CO2 laser-assisted preparation of transparent Eu2Ti2O7 thin films

We present a laser-assisted preparation of transparent europium-titanate Eu₂Ti₂O₇ thin films with tailored structural and optical properties. We have evaluated the effects of the irradiation time on the structural and the optical properties of the films. This approach allows the preparation of nanocrystalline crack-free films and micro patterns. The amorphous thin films were prepared by a sol-gel method. The films were annealed by a CO₂ laser beam for various time intervals. The laser irradiation induced a crystallization process that resulted in the formation of Eu₂Ti₂O₇ nanocrystals. The nanocrystals regularly grew with increasing irradiation time reaching the size from 25?nm to 45?nm. A film of a thickness 480?nm exhibited an optical transmission of 91.9% that is close to the maximal theoretical limit. The film's refractive index at 632?nm was 2.26. A micrometric pattern was prepared by a direct laser writing followed by a wet chemical etching. Feasibility of the demonstrated approach, together with the high film's quality, and europium-titanate chemical resistivity open up many opportunities for advanced applications. The approach can be used for a preparation of protective coatings and integrated photonic devices such as planar optical waveguides and couplers.     

Effect of neodymium ion on the structural,electrical and magnetic properties of nanocrystalline nickel ferrites

NiNd_xFe_2-xO₄ nanoferrites with different compositions of x?=?0.01, 0.03, 0.05, 0.07 and 0.09 were prepared using the sonochemical method. The structural, optical and morphological properties of the prepared nanoferrites were characterized by X-ray diffraction, ultra violet-diffuse reflectance spectroscopy, scanning electron microscopy and X-ray fluorescence techniques. The X-ray diffraction analysis of the prepared nanoferrites confirmed the presence of a cubic spinel structure. The average crystallite sizes of the prepared nanoferrites were 52, 49, 46, 44 and 40?nm for x?=?0.01, 0.03, 0.05, 0.07 and 0.09, respectively. The particle size of the prepared NiNd_xFe_2-xO₄ nanoferrites was in the range 60–40?nm. The dielectric parameters ranged from 2.9?GHz to 5.6?GHz. Decrease in the dielectric constant was observed with an increase in Nd³⁺ ions in the prepared NiNd_xFe_2-xO₄ nanoferrites. However, a reverse trend was observed in the dielectric loss. An impedance analysis of the prepared nanoferrites was carried out to explore the pseudo-capacitance behavior. The saturation magnetization and remnant magnetization values of the prepared nanoferrites decreased with an increase in the concentration of Nd³⁺ ions in NiNd_xFe_2-xO₄ nanoferrites.     

Preparation and characterization of multilayer anti-reflective coatings via sol-gel process

Single layer and multilayer films consisting of SnO₂, Ta₂O₅, SiO₂, TiO₂, indium tin oxide (ITO) and antimony tin oxide (ATO) have been prepared by sol-gel dip coating technique. All of the multilayer films contained a SiO₂ top layer, which was composed of SiO₂ nanoparticles. The other films had polymeric character. Obtained films were characterized by ellipsometry, XRD, AFM and SEM. Light transmittance values of the films were compared. Films other than SiO₂ and Ta₂O₅ were found to have crystalline structure. Thickness values of the films were in the range of 30–115 nm and roughness values were in 1.2–23 nm range. Single layer porous silica provided 95% light transmittance, whereas ITO-TiO₂-SiO₂ multilayer film provided a light transmittance of 97.2%.     

Influence of calcium concentration on formation of tetravalent chromium doped Y3Al5O12 ceramics

Yttrium Aluminium Garnet (YAG) ceramics doped with chromium were prepared by solid-state reactive sintering in a vacuum. The influence of the charge compensator Ca²⁺ concentration on microstructure, optical properties and efficacy of Cr³⁺ oxidation to Cr⁴⁺ under air annealing was investigated. A non-monotonic dependence of these features on the amount of CaO as an additive was found. The changes in ceramic transparency and microstructure were explained considering the interaction between CaO and Cr₂O₃ at the ceramic grain boundaries, which leads to a different pore evolution in distinct samples during sintering. The efficacy of the oxidation of Cr³⁺ to Cr⁴⁺ strongly depends on the concentration of Ca dissolved in the YAG. The calcium solubility decreases due to the higher oxygen partial pressure of the extra phases on the grain boundaries that decreases the amount of generated Cr⁴⁺ ions. Such phenomenon explains the lower concentration of Cr⁴⁺ ions in the sample with 0.8% of Ca against the one with 0.5%. The experiment shows that the ceramic with 0.5% of Ca has a better in-line transmission and a higher concentration of Cr⁴⁺ ions in comparison with samples with a different Ca concentration.     

Influence of fibers on the microstructure and compressive response of directional ice-templated alumina ceramics

Directional ice-templated ceramics have unique lamellar porous channels between ceramic walls which run from bottom to top of the samples. This highly oriented morphology results in the anisotropy in mechanical properties both parallel and perpendicular to freezing direction. In this research, fiber-enhanced ice-templated porous ceramics were fabricated by introducing fibers into alumina slurry for freezing. The trans-lamellar fiber bridges connecting adjacent ceramic walls were formed by adjusting the aspect ratio of fibers and freezing velocity, which greatly enhanced the compressive response in two directions and weakened the anisotropy in mechanical properties of the directional ice-templated ceramics. The results showed that the of fiber bridges increased with the increase of fiber aspect ratio and the longitudinal and transverse mechanical properties increased by 73.5% and 232.6%, respectively.     

Ferroelectric,upconversion emission and optical thermometric properties of color-controllable Er3+-doped Pb(Mg1/3Nb2/3)O3-PbTiO3-Pb(Yb1/2Nb1/2)O3 ferroelectrics

The (0.98-x)(0.6Pb(Mg_1/3Nb_1/3)O₃-0.4PbTiO₃)-xPb(Yb_1/3Nb_1/3)O₃-0.02Pb(Er_1/2Nb_1/2)O₃ ((0.98-x)(PMN-PT)-xPYN:Er³⁺) ceramics were prepared through a solid-state reaction method. The phase structure, piezoelectric response, ferroelectric performance and upconversion emission of the ceramics were systematically investigated. The phase structure, the electrical and optical properties are strongly related to the content of PYN. The optimized piezoelectric response and upconversion emissions of the ceramics were achieved near x = 0.12, which locates in the morphotropic phase boundary (MPB) composition. Furthermore, the temperature sensing behaviors of the resultant compounds based on the thermally coupled levels of ²H_11/2 and ⁴S_3/2 of Er³⁺ ions in the temperature range of 133–573 K were studied by utilizing the fluorescence intensity ratio technique. Additionally, the thermal effect, which is induced by the laser pump power, of the studied ceramics is also investigated and the produced temperature is enhanced from 268 to 348 K with the pump power rising from 109 to 607 mW.     

Distribution of carbon contamination in MgAl2O4 spinel occurring during spark-plasma-sintering (SPS) processing: I – Effect of heating rate and post-annealing

Carbon contamination from the carbon paper/dies during spark-plasma-sintering (SPS) processing was examined in the MgAl₂O₄ spinel. The carbon contamination sensitively changes with the heating rate during the SPS processing. At the high heating rate of 100 °C/min, the carbon contamination having organized structures occurred over almost the entire area from the surface to deep inside the SPSed spinel disk. In contrast, at the slow heating rate of 10 °C/min, the carbon contamination having disordered structures occurred only around the surface area. The carbon phases transform into high pressure CO/CO₂ gases by post-annealing in air and lead to pore formation along the grain junctions. The pore formation significantly occurs at the high heating rate due to the large amount of the contaminant carbon phases. This suggests that if once the carbon contamination was formed in the materials, it is very difficult to remove the carbon phases from the materials.     

Structural,electrical, optical and dielectric properties of yttrium substituted cadmium ferrites prepared by Co-Precipitation method

The yttrium substituted cadmium ferrites having composition Cd_1-xY_xFe₂O₄ (X = 0.00, 0.125, 0.250, 0.375, 0.500) were synthesized by the co-precipitation method and sintered at 1100 °C for 6 h. Structural, morphological, electrical, optical and dielectric characteristics were explored by XRD, SEM, EDS, FTIR, I–V two probes, UV–Vis and LCR techniques.XRD results confirmed the cubic structure of spinel ferrites. A decrease in lattice constants of the prepared samples was observed with the substitution of Y ions and was attributed to the difference in ionic radii of Y³⁺ (0.95 Å) and Cd²⁺ (0.97 Å) ions. Cationic distributions, ionic radii of both tetrahedral and octahedral sites, tolerance factor, oxygen positional parameters, bond lengths, interatomic distances, positional parameters and bond length angles were calculated from XRD data. The morphology of the prepared ferrites was studied using SEM and results ratified the XRD results. EDS confirmed the presence of all inserted elements in Cd_1-xY_xFe₂O₄ composition. DC resistivity and drift mobility of soft-ferrites were found to be increased from 1.047 × 10⁸–4.822 × 10¹⁰ Ω-cm and 5.87 × 10⁻¹² – 1.045 × 10⁻¹⁴ cm²V⁻¹s⁻¹, respectively, at 523 K with yttrium content confirming the behavior of semiconductor materials. The optical band gap energy calculated from the UV–Vis pattern of the Cd_1-xY_xFe₂O₄ system was decreased from 3.6011 to 2.8153 eV. DC resistivity and optical band gaps exposed inverse relation. FTIR results revealed lower and upper-frequency absorption bands in the ranges of 419.31–417.01 cm⁻¹ and 540.95–565.70 cm⁻¹, respectively. Dielectric constant and dielectric losses were in decreasing order, while ac conductivity revealed rising behavior with increasing frequency. Results showed the potential of yttrium doped Cd nanoferrites for applications in high-frequency microwave absorbing devices.     

Influence of deposition parameters on surface morphology and application of CuInS2 thin films in solar cell and photocatalysis

Copper indium disulfide (CuInS₂) thin films as an absorption layer for solar cell and photocatalytic degradation of organic pollutants, were successfully electrodeposited on the FTO coated glass substrate using the simple and inexpensive electrodeposition method and a sulfurization process. The effects of the Cu/In molar ratio, annealing temperature and kind of Cu²⁺ precursor (Cu(salen) and Cu(acac)₂ as novel Cu²⁺ precursors) on the structural and morphological properties of samples were examined. The XRD diffraction patterns and energy dispersive spectroscopy measurements exhibit that high-quality film with superior crystalline structure was formed in the presence of Cu(salen) as Cu²⁺ precursor. Also, we found that a suitable heat treatment temperature could suppress the CuS phases and form well-crystallized CIS. As we know, this is the first reported efficiency for any CuInS₂ superstrate solar cell to date that fabricated using Cu(salen) as Cu²⁺ precursor. In addition, the photocatalytic degradation of organic dye in the presence of as-synthesized CuInS₂ thin films was studied. The as-prepared semiconductor photocatalysts have a good reusability; it can be successfully reused for 5 times recycling photoactivity tests.     

Effect of Nb substitution on magnetic,ferroelectric and photocatalytic properties of Bi0.95Sm0.05Fe1-xNbxO3 (0 ≤ x ≤ 0.1) nanoparticles

The single phase Bi_0.95Sm_0.05Fe_1-xNb_xO₃ (0 ≤ x ≤ 0.1) nanoparticles were synthesized by the sol-gel route, and the effect of Nb substitution on their magnetic, ferroelectric and photocatalytic properties were studied. X-ray diffractometry confirms a phase transformation from rhombohedral to orthorhombic with an increase in Nb substitution. The grain size decreases significantly, and the morphology of grains becomes homogeneous with the increase of Nb concentration. The maximum remnant magnetization (0.014 emu/g), coercivity (565 Oe) and polarization (0.592 μC/cm²) are observed in Bi_0.95Sm_0.05Fe_0.9Nb_0.1O₃. It has been observed that the energy band gap has been slightly reduced from 2.14 to 2.03 eV with Nb substitution, indicating an improvement of photocatalytic activity. The methylene blue degradation is used to represent the photocatalytic ability of Bi_0.95Sm_0.05Fe_1-xNb_xO₃ nanoparticles. The highest degradation efficiency (~74%) of methylene blue is obtained in Bi_0.95Sm_0.05Fe_0.93Nb_0.07O₃, which is much higher than that of Bi_0.95Sm_0.05FeO₃ (~51%) and can be attributed to the optimum particle size and the smallest energy band gap.