Structural variation and near infrared luminescence in Mn5+-doped M2SiO4 (M = Ba, Sr, ca) phosphors by cation substitution

被引:12
|
作者
Zhang, Xiaowen [1 ,2 ]
Nie, Jianmin [1 ,2 ]
Liu, Shanshan [1 ,2 ]
Qiu, Jianrong [1 ,2 ,3 ]
机构
[1] South China Univ Technol, Sch Mat Sci & Technol, State Key Lab Luminescent Mat & Devices, Guangzhou, Guangdong, Peoples R China
[2] Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Guangzhou, Guangdong, Peoples R China
[3] Zhejiang Univ, Coll Opt Sci & Engn, State Key Lab Modern Opt Instrumentat, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
MN5+; COLOR; SPECTROSCOPY; CA2PO4CL; PHASE; M=BA;
D O I
10.1007/s10854-018-8622-2
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Alkaline earth orthosilicates M2SiO4 (M = Ba, Sr and Ca) phosphors doped with Mn5+ ions have been prepared by the conventional solid-state reaction method. The crystal structures were verified by X-ray diffraction. By varying the host composition from Ba to Ca, the position shifting of photoluminescence emission bands corresponding to the E-1 -> (3)A(2) transition are induced by the increasing angular distortion and covalence. The nonradiative energy transfer becomes a dominant role in the photoluminescence process with substituting Ba2+ sites for smaller cations. The structural evolution and relevant luminescence mechanisms in (Ba1-xCax)(2)SiO4 phosphors also have been investigated in detail. It reveals that the chemical composition modification and structural variation can be an efficient approach to optimize the photoluminescence behaviors.
引用
收藏
页码:6419 / 6427
页数:9
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