Lithium sulfi'/> Revealing the Electrochemical Charging Mechanism of Nanosized Li<sub>2</sub>S by in Situ and Operando X-ray Absorption Spectroscopy
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Revealing the Electrochemical Charging Mechanism of Nanosized Li2S by in Situ and Operando X-ray Absorption Spectroscopy

机译:揭示纳米型Li 2 S的电化学充电机理通过原位和Operando X射线吸收光谱法

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摘要

Lithium sulfide (Li2S) is a promising cathode material for lithium–sulfur (Li/S) cells due to its high theoretical specific capacity (1166 mAh g–1) and ability to pair with nonmetallic lithium anodes to avoid potential safety issues. However, when used as the cathode, a high charging voltage (~4 V versus Li+/Li) is always necessary to activate Li2S in the first charge process, and the voltage profile becomes similar to that of a common sulfur electrode in the following charge processes. In this report, we have prepared an electrode of nanosphere Li2S particles and investigated its charging mechanism of the initial two charge processes by in situ and operando X-ray absorption spectroscopy. The results indicate that Li2S is directly converted to elemental sulfur through a two-phase transformation in the first charge process, while it is oxidized first to polysulfides and then to sulfur in the second charge process. The origin of the different charging mechanisms and corresponding charge-voltage profiles of the first and second charge processes is found to be related to the remaining polysulfides at the end of the first discharge process: they can not only facilitate the charge-transfer process at the Li2S/electrolyte interface but also chemically react with Li2S and act as the polysulfide facilitator for the electrochemical oxidation of Li2S in the following charge processes. Our present study provides a new fundamental understanding of the charging mechanism of the Li2S electrode, which should be of help for the further development of high-performance Li/S cells.]]>
机译:<![CDATA [硫化锂(锂<子> 2 S)为锂 - 硫(李/ S)的细胞的有希望的阴极材料由于其高的理论比容量(毫安1166克 -1 )和能力,一对非金属锂阳极,以避免潜在的安全问题。然而,作为阴极使用时,高的充电电压(〜4相对于Li + / Li)的始终是必要的,以激活李<子> 2 在所述第一充电过程为S,和电压分布变得类似于在下面的电荷的处理的公共电极硫的。在本报告中,我们已经制备纳米球栗<子> 2 的极S.颗粒和通过原位和operando X射线吸收光谱法研究初始两个电荷过程的其充电机制。结果表明,锂<子> 2 S被直接通过在第一充电过程的两相变转化成元素硫,而它首先氧化成多硫化物,然后与硫在第二充电过程。不同的收费机制和相应的所述第一和第二电荷过程的电荷 - 电压曲线的原点被发现涉及到在第一放电过程结束时剩余的聚硫化物:它们不仅可以促进电荷转移过程中,在李<子> 2 S /电解质界面,而且化学上与Li <子>反应2 S和充当多硫化物促进者对Li <子> 2 S IN的电化学氧化下面的电荷的过程。我们目前的研究提供了李<子> 2 取值电极的充电机制,这应该是对高性能锂的进一步发展帮助的一个新的基本理解/ S细胞。]]>

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