Dopant Site Environment and Spectrum Blue Shift of Yellow-Emitting Solid Solution Phosphor Ba2-xSrxMg(PO4)2:Eu2+

被引:9
作者
Hu, Qingsong [1 ]
Pan, Zaifa [1 ]
Xu, Yu [1 ]
Wang, Lili [1 ]
Ning, Lixin [2 ]
机构
[1] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Zhejiang, Peoples R China
[2] Anhui Normal Univ, Dept Phys, Wuhu 241000, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
LUMINESCENCE PROPERTIES; CRYSTAL-CHEMISTRY; EU2+; EMISSION; MN2+;
D O I
10.1111/jace.13969
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
An unexpected spectrum blue shift of the yellow emission was observed for solid solution phosphors Ba2-xSrxMg(PO4)(2):Eu2+ (x=0-1.5), when bigger ions Ba2+ were substituted by smaller ions Sr2+ in Ba2Mg(PO4)(2) lattices. The solid solution phosphors were prepared by a solid-state reaction to clarify the local sites environment of activators Eu2+ and tune the anomalous long-wavelength yellow emission. BaSrMg(PO4)(2) phase was identified to be isostructural with Ba2Mg(PO4)(2) by Rietveld refinements. DFT calculation and photoluminescence show that the activator ions Eu2+ in BaSrMg(PO4)(2) occupy Sr2+ and Ba2+ sites at an equal probability and both generate an anomalous yellow emission. The yellow emission from Ba2-xSrxMg(PO4)(2):Eu2+ was gradually blue shift with increasing Sr2+ substitution concentration x from 0.1 to 1. Such unusual blue shift is interpreted based on the evolution of crystal structure parameters due to Sr2+ substitution, and subsequently, a site environmental expansion mechanism is proposed. The proposed mechanism could serve as a general model to reveal the underlying factors for spectrum shift caused by cation substitution and contribute to design new solid solution phosphors.
引用
收藏
页码:645 / 650
页数:6
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