电解质
材料科学
锂(药物)
电化学
电极
无机化学
X射线光电子能谱
共沉淀
离子
氧化物
粒子(生态学)
化学工程
化学
物理化学
冶金
有机化学
内分泌学
工程类
地质学
海洋学
医学
作者
Adrien Soloy,Delphine Flahaut,Dominique Foix,Joachim Allouche,Germain Salvato Vallverdu,Erwan Dumont,Lucille Gal,François Weill,Laurence Croguennec
标识
DOI:10.1021/acsami.2c04249
摘要
The layered oxide LiNi0.6Mn0.2Co0.2O2 is a very attractive positive electrode material, as shown by the good reversible capacity, chemical stability, and cyclability upon long-range cycling in Li-ion batteries and, hopefully, in the near future, in all-solid-state batteries. Three samples with variable primary particle sizes of 240 nm, 810 nm, and 2.1 μm on average and very similar structures close to the ideal 2D layered structure (less than 2% Ni2+ ions in Li+ sites) were obtained by coprecipitation followed by a solid-state reaction at high temperatures. The electrochemical performances of the materials were evaluated in a conventional organic liquid electrolyte in Li-ion batteries and in a gel electrolyte in all-solid-state batteries. The positive electrode/electrolyte interface was analyzed by X-ray photoelectron spectroscopy to determine its composition and the extent of degradation of the lithium salt and the carbonate solvents after cycling, taking into account the changes in particle size of the positive electrode material and the nature of the electrolyte.
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