Facile Al2O3 coating suppress dissolution of Mn2+ in Mn-substituted Na3V2(PO4)3 with outstanding electrochemical performance for full sodium ion batteries
[Display omitted] •Mn2+ substitution generates beneficial holes to accelerate electron transport while supporting the structure to stabilize the framework.•Al2O3 coating has the triple effect of reducing HClO4 concentration, inhibiting the dissolution of Mn and acting as a conductive agent.•NVMP@CNT...
Gespeichert in:
Veröffentlicht in: | Journal of colloid and interface science 2024-06, Vol.664, p.573-587 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | [Display omitted]
•Mn2+ substitution generates beneficial holes to accelerate electron transport while supporting the structure to stabilize the framework.•Al2O3 coating has the triple effect of reducing HClO4 concentration, inhibiting the dissolution of Mn and acting as a conductive agent.•NVMP@CNTs@1wt.%Al2O3 possesses a porous structure, effectively promoting the rapid Na+ transport.•The excellent structural stability is confirmed by in situ XRD.•NVMP@CNTs@1wt.%Al2O3 reveals a remarkable sodium storage property in both half and full cells.
Na3V2(PO4)3 (NVP) encounters significant obstacles, including limited intrinsic electronic and ionic conductivities, which hinder its potential for commercial feasibility. Currently, the substitution of V3+ with Mn2+ is proposed to introduce favorable carriers, enhancing the electronic conductivity of the NVP system while providing structural support and stabilizing the NASICON framework. This substitution also widens the Na+ migration pathways, accelerating ion transport. Furthermore, to bolster stability, Al2O3 coating is applied to suppress the dissolution of transition metal Mn in the electrolyte. Notably, the Al2O3 coating serves a triple role in reducing HClO4 concentration in the electrolyte, inhibiting Mn dissolution, and functioning as the ion-conducting phase. Likewise, carbon nanotubes (CNTs) effectively hinder the agglomeration of active particles during high-temperature sintering, thereby optimizing the conductivity of NVP system. In addition, the excellent structural stability is investigated by in situ XRD measurement, effectively improving the volume collapse during Na+ de-embedding. Moreover, the Na3V5.92/3Mn0.04(PO4)3/C@CNTs@1wt.%Al2O3 (NVMP@CNTs@1wt.%Al2O3) possesses unique porous structure, promoting rapid Na+ transport and increasing the interface area between the electrolyte and the cathode material. Comprehensively, the NVMP@CNTs@1wt.%Al2O3 sample demonstrates a remarkable reversible specific capacity of 122.6 mAh/g at 0.1 C. Moreover, it maintains a capacity of 115.9 mAh/g at 1 C with a capacity retention of 90.2 mAh/g after 1000 cycles. Even at 30 C, it achieves a capacity of 87.9 mAh/g, with a capacity retention rate of 84.87 % after 6000 cycles. Moreover, the NVMP@CNTs@1wt.%Al2O3//CHC full cell can deliver a high reversible capacity of 205.5 mAh/g at 0.1 C, further indicating the superior application potential in commercial utilization. |
---|---|
ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2024.03.072 |