Abstract
In this study, several borate phosphors K3Y(BO3)2:RE3+ (RE = Tb3+, Eu3+, Tb3+/Eu3+) with adjustable luminescence color were synthesized by the traditional high-temperature solid-phase method. The crystal-phase composition, particle morphology, luminescence properties, and thermal stability of phosphors were studied by XRD, SEM, PL-PLE, FLT, DRS, and variable temperature fluorescence spectrum. Results show that no impurity is produced in the phosphors. The excitation spectra of single-doped K3Y1-x(BO3)2:xTb3+ and single-doped K3Y1-y(BO3)2: yEu3+ overlap at 484 nm. K3Y0.89(BO3)2:0.11Tb3+, yEu3+ phosphors emit red and yellow–green light when excited at a wavelength of 377 nm. When Eu3+ concentration increases from 0.005 to 0.07, the emission intensity of Tb3+ decreases gradually, while that of Eu3+ increases gradually, which proves that Tb3+ → Eu3+ energy transfer exists. The Tb3+ → Eu3+ energy transfer efficiency reaches 53.54%, and energy transfer probability reaches 81.49%. At 377 nm, the co-doped phosphor color can range in the region of green, yellow, orange–red, and red. K3Y(BO3)2:Tb3+/Eu3+ phosphor can be applied in the field of LEDs excited by near-ultraviolet light.
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Data availability
The data that support the findings of this study are available from the corresponding author upon reasonable request.
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Acknowledgements
This work was supported by the Natural Science Foundation of Inner Mongolia 2018MS02002 and Inner Mongolia Autonomous Region universities basic scientific research project.
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Natural Science Foundation of Inner Mongolia Autonomous Region, 2018MS02002, Wenyu Zhao
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Chaofan Zhang (First Author): Methodology, Investigation, and Writing of the original draft; Yaming Liang: Data analysis; Qimeng Xu: Sample preparation; Wenyu Zhao (Corresponding author): Fund resources, Supervision, and Reviewing and editing of the manuscript.
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Zhang, C., Liang, Y., Xu, Q. et al. Novel color-tunable K3Y(BO3)2:RE3+ (RE = Tb3+, Eu3+, Tb3+/Eu3+) phosphors for near-UV white LEDs. J Mater Sci: Mater Electron 35, 1171 (2024). https://doi.org/10.1007/s10854-024-12918-5
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DOI: https://doi.org/10.1007/s10854-024-12918-5