期刊文献+

Co^(2+)掺杂对磷酸钒锂电化学性能的影响 被引量:4

Effects of doping Co^(2+) on the electrochemical performance of Li_3V_2(PO_4)_3
下载PDF
导出
摘要 用XRD、透射电镜(TME)和电化学性能测试,研究了Co2+掺杂对正极材料磷酸钒锂[Li3V2(PO4)3]的影响。掺杂适量的Co2+不会改变Li3V2(PO4)3的单斜晶系结构,可稳定材料结构,改善高倍率充放电性能。在室温下、3.0~4.3 V充放电,Li3(Co0.03V0.97)2(PO4)3以0.1C放电的首次放电比容量为116.8 mAh/g,电流从0.1C增加到1.0C循环80次后,容量衰减率为16.5%;Li3V2(PO4)3的首次放电比容量为128.8mAh/g,80次循环后,容量衰减率为34.8%。循环伏安和交流阻抗测试表明:Li3(Co0.03V0.97)2(PO4)3的可逆性优于Li3V2(PO4)3。 Abstract: The effects of doping Co^2+ on cathode material lithium vanadium phosphate[ LisV2 (PO4)3 ] were studied by XRD, transmission electron microscopy(TEM) and electrochemical performance test. The monoclinic structure of Li3 V2 ( POt )3 would not change, the structure was more stable,the high rate charge-discharge performance was improved. While charged-discharged in 3.0 - 4.3 V under room temperature, the initial specific capacity of Li3( Co0.03 V0.97)2( PO4)3 was 116.8 mAh/g at 0. l C discharge, the capacity fading rate was 16.5% after 80 cycles with the current increased from 0.1 C to 1.0 C. The initial specific discharge capacity of Li3V2(PO4)3 was 128.SmAh/g and the capacity fading rate was 34.8% after 80 cycles. The test of cyclic voltammo- gram and AC impedance showed that the reversibility of Li3(Co0.03V0.97)2(PO4)3 was better than that of Li3V2(PO4)3.
出处 《电池》 CAS CSCD 北大核心 2012年第3期138-141,共4页 Battery Bimonthly
基金 安徽省教育厅自然科学研究项目(050601D2)
关键词 正极材料 磷酸钒锂[Li3V2(PO4)3] 掺杂Co2+ 电化学性能 cathode material lithium vanadium phosphate[Li3V2(PO4)3] doping Co^2+ electrochemical performance
  • 相关文献

参考文献12

二级参考文献46

共引文献38

同被引文献23

  • 1张国庆,张校刚.碱性固态Zn/MnO_2电池研究[J].电池,2004,34(3):169-170. 被引量:4
  • 2袁安保,赵俊.PVA-CMC-KOH-H_2O碱性聚合物电解质研究[J].电化学,2006,12(1):40-45. 被引量:11
  • 3刘素琴,李世彩,唐联兴,黄可龙.Li_3V_2(PO_4)_3的溶胶-凝胶法合成及其性能研究[J].无机化学学报,2006,22(4):645-650. 被引量:33
  • 4Vassal N,Salmon E, Fauvarque J F. Electrochemical properties ofan alkaline solid polymer electrolyte based on P(ECH-co-EO)[ j]:Electrochim Acta,2000,45(8 - 9) : 1 527- 1 532.
  • 5Mohamad A A, Mohamed N S, Yahya M Z A, et al. Ionic conduc-tivity studies of poly (vinyl alcohol) alkaline solid polymer elec-trolyte and its use in nickel-zinc cells[j]: Solid State Ionics,2003,156(1-2):171-177.
  • 6Forsyth M, Sun J,Macfarlane D R. Enhancement of ion dissocia-tion in polyelectrolyte gels [ J]: Electrochim Acta,2003,48 (14 -16):2 129-2 136.
  • 7Yang C C.Polymer Ni-MH battery based on PEO-PVA-KOHpolymer electrolyte[j]: J Power Sources,2002,109(3):22- 31.
  • 8Cuinot S, Salmon E, Penneaub J F, et al. A new class of PEO-based SPEs: structure, conductivity and application to alkalinesecondary batteries[ j] .Electrochim Acta, 1998, 43 (10 - 11):1 163-1 170.
  • 9Yang C C, Lin S J, Hsu S T.Synthesis and characterization of al-kaline polyvinyl alcohol and poly (Cichlorohydrin) blend polymerelectrolytes and performance in electrochemical cells [ J] , J PowerSources,2003,122(2):210 - 218.
  • 10Aged E, Bouet J, Fauvarque J F.Characterization and use ofanionic membranes for alkaline fuel eUs[j]: J Power Sources,2001,101(2):267-274.

引证文献4

二级引证文献5

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