阳极
锂(药物)
电解质
材料科学
离子
石墨
纳米尺度
储能
电化学
纳米技术
化学工程
无机化学
化学
冶金
有机化学
电极
物理
工程类
物理化学
医学
功率(物理)
量子力学
内分泌学
作者
Yikang Yu,Jiayi Xu,Kaining Duanmu,V. Shutthanandan,Sungun Wi,Zhenzhen Yang,Yuzi Liu,Xingyi Lyu,Kun Qian,Mangilal Agarwal,Zhengcheng Zhang,Yugang Zhang,Tao Li,Cong Liu,Vijayakumar Murugesan,Jian Xie
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-09-20
卷期号:9 (10): 5002-5011
被引量:11
标识
DOI:10.1021/acsenergylett.4c02011
摘要
Graphite is the preferred anode material in commercial lithium-ion batteries (LIBs), but its limited compatibility with various organic molecules restricts the electrolyte solvent options. The primary challenge is solvent co-intercalation with Li ions, leading to graphite layer exfoliation. As a result, electrolyte selection often relies on ethylene carbonate (EC)-based solvents. In this study, we introduce electrolytes featuring a nanoscale anion network ordering that hinders the liquid-phase exfoliation of graphite. This network, formed from concentrated long-chain lithium salts, traps free dioxolane (DOL) molecules, reducing the interactions between graphite particles and solvents during Li intercalation. Our findings reveal a mechanism that stabilizes graphite in otherwise unstable solvents with concentrated salts like LiTFSI, providing key insights for improving LIB performance by addressing electrolyte limitations on graphite anodes.
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