材料科学
原子层沉积
锂(药物)
阴极
离子
自行车
图层(电子)
导电体
逐层
纳米技术
沉积(地质)
化学工程
复合材料
化学
物理化学
古生物学
考古
内分泌学
有机化学
工程类
历史
生物
医学
沉积物
作者
Jin Xie,Austin D. Sendek,Ekin D. Cubuk,Xiaokun Zhang,Zhiyi Lu,Yongji Gong,Tong Wu,Feifei Shi,Wei Liu,Evan J. Reed,Yi Cui
出处
期刊:ACS Nano
[American Chemical Society]
日期:2017-06-30
卷期号:11 (7): 7019-7027
被引量:336
标识
DOI:10.1021/acsnano.7b02561
摘要
Modern lithium ion batteries are often desired to operate at a wide electrochemical window to maximize energy densities. While pushing the limit of cutoff potentials allows batteries to provide greater energy densities with enhanced specific capacities and higher voltage outputs, it raises key challenges with thermodynamic and kinetic stability in the battery. This is especially true for layered lithium transition-metal oxides, where capacities can improve but stabilities are compromised as wider electrochemical windows are applied. To overcome the above-mentioned challenges, we used atomic layer deposition to develop a LiAlF4 solid thin film with robust stability and satisfactory ion conductivity, which is superior to commonly used LiF and AlF3. With a predicted stable electrochemical window of approximately 2.0 ± 0.9 to 5.7 ± 0.7 V vs Li+/Li for LiAlF4, excellent stability was achieved for high Ni content LiNi0.8Mn0.1Co0.1O2 electrodes with LiAlF4 interfacial layer at a wide electrochemical window of 2.75-4.50 V vs Li+/Li.
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