Microstructure and optical properties of electrodeposited Al-doped ZnO nanosheets

This study grew A1-doped ZnO nanosheets on polycrystalline zinc foils using cathodic electrodeposition in an aqueous solution consisting of 0.02 M Zn(NO₃)₂ and 0.001 M Al(NO₃)₃ at 90 °C. The effects of the electrodepositing potential and thermal annealing on the physical properties of the Al-doped ZnO sheets were investigated. This study observed a high quality sheet-like structure of the electrodeposited Al-doped ZnO for the applied potential larger than −1.1 V, and the sheets were interconnected over the area of interest. The X-ray diffraction patterns showed that the intensity of the Bragg reflections of the electrodeposited Al-doped ZnO sheets increases with the electrodepositing potential because a larger applied potential results in the Al-doped ZnO sheets having a larger lateral dimension and thickness. However, the appearance of the Al-doped ZnO sheets becomes coarse and rough after thermal annealing at 400 °C in ambient air for 4 h. The intensity of the Bragg reflections of the Al-doped ZnO sheets was markedly increased through the thermal annealing due to the improvement of the crystalline quality of the annealed Al-doped ZnO sheets. Annealing caused a large decrease in structural defects of the Al-doped ZnO sheets electrodeposited at −1.3 V causing the sheets to exhibit a sharp photoluminescence peak at ∼380 nm.     

Effects of oxygen concentration on the electrical properties of ZnO films

In this paper, electrical characteristics by various oxygen content in ZnO films were studied. To control the oxygen content of ZnO films, post-thermal annealing was performed in N₂ and air ambient, led to improve crystallinity and optical properties of ZnO films. The oxygen concentration was measured by Auger electron spectroscopy. The ZnO films having the deficiency of oxygen showed the electron concentrations between 10²¹ and mid 6 × 10¹⁷ cm⁻³ and resistivity at 10⁻³–10⁻¹ Ω cm. On the other hand, when the oxygen concentration of the ZnO films was up to the stoichiometry with Zn, the ZnO films showed low electron concentration at −10¹⁷ cm⁻³ and resistivity at 10 Ω cm.     

Thermal Behavior of Deteriorated Wood Waste

Abstract

This paper investigates the thermal behavior of woody biomass waste—demolition wood of Japanese cedar (Cryptomeria japonica) and insect-attacked forest residue of Japanese red pine (Pinus densiflora)—using proximate analyses, thermogravimetry (TG), and differential thermal analysis (DTA), with comparison to virgin wood. For the pine samples, there was no significant difference in thermal behavior or elemental composition between the virgin pine and pine that had been damaged by insects, indicating that insect-damaged pine received here can be treated as virgin pine in terms of energy utilization. The cedar demolition wood used here was partly degraded by termites or fungi. Its degraded part had a lower weight loss rate under nitrogen and a broader exothermic peak in the char combustion stage under air than cedar virgin wood. The changes in the relative levels of the chemical components and the resultant chemical changes that occur upon fungal degradation might complicate char formation.     

Influence of ball milling on the sintering behaviour of ZnO powder

A high purity ZnO powder was milled with either YSZ or Al₂O₃ balls. The weight losses of YSZ and Al₂O₃ balls after milling for 4 h are 10 and 40 ppm, respectively. The debris of the milling media acts as sintering aid to the ZnO powder. As a result, the grain size of the sintered ZnO specimens is reduced. The ratio of the grain boundary energy over surface energy is also decreased.     

Influence of yttrium doping on the structural,morphological and optical properties of nanostructured ZnO thin films grown by spray pyrolysis

This study reports on the deposition of highly transparent, n-type ZnO thin films on glass substrate at 450?°C using spray pyrolysis processing, with the simultaneous insertion of yttrium (Y) at different percentages (0, 2, 5, 7?at%) as a dopant. The effect of Y doping on the structure, morphology and optical properties of Y doped ZnO (ZnO:Y) was investigated for optoelectronic applications. The obtained thin films were characterized by means of X-ray diffraction, field-emission scanning electron microscopy (FESEM), UV–visible absorbance measurements, photoluminescence (PL) and cathodoluminescence (CL) spectroscopy. The as-prepared films exhibit well-defined hexagonal wurtzite structure grown along [002]. Field emission scanning electron microscope micrographs of the pure ZnO and ZnO:Y showed that the films acquired a dominance of hexagonal-like grains, the morphology was influenced by Y incorporation. All the films showed high transparency in the visible domain with an average transmittance of 83%. The band gap energy, E_g, increased from 3.12?eV to 3.18?eV by increasing the Y doping concentration up to 5?at% and then decreased to 3.15?eV for 7?at% Y content. The PL and CL measurements reveal a strong ultraviolet (UV) emission, suggesting that the as-prepared ZnO:Y thin films can potentially be used in optoelectronic devices.     

Preparation and characterization of nanocrystalline La-doped ZnO powders through a mechanical milling and their optical properties

Structural and optical properties of mechanically milled La-doped ZnO powders are presented in this paper. The Zn_1−xLa_xO phase formed when x varied in a range of 0.02-0.06 and milled at 400 rpm for 20 h. The secondary La₂O₃ phase occurred with an increase of La content. The crystallite and particle size decreased as a function of La content as x = 0-0.14 due to the effect of Zener pinning and solute drag. The absorption edge shifted to a lower wavelength when La content was increased to x = 0.14 because of the size effect. The energy band gap of Zn_1−xLa_xO powders varied in a range of 2.96-3.12 eV depending on the crystallite size. The broad emission bands in a visible region centered at about 640 nm are attributed to oxygen deficiency.     

Influence of ionic liquid on the photoelectrochemical properties of ZnO particles

ZnO particles synthesized by the microwave-assisted hydrothermal method were sensitized with different amounts of ionic liquid (IL) 1.3-dimethylimidazolium iodide (MMI.I). The structure of the modified and unmodified ZnO particles were characterized by X-ray diffraction, Raman spectroscopy, field emission gun-scanning electron microscopy (FEG-SEM), ultraviolet-visible (UV–vis) absorption spectroscopy, photoluminescence (PL), and photoelectrochemical measurements. While the sensitization of ZnO particles by the ionic liquid does not change the ZnO phase, it reduces the particle size and converts shallow defects to deep defects. These changes cause the photocurrent density of the ZnO/IL films to increase significantly from 0.05?mA?cm^?2 for pure ZnO to 0.52 and 1.24?mA?cm^?2 for the ZnO films containing 20% and 35% by mass of the IL, respectively, at 1.08?V vs. Ag/AgCl. This about 24-fold increase in the photocurrent density of the ZnO/IL35 sample may indicate that the MMI.I IL may be acting as a dye, since it is constituted by an organic part, MMI⁺. This good performance presented by this sample indicates that this is a promising material for photoanode in solar cells.     

In-situ study of electrophoretic deposition of zinc oxide nanosheets and nanorods

In the present work, the effects of two different morphologies of zinc oxide nanoparticles (nanosheets and nanorods) were investigated by in-situ measurement of deposition weight, and current density. ZnO nanosheets and nanorods were synthesized by microwave-assisted method using co-surfactant route. The average thickness of obtained nanosheets, and the average diameter of nanorods were measured to be about 26 nm and 139 nm, respectively. ZnO films were obtained by electrophoretic deposition from suspension of nanoparticles in ethanol under different voltages. Results indicated that ZnO nanosheets tend to have greater deposition rate than ZnO nanorods under similar conditions. The compactness of the film obtained from nanosheet suspension was higher than the one obtained from nanorod suspension. However, the film obtained from ZnO nanorods displayed more uniformity at different voltages in comparison to the film obtained from ZnO nanosheets, which can be due to different active surface area, and also different way of motion under hydrodynamic forces in the suspension.     

Formation of nanosize ZnO particles by thermal decomposition of zinc acetylacetonate monohydrate

Formation of ZnO particles by thermal decomposition of zinc acetylacetonate monohydrate in air atmosphere has been investigated using XRD, DTA, FT-IR, and FE-SEM as experimental techniques. ZnO as a single phase was produced by direct heating at ≥200 °C. DTA in air showed an endothermic peak at 195 °C assigned to the ZnO formation and exothermic peaks at 260, 315 and 365 °C, with a shoulder at 395 °C. Exothermic peaks can be assigned to combustion of an acetylacetonate ligand released at 195 °C. ZnO particles prepared at 200 °C have shown no presence of organic species, as found by FT-IR spectroscopy. Particles prepared for 0.5 h at 200 °C were in the nanosize range from ∼20 to ∼40 nm with a maximum at 30 nm approximately. The crystallite size of 30 nm was estimated in the direction of the a₁ and a₂ crystal axes, and in one direction of the c-axis it was 38 nm, as found with XRD. With prolonged heating of ZnO particles at 200 °C the particle/crystallite size changed little. However, with heating temperature increased up to 500 or 600 °C the ZnO particle size increased, as shown by FE-SEM observation. Nanosize ZnO particles were also prepared in two steps: (a) by heating of zinc acetylacetonate monohydrate up to 150 °C and distillation of water and organic phase, and (b) with further heating of so obtained precursor at 300 °C.     

Effect of nickel doping on structural,optical, electrical and ethanol sensing properties of spray deposited nanostructured ZnO thin films

Undoped and nickel (Ni)-doped ZnO thin films were spray deposited on glass substrates at 523 K using 0.1 M of zinc acetate dihydrate and 0.002–0.01 M of nickel acetate tetrahydrate precursor solutions and subsequently annealed at 723 K. The effect of Ni doping in the structural, morphological, optical and electrical properties of nanostructured ZnO thin film was investigated using X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), UV–vis Spectrophotometer and an Electrometer respectively. XRD patterns confirmed the polycrystalline nature of ZnO thin film with hexagonal wurtzite crystal structure and highly oriented along (002) plane. The crystallite size was found to be increased in the range of 15–31 nm as dopant concentration increased. The SEM image revealed the uniformly distributed compact spherical grains and denser in the case of doped ZnO thin films. All the films were highly transparent with average transmittance of 76%. The measured optical band gap was found to be varied from 3.21 to 3.09 eV. The influence of Ni doping in the room temperature ethanol sensing characteristics has also been reported.     

Influence of gypsum additive on the gyrolite formation process

The influence of gypsum additive on the gyrolite formation process and a sequence of intermediary compounds formation in the CaO-SiO₂·nH₂O-H₂O system was examined and explained. The synthesis has been carried out in unstirred suspensions. The molar ratios of primary mixtures were CaO/SiO₂ = 0.66. The amount of sulphate ions to be added to a raw mixture was 1-10%. The duration of isothermal curing at 200 °C was 4, 8, 16 and 72 h.It was determined that the quantity of sulphur which penetrates into the crystalline structure of gyrolite depends not only on the synthesis conditions but also on the composition of initial mixture. A larger amount of sulphate ions stimulate the formation not only of gyrolite, but also of CaSO₄. Gypsum additive has no influence on the re-crystallization temperature of C-S-H(I), Z-phase and gyrolite into wollastonite. The composition of initial mixtures is recommended to calculate according to molar ratios. In other cases, upon increasing the amount of sulphate ions, the basicity of the mixture decreases and gyrolite forms more difficult.     

Radioluminescence,thermoluminescence and dosimetric properties of ZnO ceramics

Two types of ZnO ceramics were fabricated and characterized by XRD, SEM methods. The radioluminescence spectra were measured within the 300–550 K range. The defect luminescence band peaking at ~2.35 eV is the dominant one in radioluminescence spectra in both of the fabricated ceramics. The thermostimulated luminescence (TSL) glow-curves were measured after X-ray irradiation at 300 K. It was concluded that the complex overlapping peak within the 320–450 K temperature range consists of two components (~360–375 K and 400–420 K). The ratio of component intensities differs in both ceramics. The positions of high temperature TSL components (480–520 K) also differ in both samples; therefore not only sintering conditions but also the properties of the initial powder are very important for characteristics of TSL. A linear dependence of peak intensity on irradiation dose was observed up to ~3 kGy for ceramic 1 and up to 9 kGy for ceramic 2.     

Study on the stability of different refractories during the melting process of a K4169 Ni-based superalloy

The composition of the refractory strongly affects the cleanliness of the alloy. K4169 Ni-based superalloys were melted in different types of refractories in this study. The cleanliness of the Ni-based superalloy and phase transformation of the refractory were observed by X-ray fluorescence (XRF), X-ray diffraction (XRD), and scanning electron microscopy energy dispersive spectroscopy (SEM‒EDS). The high-temperature stabilities of a Y₂O₃-based refractory, MgO-based refractory, and Al₂O₃-based refractory during melting with a Ni-based alloy were compared. The oxygen content was also lowest, and no Y₂O₃-containing inclusions were observed in the Ni-based alloy melted with the Y₂O₃-based refractory at 1823 K. Inclusions with 21%–29% MgO and a phase composed of Al, Mg and O with an area of approximately 1300 μm² were observed in the alloy. This indicates that the dissolution and erosion of the Y₂O₃-based refractory were weak, and obvious physical erosion and chemical dissolution of the MgO-based refractory occurred during the melting process of the Ni-based alloy. The width of the refractory phase adhered to the boundary of the Ni-based alloy increased in the order Y₂O₃-based refractory (15 μm- 23 μm)< Al₂O₃-based refractory (93 μm- 285 μm)< MgO-based refractory (3.5 mm–3.6 mm), indicating that the adhesive strength of the MgO-based refractory with the Ni-based alloy was strongest. The interaction between the refractory material, Ni-based alloy and inclusions was analyzed based on thermodynamic calculations by Factsage software. The effects of dissolution of the three refractory types on the formation and transformation of the new phases and inclusions were estimated. The thermodynamic results were in good agreement with the experimental results.     

Effect of carbon nanotubes and aluminum oxide on the properties of a plasma sprayed thermal barrier coating

To protect the structural components of a power generating unit from the corrosive environment, thermal spray coatings are applied to the components. In the present work, four different types of thermal barrier coating (TBC) viz. partially stabilised zirconia (8YSZ), zirconia-20% alumina (ZA) composite coating without carbon nanotube (CNT) reinforcement, and ZA with 1% and 3% CNT reinforcement. The coating was deposited on NiCrAlY coated P91 steel using a plasma spraying process. The coating microstructure and phases were characterised using field emission scanning electron microscope (FE-SEM) with energy dispersive spectroscopy (EDS). The phases of the coating were analyzed using X-ray diffraction technique. The effect of CNT reinforcement on the thermal conductivity, porosity, and hardness of the composite coatings was investigated. The protective behavior of the coatings was characterised by potentiodynamic polarization testing and electrochemical impedance measurements. The thermal conductivity of the composite coating was found to be increased with increasing CNT content. Hardness was found to be highest for 3% CNT reinforcement and the thermal conductivity was found to increase with decreasing porosity. The electrochemical measurements indicate that reinforcement of CNT in zirconia alumina composite coating improved its corrosion resistance.     

Influence of mineralogical composition of applied ball clays on properties of porcelain tiles

Relations between quality of ball clays applied in raw materials batches for manufacture of porcelain tiles, and physical properties and microstructure of obtained tiles, were investigated. Studied clays constituted 35% of the batch, while the other components were unchangeable. Stoch index, new IR 3620/3700 index and XRIR index (Stoch index multiplied by IR 3620/3700 index), were proposed to take into account crystallinity of kaolinite and contents of illite and smectites in studied clays. Relationship between XRIR index value of clay, and water absorption and abrasion resistance of the obtained ceramic material, was found. Water absorption of the tile is also correlated with grain size distribution and bending strength of used clay. Optimal ball clay for porcelain tile production should exhibit: Stoch index - min. 4.3; IR 3620/3700 index - min. 1.2; XRIR index - min. 4.8; grain size median - max. 0.27 μm; bending strength after drying - min. 8.0 MPa.     

Effects of the sulfurization temperature on sol gel-processed Cu2ZnSnS4 thin films

As a promising and alternative solar absorber material, the copper–zinc–tin–sulfide compound (Cu₂ZnSnS₄) has been drawing attention in recent years for the production of cheap thin-film solar cells owing to the high natural abundance and non-toxicity of all the constituents, a tunable direct-band-gap energy and a large optical absorption coefficient. In addition, to overcome the problem of expensive vacuum-based methods, solution-based approaches are being developed for Cu₂ZnSnS₄ deposition. In this study, we have produced Cu₂ZnSnS₄ thin films via the sol–gel technique and subsequent sulfurization. The effects of the sulfurization temperature on the structural, morphological, compositional and optical properties of the films were investigated. X-ray diffraction and Raman spectroscopy analyses confirmed the formation of phase-pure CZTS films. The crystallinity of the films increased with an increasing sulfurization temperature. From the surface images and the results of the composition analysis, it was found that the films are uniform, composed of homogenously distributed grains and have compositions with Cu deficit. The values of the optical absorption coefficients for the films were found to be 10⁴ cm^?1 based on absorbance spectroscopy. The optical band-gap values were estimated to be between 1.32 and 2.27 eV depending on the sulfurization temperature.     

Chemical solution deposition of pure and Gd-doped ceria thin films: Structural,morphological and optical properties

High quality smooth, uniform and crack-free ceria and gadolinium doped ceria (GDC) thin films were prepared on Si and Si/YSZ substrates by chemical solution deposition. The thermal behavior of Gd-Ce-O precursor was investigated by TG-DSC measurements. The phase purity and structure of deposited films were evaluated using X-ray diffraction (XRD) analysis and Raman spectroscopy. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were employed for the estimation of surface morphological features. Oxidation state of Ce ions in fabricated films was analyzed by X-ray photoelectron spectroscopy (XPS). Optical properties were evaluated by diffuse reflectance UV–vis spectrometry. Thickness of the films can be controlled by applying a certain number of spin coating cycles. A linear relation between the thickness of the films and the number of deposited layers was observed. The single-layer thickness was determined to be approximately 20 nm. The influence of annealing temperature and Gd content on the film structure, morphology and optical properties was studied and discussed. The dependence of an optical band gap as a function of grain size was demonstrated.     

Investigation of optical,structural, FTIR and magnetic properties of Sn substituted Zn0.98Mn0.02O nanoparticles

Zn_0.98Mn_0.02O and Zn_0.98−xMn_0.02Sn_xO (x=2% and 4%) nanoparticles have been successfully synthesized via sol–gel method. X-ray diffraction (XRD) confirmed the hexagonal wurtzite structure of the samples and also successful Sn doping without any secondary phases. The microstructure of ZnMnO was significantly altered where the morphology was turned from mixed plate-like structure to spherical like structure by Sn substitution which was confirmed by electron microscope images. The energy dispersive X-ray (EDX) analysis confirmed the presence of Sn and Mn in Zn–O nanoparticles. The observed narrowing of energy gap (red shift) from 3.85 eV (Sn=0%) to 3.66 eV (Sn=4%) was discussed based on size effect and generation of free carrier concentrations. The improved optical properties of Sn–Zn–Mn–O evidenced for developing opto-electronic devices with better conversion efficiency. The shift of lattice mode (position) around 527–548 cm⁻¹ and the change in shape of the band demonstrated the presence of Sn in Zn–Mn–O. The decrease of UV emission intensity and increase of defect related blue and green emissions indicated the possible generation of white light sources and display devices. The superior magnetic property of Sn doped Zn_0.98Mn_0.02O was explained by the intrinsic exchange interaction between Zn/Mn/Sn ions through the defects induced by Sn.     

Gas composition in laser pyrolysis of hydrocarbon-based mixtures: Influence on soot morphology

Laser pyrolysis of hydrocarbons leads to soots containing different carbon nanostructures. The investigations of carbon nanopowders revealed the presence of the amorphous carbon, carbon with small graphitic sheets or fullerene-like structures. The soot morphology depends on the gas mixture and experimental parameters. The role of oxygen is essential in obtaining soot particles having considerable curved-layer content.     

Influence of different bonding and fluxing agents on the sintering behavior and dielectric properties of steatite ceramic materials

The focus of the study was on providing insights into interconnections between sintering and development of the crystalline microstructure, and consequently variations in dielectric behavior of four steatites fabricated from a low-cost raw material, i.e. talc. The changes, induced by the alternations of the binders (bentonite, kaolin clay) and fluxing agents (BaCO₃, feldspar), were monitored in the temperature range 1000° to 1250 °C in which complete densification and re-crystallization of the investigated structures were accomplished. The critical points in the synthesis of steatite materials were assessed by instrumental analyses. Crystallinity changes and mineral phase transition during sintering were monitored by X-ray diffraction technique. Microstructural visualization of the samples and the spatial arrangements of individual chemical elements were achieved via scanning electron microscopy accompanied with EDS mapping. The thermal stability was observed on the green mixtures using differential thermal and thermo gravimetric analyses. Electrical measurements recorded variations of the dielectric constant (ε_r) and loss tangent (tan δ) as a function of the sintering temperature. The investigation highlighted critical design points, as well as the optimal combinations of the raw materials for production of the steatite ceramics for advanced electrical engineering applications.