Lanthanide fluorides exhibited unique luminescent properties in terms of their low phonon energy can restrict the luminescence quenching and extend luminescent lifetimes.Here,a room-temperature co-precipitation method was used to synthesize europium(III) activated La1-xGdxF3 solid phosphors.X-ray diffraction(XRD) data confirmed the crystalline phases of synthesized sample belongs to orthorhombic system.All the as-derived materials exhibited red luminescence(5D0→7F1) under the excitation at longer wavelengths(394 and 466 nm).The powder with the most intense emission was achieved in terms of 10 mol.% doping concentration(Eu content,La/Gd=1/9) and sample sintered at 700 oC.Scanning electron microscopy(SEM) investigated the morphology and crystalline of the samples,showing that many regular and large balls(5-10 μmol/L) were dispersed within the micro-meter scale composites.We proved that the above crystal growth structures were controllable and predicable based on the surface functionalization by polyvinylpyrrolidone ligand.
An investigation on the photophysical properties of the newly designed terbium imidazole-4,5-dicarboxylic acid complex encapsulated in the inert matrices (tetraethoxysilane, TEOS) was performed. The composite material was very stable and showed strong green emission in pure water. Interestingly, we discovered that the luminescence of hybrid material was selectively responsive to H2PO4-. 1H-NMR and fluorescence spectra supported that the receptor had strong affinity to dihydrogen phosphate. Meanwhile, the luminescence was quenched by Fe3+ when adding different metal ions such as Fe3+, Pd2+, Cd2+, Co2+ and Mn2+ concomitantly. Moreover, thin film was successfully pre-pared by the same materials and it also exhibited selective recognition behavior to the above two ions.
