阴极
锂(药物)
拉曼光谱
扫描电子显微镜
电化学
差示扫描量热法
X射线光电子能谱
材料科学
过渡金属
氧化物
分析化学(期刊)
氧化锂
溶解
化学工程
透射电子显微镜
电极
化学
纳米技术
物理化学
磷酸钒锂电池
复合材料
有机化学
物理
冶金
催化作用
工程类
内分泌学
热力学
医学
光学
作者
Surendra K. Martha,Boris Markovsky,Judith Grinblat,Y. Gofer,Ortal Haik,Ella Zinigrad,Doron Aurbach,Thierry Drézen,D. Wang,Gianluca Deghenghi,Ivan Exnar
摘要
nanoparticles synthesized by the polyol method were examined as a cathode material for advanced Li-ion batteries. The structure, surface morphology, and performance were characterized by X-ray diffraction, high resolution scanning electron microscopy, high resolution transmission electron microscopy, Raman, Fourier transform IR, and photoelectron spectroscopies, and standard electrochemical techniques. A stable reversible capacity up to could be measured at discharge potentials vs , with a reasonable capacity retention during prolonged charge/discharge cycling. The rate capability of the electrodes studied herein was higher than that of and (NCA) in similar experiments and measurements. The active mass studied herein seems to be the least surface reactive in alkyl solutions. We attribute the low surface activity of this material, compared to the lithiated transition-metal oxides that are examined and used as cathode materials for Li-ion batteries, to the relatively low basicity and nucleophilicity of the oxygen atoms in the olivine compounds. The thermal stability of the material in solutions (measured by differential scanning calorimetry) is much higher compared to that of transition-metal oxide cathodes. This is demonstrated herein by a comparison with NCA electrodes.
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