Alok K. Pandey a, Benoît D.L. Campéon b,c, Saad Zafar b, Toru Ishigaki d, Tsubasa Koyama e , Masanobu Nakayama e, and Naoaki Yabuuchi a,b
a Department of Chemistry and Life Science, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, Kanagawa 240–8501, Japan
b Advanced Chemical Energy Research Center, Institute of Advanced Sciences,Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama, Kanagawa 240–8501, Japan
c University Grenoble Alpes, University Savoie Mont Blanc, CNRS, Grenoble INP, LEPMI, Grenoble 38610, France
d Neutron Industrial Application Promotion Center, Comprehensive Research Organization for Science and Society (CROSS), Ibaraki Quantum Beam Center, 162-1 Shirakata, Tokai, Naka, Ibaraki 319–1106, Japan
e Frontier Research Institute for Materials Science (FRIMS), Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya, Aichi 466–8555, Japan
The global push for more sustainable and affordable energy storage has driven interest in sodium-ion batteries (SIBs), a promising alternative to lithium-ion batteries thanks to the abundance and low cost of sodium. However, developing suitable negative electrodes for SIBs remains a major challenge—conventional graphite, which works well in lithium systems, performs poorly with sodium.
In this study, researchers from Yokohama National University (Japan) and their collaborators—including contributors from LEPMI (France) and the CROSS neutron facility (Japan)—developed a novel layered electrode material: P3-type Na₀.₅Cr₀.₅Ti₀.₅O₂. This compound was designed using an innovative ion-exchange method, where potassium ions in a parent structure were replaced with sodium at room temperature, yielding a sodium-deficient but highly conductive metastable phase.
Crucially, neutron diffraction played a pivotal role in elucidating the structure of the synthesized material, results are summaries in the figure below. Unlike X-rays, neutrons are highly sensitive to light elements and can distinguish between neighboring transition metals such as chromium (Cr) and titanium (Ti), thanks to their contrasting neutron scattering lengths.1,2 This sensitivity allowed the team to precisely map the positions of potassium and the transition metals within the layered structure, confirming the disordering of cations, a key feature that facilitates fast ion movement and high electrical/ionic conductivity.
The result is a robust electrode material with exceptional performance: a high capacity of 125 mAh g⁻¹ and excellent rate capability (up to 80% capacity retention at a 20C rate), along with long-term cycling stability (70% after 1000 cycles). Its fast-charging ability and safer operating voltage (≈0.8 V) make it a strong candidate for next-generation batteries, especially for electric vehicle applications.

Figure. a) Rietveld refinement on the neutron diffraction pattern of K0.5Cr0.5Ti0.5O2, b) a schematic illustration of the P3-type layered structure, c) nuclear density distribution calculated by MEM using neutron powder diffraction data, d) HAADF-STEM image showing the orderingsequence of K0.5Cr0.5Ti0.5O2 , e) ABF-STEM image, and f) FE-SEM image and EDX maps
[1] Y. Wang, R. Xiao, Y.-S. Hu, M. Avdeev, L. Chen, Nat. Commun. 2015,6, 6954
[2] Y. Tsuchiya, K. Takanashi, T. Nishinobo, A. Hokura, M. Yonemura, T.Matsukawa, T. Ishigaki, K. Yamanaka, T. Ohta, N. Yabuuchi, Chem.Mater. 2016, 28, 7006




