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Facile synthesis, structure, and properties of Gd2O2Se.

Authors :
Tarasenko, Maria S.
Kiryakov, Alexander S.
Ryadun, Alexey A.
Kuratieva, Natalia V.
Malyutina-Bronskaya, Victoria V.
Fedorov, Vladimir E.
Wang, Hsiang-Chen
Naumov, Nikolay G.
Source :
Journal of Solid State Chemistry. Aug2022, Vol. 312, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Inorganic phosphors based on rare earth elements are commonly used as scintillation materials due to their high chemical and radiation resistance. In this work, we study gadolinium oxyselenide as a new phosphor material. The work describes a facile synthesis method for Gd 2 O 2 Se. Single crystal structure of this compound was determined for the first time: sp.gr. P ¯3 m 1 with a ​= ​3.8911(4) Å and c ​= ​6.8829(8) Å. Gd 2 O 2 Se is stable in the inert atmosphere and melts at 2075 ​± ​20 ​°C. This material is also stable when heated in air up to 720 ​°C. with the following oxidation and weight increase. This mass increase can be explained by the oxidation of Se2− to Se4+. Further temperature increase above 952°С leads to a sharp mass loss and the final mass of sample corresponds to full oxidation of Gd 2 O 2 Se to gadolinium oxide. The band gap of the material was estimated to be 3.6 ​eV. Photoluminescence spectrum for Gd 2 O 2 Se:Tb3+ shows the characteristic transitions in Tb3+ ion with the most intense green emission that corresponds 5D 4 → 7F J transitions. [Display omitted] • A powder of Gd 2 O 2 Se was obtained and the single crystal structure was determined: sp.gr. P ¯3 m 1, a ​= ​3.89Å, c ​= ​6.88 Å. • The melting point was found to be 2075 ​± ​20 ​°C. High air stability for this compound was demonstrated up to 720 ​°C. • The estimated value of the band gap is 3.6 ​eV. The photoluminescence of the Tb3+ doped sample was investigated. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00224596
Volume :
312
Database :
Academic Search Index
Journal :
Journal of Solid State Chemistry
Publication Type :
Academic Journal
Accession number :
157525697
Full Text :
https://doi.org/10.1016/j.jssc.2022.123224