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电动汽车应用中锂金属电池的互补电解质设计

Complementary Electrolyte Design for Li Metal Batteries in Electric Vehicle Applications.

作者信息

He Meinan, Su Chi-Cheung, Xu Fan, Amine Khalil, Cai Mei

机构信息

General Motors Global Research and Development Center, 30500 Mound Road, Warren, Michigan 48090, United States.

Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 S. Cass Avenue, Lemont, Illinois 60439, United States.

出版信息

ACS Appl Mater Interfaces. 2021 Jun 9;13(22):25879-25889. doi: 10.1021/acsami.1c03017. Epub 2021 May 24.

Abstract

A complementary electrolyte system with 0.8 M lithium bis(fluorosulfonylimide) (LiFSI) salt and 2 wt % lithium perchlorate (LiClO) additive in fluoroethylene carbonate (FEC)/ethyl methyl carbonate (EMC) solution enables not only stable cycling of lithium metal batteries (LMBs) with practical loading (<30 μm lithium anode, cathode loading > 4 mAh/cm) but also outstanding degradation stability toward the end of cycle life when compared to the conventional electrolyte. Although the use of LiFSI salt can increase the electrolyte conductivity and lengthen the cycle life of LMBs, the aged lithium anode morphology formed by the sacrificial decomposition of LiFSI is highly porous, leading to an abrupt cell capacity drop toward the end of cycling. Moreover, the inability to stop aluminum corrosion by the LiFSI-based electrolyte also causes cracking of the cathode tab during prolonged cycling. It is observed that a highly porous aged lithium consumed electrolyte at a higher rate, leading to the dry-out of electrolyte solvents. On the contrary, dense aged lithium anode morphology increased the localized current applied on the lithium, causing the formation of lithium dendrite. Thus, porosity control is the key to enhance battery performance. In this complementary system, LiClO was introduced as an advanced additive to not only improve the capacity retention rate but also mitigate the abrupt capacity drop toward the end of cycle life because LiClO acted as a pore astringent reducing the porosity of the aged lithium metal anode to the desired level. Moreover, the addition of LiClO can also suppress the Al corrosion, allowing stable high-voltage cycling of LMBs. The synergistic effect of combining LiFSI salt and a LiClO additive leads to an electrolyte system that can facilitate the application of high-energy LMBs with practical electrode loading.

摘要

一种互补电解质体系,在氟代碳酸乙烯酯(FEC)/碳酸甲乙酯(EMC)溶液中含有0.8 M双(氟磺酰亚胺)锂(LiFSI)盐和2 wt%高氯酸锂(LiClO)添加剂,不仅能使锂金属电池(LMBs)在实际负载(<30μm锂阳极,阴极负载>4 mAh/cm)下实现稳定循环, 而且与传统电解质相比,在循环寿命末期具有出色降解稳定性。尽管使用LiFSI盐可以提高电解质电导率并延长LMBs 的循环寿命,但LiFSI牺牲分解形成的老化锂阳极形态高度多孔,导致循环末期电池容量急剧下降, 此外,基于LiFSI 的电解质无法阻止铝腐蚀,也会导致在长时间循环过程中阴极极耳开裂。据观察,高度多孔的老化锂以更高速率消耗电解质,导致电解质溶剂干涸。相反,致密的老化锂阳极形态增加了施加在锂上局部电流,导致锂枝晶形成, 因此,孔隙率控制是提高电池性能的关键。在这种互补体系中,引入LiClO作为先进添加剂,不仅提高容量保持率,而且减轻循环寿命末期的容量急剧下降,因为LiClO起到孔隙收敛剂作用,将老化锂金属阳极的孔隙率降低至所需水平。此外,添加LiClO还可以抑制铝腐蚀,使LMBs实现稳定的高压循环。LiFSI盐和LiClO添加剂结合的协同效应产生了一种电解质体系,该体系能够促进具有实际电极负载的高能LMBs的应用

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