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.

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Journal
ACS Applied Materials & Interfaces
Published
2025-09-29
DOI
https://doi.org/10.1021/acsami.5c12505
Primary Topic
Inorganic Fluorides and Related Compounds
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article
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article

Fast Solid-State Defluorination/Fluorination of FeFx (x = 3–0) as Fluoride-Ion Battery Cathode

So Fujinami, Tomotaka Nakatani, Masahiro Shikano, Hiroki Yamamoto et al.
ACS Applied Materials & Interfaces
Inorganic Fluorides and Related Compounds
article

Fast Solid-State Defluorination/Fluorination of FeFx (x = 3–0) as Fluoride-Ion Battery Cathode

So Fujinami, Tomotaka Nakatani, Masahiro Shikano, Hiroki Yamamoto, Hikarí Sakaebe, Kazuki Yoshii, Yuta Maeyoshi, Akira Yano, Koji Nakanishi
article en

Abstract

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.

ACS Applied Materials & InterfacesVol. 17(40)
University of Hyogo (JP), Kyoto University (JP), Advance (Japan) (JP), National Institute of Advanced Industrial Science and Technology (JP)
Openalex Percentile: Top 78%
Inorganic Fluorides and Related Compounds
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