Mechanism of Carbon Nanotubes in Enhancing the Electrical Conductivity and High-Rate Performance of Na2.6Fe1.7(SO4)3/CNTs Cathode Materials
The Alluaudite-type Na2.6Fe1.7(SO4)3 cathode material used in sodium-ion batteries is limited by poor electronic conductivity and slow ionic migration, which restricts its high-rate charge-discharge performance. To confront these challenges, this study investigated various Na2.6Fe1.7(SO4)3/CNTs composite materials to elucidate how carbon nanotube composites modulate the local crystal structure, sodium storage mechanisms, and electrochemical performance. Kinetic analysis shows that introducing CNTs substantially reduces charge-transfer impedance and the apparent activation energy of Na+, thereby shifting the reaction from diffusion-controlled to pseudocapacitive behavior and greatly accelerating ion transport. In situ XRD confirms that highly reversible, single-phase, solid-solution reactions occur in all samples. The Na2.6Fe1.7(SO4)3/SWCNTs composite, containing only 1.2 wt % SWCNTs, exhibits the smallest change in unit cell volume and the greatest structural elasticity. This composition achieves a reversible specific capacity of 95.01 mAh·g-1 at 0.1C and a rate performance of 82.37 mAh·g-1 at 50C. Overall, this study reveals the key role of CNTs in facilitating synergistic electron and ion transport and stabilizing the crystal structure, providing guidance for the design of high-power sodium-ion battery cathodes.
Authors
- Qinghua Tian (ORCID: https://orcid.org/0000-0001-5695-4442)
- Jie Chen (ORCID: https://orcid.org/0000-0001-9945-9644)
- Jiafeng Zhang (ORCID: https://orcid.org/0000-0001-9057-1605)
- Zhiwei Yang (ORCID: https://orcid.org/0000-0003-0850-0512)
- Renwei Hou
- Xinming Fan
- Haojie Du
- Haonan Zhang
Institutions
- Central South University (CN)
Publication Details
- Journal
- ACS Applied Materials & Interfaces
- Published
- 2026-10-19
- DOI
- https://doi.org/10.1021/acsami.6c15754
- Primary Topic
- Advancements in Battery Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00