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Ferroelectric order driven Eu(3+) photoluminescence in BaZr(x)Ti(1−x)O(3) perovskite

The ability to tune and enhance the properties of luminescent materials is essential for enlarging their application potential. Recently, the modulation of the photoluminescence emission of lanthanide-doped ferroelectric perovskites by applying an electric field has been reported. Herein, we show th...

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Detalles Bibliográficos
Autores principales: Canu, Giovanna, Bottaro, Gregorio, Buscaglia, Maria Teresa, Costa, Chiara, Condurache, Oana, Curecheriu, Lavinia, Mitoseriu, Liliana, Buscaglia, Vincenzo, Armelao, Lidia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478923/
https://www.ncbi.nlm.nih.gov/pubmed/31015564
http://dx.doi.org/10.1038/s41598-019-42897-1
Descripción
Sumario:The ability to tune and enhance the properties of luminescent materials is essential for enlarging their application potential. Recently, the modulation of the photoluminescence emission of lanthanide-doped ferroelectric perovskites by applying an electric field has been reported. Herein, we show that the ferroelectric order and, more generally the polar order, has a direct effect on the photoluminescence of Eu(3+) in the model BaZr(x)Ti(1−x)O(3) perovskite even in the absence of an external field. The dipole arrangement evolves with increasing x from long-range ferroelectric order to short-range order typical of relaxors until the non-polar paraelectric BaZrO(3) is achieved. The cooperative polar interactions existing in the lattice (x < 1) promote the off-center displacement of the Eu(3+) ion determining a change of the lanthanide site symmetry and, consequently, an abrupt variation of the photoluminescence emission with temperature. Each type of polar order is characterized by a distinct photoluminescence behaviour.