材料科学
碳酸乙烯酯
电解质
镍
锂(药物)
碳酸盐
阴极
无机化学
阳极
钝化
碳酸二甲酯
化学工程
化学
电极
催化作用
纳米技术
有机化学
物理化学
冶金
内分泌学
工程类
医学
图层(电子)
作者
Ruijun Pan,Zehao Cui,Michael Yi,Qiang Xie,Arumugam Manthiram
标识
DOI:10.1002/aenm.202103806
摘要
Abstract Ethylene carbonate (EC) is an important component in state‐of‐the‐art electrolytes for lithium‐ion batteries (LIBs). However, EC is highly susceptible to oxidation on the surface of high‐nickel layered oxide cathodes, making it undesirable for next‐generation high‐energy‐density LIBs. In this study, a simple, yet effective, EC‐free electrolyte (20F1.5M‐1TDI) is presented by adding 20 wt% fluoroethylene carbonate (FEC) and 1 wt% lithium 4,5‐dicyano‐2‐(trifluoromethyl)imidazole (LiTDI) into 1.5 m LiPF 6 in an ethyl methyl carbonate (EMC) electrolyte. The 20F1.5M‐1TDI electrolyte is found to efficiently passivate the graphite anode and stabilize high‐nickel cathodes by a synergistic decomposition of FEC and LiTDI. The LiNi 0.9 Mn 0.05 Al 0.05 O 2 (NMA90)/graphite full cell with the 20F1.5M‐1TDI electrolyte, therefore, exhibits an enhanced cycling stability and a suppressed voltage hysteresis growth compared to that with an EC‐containing baseline electrolyte (1 m LiPF 6 in EC:EMC, 3:7 in weight, with 2 wt% vinyl carbonate). Advanced analytical tools, such as time‐of‐flight secondary ion mass spectrometry and X‐ray photoelectron spectroscopy, are employed to understand the underlying working mechanism of the EC‐free electrolyte. The present study clearly showcases the great potential of EC‐free electrolytes as a straightforward, practical approach for LIBs with high‐nickel cathodes.
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