Na+-driven enhancement of the 5D₀ → 7F₄ emission in Eu3+-activated KCa₄(BO₃)₃: photoluminescence and Judd–Ofelt study

dc.authorid0000-0001-8415-6317
dc.authorid0000-0002-3321-0341
dc.authorid0000-0002-4672-0922
dc.authorid0000-0003-3488-5284
dc.contributor.authorCan, N.
dc.contributor.authorCanımoğlu, Adil
dc.contributor.authorKarman, Tenzile
dc.contributor.authorÇin, E. Aymila
dc.contributor.authorHakami, J.
dc.contributor.authorÇoban, Mustafa Burak
dc.contributor.authorKaynar, Ümit Hüseyin
dc.contributor.authorAydın, H.
dc.contributor.authorYusan, Sabriye
dc.contributor.authorAltowyan, Abeer S.
dc.contributor.authorKarali, Elçin Ekdal
dc.contributor.authorKarman, Tenzile
dc.date.accessioned2026-03-25T07:07:07Z
dc.date.issued2026
dc.departmentFakülteler, Fen-Edebiyat Fakültesi, Fizik Bölümü
dc.descriptionÇoban, Mustafa Burak (Balikesir Author)
dc.description.abstractA series of Eu3+-activated KCa₄(BO₃)₃ (KCOB) phosphors were synthesized using a conventional solid-state re action method. The structural, morphological, and photoluminescence properties were systematically tuned via Li+ and Na+ co-doping. Rietveld-refined X-ray diffraction confirmed successful substitution of Ca2+ sites by Eu3+ and alkali ions without forming secondary phases. FTIR and Raman spectroscopy validated the stability of the [BO₃] 3− unitswhile also indicating local vibrational distortions caused by asymmetry in the crystal field envi ronment. SEM images displayed uniform microstructures with enhanced surface densification upon alkali incorporation. Photoluminescence spectra exhibited strong red emission centered at ~613 nm, attributed to the 5 D₀ → 7 F₂ electric dipole transition of Eu3+, with intensity enhancement under alkali co-doping due to increased site asymmetry. Judd–Ofelt analysis revealed significant increases in Ω₂ and Ω₄ parameters, particularly in Na+- doped samples, confirming the enhancement of electric dipole transition probabilities. CIE chromaticity analysis showed that Li+ co-doping at y = 0.02 yielded the highest color purity (84 %) and lowest correlated color temperature (CCT ≈ 1940 K), while Na+ co-doping provided moderate-to-high color purity (up to 79 %) with tunable CCT values between 1831and 2038 K. Temperature-dependent PL studies anomalous non-monotonic behavior, including partial intensity recovery at elevated temperatures, deviating from classical quenching models. This suggests the involvement of defect-mediated recombination pathways and strong local crystal field effects stabilizing emission under thermal stress. These findings demonstrate that Li+/Na+ co-doping enables precise tuning of crystal symmetry, emission intensity, chromaticity, and thermal resilience. Thus, KCOB:Eu3+ phosphors with optimized alkali content represent promising candidates for thermally robust, high-purity red emitters in near-UV-pumped warm-white solid-state lighting systems.
dc.identifier.doi10.1016/j.jphotochem.2025.116829
dc.identifier.endpage19
dc.identifier.issn1010-6030
dc.identifier.startpage1
dc.identifier.urihttps://doi.org/10.1016/j.jphotochem.2025.116829
dc.identifier.urihttps://hdl.handle.net/20.500.12462/23559
dc.identifier.volume472
dc.identifier.wos001598939400005
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElseiver
dc.relation.ispartofJournal of Photochemistry and Photobiology A: Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectKca₄(bo₃)₃ Phosphors
dc.subjectEu3+ Doping
dc.subjectPhotoluminescence
dc.subjectJudd–Ofelt Analysis
dc.subjectAnomalous Thermal Behavior
dc.titleNa+-driven enhancement of the 5D₀ → 7F₄ emission in Eu3+-activated KCa₄(BO₃)₃: photoluminescence and Judd–Ofelt study
dc.typeArticle

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