Abstract
The development of blue-excitable deep-red phosphors represents a key advancement in next-generation agricultural lighting systems. Herein, a low-coordination polyhedral engineering strategy is proposed using novel K3Y1-xLux(BO3)2:Eu2+ to enable tunable broadband emission from 650 to 690 nm via Y3+→Lu3+ substitution, achieving blue-light-excitable deep-red luminescence that is uncommon among borate phosphors. Structural analysis reveals that Lu-induced lattice compression shortens the bond lengths in KO6 and Lu/YO6 octahedra, enhancing crystal field splitting and enabling deep-red emission with a full width at half maximum (FWHM) of 147 nm. Simultaneously, the photoluminescence quantum yield and thermal stability are significantly improved due to optimized Eu2+ site occupancy and suppression of non-radiative transitions. Density functional theory calculations and Hirshfeld surface analysis confirm that the shortened bond lengths and distorted polyhedra contribute to the enhanced luminescence properties. Prototype phosphor-converted LEDs based on K3Lu(BO3)2:Eu2+ demonstrate excellent spectral overlap with chlorophyll and phytochrome absorption, accelerating wheat growth by 20% under tailored illumination. This work not only addresses the long-standing challenge of achieving deep-red emission in borate phosphors but also introduces a promising material for next-generation agricultural lighting applications.
| Original language | English |
|---|---|
| Journal | Advanced Optical Materials |
| DOIs | |
| State | Published - Nov 23 2025 |
Scopus Subject Areas
- Electronic, Optical and Magnetic Materials
- Atomic and Molecular Physics, and Optics
Keywords
- deep-red phosphor
- plant lighting
- rare-earth luminescence
- sites occupancy