4.8 Review

Proton storage chemistry in aqueous zinc-organic batteries: A review

Journal

INFOMAT
Volume 5, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1002/inf2.12382

Keywords

aqueous zinc-ion batteries; H+; Zn2+ co-storage; organic electrode materials; proton storage chemistry

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Benefiting from structural diversity and resource renewability, organic electroactive compounds have gained attention as cathode materials for aqueous Zn-ion batteries (ZIBs). This review discusses the recent developments in organic electrode materials for aqueous ZIBs, with a specific focus on the controversial proton (H+) storage chemistry. It summarizes the reported electrochemical mechanisms, including pure Zn2+ intercalation, pure H+ storage, and H+/Zn2+ co-storage, and systematically discusses the impact of H+ storage on the electrochemical performance of aqueous ZIBs. The review also highlights relevant characterization methods and outlines perspectives and directions for further understanding the charge storage mechanisms of organic materials.
Benefiting from the advantageous features of structural diversity and resource renewability, organic electroactive compounds are considered as attractive cathode materials for aqueous Zn-ion batteries (ZIBs). In this review, we discuss the recent developments of organic electrode materials for aqueous ZIBs. Although the proton (H+) storage chemistry in aqueous Zn-organic batteries has triggered an overwhelming literature surge in recent years, this topic remains controversial. Therefore, our review focuses on this significant issue and summarizes the reported electrochemical mechanisms, including pure Zn2+ intercalation, pure H+ storage, and H+/Zn2+ co-storage. Moreover, the impact of H+ storage on the electrochemical performance of aqueous ZIBs is discussed systematically. Given the significance of H+ storage, we also highlight the relevant characterization methods employed. Finally, perspectives and directions on further understanding the charge storage mechanisms of organic materials are outlined. We hope that this review will stimulate more attention on the H+ storage chemistry of organic electrode materials to advance our understanding and further its application.

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