Expanding near-infrared emission bandwidth in K2NaCrF6:Fe3+phosphors through dipole-dipole energy transfer

被引:3
作者
Yang, Juyu [1 ]
Yu, Haojun [1 ]
Liu, Yan-gai [1 ]
Mi, Ruiyu [1 ]
Xie, Ci-an [1 ]
Wang, Linlin [1 ]
Sun, Tonglu [1 ]
Liu, Jingang [1 ]
Mei, Lefu [1 ]
机构
[1] China Univ Geosci Beijing, Minist Educ Geol Carbon Storage & Low Carbon Utili, Beijing Key Lab Mat Utilizat Nonmet Minerals & Sol, Sch Mat Sci & Technol,Engn Res Ctr,Natl Lab Minera, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Near -infrared (NIR); Emission bandwidth; Dipole -dipole interaction; Energy transfer; PHOTOLUMINESCENCE;
D O I
10.1016/j.jallcom.2024.174293
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Currently, the application potential of Cr3+ doped near-infrared (NIR) fluoride phosphors excited by blue light is promising. However, the development of near-infrared fluoride phosphors with wider emission bandwidth remains a challenge. Herein, we employed the hydrothermal method to prepare K2NaCrF6:Fe3+ phosphors. Upon excitation at 432 nm, the K2NaCrF6:xFe3+ phosphors exhibited broad near-infrared emission, with the main peak ranging from 752 nm to 780 nm. As the Fe3+ concentration increased, the luminescence intensity of the K2NaCrF6:xFe3+ phosphor decreased, accompanied by a redshift in the emission band and an increase in the full width of the emission spectrum half-peak. These changes can be attributed to the dipole-dipole interaction, specifically the energy transfer between Fe3+ and Cr3+, leading to the 4T2(4F) -> 4A2(Cr3+) and 4T1(4G) -> 6A1(6S) (Fe3+) transitions.
引用
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页数:9
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