Electrochemistry
Online ISSN : 2186-2451
Print ISSN : 1344-3542
ISSN-L : 1344-3542

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UNCORRECTED PROOF
Electrode Performance of P3-type Na0.6[Mn0.9Me0.1]O2 (Me = Mn, Mg, Ti, Zn) as Lithium Intercalation Host
Sho TORIUMIShinichi KUMAKURAZachary T. GOSSAGEKodai MORIYAShinichi KOMABA
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JOURNAL OPEN ACCESS Advance online publication
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Article ID: 25-00085

UNCORRECTED PROOF: June 25, 2025
ACCEPTED MANUSCRIPT: June 10, 2025
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Abstract

Designing positive electrode materials for Li-ion and Na-ion batteries without using expensive metals is of critical importance for sustainable energy storage systems. One of the most promising candidates, P3-type layered sodium manganese oxide (P3-NaxMnO2) can be obtained via solid-state reaction. While there is no report on P3-LixMnO2 synthesis and electrochemistry because of its instability, lithium ion exchange with Na in P3-NaxMnO2 is a plausible strategy to test its Li insertion/extraction. In this study, we investigate the electrochemical activity of P3-NaxMnO2 electrode in both Li and Na cells. We found that high capacity of ca. 200 mAh/g is achieved in both cells, and P3-NaxMnO2 electrodes undergo spontaneous Na/Li ion exchange in the Li+-containing electrolyte, which can thereafter be reversibly cycled. To improve electrochemical performance, we demonstrated two approaches: partial Ti or other metal substitution for Mn in P3-NaxMnO2 and using a highly concentrated electrolyte of 5.5 mol dm−3 Li(N(SO2F)2) dimethyl carbonate solution. Particularly, the highly concentrated Li-electrolyte provides a significant enhancement on the cycle stability in the Li cell, demonstrating no apparent capacity loss up to 100 cycles.

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© The Author(s) 2025. Published by ECSJ.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License (CC BY-NC-SA, https://creativecommons.org/licenses/by-nc-sa/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium by share-alike, provided the original work is properly cited. For permission for commercial reuse, please email to the corresponding author. [DOI: 10.5796/electrochemistry.25-00085].
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