Optimization Strategies and Mechanisms of High-Concentration Electrolytes for Aqueous Rechargeable Batteries

IF 12
Lingli Chen, Yue Xu, Angran Liu, Bo Cheng, Sihan Wang, Xiaolin Zhang, Yongbin Hua, Long Jiang, Chun Fang, Jiantao Han, Paul K. Chu
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Abstract

Aqueous batteries represent a significant research area due to their low cost and high safety advantages. However, aqueous electrolytes suffer from high side-reaction activity, narrow electrochemical windows, and insufficient interface stability and are frozen at low temperatures, thus hampering practical applications. This review focuses on high-concentration brine-based aqueous electrolyte optimization strategies to address the above problems. The solvation structure, hydrogen-bond network, and interfacial components are the key factors that are altered by the appropriate salts, solvent selection, and electrode interaction. A high concentration of brine decreases the free water content, inhibits the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), and widens the electrochemical window. Additional salts and solvents in the electrolyte can further promote the formation of the solid electrolyte interphase (SEI) and the cathode electrolyte interphase (CEI) to reduce deleterious interfacial side reactions. At the same time, the synergistic effects between the cathodes/anodes and the electrolyte expand the electrochemical window, improve the interface stability, and enhance the electrochemical properties of aqueous batteries. In this review, we describe the optimization strategies and mechanisms to provide guidance to future research on high-concentration electrolytes (HCE) and the challenge of high-energy and wide-temperature-range applications.

Abstract Image

水溶液可充电电池高浓度电解液的优化策略与机理
水电池因其低成本和高安全性的优点而成为一个重要的研究领域。然而,水溶液电解质存在副反应活性高、电化学窗口窄、界面稳定性差、低温冻结等问题,阻碍了实际应用。本文综述了针对上述问题的高浓度盐水基水溶液电解质优化策略。溶剂化结构、氢键网络和界面组分是通过适当的盐、溶剂选择和电极相互作用改变的关键因素。高浓度卤水降低了游离水含量,抑制了析氢反应(HER)和析氧反应(OER),扩大了电化学窗口。电解质中附加的盐和溶剂可以进一步促进固体电解质界面相(SEI)和阴极电解质界面相(CEI)的形成,以减少有害的界面副反应。同时,阴极/阳极与电解质之间的协同作用扩大了电化学窗口,提高了界面稳定性,增强了水性电池的电化学性能。在这篇综述中,我们描述了优化策略和机制,为未来高浓度电解质(HCE)的研究以及高能和宽温度范围应用的挑战提供指导。
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