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通过电子能量损失谱研究锂镍氧化物的电子结构

Electronic structure of lithium nickel oxides by electron energy loss spectroscopy.

作者信息

Koyama Yukinori, Mizoguchi Teruyasu, Ikeno Hidekazu, Tanaka Isao

机构信息

Department of Materials Science and Engineering, Nagoya University, Furo, Chikusa, Nagoya 464-8603, Japan.

出版信息

J Phys Chem B. 2005 Jun 2;109(21):10749-55. doi: 10.1021/jp050486b.

Abstract

The electronic structures of NiO, LiNiO2, and NiO2 are studied by the electron energy loss spectroscopy at Ni L(2,3), Ni M(2,3), and O K edges. The Ni L(2,3) edge spectra suggest that the formal charge of nickel is +2 in NiO, +3 with a low-spin state in LiNiO2, and +4 with a low-spin state in NiO2. This is well confirmed by first-principles calculations. The Ni M(2,3) edge spectra show similar chemical shifts to those of the Ni L(2,3) edge. Superposition of the Li K edge spectrum, however, hinders further analysis. Although the formal charge of oxygen is -2 in all the three phases, the O K edge spectra indicate a more remarkable difference in the electronic structure of the oxygen in NiO2 than that in either NiO or LiNiO2. The spectra suggest that lithium extraction from LiNiO2 reinforces the covalent bonding between the oxygen and nickel atoms and causes a notable reduction in electron density at the oxygen atoms.

摘要

通过电子能量损失谱在镍的L(2,3)、M(2,3)边以及氧的K边对NiO、LiNiO₂和NiO₂的电子结构进行了研究。镍的L(2,3)边谱表明,在NiO中镍的形式电荷为+2,在LiNiO₂中为+3且处于低自旋态,在NiO₂中为+4且处于低自旋态。这一点通过第一性原理计算得到了很好的证实。镍的M(2,3)边谱显示出与镍的L(2,3)边谱相似的化学位移。然而,锂的K边谱的叠加阻碍了进一步分析。尽管在所有这三个相中氧的形式电荷均为-2,但氧的K边谱表明,与NiO或LiNiO₂相比,NiO₂中氧的电子结构差异更为显著。这些谱表明,从LiNiO₂中提取锂会增强氧与镍原子之间的共价键,并导致氧原子处的电子密度显著降低。

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