期刊文献+

锂离子电池电解液成膜添加剂乙烯基亚硫酸乙烯酯的电化学行为 被引量:7

Electrochemical Behavior of Vinyl Ethylene Sulfite as an Electrolyte Film-forming Additive in Lithium Ion Batteries
原文传递
导出
摘要 研究了具有不饱和双键和亚硫酸酯双官能团的乙烯基亚硫酸乙烯酯(VES)作为锂离子电池电解液成膜添加剂对中间相碳微球(CMS)和LiFePO4电极电化学性能的影响.结果表明:在1mol/LLiClO4/PC电解液体系中,少量的VES(5%)能够在电化学过程中先于PC在CMS表面还原,形成稳定的SEI膜,明显抑制PC和溶剂化锂离子共嵌入石墨层间,改善了电池的循环性能.此外,电解液1mol/LLiClO4/PC+5%VES(V∶V)在LiFePO4电极中展现出良好的电化学稳定性. A film-forming additive, vinyl ethylene sulfite (VES) with both vinylene group and sulfite group, affects the electrochemical performance of carbonaceous mesophase spherules (CMS) and LiFePO4 electrode. The results indicated that a small amount of VES (5%) could be reduced prior to the propylene carbonate (PC) solvent on the surface of CMS electrode in PC-based electrolyte to form a stable solid electrolyte interphase (SEI) layer, so co-intercalation of PC and solvated lithium ions to graphite could be suppressed. Furthermore, the electrolyte of 1 mol/L LiClO4/PC+5%VES (V: V) exhibited excellent electrochemical stability in the LiFePO4 electrode.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2009年第22期2531-2535,共5页 Acta Chimica Sinica
基金 国家自然科学基金(Nos.20473068 29985310) 国家"973"计划(No.2007CB209702)资助项目
关键词 乙烯基亚硫酸乙烯酯(VES) 电解液添加剂 固体电解质界面(SEI)膜 碳酸丙烯酯 vinyl ethylene sulfite electrolyte additive solid electrolyte interphase (SEI) layer propylene carbonate
  • 相关文献

参考文献13

  • 1Beck, F.; Ruetschi, P. Electrochim. Acta 2000, 45, 2467.
  • 2Lee, J. T.; Lin, Y. W.; Jan, Y. S, J. Power Sources 2004, 132, 244.
  • 3Fujimoto, M.; Shoji, Y.; Kida, Y.; Ohshita, R.; Nohma, T.; Nishio, K. J. Power Sources 1998, 72, 226.
  • 4Zhang, H. L.; Sun, C. H.; Li, F.; Liu, C.; Tan, J.; Cheng, H. M. J. Phys. Chem. C 2007, 111, 4740.
  • 5Fu, L.; Gao, J.; Zhang, T.; Cao, Q.; Yang, L. C.; Wu, Y. P.; Holze, R. J. Power Sources 2007, 171,904.
  • 6Jeong, S. K.; Inaba, M.; Mogi, R.; Iriyama, Y.; Abe, T.; Ogumi, Z. Langmuir 2001, 17, 8281.
  • 7Hu, Y. S.; Kong, W. H.; Hong, L.; Huang, X. J.; Chen, L. Q. Electrochem. Commun.2004, 6, 126.
  • 8Wrodnigg, G. H.; Besenhard, J. O.; Winter, M. J. Electrochem. Soc. 1999, 146, 470.
  • 9Wrodnigg, G. H.; Wrodnigg, T. M.; Besenhard, J. O.; Win- ter, M. Electrochem. Commun. 1999, 1, 148.
  • 10Yao, W. H.; Zhang, Z. R.; Gao, J.; Li, J.; Xu, J.; Wang, Z. C.; Yang, Y. Energy Environ. Sci. 2009, 2, 1102.

同被引文献109

  • 1许梦清,左晓希,李伟善,周豪杰,刘建生,袁中直.石墨电极在PC系电解液中的嵌锂行为[J].电池,2006,36(3):205-207. 被引量:5
  • 2李丽,吴锋,陈人杰,吴生先.新型成膜电解液添加剂亚硫酸丁烯酯的电化学行为[J].高等学校化学学报,2007,28(2):293-296. 被引量:9
  • 3Ping Ping, Wang Qingsong, Sun Jinhua, et al. Thermal stabilities of some lithium salts and their electrolyte solu- tions with and without contact to a LiFePO4 electrode[J]. J Electrochem Soc, 2010,157 (11) : A1170.
  • 4Xu Kang, Bridget Deveney, Kamen Nechev, et al. Evalua- ting LiBOB/lactone electrolytes in large-format lithium-ion cells based on nickelate and iron phosphate[J]. J Electro- chem Soc,2008,155(12) :A959.
  • 5Huang Jia-yuan, Liu Xing-jiang, Kang Xiao-li, et al. Study on γ-butyrolactone for LiBOB-based electrolytes[J]. J Power Sources, 2009,189 : 458.
  • 6Mestre-Aizpurua F, Hamelet S, Masquelier C, et al. High temperature electrochemical performance of nanosized LiFe- PO4 [J]. J Power Sources, 2010,195 : 6897.
  • 7Xie Bin, Li Lifei, Li Hong, et al. A preliminary study on a new LiBOB/acetamide solid phase transition electrolyte[J]. Solid State Ionics, 2009,180 : 688.
  • 8Li Jie, Xie Keyu, et al. Lithium oxalyldifluoroborate/car- bonate electrolytes for LiFePO4/artificial graphite lithium ion cells[J]. J Power Sources, 2010,195 : 5344.
  • 9Zhang Zhian, Chen Xujie, Li Fanqun, et al. LiPF6 and lithium oxalyldifluoroborate blend salts electrolyte for LiFePO4/arti- ficial graphite lithium-ion cells[J]~. J Power Sources,2010, 195:7397.
  • 10Li Lifei, Zhou Sisi, Han Hongbo, et al. Transport and elec- trochemical properties and spectral features of non-aqueous electrolytes containing LiFSI in linear carbonate solvents[J]. J Electrochem Soc, 2011,158(2) : A74.

引证文献7

二级引证文献13

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