吉首大学学报(自然科学版) ›› 2022, Vol. 43 ›› Issue (3): 72-78.DOI: 10.13438/j.cnki.jdzk.2022.03.012

• 化学化工 • 上一篇    下一篇

Li4Ti5O12材料的固相法制备及其煅烧温度

龙芮涞,吴显明,吴秀婷,尹偲硕   

  1. (吉首大学化学化工学院,湖南 吉首 416000)
  • 出版日期:2022-05-25 发布日期:2022-09-06
  • 通讯作者: 吴显明(1967—),男(苗族),湖南吉首人,吉首大学化学化工学院教授,博士,主要从事功能材料研究;E-mail:xianmingwu@163.com.
  • 基金资助:
    国家自然科学基金资助项目(51762016)

Preparation of Li4Ti5O12 by Solid-State Method and Exploration of Calcination Temperature

LONG Ruilai,WU Xianming,WU Xiuting,YIN Caishuo   

  1. (College of Chemistry and Chemical Engineering,Jishou University,Jishou 416000,Hunan China)
  • Online:2022-05-25 Published:2022-09-06

摘要:以Li2CO3,TiO2为原料,无水乙醇为分散剂,采用高温固相法,通过两步煅烧方式制备出不同煅烧温度下的Li4Ti5O12粉末材料.采用X射线衍射(XRD)、扫描电镜(SEM)表征材料的结构和形貌,采用恒电流充放电、交流阻抗和循环伏安等方法测试材料电化学性能.结果表明:在800 ℃下煅烧6 h后可得到晶型完整的纯相Li4Ti5O12,其颗粒均匀分布在200~400 nm.Li4Ti5O12在0.5C倍率下首次可逆比容量为157.67 mA·h/g,库伦效率为96.1%,经过100次循环充放电后容量保持率为98.63%;在5C倍率下首次可逆比容量为107.0 mA·h/g,经过1 000次循环充放电后容量保持率为84.1%.

关键词: 固相法, 钛酸锂, 锂离子电池, 负极材料

Abstract: Li4Ti5O12 powders were prepared by solid-state reaction and two-step calcination method with Li2CO3 and TiO2 as starting materials and anhydrous ethanol as dispersant.The microstructure and morphology of the materials were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM).The electrochemical properties of the materials were tested by constant current charge-discharge,AC impedance and cyclic voltammetry.The results show that the pure phase Li4Ti5O12 with complete crystal structure could be synthesized after calcination at 800  ℃ for 6h,and uniform dispersion with particle size of 200~400 nm.The first reversible specific capacity of the Li4Ti5O12 sample was 157.67 mA·h/g at the rate of 0.5 C,and the coulombic efficiency was 96.1%,the capacity retention was 94.3% after 100 cycles.The first reversible specific capacity was 107.0 mA·h/g at the rate of 0.5C,the coulombic efficiency was 96.1% and capacity retention was 84.1% after 1 000 cycles.

Key words: solid-state method, Lithium titanate, Li-ion battery, anode material

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