离子电导率
电解质
电致变色
电导率
聚合物
材料科学
盐(化学)
锂(药物)
无定形固体
离子键合
快离子导体
电致变色装置
离子
氧化物
无机化学
化学工程
化学
结晶学
有机化学
物理化学
电极
复合材料
冶金
内分泌学
工程类
医学
作者
Alasdair M. Christie,Scott J. Lilley,Edward Staunton,Yuri G. Andreev,Peter G. Bruce
出处
期刊:Nature
[Nature Portfolio]
日期:2005-01-01
卷期号:433 (7021): 50-53
被引量:435
摘要
Polymer electrolytes consist of salts dissolved in polymers (for example, polyethylene oxide, PEO), and represent a unique class of solid coordination compounds. They have potential applications in a diverse range of all-solid-state devices, such as rechargeable lithium batteries, flexible electrochromic displays and smart windows. For 30 years, attention was focused on amorphous polymer electrolytes in the belief that crystalline polymer:salt complexes were insulators. This view has been overturned recently by demonstrating ionic conductivity in the crystalline complexes PEO6:LiXF6 (X = P, As, Sb); however, the conductivities were relatively low. Here we demonstrate an increase of 1.5 orders of magnitude in the conductivity of these materials by replacing a small proportion of the XF6- anions in the crystal structure with isovalent N(SO2CF3)2- ions. We suggest that the larger and more irregularly shaped anions disrupt the potential around the Li+ ions, thus enhancing the ionic conductivity in a manner somewhat analogous to the AgBr(1-x)I(x) ionic conductors. The demonstration that doping strategies can enhance the conductivity of crystalline polymer electrolytes represents a significant advance towards the technological exploitation of such materials.
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