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In-Situ Constructing N,S-Codoped Carbon Heterointerface for High-Rate Cathode of Sodium-Ion Batteries. | LitMetric

In-Situ Constructing N,S-Codoped Carbon Heterointerface for High-Rate Cathode of Sodium-Ion Batteries.

ACS Appl Mater Interfaces

State Key Laboratory of Powder Metallurgy, College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.

Published: November 2024

AI Article Synopsis

  • - NaV(PO) (NVP) is a promising cathode material for sodium-ion batteries, but its poor conductivity limits its performance, prompting research for improvements.
  • - The study introduces a simple method to create N/S dual-atom doped carbon coatings that enhance Na mobility and increase conductivity by altering electron distribution and expanding interlayer spacing.
  • - The modified NVP@NSC composite achieves a high specific capacity of 90.3 mAh/g at 20 C with 94.4% capacity retention after 8000 cycles, indicating excellent stability and performance for practical battery applications.

Article Abstract

NaV(PO) (NVP) is considered one of the promising choices for cathodes of sodium-ion batteries, but the poor conductivity resulted inferior rate performance limited the practical development of NVP cathodes. In this study, we successfully synthesized N/S dual-atom doped carbon coatings in situ through a simple one-step solid-state sintering method. The uniformly coated carbon layer can inhibit the agglomeration and growth of active materials during the sintering process, shorten the Na migration path, and increase the contact area with the electrolyte, thus facilitating rapid Na migration. Notably, the doping of N elements can alter the electron distribution of carbon coating, enhancing electron conductivity. Furthermore, the introduction of S elements in the carbon layer can induce the formation of stable C-S-C bonds in the molecular layer, expanding the interlayer spacing, which is beneficial for Na transport and storage. Therefore, the modified NVP@NSC composite provides a high specific capacity of 90.3 mAh g at a rate of 20 C, with a capacity retention rate of 94.4% after 8000 cycles, demonstrating excellent stability at high current densities. Moreover, the full cell exhibits remarkable electrochemical performance at 5 C. This research contributes to the practical development of NVP cathodes.

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Source
http://dx.doi.org/10.1021/acsami.4c15311DOI Listing

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