Abstract
Highly efficient cyan-green-emitting phosphors are urgently needed for high-color-quality full-visible-spectrum white light-emitting diodes (LEDs). Herein, we report on efficient near-ultraviolet-excited cyan-green-emitting Ca2La1-xLuxHf2Al3O12:Ce3+ (CLa1-xLuxHA:Ce3+) garnet phosphors, which are developed based on the solid-solution design of chemical cation substitution. All phosphor samples present a garnet crystal structure with the Ia3‾d space group; with increasing Lu3+ ions content, the lattice could be gradually contracted, along with a high symmetry as well as rigidity. Furthermore, under the 408 nm excitation, the cyan-green emissions of CLa1-xLuxHA:Ce3+ phosphors are progressively enhanced with a slight blue-shift, due to crystal field splitting and Stokes shift. Importantly, quantum efficiency and thermal stability performances are greatly improved by introducing smaller Lu3+ ions to replace the bigger La3+ ions, owing to the high rigidity structure with high symmetry. The optimized CLa0.5Lu0.5HA:Ce3+ phosphor exhibits an intense cyan-green emission band with high internal quantum efficiency of 76.4% and external quantum efficiency of 54.4%. Through employing the as-prepared CLa0.5Lu0.5HA:Ce3+ cyan-green phosphor, we have successfully fabricated a full-visible-spectrum LED device, demonstrating a bright warm-white light emission with an extremely high color rendering index (Ra = 98.0, R9 = 95.9, and R12 = 94.3) and low correlated color temperature (3497 K) under 100 mA driving current. This study not only reveals the correlation between the crystal structure evolution and luminescent properties of phosphor materials, but also provides new strategies for the design and development of novel efficient luminescent materials for high-quality full-visible-spectrum LED lighting.
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