Indium doping effect on properties of ZnO nanoparticles synthesized by sol–gel method

Pure ZnO and indium-doped ZnO(In–ZO) nanoparticles with concentrations of In ranging from 0 to 5% are synthesized by a sol–gel processing technique. The structural and optical properties of ZnO and In–ZO nanoparticles are characterized by different techniques. The structural study confirms the presence of hexagonal wurtzite phase and indicates the incorporation of In~(3+) ions at the Zn~(2+) sites. However, the optical study shows a high absorption in the UV range and an important reflectance in the visible range. The optical band gap of In–ZnO sample varies between 3.16 e V and 3.22 e V. The photoluminescence(PL) analysis reveals that two emission peaks appear: one is located at 381 nm corresponding to the near-band-edge(NBE) and the other is observed in the green region. The aim of this work is to study the effect of indium doping on the structural, morphological, and optical properties of ZnO nanoparticles.     

Inverse magnetocaloric effect in sol–gel derived nanosized cobalt ferrite

The magnetocaloric properties of cobalt ferrite nanoparticles were investigated to evaluate the potential of these materials as magnetic refrigerants. Nanosized cobalt ferrites were synthesized by the method of sol–gel combustion. The nanoparticles were found to be spherical with an average crystallite size of 14 nm. The magnetic entropy change (ΔS _m) calculated indirectly from magnetization isotherms in the temperature region 170–320 K was found to be negative, signifying an inverse magnetocaloric effect in the nanoparticles. The magnitudes of the ΔS _m values were found to be larger when compared to the reported values in the literature for the corresponding ferrite materials in the nanoregime.     

Evolution of ZnO nanostructures in sol–gel synthesis

Evolution of the microstructure and optical properties of ZnO nanoparticles in a mild sol–gel synthesis process is studied. The ZnO nanostructures were prepared by reacting zinc acetate dihydrate with NaOH in water at 50−60 °C. Evolution of ZnO nanostructures with reaction time is studied using UV–Vis spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD), and Fourier transform infrared (FT-IR) spectroscopy techniques. During the process of Zn²⁺ hydroxylation, well defined rod-like crystals were formed within 15 min. Further hydroxylation leads to the formation of a gel-like structure within about 45 min. However, XRD, FT-IR and energy dispersive spectroscopy (EDS) confirmed that these initial products were zinc hydroxyl double salts (Zn-HDS), not ZnO. On ageing the reaction mixture, ZnO nanoparticles with wurtzite structure evolved.     

Temperature sensor based on PNR in Sagnac interferometer

A temperature sensor based on polarization non-reciprocity (PNR) in fiber-optic Sagnac interferometer (FSI) was proposed. The experimental study was made primarily and the results agree with theory well. Discussion shows that this kind of temperature sensor can achieve high precision and have great application potential.     

Temperature effect on fluorescence and UV–vis absorption spectroscopic properties of Dy(III) in molten LiCl–KCl eutectic salt

The spectroscopic properties of Dy(III) in molten LiCl–KCl eutectic salt at high temperature were investigated by time-resolved laser fluorescence spectroscopy (TRLFS) and UV–vis absorption spectroscopy. For the first time, a visible fluorescence of Dy(III) in high-temperature LiCl–KCl eutectic salt was measured due to the electronic transitions from ⁴I_13/2 and ⁴F_9/2 to ⁶H_J/2 (J=7,…,15). The effect of temperature on hypersensitivity for the electronic transitions from the ⁴I_13/2 excited state (～25700 cm^?1) of Dy(III) was confirmed by altering temperature in chloride eutectic salt in accord with optical absorption measurements. The molar absorptivity of ⁴I_13/2←⁶H_15/2 was enhanced with increasing temperature. The fluorescence intensity of Dy(III) followed a simple mono-exponential decay curve, suggesting the formation of a single chemical species in high-temperature LiCl–KCl molten salt.     

Effect of cerium doping on corrosion resistance of amorphous silica–titanium sol–gel coating

The aim of this study was to investigate the effects of ceria doping on corrosion resistance of amorphous silica–titania coating. The microstructural and phase properties of titania–silica and titania–silica–Ceria composite films were investigated by SEM, EDAX and XRD. Potentiodynamic polarization and EIS spectroscopy have been used to study the corrosion behavior of composite coating in 3.5% NaCl solution. Results showed that by cerium doping into silica–titania coating as an inhibitor, the corrosion resistance of the film increased. In addition this study revealed that cerium doping enhanced pitting resistance of the coating.     

Comparison of the effect of anti-hyperlipidemic drugs from different groups on the phase profile of liposomal membrane–a fluorescence anisotropy study

The study compares the effect of incorporation of three different groups of anti-hyperlipidemic drugs, namely niacin, simvastatin, and fenofibrate on the phase profile of liposomal membranes of dipalmitoylphosphatidylcholine (DPPC). The fluorescence anisotropy studies, using 1,6-diphenyl-1,3,5-hexatriene as fluorescent probe, have shown that the lipophilic molecule fenofibrate changes phase behavior of DPPC liposomal membrane to a greater extent compared to the changes produced by amphiphilic simvastatin and hydrophilic niacin. This variation in effect can be attributed to the nature of the drug molecules and hence their location in different parts of the liposomal membrane. We have also calculated the changes in van’t Hoff enthalpy values in all these three cases and observed that these values decreased with increase in drug concentrations in the case of simvastatin but for fenofibrate and niacin the effect is completely the reverse. In order to get a better insight, the fraction of motionally restricted lipid molecules has been calculated.     

Light absorption in Ge nanoclusters embedded in SiO2: comparison between magnetron sputtering and sol–gel synthesis

SiGeO films have been produced by a sol–gel derived approach and by magnetron sputtering deposition. Post-thermal annealing of SiGeO films in forming gas or nitrogen atmosphere between 600 and 900 °C ensured the phase separation of the SiGeO films and synthesis and growth of Ge nanoclusters (NCs) embedded in SiO₂. Rutherford backscattering spectrometry analysis evidenced a similar Ge concentration (~12 %), but a different Ge out-diffusion after annealing between the two types of techniques with the formation of a pure SiO₂ surface layer (~30 nm thick) in sol–gel samples. The thermal evolution of Ge NCs has been followed by transmission electron microscopy and Raman analysis. In both samples, Ge NCs form with similar size increase (from ~3 up to ~7 nm) and with a concomitant amorphous to crystalline transition in the 600–800 °C temperature range. Despite a similar Ge concentration, a significant lower NCs density is observed in sol–gel samples attributed to an incomplete precipitation of Ge, which probably remains still dispersed in the matrix. The optical absorption of Ge NCs has been measured by spectrophotometry analyses. Ge NCs produced by the sol–gel method evidence an optical band gap of around 2 eV, larger than that of NCs produced by sputtering (~1.5 eV). These data are presented and discussed also considering the promising implications of a low-cost sol–gel based technique towards the fabrication of light harvesting devices based on Ge nanostructures.     

Surface functionalisation of sol–gel derived aluminosilicates in simulated body fluids

Iron containing aluminosilicate systems obtained by sol–gel method are investigated as potential biomaterials for hyperthermia. The samples surface functionalisation in simulated body fluid enriched with bovine serum albumin (BSA) was studied by Fourier-transform infrared spectroscopy performed in reflectance mode and X-ray photoelectron spectroscopy (XPS). β-sheet/turns ratio estimated using the deconvolution of IR absorption band corresponding to amide I of adsorbed BSA on surface samples indicates a positive contribution to the biocompatibility of these materials. XPS results show an early attachment of albumin on sample surface that is weakly influenced by the protein concentration and prolonged immersion time in BSA–SBF solution.     

Gel stabilization in chelate sol–gel preparation of Bi-2223 superconductors

A chelating sol–gel method was used for the preparation of the superconducting Bi-2223 phase. We compared pH range of both solution and gel stability in samples with EDTA, TEA and their equimolar mixture addition. A pH range of stability (for precipitation) was extended in EDTA solutions with addition of TEA. IR spectroscopy was used to identify the type of bonding between EDTA and TEA in a stabilized solution. IR bands belonging to polyester bonding were found in the IR spectra of gels prepared at 130 °C. We describe the influence of both gel decomposition and calcinations regime on the evolution of Bi-2223 phase. The optimized temperature treatment was used for the comparison of superconducting transport and of magnetic properties of the prepared samples. Moreover, an extra 800 °C calcination step was tested to enhance the decomposition of unfavorably formed carbonates.     

TEM characterization of organic nanocrystals grown in sol–gel thin films

The tetracene molecule (2,3-benzanthracene, C₈H₁₂) was used to synthesize nanocrystals grown in sol–gel thin films, ranging from 10 to 100 nm of diameter. This confined nucleation and growth was compared to microcrystallizations of the same molecule in free solution. Transmission electron microscopy (TEM) was used to characterize these two kinds of tetracene crystals. The observation was performed under low-dose illumination to avoid amorphization of the samples during electron irradiation. Spatial confinement and size distribution of micro- and nanocrystals were compared. Using electron microdiffraction and diffraction patterns simulations, we showed that free microcrystals and nanocrystals confined in gel glasses exhibit the same triclinic structure. In addition, time-resolved spectroscopy was used to record fluorescence decays, showing a monoexponential fluorescence decay for nanocrystals while microcrystals exhibit a multiexponential decay. The simple signature of nanocrystals luminescence is promising for the future development of chemical or biological sensors.     

Temperature dependent structural and optical properties of nanocrystallineCdO thin films deposited by sol–gel process

Nanocrystallites of cadmium oxide (CdO) thin films were deposited by sol–gel dip coating technique on glass and Si substrates. XRD and TEM diffraction patterns confirmed the nanocrystalline cubic CdO phase formation. TEM micrograph of the film revealed the manifestation of nano CdO phase with average particle size lying in the range 1.6–9.3 nm. UV–Vis spectrophotometric measurement showed high transparency (nearly 75% in the wavelength range 500–800 nm) of the film with a direct allowed bandgap lying in the range 2.86–3.69 eV. Particle size has also been calculated from the shift of bandgap with that of bulk value for the films for which the particles sizes are comparable to Bohr exitonic radius. The particle size increases with the increase in annealing temperature and also the intensity of XRD peaks increases which implies that better crystallinity takes place at higher temperature.This revised version was published online in August 2005 with a corrected issue number.     

Grain boundary effect on structural,optical, and electrical properties of sol–gel synthesized Fe-doped SnO_2 nanoparticles

Tin oxide(SnO_2) and iron-doped tin oxide(Sn_(1-x)Fe_xO_2,x=0.05 wt%,0.10 wt%) nanoparticles are synthesized by the simple sol-gel method.The structural characterization using x-ray diffraction(XRD) confirms tetragonal rutile phases of the nanoparticles.The variations in lattice parameters and relative intensity with Fe-doping concentration validate the incorporation of iron into the lattice.The compressive strain present in the lattice estimated by using peak profile analysis through using Williamson-Hall plot also exhibits the influence of grain boundary formation in the lattice.The radiative recombination and quenching observed in optical characterization by using photoluminescence spectrum(PL) and the shift in the band gap estimated from UV-visible diffused reflectance spectrum corroborate the grain boundary influence.Raman spectrum and the morphological analysis by using a field emission scanning electron microscope(FESEM) also indicate the formation of grain boundaries.The compositional analysis by using energy dispersive x-ray spectrum(EDAX) confirms Fe in the SnO_2 lattice.The conductivity studies exhibit that the impendence increases with doping concentration increasing and the loss factor decreases at high frequencies with doping concentration increasing,which makes the Sn_(1-x)Fe_xO_2 a potential candidate for device applications.     

Investigation of laser ablation on hybrid sol–gel material applied to kinoform etching

Ultraviolet laser machining of a hybrid organic/inorganic material prepared via a sol–gel process has been studied for the fabrication of kinoforms or surface relief diffractive optical elements. The hybrid mixes silicon and titanium oxides and an organic network in order to improve the mechanical properties. Different material compositions have been investigated. Laser ablation of the hybrid material is observed at low laser fluence (measured threshold fluence of 125 mJ/cm² at 248 nm/6 ns) and shows that the process is well adapted to micro-patterning by laser machining means. The best observed depth resolution is 60± 20 nm and appears to be limited by the ablation setup. Finally, the fabrication of an effective diffractive optical element and its operation at 1.06 μm are described. PACS  81.20.Fw; 79.20.Ds; 42.79.-e     

Effect of heat and time-period on the growth of ZnO nanorods by sol–gel technique

Sol–gel routes to metal oxide nanoparticles in organic solvents under exclusion of water have become a versatile alternative to aqueous methods. We focus on the preparation of well-aligned ZnO nanorod arrays using non-aqueous sol–gel synthesis route, where ZnO nanorods arrays have been grown on glass substrates. This work provides a systematic study of controlled morphology and crystallinity of ZnO nanorod arrays. The investigation demonstrates that the synthesis process conditions of ZnO thin film have strong influences on the morphology and crystallinity of the ZnO nanorod arrays grown thereon, where non-aqueous process offers the possibility of better understanding and controlling the reaction pathways on the molecular level, enabling the synthesis of nanomaterials with high crystallinity and well-defined, uniform particle morphologies. Here the annealing temperature plays an important role on the growth of nanostructures of the ZnO grains and nanorod arrays. The scanning electron microscopy (SEM) image shows that the growth of ZnO nanorod arrays are high-quality single crystals growing along the c-axis perpendicular to the substrates. A detailed analysis of the growth characteristics of ZnO nanostructures as functions of growth time is also reported.     

Microwave behavior of ferrites prepared via sol–gel method

Ni-ferrites were prepared at different temperatures via sol–gel method. The electromagnetic properties of these materials, namely permittivity and permeability were measured in the 0.1–13 GHz frequency range. Following a mathematical procedure, microwave absorption diagrams were constructed including the dependence of the microwave absorption of ferrite layer on microwave frequency and layer thickness. The permeability spectra broaden and the microwave absorption improves at 9–10 GHz with increase of annealing temperature.     

Effect of the excimer laser irradiation on sol–gel derived tungsten–titanium dioxide thin films

A novel technique based on the excimer laser induced crystallization and modification of TiO₂ thin films is being reported. W⁺⁶ ions loaded TiO₂ (WTO) precursor films were prepared by a modified sol–gel method and spin-coated onto microscopic glass slides. Pulsed KrF (248 nm, 13 ns) excimer laser was used to irradiate the WTO amorphous films at various laser parameters. Mesoporous and nanostructured films consisting of anatase and rutile were obtained after laser irradiation at room temperature. The effect of varying W⁺⁶ ions concentrations on structural and optical properties the WTO films was analyzed by X-ray diffraction, field-emission scanning electron microscope, UV-Vis spectrophotometer and transmission electron microscope before and after laser treatment. Films irradiated for 10 pulses at 65–75 mJ/cm² laser fluence, exhibited anatase whereas higher parameters promoted the formation of rutile. XPS results revealed WO₃ along with minor proportion of WO₂ compounds after laser irradiation. Photo-absorbance of the WTO films was increased with increase in W⁺⁶ ions concentration in the film. TEM results exhibited a crystallite size of 15 nm which was confirmed from SEM results as well.     

Design a sensitive optical thin film sensor based on incorporation of isonicotinohydrazide derivative in sol–gel matrix for determination of trace amounts of copper (II) in fruit juice: Effect of sonication time on immobilization approach

A new selective and sensitive optical sensor based on the incorporation of new synthesized N′-(2-hydroxy-5-iodobenzylidene) isonicotinohydrazide (HIBIN) as an effective reagent into the nanoporous of a transparent glass like material through the sol–gel process was developed which was suitable for the determination of copper (II) ions in aqueous solutions. The thin film sensors were constructed by spin-coating of prepared sol onto glass plate and their surface morphology were studied by field emission scanning electron microscopy (FE-SEM) and atomic force microscope (AFM) technique. Influence of sonication time on immobilization of HIBIN into silica matrix was investigated through calculation of leaching percentage. The Results shown that sonication time of 35 min is suitable to give more stable thin films without fluctuation in sensitivity and response time of presented sensor for a long period of time. The proposed optical sensor can be used for determination of copper (II) ions in the range of 9.1 × 10⁻⁸–1.12 × 10⁻⁵ mol L⁻¹with a detection limit of 1.8 × 10⁻⁸ mol L⁻¹. It also showed relative standard deviation 3.4 and 0.72% for reproducibility and repeatability respectively, along with a fast response time about of 2 min. The constructed optode is stable in wet conditions and could be stored for at least 6 weeks without observing any change in its sensitivity. The developed sensor was successfully applied to the determination of copper (II) in fruit juice and water samples which results were confirmed by atomic absorption spectrometry method.