石油化工高等学校学报 ›› 2011, Vol. 24 ›› Issue (5): 38-40.DOI: 10.3696/j.issn.1006-396X.2011.05.010

• 石油化工 • 上一篇    下一篇

高温固相法制备LiFePO4/C 正极材料及其性能研究

杨占旭1,乔庆东1,康晓雪1,姜海波2   

  1. 1.辽宁石油化工大学石油化工学院,辽宁抚顺113001;
    2.中国石油抚顺石化公司催化剂厂,辽宁抚顺113001
  • 收稿日期:2011-10-08 修回日期:2011-10-15 出版日期:2011-10-25 发布日期:2011-10-25
  • 作者简介:杨占旭(1982-),男,辽宁铁岭县,讲师,博士。
  • 基金资助:
    辽宁省自然科学基金项目(20082187)。

The Synthesis and Properties of LiFePO4/C Prepared by Solid-State Method at High Temperatur

  1. 1.School of Petrochemical Engineering, Liaoning Shihua University, Fushun Liaoning 113001, P. R. China;
    2.Catalysts Factory of Fushun Petrochemical Company of PetroChina, Fushun Liaoning 113001, P. R. China
  • Received:2011-10-08 Revised:2011-10-15 Published:2011-10-25 Online:2011-10-25

摘要: 以Fe2O3,LiH2PO4,乙炔黑和蔗糖为原料,采用高温固相合成方法制备LiFePO4/C复合正极材料。利用X射线衍射(XRD)、扫描电镜(SEM)和电化学测试等方法对合成材料的结构、形貌以及电化学性能进行表征。结果表明,合成材料为单一晶相正交晶系结构,在电压为2.50~4.20V (vs.Li+/Li),以0.1mA/cm2 电流密度下经恒电流充放电测试,其首次放电比容量为156.3mAh/g,经过30周充放电循环后放电比容量为157.7mAh/g,表现出较大的初始放电比容量和优异的循环性能。

关键词: 锂离子电池,    , 正极材料,    , 高温固相法

Abstract: LiFePO4/C cathode material was prepared from solid-state method using Fe2O3,LiH2PO4,black carbon and sugar as the starting materials.The synthesized material was characterized by means of X-ray diffraction (XRD),scanning electron microscope (SEM) and galvanostatic charge/discharge cycling.The results show that the products are single phases and all the peaks are indexable to the orthorhombic structure.The synthesized LiFePO4/C exhibits an excellent electrochemical property with initial discharge specific capacity of 156.3 mAh/g and the discharge specific capacity of 157.7 mAh/g after 30 cycles in the voltage range 2.50~4.20V (versusLi+/Li) at a constant current density of 0.1 mA/cm2.

Key words: Lithium-ion batteries,    , Cathode material,    , Solid-state method

引用本文

杨占旭,乔庆东,康晓雪,姜海波. 高温固相法制备LiFePO4/C 正极材料及其性能研究[J]. 石油化工高等学校学报, 2011, 24(5): 38-40.

YANG Zhan-xu,QIAO Qing-,KANG Xiao-xue,et al. The Synthesis and Properties of LiFePO4/C Prepared by Solid-State Method at High Temperatur[J]. Journal of Petrochemical Universities, 2011, 24(5): 38-40.

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