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用于高性能锂金属电池的原位形成连续致密无机硼酸盐基固体电解质界面膜

In Situ Formed Continuous and Dense Inorganic Borate-Based SEI for High-Performance Li-Metal Batteries.

作者信息

Liu Yuying, Huang Tao, Huang Zhencheng, Huang Weiyuan, Chen Jing, Jia Hao, He Xuanlong, Chen Weibin, Wei Haoran, Li Liewu, Ren Xiangzhong, Ouyang Xiaoping, Liu Jianhong, Ye Shenghua, Yang Xuming, Pan Feng, Zhang Qianling, Hu Jiangtao

机构信息

Graphene Composite Research Center, College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, 518060, China.

College of Energy Engineering, Zhejiang University, Hangzhou, Zhejiang, 310027, China.

出版信息

Small. 2025 Jan;21(2):e2406400. doi: 10.1002/smll.202406400. Epub 2024 Nov 6.

DOI:10.1002/smll.202406400
PMID:39506386
Abstract

The practical application of lithium metal batteries (LMBs) is largely hindered by the notorious lithium dendrite growth, low cycle efficiency associated with insufficient electrode-electrolyte interphase dynamics, and electrolyte combustion. Here, an advanced electrolyte using a combination of three kinds of salts dissolved in carbonate-based solvents is developed. The salt anions dominate a primary solvation sheath, resulting in weak interaction between Li and the solvents, as well as the in situ formation of an inorganic-rich bilayer solid electrolyte interface (SEI). The designed electrolyte enables high cycle stability in LMBs with a high-loading NMC cathode (approximately 20 mg cm), exhibiting 89.89% capacity retention after 200 cycles with the cutoff voltage of 4.5 V. Cryo-TEM characterization and density-functional theory (DFT) calculations reveal that the borate-based bilayer SEI, characterized by an exceptional dense structure, effectively suppresses lithium dendrite growth, and certify the crucial role of inorganic component continuity and density within the SEI, which surpasses the absorption and migration energy barrier in terms of significance. This profound understanding of SEI structure holds great potential for advancing the development of high-stable LMBs and can be expanded to other battery system.

摘要

锂金属电池(LMBs)的实际应用在很大程度上受到锂枝晶生长、与电极-电解质界面动力学不足相关的低循环效率以及电解质燃烧等问题的阻碍。在此,开发了一种先进的电解质,它使用三种溶解在碳酸盐基溶剂中的盐的组合。盐阴离子主导着初级溶剂化鞘层,导致锂与溶剂之间的相互作用较弱,并原位形成富含无机成分的双层固体电解质界面(SEI)。所设计的电解质在具有高负载NMC正极(约20mg/cm²)的LMBs中实现了高循环稳定性,在截止电压为4.5V的情况下,经过200次循环后容量保持率为89.89%。低温透射电子显微镜(Cryo-TEM)表征和密度泛函理论(DFT)计算表明,具有异常致密结构的硼酸盐基双层SEI有效地抑制了锂枝晶的生长,并证明了SEI中无机成分连续性和密度的关键作用,其在重要性方面超过了吸收和迁移能垒。对SEI结构的这一深刻理解对于推进高稳定性LMBs的发展具有巨大潜力,并且可以扩展到其他电池系统。

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