dc.description.abstract |
The undoped SrSiO3/SiO2 phosphors prepared by both co-precipitation and
hydrothermal methods at different Sr/Si molar ratios are reported. Undoped and
Mn doped BaAl2O4 phosphor synthesized using combustion method are also
reported. The X-ray diffraction measurements confirmed hexagonal phases of the
SrSiO3,SiO2 and BaAl2O4:Mn in the prepared phosphors. The particle morphology
of the prepared phosphors was observed to be somewhat agglomerated partcles
in the alkaline silicate phosphors, whereas nano-sheets with uneven morphology
with both nano-rods and hexagonal particles were observed in the BaAl2O4:Mn
phosphor. EDS measurements confirmed the presence of Sr, Si, and O in the
SrSiO3/SiO2 phosphors, together with their homogenous dispersion in the
phosphors. The presence of Ba, Al, O, and Mn in the BaAl2O4:Mn phosphor was
also confirmed by EDS measurement.
PL measurements confirmed that the undoped phosphors possess room
temperature phosphorescence properties with a 2:1 Sr/Si molar ratio sample
prepared by co-precipitation method showing excellent white phosphorensce. A
combination of two emission bands (495 and 687 nm) make up a white
phosphorescence that cover a wide range of the spectrum, making this phosphor
a potential candidate in solid state lighting applications. These emission bands
were attributed to the intrinsic defects in the prepared SrSiO3/SiO2 phosphors.
PL measurements also confirmed green room temperature phosphorescence
from the BaAl2O4:Mn phosphor.
Thermoluminescence studies showed more than one overlaping peaks in all
samples except for the 2:1 Sr/Si molar ratio sample which showed only one peak
at 100 oC. For this reason, further thermoluminescence studies on this phosphor
were carried out to assess prospects of applications in dosimetry. In addition to
the observation of a single peak in this phosphor, linearity in a wide range of dose
in it also proved that this has a potential for application in dosimetry. Also, the emission band of this phosphor at 495 nm falls within the dosimetric
requirement of emission range of 400 – 500 nm. Both the methods used to
calculate the activation energy, the initial rise and variable heating rate yielded
comparable results. |
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