Light scattering and extinction in polydisperse systems

A simple approach to predict transmittance spectra of polydisperse systems is recalled and applied to various model systems (spinel-like particles in water, pores in a spinel-like matrix) and real systems (spinel in water, diamond in water, amorphous carbon soot in isopropanol) in order to investigate principal effects of size distributions (normal/lognormal, narrow/wide, monomodal/bimodal, shift of mode positions, shift of mode heights) and optical properties (refractive index contrast, with or without absorption) on the in-line transmittance. A comparison of predicted and measured spectra showed that size distributions with more small particles cause a more significant decrease in transmittance (at least for sufficiently short wavelengths) and that laser diffraction may seriously underestimate the amount of small particles (for absorbing particles, for which the influence on transmittance is enormous, a difference of up to 30% in absolute transmittance measured via spectrophotometry has been found against predictions based on laser diffraction results).     

Effect of lanthanum doping on water content and diffusion properties of corundum for producing transparent ceramics

The effect of doping corundum with lanthanum on the content of water and other gas impurities, on the diffusion characteristics, on the unit cell size and static strength of fine-crystalline corundum synthesized under thermovapours conditions in a supercritical water fluid was studied.Content, release and diffusion coefficients of water and other volatile impurities in corundum were measured by kinetic thermodesorption mass spectrometry. Water is the main volatile impurity in fine-crystalline corundum. It was found that the introduction of lanthanum into the structure of corundum reduces several times the content of water and other gas-liquid impurities. An increase in the diffusion coefficient of water during the doping of corundum with lanthanum leads to an increase in the degassing rate of fine-crystalline raw materials. When doping corundum, lanthanum, being localized in structural defects, not only displaces structural hydroxyl groups with the formation of strong aluminate-like bonds, but also decreases in the unit cell and increases in the average static strength of the crystals. La-doped corundum, due to the reduced content of water and other gas impurities, is a promising raw material for the production of transparent ceramics.     

Spray-grown highly oriented antimony-doped tin dioxide transparent conducting films

Undoped and Sb-doped tin dioxide films of varying thickness with a remarkable crystallographic orientation in the [200] direction were grown by spray-pyrolysis from tin(II) chloride solutions. Films grown on silica-coated glass substrates were completely crystalline and showed a higher degree of orientation with respect to films that were grown on uncoated glass. The presence of the silica barrier was seen to have increased the degree of orientation and to have enhanced the resulting electrical properties. Transmission electron microscopy revealed that the silica layer may have played the crucial role of a nucleation layer. Moreover, the developed microstructures were correlated with the optical and electrical behaviour of the films. Dense conducting films with thicknesses between 280–450 nm and visible transmittances of 80-70 % showed resistivities of about 10⁻³ Ωcm.     

Investigation of LSM-8YSZ cathode within an all ceramic SOFC. Part I: Chemical interactions

This work focuses on a novel, co-sintered, all-ceramic solid oxide fuel cell (SOFC) concept. The objective is the understanding of interaction and degradation mechanisms of the cathode and current collector layers within the design during co-sintering. Half cells consisting of silicate mechanical support, lanthanum strontium manganite (LSM) current collector, LSM mixed with 8 mol% yttria-stabilized zirconia (8YSZ) composite cathode and 8YSZ electrolyte were co-sintered at 1150 °C < T < 1250 °C. Crystallographically stable LSM compositions within the design were identified. However, the cathode and silicate/electrolyte interacted by interdiffusion of Zn (gas diffusion) and Mn (solid diffusion), and by the formation of several reaction phases (between silicate and cathode only). Introducing silicate poisoning decreased the electrochemical performance of the cell by around 40%. This is likely due to the formation of the Zn- and Mn-rich phase in the cathode, but may also be caused by a higher ohmic resistance of the current collector.     

Failure of high power varistor ceramic components

Ceramic varistors are electronic components which have a sharp change (over several orders of magnitude) of their electrical resistance at a well-defined voltage (switching voltage). Starting at low voltages, the resistance is large. But by exceeding the switching voltage the resistance drops dramatically and the component acts as a good conductor. Mounted parallel to a consumer, they are used as protection devices against over voltage loading. In the technical routine yearly billions of varistors are used to protect power lines, transformation stations, electronic devices, microelectronic systems or even LEDs.In service large temperature differences may come into existence, which cause severe mechanical stresses that even may destroy the components. The basic principles of the varistor behaviour are explained and examples of mechanical failure are discussed.     

Synthesis of hexacelsian barium aluminosilicate by film boiling chemical vapour process

An original oxide/oxide ceramic-matrix composite containing mullite-based fibers and a barium aluminosilicate matrix has been synthesized by the film boiling chemical vapour infiltration process. Alkoxides were used as liquid precursors for aluminum, silicon and barium oxides. The structure and microstructure of the oxide matrix were characterized by Scanning Electron Microscopy, Energy Dispersive Spectroscopy and X-ray diffraction. Apart from small residual mullite and amorphous phase amounts, the oxide matrix is composed of the hexacelsian phase, conferring to the material interesting perspectives for high-temperature electromagnetic and structural applications.     

Microfluidic synthesis of ultrasmall Co nanoparticles over reduced graphene oxide and their catalytic properties

We prepared a one-stage microfluidic-based method for continuous synthesis of cobalt (Co) nanoparticles over reduced graphene oxide (rGO) to produce Co/rGO composites. These were generated by the coreduction of Co²⁺ ions and GO with NaBH₄ which was confined within discrete aqueous plugs segmented by octane as continuous phase. Owing to the excellent transfer properties from recirculation in these plugs, ultrasmall Co nanoparticles were distributed homogeneously on the GO sheets without using any surfactants. As compared to batch methods, the average size of Co nanoparticles and the relative standard deviation decreased from 4.0 ± 1.42 nm and 35.9% to 2.0 ± 0.45 nm and 22.6%, respectively. The as-prepared Co/rGO composites exhibited superior activity towards the catalytic reduction of p-nitrophenol to p-aminophenol with NaBH₄ compared with Co nanoparticles and rGO; this enhanced activity could be attributed to the synergistic effect between Co nanoparticles and rGO.     

Electrochemical inspection of polypyrrole/chitosan/zinc oxide hybrid composites

Polymer nanocomposite composed of polypyrrole, chitosan, and zinc oxide nanoparticles has been synthesized and it has been evaluated for various electrochemical aspects of the current electrochemical industry. The polypyrrole (PPy) was synthesized by the chemical oxidative polymerization reaction by employing ammonium persulfate as oxidizing agent. Composites of polypyrrole/chitosan (PPy/Chy) and polypyrrole/chitosan/ZnO (PCZ) composites were synthesized by the solution blending method. Detailed structural, morphological, thermal characterization of PPy, PPy/Chy, and PCZ were performed to characterize the specific features of the systems. The composites exhibit better thermal stability and high surface area and the addition of ZnO nanoparticle increase the crystallinity of the composite. Electrochemical characterization of the ITO electrodes modified with PPy, PPy/Chy, and PCZ were performed using cyclic voltammetry, electrochemical impedance spectroscopy, and amperometry techniques. The present study highlights the role of a bio-compatible material with high surface area and conductive constituent for designing of various high performing electronic noninvasive sensors, biosensors, and so forth.     

Facile synthesis of Co0.5Zn0.5Fe2O4 nanoparticles decorated reduced graphene oxide hybrid nanocomposites with enhanced electromagnetic wave absorption properties

Herein, reduced graphene oxide/cobalt-zinc ferrite (RGO/Co_0.5Zn_0.5Fe₂O₄) hybrid nanocomposites were fabricated by a facile hydrothermal strategy. Results revealed that the contents of RGO could affect the micromorphology, electromagnetic parameters and electromagnetic wave absorption properties. As the contents of RGO increased in the as-synthesized hybrid nanocomposites, the dispersibility of the particles was improved. Meanwhile, numerously ferromagnetic Co_0.5Zn_0.5Fe₂O₄ particles were evenly anchored on the wrinkled surfaces of flaky RGO. Besides, the obtained hybrid nanocomposites exhibited superior electromagnetic absorption in both X and Ku bands, which was achieved by adjusting the RGO contents and matching thicknesses. Significantly, when the content of RGO was 7.4 wt%, the binary nanocomposites showed the optimal reflection loss of -73.9 dB at a thickness of 2.2 mm and broadest effective absorption bandwidth of 6.0 GHz (12.0–18.0 GHz) at a thin thickness of merely 2.0 mm. The enhanced electromagnetic absorption performance was primarily attributed to the multiple polarization effects, improved conduction loss caused by electron migration, and magnetic loss derived from ferromagnetic Co_0.5Zn_0.5Fe₂O₄ nanoparticles. Our results could provide inspiration for manufacturing graphene-based hybrid nanocomposites as high-efficient electromagnetic wave absorbers.     

Nanocrystalline transition metal oxides and their composites with reduced graphene oxide and carbon nanotubes for photocatalytic applications

Transition metal oxide nanoparticles (CuO, ZnO & Fe₂O₃) and mixed metal oxides CuO. ZnO.Fe₂O₃ were fabricated by facile co-precipitation approach for photocatalytic treatment of organic dyes. The structural features, phase purity, crystallite size and morphology of individual and mixed metal oxides were analysed by X-rays diffraction patterns (XRD) and scanning electron microscopic (SEM) analysis. Electrical behaviour of CuO, ZnO, Fe₂O₃ and mixed metal oxides CuO. ZnO.Fe₂O₃ was explored by current-voltage (I-V) measurements. Functional groups present in the synthesized metal oxides were investigated by Fourier transform infrared spectroscopy (FTIR) which ensures the existence of M-O functional groups in the samples. The optical bandgap analysis was carried out by UV–visible spectroscopic technique which revealed that the blend of three different transition metal oxides reduced the bandgap energy of mixed metal oxides. The reason behind this reduced bandgap energy is formation of new electronic state which arises due to the metal-oxygen interactions. Moreover, the nanocomposites of CuO.ZnO.Fe₂O₃ with reduced graphene oxide (rGO) and carbon nanotubes (CNTs) were prepared to study the effect of the carbonaceous materials on the rate of photodegradation. These carbonaceous nanomaterials have plethora properties which can bring advancement in sector of photocatalytic treatment of wastewater. The photocatalytic experiments were performed using methylene blue (MB) as standard dye for comparative study of metal oxides and their composites with rGO and CNTs. The percentage degradation of methylene blue (MB) by nanocomposite CuO.ZnO.Fe₂O₃/rGO is 87% which is prominent among all samples. This result ascribed the photocatalytic aspects of reduced graphene oxide along with mixed metal oxides.