Facile synthesis of flower-like T-Nb2O5 nanostructures as anode materials for lithium-ion battery
As a model quasi-2D network intercalation electrodes, niobium pentoxide (Nb 2 O 5 ) has gained numerous attention in electrochemical materials because of its structural stability and high safety. Nevertheless, Nb 2 O 5 exhibits the inherent low conductivity of transition metal oxides, which limits t...
Gespeichert in:
Veröffentlicht in: | Journal of materials science. Materials in electronics 2021, Vol.32 (1), p.875-885 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | As a model quasi-2D network intercalation electrodes, niobium pentoxide (Nb
2
O
5
) has gained numerous attention in electrochemical materials because of its structural stability and high safety. Nevertheless, Nb
2
O
5
exhibits the inherent low conductivity of transition metal oxides, which limits the rate of ionic diffusion and charge transfer. To overcome the drawbacks, the nanoscale Nb
2
O
5
can be synthesized to improve electrochemical performance. Here, we prepared the flower-like orthorhombic Nb
2
O
5
(i.e., T-Nb
2
O
5
) nanostructures to evaluate the effect of Nb
2
O
5
nanoparticle morphology associated with crystallinity for lithium-ion batteries (LIBs) anode. T-Nb
2
O
5
-2 displays superior crystallinity, pore structure, capacity, reversibility, and cycling stability. Specifically, T-Nb
2
O
5
-2 exhibits the initial charge/discharge capacity of 289 and 525 mAh g
−1
at 0.1 C, and after 100 cycles, the capacity is 178.2 mAh g
−1
at 1 C when the solvothermal time is 16 h. This study shows that Nb
2
O
5
with good crystallinity can slow down the volume expansion and structural deformation generated during the intercalation–deintercalation of Li-ions. We believe that the specified Nb
2
O
5
presented in this work has great potential as a promising candidate for high-performance LIB anodes. |
---|---|
ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-020-04865-8 |