Microwave sol–gel derived NaCaGd(MoO4)3:Er3+/Yb3+ phosphors and their upconversion photoluminescence properties

Ternary molybdate NaCaGd_1−x(MoO₄)₃:Er³⁺/Yb³⁺ phosphors with the proper doping concentrations of Er³⁺ and Yb³⁺ (x = Er³⁺ + Yb³⁺, Er³⁺ = 0, 0.05, 0.1, 0.2 and Yb³⁺ = 0, 0.2, 0.45) were successfully synthesized by microwave sol–gel method for the first time. Well-crystallized particles formed after heat-treatment at 900 °C for 16 h showed a fine and homogeneous morphology with particle sizes of 3–5 μm. The optical properties were examined comparatively using photoluminescence emission and Raman spectroscopy. Under excitation at 980 nm, the doped particles exhibited a strong 525-nm emission band, a weak 550-nm emission band in the green region, which correspond to the ²H_11/2 → ⁴I_15/2 and ⁴S_3/2 → ⁴I_15/2 transitions, and a very weak 655-nm emission band in the red region, which corresponds to the ⁴F_9/2 → ⁴I_15/2 transition. The optimal Yb³⁺:Er³⁺ ratio was obtained to be 9:1, as indicated by the composition-dependent quenching effect of Er³⁺ ions. The pump power dependence of upconversion emission intensity and Commission Internationale de L’Eclairage chromaticity coordinates of the phosphors were evaluated in detail.     

Green and red photoluminescence from ZnAl2O4:Mn phosphors prepared by sol–gel method

Luminescence investigations of Mn-activated ZnAl₂O₄ phosphors prepared by using sol–gel method were described. The phosphor was characterized by X-ray diffraction (XRD) and electronic paramagnetic resonance (EPR). The EPR spectra of the samples suggested that Mn ions possessed homogeneous distribution in ZnAl₂O₄ phosphors. Photoluminescence studies of the prepared phosphors showed green and red emissions. The red emission became weaker, and vanished at last with sintering temperature increasing from 600 to 900 °C in reducing atmosphere, while the intensity of green emission peak increased. Furthermore, when the phosphor was sintered at 900 °C in air, the intensity of red and green emissions decreased, but the value of intensity ratio increased. It suggested that the green emission resulted from Mn²⁺ and the red emission resulted from Mn⁴⁺.     

Upconversion Properties of Er3+/Yb3+ Co-doped TeO2–TiO2–K2O Glasses

The Er³⁺/Yb³⁺ co-doped TeO₂–TiO₂–K₂O glasses were prepared by conventional melting procedures, and their upconversion spectra were performed. The dependence of luminescence intensity on the ratio of Yb³⁺/Er³⁺ was studied, and the relationship between green upconversion luminescence intensity and Er³⁺ concentration is discussed in detail. The 546 nm green upconversion luminescence intensity is optimised in the studied glasses either when the Yb³⁺/Er³⁺ ratio is 25/1 and Er³⁺ concentration is 0.1 mol%, or when the Yb³⁺/Er³⁺ ratio is 10/1 and Er³⁺ concentration is 0.15 mol%. These glasses could be one of the potential candidates for LD pumping microchip solid-state lasers.     

Thermoluminescence of Al2O3:Cr3+ films synthesized by the nonaqueous sol–gel method

The thermoluminescence (TL) properties of Al₂O₃:Cr³⁺ thin films prepared by the nonaqueous sol–gel method were evaluated. The obtained thin films were characterized by scanning electron microscope and energy dispersive spectrometry. They were irradiated with ⁶⁰Co gamma rays of the different doses. TL glow curves exhibited two peaks centered at 197°C and 322°C.The heights of peaks were found to be sensitive to exposures of ionizing irradiation and the integral area of the TL signals had a linear response in the dose range of 5–60 Gy.This remarkable result suggests that Al₂O₃:Cr³⁺ films might potentially be used for radiation dosimetry.     

Electrical and optical properties of Sb-doped ZnO thin films synthesized by sol–gel method

Sb-doped ZnO thin films with different values of Sb content （from 0 to 1.1 at.%） are deposited by the sol-gel dip- coating method under different sol concentrations. The effects of Sb-doping content, sol concentration, and annealing ambient on the structural, optical, and electrical properties of ZnO films are investigated. The results of the X-ray diffraction and ultraviolet-visible spectroscopy （UV-VIS） spectrophotometer indicate that each of all the films retains the wurtzite ZnO structure and possesses a preferred orientation along the c axis, with high transmittance （〉 90%） in the visible range. The Hall effect measurements show that the vacuum annealed thin films synthesized in the sol concentration of 0.75 mol/L each have an adjustable n-type electrical conductivity by varying Sb-doping density, and the photoluminescence （PL） spectra revealed that the defect emission （around 450 nm） is predominant. However, the thin films prepared by the sol with a concentration of 0.25 mol/L, despite their poor conductivity, have priority in ultraviolet emission, and the PL peak position shows first a blue-shift and then a red-shift with the increase of the Sb doping content.     

Photoluminescent properties of Dy3+ in MgO-Ga2O3-SiO2 nano-glass-ceramic prepared by sol–gel method

The MgO-Ga₂O₃-SiO₂ (MGS) glass and glass-ceramic (GC) containing MgGa₂O₄ nanocrystals and Dy³⁺ ions were prepared by a simple sol–gel method. MgGa₂O₄ nanocrystals in MgO-Ga₂O₃-SiO₂ GC formed when the heating temperature reached 800 °C. The energy transfer from MgGa₂O₄ nanocrystals to Dy³⁺ was observed. It is important that the strong white light emission is observed corresponding to the excitation band gap of MgGa₂O₄ nanocrystals. As exciting Dy³⁺ ions, only weak yellow and blue emissions were observed.     

Synthesis and photoluminescence of core–shell structured spherical SiO2@YPO4:Tb3+ phosphors via sol–gel process

Monodispersed SiO₂@YPO₄:Tb³⁺ core–shell submicrospheres were prepared through a simply homogeneous sol–gel method. The resulted SiO₂@YPO₄:Tb³⁺ core–shell particles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), photoluminescence spectra (PL) and kinetic decays. The XRD results demonstrate that the YPO₄:Tb³⁺ layers begin to crystallize on the SiO₂ spheres after annealing at 500 °C and the crystallinity increases with raising the annealing temperature. The FTIR spectra show that the YPO₄:Tb³⁺ shell has linked to the silica surface through forming a Si–O–Y bond. SEM and TEM analysis indicate that SiO₂@YPO₄:Tb³⁺ core–shell submicrospheres have the regular microstructures and uniform size distributions. The emission spectra of the obtained submicrospheres are dominated by ⁵D₄–⁷F₅ transition of Tb³⁺ (545 nm, green), and the emission intensities of Tb³⁺ increase with increasing the annealing temperatures and the number of coating cycles. The optimum concentration for Tb³⁺ was determined to be 5 mol % of Y³⁺ in YPO₄ host.     

Efficient UV-light photocatalytic activity of TiO2@Phosphogypsum composite synthesized by sol–gel method

Optical and Quantum Electronics - All optical multiband radio transceiver is designed using Polarization Modulators. Polarization Modulators have been gaining popularity in recent times as the...     

Optical and transport properties of Sn-doped ZnMn2O4 prepared by sol–gel method

The paper describes the effect of ZnMn₂O₄ doping with different Sn ratios. Sn_x–ZnMn₂O₄ is prepared with Sol–Gel route at 700 °C. The structural, optical and electrical properties were studied. The X-ray diffraction patterns indicate the formation of pure tetragonal phase for the ratios lower than 0.03%, while for other compositions, the secondary phases were observed. The attenuated total reflectance (ATR) analysis confirmed the localization of Sn in octahedral sites. The optical properties showed not only the increase of E_g, but also the improvement of the optical characteristics such as extinction coefficient (k), optical conductivity (σ_opt), dissipation factor (tan δ) and the relaxation time (τ). The latter has been improved by 50%. The Hall measurements confirmed the transition of the conductivity mode, i.e, from p to n-type. The formation of Sn_Mn¹⁺ point defects is evidenced; however, the transport properties indicate that the charge carriers are mainly localized.     

Thermoluminescence (TL) of europium-doped ZrO2 obtained by sol–gel method

This article reports the preparation and characterization of europium-doped zirconium oxide (ZrO₂:Eu³⁺) formed by homogeneous precipitation from propoxyde of zirconium [Zr(OC₃H₇)₄]. The alkoxide sol gel process is an efficient method to prepare the zirconium oxide matrix by the hydrolysis of alkoxide precursors followed by condensation to yield a polymeric oxo-bridged ZrO₂ network. All compounds were characterized by thermal analysis and the X-ray diffractometry method. The thermoluminescence (TL) emission properties of ZrO₂:Eu³⁺ under beta radiation effects are studied. The europium-doped sintered zirconia powder presents a TL glow curve with two peaks (Tmax) centered at around 204 and around 292 ^°C, respectively. TL response of ZrO₂:Eu³⁺ as a function of beta-absorbed dose was linear from 2 Gy up to 90 Gy. The europium ion (Eu³⁺)-doped ZrO₂ was found to be more sensitive to beta radiation than undoped ZrO₂ obtained by the same method and presented a little fading of the TL signal compared with undoped zirconium oxide.     

Luminescence properties of green emission of SiO2/Zn2SiO4:Mn nanocomposite prepared by sol–gel method

Green light emitting Mn²⁺ doped Zn₂SiO₄ particles embedded in SiO₂ host matrix were synthesized by a sol–gel method. After the incorporation of ZnO:Mn nanoparticles in a silica monolith using sol–gel method with supercritical drying of ethyl alcohol in two steps, it was heat treated in air at 1200 °C for 2 h in order to obtain the SiO₂/α-Zn₂SiO₄:Mn nanocomposites. The microstructure of phosphor crystals was characterized by transmission electron microscopy (TEM) and X-ray diffraction (XRD). XRD results indicate that the pure phase α-Zn₂SiO₄ with rhombohedral structure was obtained after thermal treatment at 1200 °C. The SiO₂/α-Zn₂SiO₄:Mn nanocomposites with a Mn doping concentration of 1.5 at% exhibit two broadband emissions in the visible range: a strong green emission at around 525 nm and a second one in the range between 560 and 608 nm. This nanocomposite with a Mn doping concentration of 0.05 shows the highest relative emission intensity. Upon 255 nm excitation, the luminescence decay time of the green emission of Zn₂SiO₄:Mn around 525 nm is 11 ms. The luminescence spectra at 525 nm (⁴T₁–⁶A₁) and lifetime of the excited state of Mn²⁺ ions-doped Zn₂SiO₄ nanocrystals are investigated.     

Low-temperature photoluminescence spectra of CdO–In2O3 thin films prepared by sol–gel

(CdO)_1?x–(InO_3/2)_x thin films were deposited on glass substrates by the sol–gel method. The precursor solutions for the mixed oxide films were obtained from the mixture of the precursor solutions for CdO and In₂O₃ prepared separately. The investigated In atomic concentrations in the solution, x, were 0.0, 0.16, 0.33, 0.50, 0.67, 0.84, and 1. X-ray diffraction measurements showed that the films were mainly constituted of CdO, In₂O₃, and CdIn₂O₄. CdO and In₂O₃ were obtained for x=0 and 1, respectively. For x=0.67, which is the stoichiometric composition of the CdIn₂O₄ compound, only this oxide was formed. CdO and CdIn₂O₄ crystals were obtained in the Cd-rich region, whereas In₂O₃ and CdIn₂O₄ crystals were formed in the In-rich region. The PL spectra at 15 K for CdO showed the presence of two main emission bands at energies close to 2.2 and 3.0 eV. A blue-shift of these bands took place for increasing In concentration, which is related to the increase in the band gap energy of the mixed system in going from CdO, with a band gap energy of 2.46 eV, to CdIn₂O₄, with 3.2 eV, to In₂O₃, with 3.6 eV.     

Er3+/Yb3+:KG(WO4)2的熔盐提拉法生长及光谱性能

采用熔盐提拉法生长了尺寸达30 mm×25 mm×15 mm的Er3+/yb3+KGd(WO4)2透明晶体,从中切出5 mm×5 mm×3mm大小的激光器件,在室温下测试了吸收光谱,可以观察到晶体存在366,380,489,522,651,811,980 nm等吸收峰,并对之进行了能级归属.同时在980 nm激光激发下测试了荧光光谱,可以发现在1 024,1 535 nm处存在较宽的强发射峰,其半高宽分别为60和36 nm.研究结果表明,Er3+/yb3+KG(WO4)2适合于InGaAs LD(980 nm)泵浦,有可能产生1 024 nm波段及人眼安全的1 535 nm波段的可调谐激光.     

Electron paramagnetic resonance and photoluminescence properties of α-Al2O3:Cr3+ phosphors

The red emitting Cr³⁺ activated α-Al₂O₃ powder phosphor has been prepared by easy combustion reactions from mixed metal nitrate reactants and urea with ignition temperatures of 500 °C. The as-synthesized powder was characterized by X-ray diffraction, scanning electron microscopy, and Fourier-transform infrared techniques. The X-ray diffraction pattern reveals that the phosphor crystallized in the hexagonal α-Al₂O₃ phase directly from the combustion reaction. The EPR spectrum exhibits an intense resonance signal with effective g value at g=3.33 along with a few weak resonance signals with effective g values at g=13.7, 2.34, 1.95, 1.49, and 1.26. The spin concentration (N) and its paramagnetic susceptibility (χ) have been evaluated. The excitation spectrum consists of two broad intense bands at 415 nm and 555 nm and are assigned to ⁴A_2g (F)→⁴T_1g (F) and ⁴A_2g (F)→⁴T_2g (F) transitions, respectively. The intense fluorescence peak around 691 nm is attributed to ²E _g →⁴A_2g transition of Cr³⁺ ion. By correlating EPR and optical data, the crystal field splitting parameter (Dq), Racah inter-electronic repulsion parameter (B) have been evaluated and discussed. The EPR and optical studies reveal that Cr³⁺ ions are occupying in Al³⁺ sites in octahedral coordination.     

Particle size effects on magnetic properties of yttrium iron garnets prepared by a sol–gel method

We present detailed measurements of field—and temperature—dependence of magnetization in nanocrystalline YIG (Y₃Fe₅O₁₂) particles. The fine powders were prepared using sol–gel method. Samples with particle sizes ranging from 45 to 450 nm were obtained. We observe that the saturation magnetization decreases as the particle size is reduced due to enhancement of the surface spin effects. Below a critical diameter D_s≅190 nm, the particles become single domains and the coercive forces reaches a maximum at diameters close to the critical value. As the particle size decreases the coercivity diminishes and at D_p≃35 nm diameters the upper limit of superparamagnetic behavior is reached. A quantitative comparison of temperature and particle size dependence of coercivity shows a satisfactory agreement that is expected for an assembly of randomly oriented particles.     

Structures and local ferroelectric polarization switching properties of orthorhombic YFeO_3 thin film prepared by a sol–gel method

Orthorhombic YFeO_3 thin film was prepared on La_(0.67)Sr_(0.33)MnO_3/LaAlO_3 substrate by a sol-gel spin-coating method. The structures of the YFeO_3/La_(0.67)Sr_(0.33)MnO_3/LaAlO_3(YFO/LSMO/LAO) sample were detected by x-ray diffraction pattern, Raman spectrometer, scanning electron microscopy, and atomic force microscope. The local ferroelectric polarization switching properties of the orthorhombic YFO film were confirmed by piezoresponse force microscopy(PFM) for the first time. The results show that the YFO film deposited on LSMO/LAO possesses orthorhombic structure,with ultra-fine crystal grains and flat surface. The leakage current of the YFO film is 8.39 × 10~(-4) A·cm~(-2) at 2 V,with its leakage mechanism found to be an ohmic behavior. PFM measurements indicate that the YFO film reveals weak ferroelectricity at room temperature and the local switching behavior of ferroelectric domains has been identified. By local poling experiment, polarization reversal in the orthorhombic YFO film at room temperature was further observed.