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Simple Preparation of LaPO(4):Ce, Tb Phosphors by an Ionic-Liquid-Driven Supported Liquid Membrane System

In this work, LaPO(4):Ce, Tb phosphors were prepared by firing a LaPO(4):Ce, Tb precipitate using an ionic-liquid-driven supported liquid membrane system. The entire system consisted of three parts: a mixed rare earth ion supply phase, a phosphate supply phase, and an ionic-liquid-driven supporting...

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Detalles Bibliográficos
Autores principales: Li, Jianguo, Dong, Hongying, Yang, Fan, Sun, Liangcheng, Zhao, Zhigang, Bai, Ruixi, Zhang, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679419/
https://www.ncbi.nlm.nih.gov/pubmed/31336869
http://dx.doi.org/10.3390/ijms20143424
Descripción
Sumario:In this work, LaPO(4):Ce, Tb phosphors were prepared by firing a LaPO(4):Ce, Tb precipitate using an ionic-liquid-driven supported liquid membrane system. The entire system consisted of three parts: a mixed rare earth ion supply phase, a phosphate supply phase, and an ionic-liquid-driven supporting liquid membrane phase. This method showed the advantages of a high flux, high efficiency, and more controllable reaction process. The release rate of PO(4)(3−) from the liquid film under different types of ionic liquid, the ratio of the rare earth ions in the precursor mixture, and the structure, morphology, and photoluminescence properties of LaPO(4):Ce, Tb were investigated by inductively coupled plasma-atomic emission spectroscopy, X-ray diffraction, Raman spectra, scanning electron microscopy, and photoluminescence emission spectra methods. The results showed that a pure phase of lanthanum orthophosphate with a monoclinic structure can be formed. Due to differences in the anions in the rare earth supply phase, the prepared phosphors showed micro-spherical (when using rare earth sulfate as the raw material) and nanoscale stone-shape (when using rare earth nitrate as the raw material) morphologies. Moreover, the phosphors prepared by this method had good luminescent properties, reaching a maximum emission intensity under 277 nm excitation with a predominant green emission at 543 nm which corresponded to the (5)D(4)-(7)F(5) transition of Tb(3+).