尖晶石
分析化学(期刊)
结晶度
材料科学
电化学
离子
扫描电子显微镜
锂(药物)
八面体
结晶学
晶体结构
晶格常数
衍射
化学
电极
物理化学
冶金
医学
有机化学
色谱法
复合材料
内分泌学
物理
光学
作者
Jianbing Jiang,Wei Li,Changyun Li,Na Li
标识
DOI:10.1166/nnl.2017.2541
摘要
A series of spherical LiMg x Mn 2– x O 4 ( x ≤ 0.10) cathode materials were successfully synthesized by a co-precipitation technique and solid state route. The morphologies and crystal structures of LiMg x Mn 2– x O 4 were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD), respectively. All LiMg x Mn 2– x O 4 samples exhibited a single phase LiMn 2 O 4 spinel structure with good crystallinity. Mg 2+ ions could completely occupy the octahedral (16 d ) site to substitute Mn 3+ and Mn 4+ ions. The effect of Mg 2+ ions on the electrochemical performance of LiMg x Mn 2– x O 4 was investigated by galvanostatic charge–discharge test and electrochemical impedance spectroscopy (EIS). The results showed that the Mg-doped LiMn 2 O 4 possessed better cycling stability. For the LiMg 0.06 Mn 194 O 4 , the initial discharge capacity was 115 mAh/g and remained 111 mAh/g after 50 cycles at a constant current density of 148 mA/g (1 C-rate) during the voltage range 3.0–4.3 V. The capacity retention could reach 96.5%, which was higher than that of the LiMn 2 O 4 .
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