电解质
阳极
相间
化学
化学工程
金属
阴极
枝晶(数学)
无机化学
锂(药物)
电极
有机化学
物理化学
生物
工程类
内分泌学
医学
遗传学
数学
几何学
作者
Jing Zhang,Xinyang Yue,Zeyu Wu,Yuanmao Chen,Yu Bai,Kening Sun,Zhenhua Wang,Zheng Liang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-10-16
卷期号:23 (20): 9609-9617
被引量:11
标识
DOI:10.1021/acs.nanolett.3c03340
摘要
Lithium (Li) dendrite growth in a routine carbonate electrolyte (RCE) is the main culprit hindering the practical application of Li metal anodes. Herein, we realize the regulation of the LiPF6 decomposition pathway in RCE containing 1.0 M LiPF6 by introducing a "self-polymerizing" additive, ethyl isothiocyanate (EITC), resulting in a robust LiF-rich solid electrolyte interphase (SEI). The effect of 1 vol % EITC on the electrode/electrolyte interfacial chemistry slows the formation of the byproduct LixPOFy. Such a LiF-rich SEI with EITC polymer winding exhibits a high Young's modulus and a uniform Li-ion flux, which suppresses dendrite growth and interface fluctuation. The EITC-based Li metal cell using a Li4Ti5O12 cathode delivers a capacity retention of 81.4% over 1000 cycles at 10 C, outperforming its counterpart. The cycling stability of 1 Ah pouch cells was further evaluated under EITC. We believe that this work provides a new method for tuning the interfacial chemistry of Li metal through electrolyte additives.
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