首页> 美国卫生研究院文献>Frontiers in Chemistry >High Performance and Structural Stability of K and Cl Co-Doped LiNi0.5Co0.2Mn0.3O2 Cathode Materials in 4.6 Voltage
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High Performance and Structural Stability of K and Cl Co-Doped LiNi0.5Co0.2Mn0.3O2 Cathode Materials in 4.6 Voltage

机译:K和Cl共掺杂LiNi0.5Co0.2Mn0.3O2正极材料在4.6电压下的高性能和结构稳定性

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摘要

The high energy density lithium ion batteries are being pursued because of their extensive application in electric vehicles with a large mileage and storage energy station with a long life. So, increasing the charge voltage becomes a strategy to improve the energy density. But it brings some harmful to the structural stability. In order to find the equilibrium between capacity and structure stability, the K and Cl co-doped LiNi0.5Co0.2Mn0.3O2 (NCM) cathode materials are designed based on defect theory, and prepared by solid state reaction. The structure is investigated by means of X-ray diffraction (XRD), rietveld refinements, scanning electron microscope (SEM), XPS, EDS mapping and transmission electron microscope (TEM). Electrochemical properties are measured through electrochemical impedance spectroscopy (EIS), cyclic voltammogram curves (CV), charge/discharge tests. The results of XRD, EDS mapping, and XPS show that K and Cl are successfully incorporated into the lattice of NCM cathode materials. Rietveld refinements along with TEM analysis manifest K and Cl co-doping can effectively reduce cation mixing and make the layered structure more complete. After 100 cycles at 1 C, the K and Cl co-doped NCM retains a more integrated layered structure compared to the pristine NCM. It indicates the co-doping can effectively strengthen the layer structure and suppress the phase transition to some degree during repeated charge and discharge process. Through CV curves, it can be found that K and Cl co-doping can weaken the electrode polarization and improve the electrochemical performance. Electrochemical tests show that the discharge capacity of Li0.99K0.01(Ni0.5Co0.3Mn0.2)O1.99Cl0.01 (KCl-NCM) are far higher than NCM at 5 C, and capacity retention reaches 78.1% after 100 cycles at 1 C. EIS measurement indicates that doping K and Cl contributes to the better lithium ion diffusion and the lower charge transfer resistance.
机译:追求高能量密度的锂离子电池是因为它们广泛地用于具有大里程的电动汽车和具有长寿命的储能站。因此,增加充电电压成为提高能量密度的策略。但是它给结构稳定性带来一些危害。为了找到容量与结构稳定性之间的平衡,基于缺陷理论设计了K和Cl共掺杂的LiNi0.5Co0.2Mn0.3O2(NCM)正极材料,并通过固相反应制备。通过X射线衍射(XRD),rietveld改进,扫描电子显微镜(SEM),XPS,EDS作图和透射电子显微镜(TEM)研究了该结构。电化学性能通过电化学阻抗谱(EIS),循环伏安曲线(CV),充电/放电测试进行测量。 XRD,EDS映射和XPS的结果表明,K和Cl成功地掺入了NCM阴极材料的晶格中。 Rietveld的改进以及TEM分析表明,K和Cl共掺杂可以有效地减少阳离子混合,并使层状结构更完整。在1 C下进行100次循环后,与原始NCM相比,K和Cl共掺杂NCM保留了更完整的分层结构。这表明在反复充放电过程中,共掺杂可以有效地增强层结构并在一定程度上抑制相变。通过CV曲线可以发现,K和Cl共掺杂可以减弱电极极化,提高电化学性能。电化学测试表明,Li0.99K0.01(Ni0.5Co0.3Mn0.2)O1.99Cl0.01(KCl-NCM)在5 C时的放电容量远高于NCM,经过100次循环后容量保持率达到78.1% EIS测量表明,掺杂K和Cl有助于更好的锂离子扩散和更低的电荷转移电阻。

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