Yttrium precursors for preparation of yttrium oxide nanophosphors by

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SPECTRAL INVESTIGATION ON CERIUM ACTIVATED
YTTRIUM ALUMINATE GARNET PHOSPHORS
Amalia Hristea1, Elisabeth-Jeanne Popovici1, Laura Mureşan1,
Rodica Grecu1 and Marilena Vasilescu2
“Raluca Ripan” Institute for Research in Chemistry,
Fântânele 30, 400294 Cluj-Napoca, amaliahristea@yahoo.com
2
"I.G. Murgulescu" Institute of Physical Chemistry of the
Romanian Academy, 202 Spl. Independentei, Bucureşti,
Romania
1
Cerium activated yttrium aluminate (Y3Al5O12 : Ce) phosphor is used as a yellow
luminescent material for the manufacture of the very valuable white light emiting diodes
(LED). Usually, the synthesis of Y3Al5O12: Ce phosphor proceeds by the solid state reaction
route, at very high firing temperature (over 1400°C). Non-conventional methods were
developed in order to obtain performing phosphors in less severe thermal synthesis
conditions.
This work presents our first attempts to prepare yellow emitting cerium activated
yttrium aluminate with garnet crystalline structure. Some of our results referring to the
synthesis of Y3Al5O12: Ce phosphor by sol-gel method, inorganic route are presented.
Yttrium- aluminium-cerium precursors were prepared from the corresponding metallic nitrate
solutions, with urea, amonium carbonate or ammonia as precipitating reagents. The yttriumaluminum-cerium precursors were well washed, dried and fired at 1200 °C, in air, for 1-5 hrs.
The influence of the preparative regime on the quality of phosphors was studied in
order to select the optimal synthesis conditions for Y3Al5O12: Ce powders. Complementary
investigations were used to characterise both the precursor and phosphor samples, namely
thermal analysis, X-ray diffraction and FT-IR spectroscopy. The formation of the cubic
structure of Y3Al5O12 garnet was put in evidence. The fluorescence spectroscopy shows that,
under blue light excitation (450nm), phosphor samples emit yellow emission (λmax=525 nm)
whose intensity depend on the precipitating reagent used for precursor preparation as well as
on the the thermal synthesis regime.
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