Electrochemical Properties and Crystal and Electronic Structures of Spinel αMgCo<sub>2−</sub><i><sub>x</sub></i>Mn<i><sub>x</sub></i>O<sub>4</sub>-(1 − α)Mg(Mg<sub>0.33</sub>V<sub>1.67−</sub><i><sub>y</sub></i>Ni<i><sub>y</sub></i>)O<sub>4</sub> for Magnesium Secondary Batteries

尖晶石 结构精修 分析化学(期刊) 价(化学) X射线吸收精细结构 结晶学 八面体 晶体结构 化学 吸收光谱法 X射线晶体学 材料科学 光谱学 衍射 冶金 物理 有机化学 色谱法 量子力学 光学
作者
Yasushi Idemoto,Ren OKADA,Naoya Ishida,Chiaki Ishibashi,Toshihiko Mandai,Naoto Kitamura
出处
期刊:Electrochemistry [The Electrochemical Society of Japan]
卷期号:90 (2): 027002-027002 被引量:3
标识
DOI:10.5796/electrochemistry.21-00123
摘要

In the present study, αMgCo1.5Mn0.5O4-(1 − α)Mg1.33V1.57Ni0.1O4 was synthesized by a reverse co-precipitation method. The products were assigned to a spinel structure with a space group Fd3m based on powder X-ray diffraction analysis. Inductively coupled plasma-atomic emission spectroscopy revealed that the composition was not close to the target composition; the Mg content was higher and the V content was lower than expected. Charge/discharge cyclic tests showed that the discharge capacity exceeded 180 mAh g−1 and that the cyclability was reversible up to 60 cycles at 90 °C with a cut-off voltage of 0.945 to −1.055 V vs. Ag/Ag+ (3.545–1.545 V vs. Mg/Mg2+) for α = 0.3. The electronic structure was analyzed using the maximum-entropy method based on a Rietveld analysis, and it was found that Mg insertion was easier for α = 0.3, 0.5, 0.9 than for MgCo1.5Mn0.5O4 and Mg1.33V1.57Ni0.1O4. The strain in MO6 octahedra for α = 0.1, 0.3, 0.5, 0.7 was smaller than that for MgCo1.5Mn0.5O4 and Mg1.33V1.57Ni0.1O4, which suggests that the host structure was stabilized by forming a solid solution. A Rietveld analysis after the first discharge and second charge confirmed a partly reversible phase transition from the spinel phase to a rock-salt phase. The valence of the transition metals was examined by X-ray absorption fine structure (XAFS) measurements, and the Co and Mn K-edge spectra revealed that Co and Mn were present as Co2.67+ to Co2+ and Mn4+ to Mn3+ species for α = 0.3. Both Co and Mn redox processes are considered to contribute to Mg intercalation. Extended XAFS (EXAFS) Co K-edge and Mn K-edge spectra for the powder specimens and after the first discharge and second charge showed that bonds between Co, V atoms and nearest-neighbor O atoms were distorted after the first discharge, and that this distortion was relaxed after the second charge.
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