Sodium Rich Vanadium Oxy‐Fluorophosphate – Na3.2Ni0.2V1.8(PO4)2F2O – as Advanced Cathode for Sodium Ion Batteries

Author:

Essehli Rachid1,Yahia Hamdi Ben2,Amin Ruhul1,Li Mengya1,Morales Daniel3,Greenbaum Steven G.4,Abouimrane Ali1,Parejiya Anand1,Mahmoud Abdelfattah13456,Boulahya Khalid6,Dixit Marm1,Belharouak Ilias1ORCID

Affiliation:

1. Electrification and Energy Infrastructures Division Oak Ridge National Laboratory Oak Ridge TN 37831 USA

2. Qatar Environment and Energy Research Institute Hamad Bin Khalifa University Qatar Foundation Doha 34110 Qatar

3. Exponent, Inc. Natick MA 01760 USA

4. Department of Physics & Astronomy Hunter College of the City University of New York New York NY 10065 USA

5. Greenmat Cesam Research Unit University of Liège Department of Chemistry Liège 4000 Belgium

6. Departamento de Química Inorgánica Facultad de Químicas Universidad Complutense Madrid 28040 Spain

Abstract

AbstractConventional sodium‐based layered oxide cathodes are extremely air sensitive and possess poor electrochemical performance along with safety concerns when operating at high voltage. The polyanion phosphate, Na3V2(PO4)3 stands out as an excellent candidate due to its high nominal voltage, ambient air stability, and long cycle life. The caveat is that Na3V2(PO4)3 can only exhibit reversible capacities in the range of 100 mAh g−1, 20% below its theoretical capacity. Here, the synthesis and characterizations are reported for the first time of the sodium‐rich vanadium oxyfluorophosphate, Na3.2Ni0.2V1.8(PO4)2F2O, a tailored derivative compound of Na3V2(PO4)3, with extensive electrochemical and structural analyses. Na3.2Ni0.2V1.8(PO4)2F2O delivers an initial reversible capacity of 117 mAh g−1 between 2.5 and 4.5 V under the 1C rate at room temperature, with 85% capacity retention after 900 cycles. The cycling stability is further improved when the material is cycled at 50 °C within 2.8–4.3 V for 100 cycles. When paired with a presodiated hard carbon, Na3.2Ni0.2V1.8(PO4)2F2O cycled with a capacity retention of 85% after 500 cycles. Cosubstitution of the transition metal and fluorine in Na3.2Ni0.2V1.8(PO4)2F2O as well as the sodium‐rich structure are the major factors behind the improvement of specific capacity and cycling stability, which paves the way for this cathode in sodium‐ion batteries.

Funder

Oak Ridge National Laboratory

U.S. Department of Energy

Office of Electricity

Office of Energy Efficiency and Renewable Energy

Vehicle Technologies Office

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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