电解质
阳极
分解
锂(药物)
化学
电化学
滴定法
水溶液
无机化学
电子转移
材料科学
化学工程
电极
光化学
物理化学
有机化学
工程类
医学
内分泌学
作者
Mingyue Zhou,Xiao-Qing Ding,Jun‐Fan Ding,Li‐Peng Hou,Peng Shi,Jin Xie,Bo‐Quan Li,Jia‐Qi Huang,Xue‐Qiang Zhang,Qiang Zhang
出处
期刊:Joule
[Elsevier]
日期:2022-09-01
卷期号:6 (9): 2122-2137
被引量:39
标识
DOI:10.1016/j.joule.2022.07.003
摘要
Solid electrolyte interphase (SEI) is pivotal in dictating the stability of anodes in non-aqueous batteries. However, electrolyte decomposition mechanism as an indispensable piece of the puzzle to construct a stable SEI is with few quantitative understandings. Herein, as a quantitative descriptor, the apparent electron transfer number (ETN) is acquired by a facile yet precise methodology in working lithium metal batteries with lithium bis(fluorosulfonyl)imide (LiFSI)-dimethyl carbonate (DMC)-based localized high-concentration electrolyte. Through accurate measurements of the electrolyte evolution and concurrently accumulated inactive Li by electrolyte quantitative nuclear magnetic resonance (ely-qNMR) and titration-qNMR, respectively, the decomposition rates of different electrolyte components and ETNs that define the fate of electrolyte can all be acquired in a “one-stop” fashion. The recognition of ETNs (1.0 for DMC and 5.1 for LiFSI) provides pioneering insights into the electrolyte decomposition mechanism and affords new visions for electrolyte design to promote the continuous rise of non-aqueous rechargeable batteries.
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