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Synthesis and electrochemical performance of Ti-Fe co-doped LiMnPO4/C as cathode material for lithium-ion batteries

机译:Ti-Fe共掺杂LiMnPO4 / C作为锂离子电池正极材料的合成及电化学性能

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LiMnPO4/C, LiMn0.85Fe0.15PO4/C, LiMn0.92Ti0.08PO4/C and Li(Mn0.85Fe0.15)(0.92)Ti0.08PO4/C are prepared by a solid-state reaction route and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and electrochemical tests. All samples are single phase with similar morphologies, particle sizes and carbon contents. Ti4+ and Fe2+ co-doping at the Mn-site greatly enhances the performance of LiMnPO4/C due to the synergistic effect between Ti4+ and Fe2+, resulting in an improvement in the dynamic stability of the olivine structure, lithium ion diffusion and electrochemical kinetics. Compared with LiMn0.85Fe0.15PO4/C and LiMn0.92Ti0.08PO4/C, Li (Mn0.85Fe0.15)(0.92)Ti0.08PO4/C shows a much higher discharge capacity and a better rate capability. It delivers a capacity of 144.4 mA h g(-1) with a capacity retention ratio of approximately 100% after 50 cycles at 1 C. These results prove that Fe2+ and aliovalent ion co-doping at the Mn site is an effective way to improve the electrochemical properties of lithium manganese phosphate. (C) 2016 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
机译:通过固态反应路线制备LiMnPO4 / C,LiMn0.85Fe0.15PO4 / C,LiMn0.92Ti0.08PO4 / C和Li(Mn0.85Fe0.15)(0.92)Ti0.08PO4 / C,并通过X-射线衍射(XRD),X射线光电子能谱(XPS),扫描电子显微镜(SEM)和电化学测试。所有样品均为单相,具有相似的形态,粒径和碳含量。由于Ti4 +和Fe2 +之间的协同作用,Mn位处的Ti4 +和Fe2 +共掺杂极大地增强了LiMnPO4 / C的性能,从而改善了橄榄石结构的动态稳定性,锂离子扩散和电化学动力学。与LiMn0.85Fe0.15PO4 / C和LiMn0.92Ti0.08PO4 / C相比,Li(Mn0.85Fe0.15)(0.92)Ti0.08PO4 / C具有更高的放电容量和更好的倍率性能。它在1 C下经过50次循环后,可提供144.4 mA hg(-1)的容量,容量保持率约为100%。这些结果证明,Fe位点上的Fe2 +和aliovalent离子共掺杂是改善磁导率的有效方法。磷酸锰锂的电化学性能。 (C)2016 Elsevier Ltd和Techna Group S.r.l.版权所有。

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