首页> 外文学位 >POLYPHOSPHAZENE-BASED SOLID ELECTROLYTES: SYNTHESIS, COMPLEX FORMATION, CONDUCTIVITY, AND ION TRANSPORT (POLYMER, CONDUCTIVITY).
【24h】

POLYPHOSPHAZENE-BASED SOLID ELECTROLYTES: SYNTHESIS, COMPLEX FORMATION, CONDUCTIVITY, AND ION TRANSPORT (POLYMER, CONDUCTIVITY).

机译:基于聚磷腈的固体电解质:合成,复杂形成,电导率和离子传输(聚合物,电导率)。

获取原文
获取原文并翻译 | 示例

摘要

The focus of this thesis is the design, synthesis, and characterization of new phosphazene polymers as solid electrolyte host materials. A series of poly(alkoxy) phosphazenes, NP O(C(,2)H(,4)O)(,x)CH(,3) (,2) (,n) (x = 1, 2, 7, 12, 17; n (GREATERTHEQ) 15,000), were prepared and formed homogeneous complexes with a wide range of salts. The ionic nature of the conductivity was determined by AC complex impedance and DC potentiostatic polarization methods. The results, presented in three chapters, demonstrate that phosphazenes with short-chain polyethers, as sidegroups, are extremely good host materials.; Chapter One describes the wide range of mono-, di-, and trivalent salts which will form solvent-free, amorphous complexes with MEEP (x = 2). Also included is the characterization of the polymer-salt complexes and the effects of different cations, anions, and salt concentrations on the ionic conductivity and physical properties, such as the glass transition temperature.; Chapter Two deals with lithium salt complexes of MEEP, with emphasis on the effects of different anions on ionic conductivity and the relative contributions of the ions to the conductivity (transference numbers).; Chapter Three depicts the effects of varying the sidechain length on the ionic conductivity and physical properties of the polymers.; The phosphazene polymers exhibited ionic conductivities that were 2-3 orders of magnitude better than the corresponding poly(ethylene oxide) complexes at ambient temperatures ((LESSTHEQ) 60(DEGREES)C). Alkali-metal salt complexes were completely amorphous, single phase systems and the parent polymers exhibited chemical, thermal, and electrochemical stabilities desirable for electrolytes in high energy density batteries and other electrochemical devices.
机译:本文的重点是作为固体电解质主体材料的新型磷腈聚合物的设计,合成和表征。一系列的聚(烷氧基)磷腈,NP O(C(,2)H(,4)O)(,x)CH(,3)(,2)(,n)(x = 1,2,7,制备了12、17; n(GREATERTHEQ)15,000),并形成了具有多种盐的均质复合物。电导率的离子性质通过交流复数阻抗和直流恒电位极化方法确定。分三章介绍的结果表明,以短链聚醚为侧基的磷腈是非常好的基质材料。第一章介绍了广泛的一价,二价和三价盐,它们将与MEEP形成无溶剂的无定形络合物(x = 2)。还包括聚合物-盐配合物的表征以及不同阳离子,阴离子和盐浓度对离子电导率和物理性质(例如玻璃化转变温度)的影响。第二章讨论了MEEP的锂盐配合物,重点介绍了不同阴离子对离子电导率的影响以及离子对电导率的相对贡献(转移数)。第三章描述了改变侧链长度对聚合物的离子电导率和物理性能的影响。在环境温度下((LESSTHEQ)60(DEGREES)C),磷腈聚合物的离子电导率比相应的聚(环氧乙烷)配合物好2-3个数量级。碱金属盐配合物是完全无定形的单相体系,母体聚合物表现出化学,热和电化学稳定性,是高能量密度电池和其他电化学装置中电解质所需要的。

著录项

  • 作者

    BLONSKY, PETER MILLER.;

  • 作者单位

    Northwestern University.;

  • 授予单位 Northwestern University.;
  • 学科 Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 1986
  • 页码 159 p.
  • 总页数 159
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 无机化学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号