An ultra-fast fabrication technique for anode support solid oxide fuel cells by microwave

An effective and facile technique has been developed for high temperature anode-electrolyte co-sintering of anode support solid oxide fuel cells by using microwave activated sparking plasma. A high sintering temperature of 1600 °C can be achieved in a few minutes time by discharging effect. Anode support substrate pellet is uniaxially pressed, and then dip-coated with a 10 μm yttria stabilized zirconia electrolyte layer. After the microwave co-sintering, La_0.8Sr_0.2MnO_x cathode is screen-printed onto electrolyte and sintered by conventional thermal method. The cell has stably operated in 3% humidified hydrogen for more than 130 h.     

Preparation and electrocatalytic activity of palladium-platinum core-shell nanoalloys protected by a perfluorinated sulfonic acid ionomer

Palladium-platinum nanoalloys with a core-shell and nano-network structure were successfully synthesized by a hydrogen sacrificial protective method in an aqueous solution directly using a perfluorinated sulfonic acid (PFSA) ionomer as a protecting agent. The structure, local composition and electrocatalytic activity for the oxygen reduction reaction of the Pd/Pt/PFSA nanoalloys were investigated by transmission electron microscopy (TEM), aberration corrected scanning transmission electron microscopy (Cs-STEM), energy-dispersive X-ray spectrometry (EDS) and voltammetry. The core-shell structure was completed without contaminating reducing agents, organic solvents, useless protecting agents and a mediator. The Pd/Pt/PFSA core-shell nanoalloys realized a high electrochemical surface area and better electrocatalytic mass-activity for the oxygen reduction reaction than the Pt/PFSA nanoparticles.     

Bulk heterojunction organic solar cells utilizing 1,4,8,11,15,18,22,25-octahexylphthalocyanine

Bulk heterojunction solar cells utilizing soluble phthalocyanine derivative, 1,4,8,11,15,18,22,25-octahexylphthalocyanine (C6PcH₂) have been investigated. The active layer was fabricated by spin-coating the mixed solution of C6PcH₂ and 1-(3-methoxy-carbonyl)-propyl-1-1-phenyl-(6,6)C61 (PCBM). The photovoltaic properties of the solar cell with bulk heterojunction of C6PcH₂ and PCBM demonstrated the strong dependence of active layer thickness, and the optimized active layer thickness was clarified to be 120 nm. By inserting MoO₃ hole transport buffer layer between the positive electrode and active layer, the FF and energy conversion efficiency were improved to be 0.50 and 3.2%, respectively. The tandem organic thin-film solar cell has also been studied by utilizing active layer materials of C6PcH₂ and poly(3-hexylthiophene) and the interlayer of LiF/Al/MoO₃ structure, and a high V_oc of 1.27 V has been achieved.     

Heat and Moisture Transfer and Hygrophysical Changes in Elastoplastic Hollow Cylinder-food During Drying

There are many dried foods of hollow cylinder-shapes in the market. Hygrostress cracks form in these foods during drying without a careful process control. The objective of the present work was to develop a simulation method for heat and moisture transfer in hollow cylinder-food coupled with hygrophysical changes. A modified Luikov's model was used for the development together with a virtual work minimization principle, critical tensile stress criterion for crack formation, and critical crack-tip-opening angle criterion for crack propagation. The developed, computerized simulation model was validated through drying experiments of samples made from a starch hydrate.     

Mercury oxidation by hydrochloric acid over TiO2 supported metal oxide catalysts in coal combustion flue gas

Mercury oxidation by hydrochloric acid over the metal oxides supported by anatase type TiO₂ catalysts, 1 wt.% MO_x/TiO₂ where M = V, Cr, Mn, Fe, Ni, Cu, and Mo, was investigated by the Hg⁰ oxidation and the NO reduction measurements both in the presence and absence of NH₃. The catalysts were characterized by BET surface area measurement and Raman spectroscopy. The metal oxides added to the catalyst were observed to disperse well on the TiO₂ surface. For all catalysts studied, the Hg⁰ oxidation by hydrochloric acid was confirmed to proceed. The activity of the catalysts was found to follow the trend MoO₃ ~ V₂O₅ > Cr₂O₃ > Mn₂O₃ > Fe₂O₃ > CuO > NiO. The Hg⁰ oxidation activity of all catalysts was depressed considerably by adding NH₃ to the reactant stream. This suggests that the metal oxide catalysts undergo the inhibition effect by NH₃. The activity trend of the Hg⁰ oxidation in the presence of NH₃ was different from that observed in its absence. A good correlation was found between the NO reduction and the Hg⁰ oxidation activities in the NH₃ present condition. The catalyst having high NO reduction activity such as V₂O₅/TiO₂ showed high Hg⁰ oxidation activity. The result obtained in this study suggests that the oxidation of Hg⁰ proceeds through the reaction mechanism, in which HCl competes for the active catalyst sites against NH₃. NH₃ adsorption may predominate over the adsorption of HCl in the presence of NH₃.     

Structural analysis and transistor properties of hetero-molecular bilayers

We examined the film morphologies and transistor properties of hetero-molecular bilayer consisting of N, N’-dioctyl-3, 4, 9, 10-perylenedicarboximide (PTCDI-C₈) and quaterrylene. First, the structure and carrier conduction of PTCDI-C₈ films were studied, followed by an analysis of the carrier accumulation process in a PTCDI-C₈/quaterrylene hetero-bilayer transistor. Based on the displacement current measurement (DCM), we stress the potential of the hetero-bilayer for tuning carrier accumulation like carrier doping techniques in field-effect transistors.     

Visualization of epileptogenic phenomena using cross-correlation analysis: localization of epileptic foci and propagation of epileptiform discharges

The main objectives of the preoperative evaluation of a patient with medically intractable epileptic seizures are localization of the foci and propagation of the epileptiform discharges. Electrocorticographic (ECoG) data of intractable focal epilepsy were analyzed using an AR model, wavelet analysis, and cross-correlation analysis. In order to derive the time-shifts, the cross correlations of the epileptiform discharges were calculated between electrodes for every unit of time. Further analyses were made by means of a set of contour maps of the time-shifts and sequential two- and three-dimensional visualizations of the time-shift maps in order to localize the epileptic foci and study their propagation process. Two types of foci and propagation were revealed in the results. In the first type, epileptiform discharges were generated at localized focal sites and spread quickly to other sites. In the second type, the foci of epileptiform discharges, which appeared soon after the former bursts, were localized at more than one site, and the discharges tended to spread more slowly. The findings suggest that epileptic phenomena can be caused by at least two kinds of mechanisms in one patient: in the former, the propagation might be mediated through synaptic projections, while in the latter, the extracellular diffusion of an excitatory factor might play an important role. In addition, our newly developed visualization technique for the localization of epileptic foci and the propagation of epileptiform discharges should prove useful in the study of epileptogenesis etiology.     

Basic design of 70-MW-class superconducting generators

The application of superconductivity technology to electric power apparatus is very important from the viewpoint of energy saving. Especially, the superconducting generators using superconductors as the field windings have many merits compared with conventional generators. Super-GM has been researching and developing 70-MW-class model machines since FY 1988 for a scheduled period of eight years, aiming at a 200-MW-class superconducting generator. This paper describes the basic specifications and designs of 70-MW-class superconducting generators by Super-GM and also describes the propriety of these basic specifications and designs.     

Molecular dynamic simulation of heterogeneity and chemical states of fluorine in amorphous alkaline earth silicate systems

Chemical states of fluorine in fluorosilicate glasses in the system MF₂-MO-SiO₂ (M = Ca, Sr and Ba; SiO₂ content < 60 mol%) have been investigated by molecular dynamic (MD) simulations with a perfect ionic two-body potential. Comparison of the results with those derived by X-ray photoelectron spectra of the actual glasses demonstrates that MD simulations reproduce well the bonding states of fluorine in the systems as well as the formation of M-F clusters. The MD generated structure of imaginary glasses, or glasses not obtained by the conventional melt-quench technique, with 70 mol% SiO₂ indicates that an acidic environment induces a greater amount of F---Si bonds. Their M-F pair correlation functions plotted against normalized M-F distances suggest that relative ion positions in the clusters are very similar.