z-logo
open-access-imgOpen Access
Photoluminescence associated with the site occupations of Ho3+ ions in BaTiO3
Author(s) -
Da-Yong Lu,
Dong-Xue Guan
Publication year - 2017
Publication title -
scientific reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.24
H-Index - 213
ISSN - 2045-2322
DOI - 10.1038/s41598-017-06521-4
Subject(s) - photoluminescence , tetragonal crystal system , electron paramagnetic resonance , raman spectroscopy , materials science , ion , excitation , raman scattering , dopant , analytical chemistry (journal) , doping , ceramic , nuclear magnetic resonance , crystallography , crystal structure , chemistry , optics , physics , optoelectronics , organic chemistry , quantum mechanics , chromatography , composite material
A nominal (Ba 1− x Ho x )Ti 1− x /4 O 3 ( x  = 0.01) (BHTH) ceramic with a single-phase tetragonal structure was prepared at 1400 °C using the solid-state reaction method. The analysis on the defect chemistry revealed that the real formula of BHTH is (Ba 1− x Ho 3 x /4 )(Ti 1− x /4 Ho x /4 )O 3 with Ba vacancies via electron paramagnetic resonance (EPR). Photoluminescence (PL) was investigated on the basis of excitation with different wavelength lasers. The results indicated that under 488-nm excitation, PL and Raman scattering can occur simultaneously as two distinct optical processes for BHTH ceramic powders, and the strongest PL band at 564 nm was discovered and verified to originate from the 5 G 6 / 5 F 1  →  5 I 7 transition of Ho 3+ ions on the Ti sites in the BaTiO 3 lattice. Upon 532- and 638-nm excitations, three PL bands of 5 F 4 / 5 S 2  →  5 I 8 , 5 F 5  →  5 I 8 , and 5 F 4 / 5 S 2  →  5 I 7 transitions are attributed to the contributions from Ho 3+ ions on the Ba sites. The common Raman spectrum of BaTiO 3 can be observed without PL disturbance using 785-nm excitation wavelength. The PL effect may provide a probe for the site occupations of Ho 3+ ions in widely-used BaTiO 3 dielectric ceramics co-doped with Ho 3+ and other dopants.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here