首页> 外文会议>Batteries(General) >Electrochemical and Structural Investigations of xLiLi_(0.33)Mn_(0.66)O_2 (1-x)LiNi_(0.8)Co_(0.15)Zr_(0.05)O_2 (0.3≤ x ≤ 0.7) Composite Layered Oxide Cathode for Rechargeable Lithium Ion Batteries
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Electrochemical and Structural Investigations of xLiLi_(0.33)Mn_(0.66)O_2 (1-x)LiNi_(0.8)Co_(0.15)Zr_(0.05)O_2 (0.3≤ x ≤ 0.7) Composite Layered Oxide Cathode for Rechargeable Lithium Ion Batteries

机译:xLi Li_(0.33)Mn_(0.66) O_2(1-x)Li Ni_(0.8)Co_(0.15)Zr_(0.05) O_2(0.3≤x≤0.7)复合层状氧化物阴极的电化学和结构研究可充电锂离子电池

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摘要

The potential for high power lithium ion batteries have made them one of the most attractive candidates for electric as well as hybrid electric vehicles. As cathode material for lithium ion rechargeable batteries, the lithium based layered as well as spinel oxides remain attractive candidates. The capacity of these cathodes has so for been limited to 160 mAh/g in most cases and their electrochemical performance strongly depended on the synthesis conditions. With the aim to increase the discharge capacity beyond 160 mAh/g with the improved cycleability and rate capabilities, in the present work, we have synthesized a solid solution series of layered xLi[Li_(0.33)Mn_(0.66)]O_2(1-x)Li[Ni_(0.8)Co_(0.15Zr_(0.05)]O_2 (0.3≤x≤0.7) by wet chemical route. The XRD pattern analysis has been utilized to characterize the structural changes of the active component as a function of the inactive oxide component and XPS has been used to find oxidation/reduction behavior over the surface of cathode material. The mechanism of Li overcapacity during electrochemical charging is believed to be due to oxygen loss and the conversion of inactive material to active one.
机译:高功率锂离子电池的潜力使其成为电动以及混合动力汽车最有吸引力的候选者之一。作为锂离子可再充电电池的阴极材料,锂基层状和尖晶石氧化物仍然是有吸引力的候选物。因此,在大多数情况下,这些阴极的容量被限制在160mAh / g,并且它们的电化学性能强烈地取决于合成条件。为了将放电容量提高到160 mAh / g以上,并提高循环能力和倍率性能,在本工作中,我们合成了一系列层状xLi [Li_(Li_(0.33)Mn_(0.66)] O_2(1-通过湿化学途径制备x)Li [Ni_(0.8)Co_(0.15Zr_(0.05)] O_2(0.3≤x≤0.7),利用XRD图谱分析表征了活性成分的结构变化。非活性氧化物组分和XPS已用于发现阴极材料表面的氧化/还原行为,电化学充电过程中Li过容量的机理被认为是由于氧的损失以及非活性材料向活性材料的转化所致。

著录项

  • 来源
    《Batteries(General)》|2008年|115-122|共8页
  • 会议地点 PhoenixAZ(US);PhoenixAZ(US)
  • 作者单位

    Materials Science Center, Indian Institute of Technology, Kharagpur 721 302;

    Department of Physics, University of Puerto Rico, San-Juan, PR 00931;

    Materials Science Center, Indian Institute of Technology, Kharagpur 721 302;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 表面处理;
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