Precipitates of Cr at Σ3 <110> {112} GB in α-Fe have been studied using molecular dynamics with a two-band embedded atomic model potential. The accumulation and segregation of Cr atoms and the evolution of the GB depend on local Cr concentration and temperature. At the early stage, with the existence of vacancies, the strong attraction of Cr with the GB core provides a pathway for Cr atoms to quickly accumulate within the GB core. With the increase of Cr concentration, the size of Cr dilute precipitates increases dramatically. And the strong segregation of Cr at the GB is observed, when Cr concentration reach 20%. Also, the size of Cr precipitates increases with increasing the temperatures from 300 K to 1000 K. The accumulation and segregation of Cr atoms at the GB lead to significant deformation of the GB structure and the formation of GB steps, causing the displacement and broadening of the GB.

In this paper, single crystal 4H-SiC MEMS devices with n-p-n epitaxial structure was fabricated. A dopant-selective photoelectrochemical etching technique was applied to etch the sacrificial p-type SiC layer to release n-type SiC suspended structures on n-type SiC substrate. The selective etching was achieved by applying a bias which employs the different flat-band potentials of n-SiC and p-SiC in KOH solution. Such MEMS devices have the potential to fully exploit the superior properties of single crystal SiC for harsh environment operation, as well as mature epitaxial growth and device fabrication of 4H-SiC. The n-p-n structure, together with the previously reported p-n structure, extends the capability of monolithic integration between MEMS with electronic devices and circuits on SiC platform.

We studied the structure and mechanical properties of DNA i-motif nanowires by means of molecular dynamics computer simulations. We built up to 230 nm-long nanowires, based on a repeated TC5 sequence from NMR crystallographic data, fully relaxed and equilibrated in water. The unusual C●C+ stacked structure, formed by four ssDNA strands arranged in an intercalated tetramer, is here fully characterized both statically and dynamically. By applying stretching, compression and bending deformations with the steered molecular dynamics and umbrella sampling methods, we extract the apparent Young’s and bending moduli of the nanowire, as well as estimates for the tensile strength and persistence length. According to our results, i-motif nanowires share similarities with structural proteins, as far as their tensile stiffness, but are closer to nucleic acids and flexible proteins, as far as their bending rigidity is concerned. Curiously enough, their tensile strength makes such DNA fragments tough as mild steel or a nickel alloy. Besides their yet to be clarified biological significance, i-motif nanowires may qualify as interesting candidates for nanotechnology templates, due to such outstanding mechanical properties.

It is biologically and clinically important to understand and explain the functional properties of cartilage, such as its load bearing and lubricating ability, in terms of the structure, organization, components and their interactions. Our approach tries to explain functional material properties of these tissues as arising from polymeric interactions between and among the different molecular constituents within the tissues at different hierarchical lengthscales. We treat the tissue effectively as a complex molecular composite containing highly charged polysaccharide microgels trapped within a fine collagen meshwork. We have been developing a multi-scale experimental and theoretical framework to explain key material properties of cartilage by studying those of its constituents and the interactions among them at a variety of length and time scales. We use this approach to address important biological questions. One novel application we highlight here is the use of non-invasive magnetic resonance imaging (MRI) methods to characterize different components and compartments within cartilage and the different water environments associated with each one, in an attempt to provide a comprehensive picture of the mechanical/chemical state of cartilage.

Nax CoO2 has a particularly high contact resistance because it forms an insulated layer of NaHCO3 and Na2CO3, which are produced in a chemical reaction with carbon dioxide and water in air on the surface. In this study, we tried to improve the interface resistance between Nax CoO2 and Ag sheet electrodes by connecting these materials with the spark plasma sintering (SPS) technique. The interface resistance between Nax CoO2 and Ag sheet electrodes connected by SPS is compared with that connected with Ag paste. In an experiment, the interface resistance of a sample treated by decrease to less than 1/600 of the former value. It is thought that the NaHCO3 and Na2CO3 insulated layer is decomposed through the application of a large value of applied DC current by using the SPS technique.

We report on the preparation and characterization of crystalline bismuth oxide thin films via Biased Target Ion Beam Deposition method. A focused blue laser (405nm) is used to write an array of dots in the bismuth oxide thin film and demonstrate clear and circular recording marks in form of “bubbles” or “little volcanos” (FWHM ∼500nm). Results indicate excellent static recording characteristics, writing sensitivity and contrast. The recording mechanism is investigated and is believed to be related to laser-induced morphology change.

Poly(glycerol sebacate) (PGS) is a biodegradable and biocompatible elastomer that has been used in a wide range of biomedical applications. While a porous format is common for tissue engineering scaffolds, to allow cell ingrowth, PGS degradation has been primarily studied in a nonporous format. The purpose of this research was to investigate the degradation of porous PGS at three frequently used cure temperatures: 120°C, 140°C, and 165°C. The thermal, chemical, mechanical, and morphological changes were examined using thermogravimetric analysis, differential scanning calorimetry, Fourier transform infrared spectroscopy, compression testing, and scanning electron microscopy. Over the course of the 16-week degradation study, the samples’ pores collapsed. The specimens cured at 120°C demonstrated the most degradation and became gel-like after 16 weeks. Thermal changes were most evident in the 120°C and 140°C cure PGS specimens, as shifts in the melting and recrystallization temperatures occurred. Porous samples cured at all three temperatures displayed a decrease in compressive modulus after 16 weeks. This in vitro study helped to elucidate the effects of porosity and cure temperature on the biodegradation of PGS and will be valuable for the design of future PGS scaffolds.

The n-type GaN has stability problem of the surface anodic corrosion during the photoelectrochemical reaction for H2 generation. The photoelectrochemical surface stabilities of n-type GaN dependent on the electrolytes were investigated. The flatband potential in HCl obtained from Mott-Schottky plot shifted 0.1 V to positive direction compared with that in H2SO4. The variation of saturated photocurrent of 1 to 3 cycles in H2SO4 was much larger than that of HCl, NaOH and KOH. The surface morphologies also changed by the electrolytes. These results show the absorbed materials on the GaN electrode surface during the photoelectrochemical reactions were changed by the electrolyte and affected the surface reactions.

Scanning acoustic microscopy (SAM), when applied to biological samples has the potential to resolve the longitudinal acoustic wave speed and hence stiffness of discrete tissue components. The heterogeneity of biological materials combined with the action of cryosectioning and rehydrating can, however, create variations in section topography. Here, we set out to determine how variations in specimen thickness influence apparent acoustic wave speed measurements

Cryosections (5μm nominal thickness) of human skin biopsies were adhered to glass slides before washing and rehydrating in water. Multiple regions (200x200 μm; n = 3) were imaged by SAM to generate acoustic wave speed maps. Subsequently co-localised 30x30 μm sub-regions were imaged by atomic force microscopy (AFM) in fluid. The images were then registered using Image J. Each pixel was allocated both a height and wave speed value before their relationship was then plotted on a scattergram. The mean section thickness measured by AFM was 3.48 ± 1.12 (SD) μm. Regional height variations influenced apparent wave speed measurements. A 3.5 μm height difference was associated with a 400 ms-1 increase in wave speed. In the present study we show that local variations in specimen thickness influence apparent wave speed. We also show that a true measure of wave speed can be calculated if the thickness of the specimen is known at each sampling point.

We report successful tuning of laser wavelength from ∼420 nm to ∼600 nm in epitaxially aligned nanofibers grown by periodic deposition of para-sexiphenyl (p6P) and sexithiophene (6T) on p-6P/muscovite mica templates. The nanofibers were photoexcited by subpicosecond pulses tuned to the lowest p6P absorption band, and the emission of 6T, whose coverage was kept in the submonolayer regime, was efficiently sensitized through resonance energy transfer (RET).

The 6T lasing was achieved at room temperature with threshold fluences as low as 10 μJ/cm2 per pulse. Transient photoluminescence measurements, with picosecond resolution, showed that at these pump fluences the decay dynamics of 6T emission is independent of the excitation density, thereby demonstrating the attainment of room-temperature monomolecular lasing from epitaxially oriented 6T submonolayer aggregates. Main lasing properties remained unaltered upon direct photoexcitation of 6T below the p6P absorption edge.

We report, for the first time, effects of annealing of ZnO NWs grown on p-Si substrates. ZnO NWs are grown using metalorganic chemical vapor deposition (MOCVD) and thermal annealing was performed in situ under nitrogen ambient at different stages of the growth process. Increasing the annealing temperature of the ZnO seed epi-layer from 635 °C to 800 °C does not affect the morphology of the grown NWs. In contrast, annealing the NWs themselves at 800 °C results in a 48% decrease of the surface area to volume ratio of the grown NWs. The optical quality can be improved by annealing the seed layer at a higher temperature of 800 °C, although annealing the NWs themselves does not affect the defect density.

Excimer fluorescence of two-component thin films made of pyrene (Py) and polystyrene (PS) can be quenched by the vapor of nitro-aromatic and nitro-ester explosives with a high selectivity and sensitivity. Normally, an electrospun film can be quenched in minutes by the vapor of the explosives. In order to understand the origin of the mechanism, we have investigated the fluorescence quenching rate of the binary thin films as functions of the molecular weights (MW) of the polystyrene (from 2,500 to 900,000 g/mol) and film thicknesses (110nm and 610 nm) in presence of the vapor of 2,4-dinitrotoluene (2,4-DNT, a type of nitro-explosives). The diffusion coefficients of 2, 4-DNT in the solid films are found nearly independent of MW but have strong dependence on the film thicknesses.

The potential effect of high pH plume caused by cementitious materials must be evaluated in the performance assessment for HLW geological disposal. Alkaline plume would lead to change sorption properties of host rock by primary mineral dissolution, secondary mineral precipitation and sequential change of pore water chemistry. In this study, the effect of alkaline alteration on sorption of Cs, Ni and Th was investigated using rock samples from the Horonobe Underground Research Laboratory. Crushed rock samples were reacted in high pH alkaline solution at 90 °C for 45 days, 95 days and 1,383 days, respectively. As a result of sample analysis, it was supposed that zeolitic mineral was precipitated as secondary mineral. The cation exchange capacity slightly increased in comparison with the unaltered sample. Distribution coefficients (Kd) of Cs, Ni and Th on unaltered and altered rock sample were measured by batch sorption experiment in synthetic groundwater. Kd of Cs increased with the alteration period. These results show that secondary minerals contribute to the increase in Cs sorption. By contrast, Kd of Ni and Th decreased with the alteration period. This change might be caused by dissolution of clay minerals and amorphous silicates controlling Ni and Th sorption by surface complexation. These results imply that effects of alkaline alteration on Kd of rocks depend on the dissolution/precipitation of minerals, their surface properties and sorption mechanisms.

The self-assembly of a hydrophobically modified biopolymer (chitosan) is described with particular reference to gelation of these systems. The hydrophobic modification consists of the attachment of long chain alkyl groups inserted randomly along the polysaccharide backbone. The attachment of these alkyl groups to hydrophobic surfaces or the insertion into nonpolar liquids provides a ubiquitous and versatile way to create hierarchical structures, particularly the formation of self-assembled gels. Such self-assembly can be used in a variety of new technologies relating to chromatography, lubrication and the environmental remediation of oil spills through gelation of surface layers.

The detection of hydrogen peroxide has been shown to be very important in recent years due to its role in many industrial applications, as well as in biological reactions. Previously, a commercial silver flake-based ink (PF-410, Acheson®), when screen-printed as films to substrate and subsequently coated with surfactant and salt (sodium dodecylbenezene sulphonate (SDBS) and KCl), have been shown to significantly enhance the electrochemical reduction of hydrogen peroxide – up to 80-fold over non-modified films. In this study, an attempt to understand the effect of the silver material within the ink on the catalytic behaviour of the films, as well as the distinct change in behaviour upon modification with surfactant/salt are examined. Factors including Ag morphology, presence of dispersant and Ag material supplier are all investigated to assess their effects on the electrocatalytic breakdown of hydrogen peroxide. To do this, a range of inks were formulated from various Ag materials, e.g., flakes and nanoparticles of various sizes. These inks were then cast as coatings onto conventional glassy carbon (GC) electrodes, and their electrocatalytic behaviours, both as modified and non-modified films were studied.

Thermoelectric materials based on non-toxic and earth-abundant elements are important from the viewpoint of energy harvesting from the widely-spread waste heat. We have investigated the thermoelectric properties of Cu9Fe9S16, known as the natural mineral mooihoekite or talnakhite. Seebeck coefficient shows a large negative value of about -140 μV/K around room temperature. Thermal conductivity is found to be as small as 2.0 W/Km above 100 K, which is attributed to the large unit cell and the complicated crystal structure. Our results indicate that Cu9Fe9S16 can make a high-performance and environmentally-friendly thermoelectric material if the concentration of carriers, especially holes, is reduced.

Magnetite nanoparticles were produced by the chemical co-precipitation of iron sulfates at alkaline conditions and were tested as a Cr(VI) adsorbent from water. Batch adsorption experiments showed a high removal efficiency, which is maximized at pH values below 6. This behavior was also verified in a continuous flow reactor, where nanoparticles were in contact with the polluted water. In particular, using a particle concentration of 1 g/L in water containing 100 μg Cr(VI)/L, a contact time of at least 2 h was required to achieve complete removal of Cr(VI). The recovery of nanoparticles after their use was accomplished using their magnetic nature. Application of an external magnetic field at the sides of the tube in which the suspension was flowing was sufficient to completely collect the nanoparticles in the outflow of the contact reactor, thus, providing water free of Cr(VI) and a solid phase.

With increasing attention towards long-term health monitoring, there is a pressing need to create noninvasive sensors that monitor vital bioelectronic signals. Particular importance is placed on measuring electrocardiogram (ECG) signals as heart issues are widespread and can be prevented with the proper warning and care of potential problems. Currently, ECGs are taken in a hospital setting using disposable silver-silver chloride (Ag/AgCl) pre-gelled electrodes. Unfortunately, this cannot translate to a long-term monitoring setting due to the electrolytic gel of the electrodes drying and causing skin irritation. This paper presents a soft, skin-mountable dry electrode based on silver nanowires (AgNWs) for measuring ECG signals that can be used in long-term, wearable health monitoring due to the elimination of the electrolytic gel. The AgNWs are embedded in polydimethylsiloxane (PDMS), which creates a robust design that will not suffer from delamination or cracking problems that can eventually lead to loss of conductivity. The electrode is characterized by electrode-skin impedance as a function of frequency and by the surface resistance as the electrode is stretched. The performance of the dry electrode is evaluated and comparable to that of conventional Ag/AgCl electrodes. The ability of the dry electrode to conform to skin is believed to compensate for the lack of an electrolytic gel.