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Orange‐to‐Red Emission from Bi 2+ and Alkaline Earth Codoped Strontium Borate Phosphors for White Light Emitting Diodes
Author(s) -
Peng Mingying,
Wondraczek Lothar
Publication year - 2010
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1551-2916.2009.03590.x
Subject(s) - phosphor , luminescence , alkaline earth metal , dopant , analytical chemistry (journal) , strontium , materials science , boron , excited state , quantum yield , excitation , absorption band , mineralogy , chemistry , optoelectronics , doping , fluorescence , optics , atomic physics , physics , organic chemistry , chromatography , quantum mechanics , metal , metallurgy
SrB 4 O 7 and SrB 6 O 10 were considered as host materials for Bi 2+ dopants with luminescence in the orange‐to‐red spectral range. Based on the predominance of tetrahedral anion groups, both compounds are highly efficient for stabilizing the Bi 2+ ‐ion over its trivalent form. SrB 4 O 7 : Bi 2+ exhibits a broad blue excitation band while SrB 6 O 10 : Bi 2+ can be excited in the yellow spectral range. These bands suggest high interest for application in light emitting diode devices such as InGaN (SrB 4 O 7 :Bi 2+ ) and YAG:Ce 3+ (SrB 6 O 10 :Bi 2+ ) with improved color rendering index. Absorption due to strongly allowed 2 P 1/2 → 2 S 1/2 occurs at 245 and 286 nm, respectively. By substituting Sr 2+ with other alkaline earth species, the parity selection rule for transitions to 2 P 3/2 (blue and yellow excitation) can be lifted to a large extent, in this way increasing the transition probability from both bands and, thus, improving quantum yield for visible excitation. Analyses of the temperature dependence of luminescence reveal superior performance for SrB 4 O 7 :Bi 2+ .