Journal
JOURNAL OF LUMINESCENCE
Volume 161, Issue -, Pages 257-263Publisher
ELSEVIER
DOI: 10.1016/j.jlumin.2015.01.033
Keywords
Ce3+; Tb3+; GdAl3(BO3)(4); Optical material; Luminescence
Categories
Funding
- National Natural Science Foundation of China [21171176, U1232108, U1432249]
- Guangzhou Science and Technology Project [2013Y2-00118]
- Science and Technology Project of Guangdong Province [2013B010403010]
- Natural Science Foundation of Guangdong Province [S2013030012842]
- European Social Fund's Doctoral Studies and Internationalization Program DoRa
- European Regional Development Fund (Center of Excellence 'Mesosystems: Theory and Applications') [TK114]
- Marie Curie Initial Training Network LUMINET [316906]
- Program for the Foreign Experts
- Ministry of Education and Research of Estonia [PUT430]
- STFC [ST/J001465/1] Funding Source: UKRI
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Ce3+ and/or Tb3+ doped GdAl3(BO3)(4) phosphors were prepared via a high-temperature solid-state reaction method. The band gap of GdAl3(BO3)(4) is determined from the VUV excitation spectrum of a Ce3+ doped sample at 14 K and further confirmed by that of undoped and Tb3+ doped samples at RT. X-ray excited luminescence (XEL) of GdAl3(BO3)(4): Ce3+ was measured. The main electron-vibrational interaction (EVI) parameters for Ce3+ in GdAl3(BO3)(4) were simulated. The vacuum referred binding energy (VRBE) scheme of lanthanide 4f/5d states in GdAl3(BO3)(4) was constructed. Using this scheme, the lowest 5d excitation band of Pr3+ in GdAl3(BO3)(4) was predicted, showing that the estimation is in agreement with the experimental result. The occurrence of multi-step energy transfer processes which include Gd3+->+Ce3+, Gd3+-> Tb3+,Ce3+-> Tb3+, and Tb3+-> Gd3+, Tb3+-> Ce3+ under different excitations was derived from excitation, emission, and fluorescence decay spectra. (C) 2015 Elsevier B.V. All rights reserved.
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