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Название: Novel Red Phosphor of Gd3+, Sm3+ co-Activated AgxGd((2−x)/3)−0.3−ySmyEu3+0.30☐(1−2x−2y)/3WO4 Scheelites for LED Lighting
Авторы: Morozov, V. A.
Lazoryak, B. I.
Savina, A. A.
Khaikina, E. G.
Leonidov, I. I.
Ishchenko, A. V.
Deyneko, D. V.
Дата публикации: 2023
Издатель: MDPI
Библиографическое описание: Morozov, VA, Lazoryak, BI, Savina, AA, Khaikina, EG, Leonidov, II, Ishchenko, AV & Deyneko, DV 2023, 'Novel Red Phosphor of Gd3+, Sm3+ co-Activated AgxGd((2−x)/3)−0.3−ySmyEu3+0.30☐(1−2x−2y)/3WO4 Scheelites for LED Lighting', Materials, Том. 16, № 12, 4350. https://doi.org/10.3390/ma16124350
Morozov, V. A., Lazoryak, B. I., Savina, A. A., Khaikina, E. G., Leonidov, I. I., Ishchenko, A. V., & Deyneko, D. V. (2023). Novel Red Phosphor of Gd3+, Sm3+ co-Activated AgxGd((2−x)/3)−0.3−ySmyEu3+0.30☐(1−2x−2y)/3WO4 Scheelites for LED Lighting. Materials, 16(12), [4350]. https://doi.org/10.3390/ma16124350
Аннотация: Gd3+ and Sm3+ co-activation, the effect of cation substitutions and the creation of cation vacancies in the scheelite-type framework are investigated as factors influencing luminescence properties. AgxGd((2−x)/3)−0.3−ySmyEu3+0.3☐(1−2x)/3WO4 (x = 0.50, 0.286, 0.20; y = 0.01, 0.02, 0.03, 0.3) scheelite-type phases (AxGSyE) have been synthesized by a solid-state method. A powder X-ray diffraction study of AxGSyE (x = 0.286, 0.2; y = 0.01, 0.02, 0.03) shows that the crystal structures have an incommensurately modulated character similar to other cation-deficient scheelite-related phases. Luminescence properties have been evaluated under near-ultraviolet (n–UV) light. The photoluminescence excitation spectra of AxGSyE demonstrate the strongest absorption at 395 nm, which matches well with commercially available UV-emitting GaN-based LED chips. Gd3+ and Sm3+ co-activation leads to a notable decreasing intensity of the charge transfer band in comparison with Gd3+ single-doped phases. The main absorption is the 7F0 → 5L6 transition of Eu3+ at 395 nm and the 6H5/2 → 4F7/2 transition of Sm3+ at 405 nm. The photoluminescence emission spectra of all the samples indicate intense red emission due to the 5D0 → 7F2 transition of Eu3+. The intensity of the 5D0 → 7F2 emission increases from ~2 times (x = 0.2, y = 0.01 and x = 0.286, y = 0.02) to ~4 times (x = 0.5, y = 0.01) in the Gd3+ and Sm3+ co-doped samples. The integral emission intensity of Ag0.20Gd0.29Sm0.01Eu0.30WO4 in the red visible spectral range (the 5D0 → 7F2 transition) is higher by ~20% than that of the commercially used red phosphor of Gd2O2S:Eu3+. A thermal quenching study of the luminescence of the Eu3+ emission reveals the influence of the structure of compounds and the Sm3+ concentration on the temperature dependence and behavior of the synthesized crystals. Ag0.286Gd0.252Sm0.02Eu0.30WO4 and Ag0.20Gd0.29Sm0.01Eu0.30WO4, with the incommensurately modulated (3 + 1)D monoclinic structure, are very attractive as near-UV converting phosphors applied as red-emitting phosphors for LEDs. © 2023 by the authors.
Ключевые слова: EUROPIUM
GADOLINIUM
INCOMMENSURATELY MODULATED STRUCTURES
LUMINESCENCE
PHOSPHORS
SAMARIUM
SCHEELITE
SILVER
TUNGSTATES
WHITE LIGHT-EMITTING DIODES
CHARGE TRANSFER
CHEMICAL ACTIVATION
EMISSION SPECTROSCOPY
EUROPIUM
GADOLINIUM
GALLIUM NITRIDE
III-V SEMICONDUCTORS
LIGHT EMITTING DIODES
LUMINESCENCE OF INORGANIC SOLIDS
PHOSPHORS
PHOTOLUMINESCENCE
POSITIVE IONS
SAMARIUM
TUNGSTATE MINERALS
CO ACTIVATION
CO-ACTIVATION
GADOLINIA
INCOMMENSURATELY MODULATED STRUCTURE
LUMINESCENCE PROPERTIES
MODULATED STRUCTURES
SCHEELITE
SYNTHESISED
TUNGSTATE
WHITE LIGHT EMITTING DIODES
SILVER
URI: http://elar.urfu.ru/handle/10995/130601
Условия доступа: info:eu-repo/semantics/openAccess
cc-by
Текст лицензии: https://creativecommons.org/licenses/by/4.0/
Идентификатор SCOPUS: 85163836662
Идентификатор WOS: 001017399200001
Идентификатор PURE: 41559509
ISSN: 1996-1944
DOI: 10.3390/ma16124350
Сведения о поддержке: AAAA-A21-121011590086-0; Ministry of Education and Science of the Russian Federation, Minobrnauka: 0273-2021-0008, FEUZ–2023–0014; Institute of Solid State Chemistry, Ural Branch, Russian Academy of Sciences, ISSC UB RAS; 122011300125-2
The study was supported by the Development Program of the Interdisciplinary Scientific and Educational School of Lomonosov Moscow State University’s “The future of the planet and global environmental change”, and the state assignment of the Chemistry Department of Moscow State University (Agreement No. AAAA-A21-121011590086-0) and state of the Russian Federation (122011300125-2). A.A.S. and E.G.K. are grateful to the support from the Ministry of Science and Higher Education of the Russian Federation (project No. 0273-2021-0008). A.V.I. is grateful to the scientific project of the Ministry of Education and Science of the Russian Federation FEUZ–2023–0014. I.I.L. acknowledges the support from the Research Program No. AAAA–A19–119031890025–9 (ISSC UB RAS).
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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