Overview
- A Tokyo University of Science team led by Shinichi Komaba, with Yuki Fujii and Zachary T. Gossage, reports the findings in Chemical Science.
- The diluted-electrode method mixes hard carbon with inactive aluminum oxide to remove ion transport limits that mask intrinsic behavior in dense electrodes.
- Measurements show a higher apparent diffusion coefficient for sodium than for lithium in hard carbon, confirming faster intrinsic sodiation.
- Pore-filling involving pseudo-metallic cluster formation is the rate-determining step, with sodium requiring less activation energy and showing reduced temperature sensitivity.
- The results indicate that hard‑carbon sodium‑ion cells could be viable for high‑power use cases, though further development and validation remain necessary.