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Dense thin β/β’’-alumina electrolyte films of less than 50 μm thickness were fabricated using vacuum dip-coating on porous substrate tubes. The porous substrate tubes were fabricated using a slip casting method. Fine Na-β/β’’-alumina powder was obtained via traditional solid state reaction processing. It was found that vacuum dip-coating is an effective method for fabricating thin dense layers coated on the porous tube. The mechanical properties of the porous tube, with and without the dense layer, were tested using a C-ring method. The optimized sintering process was also studied.
We investigated carrier dynamics in both proton-irradiated InAs-GaAs quantum dot laser structures and in high power broad-area InAs-GaAs quantum dot lasers with windowed n-contacts using time-resolved PL (TR-PL) techniques.
Cu2ZnSnS4 (henceforth CZTS) absorber layers are successfully synthesized by a sulfurization technique of physical vapor deposited precursors. In our previous report, we have clarified that the off-stoichiometry composition of Cu-poor and Zn-rich is desirable to achieve high conversion efficiency. By using CZTS compound target that provide such active composition, we could conduct a simple single sputtering method to prepare CZTS absorber. In our laboratory, a two-stage process of precursor preparation followed by sulfurization is a major fabrication method from the start of this study. We think that this method is suitable for a mass production. An optimization of the sulfurization process is a quite important issue because the active composition was already revealed. In this paper, TG/DTA system available in the H2S atmosphere is introduced to optimize the sulfurization condition. As a result, bump-free CZTS films were prepared successfully and the fluctuation of J-V properties in one substrate was drastically suppressed.
The mechanical characteristics of ionic-covalent entanglement hydrogels consisting of combinations of the biopolymers gellan gum and kappa-carrageenan, and the synthetic polymers polyacrylamide and an epoxy amine were investigated. Compression testing showed that these gels exhibited “double network” behavior, i.e. strong tough gels.
We examine the electron transport that occurs within a zinc-oxide-based two-dimensional electron gas using Monte Carlo simulations. The sensitivity of the results to variations in the lowest energy conduction band valley electron effective mass is examined. Increased values of the electron effective mass result in diminished electron drift velocities and reduced sensitivity to the free electron concentration. In agreement with our previous studies for a fixed value of the electron effective mass [11], we find that the reduced scattering due to the screening of the impurity and polar optical scattering leads to a slightly higher mobility of the 2DEG at low-fields but reduces the peak velocity, since gaining a higher energy due to the reduced polar optical phonon scattering enhances the effects of the non-parabolicity within this material.
To evaluate a change of chemical species of groundwater composition by the metabolism of microbes, which will be introduced to deep underground from the surface and be in a deep underground, is important for the discussion of the microbial effects on the performance assessment of the high-level radioactive waste repository. The purpose of this study is to develop of a microbial kinetics database to evaluate their activities in the deep underground environment.
Some microbial metabolism data were collected and constructed their kinetics database for aerobic, denitrifying, manganese reducing, iron reducing, sulfate reducing, methanogenic and acetogenic bacteria to evaluate above groundwater chemistry. About 1260 data were selected by literature survey for some journals and books published from 1960s and summarized in this microbial kinetics database. Some sensitivity analyses were performed for some parameter of metabolism of microbes.
The rapid release of fission products segregated either to the gap between the fuel and the cladding or to the UO2 grain boundaries from spent nuclear fuel in contact with water (often referred to as the instant release fraction - IRF) is of interest for the safety assessment of geological repositories for spent fuel due to the potential dose contribution. In September 2012 a study was initiated with the aim of comparing the instant release behavior of fuels with and without additives/dopants. Preliminary results from this (ongoing) study indicate that the release of uranium during the first contact periods was higher than during the tests with fuel segments, even though the fuel was cut open recently [1]. This could be due to the sample preparation method which included axial cutting of the cladding in order to remove the fuel fragments used in the study. In the present work, leaching data from both studies are presented and the releases are discussed comparing the two sample preparation methods and considering the effect of matrix composition. The leaching studies have been performed in air using 10 mM NaCl + 2 mM NaHCO3 as leaching solution.
Multi-functionalization of catalytically-active nanomaterials provides a valuable tool for enhancing reaction yield by shifting reaction equilibrium, and potentially also by adjusting reaction-diffusion kinetics. For example, multi-functionalization of mesoporous silica to make the interior pore surface hydrophobic can enhance yield in dehydration reactions. Detailed molecular-level modeling to describe the pore environment, as well as the reaction and diffusion kinetics is challenging, although we briefly discuss current strategies. Our focus, however, is on coarse-grained stochastic modeling of the overall catalytic process for highly restricted transport within narrow pores (with single-file diffusion), while accounting for a tunable interaction of the pore interior with reaction products. We show that making the pore interior unfavorable to products can significantly enhance yield due to both thermodynamic and kinetics factors.
The effects of N2O gas addition on the properties of zinc oxide films grown on a-plane (11-20) sapphire (a-Al2O3) substrates were investigated, using a chemical vapor deposition method based on the reaction between dimethylzinc and high-energy H2O produced by a Pt-catalyzed H2-O2 reaction. By employing an optimal N2O gas pressure, both the film crystallinity and crystal orientation were improved. Subsequent to treatment with N2O, the electron mobility of films at room temperature increased from 207 to 234 cm2/Vs while the electron concentration decreased at low temperatures. In addition, the photoluminescence peak intensity of the nearband-edge emission was increased.
Adsorption of charged biomolecules onto atomically flat mica substrates is facilitated by the deposition of metal ions. Despite successfully acting as preferential anchoring sites, the presence of ions on the mica surface also changes its physicochemical characteristics something that is rarely quantified from a nanoscale point of view. In this study the nanoscale physicochemical properties of nickel-functionalized Muscovite mica are investigated by reconstructing the conservative force profile between an atomic force microscopy (AFM) tip and the surface. Various nickel ion concentrations (i.e. 1.0 mM to 20.0 mM) along with different incubation times (30 seconds and 5 minutes) are directly analyzed. Details in the spatial and temporal variations in surface properties due to the ion mediated adsorption of water are presented in details and in light of the binding efficiency of the metal ions. This insight benefits our understanding in the behavior of ion distribution that plays a crucial role in biomolecule imaging using AFM.
Carbon fine particles including single-walled carbon nanotubes (SWNTs) were synthesized by hot-filament and plasma assisted chemical vapor deposition. Specific surface area was evaluated for carbon fine particles synthesized under optimized conditions along with purified SWNTs and multi-walled carbon nanotubes (MWNTs) for comparison. The value of specific surface area for the synthesized carbon fine particles was smaller than the SWNTs, but larger than the MWNTs. Pore size distribution was analyzed with desorption isotherms by the DH method. Although smaller pores are included in the purified SWNTs than the synthesized carbon fine particles, pores of size larger than several nm were included more in the synthesized carbon fine particles.
In this contribution we report on the optical properties of cubic AlN/GaN asymmetric multi quantum wells (MQW) structures on 3C-SiC/Si (001) substrates grown by radio-frequency plasma-assisted molecular beam epitaxy (MBE). Scanning transmission electron microscopy (STEM) and spatially resolved cathodoluminescence (CL) at room temperature and at low temperature are used to characterize the optical properties of the cubic AlN/GaN MQW structures. An increasing CL emission intensity with increasing film thickness due to the improved crystal quality was observed. This correlation can be directly connected to the reduction of the linewidth of x-ray rocking curves with increasing film thickness of the c-GaN films. Defects like stacking faults (SFs) on the {111} planes, which also can be considered as hexagonal inclusions in the cubic crystal matrix, lead to a decrease of the CL emission intensity. With low temperature CL line scans also monolayer fluctuations of the QWs have been detected and the observed transition energies agree well with solutions calculated using a one-dimensional (1D) Schrödinger-Poisson simulator.
This work reports a carbon-free, blue-enhanced a-Si:H n-i-p photodiode with an optimized protocrystalline p-layer. Although the used deposition conditions for the p-layer correspond to the microcrystalline regime, thin layers are mostly protocrystalline due to the amorphous underlying undoped layer. This conclusion is supported by Raman spectroscopy measurements. We have also found that the optical band gap of the p-layer can be varied by adjusting the rf power. By widening the band gap and tuning the impurity concentration in the p-layer, absorption and recombination losses at the p-i interface were reduced. The current-voltage, capacitance-voltage, and spectral-response characteristics of fabricated photodiodes are correlated with the doping level, optical band gap, and deposition conditions for p-layers. The optimized device exhibits a leakage current of about ∼80 pA/cm2 at 5 V reverse bias. The external quantum efficiency reaches a peak value of 92% at a wavelength of 510 nm, and, at shorter wavelengths, decreases down to 66%@400nm.
The formation of the structure of geopolymer binders based on low-calcium fly ash is a multifactorial process that depends on the degree of solubility of aluminosilicate components in the solution of alkali activator. It is observed that the geopolymer binders based on fly ash with an identical chemical and mineral composition, the same grain size, and also activated by the same alkalis can result in a different strength.
This study is based on the assumption that there is dependence between the solubility of aluminosilicate components and the degree of polymerization of the silicates in glass phase. The degree of SiO2-polymerization is an integral parameter that is equal to the Si molar ratio (fSi) of the silicate component in the glass phase of fly ash. The degree of SiO2-polymerization can be estimated from the molar composition of glass phase, which is determined from the chemical composition and quantitative X-ray diffraction analysis including identification of the amorphous phase composition.
The SiO2 polymerization rates of investigated fly ash specimens are confirmed by the IR results, specifically, by comparison of absorption bands of silicate fragments with varying levels of connectivity (Q0-4) in the range of wave numbers of 650–1350 cm-1.
The comparative analysis of the correlation of 28-day strength of geopolymer binders based on fly ash from different sources and level of SiO2-polymerization demonstrated an inverse relationship with fSi molar ratio and compressive strength.
To provide a counter electrode with lower-cost and simple production method for dye-sensitized solar cells (DSSCs), we developed polyaniline/graphene nanoplatelet/multi-walled carbon nanotube (PANi/GNP/MWCNT) composite films growing on glass substrates by using chemical/electrochemical deposition method and on fluorine-doped tin oxide (FTO)/glass substrates by using electrochemical deposition method respectively. A proper weight ratio of PANi/GNP/MWCNT (1/0.0030/0.0045) composite film depositing on FTO substrate as counter electrode with sheet resistance of 8.25±0.13 Ω/sq for DSSCs yielded power conversion efficiency (PCE) up to 7.45±0.08%, which has potential to replace the conventional Pt cell (7.62±0.07%). In addition, we also fabricated the DSSCs composed of a proper weight ratio of PANi/GNP/MWCNTs (1/0.0045/0.0060) composite film depositing on glass substrate as counter electrode. The sheet resistance of resulting composite film was 59.34±12.34 Ω/sq. These solar cells with FTO-free counter electrode exhibited a PCE of 2.90±0.09%.
Duplex stainless steels are commonly used for various applications owing to their superior corrosion resistance and/or strength. They have ferromagnetic behavior together with a good thermal conductivity and a lower thermal expansion as a result of higher ferrite content than austenitic steels. Their ferrite matrix suffers a decomposition process during aging in the temperature range 650-950° C producing precipitation of austenite, σ and χ, carbides and nitrides. These intermetallic phases are known to be deleterious for corrosion resistance and mechanical properties.
In this work the effect of aging time during isothermal treatment at 850°C and 900°C on the microstructure of SAF 2205 Duplex Stainless Steels welded plates has been investigated. The aim of this work is to determine the morphology of σ phase, and perform a quantitative analysis of the precipitation process.
Submerged Arc Welding is used for processing. It produces a high content of δ ferrite in the heat affected zone and low content of austenite in the weld. Microstructural examination shows that the σ phase precipitates at δ ferrite/γ interphases. Longer aging treatments give rise to an increase of volume fraction together with a coarser morphology.
This paper presents the first attempts to study the large conductance mechano-sensitive channel (MscL) activity in an artificial droplet interface bilayer (DIB) system. A novel and simple technique is developed to characterize the behavior of an artificial lipid bilayer interface containing mechano-sensitive (MS) channels. The experimental setup is assembled on an inverted microscope and consists of two micropipettes filled with PEG-DMA hydrogel and containing Ag/AgCl wires, a cylindrical oil reservoir glued on top of a thin acrylic sheet, and a piezoelectric oscillator actuator. By using this technique, dynamic tension can be applied by oscillating axial motion of one droplet, producing deformation of both droplets and area changes of the DIB interface. The tension in the artificial membrane will cause the MS channels to gate, resulting in an increase in the conductance levels of the membrane. The results show that the MS channels are able to gate under an applied dynamic tension. Moreover, it can be concluded that the response of channel activity to mechanical stimuli is voltage-dependent and highly related to the frequency and amplitude of oscillations.
In the recent time spinel ferrite magnetic nanoparticles have been largely studied owing to various applications of these materials in the information storage, ferro-fluid technology, magnetocaloric effect, refrigeration and medical diagnostics. In this category cobalt ferrite (CoFe2O4) nanoparticles specifically gained huge research attention and prepared by various chemical methods. However, further investigations are still needed on the substituted CoFe2O4 (CFO) nanoparticles to explore their various characteristics. In this paper we present our results on Mn and Zn substituted cobalt ferrite (Co0.6Zn0.4Mn0.3Fe1.7O4 ) nanoparticles prepared by chemical co precipitation method. The x ray diffraction pattern of as prepared Co0.6Zn0.4Mn0.3Fe1.7O4 (CZFMO) nanoparticles indicated their average particle size =20 nm. Magnetic properties of these nanoparticles before and after thermal annealing have been compared. Magnetization (M) vs. field (H) loop measurements at T = 293 K on as prepared and thermally annealed CZFMO nano powders revealed an unusual feature contrary to CFO nanoparticles prepared under same conditions. The saturation magnetization (Ms) decreases after the thermal annealing unlike the usual increase in Ms observed for CFO nanoparticles. These nano sized CZFMO powder samples are further characterized by low temperature magnetic measurements; Raman spectroscopy and Fourier transform infrared spectroscopy.
Physically crosslinked polyvinyl alcohol (PVA) hydrogels with high mechanical properties can be made by a low temperature crystallization method using a mixed solvent of dimethyl sulfoxide (DMSO) and water. Such hydrogels are studied as the artificial articular cartilage material. But DMSO shows cytotoxycity, and it is also have the effect of accelerating the absorption of harmful substances. Therefore completely elimination must be required for clinical application but the process is difficult.
However, PVA hydrogel made by water as a sole solvent by freeze-thawing method became cloudy because of micro-heterogeneous structure, and shows low mechanical properties.
Therefore, in this study, we developed the novel hot pressing method for preparing transparent and uniformly cross-linked PVA hydrogels without DMSO from highly concentrated aqueous solution. By this method, PVA hydrogels with high mechanical property and high transparency can be obtained without any harmful organic solvent because of the fast crystallization even at room temperature. The mechanical properties of PVA hydrogels were remarkably depended on their water contents after gelation, regardless of solution concentration.