Unique double-layer solid electrolyte interphase formed with fluorinated ether-based electrolytes for high-voltage lithium metal batteries

IF 3.784 3区 化学 Q1 Chemistry ACS Combinatorial Science Pub Date : 2023-10-13 DOI:10.1016/j.jechem.2023.10.002
Ruo Wang , Jiawei Li , Bing Han , Qingrong Wang , Ruohong Ke , Tong Zhang , Xiaohu Ao , Guangzhao Zhang , Zhongbo Liu , Yunxian Qian , Fangfang Pan , Iseult Lynch , Jun Wang , Yonghong Deng
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Abstract

Li metal batteries using high-voltage layered oxides cathodes are of particular interest due to their high energy density. However, they suffer from short lifespan and extreme safety concerns, which are attributed to the degradation of layered oxides and the decomposition of electrolyte at high voltage, as well as the high reactivity of metallic Li. The key is the development of stable electrolytes against both high-voltage cathodes and Li with the formation of robust interphase films on the surfaces. Herein, we report a highly fluorinated ether, 1,1,1-trifluoro-2-[(2,2,2-trifluoroethoxy) methoxy] ethane (TTME), as a co-solvent, which not only functions as a diluent forming a localized high concentration electrolyte (LHCE), but also participates in the construction of the inner solvation structure. The TTME-based electrolyte is stable itself at high voltage and induces the formation of a unique double-layer solid electrolyte interphase (SEI) film, which is embodied as one layer rich in crystalline structural components for enhanced mechanical strength and another amorphous layer with a higher concentration of organic components for enhanced flexibility. The Li||Cu cells display a noticeably high Coulombic efficiency of 99.28% after 300 cycles and Li symmetric cells maintain stable cycling more than 3200 h at 0.5 mA/cm2 and 1.0 mAh/cm2. In addition, lithium metal cells using LiNi0.8Co0.1Mn0.1O2 and LiCoO2 cathodes (both loadings ∼3.0 mAh/cm2) realize capacity retentions of >85% over 240 cycles with a charge cut-off voltage of 4.4 V and 90% for 170 cycles with a charge cut-off voltage of 4.5 V, respectively. This study offers a bifunctional ether-based electrolyte solvent beneficial for high-voltage Li metal batteries.

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采用氟化醚基电解质形成独特的双层固体电解质界面,用于高压锂金属电池
使用高压层状氧化物阴极的锂金属电池由于其高能量密度而受到特别关注。然而,由于层状氧化物的降解和电解液在高压下的分解,以及金属锂的高反应性,它们的寿命短,安全问题严重。关键是在高压阴极和锂表面形成坚固的界面膜,从而开发出稳定的电解质。本文报道了一种高氟醚1,1,1-三氟-2-[(2,2,2-三氟乙氧基)甲氧基]乙烷(TTME)作为助溶剂,它不仅可以作为稀释剂形成局域高浓度电解质(LHCE),而且还参与了内部溶剂化结构的构建。基于ttme的电解质本身在高压下稳定,并诱导形成独特的双层固体电解质界面(SEI)膜,其表现为一层富含晶体结构成分以增强机械强度,另一层具有较高浓度的有机成分以增强柔韧性。经过300次循环后,Li||铜电池的库仑效率高达99.28%,而Li对称电池在0.5 mA/cm2和1.0 mAh/cm2下稳定循环3200 h以上。此外,使用LiNi0.8Co0.1Mn0.1O2和LiCoO2阴极(两种负载均为3.0 mAh/cm2)的锂金属电池在充电截止电压为4.4 V时,240次循环的容量保留率为85%,在充电截止电压为4.5 V时,170次循环的容量保留率为90%。本研究提供了一种有利于高压锂金属电池的双功能醚基电解质溶剂。
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ACS Combinatorial Science
ACS Combinatorial Science CHEMISTRY, APPLIED-CHEMISTRY, MEDICINAL
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审稿时长
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期刊介绍: The Journal of Combinatorial Chemistry has been relaunched as ACS Combinatorial Science under the leadership of new Editor-in-Chief M.G. Finn of The Scripps Research Institute. The journal features an expanded scope and will build upon the legacy of the Journal of Combinatorial Chemistry, a highly cited leader in the field.
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