Activating fast and reversible sodium storage in NASICON cationic defect sites through fluorine doping

Cycling positive electrode materials with high voltages and long lifetimes remains a challenge. On the one hand, operating electrodes at high voltages is usually accompanied by severe structural distortions and irreversible reactions. On the other hand, the significant volume variation upon Na<sup>+</sup> insertion/extraction limits the long cycling life. Here, we report a defective positive electrode material with a chemical formula of Na<sub>3.2</sub>□<sub>0.8</sub>Co<sub>0.5</sub>Fe<sub>0.5</sub>V(PO<sub>3.9</sub>F<sub>0.1</sub>)<sub>3</sub> (□ represents Na vacancy) through fluorine doping with activated reversible and fast Na<sup>+</sup> intercalation/deintercalation to increase the energy and power densities. Notably, this positive electrode material achieves a high reversible specific capacity of 151 mAh g<sup>-1</sup> and prominent rate performance ranging from 1.5-4.2 V vs. Na<sup>+</sup>/Na, as well as a long lifespan of 6000 cycles under a high rate of 5 A g<sup>-1</sup> with a capacity retention of ~94%, due to the activated cationic defect sites which reduces the transport barrier at the Na(1) site. This approach is expected to be applied to the rational design of polyanionic materials for batteries.

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Publication Details

Journal
Nature Communications
Published
2025-03-25
DOI
https://doi.org/10.1038/s41467-025-58012-0
Citations
18
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
13.15

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article

Activating fast and reversible sodium storage in NASICON cationic defect sites through fluorine doping

Tsung‐Yi Chen, Jingrong Hou, Mohammed Hadouchi, Mohamed Ait Tamerd et al.
18 citations
Nature Communications
Advancements in Battery Materials
13.15
article

Activating fast and reversible sodium storage in NASICON cationic defect sites through fluorine doping

Tsung‐Yi Chen, Jingrong Hou, Mohammed Hadouchi, Mohamed Ait Tamerd, Yiming Zhu, Xinyue Shi, Jiwei Ma, Yongchao Shi, Menghao Yang, Wei‐Hsiang Huang, Shasha Guo, Jie Liu, Mingxue Tang
article en
18 citations

Abstract

Cycling positive electrode materials with high voltages and long lifetimes remains a challenge. On the one hand, operating electrodes at high voltages is usually accompanied by severe structural distortions and irreversible reactions. On the other hand, the significant volume variation upon Na<sup>+</sup> insertion/extraction limits the long cycling life. Here, we report a defective positive electrode material with a chemical formula of Na<sub>3.2</sub>□<sub>0.8</sub>Co<sub>0.5</sub>Fe<sub>0.5</sub>V(PO<sub>3.9</sub>F<sub>0.1</sub>)<sub>3</sub> (□ represents Na vacancy) through fluorine doping with activated reversible and fast Na<sup>+</sup> intercalation/deintercalation to increase the energy and power densities. Notably, this positive electrode material achieves a high reversible specific capacity of 151 mAh g<sup>-1</sup> and prominent rate performance ranging from 1.5-4.2 V vs. Na<sup>+</sup>/Na, as well as a long lifespan of 6000 cycles under a high rate of 5 A g<sup>-1</sup> with a capacity retention of ~94%, due to the activated cationic defect sites which reduces the transport barrier at the Na(1) site. This approach is expected to be applied to the rational design of polyanionic materials for batteries.

Nature CommunicationsVol. 16(1)
Tongji University (CN), Mohammed V University (MA), National Synchrotron Radiation Research Center (TW), Center for High Pressure Science & Technology Advanced Research (CN), University of Science and Technology Beijing (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 1%
Advancements in Battery Materials
13.15
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