X射线吸收光谱法
尖晶石
阴极
材料科学
透射电子显微镜
溶解
电子能量损失谱
吸收光谱法
光谱学
价(化学)
相变
化学物理
化学工程
分析化学(期刊)
离子
纳米技术
化学
凝聚态物理
冶金
物理化学
光学
量子力学
色谱法
有机化学
工程类
物理
作者
Biwei Xiao,Hanshuo Liu,Ning Chen,Mohammad Norouzi Banis,Haijun Yu,Jianwen Liang,Qian Sun,Tsun‐Kong Sham,Ruying Li,Mei Cai,Gianluigi A. Botton,Xueliang Sun
标识
DOI:10.1002/anie.202005337
摘要
Li- and Mn-rich layered oxides are among the most promising cathode materials for Li-ion batteries with high theoretical energy density. Its practical application is, however, hampered by the capacity and voltage fade after long cycling. Herein, a finite difference method for near-edge structure (FDMNES) code was combined with in situ X-ray absorption spectroscopy (XAS) and transmission electron microscopy/electron energy loss spectroscopy (TEM/EELS) to investigate the evolution of transition metals (TMs) in fresh and heavily cycled electrodes. Theoretical modeling reveals a recurring partially reversible LiMn2 O4 -like sub-nanodomain formation/dissolution process during each charge/discharge, which accumulates gradually and accounts for the Mn phase transition. From the modeling of spectra and maps of the valence state over large regions of the cathodes, it was found that the phase change is size-dependent. After prolonged cycling, the TMs displayed different levels of inactivity.
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