Open AccessPhotoluminescent ZrO2:Tb3+ thin films synthesized by USP technique using a metal-organic precursor
Author(s) -
G. Juárez-López,
R. Martínez Martínez,
I. I. Rojas-Velasco,
M. Garcı́a-Hipólito,
F. Ramos-Brito,
E. I. Velázquez-Cruz,
M. Aguilar-Frutis,
C. Falcony-Guajardo
Publication year - 2021
Publication title -
materials research express
Language(s) - English
Resource type - Journals
ISSN - 2053-1591
DOI - 10.1088/2053-1591/abe5f1
Subject(s) - photoluminescence , materials science , zirconium , thin film , analytical chemistry (journal) , tetragonal crystal system , spectroscopy , crystal structure , crystallography , nanotechnology , chemistry , metallurgy , optoelectronics , organic chemistry , physics , quantum mechanics
Photoluminescent ZrO 2 and ZrO 2 :Tb 3+ thin films were synthesized from metal-organic precursor, zirconium acetylacetonate [Zr(C 5 H 7 O 2 ) 4 ], using Ultrasonic Spray Pyrolysis method. These thin films were deposited on Corning glass substrates at several deposition temperatures. ZrO 2 and ZrO 2 :Tb 3+ (X a/o) films were characterized by x-ray diffraction to identify the crystalline structure; results showed tetragonal phase of zirconia; with a crystalline size of approximately 4 nm according to Scherrer’s formula. Also, SEM micrographs revealed that surface morphology of these films is very flat. Chemical composition microanalysis showed presence of oxygen and zirconium as major species. Analysis by Infrared spectroscopy demonstrates that 900 and 760 nm bands correspond to presence of ZrO 2 . In addition, these films showed optical transmittances from 75 to 98 % in the visible range. Photoluminescent features varied as a function of excitation wavelength; when excited at λ ex = 286 nm strong green emission is observed, which is associated to electronic transitions 5 D 4 → 7 F n (n = 6, 5, 4, 3) corresponding to Tb 3+ ions. Excitation with λ ex = 336 nm exhibits spectra with simultaneous emissions from host lattice and Tb 3+ ions; here, observed color was blue-green.