Improving lithium-sulfur battery performance by protecting lithium anode with Li2S

IF 2.4 4区 化学 Q3 CHEMISTRY, PHYSICAL Ionics Pub Date : 2024-08-21 DOI:10.1007/s11581-024-05763-3
Yu Sun, Ting Zhang, Guo Ai, Birong Luo, Dejun Li, Bo Zhang
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Abstract

Lithium-sulfur batteries have become a research hotspot in the field of energy storage due to their high capacity and low cost. However, lithium metal anodes' short cycle life and safety performance severely limit their commercial application. Here, we used an “in situ” method to form a stable artificial solid electrolyte interface on the surface of the metal lithium, which can control the electrochemical behavior of the interface between the lithium metal and the electrolyte and inhibit the growth of lithium dendrites. The electrochemical performance of lithium-sulfur batteries with protected lithium anode is greatly enhanced. The discharge capacity remains at 1519.6 mAhg−1 after 100 cycles at 0.1 C. In addition, the rate capability of lithium-sulfur batteries is also significantly improved, delivering a reversible capacity of 685.7 mAh g−1 at 0.5 C.

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用 Li2S 保护锂阳极,提高锂硫电池性能
锂硫电池因其容量大、成本低而成为储能领域的研究热点。然而,锂金属阳极较短的循环寿命和安全性能严重限制了其商业应用。在此,我们采用 "原位 "方法在金属锂表面形成了稳定的人工固体电解质界面,从而控制了金属锂与电解质界面的电化学行为,抑制了锂枝晶的生长。采用保护锂负极的锂硫电池的电化学性能大大提高。此外,锂硫电池的速率能力也得到了显著提高,在 0.5 摄氏度时的可逆容量为 685.7 mAh g-1。
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来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
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