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Intense red photoluminescence from Mn^2+-doped (Na^+; Zn^2+) sulfophosphate glasses and glass ceramics as LED converters
Author(s) -
De Ning,
Mingying Peng,
Sebastian Krolikowski,
Lothar Wondraczek
Publication year - 2010
Publication title -
optics express
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.394
H-Index - 271
ISSN - 1094-4087
DOI - 10.1364/oe.18.002549
Subject(s) - materials science , raman spectroscopy , photoluminescence , analytical chemistry (journal) , doping , dopant , crystallization , spectroscopy , mineralogy , optics , optoelectronics , chemical engineering , chemistry , physics , chromatography , quantum mechanics , engineering
We report on intense red fluorescence from Mn(2+)-doped sulfophosphate glasses and glass ceramics of the type ZnO-Na(2)O-SO(3)-P(2)O(5). As a hypothesis, controlled internal crystallization of as-melted glasses is achieved on the basis of thermally-induced bimodal separation of an SO(3)-rich phase. Crystal formation is then confined to the relict structure of phase separation. The whole synthesis procedure is performed in air at <or= 800 degrees C. Electron spin resonance and Raman spectroscopy indicate that Mn(2+) species are incorporated on Zn(2+) sites with increasingly ionic character for increasing concentration. Correspondingly, in the glasses, increasing MnO content results in decreasing network polymerization. Stable glasses and continuously increasing emission intensity are observed for relatively high dopant concentration of up to 3 mol.%. Recrystallization of the glass results in strongly increasing emission intensity. Dynamic emission spectroscopy reveals only on type of emission centers in the glassy material, whereas three different centers are observed in the glass ceramic. These are attributed to octahedrally coordinated Mn(2+) in the residual glass phase and in crystalline phosphate and sulfate lattices, respectively. Relatively low crystal field strength results in almost ideal red emission, peaking around 625 nm. Excitation bands lie in the blue-to-green spectral range and exhibit strong overlap. The optimum excitation range matches the emission properties of GaN- and InGaN-based light emitting devices.

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