荧光粉
余辉
发光
材料科学
分析化学(期刊)
紫外线
兴奋剂
持续发光
发射光谱
激发
激活剂(遗传学)
谱线
化学
热释光
光电子学
物理
生物化学
伽马射线暴
色谱法
量子力学
天文
基因
作者
Runze Li,Hui Cao,Huahui Li,Dongyun Zhang,Chengkang Chang
标识
DOI:10.1016/j.ceramint.2022.04.019
摘要
A long persistent phosphor LiSr4(BO3)3: Eu2+, Dy3+ shows a typical 5d–4f transition of Eu2+ under ultraviolet activation with an emission centered at 632 nm. Herein, the lattice site of Sr2+ is partially replaced with Mg2+ and Ba2+ and co-doping is performed using Eu2+ and Dy3+ to successfully synthesize several LiSr4−xBax(BO3)3:2% Eu2+, Dy3+ and LiSr4−yMgy(BO3)3:2% Eu2+, Dy3+ phosphors with multicolor luminescence using a high-temperature solid-phase approach. When x or y = 0.4, the samples exhibit bright yellow or orange–red luminescence under ultraviolet (UV) excitation, with the emission spectra showing blue (611–632 nm) or red (632–648 nm) shifts, respectively. Such shifts in the peak position are ascribed to the weakened or enhanced crystal field strength. Under UV excitation, an afterglow phenomenon is also observed. The afterglow profiles can be simulated using an empirical double decay model. The LiSr3.76Mg0.2(BO3)3: 2% Eu2+, Dy3+ sample exhibits the best afterglow phenomenon, which is potentially attributed to the formation of numerous electron traps with suitable trap depths after the incorporation of Mg2+ into the phosphor lattice.
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