Enhanced green emission from UV down-converting Ce3+-Tb3+ co-activated ZnAl2O4 phosphor

Authors
Tshabalala, K. G.Nagpure, I. M.Swart, H. C.Ntwaeaborwa, O. M.Cho, S. -H.Park, J. -K.
Issue Date
2012-05
Publisher
A V S AMER INST PHYSICS
Citation
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY B, v.30, no.3
Abstract
Ce3+-Tb3+ co-activated ZnAl2O4 powder phosphors were prepared by a solution combustion method using urea as a fuel. X-ray diffraction characterization showed that all the powders crystallized in the well known cubic spinel phase of ZnAl2O4. An enhanced down-converted green emission associated with the (D4 -> F5)-D-5-F-7 transitions of Tb3+ ions was observed at 543 nm from the ZnAl2O4:Ce3+, Tb3+ powders with different concentrations of Ce3+ and Tb3+. It was inferred from the fluorescence decay data that the enhancement was due to energy transfer from Ce3+ to Tb3+. Further, cathodoluminescence intensity degradation of the ZnAl2O4:Ce3+, Tb3+ powder phosphors was investigated when the powders were irradiated with 2 keV electrons. X-ray photoelectron spectroscopy was used to analyze the chemical and electronic states of individual elements before and after electron irradiation. The ZnAl2O4:Ce3+, Tb3+ phosphor was evaluated to be used as a UV down-converting layer in conventional silicon photovoltaic cells or as a source of green light in field emission display technologies. (C) 2012 American Vacuum Society. [http://dx.doi.org/10.1116/1.3696720]
Keywords
PHOTOLUMINESCENCE; LUMINESCENCE; DEGRADATION; OXIDES; XPS; PHOTOLUMINESCENCE; LUMINESCENCE; DEGRADATION; OXIDES; XPS; phosphor; ZnAl2O4; down conversion; Ce Tb
ISSN
1071-1023
URI
https://pubs.kist.re.kr/handle/201004/129315
DOI
10.1116/1.3696720
Appears in Collections:
KIST Article > 2012
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