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Synthesis, structure, and electrochemical performance of magnesium-substituted lithium manganese orthosilicate cathode materials for lithium-ion batteries

机译:锂离子电池用镁取代原硅酸锰锂正极材料的合成,结构和电化学性能

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摘要

Magnesium-substituted lithium manganese orthosilicate (Li2MnSiO4) cathode materials with a nominal composition of Li2MgxMn1−xSiO4, for x = 0.4 and 0.5 are synthesized by a solid-state route, at 700 °C in argon. The samples are characterized using powder X-ray and neutron diffraction, scanning electron microscopy, and galvanostatic cell-cycling. Rietveld analyses of the powder X-ray and neutron diffraction data show the formation of a monoclinic P21/n structure related to gamma lithium phosphate with no significant impurity peaks. This structure of the Mg-substituted samples is in contrast to the unsubstituted Li2MnSiO4 compound that has a Pmn21 structure when synthesized under the same conditions. Unit-cell volumes of the Mg-substituted materials are intermediate between those of the P21/n structure of Li2MnSiO4 and the isostructural low-temperature form of Li2MgSiO4, indicating the formation of a solid solution. The Mg-substituted materials feature mixed Mg/Mn cation sites, although no evidence of Li/Mn, Li/Mg or Li/Mg/Mn mixed sites are found. The Li2MgxMn1−xSiO4 cathodes show improved electrochemical performance over that reported for the unsubstituted Li2MnSiO4P21/n phase. The Li2MgxMn1−xSiO4 cathode performance remains limited by its poor electronic properties and the large particle size of the solid-state synthesized products. Optimization of the synthesis conditions is likely to lead to enhanced electrochemical performance.
机译:在700℃的氩气中,通过固态途径合成了标称成分为Li2MgxMn1-xSiO4的镁取代的原硅酸锂锰硅酸盐(Li2MnSiO4)正极材料。使用粉末X射线和中子衍射,扫描电子显微镜和恒电流细胞循环对样品进行表征。粉末X射线和中子衍射数据的Rietveld分析表明,与γ磷酸锂有关的单斜P21 / n结构的形成没有明显的杂质峰。 Mg取代样品的这种结构与在相同条件下合成时具有Pmn21结构的未取代Li2MnSiO4化合物相反。 Mg取代的材料的晶胞体积介于Li2MnSiO4的P21 / n结构和Li2MgSiO4的等温低温形式的晶胞体积之间,表明形成了固溶体。尽管没有发现Li / Mn,Li / Mg或Li / Mg / Mn混合位点的证据,但Mg取代的材料具有Mg / Mn混合位点。 Li2MgxMn1-xSiO4阴极的电化学性能优于未取代的Li2MnSiO4P21 / n相。 Li2MgxMn1-xSiO4的阴极性能仍然受到其不良的电子性能和固态合成产物大粒径的限制。合成条件的优化可能导致增强的电化学性能。

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