电解质
碳酸乙烯酯
材料科学
阴极
电化学
无机化学
溶解
介电谱
化学工程
溶剂
反应性(心理学)
X射线光电子能谱
电极
化学
有机化学
物理化学
病理
医学
工程类
替代医学
作者
Wesley M. Dose,Israel Temprano,Jennifer P. Allen,Erik Björklund,Christopher A. O’Keefe,Weiqun Li,B. Layla Mehdi,Robert S. Weatherup,Michael F. L. De Volder,Clare P. Grey
标识
DOI:10.1021/acsami.1c22812
摘要
(LTO) cells, this is not the case for NMC811. Online gas analysis reveals that the solvent-dependent reactivity for Ni-rich cathodes is related to the extent of lattice oxygen release and accompanying electrolyte decomposition, which is higher for EC-containing than EC-free electrolytes. Combined findings from electrochemical impedance spectroscopy (EIS), TEM, solution NMR, ICP, and XPS reveal that the electrolyte solvent has a profound impact on the degradation of the Ni-rich cathode and the electrolyte. Higher lattice oxygen release with EC-containing electrolytes is coupled with higher cathode interfacial impedance, a thicker oxygen-deficient rock-salt surface reconstruction layer, more electrolyte solvent and salt breakdown, and higher amounts of transition metal dissolution. These processes are suppressed in the EC-free electrolyte, highlighting the incompatibility between Ni-rich cathodes and conventional electrolyte solvents. Finally, new mechanistic insights into the chemical oxidation pathways of electrolyte solvents and, critically, the knock-on chemical and electrochemical reactions that further degrade the electrolyte and electrodes curtailing battery lifetime are provided.
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