Abstract
The Dy3+ doped (Lu,Gd)3Al5O12 garnet phosphors with spherical morphology were obtained via homogeneous precipitation method, followed by calcination at 1100 °C. The particle morphology does not change significantly, but can be controlled by adjusting the urea content. The synthesis, structure, luminescent properties of precursor and resultant particles were analyzed by the combined technologies of XRD, FE-SEM, PLE/PL decay behavior. The (Lu0.975Dy0.025)AG phosphors display strong blue and yellow emission at ~481 nm (4F9/2 → 6H15/2 transition of Dy3+) and ~582 nm 4F9/2 → 6H13/2 transition of Dy3+), respectively. The phosphors have similar color coordinate and temperature of (~0.33, ~0.34), ~5517 K, respectively, which are closed to the white emission. The particle size and luminescent intensity decreased while the lifetime increased with the urea concentration increasing. The Gd3+ addition does not alter the shape/position of emission peaks, but enhance the blue and yellow emission of Dy3+ owing to the efficient Gd3+ → Dy3+ energy transfer. The [(Lu1-xGdx)0.975Dy0.025]3Al5O12 phosphors are expected to be widely used in the lighting and display areas.
Highlights
In the powder form, Ce3+ doped Ln3Al5O12 (LnAG) garnet phosphors, especially Ce3+ doped YAG (YAG:Ce), have become one of the most efficient yellow phosphors
Phase evolution of the precursors upon calcination and photoluminescence behaviors of the oxide phosphors were studied in detail via the combined techniques of fourier transform infrared spectroscopy (FT-IR), X-ray diffractometry (XRD), field emission scanning electron microscopy (FE-SEM), photoluminescence excitation/photoluminescence (PLE/PL) spectroscopy, and fluorescence decay analysis
From which it can be seen that all the XRD diffraction peaks are well agreement with the standard PDF card of LuAG
Summary
In the powder form, Ce3+ doped Ln3Al5O12 (LnAG) garnet phosphors, especially Ce3+ doped YAG (YAG:Ce), have become one of the most efficient yellow phosphors. Phase evolution of the precursors upon calcination and photoluminescence behaviors of the oxide phosphors were studied in detail via the combined techniques of fourier transform infrared spectroscopy (FT-IR), X-ray diffractometry (XRD), field emission scanning electron microscopy (FE-SEM), photoluminescence excitation/photoluminescence (PLE/PL) spectroscopy, and fluorescence decay analysis.
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