Recent Progress and Future Advances on Aqueous Monovalent-Ion Batteries towards Safe and High-Power Energy Storage

Fangli Zhang, Wenchao Zhang*, David Wexler, Zaiping Guo*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

16 Downloads (CityUHK Scholars)

Abstract

Aqueous monovalent-ion batteries have been rapidly developed recently as promising energy storage devices in large-scale energy storage systems owing to their fast charging capability and high power densities. In recent years, Prussian blue analogues, polyanion-type compounds, and layered oxides have been widely developed as cathodes for aqueous monovalent-ion batteries because of their low cost and high theoretical capacity. Furthermore, many design strategies have been proposed to expand their electrochemical stability window by reducing the amount of free water molecules and introducing an electrolyte addictive. This review highlights the advantages and drawbacks of cathode and anode materials, and summarizes the correlations between the various strategies and the electrochemical performance in terms of structural engineering, morphology control, elemental compositions, and interfacial design. Finally, this review can offer rational principles and potential future directions in the design of aqueous monovalent-ion batteries. © 2022 The Authors. Advanced Materials published by Wiley-VCH GmbH.
Original languageEnglish
Article number2107965
Number of pages16
JournalAdvanced Materials
Volume34
Issue number24
Online published26 Mar 2022
DOIs
Publication statusPublished - 16 Jun 2022
Externally publishedYes

Funding

Financial support from the Australian Research Council (ARC) (LP160101629, DP210101486, and DP200101862) and the National Natural Science Foundation of China (Grant No. 52104315) is acknowledged.

Research Keywords

  • anodes
  • aqueous monovalent-ion batteries
  • cathodes
  • electrolytes
  • the correlations between the strategies and the performance

Publisher's Copyright Statement

  • This full text is made available under CC-BY-NC-ND 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/

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