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Öğe Beta-irradiated ZnGa2O4:Sm3+phosphor: Thermoluminescence glow curves and kinetic parameters via gel combustion synthesis(Elsevier Science Sa, 2024) Barad, A.; Topaksu, M.; Hakami, J.; Kaynar, U. H.; Akca-Ozalp, S.; Altowyan, Abeer S.; Aydin, H.This study examines the X-ray Diffraction (XRD) characteristics of Sm 3+-doped ZnGa 2 O 4 phosphor, shedding light on its structural characteristics. The XRD data reveal distinctive peaks that represent the crystal 's lattice structure. This provides the basis for a more detailed analysis of thermoluminescence (TL). Initially, the TL glow curves corresponding to different concentrations of Sm were analysed, leading to the identification of the most favorable Sm concentration. Subsequently, an investigation was conducted into the TL behavior of the material in response to varying doses within a broad spectrum of beta radiation, revealing a linear characteristic (b=1.075) across doses ranging from 0.1 Gy to 50 Gy. Following this, a reusability assessment was executed over three measurement sets, wherein it was ascertained that the deviation in peak area across ten cycles did not surpass 2 %. Furthermore, it was investigated how different heating rates ranging from 0.5 degrees C/s to 7 degrees C/s affect the TL curve of the material. To determine the TL trap parameters of the sample, Initial Rise (IR) and Computerized Glow Curve Deconvolution (CGCD) methods were employed. A consistent pattern of activation energy values was observed in both IR in the T M-T stop experiment and CGCD analyses, indicating a uniform response to distinct energy levels within the sample. In terms of providing valuable insights into the characteristics of TL, these methods were found to be very effective. This contributed to a comprehensive understanding of charge carrier dynamics within the crystal lattice. Moreover, Peaks I, II, and III showed a linear response to applied doses, indicating the material 's potential for dosimetry applications. The findings of this study not only provide insights into Sm 3+-doped ZnGd 2 O 4 phosphors ' TL properties, but also enhance our understanding of how to optimize their radiation response.Öğe Enhanced luminescence and quenching mechanisms in Na⁺ Co-doped K₇CaY₂(B₅O₁₀)₃:Tb3+ phosphors under UV radiation(Elsevier Ltd, 2025) Alsam, Amani A.; Kaynar, U.H.; Aydin, H.; Coban, M.B.; Canimoglu, A.; Can, N.This study investigates the structural and luminescent properties UV radiation of Tb³⁺-doped K₇CaY₂(B₅O₁₀)₃ (KCYBO) phosphors prepared using a microwave-assisted sol-gel method, with a focus on the impact of Na⁺ co-doping. Tb³⁺ ions were effectively integrated as evidenced by X-ray diffraction (XRD) and Rietveld analysis, without disrupting the crystal structure. Photoluminescence (PL) analysis showed intense green emissions at 542 nm, which are due to the 5D₄ → 7F₅ transition in Tb³⁺. Optimal luminescence was observed at 3 wt% Tb³⁺, beyond which concentration quenching effect was driven by non-radiative cross-relaxation between adjacent Tb³⁺ ions. Na⁺ co-doping enhanced PL intensity by improving energy transfer and reducing non-radiative losses. CIE chromaticity coordinates demonstrated a tunable color shift towards warmer tones with increasing Na⁺ concentration. Thermal stability was assessed through the Arrhenius equation, with an activation energy of 0.31 eV, indicating the material's potential for high-temperature optoelectronic applications. © 2024 Elsevier LtdÖğe Enhanced luminescence of Eu3+ in LaAl2B4O10 via energy transfer from Dy3+ doping(Pergamon-Elsevier Science Ltd, 2024) Kaynar, Ümit Hüseyin; Coban, M. B.; Hakami, Jabir; Altowyan, Abeer S.; Aydin, H.; Ayvacikli, M.; Can, N.In this study, an investigation was conducted on the structural and photoluminescence (PL) characteristics of LaAl2B4O10 (LAB) phosphors initially incorporated with Dy3+ and Eu3+ ions. Subsequently, the impact of varying Eu3+ concentration while maintaining a constant Dy3+ concentration was examined. Structural characterization was performed using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and energy-dispersive X-ray spectroscopy (EDS). XRD analysis confirmed the effective embedding of both dopants into the hexagonal framework of the LAB. The PL emission spectra revealed characteristic emissions of Dy3+ (blue and yellow) and Eu3+ (red) ions. The optimized dopant concentrations of both Dy3+ and Eu3+ were observed to be 3 wt%. The dominant mechanism for concentration quenching in doped LAB phosphors was determined to be the electric dipole-dipole interaction. Co-doping with Eu3+ led to a substantial decrease in Dy3+ emission intensity (similar to 0.18-fold) while enhancing Eu3+ emission intensity (similar to 3.72-fold). The critical energy transfer distance (R-C = 11.64 & Aring;) and the analysis based on the Dexter theory confirmed that the energy transfer mechanism corresponds to dipole-dipole interaction. The color purities and correlated color temperatures (CCT) were estimated, suggesting the potential of these phosphors for warm white and red lighting applications, respectively. The observed energy transfer and luminescence properties, along with the structural and compositional characterization, highlight the promising potential of LAB:Dy3+/Eu3+ co-doped phosphors for advanced lighting and display technologies.Öğe Enhancement of luminescence and thermal stability in Eu3+-doped K3Y (BO2)6 with Li+ and Na+ co-doping(Elsevier, 2024) Kaynar, U. H.; Aydin, H.; Altowyan, A. S.; Hakami, J.; Coban, M. B.; Ayvacikli, M.; Karali, E. EkdalEu3+-doped and Li+/Na+ co-doped K3Y(BO2)6 (KYBO) phosphors were synthesized through a microwave- assisted sol-gel method, and their structural and photoluminescent (PL) characteristics were examined. X-ray diffraction (XRD) and Rietveld refinement confirm effective dopant incorporation and preservation of the crystalline structure. Fourier Transform Infrared (FTIR) spectroscopy indicates the maintenance of the borate structure, confirming the structural integrity of the phosphors upon doping. The addition of Li+ and Na+ co-dopants notably enhances luminescent efficiency and thermal stability, making these phosphors promising candidates for solid-state lighting (SSL) applications. PL analysis reveals strong red emission peaks at 612 nm, attributed to the 5 D o ? 7 F 2 transition of Eu3+ ions. The study indicates that electric dipole-quadrupole interactions are the primary mechanism for energy migration, with a critical distance of approximately 22.68 & Aring;. This mechanism contributes to concentration quenching at higher doping levels. High temperature PL measurements indicated an activation energy of 0.1389 eV for thermal quenching in the Li+ co-doped sample. Additionally, the Na+ co-doped sample exhibited an abnormal thermal stability behavior, with an even higher activation energy of 0.2536 eV. This suggests that Na+ co-doping significantly enhances the thermal resilience of the phosphor, making it more suitable for high-power light-emitting applications that operate under extreme conditions. CIE chromaticity diagrams highlight the potential for optimizing Eu3+ doping levels, combined with Li+ and Na+ co-doping, to improve luminescent performance and thermal stability for advanced SSL applications. (c) 2024 The Society of Powder Technology Japan. Published by Elsevier BV and The Society of Powder Technology Japan. All rights are reserved, including those for text and data mining, AI training, and similar technologies.Öğe Enhancement of luminescence and thermal stability in Eu3+-doped K3Y(BO2)6 with Li+ and Na+ co-doping (vol 35, 104695, 2024)(Elsevier, 2024) Kaynar, U. H.; Aydin, H.; Altowyan, Abeer S.; Hakami, J.; Coban, M. B.; Ayvacikli, M.; Karali, E. Ekdal[No abstract available]Öğe High temperature photoluminescence dependence and energy migration of Tb3+-Incorporated K3Y(BO2)6 phosphors(Pergamon-Elsevier Science Ltd, 2024) Souadi, G.; Hakami, O.; Kaynar, U. H.; Coban, M. B.; Aydin, H.; Madkhali, O.; Zelai, T.This study investigates the structural and photoluminescence (PL) characteristics of Tb3+-incorporated K3Y(BO2)(6) (KYBO) phosphors synthesized via a microwave-assisted sol-gel technique. X-ray diffraction (XRD) and Rietveld refinement confirmed the formation of a pure hexagonal phase, with lattice expansion due to Tb3+ doping. PL studies revealed strong green emissions centered at 541 nm, attributed to the D-5(4) -> F-7(5) transitions of Tb3+ ions, with the highest intensity observed at 5 wt% Tb3+. A decrease in emission was observed at higher concentrations due to concentration quenching. Temperature-dependent PL measurements revealed reverse thermal quenching enhancing PL intensity. Chromaticity analysis based on CIE 1931 coordinates showed stable green emission across all concentrations, with a maximum color purity of 89.74% observed for the KYBO:3 wt% Tb3+ sample. The results, along with reverse thermal quenching behavior observed between 470K and 550K, suggest that these phosphors exhibit excellent potential for lighting and display technologies.Öğe Integrating K plus into Eu and Tb doped GdCa 4O(BO3)3: A dual study on photoluminescence and structure(Elsevier Science Sa, 2024) Altowyan, Abeer S.; Kaynar, U. H.; Hakami, Jabir; Coban, M. B.; Ayvacikli, M.; Aydin, H.; Canimoglu, A.In this study, we investigate the structural and photoluminescence (PL) properties of rare -earth -doped GdCa 4 O (BO 3 ) 3 (GdCOB) phosphors, specifically focusing on the spectral behaviour induced by doping with Eu 3 + and Tb 3 + ions. The powder X-ray diffraction (XRD) spectra confirm the formation of a monoclinic phase. The XRD data were also refined by a Rietveld refinement method. The existence of B, O, Ca, Gd, Tb, Eu and K elements was verified by EDS spectra. We introduce a detailed examination of the charge compensation process using Kro ger- Vink notation to clarify the mechanisms essential for tailoring the optical properties of the phosphors. The PL excitation spectrum of GdCOB:Eu 3 + , monitored at 611 nm, reveals sharp excitation peaks at 319, 361, 380, and 392 nm, corresponding to 7 F 0 -> 5 H 3 , 7 F 0 -> 5 D 4 , 7 F 0 -> 7 F 0 , and 7 F 0 -> 5 L 6 transitions, respectively. The PL spectrum under excitation of 392 nm exhibits that phosphors doped with Eu 3 + a significant red emission at 611 nm, which is attributed to the 5 D 0 -> 7 F 2 transition. This emission intensity is particularly enhanced at non-centrosymmetric sites of the Eu 3 + ions. Similarly, the PL excitation spectrum of GdCOB:Tb 3 + , monitored at 552 nm, displays distinct excitation peaks at 316, 341, 353, and 379 nm, which correspond to the transitions 7 F 6 -> 5 D 0, 7 F 6 -> 5 L 7, 7 F 6 -> 5 D 2, and 7 F 6 -> 5 D 3, respectively. Tb 3 +-doped phosphors display a bright green emission, with a dominant peak at 552 nm, resulting from the 5 D 4 -> 7 F 5 transition. Additionally, the introduction of K + ions as co-dopants results in modifications to the local environments of Eu 3 + and Tb 3 + ions. These changes allow for fine-tuning of the emission peaks, significantly enhancing the luminescent output of the phosphors. Optimal doping concentrations of 5 mol% for Eu 3 + and 1 mol% for Tb 3 + enhance luminescent intensity and prevent concentration quenching. This phenomenon, often resulting in reduced PL intensity at higher dopant levels, is primarily due to dipole -dipole interactions, consistent with Dexter's theory of energy transfer. Strategic modulation of doping concentrations, coupled with a deep understanding of energy transfer mechanisms are critical for the development of advanced luminescent materials Our analysis of the Commission de l ' Eclairage (CIE) chromaticity coordinates reveals enhanced energy transfer dynamics in rare -earth -doped borates, facilitating the tuning of luminescent properties. These results not only deepen our understanding of the fundamental physics governing such phosphors but also open pathways for the development of optoelectronic applications requiring consistent color output, such as LED technologies and solid-state lighting.Öğe Novel Tb3+-Doped LaAl2 B4 O10 phosphors: Structural analysis, luminescent properties, and energy transfer mechanism(Pergamon-Elsevier Science Ltd, 2024) Kaynar, U. H.; Aydin, H.; Hakami, Jabir; Altowyan, Abeer S.; Coban, M. B.; Ayvacikli, M.; Canimoglu, A.This study explores the structural and luminescent properties of terbium (Tb3+)-doped lanthanum aluminium borate (LaAl2B4O,0, abbreviated as LAB) phosphors, a novel host lattice for Tb3+ doping. LAB:Tb3+ phosphors, with varying dopant concentrations, were synthesized using a microwave-assisted combustion synthesis approach and characterized using X-ray diffraction (XRD), Rietveld refinement, and photoluminescence spectroscopy at both room and low temperatures. The structural analysis confirmed the hexagonal crystal structure of LAB and revealed successful incorporation of Tb3+ ions without altering the fundamental lattice. Luminescence studies demonstrated that the LAB:Tb3+ phosphors show strong green emission primarily attributed to the 5D4 -> 7F5 transition of Tb3+. The optimal doping concentration was determined to be 5 wt% Tb3+, which provided maximum luminescence efficiency. This concentration also allowed for a critical study of energy transfer mechanisms within the phosphor, revealing dipole-dipole interactions with a critical distance of 9.80 & Aring; between Tb3+ ions. Additionally, the CIE chromaticity coordinates of LAB:0.05 Tb3+ were precisely determined to be (0.289, 0.4460), indicating the potential for high-quality green emission suitable for solid-state lighting and display technologies. This work not only demonstrates the potential of LAB:Tb3+ as a highly efficient green luminescent material, but also sheds light on the mechanisms responsible for energy transfer and concentration quenching.Öğe Optical performance and luminescence properties of Dy3+-doped LaMgB5O10 phosphors(Elsevier, 2025) Hakami, Jabir; Kaynar, U. H.; Coban, M. B.; Aydin, H.; Alamri, R.; Jabali, D. A.; Can, N.Despite significant advancements in borate-based phosphors, improving luminescent efficiency and thermal stability, particularly at high temperatures, remains a persistent challenge. In this study, Dy3+-doped LaMgB5O10 (LMBO) phosphors were synthesized and characterized for their photoluminescent properties to address these issues. Under 344 nm excitation, the Dy3+-activated LMBO phosphors exhibited strong luminescence with characteristic peaks at 482 nm (blue), 578 nm (yellow), and 663 nm (red), corresponding to specific Dy3+ transitions. Optimal luminescence was achieved at a doping level of 2 wt% Dy3+, beyond which quenching effects reduced emission intensity. The critical quenching distance (Rc) was estimated at 24.66 & Aring;, indicating predominant non-radiative energy transfer. Moreover, thermal quenching was reduced, with the activation energy for thermal quenching determined to be 0.1975 eV, demonstrating that the material can maintain reasonable luminescence efficiency at elevated temperatures. Time-resolved photoluminescence spectroscopy revealed multi-exponential decay behavior, indicating the presence of multiple decay processes. The average luminescence lifetimes were calculated as 632 mu s for the 2 wt% Dy3+ sample and 539 mu s for the 3 wt% Dy3+ sample, with a clear concentration quenching effect observed at higher dopant levels. Colorimetric analysis in the CIE 1931 color space revealed a shift toward yellow with increasing Dy3+ concentration, achieving a correlated color temperature (CCT) of 6595 K at 2 wt% Dy3+. This shift supports the material's potential for photonic and lighting applications. These findings highlight a significant advancement in addressing the thermal stability issue in phosphor materials, making Dy3+-doped LMBO phosphors promising candidates for advanced photonic technologies.Öğe Photoluminescence properties and structural analysis of Tb3+-doped K3Gd (BO2)6: A first study on negative thermal quenching(Elsevier Science Sa, 2025) Souadi, G.; Madkhli, A. Y.; Kaynar, U. H.; Gok, C.; Aydin, H.; Coban, M. B.; Kaynar, S. CamIn this study, Tb3+-doped K3Gd(BO2)6 phosphors were synthesized using the microwave-assisted sol-gel method to explore their photoluminescence (PL) properties and thermal stability. XRD and Rietveld refinement confirmed the incorporation of Tb3+ions, without secondary phases. PL analysis revealed a strong green emission near 542 nm, attributed to the 5 D 4 -> 7 F 5 transition of Tb3+ions. An optimal Tb3+concentration of 3 wt% was identified, beyond which concentration quenching significantly reduced luminescence intensity. Radiative energy transfer, occurring via reabsorption, was observed at lower concentrations, facilitating efficient energy migration. Conversely, at higher concentrations, non-radiative processes such as cross-relaxation dominated. Remarkably, negative thermal quenching (NTQ) was observed up to 470 K, with an activation energy of 0.96 eV. Additionally, Na+ co- doping introduced lattice distortions that enhanced energy transfer between Tb3+ions and improved luminescence efficiency. The chromaticity diagram highlighted a shift towards the yellow-green region with increasing the Tb3+concentration, demonstrating tunable emission properties for solid-state lighting applications.Öğe Structural and thermal insights into the luminescent behavior of Dy3+-Doped BaZrO3 with alkali metal codopants under UV radiation(Pergamon-Elsevier Science Ltd, 2025) Arslanlar, Y. Tuncer; Alajlani, Y.; Coban, M. B.; Kaynar, U. H.; Aydin, H.; Orucu, H.; Guinea, J. GarciaThis study investigates the structural, thermal, and photoluminescent properties of Dy3+-doped BaZrO3 (BZO) perovskites, synthesized via a co-precipitation method, incorporating alkali metal codopants (Li+, Na+, and K+). Xray diffraction (XRD) analysis confirmed the retention of the cubic perovskite phase following doping, with Rietveld refinement further revealing minor lattice distortions due to Dy3+incorporation. The Williamson-Hall (W-H) analysis revealed average crystallite sizes of 53 nm and 66 nm for undoped and 0.01 Dy3+-doped BaZrO3, respectively, with corresponding micro-strain values of 1.79 x 10-3 and 1.81 x 10-3, suggesting lattice distortions due to incorporation of Dy3+. Fourier transform infrared (FTIR) spectroscopy confirmed the cubic perovskite structure and subtle structural modifications upon doping. Notably, the absence of moisture-related peaks highlights the effectiveness of the synthesis process, including rigorous drying and calcination steps that prevented hydrous species. Photoluminescence (PL) analysis of Dy3+-doped BaZrO3 exhibited three prominent emission peaks at 452 nm, 573 nm, and 656 nm under 368 nm excitation. These peaks correspond to the characteristic intra-4f electronic transitions of Dy3+ ions, specifically, 4I13/2 to 6H15/2, 4F9/2 to 6H13/2, and 4F9/2 to 6H11/2, representing blue, yellow, and red emissions, respectively. Photoluminescence decay studies showed multi-exponential behavior, with the average lifetime decreasing from 641 mu s in undoped BZO to 492 mu s in Dy3+- doped samples attributed to enhanced non-radiative recombination pathways. Among the codopants, Li+ demonstrated the most significant improvement in luminescence intensity and thermal stability by mitigating defects and optimizing charge compensation.
