Photoluminescence properties of ‘red’ emitting La2Zr2O7:Eu pyrochlore ceramics for potential phosphor application

• Published in: Journal of luminescence 2015-10, Vol.166, p.1-7
• Main Authors: Mohapatra, M., Rajeswari, B., Hon, N.S., Kadam, R.M., Natarajan, V.
• Format: Article
• Language: English
• Subjects: Europium; Judd–Ofelt parameters; La2Zr2O7; Phosphor; Photoluminescence
• ISSN: 0022-2313; 1872-7883
• DOI: 10.1016/j.jlumin.2015.04.034

Lanthanum zirconate (La2Zr2O7=LZO) pyrochlores doped with varying concentrations of Eu were synthesized using a low temperature gel-combustion synthesis route and characterized using X-ray diffraction, scanning electron microscopic and photoluminescence techniques. The final annealing temperature of the system could be brought down to 700°C to produce a single phase compound. In addition, the optimum activator ion concentration for maximum luminescence yield was evaluated for the system. The site occupancy for the Eu ions was also investigated which suggested that at 500°C, the ions were on the surface of the LZO host and later diffused into the lattice and replaced the La3+ ions on annealing at 700°C 5h. However, due to difference in the ionic radii, the doped RE ions were of the inversion center forming a D2d symmetry around them. For the first time the radiative properties and the commercial utility of the LZO system have been investigated. These parameters were used to get an idea about the M–L bond covalency in the system. The radiative properties suggested the system can be used as a potential ‘red’ emitting phosphor. •Synthesis of lanthanum zirconate pyrochlores doped with Eu using gel-combustion route.•Optimization of dopant ion concentration and annealing temperature and evaluation of its local site symmetry.•Evaluation of various photo-physical properties for the Eu-LZO system to investigate the M–L bond covalency.•Investigation of the commercial utility of the system by calculating the color coordinates.•Comparison of the emission properties with commercial sample.