Abstract
In this paper, we report on structural and optical properties of terbium and europium doped barium stannate phosphors (BaSnO3) synthesised by conventional solid state reaction method. We have studied those materials by using X-ray diffraction (XRD), radioluminescence (RL) and photoluminescence (PL) techniques. XRD patterns confirm that the BaSnO3 sintered at 1400°C exhibit orthorhombic structure and that the Tb3+ and Eu3+ substitution of Ba2+ does not change the structure of the BaSnO3 host. The optical emission spectrum is characterized a broad band centered at 897nm (1.38eV), with a high-energy tail approximately 750nm from the host lattice. Other emission signals that are characteristic of the 3+oxidation state of rare earth elements were generated by Eu and Tb doping. Luminescence measurements show that the series of emission states 5D4→7F6, 5D4→7F5, 5D4→7F4 and 5D4→7F3 corresponding to the typical 4f→4f infra-configuration forbidden transitions of Tb3+ are appeared and the major emission peak at 540nm is due to 5D4→7F5 transitions of Tb3+. On the other hand, the emission spectrum of Eu doped BaSnO3 phosphor exhibits a series of emission bands, which are attributed to the 5D0→7Fj (j=0–4) transitions of Eu3+ ions. The dominant emission of Eu3+corresponding to the electric dipole transition5D0→7F2is located at 613nm. The sharp emission properties exhibited demonstrate that the BaSnO3 is a suitable host for rare-earth ion doped phosphor material. This work clearly confirms the unusual near infrared (NIR) PL discovered by H. Mizoguchi et al. in BaSnO3 at room temperature.