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首页> 外文期刊>Ionics >Solvothermal synthesis of LiCo_(1-x)Mn_xPO4/C cathode materials for lithium-ion batteries
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Solvothermal synthesis of LiCo_(1-x)Mn_xPO4/C cathode materials for lithium-ion batteries

机译:溶剂热合成锂离子电池LiCo_(1-x)Mn_xPO4 / C正极材料

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摘要

LiCo_(1-x)Mn_xPO4/C cathode materials are selectively synthesized by a solvothermal method in ethylene glycol solvent using glucose, LiCl, H3PO4, MnCl2·4H2O, and Co(NO3)2·6H2O as precursors. The obtained samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) and the electrochemical performances are also evaluated using a LAND CT2001A battery test system at room temperature. XRD result demonstrates the formation of LiCo_(1-x)Mn_xPO4 solid solution and the enlarged channels are benefit for Li~+ migration. SEM graph indicates that the particle size of LiCo_(0.5)Mn_(0.5)PO4/C is about several hundred nanometers and aggregates to large particles located in the range of 2-3 μm. TEM image illustrates that the core/ shell-structured LiCo_(0.5)Mn_(0.5)PO4/C solid solution is indeed obtained by this method. The high specific surface area (35 m~2/g) of LiCo_(0.5)Mn_(0.5)PO4/C could make this solid solution contact with the electrolyte more sufficiently and benefit for Li~+ transportation. The capacity, flat voltage, and cyclical stability of LiCo_(1-x)Mn_xPO4/C are improved compared to LiMnPO4 and LiCoPO4 due to the improved electronic conductivity and lithium-ion conductivity which resulted from carbon coating and foreign element incorporation.
机译:以乙二醇,LiCl,H3PO4,MnCl2·4H2O和Co(NO3)2·6H2O为前驱体,在乙二醇溶剂中通过溶剂热法选择性合成LiCo_(1-x)Mn_xPO4 / C正极材料。通过X射线衍射(XRD),扫描电子显微镜(SEM)和透射电子显微镜(TEM)对获得的样品进行表征,并且还在室温下使用LAND CT2001A电池测试系统评估电化学性能。 XRD结果表明形成了LiCo_(1-x)Mn_xPO4固溶体,增大的通道有利于Li〜+的迁移。 SEM图表明,LiCo_(0.5)Mn_(0.5)PO4 / C的粒径约为几百纳米,并且聚集成位于2-3μm范围内的大颗粒。 TEM图像表明,通过该方法确实获得了核/壳结构的LiCo_(0.5)Mn_(0.5)PO4 / C固溶体。 LiCo_(0.5)Mn_(0.5)PO4 / C的高比表面积(35 m〜2 / g)可使该固溶体更充分地与电解质接触,有利于Li +的运输。与LiMnPO4和LiCoPO4相比,LiCo_(1-x)Mn_xPO4 / C的容量,平坦电压和循环稳定性得到了改善,这归因于碳涂层和异物掺入带来的电子电导率和锂离子电导率的提高。

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