阳极
阴极
电解质
电化学
电极
相间
溶解
金属锂
锂(药物)
吡咯烷
材料科学
化学工程
化学
无机化学
分析化学(期刊)
物理化学
有机化学
工程类
医学
遗传学
生物
内分泌学
作者
Chao Qiu,Zhiqiang Li,Jiajie Pan,Yeon Ki Hong,Junhao Li,Yongxian Lin,Kaixiang Shi,Quanbing Liu
标识
DOI:10.1021/acs.iecr.2c02541
摘要
LiNi0.8Co0.1Mn0.1O2 (NCM 811) has superior capacity but meanwhile also faces continuous electrolyte decomposition and transition metal dissolution induced by unstable cathode electrolyte interphase (CEI) films. The poor compatibility of the traditional electrolyte and lithium anode and the uncontrollable growth of the lithium (Li) dendrite also hinder the application of the lithium anode. Based on this, we designed the 1-methyl-1-cyanopropylpyrrolidine bisfluoromethanesulfonimide salt (PYR1(4CN)TFSI) to reduce the interface impedance on the cathode side and enhance the compatibility between the electrolytes and the lithium metal anode. A uniform and thin CEI was formed on the cathode side, and a dense and stable solid–electrolyte interphase was formed on the anode side, which effectively inhibited the side reaction and further promoted the electrochemical performance. The symmetrical cells with the addition of 0.5 wt % PYR1(4CN)TFSI can be maintained from 400 h to more than 750 h at a current density of 0.5 mA cm–2. After 200 cycles, the discharge specific capacity delivered by Li||LiNi0.8Co0.1Mn0.1O2 cells was 107 mA h g–1 at 1 C.
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