共晶体系
材料科学
电解质
电化学窗口
阴极
化学工程
锂(药物)
容量损失
电化学
三元运算
法拉第效率
电极
无机化学
水溶液
离子电导率
化学
复合材料
有机化学
微观结构
物理化学
内分泌学
工程类
计算机科学
程序设计语言
医学
作者
Feng Xu,Xiao Ji,Jiaxun Zhang,Chongyin Yang,Pengfei Wang,Sufu Liu,Kyle B. Ludwig,Fu Chen,Peter Kofinas,Chunsheng Wang
出处
期刊:Nature Energy
[Springer Nature]
日期:2022-02-07
卷期号:7 (2): 186-193
被引量:170
标识
DOI:10.1038/s41560-021-00977-5
摘要
To compete with commercial organic electrolytes, aqueous electrolytes beyond water-in-salt electrolytes with a lower salt concentration of <5.0 m (mol kgsolvent–1) and wider electrochemical stability window of >3.0 V are urgently needed. Here we report a 4.5 m lithium bis(trifluoromethanesulfonyl) imide (LiTFSI)–KOH–CO(NH2)2–H2O non-flammable ternary eutectic electrolyte that expands the electrochemical stability window to >3.3 V by forming a robust solid–electrolyte interphase. The ternary eutectic electrolyte enables Li1.5Mn2O4 || Li4Ti5O12 pouch cells to achieve a high average Coulombic efficiency of 99.96% and capacity retention of 92% after 470 cycles at an areal capacity of 2.5 mAh cm–2, a low positive/negative capacity ratio of 1.14 and a lean electrolyte (3 g Ah–1). The Li loss due to the solid–electrolyte interphase formation in the initial charge/discharge cycles is compensated by an excess 0.5 Li in the Li1.5Mn2O4 cathode, which converts the Li1.5Mn2O4 || Li4Ti5O12 cell into LiMn2O4 || Li4Ti5O12 after solid–electrolyte interphase formation. The 2.5 V aqueous Li1.5Mn2O4 || Li4Ti5O12 pouch cells with practical settings demonstrate a promising approach towards safe, low-cost and high-energy aqueous Li-ion batteries.
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