Preparation and characterization of rare-earth-doped Y2O3 luminescent ceramics by the use of reverse micelles
✍ Scribed by Olivia A. Graeve; Jessica O. Corral
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 470 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0925-3467
No coin nor oath required. For personal study only.
✦ Synopsis
The objective of this project was to study luminescent powders of Y 2 O 3 :Eu 3+ (5 at%), Y 2 O 3 :Tb 3+ (5 at%), and Y 2 O 3 :Tm 3+ ,Yb 3+ (Tm: 2 at%, Yb: 1 at%), prepared by the use of reverse micelles. This report describes the phase stability, crystallite size, and luminescence properties of these powder materials as a function of heat treatment time and temperature. The Y 2 O 3 phase produced during synthesis can be controlled by the heat treatment temperature and time. Monoclinic and cubic phases of Y 2 O 3 are obtainable, with the monoclinic powders produced at the smaller crystallite sizes. Photoluminescence properties of the Y 2 O 3 :Eu 3+ and Y 2 O 3 :Tb 3+ were evaluated and sharp emission was observed for the Eu 3+ powders at 610 nm and the Tb 3+ powders at 544 nm. The maximum emission intensity of both phosphors increased as annealing temperature and time increased. This, however, was not seen for the case of the Y 2 O 3 :Tm 3+ ,Yb 3+ powders, which exhibited emission at 454 nm. For this phosphor, as heat treatment temperature increased the luminescence intensity decreased.
📜 SIMILAR VOLUMES
Glass-ceramics with composition of 89.9SiO 2 -10LaF 3 -0.1EuF 3 (mol%) were prepared by sol-gel method. LaF 3 nanocrystals, precipitated by heat-treatments, were identified by X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). Besides the well-known red emission of
The structural characteristics of tin-and titanium-doped -Fe 2 O 3 prepared by hydrothermal methods have been investigated by Rietveld structure refinement of the X-ray powder diffraction data. The analysis reveals that the dopant ions adopt two distinct sites: in addition to partially substituting
The crystal structure of the known compounds Ln 5 Re 2 O 12 (Ln = Y, Gd, Dy±Lu) and the new isotypic terbium rhenate Tb 5 Re 2 O 12 was determined from X-ray data of a twinned crystal of Ho 5 Re 2 O 12 : B2/m, a = 1236.5(4) pm, b = 748.2(2) pm, c = 563.8(1) pm, c = 107.73(3)°, Z = 2, R = 0.034 for 3