基于 NO3 的电解质添加剂在锂金属电池中的表现

IF 4.6 4区 化学 Q2 ELECTROCHEMISTRY
Jeongmin Kim, Taeho Yoon, Oh B. Chae
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引用次数: 0

摘要

虽然锂金属因其理论上的最高容量和最低电极电位而被寄予厚望,成为下一代电池材料,但其实际应用却因枝晶形成和循环寿命短等稳定性问题而受到阻碍。目前正在进行的研究旨在提高锂金属电池的稳定性,以实现商业化。其中,N 基电解质添加剂的研究大有可为,它可以稳定固体电解质界面(SEI)层,并为锂金属表面提供稳定性。N 基电解质添加剂中的 NO3- 阴离子会使锂金属表面的 SEI 层含有 Li3N 和 Li2O 等化合物,这不仅有利于 Li+ 离子在 SEI 层中的传导,还能提高其机械强度。然而,由于 N 基电解质添加剂在碳酸盐基电解质中的溶解性问题,人们对基于醚的电解质进行了广泛的研究。然而,醚基电解质的氧化稳定性较低,阻碍了其实际应用。因此,我们需要一种策略,将 N 基电解质添加剂加入碳酸盐基电解质中。在本综述中,我们探讨了锂金属电池所面临的挑战,并提出了应用和开发 N 基电解质添加剂的实用方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Behavior of NO3−-Based Electrolytes Additive in Lithium Metal Batteries
While lithium metal is highly desired as a next-generation battery material due to its theoretically highest capacity and lowest electrode potential, its practical application has been impeded by stability issues such as dendrite formation and short cycle life. Ongoing research aims to enhance the stability of lithium metal batteries for commercialization. Among the studies, research on N-based electrolyte additives, which can stabilize the solid electrolyte interface (SEI) layer and provide stability to the lithium metal surface, holds great promise. The NO3− anion in the N-based electrolyte additive causes the SEI layer on the lithium metal surface to contain compounds such as Li3N and Li2O, which not only facilitates the conduction of Li+ ions in the SEI layer but also increases its mechanical strength. However, due to challenges with the solubility of N-based electrolyte additives in carbonate-based electrolytes, extensive research has been conducted on electrolytes based on ethers. Nonetheless, the low oxidative stability of ether-based electrolytes hinders their practical application. Hence, a strategy is needed to incorporate N-based electrolyte additives into carbonate-based electrolytes. In this review, we address the challenges of lithium metal batteries and propose practical approaches for the application and development of N-based electrolyte additives.
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来源期刊
Batteries
Batteries Energy-Energy Engineering and Power Technology
CiteScore
4.00
自引率
15.00%
发文量
217
审稿时长
7 weeks
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