Micro-length anodic porous niobium oxide for lithium-ion thin film battery applications
The anodization of niobium in an aqueous mixture of H3PO4 and HF in the potential range from 2.5 to 30V for 2h at 5°C was performed, demonstrating that anodic porous niobium oxide film with a thickness of up to 2000nm, including a surface dissolution layer, can be obtained by controlling the applied...
Gespeichert in:
Veröffentlicht in: | Thin solid films 2013-03, Vol.531, p.583-587 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The anodization of niobium in an aqueous mixture of H3PO4 and HF in the potential range from 2.5 to 30V for 2h at 5°C was performed, demonstrating that anodic porous niobium oxide film with a thickness of up to 2000nm, including a surface dissolution layer, can be obtained by controlling the applied potential and composition of the electrolytes. Specifically, surface dissolution-free porous niobium oxide film with a thickness of 800nm can be prepared in a low electrolyte concentration. The surface dissolution is observed when the concentration ratio of HF (wt.%):H3PO4 (M) was more than 2:1. The discontinuous layers in the niobium oxide film were observed when the thickness was higher than 500nm, which was ascribed to the large volume expansion of the niobium oxide grown from the niobium metal. The anodic porous niobium oxide film was used as the cathode for lithium-ion batteries in the potential range from 1.2 to 3.0V at a current density of 7.28×10−6Acm−2. The first discharge capacity of ca. 53μAhcm−2 was obtained in 800nm thick niobium oxide without a surface dissolution layer.
► Anodic porous niobium oxide film with a thickness of 2000nm was obtained. ► Surface dissolution-free porous niobium oxide film was prepared. ► The niobium oxide film was used as the cathode for lithium-ion batteries. |
---|---|
ISSN: | 0040-6090 1879-2731 |
DOI: | 10.1016/j.tsf.2013.01.062 |