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Crystal structure and morphology evolution in the LaXO3, X = Al, Ga, In nano-oxide series. Consequences for the synthesis of luminescent phosphors
Authors:Pazik Robert  Seisenbaeva Gulaim A  Wiglusz Rafal J  Kepinski Leszek  Kessler Vadim G
Affiliation:Department of Chemistry, SLU, Uppsala, Sweden. robert.pazik@kemi.slu.se
Abstract:The LaXO(3):Tb(3+) (X = Al(3+), Ga(3+), In(3+)) perovskite nanoparticles were obtained using the nonhydrolytic treatment (Bradley reaction) of the molecular precursors of the La(O(i)Pr)(3), Al(O(i)Pr)(3), Ga(O(i)Pr)(3), In(5)O(O(i)Pr)(13), and Tb(acac)(3), respectively. It was shown that crystal structure and morphology evolution in the LaXO(3), X = Al, Ga, In nano-oxide series depended on the size and chemical properties of the X-metal atom. Formation of the LaInO(3):Tb(3+) nanoparticles is distinctly less thermodynamically demanding on contrary to the LaAlO(3):Tb(3+) and LaGaO(3):Tb(3+) since it provided crystalline product directly in the solution synthesis at 202 °C, which is the lowest reported synthesis temperature for this compound up-to-date. This behavior was ascribed to the effects directly connected with the dopant substitution (exchange of bigger La(3+) cation with smaller Tb(3+)) as well as reduction of the particle size. The size effects are mostly reflected in the expansion of the cell volume, changes of the cell parameters as well as shifting and broadening of the Raman bands. Indirectly, size reduction has also an effect on the luminescence properties through the higher probability of presence of surface and net defects as well as heterogeneous distribution of the Tb(3+) ions caused by high surface-to-volume ratio. The prepared nanophosphors show basically green emission with exception of white-green in case of the LaInO(3):Tb(3+). Strong emission quenching was found in the latter case being most likely a consequence of the nonradiative energy transfer between Tb(3+) and In(3+) as well as the presence of defects. In comparison to the Pechini's method, the LaXO(3) nanoparticles required significantly lower annealing temperature (700 °C) necessary for complete crystallization. Generally the resulting particles are distinctly smaller (5 to 25 nm) and less agglomerated (50-100 nm) depending on the reaction conditions as well as thermal treatment. For the first time, it was shown that the LaGaO(3):Tb(3+) nanopowder has crystallized in the high-temperature rhombohedral R3c phase.
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