Advanced Aqueous Zn-Halogen Batteries with Multi-electron Transfer Chemistry Catalyzed by Organic Compounds: Insights into Mechanisms and Prospects

Abstract

Rechargeable aqueous zinc-halogen batteries (ZHBs) have regarded as promising candidates for next-generation energy storage, due to their intrinsic safety, multi-electron redox chemistry, low redox potential, and high theoretical capacity. Nevertheless, their practical implementation is hindered by several critical challenges, such as sluggish reaction kinetics, unexpected polyhalide shuttle effect, and poor electrode stability. In this review, we comprehensively summarize recent advances halogen conversion chemistry facilitated by organic compounds, with a focus on their roles as cathode host materials and functional electrolyte additives in AZHBs. Detailed analyses are provided on the electrochemical charge storage mechanisms and the selection criteria for organic compounds, emphasizing electrochemical stability, precise energy-level matching, dynamic interfacial adaptability, and the synergistic optimization of capacity and stability. Furthermore, recent developments of representative organic compounds that enhance ZHBs performance are summarized. For practical applications, current challenges and potential strategies to improve the electrochemical performance of ZHBs, specifically in terms of specific capacity, output voltage, cycle life, and rate capability, are proposed. Finally, perspectives on developing high-efficiency and high-energy ZHBs catalyzed by organic compounds with multi-electron transfer are discussed.

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Article information

Article type
Review Article
Submitted
07 Oct 2025
Accepted
17 Dec 2025
First published
18 Dec 2025

J. Mater. Chem. A, 2026, Accepted Manuscript

Advanced Aqueous Zn-Halogen Batteries with Multi-electron Transfer Chemistry Catalyzed by Organic Compounds: Insights into Mechanisms and Prospects

Y. Ma, M. Liu, X. Zhang, T. Zhao, Y. Zheng, J. Xiong, M. Muhammad, Z. Song, W. Wang, S. Yang and Y. Zhao, J. Mater. Chem. A, 2026, Accepted Manuscript , DOI: 10.1039/D5TA08175K

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