MCBÜ Açıkerişim Sistemi :: Browsing by Author "Garcia Guinea J."

Browsing by Author "Garcia Guinea J."

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Luminescence behaviour and Raman characterization of dendritic agate in the Dereyalak village (Eskiehir), Turkey
(2011) Paral L.; Garcia Guinea J.; Kibar R.; Cetin A.; Can N.
Results are presented for the cathodoluminescence (CL), X-ray diffraction (XRD), inductively coupled plasma-atomic emission spectrometry (ICP-AES) and simultaneously two thermal analyses of (DTA/TGA) spectroscopy of dendritic agate which occurs in the Pliocene polymictic conglomerates of the Höyüklü Formation, North West of the Dereyalak village (Eskisehir, Turkey). Micro-Raman measurements were performed on dendritic agate and then strong quartz and moganite peaks were identified at 465 and 501 cm -1, respectively. Thermal analysis shows the loss of water and hydroxyl units occurs in 2 distinct stages; at 796 and 808 °C. Spatially resolved CL results at room temperature were recorded for chosen 3 different areas. Grey area (100% SiO2) displays the lowest CL emission. Brown area (99.7% SiO2 and 0.3% Fe2O3) contains exsolved non-detected ironed phases such as goethite-lepidochrocite to explain the brown colour and the iron point substitutional defects attributed to the 643 nm CL emission. White outer (98.7% SiO2 and 1.3% Al 2O3) would be strongly disordered as observed in the amorphous Raman spectrum containing as inferred from the spectrum CL on the outer areas, particularly non-bridging oxygen hole centres (NBOHC) (317 nm) and [AlO4]°/H (380 nm) centres produced by large amounts of aluminium in the lattice (1.33% Al2O3). When it comes to collect the data in the time resolved CL spectrum, at least three broad emission bands were detected in: a green band of low intensity at about 496 nm, intense orange band at about 600 nm, and a red band at 670 nm. The CL emission at 670 nm shows some relationships between the hydroxyl or alkali content and the abundance of O2 (super 3-) centres and E′1 centres. Another conspicuous observed feature in the CL spectra of agates is the existence of an orange emission band centred at around 600 nm. The predominance of the yellow CL emission band and the high concentration of E′1 centres are typical for agates formed by acidic volcanism processes. © 2011 Elsevier B.V. All rights reserved.
Solid state synthesis of SrAl2O4:Mn2+ co-doped with Nd3+ phosphor and its optical properties
(2013) Ayvacikli M.; Kotan Z.; Ekdal E.; Karabulut Y.; Canimoglu A.; Garcia Guinea J.; Khatab A.; Henini M.; Can N.
The optical properties of alkaline earth aluminates doped with rare earth ions have received much attention in the last years and this is due to their chemical stability, long-afterglow (LAG) phosphorescence and high quantum efficiency. However, there is a lack of understanding about the nature of the rare earth ion trapping sites and the mechanisms which could activate and improve the emission centers in these materials. Therefore a new phosphor material composition, SrAl2O4:Mn2+, co-doped with Nd3+ was synthesized by a traditional solid-state reaction method. The influence of transition metal and rare earth doping on crystal structure and its luminescence properties have been investigated by using X-ray diffraction (XRD), Raman scattering, Photoluminescence (PL) and Radioluminescence (RL). Analysis of the related diffraction patterns has revealed a major phase characteristic of the monoclinic SrAl2O 4 compound. Small amounts of the dopants MnCO3 and Nd 2O3 have almost no effect on the crsytalline phase composition. Characteristic absorption bands from Nd3+ 4f-4f transitions in the spectra can be assigned to the transitions from the ground state 4I9/2 to the excited states. The luminescence of Mn2+ activated SrAl2O4 exhibits a broad green emission band from the synthesized phosphor particles under different excitation sources. This corresponds to the spin-forbidden transition of the d-orbital electron associated with the Mn2+ ion. In photo- and radio-luminescence spectra, Nd3+ 4f-4f transition peaks were observed. The emitted radiations for different luminescence techniques were dominated by 560, 870, 1057 and 1335 nm peaks in the visible and NIR regions as a result of 4I9/2→4G7/2 and 4F3/2→4IJ (J=9/2, 11/2 and 13/2) transitions of Nd3+ ions, respectively. Multiple emission lines observed at each of these techniques are due to the crystal field splitting of the ground state of the emitting ions. The nature of the emission lines is discussed. © 2013 Elsevier B.V.
Studies on luminescence from a cerium-doped strontium stannate phosphor
(John Wiley and Sons Ltd, 2015) Karabulut Y.; Ayvacikli M.; Canimoglu A.; Garcia Guinea J.; Can N.
The crystal structure and morphology of Ce3+-doped SrSnO3 materials prepared using the solid-state reaction method were extensively characterized using experimental techniques. X-Ray diffraction results show that the cerium substitution of strontium does not change the structure of the strontium stannate. Raman spectroscopy was used to investigate the microstructures and lattice vibrations. Environmental scanning electron microscopy images showed that phosphors aggregate and their particles form irregular shapes. SrSnO3 exhibits an intense green emission with a broad band originating from the 5d1 → 4f1 transition of cerium. It was observed that, after exposure to beta-irradiation, the glow curve of this material has two broad thermoluminescence peaks, one centered at ∼ 127C and the other at ∼ 245C for a heating rate of 5 K/s. The kinetic parameters, which include the frequency factor and the activation energy of the material, were calculated using Chen's method, after beta-irradiation. The fading and reusability of the phosphor were also studied and it was found that the phosphor is suitable for radiation dosimetry. Copyright © 2014 John Wiley & Sons, Ltd. Copyright © 2014 John Wiley & Sons, Ltd.
Characterisation and luminescence studies of Tm and Na doped magnesium borate phosphors
(Elsevier Ltd, 2015) Ekdal E.; Garcia Guinea J.; Karabulut Y.; Canimoglu A.; Harmansah C.; Jorge A.; Karali T.; Can N.
In this study, structural and luminescence properties of magnesium borate of the form MgB4O7 doped with Tm and Na were investigated by X-ray diffraction (XRD), Raman spectroscopy and cathodoluminescence (CL). The morphologies of the synthetised compounds exhibit clustered granules and road-like materials. As doping trivalent ions into a host with divalent cations requires charge compensation, this effect is discussed. The CL spectra of undoped MgB4O7 shows a broad band emission centred around 350nm which is postulated to be produced by self-trapped excitons and some other defects. From the CL emission spectrum, main emission bands centred at 360, 455, 475nm due to the respective transitions of 1D2→3H6,1D2→3F4 and 1G4→3H6 suggest the presence of Tm3+ ion in MgB4O7 lattice site. CL mechanism was proposed to explain the observed phenomena which are valuable in possibility of the developing new luminescent materials for different applications. In addition, the experimental Raman spectrum of doped and undoped MgB4O7 were reported and discussed. © 2015 Elsevier Ltd.
Optical spectroscopy of the Ce-doped multicomponent garnets
(Elsevier Ltd, 2016) Canimoglu A.; Karabulut Y.; Ayvacikli M.; Muresan L.E.; Perhaita I.; Barbu-Tudoran L.; Garcia Guinea J.; Karali T.; Can N.
Here, we report our results referring to the preparation of Ce doped Y2.22MgGa2Al2SiO12, Y1.93MgAl4SiO12 and Y2.22Gd0.75Ga2Al3O12 using solid state reaction at high temperature. Several complementary methods (i.e. powder x-ray diffraction (XRPD), energy dispersive analysis of X-rays (EDX), scanning electron microscopy (SEM) and Fourier transforms infrared spectroscopy (FTIR)) were studied to examine the effects of the synthesis procedure on the morphology and structure. XRD analyses revealed that all compounds include yttrium aluminate phase with garnet structure. Cathodoluminescence (CL), radioluminescence (RL) and photoluminescence (PL) measurements were carried out for clarification of relationship between host lattice defects and the spectral luminescence emissions. Luminescence emission of phosphors is peaked at 530 nm assigned to 5d-4f transitions of the dopant Ce3+ ions with a broad emission band in 400-700 nm range. Under electron irradiation, the emission spectrum of Ce doped (YGd)3Ga2Al3O12 is well defined and has a characteristic fairly narrow and sharp emission band peaking at 312 nm and 624 nm corresponding to transition of 6P7/2 →8S7/2 and 6GJ→6PJ (Gd3+), respectively. We suggest some of phosphors might be excellent phototherapy phosphor materials under electron excitation. © 2016 Elsevier Ltd.
Study of luminescence of Mn-doped CaB4O7 prepared by wet chemical method
(Elsevier Ltd, 2016) Oguz K.F.; Ekdal E.; Aslani M.A.A.; Canimoglu A.; Garcia Guinea J.; Can N.; Karali T.
In this study, manganese (Mn) doped Calcium Tetraborate (CaB4O7) samples were prepared by the wet chemical method. Under beta irradiated, CaB4O7:Mn showed thermally stimulated luminescence (TSL) glow peaks at approximately 85 °C and 220 °C with a heating rate of 5 °C/s. Peak shape (PS) and various heating rates (VHR) methods were applied for determining the trap parameters such as order of kinetic (b), activation energy (E) and frequency factor (s). The results indicate that the main dosimetric peak of CaB4O7:Mn follows the second-order kinetic model. The thermal fading ratio of the material is around 15% at the end of one month period of storage. The results of the TL studies carried out on the CaB4O7:Mn dosimeter revealed that it has high sensitivity, which makes it very valuable in various dosimetric applications like space, medical, personal dosimetry and dating. Radioluminescence (RL) of CaB4O7:Mn was also studied. It is shown that the RL spectrum contains a wide band centered at 530 nm assigned to Mn2+ ion emission. A broad band emission feature peaked at 350 nm assigned to the non-bridging oxygen hole center (NBOHC) is also discussed and a model is proposed to explain this broad band feature. © 2016 Elsevier B.V. All rights reserved.
Structural and luminescence effects of Ga co-doping on Ce-doped yttrium aluminate based phosphors
(Elsevier Ltd, 2016) Ayvacikli M.; Canimoglu A.; Muresan L.E.; Barbu Tudoran L.; Garcia Guinea J.; Karabulut Y.; Jorge A.; Karali T.; Can N.
Herein, we primarily focus on luminescence spectrum measurements of various types of green emitting yttrium aluminate phosphors modified with gallium (Y3Al5-xGaxO12) synthesised by solid state reaction. The luminescent emission of samples depends on sample temperature and excitation radiation such as incident X-ray, electron and laser beam. Here, we measured radioluminescence (RL), cathodoluminescence (CL), photoluminescence (PL) along with XRD in order to clarify relationship between lattice defects and the spectral luminescence emissions. The RL and CL spectra of YAG:Ce exhibit an emission band ranging from 300 to 450 nm related to YAl antisite defects. The broad emission band of garnet phosphors is shifted from 526 nm to 498 nm with increasing of Ga3+ content, while full width at half maximum (FWHM) of the band tends to be greater than the width of unmodified YAG:Ce garnet. Deconvolution of the spectrum reveals that three emission bands centred at 139, 234 and 294°C occur in aluminate host garnets. © 2016 Elsevier B.V. All rights reserved.
Tunable luminescence of broadband-excited and narrow line green emitting Y2SiO5:Ce3+, Tb3+ phosphor
(Elsevier Ltd, 2016) Muresan L.E.; Karabulut Y.; Cadis A.I.; Perhaita I.; Canimoglu A.; Garcia Guinea J.; Barbu Tudoran L.; Silipas D.; Ayvacikli M.; Can N.
Cerium and terbium activated white emitting yttrium silicate phosphors (Y2-x-yCexTbySiO5) having average size between 96 and 123 nm were synthesised by a gel-combustion, and their phase and crystal structures, morphologies and ultraviolet (UV)-visible spectroscopic properties were studied. All rare earth doped yttrium silicate (YSO) phosphors are well crystallized powders containing only monoclinic X2-Y2SiO5 phase. No significant changes in the cell parameters were observed with increasing of Tb amount as ionic radii of Tb3+ (0.923 Å) and Y3+ (0.9 Å) have almost the same. Under different excitations, YSO:Ce3+ exhibits blue emission due to the 5d-4f transitions of Ce3+ ions. The series of emission states at different wavelengths of YSO:Tb3+ associated to f-f transition of Tb3+ ion were detected from luminescence measurements. The emission observed at 544 nm (green) corresponding to 5D4 → 7F5 of Tb3+ is strongest one. Incorporation of variable amounts of Tb3+ in the YSO host lattice determines the modification of emission colour from blue through light blue and eventually to bluish green. A possible energy transfer mechanism taking place from Ce3+ to Tb3+ was also discussed in terms of excitation and emission spectra. © 2015 Elsevier B.V.
Preparation and characterization of Yttrium based luminescence phosphors
(Elsevier B.V., 2017) Muresan L.E.; Ayvacikli M.; Garcia Guinea J.; Canimoglu A.; Karabulut Y.; Can N.
Ce doped Yttrium aluminate modified by replacing different molar part of aluminium or gallium (Y3Al5−xGaxO12) and Yttrium silicate phosphors activated with Ce and Tb (Y2SiO5:Ce3+,Tb3+) were synthesized by solid state reaction and a gel combustion method, respectively. X-ray diffraction and Scanning electron microscope (SEM) techniques are used to identify their structures and morphologies. Luminescence characteristics are measured and spectroscopic data confirm that Y2SiO5:Ce3+, Tb3+ phosphors can be effectively excited upon UV excitation light and X-ray irradiation, resulting in intense blue and green emissions, respectively. This energy transfer takes place by means of a non-radiative process inside Ce3+-Tb3+ clusters formed in the host matrix. Tb3+ doped Y2SiO5 yields both blue emission 5D3 → 7Fj (j = 3,4,5,6) and green emission 5D4 → 7FJ (J = 3,4,5,6) of Tb3+. Y3Al5−xGaxO12:Ce3+ phosphors exhibit a broad blue emission band originating from allowed 5d-4f transition of the Ce3+ ions under different excitation sources but the broad emission band shifts with increasing of Ga3+ content. This work presents a quantitative understanding of host material's on dopant's luminescence properties and thereby provides an optimization guideline, which is extremely demanding for the development of new luminescent materials. © 2017 Elsevier B.V.
Synthesis and influence of ultrasonic treatment on luminescence of Mn incorporated ZnS nanoparticles
(Elsevier B.V., 2017) Cadis A.-I.; Muresan L.E.; Perhaita I.; Munteanu V.; Karabulut Y.; Garcia Guinea J.; Canimoglu A.; Ayvacikli M.; Can N.
Manganese (Mn) doping of ZnS phosphors was achieved by precipitation method using different ultrasound (US) maturation times. The structural and luminescence properties of the samples were carried out by means of X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive spectroscopy (EDS), photoluminescence (PL), and cathodoluminescence (CL). The real amount of manganese incorporated in ZnS lattice was calculated based on ICP-OES results. According with XRD patterns, the phase structure of ZnS:Mn samples is cubic. EDS spectra reveal deviations of the Mn dopant concentration from the target composition. Both 300 K PL and CL emission spectra of the Mn doped ZnS phosphors display intense orange emission at 590 and 600 nm, respectively, which is characteristic emission of Mn ion corresponding to a 4T1→6A1 transition. Both PL and CL spectra confirmed manganese is substitutionally incorporated into the ZnS host as Mn2+. However, it is suggested that the origin of broad blue emission around 400 nm appeared in CL is due to the radiative recombination at deep level defect states in the ZnS. The ultrasound treatment at first enhances the luminescent intensity by ∼3 times in comparison with samples prepared by classical way. This study gives rise to an optimization guideline, which is extremely demanded for the development of new luminescent materials. © 2017 Elsevier B.V.
Doping Sm3+ into ZnB2O4 phosphors and their structural and cathodoluminescence properties
(Elsevier Ltd, 2018) Kucuk N.; Bulcar K.; Dogan T.; Garcia Guinea J.; Portakal Z.G.; Karabulut Y.; Ayvacikli M.; Canimoglu A.; Topaksu M.; Can N.
In this study, ZnB2O4:xSm3+ (0.01 ≤ x ≤ 0.05 mol) powder phosphors have been synthesized by low temperature chemical synthesis method. The structure and morphological observation of the phosphor samples were systematically monitored by X-ray powder diffraction (XRD) and environmental scanning electron microscope (ESEM) coupled to an energy dispersive X-ray spectrometer (EDS). The all diffraction peaks are well assigned to standard data card (PDF#39-1126). Emission properties of the samples were explored using light emission induced by an electron beam (i.e cathodoluminescence, CL) at room temperature (RT). When excited with electron beam, CL spectral measurements of scrutinized phosphors exhibit orange-red luminescence at 572 nm, 606 nm and 658 nm due to various transition from ground state to 6H5/2,6H7/2 and 4G5/2 states, respectively. The transition 4G5/2 → 6H7/2 located at 606 nm can occur as hypersensitive transition having the selection rule ΔJ = ±1. The observed peaks are in the region of yellow reddish light of Sm3+. Experimental results verify that the optimum Sm3+ content in terms of intense luminescence for this series of phosphors was 2%. Beyond 2% of Sm3+ ions concentration, luminescence quenching occurs due to an enhanced probability of the energy transfer from one Sm3+ to another that matches in energy via cross-relaxation and dipole-dipole interactions according to Dexter theory. A suitable energy transfer model between two adjacent Sm3+ ions in the ZnB2O4 phosphors was accomplished by the electric dipole-dipole interaction. The critical transfer distance (Rc) for non-radiative energy transfer was found to be 21.52 Å at 2 mol % Sm3+ doped ZnB2O4. Additionally, thermoluminescence (TL) glow curves of undoped and Sm activated ZnB2O4 under beta irradiation of 10 Gy are also discussed here. © 2018 Elsevier B.V.
Enhancing the blue luminescence behaviour of the Li co-doped novel phosphor ZnB2O4: Tm3+
(Elsevier Ltd, 2020) Kucuk N.; Kaynar Ü.H.; Akca S.; Alajlani Y.; Yin L.; Wang Y.; Garcia Guinea J.; Bulcar K.; Dogan T.; Karabulut Y.; Ayvacikli M.; Canimoglu A.; Topaksu M.; Can N.
Here we report a detailed structural analysis, and properties of the cathodoluminescence (CL), photoluminescence (PL) and 3D thermoluminescence spectra of the Tm3+ incorporated ZnB2O4 phosphor successfully synthesized through wet-chemical synthesis. The formation of a single-phase compound is verified through X-ray diffraction (XRD) studies. The phosphor shows an efficient blue emission located at 458 nm corresponding to 1D2→3F4 under both a low voltage electron beam and UV excitation. The optimal concentration of the doped Tm3+ is 0.5 mol% in CL and PL measurements. The corresponding concentration quenching mechanism is confirmed to be a multipole-multipole interaction, and the critical distance between Tm3+ ions is estimated to be 34 Å. Incorporating Li+ remarkably enhances the luminescence intensity probably because of the charge compensation effect. Li ions are speculated to fill the defects in the ZnB2O4 host and then the excitation energy transfers from the host to Tm3+. Surprisingly, the thermoluminescence spectra of ZnB2O4:Tm3+ and Li+ co-doped ZnB2O4:Tm3+ recorded in the temperature range 30–400 °C follow a different pattern compared with PL and CL data. The dominant signals come from Tm3+ sites. Above room temperature, the Tm3+ ions do not show the peak temperature movement, but do exhibit a different pattern with the addition of co-doped Li+ ions. These results indicate that these phosphors are promising candidates for luminescence-based optoelectronic devices. © 2020 Elsevier B.V.
Synthesis, characterization and enhanced photoluminescence and temperature dependence of ZrO2:Dy3+ phosphors upon incorporation of K+ ions
(Elsevier Ltd, 2023) Can N.; Coban M.B.; Souadi G.; Kaynar Ü.H.; Ayvacikli M.; Garcia Guinea J.; Ekdal Karali E.
This study reports the successful synthesis and comprehensive characterization of ZrO2:Dy3+ phosphors with the incorporation of K+ ions. The introduction of Dy3+ and K+ in the ZrO2 lattice as lanthanide activators demonstrates its potential as an efficient host material. The structural integrity of ZrO2 remains unaltered following the doping process. Fourier-transform infrared spectroscopy (FTIR) analysis confirms the presence of Zr-O and O-H stretching, along with H2O bending modes in the phosphor sample. The wide luminescence band seen at 460 nm is attributed to luminescence defects in the ZrO2 induced by oxygen, and the presence of water molecules. Photoluminescence (PL) spectra analysis reveals pronounced emission peaks at 491 and 578 nm, corresponding to 4F9/2 → 6H15/2 and 4F9/2 → 6H13/2 transitions, respectively, upon excitation at 349 nm. Optimizing the Dy3+ doping concentration to 0.4 wt% and achieving a critical distance of 31.82 Å resulted in efficient energy transfer. Notably, co-doping K+ as a charge compensator significantly enhances the luminescence intensity. Moreover, at lower temperatures, direct excitation of Dy3+ ions through our pump wavelength, coupled with exciton-mediated energy transfer, leads to a remarkable increase in PL intensity. Tailoring the doping concentrations effectively shifts the emission spectrum of the phosphor mixture, aligning with the standard white light illumination coordinates (0.333, 0.333). This property positions the material as a promising candidate for applications in white light-emitting diodes (WLEDs) and various high-quality lighting applications. The enhanced photoluminescence and temperature dependence observed in ZrO2:Dy3+ phosphors upon the incorporation of K+ ions pave the way for their potential utilization in advanced luminescent devices. © 2023 Elsevier Ltd and Techna Group S.r.l.

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