金属锂
材料科学
锂(药物)
图层(电子)
吸附
固态
电压
金属
光电子学
纳米技术
电极
化学
电气工程
物理化学
阳极
冶金
医学
工程类
内分泌学
作者
Qingjie Zhou,Huaian Zhao,Chuankai Fu,Jiyuan Jian,Hua Huo,Yulin Ma,Chunyu Du,Yunzhi Gao,Geping Yin,Pengjian Zuo
标识
DOI:10.1002/anie.202402625
摘要
Abstract The interfacial instability of high‐nickel layered oxides severely plagues practical application of high‐energy quasi‐solid‐state lithium metal batteries (LMBs). Herein, a uniform and highly oxidation‐resistant polymer layer within inner Helmholtz plane is engineered by in situ polymerizing 1‐vinyl‐3‐ethylimidazolium (VEIM) cations preferentially adsorbed on LiNi 0.83 Co 0.11 Mn 0.06 O 2 (NCM83) surface, inducing the formation of anion‐derived cathode electrolyte interphase with fast interfacial kinetics. Meanwhile, the copolymerization of [VEIM][BF 4 ] and vinyl ethylene carbonate (VEC) endows P(VEC‐IL) copolymer with the positively‐charged imidazolium moieties, providing positive electric fields to facilitate Li + transport and desolvation process. Consequently, the Li||NCM83 cells with a cut‐off voltage up to 4.5 V exhibit excellent reversible capacity of 130 mAh g −1 after 1000 cycles at 25 °C and considerable discharge capacity of 134 mAh g −1 without capacity decay after 100 cycles at −20 °C. This work provides deep understanding on tailoring electric double layer by cation specific adsorption for high‐voltage quasi‐solid‐state LMBs.
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