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Tuning the Mn-based NASICON cathodes: A perspective on stabilizing high working voltage for sustainable sodium-ion batteries AITranslate

MOE Key Laboratory for UV Light-Emitting Materials and Technology, Northeast Normal University, Changchun 130024, China
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Abstract AITranslate

Manganese-based NASICON materials are promising cathodes for sodium-ion batteries owing to their open three-dimensional framework and high Na⁺ mobility. However, their cycling performance is hindered by Jahn–Teller distortions and anti-site defects that destabilize the lattice. Recent studies show that rational electronic structure and defect engineering can effectively address these challenges. High-valent cation doping, such as Ti4+ or Zr4+, reduces lattice strain and stabilizes Mn redox reactions, while controlled synthesis suppresses Mn–Na anti-site defects and enhances Na+ transport. Furthermore, partial anion substitution with fluorophosphate or silicate units strengthens Mn–O bonding and increases operating voltage. Integrating these strategies enables improved structural stability and long-term reversibility, offering a feasible pathway toward durable, high-energy sodium-ion batteries for large-scale energy storage.

KeyWords AITranslate

manganese-based NASICON Jahn–Teller distortion high-voltage structural stability

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Basic Information:

DOI:10.23919/CHAIN.2025.000019

Chinese Library Classification Number:

Citation Information:

Manganese-based NASICON materials are promising cathodes for sodium-ion batteries owing to their open three-dimensional framework and high Na⁺ mobility. However, their cycling performance is hindered by Jahn–Teller distortions and anti-site defects that destabilize the lattice. Recent studies show that rational electronic structure and defect engineering can effectively address these challenges. High-valent cation doping, such as Ti4+ or Zr4+, reduces lattice strain and stabilizes Mn redox reactions, while controlled synthesis suppresses Mn–Na anti-site defects and enhances Na+ transport. Furthermore, partial anion substitution with fluorophosphate or silicate units strengthens Mn–O bonding and increases operating voltage. Integrating these strategies enables improved structural stability and long-term reversibility, offering a feasible pathway toward durable, high-energy sodium-ion batteries for large-scale energy storage.

quote

GB/T 7714-2015 [1] Heng Zhang, Xinglong Wu. Tuning the Mn-based NASICON cathodes: A perspective on stabilizing high working voltage for sustainable sodium-ion batteries[J]. Chain, 2025, 2(4): 267-271. DOI:10.23919/CHAIN.2025.000019.
MLA [1] Heng Zhang, and Xinglong Wu. "Tuning the Mn-based NASICON cathodes: A perspective on stabilizing high working voltage for sustainable sodium-ion batteries." Chain, vol. 2, no. 4, 2025, pp. 267-271, https://doi.org/10.23919/CHAIN.2025.000019.
APA [1] Heng Zhang, & Xinglong Wu. (2025). Tuning the Mn-based NASICON cathodes: A perspective on stabilizing high working voltage for sustainable sodium-ion batteries. Chain, 2(4), 267-271. https://doi.org/10.23919/CHAIN.2025.000019
IEEE [1] Heng Zhang and Xinglong Wu, "Tuning the Mn-based NASICON cathodes: A perspective on stabilizing high working voltage for sustainable sodium-ion batteries," Chain, vol. 2, no. 4, pp. 267-271, 2025, doi: 10.23919/CHAIN.2025.000019. keywords: {manganese-based NASICON;Jahn–Teller distortion;high-voltage structural stability}