离子电导率
电解质
无定形固体
环氧乙烷
聚合物
化学
电导率
离子键合
微晶
快离子导体
玻璃化转变
氧化物
锂(药物)
化学工程
高分子化学
无机化学
结晶学
离子
物理化学
有机化学
电极
医学
共聚物
工程类
内分泌学
作者
Zlatka Stoeva,Isabelle Martin‐Litas,Edward Staunton,Yuri G. Andreev,Peter G. Bruce
摘要
Ionically conducting polymers (salts dissolved in a polymer matrix) are of great interest because they uniquely exhibit ionic conductivity in a soft but solid membrane. As such, they are critical to the development of devices such as all-solid-state lithium batteries. The established view of ionic conductivity in polymer electrolytes is that this occurs in amorphous materials above their glass transition temperature and that crystalline polymer electrolytes are insulators. In contrast, we show that three crystalline polymer electrolytes, poly(ethylene oxide)(6):LiXF(6), X = P, As, Sb, not only conduct but do so better than the analogous amorphous phases! It is also shown that the conductivities of all three 6:1 complexes are similar, consistent with the dimension of the bottlenecks to conduction derived from their crystal structures. An increase in ionic conductivity with reduction of molecular weight of the crystalline polymer electrolyte (from 2000 to 1000) is reported and shown to relate to the increase in crystallite size on reducing molecular weight.
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