Effect of Annealing Temperature on the Structure, Morphology and Photoluminescence Properties of MgAl2O4:0.1% Eu3+ Nanophosphor Prepared by Sol–Gel Method

• Published in: Journal of electronic materials Vol. 48; no. 1; pp. 494 - 502
• Main Authors: Melato, L. T., Koao, L. F., Motaung, T. E., Swart, H. C., Motloung, S. V.
• Format: Journal Article
• Language: English
• Published: New York Springer US 01-01-2019; Springer Nature B.V
• Subjects: Annealing; Characterization and Evaluation of Materials; Chemistry and Materials Science; Crystal defects; Crystal structure; Crystallites; Electron microscopes; Electronics and Microelectronics; Energy dispersive X ray spectroscopy; Europium; Image transmission; Instrumentation; Luminescence; Magnesium aluminate; Materials Science; Morphology; Nanomaterials; Nanophosphors; Optical and Electronic Materials; Phosphors; Photoluminescence; Sol-gel processes; Solid phases; Solid State Physics; X ray powder diffraction; Eu; MgAl; photoluminescence; sol–gel; doping; annealing temperature; O
• ISSN: 0361-5235; 1543-186X
• DOI: 10.1007/s11664-018-6729-0

Un-doped and 0.1% Eu
3+
-doped magnesium aluminate (MgAl
2
O
4
) nanomaterials were synthesized using the sol–gel method. The effects of annealing temperature (AT) from 600–1300°C on the crystal structure, morphology and photoluminescence properties were investigated. X-ray powder diffraction showed that below 650°C the structure consists of poorly crystalline and amorphous phases. A cubic phase structure corresponding to MgAl
2
O
4
was formed at AT above 700°C. Generally, the crystallite sizes increased with an increase in AT. Energy-dispersive x-ray spectroscopy results confirmed the presence of the anticipated elementary composition. The scanning electron microscope and transmission electron microscope images suggested that the AT influenced the morphology, crystallite sizes and shape of the prepared phosphors. Photoluminescence (PL) results showed that the emissions peaks at 384 and 561 nm originate from defects located at different levels within the host material. The emission peaks at 561 nm, 581 nm, 594 nm, 618 nm, 655 nm and 701 nm were attributed to the (
5
D
1
 → 
7
F
4
) (
5
D
0
 → 
7
F
0
), (
5
D
0
 → 
7
F
1
), (
5
D
0
 → 
7
F
2
), (
5
D
0
 → 
7
F
3
) and (
5
D
0
 → 
7
F
4
) transitions of Eu
3+
ion. Emission peaks from Eu
3+
were observed to increase in intensity as the AT was increased. Luminescence enhancement was observed when increasing the AT to 650°C, while further increase lead to luminescence quenching. The Commision Internationale de l’Eclairage (CIE) coordinates results showed that the emission colour shift can be tuned from bluish to reddish by varying the AT.