Synthesis of Y2O2S:Eu3+ luminescent nanobelts via electrospinning combined with sulfurization technique
Y 2 O 2 S:Eu 3+ nanobelts were successfully prepared via electrospinning method and sulfurization process using the as-prepared Y 2 O 3 :Eu 3+ nanobelts and sulfur powders as sulfur source by a double-crucible method for the first time. X-ray diffraction analysis indicated that the Y 2 O 2 S:Eu 3+ n...
Gespeichert in:
Veröffentlicht in: | Journal of materials science 2013, Vol.48 (2), p.644-650 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Y
2
O
2
S:Eu
3+
nanobelts were successfully prepared via electrospinning method and sulfurization process using the as-prepared Y
2
O
3
:Eu
3+
nanobelts and sulfur powders as sulfur source by a double-crucible method for the first time. X-ray diffraction analysis indicated that the Y
2
O
2
S:Eu
3+
nanobelts were pure hexagonal in structure with space group
P
m
1. Scanning electron microscope images showed that the width and thickness of the Y
2
O
2
S:Eu
3+
nanobelts were ca. 6.7 μm and 125 nm, respectively. Under the excitation of 325-nm ultraviolet light, Y
2
O
2
S:Eu
3+
nanobelts exhibited red emissions of predominant peaks at 628 and 618 nm, which are attributed to the
5
D
0
→
7
F
2
transition of the Eu
3+
ions. It was found that the optimum doping concentration of Eu
3+
ions in the Y
2
O
2
S: Eu
3+
nanobelts was 3 %. Compared with bulk particle, Eu
3+
–O
2−
/S
2−
charge transfer bands (260 and 325 nm) of the Y
2
O
2
S:Eu
3+
nanobelts showed a blue-shift significantly. The formation mechanism of the Y
2
O
2
S: Eu
3+
nanobelts was also proposed. This new sulfurization technique is of great importance, not only to inherit the morphology of rare earth oxides but also to fabricate pure-phase rare earth oxysulfides at low temperature compared with conventional sulfurization method. |
---|---|
ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-012-6768-5 |