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In operando infrared spectroscopy of lithium polysulfides using a novel spectro-electrochemical cell

机译:使用新型光谱电化学电池的多硫化锂的操作红外光谱

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A new in operando spectro-electrochemical Li-S cell has been demonstrated. The novel design allows investigations of the liquid electrolyte phase, in a commercial coin cell geometry, at C rates much higher than conventional in situ cells. We use ATR FT-IR spectroscopy, coupled with a previously developed polysulfide diagnostic to quantify the evolution of lithium polysulfides during the discharge and charge cycles of a Li-S cell. The trends observed in the polysulfide order and concentration with respect to state of charge are consistent with prevailing understanding of the electrochemical mechanisms of Li-S battery operation. During discharge, we observe the reduction of elemental sulfur to dissolved Li2S8 polysulfides, and their cascading conversion to smaller polysulfides until insoluble species (Li2S2 and Li2S) are formed. During cell charging, we observe the oxidation of insoluble polysulfides to larger, soluble polysulfides (Li2Sn, n>3), and infer an eventual recovery of crystalline sulfur, from changes in polysulfides. Long-term evolution of polysulfides is observed over 7 discharge/charge cycles. Capacity fading is evident in the decay of polysulfide order and concentration at the same state of charge between cycles. Sulfur is not recovered by charging the cell in the latter cycles, and the active material is lost as solid Li2S. (C) 2017 Elsevier B.V. All rights reserved.
机译:已经证明了一种新的操作光谱电化学Li-S电池。新颖的设计允许以比传统的原位电池高得多的C速率研究商业纽扣电池几何形状中的液体电解质相。我们使用ATR FT-IR光谱技术,再结合先前开发的多硫化物诊断程序,以量化Li-S电池放电和充电周期中多硫化锂的演变。相对于充电状态,以多硫化物顺序和浓度观察到的趋势与对Li-S电池运行的电化学机理的普遍理解相一致。在放电过程中,我们观察到元素硫还原为溶解的Li2S8多硫化物,并将其级联转化为较小的多硫化物,直至形成不溶物(Li2S2和Li2S)。在电池充电过程中,我们观察到不溶性多硫化物氧化为较大的可溶性多硫化物(Li2Sn,n> 3),并从多硫化物的变化推断出最终回收的结晶硫。在7个放电/充电周期中观察到多硫化物的长期放出。在循环之间相同电荷状态下,多硫化物级次和浓度的衰减中,容量衰减明显。在后面的循环中,无法通过给电池充电来回收硫,并且活性物质以固态Li2S的形式损失。 (C)2017 Elsevier B.V.保留所有权利。

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