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Model alloys have been made of pure W and 1% & 5% W-Ta and W-Re. Indentation hardness and modulus data were obtained by nanoindentation to assess the effect of composition on mechanical properties. Results showed that both the Ta and Re compositions hardened with increasing alloy content, greater in the W-5%Ta composition which showed an increase of 1.03GPa (17%), compared to a 0.43GPa (7%) increase in W-5%Re. The samples also showed very small increases in modulus of ∼ 25GPa (6%) in both W-5%Re and W-5%Ta. The samples were implanted with 3000appm concentration of helium. All samples show a substantial increase in hardness of up to 107% in the case of pure W. An appreciable difference in modulus is also seen in all samples. Initial TEM work has shown no visible He bubbles, suggesting that the mechanical properties changes are due to He-vacancy cluster formation below the resolvable limit.
Deoxyribonucleic acid (DNA) immobilization on nanoscale architectures is critical for developing bio-compatible devices and clinical diagnoses. In this study, silicon nanowires (SiNWs) were combined with gold nanoparticles encapsulated in graphitic shells (GNPs). The resulting SiNWs-GNPs heterostructures were plasma oxidized to create carboxylic (-COOH) functionality on the surface of the graphitic carbon shell. These heterostructures and their surface chemistries were studied using electron microscopy, Fourier transform infrared spectroscopy (FT-IR), and Raman spectroscopy. The –COOH terminated graphitic shells in heterostructures were covalently linked with DNA. The DNA molecules on these heterostructures were detected by linking with fluorescent streptavidin and observed under a fluorescence microscope. Such inorganic heterostructure-biomolecule assemblies can be very useful in the development of biomolecule analysis and detection devices.
Very recently, Cu3BiS3 has been suggested as an alternative material for photovoltaic (PV) thin-film technologies. In this work, we analyze the electronic and optical properties of Cu3BiY3 with the anion elements Y = S, Se, and Te, employing a first-principles approach within the density function theory. We find that the three Cu3BiY3 compounds have indirect band gaps and the gap energies are in the region of 1.2–1.7 eV. The energy dispersions of the lowest conduction bands are small, and therefore the direct gap energies are only ∼0.1 eV larger than the fundamental gap energies. The flat conduction bands are explained by the presence of localized Bi p-states in the band gap region. Flat energy dispersion implies a large optical absorption, and the calculations reveal that the absorption coefficient of Cu3BiY3 is larger than 105 cm−1 for photon energies of ∼2.5 eV. The absorption is stronger than other Cu-S based materials like CuInS2 and Cu2ZnSnS4. Thereby, Cu3BiY3 has the potential to be a suitable material in thin-film PV technologies.
We have investigated BisGMA-TEGDMA dental composites with varying mass fractions of hydroxyapatite and silica filler. Commercially available dental composites with 60% silica filler were synthesized in the presence of nanometer-sized hydroxyapatite crystals. We have compared the mechanical properties of BisGMA-TEGDMA samples filled with silica only and those filled with silica and hydroxyapatite particles. We report on hardness as a function of crystalline content as determined by nanoindentation and microindentation.
Oblique-angle deposition is used to fabricate indium tin oxide (ITO) optical coatings with a porous, columnar nanostructure. Nanostructured ITO layers with a reduced refractive index are then incorporated into antireflection coating (ARC) structures with a step-graded refractive index design, enabling increased transmittance into an underlying semiconductor over a wide range of wavelengths of interest for photovoltaic applications. Low-refractive index nanostructured ITO coatings can also be combined with metal films to form an omnidirectional reflector (ODR) structure capable of achieving high internal reflectivity over a broad spectrum of wavelengths and a wide range of angles. Such conductive high-performance ODR structures on the back surface of a thin-film solar cell can potentially increase both the current and voltage output by scattering unabsorbed and emitted photons back into the active region of the device.
We demonstrate the superior inductive properties of coiled carbon nanotubes (CCNTs) through numerical computation and analytical modeling, for the next generation of nanoscale, on-chip inductors. Taking advantage of the kinetic inductance (Lk), particularly evident at the nanoscale we find that the inductance can be increased by three orders of magnitude through changing the tube radius as well as the coil radius while the device footprint of the CCNTs can be reduced by 60%. By varying the geometric parameters of the coiled structure, the external magnetic inductance (LM,ext) can be as high as 20% of the Lk. We also report that the self resonant frequency (fSR) of CCNTs can be as much of the order of THz whereas the fSR of conventional copper(Cu) spiral inductors are limited to around 40GHz. Moreover when the material volume is considered, CCNTs have the potential to achieve Quality Factor (Q) eight times as Cu and when the footprint volume is considered Q can be twice as Cu All these promising properties of CCNTs make them a potential candidate for the entire frequency spectrum.
Carbon/carbon composites (C/C composites) possess superior characteristics of low density, high strength, extremely low coefficient of thermal expansion, high fatigue resistance. In carbonization process, the high temperature pyrolysis made of carbon, hydrogen, oxygen and other elements, results in a lot of voids and cavities generated in the interior of C/C composites. Therefore, the C/C composites are densified to fill the void by using repeated impregnation. But densification is a time-wasting and complex process, which increases production costs in the manufacturing process.
In this study, the Multi-Wall Carbon Nanotubes (MWNTs) were adopted as reinforcement material for C/C composites to reduce the existence of voids or cavities and enhance the mechanical properties of C/C composites under environment aging effects. Three different temperature with high moisture conditions are used to be tested, including high temperature (150°C/ 90%RH), room temperature (25°C/90%RH), and low temperature (-15°C/90%RH) to analyze the mechanical properties of C/C composites, such as flexural and Interlaminar Shear Strength (ILSS).
We used sporopollenin prepared from Lycopodium Clavatum to encapsulate living yeast cells as a model for probiotics. The microencapsulation of cells was achieved by using the trilite scars of the sporopollenin microcapsules which can open up by compressing the sporopollenin into a pellet. Such compressed pellets were exposed to an aqueous suspension of yeast cells in the presence of a biocompatible surface active agent which allowed living cells to be loaded inside the sporopollenin particles by the influx of liquid to the sporopollenin interior as the deformed microcapsules re-inflated to their original state. We demonstrated that the cells viability and biological activity is preserved after the microencapsulation in the sporopollenin. Such microencapsulation technology could find application in preserving cells from mechanical stress and aggressive environments which can be used in protection of probiotics in food formulations.
In situ imaging using (scanning) transmission electron microscopy has proven to be an extremely important and powerful cross-disciplinary scientific technique. In particular nanotechnology and materials sciences have special interest in assembly and disintegration processes, in growth and shape-tuning of (nano)-particles, and, furthermore in mechanistic studies of chemical reactions underlying these processes. However, limitations for in liquid and in situ imaging using electron microscopy arise from the stringent experimental conditions required with respect to electron scattering.
Here, we present a nanofluidic sample cell allowing for controlled fluidic conditions which preserve the highest possible spatial resolution for in-liquid electron microscopy. The nanocell allows for liquid flow with a flow control mechanism operated external to the microscope column enabling on-the-fly sample exchange within the imaging area. A well-defined flow path allows us to direct the motion of gold nanorods through fluid flow. Further a particle’s Brownian motion becomes evident once the external flow is terminated. In addition to quantitatively showing the resolution capabilities of our nanofluidic design, we show preliminary results of in situ imaging of gold nanorods and unstained amyloid fibrils to emphasize the significance of this imaging modality for both material sciences and biology.
The efficacy of vertically aligned defect engineered multi-walled carbon nanotube (MWCNT) arrays as electrochemical double layer capacitors (EDLCs) was investigated using standard electrochemical techniques such as cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). We report a ∼ 200% improvement in specific double layer capacitance of MWCNT arrays by extrinsically introducing defects using argon plasma irradiation. The capacitance-voltage characteristics of argon irradiated MWCNTs provide insights into the nature of the defects and their influence on the specific capacitance (capacitance/area).
The general public is typically positive towards ‘Nano’, but often have limited and anecdotal information from which to draw informed conclusions. We present lessons learned from a new demonstration for 1-on-1 and small group science expo table use that appears to captivate and lead to active learning for ages seven to adult. ‘Making Nanoparticles with Ouzo’ covers: 1. issues in measuring and seeing small particles; 2. light as having wave properties with wavelengths in the nm range; 3. using green (510 nm) and red (650 nm) laser pointers as ‘rulers’; 4. using the liqueur Ouzo (a blend of water, alcohol and water insoluble anethole oil) to illustrate and ‘illuminate’ nanoparticles invisible to the naked eye; 5. demonstrating that the anethole particles do not initially scatter laser light, but do as water is added and particle sizes increase; 6. allowing a visitor to ‘make nanoparticles’ by warming up a cold dispersion of cloudy anethole particles (micron size) in warm water until they vanish.
Although a lot of information is presented, a surprising amount of it seems to stick, if it is presented and built in story form from widely appreciated concepts, with samples and props people can see and hold, and with a few diagrams and written descriptions.
The synthesis of hierarchically assembled Al-doped ZnO layers by Pulsed Laser Deposition (PLD) at room temperature was investigated. PLD was performed in a background pressure of 100 Pa O2 to deposit clusters in a low energy regime and obtain nano- and mesostructures resulting from a hierarchical assembly of nanoclusters. We here analyzed the effects of varying the gas flow rate on mesoscale morphology, mass density and optical properties. The variation of the target-to-substrate distance was also investigated, identifying its effects on mass density and film morphology. The optimization of optical properties in terms of transparency and light scattering capability is of potential interest for photovoltaic applications.
The symmetry properties of many inorganic two-dimensional monolayer crystals make them piezoelectric, whereas their three-dimensional parent crystals are not. The emergence of piezoelectricity in the single-layer limit points toward intriguing electromechanical effects and applications in the single- or few-layer regime. We use density functional theory to calculate the piezoelectric coefficients of BN, MoS2, MoSe2, MoTe2, WS2, WSe2 and WTe2. These coefficients are found to be comparable to, and in some cases greater than those of commonly used wurtzite piezoelectrics. The centrosymmetry of a BN bilayer prevents a piezoelectric effect for this structure. However, by developing an elastic model, we find that the bilayer exhibits an unusual electromechanical coupling to the curvature, similar to that of a bimorph. A BN bilayer is found to amplify the constituent monolayers’ in-plane piezoelectric displacements by factors on the order of 103-104 into out-of plane deflections.
Organic single crystals are an established part of the emerging field of organic optoelectronics, because they provide an ideal platform for the studies of the intrinsic physical properties of organic semiconductors. As organic crystals have low melting temperatures and high vapor pressures and are soluble in numerous organic solvents, both solution and gas-phase methods can be used for crystal growth. The nature of the individual molecules and the interactions between molecules determine which growth method is preferred for particular materials. Organic semiconductors with very low decomposition or melting temperatures can be grown from solutions, whereas semiconductors with high vapor pressures can be grown using physical vapor transport methods. High-quality crystals can be obtained using both methods. Crystal growth and crystal engineering of multicomponent organic compounds are emerging fields that can provide a variety of new materials with different physical properties. The growth of large crystals from the melt by zone melting, the Bridgman, or the Czochralski methods has been used to produce stable materials used in wafer manufacturing or large scintillator detectors. In this article, single-crystal growth methods for organic semiconductors are discussed with the aim of preparing high-quality specimens for determination of the basic properties of organic semiconductors.
An effective n-type doping of ZnO using Cl was demonstrated in thin films electrochemically synthetized by adding different amounts of chlorine ions in the starting electrolyte. The ratio between chlorine and zinc cations was varied between 0 and 2 while the zinc concentration in the solution was kept constant. When the concentration of chloride in the bath increases an effective n-type doping of ZnO films takes place. n-type doping is evidenced by the rise of donors concentration, obtained from Mott-Schottky measurements, as well as from the blue shift observed in the optical gap owing to the Burstein-Moss effect.
Mesoporous carbon aerogel has been impregnated with iron (10 and 15 wt. %) as a catalyst for graphitization by wet incipient method. The iron modified and non-modified carbon aerogels were heat treated at 900°C, 1200°C, and 1400°C in argon. The crystal structure, morphology, and electro catalytic activity of the resulting nano-composites have been studied. It was found that, the degree of graphitization was proportional to the concentration of Iron phase and the ratio of iron to iron nitride phase in the heat-treated samples. In carbon aerogel sample sintered at 1200°C with 15 wt. % of iron phase, mesoporosity in the range of 3-4 nm and microporosity (< 2nm) was significantly improved by graphitization without affecting the Carbon Aerogels mesoporosity in 10-30 nm range. In this case of 15 wt. % iron doped samples, HRTEM analysis confirms the presence of uniformly distributed ∼43.5nm iron nanoparticles surrounded by graphene layers. Correspondingly, improved graphitization and presence of iron nitride resulted in 3.65 electron assisted oxygen reduction reaction.
The ability to efficiently harvest heat as a source of sustainable energy would make a significant contribution to reducing our current reliance on fossil fuels. Waste heat sources, such as those produced in industrial processes or through geothermal activity, are extensive, often continuous, and at present severely underutilised. Thermoelectrochemical cells offer an alternative design to the traditional semiconductor-based thermoelectric devices and offer thepromise of continuous and cheap operation at moderate temperatures, low maintenance and with no carbon emissions. They utilise two electrodes, held at different temperatures, separated by an electrolyte containing a redox couple. It is the temperature dependence of the electrochemical redox potential that generates the potential difference across the device as a result of the appliedtemperature difference. The magnitude of this redox potential temperature dependence is given by the Seebeck coefficient, Se. Until recently, research into thermoelectrochemical cells had primarily focused on aqueous media, predominantly with the Fe(CN)63-/4- redox couple.[1] However, the good thermal and electrochemical stability, non-volatility and non-flammability ofmany ionic liquids make them promising alternative electrolytes for these devices. The use of ionic liquid (IL) electrolytes offers potential advantages that include increased thermoelectrochemical device efficiencies and lifetimes and the ability to utilise low temperature (often “waste”) heat sources in the 100 – 200 °C temperature range.[2] Here we discuss our research into the use of the Fe(CN)63-/4- redox couple in protic IL electrolytes, with different amounts of added water, in a thermoelectrochemical device with platinum and single walled carbon nanotube (SWNT) electrodes.
In this study, in order to investigate biocompatibility of nitrogen-doped hydrogenated amorphous carbon (a-C:H:N) film coating segmented polyurethane (SPU) scaffold fiber sheet (a-C:H:N-Scaffold) in in-vitro test, mouse fibroblasts (NIH 3T3) cells were grown on the a-C:H:N-Scaffold. The cell behavior was monitored by time-lapse imaging system. Additionally, the a-C:H:N-Scaffold was implanted at partial aorta descendens of a goat for 35 days. The surface morphology, composition, and wettability of the a-C:H:N-scaffold was estimated by Scanning Electron Microscope (SEM), X-ray photoelectron spectrometer (XPS), and contact angle measurement. In in-vitro test, it was observed that a-C:H:N film coating had a facilitatory effect on cell motility and cell growth. In in-vivo test, it was observed that the a-C:H:N-Scaffold surface was uniformly covered by neointima. The a-C:H:N-Scaffold surface had no thrombus formation as an inflammatory reaction and it was shown that the a-C:H:N film coating had a good blood compatibility. These results suggest that a-C:H:N film coating has good cytocompatibility and blood compatibility and it is a promising approach for improvement of biocompatibility of biomaterial surfaces.
Light-emitting electrochemical cells (LECs) are one of the simplest electroluminescent devices. The possibility to be processed from solution and to operate with air-stable materials makes them an attractive alternative to organic light emitting diodes (OLEDs). Still their efficiencies are below those obtained in OLEDs. Additionally the best efficiencies were reported at low luminances and sustained for a short period of time. Here we show that for a LEC employing an orange-emitting charged iridium complex that is driven using a pulsed driving scheme high efficiencies of up to 20.5 cd A-1 can be obtained at high luminance and sustained over the device lifetime. It is also shown that the efficiency depends strongly on the current density applied.
Highly transparent conductive Ga-doped ZnO (GZO) films are one of the promising transparent conductive oxide (TCO) films for use in electrodes of flat display panels and window layers of thin film solar cells. For the ZnO-based TCO films, the stability to damp-heat environment is a crucial issue for practical applications. We will report moisture resistant GZO codoped with indium films (GZO:In) on the basis of analysis of data obtained a damp-heat test for solar cells (85°C and 85% relative humidity for 1000 hours).
We used ZnO sintered targets with contents of 3 wt% Ga2O3 and 0.25 wt% In2O3 to grow GZO:In films in ion plating with direct current arc-discharge system. GZO:In films with different thicknesses (0.1-1 μm) were deposited on glass substrates at 200°C under the O2 flow rate of 15 sccm. As the film thickness increased from 0.1 to 1 μm, the resistivity and sheet resistance decreased from 4.3 μΩm to 2.6 μΩm and from 42.7 Ω/Sq. to 2.6 Ω/Sq., respectively. And the average optical transmittance (Tav) in the range from 0.4 to 1 μm decreased from ∼ 86% to ∼ 75%. The GZO:In film with a thickness of ∼300 nm had a low sheet resistance of 10.5 Ω/Sq. and a Tav of 82.5%. After 1000 hours damp-heat (DH) test under 85°C and 85% relative humidity, the relative change of sheet resistance is 3.4% with a Hall mobility of 26.4 cm2/V.s and a Tav of 82.7% after test. The film thicker than 300 nm has a sheet resistance lower than 10 Ω/Sq. and a relative change of resistance of ∼3% after DH test.