原位电化学沉积Mg种子稳定锂金属阳极

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY
Wenzheng Nan, Shaojiu Yan, Xiang Chen, Sheng Long Dai
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引用次数: 0

摘要

金属锂因其极低的反应电位和超高的理论比容量而被公认为负极材料的“圣杯”。然而,锂枝晶的形成导致电池容量的快速退化和相当大的安全性问题,阻碍了其进一步发展。在本研究中,通过将MgCl2加入电解质中,在循环过程中在锂金属表面原位生成Mg种子。这些Mg种子作为亲硫位点,降低了Li成核屏障,促进了Li的均匀成核和生长。因此,用碳酸盐电解质构建的对称电池可以在电流密度为1ma cm - 2和容量为1mah cm - 2的情况下稳定循环400小时以上。值得注意的是,使用Li4Ti5O12作为阴极的完整电池可以保持300次循环的稳定循环,实现71.9%的容量保持率。该方法在减少锂枝晶形成和提高锂金属电池性能方面具有较好的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In Situ Electrochemically Deposited Mg Seeds Stabilizing the Lithium Metal Anode

In Situ Electrochemically Deposited Mg Seeds Stabilizing the Lithium Metal Anode

Lithium metal, recognized for its extremely low reaction potential and ultrahigh theoretical specific capacity, is regarded as the “Holy Grail” of anode materials. However, the formation of lithium dendrites result in rapid cell capacity degradation and considerable safety issues, hindering its further advancement. In this study, in situ Mg seeds are generated on the lithium metal surface during cycling by incorporating MgCl2 into the electrolyte. These Mg seeds function as thiophilic sites, which lower the Li nucleation barrier and promote uniform Li nucleation and growth. Consequently, symmetric cells constructed with the carbonate electrolyte can cycle stably for over 400 h at a current density of 1 mA cm−2 and a capacity of 1 mAh cm−2. Notably, full cells using Li4Ti5O12 as the cathode can maintain stable cycling for 300 cycles, achieving a capacity retention rate of 71.9 %. This method has demonstrated its effectiveness in mitigating lithium dendrites formation and enhancing the performance of lithium metal batteries.

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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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