节点文献

PEO与Li1.3Al0.3Ti1.7(PO43络合的离子导体聚合物电解质

A New Polymer Electrolyte Based on Poly(ethylene oxide) Complexed with Li1.3Al0.3Ti1.7(PO43 Salt

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 王利王严杰庞明杰潘颐

【Author】 WANG Li, WANG Yan-jie, PANG Ming-jie, PAN Yi (Department of Materials Science and Engineering,Zhejiang Universtiy, Hangzhou 310027,China)

【机构】 浙江大学材料科学与工程系浙江大学材料科学与工程系 杭州310027杭州310027杭州310027

【摘要】 将实验室经固相反应的精细Li1.3Al0.3Ti1.7(PO43盐与聚氧化乙烯(PEO)按照不同nEO/nLi摩尔比,通过溶液浇铸法制备了固态聚合物电解质。红外光谱分析表明Li1.3Al0.3Ti1.7(PO43盐与PEO之间有络合产生。SEM照片显示PEO晶体外层为无定形相所包覆形成的胞状结构。经电化学阻抗(简称EIS)法测试发现聚合物电解质膜的室温阻抗谱图是由高频处一压缩的半圆和低频下一条直线组成,而高温时的阻抗谱主要为一条直线。离子电导率的测试结果得到当nEO/nLi=16时,聚合物电解质室温下电导率约为10-6S/cm,343K时达到10-4S/cm。离子迁移率的数据表明聚合物电解质为离子和电子共混的导体,但在聚合物电解质体系中电荷的迁移主要是由离子作为载流子导电造成的,由测试结果可得此电解质为离子导体。

【Abstract】 Solid polymer electrolyte films were prepared from poly (ethylene oxide) (PEO) and fine Li<sup>1.3 Al<sup>0.3 Ti<sup>1.7 (PO43 salt in appropriate ratios of n<sup>EO /n<sup>Li =8-50 by a solution-cast technique. The complexation of Li<sup>1.3 Al<sup>0.3 Ti<sup>1.7 (PO43 salt with PEO was directly detected by infrared (IR) spectroscopy. A cellular structure formed by the PEO crystallites, which were covered by the amorphous complexed layer, was observed under SEM. The room temperature impedance spectra of the polymer films exhibited a shape of depressed semicircle in high frequency range and inclined line in low frequency range by Electrochemical Impedance Spectroscopy (EIS) measurement, but the high temperature ones were mainly the inclined lines. Measurements of ionic conductivity show that, with n<sup>EO /n<sup>Li  = 16, the conductivity of the film is 10-6 S/cm at room temperature and 10-4 S/cm at above 343K. The transference number data show that the polymer films is a mixed (ionic + electronic) conductor, and that the charge transport in the polymer electrolyte system is predominantly due to the ions.

  • 【文献出处】 功能高分子学报 ,Journal of Functional Polymers , 编辑部邮箱 ,2005年02期
  • 【分类号】O631.3
  • 【被引频次】1
  • 【下载频次】197
节点文献中: 

本文链接的文献网络图示:

本文的引文网络