期刊文献+

Li4Ti5O12-聚苯胺复合材料的制备与电化学性能

Synthesis and electrochemical properties of Li4Ti5O12-PAn composites
下载PDF
导出
摘要 以醋酸锂和钛酸四丁酯为原料,以乙醇为溶剂,采用溶胶.凝胶法制备Li4Ti5O12;以苯胺、过硫酸铵为原料,以盐酸为溶剂,采用原位聚合法合成Li4Ti5O12-聚苯胺复合材料。采用x射线衍射、红外光谱和电化学测试等对复合材料进行了表征。结果表明,聚苯胺的加入明显提高了Li4Ti5O12的电子导电性能,Li4rri5O12-PAn复合材料具有比Li4Ti5O12更好的高倍率性能和循环稳定性。0.1C和2.0C放电时Li4Ti5O12-PAn的放电容量达到了191.3和148.9mAh.g^-1,经80次循环后二者平均每次循环容量衰减率分别为0.13%和0.61%。 Li4Ti5Ol2 powders were prepared by so-gel method using tetrabutyl titanate, lithium acetate and absolute alcohol as starting materials. Li4Ti5Ol2-polyaniline (Li4Ti5O12-PAn) composites were prepared by in situ polymerization method using aniline, ammonium persulfate and hydrochloricarried as starting materials. Li4Ti5O12-PAn composites were characterized by XRD, IR combined with electrochemical tests. Results show that the electrical conductivity is enhanced obviously due to the introduction of PAn to Li4Ti5O12. Li4Ti5O12-PAn composites exhibit better high rate capability and cyclability than Li4Ti5O12. The composites can deliver a specific capacity of 191.3 and 148.9 mAh/g, only 0.13% and 0.61% of the capacity is lose after discharged for 80 times at 0.1C and 2.0C,respectively.
出处 《功能材料》 EI CAS CSCD 北大核心 2007年第A04期1419-1422,共4页 Journal of Functional Materials
基金 基金项目:国家自然科学基金资助项目(20376086) 中国博士后科学基金资助项目(2005037700) 中南大学博士后科学基金资助项目(2004107)
关键词 溶胶-凝胶法 原位聚合合成法 LI4TI5O12 聚苯胺 锂离子电池 sol-gel method in situ polymerization method Li4Ti5O12 polyaniline lithium ion batteries
  • 相关文献

参考文献25

  • 1Fu L J, Liu H, Wu Y P, et al. [J]. Prog Mater Sci, 2005, 50: 881-887.
  • 2Wu Y P, Dai X B, Ma J Q, et al. Lithium Ion Batteeries-Practice and Application [M]. Beijing: Chemical Industry Press, 2004.
  • 3Amatucci G, Badway F, Pasquier A D, et al. [J]. J Electrochem Soc, 2001, 148(8): A930-939.
  • 4Singhal A, Skandan G, Amatucci G, et al. [J]. J Power Sources, 2004, 129(1): 38-44.
  • 5Ohzuku T, Ueda A, Yamamoto N. [J]. J Electrochem Soc, 1995, 142:1431-1436.
  • 6Prosini P P, Mancini R, Petrucci L, et al. [J]. Solid State Ionics, 2001,144:185-189.
  • 7Kavan L, Prochazka J, Spitler T M, et al. [J]. J Electrochem Soc, 2003, 150:A1000-1005.
  • 8Huang S H, Wen Z Y, Zhu X J, et al. [J]. Electrochem Commun, 2004, 6:1093-1097.
  • 9Guerfi A, Charest Pa, Kinoshita K, et al. [J]. Journal of Power Sources, 2004, 126:163-168.
  • 10Guerfi A, Se'vigny S, Lagace' M, et al. [J]. Journal of Power Sources, 2003, 119-121:88-94.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部