Abstract
Tb3+-doped CaMoO4 (Tb3+ = 1, 3, 5, 7, 10, 15 and 20 atom%) core and core-shell nanoparticles have been prepared by urea hydrolysis in ethylene glycol (EG) as capping agent as well as reaction medium at low temperature similar to 150 degrees C. As-prepared samples were annealed at 500 and 900 degrees C for 4 h to eliminate unwanted hydrocarbons and/or H2O present in the sample and to improve crystallinity. The synthesised nanophosphors show tetragonal phase structure. The crystallite size of as-prepared sample is found to be similar to 18 nm. The luminescence intensity of the D-5(4) -> F-7(5) transition at 547 nm of Tb3+ is much higher than that of the D-5(4) -> F-7(6) transition at 492 nm. 900 degrees C annealed samples show the highest luminescence intensity. The intensity ratio R (I[D-5(4) -> F-7(6)]/I[D-5(4) -> F-7(5)]) lies between 0.3-0.6 for as-prepared, 500 and 900 degrees C annealed samples. The luminescence decay of D-5(4) level under 355 nm excitation shows biexponential behaviour indicating availability of Tb3+ ions on surface and core regions of particle; whereas, contribution of Mo-O charge transfer to lifetime is obtained under 250 nm excitation. The CIE coordinates of as-prepared, 500 and 900 degrees C annealed 5 atom% Tb3+-doped CaMoO4 samples under 250 nm excitation are (0.28, 0.32), (0.22, 0.28) and (0.25, 0.52), respectively. The dispersed particles in polar medium and its polymer film show green light emission. The luminescence intensity is improved significantly after core-shell formation due to extent of decrease of non-radiative rates arising from surface dangling bonds and capping agent. Quantum yields of as-prepared samples of 1, 5 and 7 atom% Tb3+-doped CaMoO4 samples are found to be 10, 3 and 2, respectively.