金属锂
制作
锂(药物)
电解质
固态
聚合物电解质
聚合物
溶剂
原位
材料科学
化学工程
金属
快离子导体
无机化学
化学
纳米技术
电极
离子电导率
有机化学
物理化学
冶金
医学
替代医学
病理
工程类
内分泌学
作者
Huihui Gan,Mingyu Cui,Li Liang,Pengyuan Qiu,Xia Ye,Jiajun Sun,Wen Zhu
出处
期刊:Langmuir
[American Chemical Society]
日期:2024-09-20
卷期号:40 (39): 20745-20754
被引量:5
标识
DOI:10.1021/acs.langmuir.4c02845
摘要
All-solid-state lithium metal batteries (ASSLMBs) have been regarded as promising candidates to settle the safety issues of liquid electrolytes for rechargeable lithium batteries. However, the currently reported gel polymer electrolytes still have flammable liquid solvents, thus leading to the potential safety hazard. Here, solvent-free deep eutectic solid polymer electrolytes (SPEs) are designed and fabricated via an in situ polymerization, which are composed of a poly(vinylidene fluoride–hexafluoropropylene) (PVDF–HFP) electrospun membrane, succinonitrile (SN), poly(ethylene glycol) diacrylate (PEGDA200, M n = 200 g mol –1 ), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and lithium difluoro(oxalato)borate (LiDFOB). The deep eutectic solvent (DES) with SN/LiTFSI provides a superior room-temperature ionic conductivity, while the PEGDA200 precursor acts as cross-linking network to form SPEs under thermal initiation for free radical polymerization, and LiDFOB can form a stable solid electrolyte interface (SEI) layer. The PVDF–HFP electrospun membrane with a three-dimensional nanofibrous network structure for SN/PEGDA200/LiTFSI/LiDFOB SPEs exhibits a wide electrochemical stability window, high lithium-ion transference number, and good compatibility with the lithium metal anode. Furthermore, the obtained SPEs assembled with Li//LiMn 0.6 Fe 0.4 PO 4, Li//LiFePO 4, and Li//LiNi 0.8 Co 0.1 Mn 0.1 O 2 asymmetric cells show excellent cycling performance and rate capability at a wide temperature. This strategy provides a promising path in designing high-energy-density ASSLMBs for practical application.
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