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Structure and fluorescence properties of Dy‐doped alkaline‐earth borophosphate glasses
Author(s) -
Griebenow Kristin,
Muñoz Francisco,
Tagiara Nagia S.,
Klement Róbert,
Prnová Anna,
Wolfrum Bruno,
Kamitsos Efstratios I.,
Duran Alicia,
Galusek Dušan
Publication year - 2021
Publication title -
international journal of applied glass science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.383
H-Index - 34
eISSN - 2041-1294
pISSN - 2041-1286
DOI - 10.1111/ijag.16105
Subject(s) - dysprosium , raman spectroscopy , materials science , ionic bonding , analytical chemistry (journal) , quenching (fluorescence) , fluorescence , doping , alkaline earth metal , molar volume , infrared , divalent , ion , inorganic chemistry , chemistry , optics , metal , physics , optoelectronics , organic chemistry , chromatography , metallurgy , thermodynamics
Dysprosium‐doped borophosphate glasses, containing the divalent cations Mg 2+ , Ca 2+ , Sr 2+ , Ba 2+ , and Zn 2+ , are prepared by the melt‐quenching technique. The structure of the glasses is investigated by Raman, infrared, and nuclear magnetic resonance (NMR) spectroscopies and the fluorescence properties are determined. The Dy 3+ emission lifetime increases with an increasing ionic field strength and its maximum is observed in the Mg 2+ and Zn 2+ containing glasses. This result can be explained by the stronger M‐O bonding which causes a rearrangement of the borophosphate network and creates a local Dy 3+ environment of comparably low symmetry. This is in agreement with the Raman spectra and the evolution of the molar volume. The effect of the B/P variation on the emission properties of Dy 3+ is investigated in a second series of glasses where the emission lifetime is found to be maximum at 10 mol% B 2 O 3 .
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