密度泛函理论
电子结构
光电发射光谱学
锂(药物)
价(化学)
化学
插层(化学)
态密度
离子
阴极
共价键
光谱学
材料科学
结晶学
X射线光电子能谱
无机化学
物理化学
凝聚态物理
计算化学
核磁共振
有机化学
内分泌学
物理
医学
量子力学
作者
Shodai Kurosumi,Naoka Nagamura,Satoshi Toyoda,Koji Horiba,Hiroshi Kumigashira,Masaharu Oshima,Sho Furutsuki,Shin‐ichi Nishimura,Atsuo Yamada,Noritaka Mizuno
摘要
The change of Fe 3d states accompanied with the Li intercalation/deintercalation process has been successfully revealed by resonant photoemission spectroscopy. The main peak shift and expansion of Fe 3d bands through the Li deintercalation reflect the strong hybridization between Fe 3d states and O 2p states as the Fe–O bond lengths decrease. From the antiresonance spectra, O 2p partial density of states also changes, suggesting the interaction between Fe and O atoms still remains in LiFePO4. Furthermore, density functional theory calculations results strongly support these experimental results. The framework structure of LiFePO4 is more suitable than that of LiCoO2 for the good rechargeable battery, because the change of the electronic structure in LiFePO4 valence band is rather small because of the strong covalent P–O bond.
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