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Microwave-assisted fast synthesis and red-emitting properties of a borotellurate-based phosphor with excellent thermostability

At present, with the increasing application needs of phosphor-converted white light-emitting diode (w-LED), the synthetic efficiency and thermal stability of phosphor become urgent problems. Herein, this research reports a microwave-assisted fast synthesis approach to obtain a Sm3+-activated borotel...

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Bibliographic Details
Published in:Journal of rare earths 2024-06, Vol.42 (6), p.1036-1045
Main Authors: Xiang, Yuefei, Li, Hong, Zhang, Hongzhi, Yang, Lin, Liao, Canyuan, Yang, Tongsheng, Li, Junpeng, Guo, Zewen, Zhu, Jing
Format: Article
Language:English
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Summary:At present, with the increasing application needs of phosphor-converted white light-emitting diode (w-LED), the synthetic efficiency and thermal stability of phosphor become urgent problems. Herein, this research reports a microwave-assisted fast synthesis approach to obtain a Sm3+-activated borotellurate Na2Y2TeO4(BO3)2 (NYTB) red phosphor with high crystallinity, excellent thermostability, and low chromaticity shift. For the NYTB-based phosphor, in contrast to the conventional solid-state synthesis, the microwave-assisted synthesis method involves lower synthesis temperature and shorter processing time. Additionally, the concentration quenching mechanism was determined. The w-LED device packaged with the studied phosphor exhibits a near-standard white light with proper CCT and high Ra parameters. [Display omitted] A microwave-assisted fast synthesis approach was used to synthesize the borotellurate-based Na2Y2TeO4(BO3)2:Sm3+ red phosphor with high crystallinity, excellent thermostability, and low chromaticity shift. The red phosphor demonstrates potential solid-state lighting applications. •A microwave-assisted fast synthesis is used to construct a Na2Y2TeO4(BO3)2:Sm3+ phosphor.•Na2Y2TeO4(BO3)2:Sm3+ with high CP and suitable IQE exhibits high thermal stability.•The fabricated w-LED device exhibits proper CCT and high Ra.
ISSN:1002-0721
2509-4963
DOI:10.1016/j.jre.2023.03.012