2644
Synthesis and Photoluminescence Properties of (Sr, Ba)2-XEuxSiO4 Phosphors with High Eu2+ Concentration for White LED Applications

Wednesday, 16 May 2018: 11:40
Room 307 (Washington State Convention Center)
Y. Sato (Department of Chemistry, Okayama University of Science), K. Tomita (Department of Chemistry, Tokai University), and M. Kakihana (IMRAM, Tohoku University)
Recently, several oxide-based phosphors with excellent luminescence properties have been reported. Especially, the deep-red emitting Ca1.2Eu0.8SiO4 has been prepared by the basis on crystal-site engineering, which shows an emission peak at 653 nm under excitation at 450 nm [1]. The emission wavelength of Ca1.2Eu0.8SiO4 is quite similar to those of commercial red-emitting CaAlSiN3:Eu2+ and Sr2Si5N8:Eu2+. The crystal structure of Ca2-xEuxSiO4 is analogous to those of Sr2-xEuxSiO4 and Ba2-xEuxSiO4. Therefore, it is expected that the addition of large amounts of Eu2+ ions to Sr2-xEuxSiO4 and Ba2-xEuxSiO4 can also lead to large redshifts in their emission and excitation spectra. In this study, we prepared and characterized Sr2-xEuxSiO4 and Ba2-xEuxSiO4 with a high concentration of Eu2+ ions. In the case of Sr2-xEuxSiO4, the emission peak was shifted from 585 nm for Sr1.9Eu0.1SiO4 to 611 nm for Sr1.2Eu0.8SiO4. On the other hand, in the case of Ba2-xEuxSiO4, the emission peak was shifted from 513 nm for Ba1.9Eu0.1SiO4 to 545 nm for Ba1.2Eu0.8SiO4. The right-hand edges of the excitation spectra for both the samples were significantly shifted, by 40-55 nm, to longer wavelengths, allowing for excitation by blue light. The induction of large redshifts in the emission and excitation spectra of both samples could be attributed to the occupancy of Eu2+ ions in the polyhedra of Sr(2) or Ba(2) sites, which are smaller and more distorted than the Sr(1) or Ba(1) sites. These results indicate that Sr1.2Eu0.8SiO4 and Ba1.2Eu0.8SiO4 are suitable as red- and green-emitting phosphors for next-generation white-LED applications.

[1] Y. Sato and M. Kakihana et al., Angew. Chem. Int. Ed. 53 (2014) 7756.