Fast Solid-State Defluorination/Fluorination of FeF<sub><i>x</i></sub> (<i>x</i> = 3–0) as Fluoride-Ion Battery Cathode
Fluoride-ion batteries, which use fluoride ions as charge carriers, are potential candidates for surpassing conventional lithium-ion batteries. Iron fluoride (FeF<sub><i>x</i></sub>, <i>x</i> = 3-0) is a cathode material with a high theoretical capacity of 712 mAh g<sup>-1</sup>. However, its electrochemical properties and reaction mechanism remain largely unexplored. In this study, a FeF<sub><i>x</i></sub> thin film was fabricated to investigate its discharge/charge capability and defluorination/fluorination mechanism as a cathode for all-solid-state fluoride-ion batteries. At room temperature, the FeF<sub><i>x</i></sub> cathode exhibited a reversible capacity that is 88-72% of the theoretical value at current rates of 0.1-1C. In addition, the cathode demonstrated excellent cyclability without any overvoltage increase or capacity degradation. The FeF<sub><i>x</i></sub> cathode could be discharged/charged even at a very low temperature of -30 °C, suggesting that the activation energy required for defluorination/fluorination is low. Operando X-ray absorption spectroscopy quantitatively demonstrated that the reversible discharge/charge of the FeF<sub><i>x</i></sub> cathode at room temperature was due to defluorination/fluorination between FeF<sub>3</sub>, FeF<sub>2</sub>, and Fe. The scanning electron microscopy and X-ray photoelectron spectroscopy results revealed that the electrode structure comprising uniformly distributed FeF<sub>3</sub> fine grains approximately 10 nm in size was maintained throughout the discharge/charge cycle, suggesting that this nanometer-scale structure is related to the excellent cyclability of the FeF<sub><i>x</i></sub> cathode. Electrochemical analysis revealed that the defluorination/fluorination reaction of FeF<sub>2</sub>/Fe was rate-limited by the charge transfer process, indicating the kinetic advantage of the solid-state FeF<sub><i>x</i></sub> reaction. This study provides significant improvements in the practical properties of the fluoride-ion electrode and insights into solid-state defluorination/fluorination.
Authors
- So Fujinami (ORCID: https://orcid.org/0000-0001-5151-7008)
- Tomotaka Nakatani (ORCID: https://orcid.org/0000-0003-4085-6236)
- Masahiro Shikano (ORCID: https://orcid.org/0000-0002-8710-9759)
- Hiroki Yamamoto (ORCID: https://orcid.org/0000-0003-3751-6978)
- Hikarí Sakaebe (ORCID: https://orcid.org/0000-0002-2520-1621)
- Kazuki Yoshii (ORCID: https://orcid.org/0000-0001-8904-6790)
- Yuta Maeyoshi (ORCID: https://orcid.org/0000-0002-4612-8283)
- Akira Yano (ORCID: https://orcid.org/0000-0002-5922-7897)
- Koji Nakanishi
Institutions
- University of Hyogo (JP)
- Kyoto University (JP)
- Advance (Japan) (JP)
- National Institute of Advanced Industrial Science and Technology (JP)
Publication Details
- Journal
- ACS Applied Materials & Interfaces
- Published
- 2025-09-29
- DOI
- https://doi.org/10.1021/acsami.5c12505
- Primary Topic
- Inorganic Fluorides and Related Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00