1. Expanding near-infrared emission bandwidth in K2NaCrF6:Fe3+ phosphors through dipole-dipole energy transfer.
- Author
-
Yang, Juyu, Yu, Haojun, Liu, Yan-gai, Mi, Ruiyu, Xie, Ci-an, Wang, Linlin, Sun, Tonglu, Liu, Jingang, and Mei, Lefu
- Subjects
- *
ENERGY transfer , *PHOSPHORS , *DIPOLE-dipole interactions , *BLUE light , *BANDWIDTHS , *CHROMIUM isotopes , *PHOTOTHERMAL effect , *LUMINESCENCE - Abstract
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 K 2 NaCrF 6 :Fe3+ phosphors. Upon excitation at 432 nm, the K 2 NaCrF 6 :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 K 2 NaCrF 6 :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 4T 2 (4F) → 4A 2 (Cr3+) and 4T 1 (4G) → 6A 1 (6S) (Fe3+) transitions. • K 2 NaCrF 6 :Fe3+ phosphors display application potential for near-infrared (NIR) fluorescence when excited by blue light. • The developed phosphors exhibit a broad near-infrared emission bandwidth (752–780 nm) under 432 nm excitation. • Increasing Fe3+ concentration leads to redshift and broadening of the emission spectrum. • Luminescent changes are attributed to dipole-dipole interactions and efficient energy transfer. • Cr3+ and Fe3+ enables synchronous excitation processes, offering versatility for applications in spectroscopy. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF