期刊文献+

尿素作为造孔剂对聚乙烯支撑的PAMS聚合物电解质性能的改进 被引量:2

Performance Improvement of Polyethylene-Supported PAMS Electrolyte Using Urea as Foaming Agent
下载PDF
导出
摘要 采用乳液聚合法合成聚(丙烯腈-甲基丙烯酸甲酯-笨乙烯)(P(AN-MMA-ST)或者共聚物PAMS),并利用尿素作为造孔剂制备了聚乙烯(PE)支撑的PAMS聚合物膜(PE-PAMS-U)及凝胶聚合物电解质(GPE).利用傅里叶变换红外(FTIR)光谱、X射线衍射(XRD)、扫描电子显微镜(SEM)、热重(TG)分析、线性电位扫描(LSV)、电化学阻抗谱(EIS)以及充放电等方法对PAMS聚合物以及PE支撑的聚(丙烯腈-甲基丙烯酸甲酯-苯乙烯)(PE-PAMS)聚合物隔膜及凝胶聚合物电解质的性能进行了研究.结果表明,利用尿素作为造孔剂可以提高PE-PAMS凝胶聚合物的性能.由于尿素的加入,聚合物膜呈现均匀的微孔结构,室温下的电导率从1.1×10^(-3)S·cm^(-1)提高到2.15×10^(-3)S·cm^(-1).同时,锂电极/聚合物电解质界面上的电荷传递电阻也从480Ω·cm^2降低到250Ω·cm^2.电化学稳定窗口为5.0V.电池(Li/PE支撑的GPE/LiCoO_2)的测试证明,用尿素作为造孔剂的凝胶聚合物锂离子电池表现出优良的倍率性能和循环性能. Poly(acrylonitrile-methyl methacrylate-styrene) (PAMS) was synthesized by emulsion polymerization and a polyethylene (PE)-supported membrane was prepared using urea as foaming agent (PE-PAMS-U). The structure and performance of the PAMS copolymer, PE-PAMS-U membrane and corresponding gel polymer electrolyte (GPE) were characterized by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetry (TG), linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS) and by a charge/discharge test. We found that the performance of the PE-PAMS-U based GPE could be improved when using urea as a foaming agent. With the use of urea the pore size of the membrane becomes uniform, the ionic conductivity of the GPE improves from 1.1×10^-3S·cm^-1 to 2.15×10^-3S·cm^-1 at room temperature and the interfacial resistance between the GPE and lithium is reduced from 480 to 250 Ω. cm2. The GPE is stable up to 5.0 V (vs Li/Li+) at room temperature and the battery made using the Li/PE-supported GPE/LiCoO2 shows a good rate andgood cycle performance.
出处 《物理化学学报》 SCIE CAS CSCD 北大核心 2011年第7期1689-1694,共6页 Acta Physico-Chimica Sinica
基金 国家自然科学基金(20873046) 广东省自然科学基金(10351063101000001)资助项目~~
关键词 锂离子电池:凝胶聚合物电解质:聚(丙烯腈-甲基丙烯酸甲酯-苯乙烯) 尿素 造孔剂 Lithium ion battery Gel polymer electrolyte Poly((acrylonitrile-methylmethacrylate-styrene) Urea Foaming agent
  • 相关文献

参考文献31

  • 1Liao, Yr. H.; Zhou, D. Y.; Rao, M. M.; Li, W. S.; Cai, Z. E; Liang, Y.; Tan, C. L. J. Power Sources 2009, 189, 139. 被引量:1
  • 2Tarascon, J. M.; Armand, M. Nature 2001, 414, 359. 被引量:1
  • 3Subba, C. V. R.; Wu, G. P.; Zhao, C. X.; Zhu, Q. Y.; Chen, W.; Kalluru Rajamohan, R. J. Non-Cryst. Solids 2007, 353, 440. 被引量:1
  • 4Sundaram, N. T. K.; Subramania, A. J. Membr Sci. 2007, 289, 1. 被引量:1
  • 5Zuo, X. X.; Xu, M. Q.; Li, W. S.; Su, D. G.; Liu, J. S. Electrochem. Solid-State Lett. 2006, 9, A 196. 被引量:1
  • 6Jeon, J. D.; Kim, M. J.; Kwak, S. Y. J. Power Sources 2006, 162, 1304. 被引量:1
  • 7Xie, H.; Tang, Z. Y.; Li, Z. Y.; He, Y. B.; Liu, Y.; Wang, H. J. Solid State Electrochem. 2008, 12, 1497. 被引量:1
  • 8Chen-Yang, Y. W.; Chen, H. C.; Lin, F. J.; Chen, C. C. SolidState lonics 2002, 150, 327. 被引量:1
  • 9Pu, W. H.; He, X. M.; Wang, L.; Tian, Z.; Jiang, C. Y.; Wan, C. R. J. Membr. Sci. 2006, 280, 6. 被引量:1
  • 10张国庆,马莉,吴忠杰,张海燕,倪佩.P(VDF-HFP)-PMMA/CaCO3(SiO2)复合聚合物电解质的电化学性质[J].物理化学学报,2009,25(3):555-560. 被引量:8

二级参考文献21

  • 1Yang, M. J.; Li, W. L.;Wang, G. G.; Zhang, J. Q. Solid State lonics, 2005, 176:2829 被引量:1
  • 2Croce, F.; Appetecchi, G. B.; Mustarelli, P.; Quartarone, E.; Tomasi, C.; Cazzanelli, E. Electrochim. Acta, 1998, 43:1441 被引量:1
  • 3Croce, F.; Fiory, F. S.; Persi, L.; Scrosati, B. Electrochem. Solid State Letters, 2001, 4:A121 被引量:1
  • 4Nan, C. W.; Fan, L. Z.; Lin, Y. H.; Cai, Q. Phys. Rev. Lett., 2003, 91:266104 被引量:1
  • 5Fan, L. Z. ; Dang, Z. M.; Nan, C. W.; Li, M. Chem. Phys. Lett., 2003, 369:698 被引量:1
  • 6Zhang, S. S.; Xu, K.; Jow, T. R. J. Power Sources, 2005, 140:361 被引量:1
  • 7Stygar, J.; Biemat, A.; Kwiatkowska, A.; Lewandowski, P.; Rusiecka, A.; Zalewska, A.; Wieczorek, W. J. Phys. Chem. B, 2004, 108:4263 被引量:1
  • 8Kim, K. M.; Ko, J. M.; Park, N. G.; Kwang, S. R.; Soon, H. C. Solid State lonics, 2003, 161:121 被引量:1
  • 9Rajendran, S.; Babu, R. S.; Sivakumar, P. Journal of Membrane Science, 2008, 315:67 被引量:1
  • 10Wang, B. B.; Gu, L. X. Materials Letters, 2002, 57:361 被引量:1

共引文献7

同被引文献12

引证文献2

二级引证文献23

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