 ), and excellent full-cell performance with LiFePO 4 and NCM811 cathodes. The pouch cell demonstrated remarkable stability across a wide temperature range, retaining a capacity of 79.2% after 150 cycles of charge and discharge at 0.5 C). This work presents an approach for constructing stable interfaces in solid-state batteries.
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