Abnormal upconversion luminescence induced by defects and Er3+–Yb3+ distance change in Cs3GdGe3O9:Er3+/Yb3+ phosphors

A series of Er³⁺/Yb³⁺ co-doped Cs₃GdGe₃O₉ (CGG) phosphors were prepared by solid-phase sintering method, and the microstructure and upconversion luminescence (UCL) properties were tested by variable-temperature X-ray diffractometry and variable-temperature spectrometer. Abnormal UCL phenomena were found, which include UCL intensity continuously increasing under 980 nm laser continuous irradiation and UCL thermal enhancement. After 10 min of continuous irradiation by 980 nm laser at 513 K, the UCL intensity increased 2.91 times compared with the initial UCL intensity. The phenomenon is due to the electron releasing of host defects. The green UCL intensity of CGG:0.1Er³⁺/0.2Yb³⁺ decreases at 303–423 K and increases at 423–723 K, which reaches 13.23 times compared with that at 423 K. The phenomenon is due to Er³⁺–Yb³⁺ distance change by temperature and phonon-assisted transitions. In addition, the absolute temperature sensitivities of samples are calculated by luminescence intensity ratio technology, the maximum absolute sensitivity of CGG:0.1Er³⁺/0.4Yb³⁺ is 0.00691 K⁻¹ at 546 K, and the maximum relative sensitivity of CGG:0.1Er³⁺/0.1Yb³⁺ is 0.01224 K⁻¹ at 303 K. These results indicate that CGG:Er³⁺/Yb³⁺ phosphors can be used as a high-temperature optical thermometer.     

Er3+:Yb3+:Y3Al5O12单晶中Er3+离子光谱参数的计算

采用提拉法生长出光学质量的Er3 :Yb3 :Y3Al5O12(YAG)单晶,测定了晶体的吸收光谱和上转换荧光光谱,根据Judd-Ofelt理论,计算出Er3 在YAG晶体中的强度参数Ω2=1.074 1×10-20cm2,Ω4=1.295 3×1020cm2,Ω6=0.923 8×1020cm2.由此得到部分波段跃迁的荧光分支比、辐射寿命和积分发射截面积.提出将679 nm波段的4F9/2→4I15/2跃迁作为激光输出进一步研究的新通道.     

Structural-phase state and lasing of 5–15 at% Yb3+:Y3Al5O12 optical ceramics

Yttrium aluminum garnet (Yb³⁺:Y₃Al₅O₁₂) laser ceramics doped by 5, 10 and 15 at% of ytterbium ions were obtained by reactive sintering. Optimal sintering temperature range for the formation of highly-dense transparent Yb³⁺:Y₃Al₅O₁₂ ceramics under normal recrystallization conditions was found to be T = 1750–1800 °C. The influence of Yb³⁺ ions on structural-phase state, phase composition, microstructure, optical and luminescent properties of sintered samples was experimentally investigated. It was shown that lattice parameter a of Yb³⁺:Y₃Al₅O₁₂ ceramics decreases linearly with increasing of Yb³⁺ concentration in a good agreement with L. Vegard’s rule, that indicates to the formation of (Y_1−xYb_x)₃Al₅O₁₂ (х = 0.05–0.15) substitutional solid solutions. No concentration quenching of Yb³⁺ luminescence was observed in Yb³⁺:Y₃Al₅O₁₂ within the 5–15 at% doping range. Quasi-CW lasing of Yb³⁺:Y₃Al₅O₁₂ ceramics was studied under diode-pumping at 970 nm. A highest slope efficiency of about 50% was obtained for 15 at%-doped Yb³⁺:Y₃Al₅O₁₂ ceramics sintered at T = 1800 °C for 10 h.     

Mullite fibres prepared by sol–gel method using polyvinyl butyral

Mullite fibres with uniform diameter and smooth surface have been synthesized using commercial grade polyvinyl butyral (PVB) as binder. The sol with good spinnablity was obtained at reaction temperature of 60 °C for 1 h. The results of X-ray diffraction indicated that the Al–Si spinel was obtained before complete mullization, which implied the addition of PVB retarded the phase transformation of mullite. The fibres showed a rough surface and lateral cracks at 800 °C. Smooth and dense surface was observed when fibres were sintered at 1200 °C and completed transformation to mullite was achieved. This technique offered the possibility of synthesizing mullite fibres at considerably lower cost than at present.     

Structure and optical properties of transparent Er3+-doped CaF2–silica glass ceramic prepared by controllable sol–gel method

Transparent Er³⁺-doped CaF₂–silica glass ceramics were prepared by the direct physical introduction of Er³⁺ doped CaF₂ nanocrystals into acid-catalyzed sol–gel silica glass. The physical methods of ball milling, ultrasonic baths, and stirring were investigated to disperse Er³⁺ doped CaF₂ nanocrystals in the silica sols. The CaF₂–silica sol mixture went through gelation and heat-treatment to form Er³⁺-doped CaF₂–silica glass ceramics. The morphology of Er³⁺ doped CaF₂ in silica glass did not change after heat-treatment at 600 °C for 10 h. The experimental results showed that Er³⁺ doped CaF₂ in the glass ceramic prepared with the assistance of ball milling possesses the best dispersity and homogeneity. The highest in-line transmittance of the glass ceramic reached up to 85% in visible region. Glass ceramic exhibits efficient up-conversion emissions corresponding to the Er³⁺:⁴F_9/2→⁴I_15/2 transition and long lifetime of ⁴F_9/2 level (1.73 ms) under 980 nm excitation.     

Laser-induced birefringence of methyl red in a polymeric nanocomposite prepared by sol–gel method

Non-linear optical (NLO) dyes used as guests in polymeric films have recently attracted interests in optical applications. In this regard, dye-grafted polymeric systems can outperform conventional guest?Chost dye-containing films because they have lower loading limitations and aggregation problems. These give rise to enhanced molecular orientation. The work presented here is an attempt to study the laser-induced birefringence for a novel sol?Cgel based polymeric nanocomposite prepared by reacting an NLO dye (methyl red) and an epoxy silane coupling agent at different concentrations of dye. 3-Glycidoxy propyltrimethoxysilane was hydrolyzed and condensed to prepare a siloxane structure from which a dye-containing hybrid was obtained. The structural and morphological properties of the resulting nanocomposites were studied by FTIR spectroscopy, differential scanning calorimetry and transmission electron microscopy. Results showed that the dye was chemically attached to the siloxane structure built through sol?Cgel processing. This chemical modification leads to nanostructured morphology in which inorganic phase was entangled to the organic phase. The size of clusters formed was 60?C80?nm in dimension. The optical responses of nanocomposites were investigated at different process parameters, including dye concentration, film thickness and curing regimes. These were then discussed based on the photochemical and photothermal properties of the dye molecules, the rotation dynamic of which was shown to strongly depend on the physical and chemical properties of the host. The samples with 8 wt% of dye revealed the maximum birefringence, while the sample with 10 wt% showed the best memory effect. The best condition for curing was found to be 24?h. By increasing the film thickness, there was an increase in the amount of induced birefringence.     

Multilayer zirconium titanate thin films prepared by a sol–gel deposition method

Zirconium titanate multilayer thin films were prepared by an aqueous particulate sol–gel process followed by spin coating. The obtained structures were studied by transmission electron microscope, scanning electron microscope, atomic force microscope, and spectroscopic reflection analyses. According to the results, sound thin films up to three layers were developed, accompanied by an increase in thickness and roughness by increasing the number of the layers. It was also found that the coatings consist of globular nanoparticles with an average diameter of 50 nm. Considering the contribution of roughness to biological responses, the optimization of the surface characteristics to meet an optimal performance seems to be a challenging issue, which demands future studies.     

Structural properties and hyperfine interactions in Co–Zn Y-type hexaferrites prepared by sol–gel method

Y-type barium hexaferrites Ba₂Co_2−xZn_xFe₁₂O₂₂ (0.0≤x≤2.0) were prepared using sol–gel method and then sintering at temperatures between 900 and 1100 °C. The properties of the prepared samples were investigated using X-ray diffraction, scanning electron microscopy, and Mössbauer spectroscopy. XRD patterns revealed the presence of a single Y-type hexaferrite phase in the samples sintered at temperatures above 1000 °C. Mössbauer data indicated that Co²⁺ ions occupied octahedral sites in the T blocks, while Zn²⁺ ions were distributed between the two tetrahedral sites. This trend for cationic distribution resulted in weakening the superexchange interactions between spin-up and spin-down sublattices with increasing Zn content, and a consequent reduction in the hyperfine fields in Zn rich compounds.     

Characterization and X-ray peak broadening analysis in PZT nanoparticles prepared by modified sol–gel method

Lead zirconate titanate nanoparticles (PZT-NPs) were synthesized by a modified sol–gel method and were calcinated at temperatures of 600, 650 and 700 °C. Fourier transform infrared (FTIR), powder X-ray diffraction (XRD) and thermal analysis (TGA/DTA), indicate that single-phase perovskite PZT-NPs are obtained after heat treatment at a temperature of 650 °C. The TEM results obtained from the PZT-NPs confirm that the morphology of the PZT nanoparticles is spherical, with an average diameter size of 17 nm. We also investigated the crystallite development in the nanostructured PZT by X-ray peak broadening analysis. The individual contribution of many small crystallite sizes and lattice strains to the peak broadening in the PZT nanoparticles prepared at different temperatures were studied using Williamson–Hall (W–H) analysis in the range of 2θ = 15–80°.     

Electrochromic properties of Al doped B-subsituted NiO films prepared by sol–gel

In this paper, Al doped B-substituted NiO films were prepared by sol–gel method. The effect of the Al content on the structure of the Al_xB_0.15NiO films were studied with X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical and EC properties were examined by cyclic voltammetric (CV) measurements and UV–Vis spectrophotometry, respectively. Al doping could prevent the crystallization of the films, which exhibited much better electrochemical and electrochromic properties than undoped samples. The bleached state absorbance could be significantly lowered when the Al added. EC efficiencies measured at λ = 500 nm of the films with different Al doping content reach ～30 cm² C^?1, with a change in transmittance up to 70%.     

Optical properties of Nb-doped TiO2 thin films prepared by sol–gel method

In this work, we studied optical properties of pure and Nb-doped TiO₂ synthesized using a sol–gel method and deposited as thin films by spin-coating followed by annealing in air at 500 °C for 1 h. The surface elemental composition was derived from X-ray photoelectron spectra, while structure and surface morphology were investigated using X-ray diffraction and atomic force/scanning electron microscopy. Finally, the optical properties were investigated by means of UV–vis spectrophotometry and spectroscopic ellipsometry.The Nb content was determined from XPS measurements to vary between 1.8 and 4.3 at%. The XRD patterns of the deposited thin films, with a maximum thickness of about 56 nm, showed no diffraction peaks. As proven both by microscopy and spectroscopic ellipsometry studies doping TiO₂ with Nb modified the surface morphology of the samples; the grain size is increasing while the surface roughness decreases with the increase in Nb content. This is accompanied by a decrease in the refractive index and an increase of the extinction coefficient.     

Hybrid nanocomposite coating by sol–gel method: a review

The development of environmentally friendly process for pretreatments of metallic substrates is a field of growing research due to the ban against chromates used as protective pretreatments. Among the possible candidates for environmentally friendly pretreatments of aluminum alloys are the silica-based sol–gel coatings. Such coatings are able to form an Si–O–Al conversion layer providing a stable alumina/sol–gel film interface, which inhibits the onset of corrosion. Sol–gel technology offers a wide range of chemical mechanisms and exhibits high potential substitutes for the environmentally unfriendly chromate metal-surface pretreatment. Sol–gel derived organo-silicate hybrid coatings, preloaded with organic corrosion inhibitors, have been developed to provide active corrosion protection when integrity of the coating is compromised. The incorporation of organic corrosion inhibitors into hybrid coatings has been achieved as a result of physical entrapment of the inhibitor within the coating material at the stage of film formation and cross-linking. Sol–gel derived coatings, especially the hybrid films, provide a dense barrier against electrolyte uptake, and offer a wide range of applications as corrosion protective, hydrophilic coatings, hydrophobic anti-reflective coatings, migration barriers against liquid and volatile compounds, antibacterial modification of textiles and water-repellent antistatic textiles. In this paper, the novel applications of the sol–gel derived coatings are presented and discussed.     

Antireflective coatings prepared by sol–gel processing: Principles and applications

Sol–gel processing is a powerful tool to prepare antireflective (AR) coatings on optical surfaces. In this paper the different strategies to obtain antireflective properties are reviewed: porous λ/4 layers, multilayer interference-type films and index-gradient materials such as “moth eye” structures. The processing of the respective films is described and evaluated; references to respective commercial products on glass substrates are given.AR coatings may have a particularly high importance for transparent ceramics as their index of refraction is significantly higher than that of common glass types. Reflective losses therefore are higher which is especially unpleasant for materials with a yet improvable intrinsic transparency.Recent studies indicate that specific porous λ/4 layers may exhibit pronounced anti-soiling features. Laboratory experiments as well as outdoor exposure tests were used to demonstrate the dust-repellant properties.     

Highly stable and selective ethanol sensor based on α-Fe2O3 nanoparticles prepared by Pechini sol–gel method

In the present work, α-Fe₂O₃ nanoparticles were successfully synthesized by Pechini sol–gel (PSG) method following annealing at 550 °C. The morphology and microstructure of the prepared α-Fe₂O₃ nanoparticles were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Raman analysis. The electrical and sensing properties were also investigated. The α-Fe₂O₃ based sensor showed good sensitivity and selectivity towards ethanol at the optimal temperature of 225 °C. Moreover, the sensor displayed good electrical and sensing stability. These results suggest the potential applications of α-Fe₂O₃ synthesized by Pechini sol–gel method as a sensor material for ethanol detection.     

Surface modification of polyester nonwoven fabrics by Al2O3 sol–gel coating

Nonwoven polyester (PET) fabrics have been extensively studied for various applications. However, the nonwoven PET fabrics have poor wettability. In this work, nonwoven PET fabrics were impregnated in a stable and transparent alumina sol that was prepared by the hydrolysis of aluminium isopropoxide using the sol–gel technique. The Al₂O₃ particles were coated on nonwoven PET fabrics after the rolling-drying process. The surface morphology of modified nonwoven PET fabrics was characterized by scanning electronic microscopy (SEM) and atomic force microscopy (AFM). The SEM and AFM observations revealed the formation of the Al₂O₃ particles on the fiber surface. The Al₂O₃ coating was also confirmed by Fourier transform infrared (FTIR). The mechanical properties of the coated nonwoven PET fabrics were investigated using a tensile strength test, and the results showed that the mechanical properties were improved after surface sol–gel coating. The effect of Al₂O₃ on the wetting behavior of the fabric was also significantly improved.     

Effect of carbon nanotubes on sintering behavior of alumina prepared by sol–gel method

Alumina (Al2O3)/carbon nanotube (CNT) (99/1 by weight) composite was prepared by mixing CNT dispersion with AlCl₃-based gel, followed by high temperature sintering at a temperature up to 1150 °C in argon. Composite alumina precursor showed phase transition order from amorphous to γ-Al₂O₃ after sintered at 900 °C for 2 h, partially to θ-Al₂O₃ after sintered at 1000 °C for 2 h, and then partially to α-Al₂O₃ after sintered at 1150 °C for 2 h. By comparison, control alumina precursor directly transformed from amorphous to α-Al₂O₃ after sintered at a relatively low temperature of 600 °C for 2 h. Composite alumina showed porous structure with pore diameter ranging from 100 nm to 2 µm, whereas control alumina was relatively pore-free. The elevated alumina-crystal phase transition temperatures and the formation of porous structure were ascribed to the presence of CNTs in alumina precursor. The composite alumina sintered at 900 °C for 2 h containing only γ-Al₂O₃ had a BET surface area of 138 m²/g, which was significantly higher than that of control alumina sintered at 1150 °C for 2 h containing only α-Al₂O₃, ~15 m²/g.     

Preparation of nanocrystalline SrTiO3 powder by sol–gel combustion method

In this research a sol–gel combustion route has been presented to synthesize strontium titanate (SrTiO₃:ST) nanocrystalline, using citric acid as fuel. The synthesis procedure was optimized by systematically varying the molar ratios of total metal nitrate to citric acid (MN:CA) from 1:1 to 1:3. The effect was investigated through XRD, SEM and TEM analysis. Analysis of XRD spectrum shows the complete of SrTiO₃ nanocrystalline, however, a minor phase of SrCO₃ impurity was found. Hence, an acid treatment process, with 1 mol/l HNO₃ solution and deionized water, was applied to remove the impurity. The results show that the appropriate condition to prepare the single phase nanocrystalline SrTiO₃ powders is MN:CA molar ratio of 1:3, coupled with an acid treatment process and at the lower calcination temperature of 500 °C. The particle size of powders was in nanometer ranges. The average crystallite size calculated from FWHM was about 23 nm. Morphology of powders was identified by SEM analysis. However, TEM estimated the average particle size about 7.5 nm after applying an acid treatment technique at 600 °C.     

Yb3Al5O12激光晶体的生长

采用中频感应提拉法成功生长出Yb3Al5O12(YbAG)激光晶体.通过X射线粉末衍射分析,得出了YbAG晶体的晶胞参数a=1.193799nm,β=90°,V=1.70135nm3;密度为6.62g/cm3.测量了室温下YbAG晶体的吸收光谱和发射光谱特性.研究表明在938nm和968nm处存在Yb3+离子的2个吸收带,能与InGaAs激光二极管(LD)有效耦合,适合激光二极管泵浦;其荧光主峰位于1036nm附近,YbAG晶体的荧光寿命为270μs.     

Pre-evaluation method for the spectroscopic properties of YAG bulk materials by sol–gel synthetic YAG powder

We propose a convenient method for pre-evaluating the spectroscopic properties of luminescent impurity doped YAG by sol–gel synthetic powder. Three synthetic methods, the sol–gel, normal-strike, and reverse-strike methods, are examined for their ability as a predictor and the sol–gel method proved the most effective of the three in experiments on crystallinity, particle size, and spectroscopic properties. The sol–gel Nd:YAG powder agrees well with that of a single crystal or ceramic YAG regarding the luminescent spectrum, the intensity, and the lifetime, even though the powder sintered at a low temperature of 1100 °C in comparison with the YAG crystal melting point of 1970 °C. These facts suggest that the sol–gel synthetic powder is the most effective and the easiest technique for evaluating spectroscopic properties of bulk YAG materials before fabricating the final materials.