4.7 Article

Co-substitution strategy to achieve a novel efficient deep-red-emitting SrKYTeO6:Mn4+ phosphor for plant cultivation lighting

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 906, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2022.164243

关键词

Red phosphor; SrKYTeO6:Mn4+; Co-substitution; Photoluminescence; Plant cultivation

资金

  1. National Natural Science Foundation of China [11564025, 51762008]

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In this study, an efficient deep-red-emitting SrKYTeO6:Mn4+ phosphor was synthesized, exhibiting superior luminescent properties and thermal stability, which holds potential application value in plant cultivation lighting.
Mn4+-doped oxide phosphors with bright red emission show promising application potential in plant cultivation lighting. However, finding suitable oxide hosts for Mn4+ ions incorporation is still a challenge. Herein, an efficient deep-red-emitting SrKYTeO6:Mn4+ phosphor was achieved through the co-substitution of [K+-Y3+] for [Sr2+-Ca2+] in non-luminous Sr2CaTeO6:Mn4+ for the first time. Crystal structure analysis reveals that the new SrKYTeO6 compound is isostructural to Sr2CaTeO6, which belongs to the monoclinic P2(1)/n (14) space group. Upon 338 nm excitation, the SrKYTeO6:Mn4+ phosphor exhibits a deep-red emission band peaking at 680 nm, resulting from the E-2(g) -> (4)A(2) g transition of Mn4+ ion. The concentration of Mn4+ ion in SrKYTeO6 is optimized to be 0.4 mol%, and color purity and internal quantum efficiency (IQE) of this phosphor reach as high as 98.5% and 44.3%, respectively. The phosphor also possesses good thermal stability with the emission intensity at 423 K maintaining 56% of the initial value at 298 K. These superior lumi-nescent properties could be attributed to the change of local crystal environment induced by distorting the internal [TeO6] octahedra. This work not only acquires an efficient SrKYTeO6:Mn4+ phosphor for application in plant cultivation lighting but also offers a replicable strategy for further exploring novel Mn4+-doped perovskite phosphors. (C) 2022 Elsevier B.V. All rights reserved.

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