Journal
DALTON TRANSACTIONS
Volume 44, Issue 9, Pages 4080-4087Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4dt03906h
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Funding
- National Natural Science Foundation of China [21271167, 11304309]
- Fund for Creative Research Groups [21221061]
- National Basic Research Program of China (973 Program) [2014CB643803]
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A new langbeinite-type phosphate KSrSc2(PO4)(3) has been synthesized by conventional high temperature solid state reaction. Rietveld structure refinement, a field emission scanning electron microscope, photoluminescence spectra, quantum efficiency as well as lifetimes were used to characterize the samples. Structure refinement reveals that KSrSc2(PO4)(3) has two kinds of Sr2+ and Sc3+ sites for the doped ions to occupy, forming emission centers. The KSrSc2(PO4)(3):Ce3+ and KSrSc2(PO4)(3): Eu2+ phosphors both have broad excitation and emission bands due to spin-and orbit-allowed electron transitions. Phosphors with tunable blue to blue-green colors were obtained by codoping the Tb3+ ions into the KSrSc2(PO4)(3):0.03Ce(3+) and KSrSc2(PO4)(3):0.03Eu(2+) phosphors with varying contents. The mechanism of Eu2+ --> Tb3+ energy transfer is determined to be a dipole-quadrupole interaction in terms of the experimental results and analysis of photoluminescence spectra and decay curves of the phosphors by using the Inokuti-Hirayama theoretical model. Our prepared KSrSc2(PO4)(3):Ce3+, Tb3+ and KSrSc2(PO4)(3):Eu2+, Tb3+ phosphors are of potential value for UV excited WLEDs.
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