Abstract
Na3V2(PO4)3, a highly promising cathode material for sodium-ion batteries, often suffers from limited electronic conductivity, impeding its overall performance. To address this issue, a study was conducted to synthesize graphene-attached hierarchical porous Na3V2(PO4)3 microspheres (NVP/GO). Using a hydrothermal method and high temperature sintering process with 1,4-naphthalene dicarboxylic acid (NDC) as a carbon source, this study successfully improved the transport dynamics of NVP/GO, resulting in enhanced rate capability and cycling performance. The NVP/GO microspheres exhibited an initial discharge capacity of 108.6 mAh g−1 at 0.5 C, and even at a high rate of 20 C, the capacity remained at 81.2 mAh g−1. Impressively, after 10,000 cycles at 10 C, the capacity only experienced a minimal decay of 0.006% per cycle, indicating excellent cycling stability. Ex-situ XRD analysis further confirmed the reversible Na ion extraction/insertion process of the NVP/GO electrode. Moreover, when NVP/GO was assembled into full cells with NVP/GO as both the cathode and anode, the electrochemical performance remained highly satisfactory. These findings provide valuable insights for advancing the practical application of sodium-ion cathode materials.
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The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
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Acknowledgements
This work was supported by the Natural Science Foundation of Hunan Province [2020JJ4117].
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This work was supported by the Natural Science Foundation of Hunan Province [2020JJ4117].
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All authors contributed to the study’s conception and design. Material preparation, data collection, and analysis were performed by HC, SX, MZ, XZ. The first draft of the manuscript was written by HC and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
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Chen, H., Xu, S., Zhou, M. et al. Hierarchical porous Na3V2(PO4)3/graphene microspheres with enhanced sodium-ion storage properties. J Mater Sci: Mater Electron 34, 2196 (2023). https://doi.org/10.1007/s10854-023-11633-x
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DOI: https://doi.org/10.1007/s10854-023-11633-x