Journal
JOURNAL OF ALLOYS AND COMPOUNDS
Volume 827, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2020.154216
Keywords
Red-orange emitting phosphors; Photoluminescence; Solid state lighting; Intensity parameters
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Funding
- Ministry of Science and Higher Education (Ethiopia)
- National Research Foundation (NRF), South Africa
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In this study, Ba1.3Ca0.7SiO4: Eu3+ red-orange phosphors were synthesized by the solution combustion method. The effect of varying Eu3+ molar percentages on the material properties including its intrinsic quantum efficiency (IQE) was investigated. XRD results showed synthesized phosphor is hexagonal T-phase Ba1.3Ca0.7SiO4 and the average crystallite size calculated using the Scherer's formula was estimated to be similar to 33 nm. SEM result showed the synthesized Ba1.3Ca0.7SiO4: Eu3+ phosphor had granular shaped and slightly agglomerated particles. The EDS shows that prepared samples contain Ba, Ca, Eu, Si, and O as expected. UV-vis measurement confirms the percent reflectance in the UV-region to be dependents on Eu3+ ions and the estimated bandgap vary between 3.80 and 4.23 eV. Photoluminescence emission measurements of all prepared samples at room temperature appeared to be entirely from inter configurational Eu3+ emission and depend both on the site symmetry as well as ion concentration. Hence, the peak centred at 592 nm is due to transition D-5(0) -> F-7(1), while the peak centred at 615 nm is due to transition D-5(0) -> F-7(2). The quadrupole-quadrupole multipolar interaction was found to be exclusively responsible for luminescence quenching. The Judd-Ofelt intensity parameters (Omega(2), Omega(4)), asymmetry ratio (R-0), and average decay lifetime of the nanocrystals showed dependence on concentration. High IQE values were obtained at low Eu3+ ion concentrations but the efficiency decreased with increasing ion concentration. The CIE color coordination confirmed that the emitted color fall in the strong orange-red region of the emission spectrum. (C) 2020 Elsevier B.V. All rights reserved.
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