荧光粉
烧结
材料科学
激光器
光电子学
光源
选择性激光烧结
复合材料
光学
物理
作者
Pengfei Wang,Hang Lin,Guoxin Chen,W.T. Weng,Yue Xu,Yi Lin,Ju Xu,Yao Cheng,Yuansheng Wang
标识
DOI:10.1038/s41467-025-58099-5
摘要
The development of advanced high-power-density laser-driven light source requires durable and color-tunable inorganic phosphor-in-glass film composites as color converter. One challenge remains for the phosphor-in-glass film is the thermal erosion and degradation of phosphor, as harsh condition or long duration time is required to densify the film for conventional sintering. Here we develop a rapid thermal annealing technique that achieves high film densification (porosity < 3%) within seconds utilizing high-power (>10 kW) infrared irradiation. As demonstrated by high-resolution electron microscopy observation, a trivial interfacial reaction occurs, leading to almost intact phosphor particles and thus restrained luminous loss. For instance, the red-emitting Sr0.8Ca0.2AlSiN3:Eu2+ exhibits a record internal quantum efficiency of 91.2% in the processed film and achieves a luminous flux of 2379 lm and efficacy of 140 lm W−1 after fabricating a phosphor wheel. This method reduces energy consumption, enables high-throughput screening, and offers material universality and design flexibility, paving the way for new opto-functional materials and applications. High-power laser lighting requires stable phosphor-in-glass films, but conventional sintering damages phosphors. Here, the authors develop infrared annealing which enables seconds-scale fabrication, minimizes interfacial damage and retains luminescence.
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