Nonstoichiometric LaO_0.65F_1.7 Structure and Its Green Luminescence Property Doped with Bi³⁺ and Tb³⁺ Ions for...

Red-green-blue phosphors excited by ultraviolet (UV) radiation for white light LEDs have received much attention to improve the efficiency, color rendering index (CRI), and chromatic stability. The spectral conversion of a rare-earth ion-doped nonstoichiometric LaO_0.65F_1.7 host was explored with structural analysis in this report. The nonstoichiometric structure of a LaO_0.65F_1.7 compound, synthesized by a solid-state reaction using La₂O₃ and excess NH₄F precursors, was analyzed by synchrotron X-ray powder diffraction. The crystallized LaO_0.65F_1.7 host, which had a tetragonal space group of P4/nmm, contained 9- and 10-coordinated La³⁺ sites. Optical materials composed of La_1-BiTbO_0.65F_1.7 (p = 0 and 0.01; q = 0-0.2) were prepared at 1050 °C for 2 h, and the single phase of the obtained phosphors was indexed by X-ray diffraction analysis. The photoluminescence spectra of the energy transfer from Bi³⁺ to Tb³⁺ were obtained upon excitation at 286 nm in the nonstoichiometric host lattice. The desired Commission Internationale de l'Eclairage (CIE) values of the phosphors were calculated. The intense green La_0.89Bi_0.01Tb_0.1O_0.65F_1.7 phosphor with blue and red optical materials was fabricated on a 275 nm UV-LED chip, resulting in white light, and the internal quantum efficiency, CRI, correlated color temperature, and CIE of the pc LED were characterized.