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Deep eutectic solvents based on N-methylacetamide and a lithium salt as suitable electrolytes for lithium-ion batteries

机译:基于N-甲基乙酰胺和锂盐的深共熔溶剂,适合作为锂离子电池的电解质

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In this work, we present a study on the physical and electrochemical properties of three new Deep Eutectic Solvents (DESs) based on N-methylacetamide (MAc) and a lithium salt (LiX, with X = bisl(trifluoro-methyl)sulfonyl]imide, TFSI; hexafluorophosphate, PF6; or nitrate, NO3). Based on DSC measurements, it appears that these systems are liquid at room temperature for a lithium salt mole fraction ranging from 0.10 to 0.35. The temperature dependences of the ionic conductivity and the viscosity of these DESs are correctly described by using the Vogel-Tammann-Fulcher (VTF) type fitting equation, due to the strong interactions between Li~+, X~- and MAc in solution. Furthermore, these electrolytes possess quite large electrochemical stability windows up to 4.7-5 V on Pt, and demonstrate also a passivating behavior toward the aluminum collector at room temperature. Based on these interesting electrochemical properties, these selected DESs can be classified as potential and promising electrolytes for lithium-ion batteries (LIBs). For this purpose, a test cell was then constructed and tested at 25 °C, 60 °C and 80 °C by using each selected DES as an electrolyte and LiFePO4 (LFP) material as a cathode. The results show a good compatibility between each DES and LFP electrode material. A capacity of up to 160 mA h g~(-1) with a good efficiency (99%) is observed in the DES based on the LiN03 salt at 60 °C despite the presence of residual water in the electrolyte. Finally preliminary tests using a LFP/DES/LTO (lithium titanate) full cell at room temperature clearly show that LiTFSI-based DES can be successfully introduced into LIBs. Considering the beneficial properties, especially, the cost of these electrolytes, such introduction could represent an important contribution for the realization of safer and environmentally friendly LIBs.
机译:在这项工作中,我们介绍了三种基于N-甲基乙酰胺(MAc)和锂盐(LiX,X =双(三氟-甲基)磺酰基]亚胺的新型深共晶溶剂(DES)的物理和电化学性质的研究。 ,TFSI;六氟磷酸盐,PF6;或硝酸盐,NO3)。基于DSC测量,看来这些系统在室温下为0.10至0.35的锂盐摩尔分数是液体。由于溶液中Li〜+,X〜-和MAc之间的强相互作用,使用Vogel-Tammann-Fulcher(VTF)型拟合方程可正确描述这些DES的离子电导率和粘度的温度依赖性。此外,这些电解质在Pt上具有高达4.7-5 V的相当大的电化学稳定性窗口,并且在室温下还表现出对铝收集器的钝化行为。基于这些有趣的电化学特性,可以将这些选定的D​​ES归类为锂离子电池(LIB)的潜在和有前途的电解质。为此,然后使用所选的每种DES作为电解质,并使用LiFePO4(LFP)材料作为阴极,构建测试电池并在25°C,60°C和80°C下进行测试。结果表明每种DES和LFP电极材料之间具有良好的兼容性。尽管在电解液中存在残留水,但在60°C的基于LiNO3盐的DES中,观察到的容量高达160 mA h g〜(-1),效率良好(99%)。最后,在室温下使用LFP / DES / LTO(钛酸锂)全电池进行的初步测试清楚地表明,基于LiTFSI的DES可成功引入LIB。考虑到这些电解质的有益特性,尤其是成本,这种引入可能代表了对实现更安全和环保的LIB的重要贡献。

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