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Study on a Highly Thermostable Dy 3+ -Activated Borophosphate Phosphor.

Authors :
Liu C
Zheng Y
Qin Y
Liang L
Yang S
Li H
Jiang H
Zhao X
Liu S
Zhang H
Zhu J
Source :
Inorganic chemistry [Inorg Chem] 2024 Apr 08; Vol. 63 (14), pp. 6483-6492. Date of Electronic Publication: 2024 Mar 26.
Publication Year :
2024

Abstract

Constructing a phosphor with multifunctional applications is an imperative challenge. Especially, highly thermostable luminescence of phosphor is indispensable for stable white-light-emitting diodes (LEDs). Nevertheless, good thermal quenching resistance behavior is unfavorable for a fluorescence intensity ratio (FIR)-based optical temperature sensor. Herein, a highly thermostable Ba <subscript>3</subscript> (ZnB <subscript>5</subscript> O <subscript>10</subscript> )PO <subscript>4</subscript> (BZBP)-based phosphor is successfully achieved via replacing Ba <superscript>2+</superscript> with Dy <superscript>3+</superscript> , demonstrating simultaneously promising lighting and thermometry utilizations. Under the excitation of 350 nm, the title phosphor only loses 12% of the initial intensity when the temperature is up to 473 K, ensuring sufficient luminescence thermostability for white-LED lighting. The white-LED device fabricated using the title phosphor emits high-quality white light with a high color rendering index ( R <subscript>a</subscript> = 93) and low correlated color temperature (CCT = 3996 K). Meanwhile, the yellow and blue emission intensities demonstrate a downtrend difference with rising temperature. Temperature sensing properties are assessed through FIR technology. The maximal relative sensitivity reaches as high as 0.0379 K <superscript>-1</superscript> at 298 K. These results reveal that the title phosphor has a great potential for indoor lighting and thermometry applications.

Details

Language :
English
ISSN :
1520-510X
Volume :
63
Issue :
14
Database :
MEDLINE
Journal :
Inorganic chemistry
Publication Type :
Academic Journal
Accession number :
38531042
Full Text :
https://doi.org/10.1021/acs.inorgchem.4c00358