Influence of Molecular Weight and End Groups on Ion Transport in Weakly and Strongly Coordinating Polymer Electrolytes

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY
Rassmus Andersson, Samuel Emilsson, Guiomar Hernández, Mats Johansson, Jonas Mindemark
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Abstract

In the development of polymer electrolytes, the understanding of the complex interplay of factors that affect ion transport is of importance. In this study, the strongly coordinating and flexible poly (ethylene oxide) (PEO) is compared to the weakly coordinating and stiff poly (trimethylene carbonate) (PTMC) as opposing model systems. The effect of molecular weight (Mn) and end group chemistry on the physical properties: glass transition temperature (Tg) and viscosity (η) and ion transport properties: transference number (T+), ion coordination strength and ionic conductivities were investigated. The cation transference number (T+) showed the opposite dependence on Mn for PEO and PTMC, decreasing at low Mn for PTMC and increasing for PEO. This was shown to be highly dependent on the ion coordination strength of the system regardless of whether the end group was OH or if the chains were end-capped. Although the coordination is mainly of the cations in the systems, the differences in T+ were due to differences in anion rather than cation conductivity, with a similar Li+ conductivity across the polymer series when accounting for the differences in segmental mobility.

Abstract Image

分子量和端基对弱配位和强配位聚合物电解质中离子迁移的影响
在开发聚合物电解质的过程中,了解影响离子传输的各种因素之间复杂的相互作用非常重要。在本研究中,强配位柔性聚(环氧乙烷)(PEO)与弱配位刚性聚(三亚甲基碳酸酯)(PTMC)作为对立模型系统进行了比较。研究了分子量(Mn)和端基化学性质对物理特性:玻璃化转变温度(Tg)和粘度(η)以及离子传输特性:转移数(T+)、离子配位强度和离子电导率的影响。PEO 和 PTMC 的阳离子转移数(T+)与锰的关系相反,PTMC 的阳离子转移数在锰含量低时减少,而 PEO 的阳离子转移数则增加。研究表明,无论末端基团是羟基还是链的末端被封盖,这在很大程度上取决于系统的离子配位强度。虽然体系中的配位主要是阳离子,但 T+ 的差异是由于阴离子而非阳离子电导率的差异造成的,在考虑到段移动性差异的情况下,整个聚合物系列的 Li+ 电导率相似。
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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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