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Stabilizing Oxygen Framework in P3-Type Cathodes for Highly Reversible Sodium-Ion Batteries.

Xin-Yu Zhang1, Wen-Ye Wang1, Guang-Xu Wei1

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Summary

Cosubstitution with Zn2+ and Ti4+ stabilizes P3-layered oxide cathodes for sodium-ion batteries by preventing oxygen loss. This strategy enhances cycling stability and capacity retention, crucial for advanced battery performance.

Keywords:
P3 cathodeco-substitution strategyhigh reversibilityoxygen frameworkoxygen vacanciessodium-ion batteries

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Area of Science:

  • Materials Science
  • Electrochemistry
  • Energy Storage

Background:

  • P3-type layered oxides are promising cathode materials for sodium-ion batteries.
  • These materials suffer from voltage decay and capacity fading due to oxygen vacancies and oxygen loss during cycling.

Purpose of the Study:

  • To develop a cosubstitution strategy to stabilize the oxygen framework of P3-Na0.67Ni0.25Mn0.75O2 cathode material.
  • To suppress oxygen vacancies and improve the overall electrochemical performance.

Main Methods:

  • Incorporation of Zn2+ and Ti4+ into the P3-Na0.67Ni0.25Mn0.75O2 structure.
  • Investigation of the effects of cosubstitution on oxygen stability, anionic overoxidation, and Mn3+ generation.
  • Electrochemical cycling tests to evaluate capacity retention and structural evolution.

Main Results:

  • Cosubstitution effectively stabilized the oxygen framework by suppressing anionic overoxidation and restraining oxygen vacancy formation and diffusion.
  • The Ti-O bonding anchored the oxygen sublattice, reducing Mn3+ generation and Jahn-Teller distortion.
  • The modified cathode demonstrated highly reversible structural evolution and retained 90.0% of its capacity after 50 cycles.

Conclusions:

  • Oxygen vacancy management through cosubstitution is an effective strategy for enhancing the stability of P3 cathodes.
  • The Zn2+/Ti4+ cosubstitution approach offers a pathway to achieve stable and high-performance sodium-ion batteries.