Synthesis and luminescence spectra of poly(methyl methacrylate)/CdS:Ln(III) composites

Cadmium sulfide was prepared by colloidal synthesis in methyl methacrylate (MMA). Europium and terbium salts were added to the colloidal solutions. Using MMA radical polymerization, we synthesized PMMA/CdS:Eu(III), PMMA/CdS:Tb(III), and PMMA/CdS:Eu(III):Tb(III) luminescent composites. Their luminescence is due to defects in the CdS crystals and the ⁵ D _о → 7Fj and ⁵ D ₄ → ⁷ F _j electronic transitions of the Eu³⁺ and Tb³⁺ ions, respectively. It depends on the composition of the materials, complexation on the surface of the colloidal particles, heat treatment time during synthesis, excitation wavelength, and other factors.     

Synthesis and luminescence spectra of (Y<Subscript>2</Subscript>O<Subscript>3</Subscript>–YOF):Ln(III) composites

Sols were prepared by reacting yttrium, europium, and terbium trifluoroacetates with thioacetamide in ethyl acetate. The Eu³⁺ and Tb³⁺ concentrations in the sols were 0.10 to 10 wt % relative to yttrium, which corresponded to 0.061 (0.059) to 6.1 (5.9) at % Eu (Tb). The sols were converted into a gel-like state by slowly evaporating the solvent. After ripening, the gels were heat-treated at a temperature of 800°C. X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, and IR spectroscopy results showed that the resultant composites consisted predominantly of a mixture of Y₂O₃ and YOF. The Eu³⁺ and Tb³⁺ ions were shown to substitute for Y³⁺ ions in the crystal lattices of the yttrium oxide and yttrium oxyfluoride. The formation of the (Eu_0.6Y_0.4)₂O₃, Eu₂O₃, and EuOF phases was demonstrated. We determined the types and parameters of the crystal lattices of the synthesized materials in relation to activator concentrations. The luminescence of the composites is due to the ⁵ D ₀ → ⁷ F _j and ⁵ D ₄ → ⁷ F _j electronic transitions of the Eu³⁺ and Tb³⁺ ions and depends on the host and activator compositions, the excitation wavelength, and other factors.     

Photoluminescence and electrical properties of Eu3+-doped Na0.5Bi4.5Ti4O15-based ferroelectrics under blue light excitation

Na_0.5Bi_4.5?x Eu _x Ti₄O₁₅ (NBT- _x Eu³⁺) ceramics with x = 0, 0.05, 0.10, 0.15, 0.20, 0.25, 0.30 and 0.40 were prepared by conventional ceramics processing. NBT-0.25Eu³⁺ ceramics show the strongest red and orange emissions corresponding to the ⁵D₀ → ⁷F₂ (617 nm) and ⁵D₀ → ⁷F₁ (596 nm) transitions, respectively. The strongest excitation band around 465 nm matches well with the emission wavelength of commercial InGaN-based blue LED chip, indicating that Eu³⁺-doped NBT ceramics may be used as potential environmental friendly red-orange phosphor for W-LEDs application. As an inherent ferroelectric and piezoelectric material, the electrical properties of this potentially multifunctional electro-optical material have been also studied. The introduction of Eu³⁺ distinctly increased the Curie temperature (T _C ) of NBT- _x Eu³⁺ ceramics from 640°C to 711°C as x ranges from 0 to 0.40. For higher temperature applications, the electrical conductivity was also investigated. The conduction of charge carriers in high-temperature range originates from the conducting electrons from the ionization of oxygen vacancies. High T _C and low tanδ makes Eu³⁺-doped NBTceramic also suitable for high temperature piezoelectric sensor applications and electro-optical integration.     

Green electroluminescence from AlN:Tb thin film devices on glass

Electroluminescence (EL) properties of AlN:Tb thin film EL device (TFELD) prepared on a glass substrate by a rf-magnetron sputtering method have been studied. The AlN:Tb emission layer consists of hexagonal (110)-oriented poly-crystals of AlN with a high transparency in visible region. Four emission peaks originating from ⁵D₄ → ⁷F _j (j = 6, 5, 4, 3) transitions of Tb³⁺ were found in both photoluminescence (PL) and EL spectra of the AlN:Tb thin film. The peak emission intensity of the ⁵D₄ → ⁷F₆ transitions is almost the same magnitude with that of the ⁵D₄ → ⁷F₅ transitions, being largely different from the intensity ratio of Tb³⁺in other host materials.     

Luminescent properties of europium-activated yttrium gadolinium phosphates

Nanocrystalline Y_{1 ? x ? y} Gd _x Eu _y PO₄ phosphors have been prepared via precipitation from aqueous solutions. From their luminescence and excitation spectra, the intensity ratio I ₆₁₅/I ₅₉₄ of the Eu³⁺ luminescence bands corresponding to electric dipole and magnetic dipole transitions has been determined as a function of Gd³⁺ content. The critical concentration and effective energy transfer radius in Y_{1 ? x ? y} Gd _x Eu _y PO₄ have been evaluated. Excitation of Gd³⁺⁸ S _J ?⁶ D _J and ⁸ S _J ?⁶ J _J transitions to Eu³⁺ luminescence excitation levels in Y_{0.99 ? x} Gd _x Eu_0.01PO₄ involves efficient energy transfer. Under 250-nm excitation, the Eu³⁺ luminescence yield in Y_{0.99 ? x} Gd _x Eu_0.01PO₄ is a factor of 2.5–3 higher than that in Y_0.99Eu_0.01PO₄.     

Optical properties of europium-activated hafnium fluoride-based glasses

We have studied the optical absorption, luminescence, and electron paramagnetic resonance of EuF₃- and EuF₂-activated fluorohafnate glasses. The glasses prepared with EuF₂ contain both di- and trivalent europium. The fraction of divalent europium clusters in the glass host decreases with decreasing EuF₂ concentration. Eu²⁺ luminescence in the fluorohafnate glasses is quenched, which is due the overlap of Eu²⁺ excited state levels with the conduction band of the glass, resulting in nonradiative relaxation through Hf³⁺ levels in the conduction band. The Eu³⁺ luminescence spectra contain lines corresponding to transitions from several levels of the ⁵D multiplet to levels of the ⁷F multiplet. The relationship between transitions from different ⁵D levels depends on europium concentration and temperature.     

Temperature effect on the photoluminescence intensity and Eu<Superscript>2+</Superscript> excited state lifetime in EuGa<Subscript>2</Subscript>S<Subscript>4</Subscript> and EuGa<Subscript>2</Subscript>S<Subscript>4</Subscript>:Er<Superscript>3+</Superscript>

The photoluminescence (PL) spectra and Eu²⁺ excited state lifetime of EuGa₂S₄ and EuGa₂S₄:Er³⁺ have been studied in the range 78–500 K. The spectra show a band at 545 nm, due to the 4f ⁶5d → 4f ⁷(⁸ S _7/2) transition. With increasing temperature, the full width at half maximum Γ(T) of the PL band of EuGa₂S₄ and EuGa₂S₄:Er³⁺ crystals increases from 0.15 to 0.22 and from 0.13 to 0.19 eV, respectively. Over the entire temperature range studied, Γ(T) is a linear function of T ^1/2. The 545-nm emission intensity and Eu²⁺ excited state lifetime in EuGa₂S₄ and EuGa₂S₄:Er³⁺ vary exponentially with temperature. The luminescence quenching energies evaluated from the Arrhenius plots of I(10³/T) and τ(10³/T) coincide (0.10 eV) within the error of determination.     

Effect of precursor morphology on the structural properties,optical absorption,and luminescence of BaI<Subscript>2</Subscript>:Eu<Superscript>2+</Superscript>,Eu<Superscript>3+</Superscript>

BaI₂:Eu²⁺,Eu³⁺ powders have been prepared by heat-treating BaCO₃:Eu³⁺ precursor powders of various morphologies in an iodinating agent atmosphere and their structural properties, morphology, optical absorption, and luminescence have been studied. The results demonstrate that the powders thus prepared consist of a mixture of crystalline hydrates of various compositions, dominated by BaI₂ ? 2Н₂О (sp. gr. C2/c), and that the Eu²⁺: Eu³⁺ ratio in the powders is determined by the morphology of the precursor.     

Luminescence performance of Eu<Superscript>3+</Superscript>-doped lead-free zinc phosphate glasses for red emission

In this study, the luminescence performance of zinc phosphate glasses containing Eu³⁺ ion with the chemical compositions (60–x)NH₄H₂PO₄-20ZnO-10BaF₂-10NaF–x Eu₂O₃ (where x = 0.2, 0.5, 1.0 and 1.5 mol%) has been studied. These glasses were characterized by several spectroscopic techniques at room temperature. All the glasses showed relatively broad fluorescence excitation and luminescence spectra. Luminescence spectra of these glasses exhibit characteristic emission of Eu³⁺ ion with an intense and most prominent red emission (614 nm), which is attributed to ⁵D₀ → ⁷F₂ transition. Judd-Ofelt (Ω₂, Ω₄) parameters have been evaluated from the luminescence intensity ratios of ⁵D₀ → ⁷F_J (where J = 2 and 4) to ⁵D₀ → ⁷F₁ transition. Using J-O parameters and excitation spectra, the radiative parameters are calculated for different Eu³⁺-doped glasses. Effect of γ-irradiation at fixed dose has been studied for all the Eu³⁺-doped glass matrices. The lifetimes of the excited level, ⁵D₀, have been measured experimentally through decay profiles. The colour chromaticity coordinates are calculated and represented in the chromaticity diagram for Eu³⁺-doped zinc phosphate glasses for all concentrations.     

Recombination luminescence of activated CaI<Subscript>2</Subscript> crystals

Data are presented on the recombination luminescence of CaI₂:Eu²⁺, CaI₂:Gd²⁺, CaI₂:Tl⁺, CaI₂:Pb²⁺, and CaI₂:Mn²⁺ crystals grown by the Bridgman-Stockbarger method. It follows from their photostimulated luminescence, roentgenoluminescence, and thermostimulated luminescence spectra that the activation of CaI₂ with Gd²⁺, Eu²⁺, Tl⁺, Pb²⁺, and Mn²⁺ cations, which produce anion defects, leads to the formation of defect complexes which act as electron traps and determine the 90-K photostimulation spectra of the crystals. The observed effect of the nature of the dopant on the photostimulation spectrum indicates that the doped calcium iodide crystals contain near-activator F- and F _A -type electron centers. Under x-ray and optical excitation, the trapping levels in the crystals are filled mainly by charge carriers delocalized from hydrogen- and oxygen-containing centers. The activation increases the decay probability of impurity-bound excitons.     

Conductivity in Cuprates Arises from Two Different Sources: One-Electron Exchange and Disproportionation

Simulation of the resistivity in the normal state of doped La_2?x Sr _x CuO₄ has been performed using a hopping model based on Marcus theory. The results are in substantial agreement with experimental results. At oxidative doping, Cu(III) sites are formed and electron mobility possible due to hopping: Cu(III)Cu(II) → Cu(II)Cu(III) (one-electron exchange). In the underdoped, non-metallic region, the resistivity (ρ) decreases from almost insulation at T = 0 to a minimum at about T = 100 K. ρ then increases more than linearly with T (～T ^3/2) in the region 100 < T < 500 K. A photo-induced metal-metal (MM) charge transfer transition at 2 eV 2Cu(II) + h ν→ Cu(I) + Cu(III) is responsible for the strong absorption in the visible spectrum of La₂CuO₄. The down-shift of spectral density with doping (x) in La_2?x Sr _x CuO₄ depends on the appearance of Cu(III) sites which makes optical as well as thermal one-electron exchange transitions possible with lower energy. Disproportionation occurs spontaneously for x > 0.06, opening up for electron pair formation. Configuration interaction between two-electron states of low chemical potential, but strong vibrational coupling, gives rise to the superconductor and pseudogaps. Data from photo-induced conductivity and absorption spectra are used in the simulation, which gives results in good agreement with experiments. Possible explanations for Raman and MIR absorption suggest themselves.     

Growth of LiF/LiBaF<Subscript>3</Subscript> eutectic scintillator crystals and their optical properties

Li-containing materials can be applied as neutron scintillators, and LiBaF₃ can discriminate neutron and gamma rays. Moreover, LIF/LiBaF₃ can have higher cross section of thermal-neutron capture compared with LiBaF₃. In this study, LiF (82.5 mol%) and (Ba_1?x RE _x )F₂ (17.5 mol%, RE = Ce and Eu, x = 0.002) eutectic crystals, LiF/RE:LiBaF₃, were grown by the micropulling down method with different pulling rates (growth rate) in order to observe the eutectic structure. Lamellar microstructure was formed for each pulling rate. LiF/Ce:LiBaF₃ excited by 5.5-MeV alpha rays had a broad peak at ~350 nm corresponding to 5d–4f transition of Ce³⁺. On the other hand, LiF/Eu:LiBaF₃ had two scintillation processes; a sharp emission was originated from ⁶P_7/2 → ⁸S_7/2 transitions in the 4f electronic configuration of Eu²⁺ at 360 nm, and a broad one was attributed to Eu²⁺ trapped exciton recombination at 400–450 nm. Since scintillation light was observed for these materials, these scintillators are sensitive to neutrons.     

Effect of Blocking and Superconducting Layer Doping on the Superconductivity and Magnetic Properties of Polycrystalline Sr<Subscript>2</Subscript>CaCu<Subscript>2</Subscript>O<Subscript>6</Subscript>

The possible difference in the properties upon doping the Sr₂CaCu₂O₆ superconducting or blocking layers with Fe and Eu respectively was investigated in this work. The homogeneous Sr_2?yEu_yCaCu₂O_6+δ and Sr₂CaCu_2?xFe_xO_6+δ (y = 0, 0.1, 0.5, x = 0, 0.05) compounds were produced by a high-pressure synthesis route. Judging by the magnetic susceptibility measurements, all samples exhibit a superconductivity transition and the Eu/Fe concentration dependencies on the diamagnetic moment and average T_c have been constructed using the experimental data. As a result, an unusual behavior of the T_c value was observed for the samples with doped Eu: a fivefold reduction in the europium concentration in the sample does not give a noticeable effect on the transition temperature value while the diamagnetic signal becomes more stronger. Complex superconducting dome was found for Eu-doped material: 0.1 ≤ y ≤ 0.5 region T_c vs. concentration data were approximated by inverted parabola-like curve with a maximum at y = 0.3. Difference in properties of the Eu and Fe-doped samples was also found in the behavior of the hysteresis loops showed the opposite orientations.     

Critical Temperature of Smart Meta-superconducting MgB<Subscript>2</Subscript>

Enhancing the critical temperature (T _C ) is important not only to widen the practical applications but also to expand the theories of superconductivity. Inspired by the meta-material structure, we designed a smart meta-superconductor consisting of MgB₂ microparticles and Y₂O₃/Eu³⁺ nanorods. In the local electric field, Y₂O₃/Eu³⁺ nanorods generate an electroluminescence (EL) that can excite MgB₂ particles, thereby improving the T _C by strengthening the electron–phonon interaction. An MgB₂-based superconductor doped with one of four dopants of different EL intensities was prepared by an ex situ process. Results showed that the T _C of MgB₂ doped with 2 wt% Y₂O₃, which is not an EL material, is 33.1 K. However, replacing Y₂O₃ with Y₂O₃/Eu³⁺II, which displays a strong EL intensity, can improve the T _C by 2.8 to 35.9 K, which is even higher than that of pure MgB₂. The significant increment in T _C results from the EL exciting effect. Apart from EL intensity, the micromorphology and degree of dispersion of the dopants also affected the T _C . This smart meta-superconductor provides a new method to increase T _C .     

Synthesis and luminescence properties of Tb<Superscript>3+</Superscript>-doped LiMgPO<Subscript>4</Subscript> phosphor

Polycrystalline sample LiMg_(1?x)PO₄:xTb³⁺ (x = 0.001, 0.002, 0.005, 0.01, 0.02) phosphor was synthesized via modified solid state method (MSSM). The prepared sample was characterized through XRD pattern (X-ray diffraction) and SEM (scanning electron microscope). Additionally, photoluminescence (PL), optically stimulated luminescence (OSL), thermoluminescence (TL) and other dosimetric properties including dose linearity, reusability and fading were studied. In OSL mode, sensitivity of prepared phosphor was found to be 2.7 times that of LiMgPO₄:Tb³⁺, B (BARC) phosphor and 4.3 times that of α-Al₂O₃:C (BARC) phosphor. The TL glow consists of overlapping peaks in temperature range of 50–400^°C and first peak (P₁) was observed at 150^°C, second peak (P₂) at 238^°C, third peak (P₃) at 291^°C and fourth peak (P₄) at 356^°C. The TL sensitivity of second peak (P₂) of LiMgPO₄:Tb³⁺ phosphor was compared with α-Al₂O₃:C (BARC) phosphor and found to be 100 times that of the α-Al₂O₃:C (BARC) phosphor. The minimum detectable dose (MDD) was found to be 5.6 μGy. Moreover, photoionization cross-sections, linearity, reusability, fading and kinetic parameters were calculated. Also, photoluminescence spectra of LiMgPO₄: Tb³⁺ shows characteristic green–yellow emission exciting at 224 nm UV source.     

A magnetooptical study of the odd crystal field component in a terbium-yttrium aluminum garnet

We have studied the photoluminescence spectra and the luminescence magnetic circular polarization (LMCP) spectra in the region of the 4f-4f radiative transition ⁵D₄→⁷F₆ in the rare earth Tb³⁺ ion in a Y₃Al₅O₁₂ garnet matrix. A comparison of the experimental and theoretically calculated LMCP spectra allowed parameters of the odd crystal field component to be determined that removes the prohibition with respect to parity from the 4f-4f transitions in Tb³⁺ ion in the garnet structure. The energy spectra and wave functions of ⁵D₄ and ⁷F₆ multiplets of Tb³⁺ ion in a crystal field with the D₂ symmetry have been calculated.     

Improving the Critical Temperature of MgB<Subscript>2</Subscript> Superconducting Metamaterials Induced by Electroluminescence

The MgB₂ superconductor was doped with electroluminescent Y₂O₃:Eu, to synthesise a superconducting metamaterial. The temperature dependence of the resistivity of the superconductor indicates that the critical temperature (T _C) of samples decreases when increasing the amount of doped Y ₂ O ₃ nanorods, due to impurity (Y ₂ O ₃, MgO and YB ₄). However, the T _C of the samples increase with increasing amount of doped Y ₂ O ₃:Eu ³⁺ nanorods, which are opposite to doped Y ₂ O ₃ nanorods. Moreover, the transition temperature of the sample doped with 8 wt % Y ₂ O ₃:Eu ³⁺nanorods is higher than those of doped and pure MgB ₂. The T _C of the sample doped with 8 wt % Y ₂ O ₃:Eu ³⁺ nanorods is 1.15 K higher than that of the sample doped with 8 wt % Y ₂ O ₃. The T _C of sample doped with 8 wt% Y ₂ O ₃:Eu ³⁺ is 0.4 K higher than that of pure MgB ₂. Results indicate that doping electroluminescent materials into MgB ₂ increases the transition temperature; this novel strategy may also be applicable to other superconductors.     

On VLSI interconnect optimization and linear ordering problem

Some well-known VLSI interconnect optimizations problems for timing, power and cross-coupling noise immunity share a property that enables mapping them into a specialized Linear Ordering Problem (LOP). Unlike the general LOP problem which is NP-complete, this paper proves that the specialized one has a closed-form solution. Let f(x,y):?²→? be symmetric, non-negative, defined for x≥0 and y≥0, and let f(x,y) be twice differentiable, satisfying ? ² f(x,y)/?x?y<0. Let π be a permutation of {1,…,n}. The specialized LOP comprises n objects, each associated with a real value parameter r _i , 1≤i≤n, and a cost f(r _i ,r _j ) associated to any two objects if |π(i)?π(j)|=1,1≤i,j≤n, and f(r _i ,r _j )=0 otherwise. We show that the permutation π which minimizes \(\sum_{i= 1}^{n - 1} f( r_{\pi^{ - 1}( i )},r_{\pi^{ - 1}( i + 1 )} )\), called “symmetric hill”, is determined upfront by the relations between the parameter values r _i .     

Stability region of Eu<Subscript>2−<Emphasis Type="Italic">x</Emphasis></Subscript>Mn<Subscript>x</Subscript>O<Subscript>3+δ</Subscript> solid solutions in air

The homogeneity range of EuMnO₃ has been determined using x-ray diffraction analysis of single-and mixed-phase Eu_2?x Mn_xO_3+δ samples (0.90≤x≤1.20, Δx = 0.02) prepared from oxide mixtures by solid-state reactions in air between 900 and 1400°C. The results have been used to construct a partial phase diagram of the Eu-Mn-O system in air. The dependences of unit-cell parameters on x and synthesis temperature are presented for the samples synthesized at 1100 and 1400°C and for EuMnO₃, respectively. The solubility of europium oxide in EuMnO₃ is tentatively attributed to structural defects, and that of managanese oxides is interpreted in terms of structural defects, oxygen nonstoichiometry of europium manganite, the disproportionation reaction 2Mn³⁺ = Mn²⁺ + Mn⁴⁺, and partial substitution of the resulting Mn²⁺ for Eu³⁺ on the cuboctahedral site of the perovskite-like structure. To check these assumptions, systematic studies of the oxygen nonstoichiometry and structure of Eu_2?x Mn_xO_3+δ solid solutions synthesized at different temperatures are needed.     

New NaSrPO<Subscript>4</Subscript>:Sm<Superscript>3+</Superscript> phosphor as orange-red emitting material

Sm³⁺-activated NaSrPO₄ phosphors could be efficiently excited at 403 nm, and exhibited a bright red emission mainly including four wavelength peaks of 565, 600, 646 and 710 nm. The highest emission intensity was found for NaSr _1?x PO₄: xSm³⁺ with a composition of x = 0.007. Concentration quenching was observed as the composition of x exceeds 0.007. The decay time values of NaSr_1?x PO ₄ : xSm³⁺ phosphors range from around 2.55 to 3.49 ms. NaSr_1?x PO₄: xSm³⁺ phosphor shows a higher thermally stable luminescence and its thermal quenching temperature T ₅₀ was found to be 350°C, which is higher than that of commercial YAG:Ce³⁺ phosphor and ZnS:(Al, Ag) phosphor. Because NaSr_1?x PO₄: xSm³⁺ phosphor features a high colour-rendering index and chemical stability, it is potentially useful as a new scintillation material for white light-emitting diodes.