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作 者:吴桂贤[1] 赵海峰[2] 黄伟峰[3] 陶石[1] 张凌铭 余蓁[1] 储旺盛[1] 韦世强[1]
机构地区:[1]中国科学技术大学国家同步辐射实验室,安徽合肥230026 [2]中国科学院高能物理研究所,北京100049 [3]北京大学工程学院,高能电池材料理论技术重点实验室,北京100871
出 处:《中国科学技术大学学报》2017年第5期369-376,391,共9页JUSTC
基 金:Supported by the National Natural Science Foundation of China(11179001,11275227)
摘 要:利用共沉淀法合成出了一系列化合物LiFe_xMn_(1-x)O_2(0≤x≤1),电化学测试表明LiFe_(0.25)Mn_(0.75)O_2可逆容量最高,当倍率为0.1C(1C=140mA/g)时,可逆容量可达180mAh/g.通过X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线吸收谱(XAS)对所制备的材料的组成、形貌和精细结构进行了表征.XRD和XAS的结果显示LiFe_xMn_(1-x)O_2(0<x<1)含有三重晶体相即尖晶石相(LiMn_2O_4)、富锂相(Li_2MnO_3)和层状相(LiFeO_2).另外,XAS结果证明材料中的Mn相和Fe相是随机堆叠的.该研究表明Fe的替代影响了晶体相的组成和Mn相的局域结构,进而调节了该正极材料的电化学性能,得到当x=0.25时最优的电化学性能.LiFexMn1-xO2(0≤x≤1) compounds were synthesized by the co-precipitation method. Electrochemical tests show that the LiFe0.25Mn0.75O2 composite has a maximum reversible capacity of 180 mAh/g at 0.1 C(1 C=140 mA/g). These as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray absorption spectroscopy (XAS). XRD and XAS results show that the LiFex Mn1-xO2 (0〈x〈1) samples actually have multiple crystal phases, especially the spinel phase (LiMn2O4), Li-rich phase (Li2MnOa) and layered phase (LiFeO2). Moreover, XAS reveals that the Mn-phase and the Fe-phase are randomly stacked in the samples. The work shows the doping of Fe influences the crystal phase and local structure of the Mn-phase upon the samples and then adjusts the electrochemical performances of the cathode materials, giving an optimal proportion (x =0.25) of the spinel and Li-rich and layered phase.
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