首页> 外文期刊>Electrochimica Acta >Ionic liquid electrolyte of lithium bis(fluorosulfonyl)imide/N-methyl-N-propylpiperidinium bis(fluorosulfonyl)imide for Liatural graphite cells: Effect of concentration of lithium salt on the physicochemical and electrochemical properties
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Ionic liquid electrolyte of lithium bis(fluorosulfonyl)imide/N-methyl-N-propylpiperidinium bis(fluorosulfonyl)imide for Liatural graphite cells: Effect of concentration of lithium salt on the physicochemical and electrochemical properties

机译:锂/天然石墨电池双(氟磺酰基)酰亚胺锂/ N-甲基-N-丙基哌啶双(氟磺酰基)酰亚胺离子液体电解质:锂盐浓度对理化性质和电化学性质的影响

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摘要

Binary electrolytes, comprising of lithium bis(fluorosulfonyl) imide (LiFSI) and ionic liquids (ILs) of N-methyl-N-propylpiperidinium bis(fluorosulfonyl) imide (PI13FSI) with various concentrations of LiFSI (i.e., LiFSI/PI13FSI in 0.05:1, 0.1:1, 0.2:1, 0.5:1, 0.8:1 and 1:1, by mole) have been investigated as electrolyte for Li-ion cells, in terms of phase behavior, thermal stability, density, viscosity, ionic conductivity, lithium-ion transference number, and electrochemical behaviors on Al, Pt, Ni, and composite natural graphite electrodes, with particular attention to the effect of concentration of LiFSI in PI13FSI on these properties. The stability of Al in the high potential region (3.05.0 V vs. Li/Li+) has been confirmed in these electrolytes using cyclic voltammetry, chronoamperometry and SEM morphology. The anodic stability of these electrolytes on Pt electrode has been little affected by addition of LiFSI. Li deposition/stripping on Ni electrode shows low columbic efficiencies (< 45%) in these electrolytes, due to the continuous reduction of FSI-anions and PI13+ cations. Reduction of FSI-anions for forming solid electrolyte interphase (SEI) films on the graphite is observed at ca. 2.0 V (vs. Li/Li+), followed by intercalation of Li+ ions and IL cations into graphite in these electrolytes at the first cathodic scan in CV measurements. The performances of SEI films formed on the graphite highly depend on the concentration of LiFSI, and a stable Li-ion conducting SEI film can only be formed in the electrolyte containing a high concentration of LiFSI. Liatural graphite cell using LiFSI-PI13FSI (1:1, by mole) as electrolyte displays high specific capacities (> 360 mAh g(-1)) and columbic efficiencies (> 99%) after conditioning, except for a large irreversible capacity (139 mAh g(-1)) observed at the first cycle. Analyses of XPS and electrochemical impedance spectra reveal that a stable Li-ion conducting SEI film, mainly comprising reduction products of FSI-anions (e.g., LiF, LiOH, Li2SO3, and species containing NSO2-, FSO2-, and N-), has been formed on the graphite.
机译:二元电解质,由双(氟磺酰基)酰亚胺锂(LiFSI)和N-甲基-N-丙基哌啶双(氟磺酰基)酰亚胺(PI13FSI)的离子液体(ILs)和各种浓度的LiFSI(即LiFSI / PI13FSI为0.05)组成:已经研究了1,0.1:1、0.2:1、0.5:1、0.8:1和1:1(摩尔)作为锂离子电池的电解质,包括相行为,热稳定性,密度,粘度,离子性电导率,锂离子转移数以及在Al,Pt,Ni和复合天然石墨电极上的电化学行为,尤其要注意PI13FSI中LiFSI浓度对这些性能的影响。使用循环伏安法,计时安培法和SEM形态学已证实了这些电解质中Al在高电势区域(3.05.0 V vs. Li / Li +)的稳定性。这些电解质在Pt电极上的阳极稳定性几乎不受LiFSI的影响。由于FSI阴离子和PI13 +阳离子的连续还原,在Ni电极上的Li沉积/剥离在这些电解质中显示出低的哥伦布效率(<45%)。在大约200℃下观察到了还原FSI-阴离子以在石墨上形成固体电解质中间相(SEI)膜。 2.0 V(vs. Li / Li +),然后在CV测量的第一次阴极扫描中,将Li +离子和IL阳离子嵌入这些电解质中的石墨中。在石墨上形成的SEI膜的性能高度依赖于LiFSI的浓度,并且稳定的锂离子导电SEI膜只能在含有高浓度LiFSI的电解质中形成。使用LiFSI-PI13FSI(1:1,以摩尔计)作为电解质的锂/天然石墨电池在调理后显示出高的比容量(> 360 mAh g(-1))和哥伦比亚的效率(> 99%),除了不可逆的容量大(139 mAh g(-1))在第一个循环中观察到。 XPS和电化学阻抗谱分析表明,稳定的锂离子导电SEI膜具有以下特征:主要包含FSI阴离子的还原产物(例如LiF,LiOH,Li2SO3和含有NSO2-,FSO2-和N-的物质)在石墨上形成。

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