Recent progress in structural modification of polymer gel electrolytes for use in solid-state zinc-ion batteries

电解质 聚合物电解质 固态 聚合物 材料科学 离子 化学工程 无机化学 纳米技术 化学 冶金 有机化学 复合材料 离子电导率 工程类 电极 物理化学
作者
Yifan Li,Jingjing Yuan,Yifan Qiao,Hui Xu,Zhihao Zhang,Wenyao Zhang,Guangyu He,Haiqun Chen
出处
期刊:Dalton Transactions [Royal Society of Chemistry]
卷期号:52 (34): 11780-11796 被引量:17
标识
DOI:10.1039/d3dt01764h
摘要

Zinc-ion batteries are one of the promising energy storage devices, which have the advantages of environmental friendliness, high safety and low price and are expected to be used in large-scale battery application fields. However, four prominent water-induced adverse reactions, including zinc dendrite formation, zinc corrosion, passivation and the hydrogen evolution reaction in aqueous systems, seriously shorten the cycling life of zinc-ion batteries and greatly hinder their development. Based on this, polymer gel electrolytes have been developed to alleviate these issues due to their unique network structure, which can reduce water activity and suppress water-induced side reactions. Based on the challenges of polymer gel electrolytes, this review systematically summarizes the latest research progress in the use of additives in them and explores new perspectives in response to the existing problems with polymer electrolytes. In order to expand the performance of polymer gel electrolytes in zinc-ion batteries, a range of different types of additives are added via physical/chemical crosslinking, such as organic or inorganic substances, natural plants, etc. In addition, different types of additives and polymerization crosslinking from different angles essentially improve the ionic conductivity of the gel electrolyte, inhibit the growth of zinc dendrites, and reduce hydrogen evolution and oxygen-absorbed corrosion. After these modifications of polymer gel electrolytes, a more stable and superior electrochemical performance of zinc-ion batteries can be obtained, which provides some strategies for solid-state zinc-ion batteries.
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