电解质
溶剂化
锂(药物)
材料科学
金属锂
电化学
离子
电极
金属
电压
化学物理
纳米技术
化学
物理化学
有机化学
内分泌学
物理
冶金
医学
量子力学
作者
Fangyuan Cheng,Wen Zhang,Qing Li,Chun Fang,Jiantao Han,Yunhui Huang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-11-27
卷期号:17 (23): 24259-24267
被引量:15
标识
DOI:10.1021/acsnano.3c09759
摘要
The optimal electrolyte for ultrahigh energy density (>400 Wh/kg) lithium-metal batteries with a LiNi0.8Co0.1Mn0.1O2 cathode is required to withstand high voltage (≥4.7 V) and be adaptable over a wide temperature range. However, the battery performance is degraded by aggressive electrode–electrolyte reactions at high temperature and high voltage, while excessive growth of lithium dendrites usually occurs due to poor kinetics at low temperature. Accordingly, the development of electrolytes has encountered challenges in that there is almost no electrolyte simultaneously meeting the above requirements. Herein, a high chaos electrolyte design strategy is proposed, which promotes the formation of weak solvation structures involving multiple anions. By tailoring a Li+-EMC-DMC-DFOB–-PO2F2–-PF6– multiple-anion-rich solvation sheath, a robust inorganic-rich interphase is obtained for the electrode–electrolyte interphase (EEI), which is resistant to the intense interfacial reactions at high voltage (4.7 V) and high temperature (45 °C). In addition, the Li+ solvation is weakened by the multiple-anion solvation structure, which is a benefit to Li+ desolventization at low temperature (−30 °C), greatly improving the charge transfer kinetics and inhibiting the lithium dendrite growth. This work provides an innovative strategy to manipulate the high chaos electrolyte to further optimize solvation chemistry for high voltage and wide temperature applications.
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