材料科学
尖晶石
阴极
电解质
降级(电信)
化学工程
表层
电池(电)
表面改性
容量损失
阳离子聚合
电化学
结构稳定性
不稳定性
曲面(拓扑)
图层(电子)
工作(物理)
化学稳定性
替代(逻辑)
铝
限制
限制电流
作者
Beth E. Murdock,Liang Zhao,Ashok S. Menon,Samuel G. Booth,Jack R. Fitzpatrick,Li Zhang,Louis F. J. Piper,Serena A. Cussen,Nuria Tapia‐Ruiz
标识
DOI:10.1002/adfm.202501660
摘要
Abstract LiNi 0.5 Mn 1.5 O 4 (LNMO) cathodes offer a cobalt‐free, high‐voltage alternative to current state‐of‐the‐art Li‐ion battery cathodes, and are particularly well‐suited for high‐power applications due to their 3D lithium‐ion pathways and structural stability. However, degradation of commercial electrolytes at high voltages exacerbates capacity decay, as instability at the cathode surface causes active material loss, surface reconstructions, thickening surface layers, and increases in internal cell resistance. Cationic substitution has been proposed to enhance surface stability, thus limiting capacity decay. Here, we demonstrate the stabilizing effect of Mg on the LNMO cathode surface, which is most evident during the early stages of cycling. This study indicates that improved O 2 p ‐TM 3 d hybridization in Mg‐substituted LNMO, facilitated by Li‐site defects, leads to the formation of a stable surface layer that is corrosion‐resistant at high voltage. Examination of Fe‐substituted and unsubstituted LNMO further confirms that the surface stability is uniquely enabled by Mg substitution. This work offers valuable insights into surface design for reducing degradation in high‐voltage spinel cathodes.
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