Tuning the emission half-peak width of CaMgSi2O6:Cr3+ from 138 nm to 393 nm by controlling the Cr3+ concentration

荧光粉 半最大全宽 光致发光 离子 八面体 兴奋剂 材料科学 发光二极管 发光 分析化学(期刊) 光电子学 化学 色谱法 有机化学
作者
Xiaoqian Dong,Zhibin Chen,Lehui Liu,Feifei Yuan,Yisheng Huang,Lizhen Zhang,Zhoubin Lin
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:981: 173746-173746 被引量:12
标识
DOI:10.1016/j.jallcom.2024.173746
摘要

Broadband near-infrared (NIR) phosphors play a crucial role in the development of next-generation smart NIR light sources based on blue light-emitting diodes (LEDs). The emission bandwidth is an important parameter for evaluating the performance of these phosphors. Herein, an ultra-broadband NIR phosphor CaMgSi2O6:Cr3+ (CMSO:Cr), with a tunable emission band and a full width at half maximum (FWHM) ranging from 138 nm to 393 nm, is obtained by adjusting the doping concentration of Cr3+. In the low-concentration doped sample, a single emission peak at 785 nm is observed. When the concentration of Cr3+ exceeds 1.0 at%, emissions at both 785 nm and 980 nm are detected. The emission peak at 785 nm originates from the [MgO6](Ⅰ) octahedron within the CMSO structure. On the other hand, the emission peak at 980 nm is attributed to the presence of a twisted octahedron [MgO6](Ⅱ), which is caused by defects and vacancies resulting from the charge imbalance when Mg2+ ions are replaced by Cr3+ ions. The Cr3+ ion primarily occupies the [MgO6](Ⅰ) site in the lower-concentration doped sample, which explains the photoluminescence peak at 785 nm. With the increase in the concentration of Cr3+ ions, more and more Cr3+ ions preferentially occupy the [MgO6](Ⅱ) octahedral sites, leading to the broad emission at 980 nm. A novel NIR phosphor light source was fabricated by combining a blue chip with CMSO:Cr phosphor. Driven by a current of 60 mA, the NIR light output power of 5.89 mW and 0.76 mW is achieved by using CMSO:0.015Cr and CMSO:0.04Cr, respectively. This work demonstrates that new luminescent centers can be generated by substituting heterovalent ions, resulting in broadened emission spectra.
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