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用于4.6V无阳极锂金属电池的电解质配方

Formulating Electrolytes for 4.6 V Anode-Free Lithium Metal Batteries.

作者信息

Deng Jiaojiao, Lin Hai, Hu Liang, Zhan Changzhen, Weng Qingsong, Yu Xiaoliang, Sun Xiaoqi, Zhang Qianlin, Mo Jinhan, Li Baohua

机构信息

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

Shenzhen Key Laboratory on Power Battery Safety Research and Shenzhen Geim Graphene Center, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, China.

出版信息

Molecules. 2024 Oct 12;29(20):4831. doi: 10.3390/molecules29204831.

Abstract

High-voltage initial anode-free lithium metal batteries (AFLMBs) promise the maximized energy densities of rechargeable lithium batteries. However, the reversibility of the high-voltage cathode and lithium metal anode is unsatisfactory in sustaining their long lifespan. In this research, a concentrated electrolyte comprising dual salts of LiTFSI and LiDFOB dissolved in mixing solvents of dimethyl carbonate (DMC) and fluoroethylene carbonate (FEC) with a LiNO additive was formulated to address this challenge. FEC and LiNO regulate the anion-rich solvation structure and help form a LiF, LiN-rich solid electrolyte interphase (SEI) with a high lithium plating/stripping Coulombic efficiency of 98.3%. LiDFOB preferentially decomposes to effectively suppress the side reaction at the high-voltage operation of the Li-rich LiMnNiCoO cathode. Moreover, the large irreversible capacity during the initial charge/discharge cycle of the cathode provides supplementary lithium sources for cycle life extension. Owing to these merits, the as-fabricated AFLMBs can operate stably for 80 cycles even at an ultrahigh voltage of 4.6 V. This study sheds new insights on the formulation of advanced electrolytes for highly reversible high-voltage cathodes and lithium metal anodes and could facilitate the practical application of AFLMBs.

摘要

高压初始无阳极锂金属电池(AFLMBs)有望实现可充电锂电池的最大能量密度。然而,高压正极和锂金属负极在维持其长寿命方面的可逆性并不理想。在本研究中,配制了一种由双盐LiTFSI和LiDFOB溶解于碳酸二甲酯(DMC)和氟代碳酸乙烯酯(FEC)的混合溶剂中,并添加LiNO的浓电解质,以应对这一挑战。FEC和LiNO调节富阴离子溶剂化结构,并有助于形成富含LiF、LiN的固体电解质界面(SEI),其锂电镀/剥离库仑效率高达98.3%。LiDFOB优先分解,有效抑制富锂LiMnNiCoO正极在高压运行时的副反应。此外,正极在初始充放电循环期间的大不可逆容量为延长循环寿命提供了补充锂源。由于这些优点,所制备的AFLMBs即使在4.6 V的超高电压下也能稳定运行80个循环。本研究为高可逆性高压正极和锂金属负极的先进电解质配方提供了新的见解,并可能促进AFLMBs的实际应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/734f/11510016/8a5d78f52889/molecules-29-04831-g001.jpg

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