Issue 6, 2024

Co-intercalation strategy for simultaneously boosting two-electron conversion and bulk stabilization of Mn-based cathodes in aqueous zinc-ion batteries

Abstract

Zinc-ion batteries (ZIBs) have emerged as a promising candidate due to the abundance, low cost and high energy density. However, the performance of ZIBs needs to be improved to meet the practical requirements of energy storage systems. This work probes the efficacy of co-intercalation as a strategy for enhancing the electrochemical performance of ZIBs through the fabrication of sodium and copper co-intercalated birnessite manganese oxide (NCMO) cathodes. The results show that the co-intercalation of sodium and copper ions catalyzes the activation of copper cations on the surface Mn2+/Mn4+ redox pair, leading to improved specific capacity and cycling stability. The NCMO cathode exhibits a remarkable specific capacity of 576 mA h g−1 after 100 cycles at a low loading of around ∼1 mg cm−2 and a high areal capacity of 2.10 mA h cm−2 at a high loading of ∼10.9 mg cm−2. The mechanism of copper ions to promote the manganese-based cathode conversion reaction is thoroughly investigated. These findings suggest that developing catalytic effects is a promising approach for developing high-performance cathode materials for ZIBs with practical and efficient energy storage systems.

Graphical abstract: Co-intercalation strategy for simultaneously boosting two-electron conversion and bulk stabilization of Mn-based cathodes in aqueous zinc-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
22 Dec 2023
Accepted
16 Feb 2024
First published
16 Feb 2024
This article is Open Access
Creative Commons BY license

Energy Environ. Sci., 2024,17, 2287-2297

Co-intercalation strategy for simultaneously boosting two-electron conversion and bulk stabilization of Mn-based cathodes in aqueous zinc-ion batteries

X. Gao, C. Shen, H. Dong, Y. Dai, P. Jiang, I. P. Parkin, H. Zhang, C. J. Carmalt and G. He, Energy Environ. Sci., 2024, 17, 2287 DOI: 10.1039/D3EE04492K

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