热重分析
X射线光电子能谱
材料科学
锂(药物)
纳米颗粒
烧结
透射电子显微镜
电化学
复合数
扫描电子显微镜
化学工程
分析化学(期刊)
核化学
化学
电极
纳米技术
复合材料
色谱法
物理化学
内分泌学
工程类
医学
标识
DOI:10.1016/j.ssi.2008.05.005
摘要
LiFePO4/C nanoparticles were prepared using raw Fe2O3 and Fe materials by rheological phase reaction under nitrogen atmosphere. Thermogravimetric analysis (TGA) was employed to analyze the precursor. The effect of the sintering temperature on its structure was investigated by X-ray diffraction (XRD). The chemical composition, surface morphology and valance states of the as-prepared product sintered at 700 °C has been characterized by X-ray photoelectron spectrometry (XPS), transmission electron microscopy (TEM). The content of carbon in LiFePO4/C was determined by the elemental analyzer. The cyclic voltammogram(CV) and the charge–discharge test are adopted to study the electrochemical performance of the LiFePO4/C prepared at 700 °C. The initial discharge capacity was 162.4 mAh g− 1, and the discharge capacity was 166.6 mAh g− 1 after the 30th cycle at a rate of 240 mA g− 1 in a potential range of 2.0 and 4.4 V.
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