Surpassing water-splitting potential in aqueous redox flow batteries: insights from kinetics and thermodynamics

EES catalysis Pub Date : 2024-01-04 DOI:10.1039/D3EY00231D
Vithiya Muralidharan, S. Jayasubramaniyan and Hyun-Wook Lee
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Abstract

Aqueous redox flow batteries (AQRFBs) employing non-flammable electrolytes are recognized for their inherent safety and eco-friendliness, making them promising candidates for large-scale energy storage systems. Furthermore, the unique architecture of this battery technology enables autonomous decoupling of power and energy, resulting in higher capacity and enhanced cost-effectiveness compared to other battery technologies. Nonetheless, the limited electrochemical stability of water leads to water electrolysis during the electrochemical process, triggering undesired parasitic reactions, namely, the hydrogen evolution reaction, and ion-cross-over. These reactions significantly affect the electrochemical performance of the system, giving rise to several challenges, including low Coulombic efficiency and a short cycle life, hindering the advancement of AQRFBs. To overcome these obstacles and achieve high-potential AQRFBs, it becomes essential to incorporate a reaction-inhibitor to encounter water electrolysis during battery operation. This perspective review focuses on addressing and mitigating the thermodynamic limitations through improved strategies, proposing effective approaches to suppress aforementioned side reactions.

Abstract Image

超越水氧化还原流动电池中的分水势:动力学和热力学的启示
采用不易燃电解质的水氧化还原液流电池(AQRFB)因其固有的安全性和生态友好性而备受认可,是一种前景广阔的大规模储能系统。此外,与其他电池技术相比,这种电池技术的独特结构可实现功率和能量的自主解耦,从而实现更高的容量和更优越的成本效益。然而,水的电化学稳定性有限,导致水在电化学过程中发生电解,引发了不希望发生的寄生反应,即氢进化反应和离子交叉。这些反应严重影响了系统的电化学性能,从而带来了一些挑战,包括库仑效率低和循环寿命短,阻碍了 AQRFB 的发展。为了克服这些障碍,实现高潜力的 AQRFB,必须加入反应抑制剂,以应对电池运行过程中的水电解问题。本视角综述集中探讨了如何通过改进策略来解决和缓解热力学限制,并提出了抑制上述副反应的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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