离子液体
聚合
差示扫描量热法
聚合物
介电谱
高分子化学
离子电导率
放松(心理学)
化学
电导率
化学物理
电介质
动态光散射
化学工程
离子
离子键合
材料科学
物理化学
电化学
有机化学
纳米技术
热力学
纳米颗粒
工程类
光电子学
电极
物理
催化作用
心理学
社会心理学
电解质
作者
Fei Fan,Weiyu Wang,Adam P. Holt,Hongbo Feng,David Uhrig,Xinyi Lu,Tao Hong,Yangyang Wang,Nam‐Goo Kang,Jimmy W. Mays,Alexei P. Sokolov
出处
期刊:Macromolecules
[American Chemical Society]
日期:2016-06-07
卷期号:49 (12): 4557-4570
被引量:120
标识
DOI:10.1021/acs.macromol.6b00714
摘要
The unique properties of ionic liquids (ILs) have made them promising candidates for electrochemical applications. Polymerization of the corresponding ILs results in a new class of materials called polymerized ionic liquids (PolyILs). Though PolyILs offer the possibility to combine the high conductivity of ILs and the high mechanical strength of polymers, their conductivities are typically much lower than that of the corresponding small molecule ILs. In the present work, seven PolyILs were synthesized having degrees of polymerization ranging from 1 to 333, corresponding to molecular weights (MW) from 482 to 160 400 g/mol. Depolarized dynamic light scattering, broadband dielectric spectroscopy, rheology, and differential scanning calorimetry were employed to systematically study the influence of MW on the mechanism of ionic transport and segmental dynamics in these materials. The modified Walden plot analysis reveals that the ion conductivity transforms from being closely coupled with structural relaxation to being strongly decoupled from it as MW increases.
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