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Electrochemical Analysis for Enhancing Interface Layer of Spinel Li4Ti5O12: p-Toluenesulfonyl Isocyanate as Electrolyte Additive

机译:尖晶石Li4Ti5O12界面层增强的电化学分析:对甲苯磺酰基异氰酸酯作为电解质添加剂

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摘要

An electrolyte additive, p-toluenesulfonyl isocyanate (PTSI), is evaluated in our work to overcome the poor cycling performance of spinel lithium titanate (Li4Ti5O12) lithium-ion batteries. We find that the cycling performance of a Li/Li4Ti5O12 cell with 0.5 wt % PTSI after 400 cycles is obviously improved. Remarkably, we also find that a solid electrolyte interface (SET) film is formed about 1.2 V, which has higher potential to generate a stable SEI film than do carbonate solvents in the voltage range of 3.0-0 V. The stable SET film derived from PTSI can effectively suppress the decomposition of electrolyte, HF generation, interfacial reaction, and LiF formation upon cycling. These observations are explained in terms of PTSI including SO3. The S=0 groups can delocalize the nitrogen core, which acts as the weak base site to hinder the reactivity of PF5. Hence, HF generation and LiF formation are suppressed.
机译:为了克服尖晶石钛酸锂(Li4Ti5O12)锂离子电池的不良循环性能,在我们的工作中对电解质添加剂对甲苯磺酰基异氰酸酯(PTSI)进行了评估。我们发现具有0.5 wt%PTSI的Li / Li4Ti5O12电池在400次循环后的循环性能得到明显改善。值得注意的是,我们还发现,固体电解质界面(SET)膜形成于1.2 V左右,与在3.0-0 V电压范围内的碳酸盐溶剂相比,它具有更高的电势来产生稳定的SEI膜。 PTSI可以有效地抑制电解质的分解,HF的产生,界面反应以及循环时LiF的形成。这些观察结果是根据PTSI包括SO3来解释的。 S = 0基团可以使氮核离域,氮核作为弱碱位,阻碍了PF5的反应性。因此,抑制了HF的产生和LiF的形成。

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