Materials Futures (Jan 2024)

Improving cycling performance of the NaNiO2 cathode in sodium-ion batteries by titanium substitution

  • Siyu An,
  • Leonhard Karger,
  • Sören L Dreyer,
  • Yang Hu,
  • Eduardo Barbosa,
  • Ruizhuo Zhang,
  • Jing Lin,
  • Maximilian Fichtner,
  • Aleksandr Kondrakov,
  • Jürgen Janek,
  • Torsten Brezesinski

DOI
https://doi.org/10.1088/2752-5724/ad5faa
Journal volume & issue
Vol. 3, no. 3
p. 035103

Abstract

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O3-type layered oxide cathodes, such as NaNi _0.5 Mn _0.5 O _2 , have garnered significant attention due to their high theoretical specific capacity while using abundant and low-cost sodium as intercalation species. Unlike the lithium analog (LiNiO _2 ), NaNiO _2 (NNO) exhibits poor electrochemical performance resulting from structural instability and inferior Coulomb efficiency. To enhance its cyclability for practical application, NNO was modified by titanium substitution to yield the O3-type NaNi _0.9 Ti _0.1 O _2 (NNTO), which was successfully synthesized for the first time via a solid-state reaction. The mechanism behind its superior performance in comparison to that of similar materials is examined in detail using a variety of characterization techniques. NNTO delivers a specific discharge capacity of ∼190 mAh g ^−1 and exhibits good reversibility, even in the presence of multiple phase transitions during cycling in a potential window of 2.0‒4.2 V vs. Na ^+ /Na. This behavior can be attributed to the substituent, which helps maintain a larger interslab distance in the Na-deficient phases and to mitigate Jahn–Teller activity by reducing the average oxidation state of nickel. However, volume collapse at high potentials and irreversible lattice oxygen loss are still detrimental to the NNTO. Nevertheless, the performance can be further enhanced through coating and doping strategies. This not only positions NNTO as a promising next-generation cathode material, but also serves as inspiration for future research directions in the field of high-energy-density Na-ion batteries.

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