A temperature dependent Hall Effect measurement system with software based data acquisition and control was built and tested. Transport measurements are shown for boron-doped single crystal diamond (SCD) films deposited in a microwave plasma-assisted chemical vapor deposition (MPCVD) reactor. The influence of Ohmic contacts and temperature control accuracy are studied. For a temperature range of 300K-700K IV curves, Hall mobilities and carrier concentrations are presented.

Periodically textured back reflectors with hexagonal dimple arrays are applied to thin-film microcrystalline silicon (μc-Si:H) solar cells for enhancing light trapping. The period and aspect ratio of the honeycomb textures have a big impact on the photovoltaic performance. When the textures have a moderate aspect ratio, the optimum period for obtaining a high short circuit current density (J SC ) is found to be equal to or slightly larger than the cell thickness. If the cell thickness exceeds the texture period, the cell surface tends to be flattened and texture-induced defects are generated, which constrain the improvement in J SC . Based on these findings, we have fabricated optimized μc-Si:H cells achieving a high active-area efficiency exceeding 11% and a J SC of 30 mA/cm2.

In this paper, the Lattice Statics formalism is used to perform Monte Carlo simulations of alloy microstructures when elastic effects are present. It provides sets of long-range effective pair interactions (EPIs), defined in a rigid average reference state, that allow us to compute microstructural evolutions on diffusion time scale. A wide composition range is investigated in order to characterize the different precipitation processes with elasticity (nucleation and growth, spinodal decomposition). An advantage of the approach is to include the concentration dependence of both the effective chemical interactions and the elastic properties of the reference state. The importance of this point is illustrated by comparing the precipitation sequences in two alloys with symmetric average concentrations.

Flexible substrates, like plastic, paper and cotton fabrics can be of interest for several reasons in connection to the appealing issue of generating voltage-current from piezoelectric ZnO nanowires (NWs). Zinc oxide NWs have shown very high voltage generation and they are possible to grown on plastic, paper and cotton. Since we with these substrates can get a new freedom to bend and also stretch the NWs and to incorporate them into new applications they are of great potential. Here we will describe the mechanical and piezoelectric properties of ZnO NWs grown on ordinary clean room paper and on cotton fabrics substrates as well as possibility of coating the ZnO NWs to maximize the output generated power. An enhancement of 160 times in the piezo-potential was observed from ZnO NWs coated with P3HT p-type polymer compared to non-coated NWs.

To investigate template releasing process in nanoimprint lithography, template releasing energy (i.e. surface energy between the template and the resist polymer) in various releasing conditions is evaluated using multi-axial controlled releasing system. The releasing energy is in proportion to the surface free energy of the template, but does not depend on the velocity of releasing. Also, a peeling mode where the template is released from a single side and a lift-off mode where the template is removed in the perpendicular direction to the resist are examined. The result shows that the releasing energy by peeling mode is lower than that by lift-off modes.

Quaternary semiconductors, Cu2ZnSnS4 and Cu2ZnSnSe4 which contain only earth-abundant elements, have been considered as the alternative absorber layers to Cu(In,Ga)Se2 (CIGS) for thin film solar cells although CIGS-based solar cells have achieved efficiencies over 20 %. In this work we report an air-stable route for preparation of Cu2ZnSn(Sx,Se(1-x))4 (CZTSSe) thin film absorbers by a solution process based on the binary and ternary chalcogenide nanoparticle precursors dispersed in organic solvents. The CZTSSe absorber layers were achieved by spin coating of the ink precursors followed by annealing under Ar/Se atmosphere at temperature up to 580°C. We have investigated the influence of the annealing temperature on the reduction or elimination of detrimental secondary phases. X-ray diffraction combined with Raman spectroscopy was utilized to better identify the secondary phases existing in the absorber layers. Solar cells were completed by chemical bath deposited CdS buffer layer followed by sputtered i-ZnO/ZnO: Al bi-layers and evaporated Ni/Al grids.

Electronic systems are a very good platform for sensing biological signals for fast point-of-care diagnostics or threat detection. One of the solutions is the lab-on-a-chip integrated circuit (IC), which is low cost and high reliability, offering the possibility for label-free detection. In recent years, similar integrated biosensors based on the conventional complementary metal oxide semiconductor (CMOS) technology have been reported. However, post-fabrication processes are essential for all classes of CMOS biochips, requiring biocompatible electrode deposition and circuit encapsulation.

In this work, we present an amorphous silicon (a-Si) thin film transistor (TFT) array based sensing approach, which greatly simplifies the fabrication procedures and even decreases the cost of the biosensor. The device contains several identical sensor pixels with amplifiers to boost the sensitivity. Ring oscillator and logic circuits are also integrated to achieve different measurement methodologies, including electro-analytical methods such as amperometric and cyclic voltammetric modes. The system also supports different operational modes. For example, depending on the required detection arrangement, a sample droplet could be placed on the sensing pads or the device could be immersed into the sample solution for real time in-situ measurement. The entire system is designed and fabricated using a low temperature TFT process that is compatible to plastic substrates. No additional processing is required prior to biological measurement. A Cr/Au double layer is used for the biological-electronic interface. The success of the TFT-based system used in this work will open new avenues for flexible label-free or low-cost disposable biosensors.

Supersulphated cements (SSC) are environmentally friendly binders that incorporate several raw materials, including byproducts. A systematic study was considered opportune considering the wide range of formulations found in the literature. The effect of the type and proportioning of components in the strength of SC was investigated using the Taguchi method to optimize the experimental work and to define the optimal conditions. The factors were: [A] %blast furnace slag (82.5-90%), [B] CaSO4 - alkaline activator ratio (1:0, 3:1, 1:1, 1:3 and 0:1), [C] type of CaSO4 (5 types) and [D] type of alkaline activator (portland cement, Ca(OH)2, KOH and NaCO3 and 2 combinations of these). Pastes were prepared and characterized for up to 28 days at 20°C. In general, for all values of [A] the best strength was for levels of [C] at 3:1, followed by the 1:1 and 1:0 ratios. The optimal conditions using the 28 day strength consisted of [A]= 82.5%, [B]= 3:1, [C]= flyorgypsum and [D] = portland cement, which developed excellent strength from day one and 35MPa. X-ray diffraction showed ettringite and C-S-H formation from the early ages. The microstructures showed dense matrices of reaction products well bonded to partially reacted slag grains, which in some cases showed rims of hydration products.

Environmental issues related to CO2 emissions have become a key focus for many different industries, including the cement and concrete industry. An environmentally optimized ‘green’ concrete can provide a much needed alternative to conventional concrete to reduce the carbon foot-print of the construction industry. This can be achieved through high Portland cement replacement by fly ash and with the inclusion of activators to enhance the rate of development of strength and other properties. This study evaluates different fly ashes and different activators (Na2SO4, lime and quicklime) that are added to enhance the reaction of the fly ash to achieve a comparable performance to that of standard Portland cement in mixes of much lower CO2 emissions. TGA, XRD and SEM are used to determine the development of hydration products and the consumption of portlandite by the fly ash. It is found that the amorphous content of the fly ash is an important parameter influencing compressive strength evolution. Based on the results, Na2SO4 as an activator, and a fly ash with high reactive SiO2 and Al2O3 contents and low Fe2O3 are found to provide the best options for producing a high volume fly ash matrix with the potential to show comparable behavior to a Portland cement control mix.

3D integration enabled by through-silicon-via (TSV) allows continued performance enhancement and power reduction for semiconductor devices, even without further scaling. For TSV wafers with all Applied Materials unit processes, we evaluate the integrity of oxide liner and copper barrier by capacitance-voltage (C-V) and current-voltage (I-V) measurements, from which oxide capacitance, minimum TSV capacitance, and leakage current are extracted. The capacitance values match well with model predictions. The leakage data also demonstrate good wafer-scale uniformity. The liner and barrier quality are further verified with microanalysis techniques.

A fast proton conducting glass with proton transport number t H = 1 was successfully prepared by using conventional melting method. In-situ FTIR (Fourier transform infrared) measurements under hydrogen atmosphere, temperature of 300°C and applying 1 V between Pt electrodes were carried out in order to monitor the proton concentration. The electrode reaction on Pt in these conditions is similar to that under intermediate-temperature fuel cell operation. It was found from the in-situ FTIR measurements that the absorbance around 2900 cm-1 increases clearly after applying 1 V, whereas no significant change was observed around 3400 cm-1. Proton infiltration into the glass is discussed based on the in-situ FTIR and impedance results.

Wafer level metal bonding involving copper material is widely used to achieve 3D functional integration of ICs and ensure effective packaging sealing for various applications. In this paper we focus on thermocompression bonding technology where temperature and pressure are used in parallel to assist the bonding process. More specifically a broad range of conditions was explored and interesting results were observed and are reported. Indeed, despite a relatively high roughness, the presence of a native oxide and the lack of surface preparation, there still exists a process window where wafer level bonding is allowed. In these conditions, limiting the bonding mechanisms to basic copper diffusion is no longer satisfactory. In this study, a specific scenario inspired by both wafer bonding and metal welding state of the art is put forward. Accordingly, pure copper diffusion through the bonding interface is lined with plastic deformation and metallic oxide fracture. In addition, polycrystalline film deformation due to thermomechanical stress is highlighted and grain growth and voiding formation are observed and confirmed.

Valence state and local environment of Fe in complex glasses related to the system Al2O3-B2O3-Fe2O3-Na2O-SiO2 were studied. In all the glasses, the major fraction of Fe exists as Fe3+ ions but a minor fraction of Fe2+ ions especially in the glass with the lowest K=[SiO2]/[B2O3] ratio was also present. Average Fe—O distance in the first shell is 1.80-1.85 Å and coordination number is 4-6. The intensity due to the second sphere is rather weak demonstrating homogeneous distribution of Fe ions in the glass.

Laves-type intermetallic phases have been observed to be the dominant phases in a series of alloy compositions being designed for the immobilization of technetium in a metallic waste form. The dominant metals in the alloy compositions were Fe-Mo and Fe-Mo-Zr. The alloy composition, Fe-Mo-Zr, also contained Pd, Zr, Cr, and Ni. Both non-radioactive rhenium-containing and radioactive technetium-bearing alloy compositions were investigated. In the Fe-Mo series, the phases observed were Fe2Mo (C14 Laves phase) and ferrite in agreement with predictions. Both Tc and Re resided predominantly in the Laves phases. In the Fe-Mo-Zr system, the phases included hexagonal C14 with the composition (Fe,Cr)2Mo, cubic C15 phase with a (Fe,Ni)2Zr composition, and the hcp phase Pd2Zr. The observation of these phases was in agreement with predictions. Re was found in the C14 intermetallic, (Fe,Cr)2Mo. Technetium was also observed to be partitioned preferentially into the (Fe,Cr)2Mo phase; however, this phase exhibited a cubic structure consistent with the C15 structural type. The composition of Laves phases is influenced by both the atomic size and electro-negativity of the constituent elements. The long-term release behavior of technetium under nuclear waste disposal conditions may be more dependent on the corrosion characteristics of these individual Laves phases containing Tc than the other metallic phases.

A calcium phosphate ceramic waste-form has been developed at AWE for the immobilisation of chloride containing wastes arising from the pyrochemical reprocessing of plutonium. In order to determine the long term durability of the waste-form, aging trials have been carried out at PNNL. Ceramics were prepared using Pu-239 and -238, these were characterised by PXRD at regular intervals and Single Pass Flow Through (SPFT) tests after approximately 5 yrs.

While XRD indicated some loss of crystallinity in the Pu-238 samples after exposure to 2.8 x 1018 α decays, SPFT tests indicated that accelerated aging had not had a detrimental effect on the durability of Pu-238 samples compared to Pu-239 waste-forms.

The corrosion behavior of simulated spent nuclear fuel (SIMFUEL) was investigated using electrochemical impedance spectroscopy and solution chemistry analyses. The SIMFUEL was exposed to aerated solutions of NaCl+NaHCO3 with and without calcium (Ca) and silicate. Two SIMFUEL compositions were studied, representing spent nuclear fuel (SNF) corresponding to 3 or 6 at % burnup in terms of fission product equivalents of surrogate elements. For all tested cases, the polarization resistance increased with increased immersion time, indicating possible blocking effects due to accumulation of corrosion products on the SIMFUEL surface. The potential-pH diagram suggests formation of schoepite that may cause the increase in the polarization resistance. The addition of Ca and silicate produced no measureable change in the polarization resistance measured at the corrosion potential. The dissolution rate ranged from 1 to 3 mg/m2-day, which is similar to the range of dissolution rates for SIMFUEL and SNF reported in the literature for comparable conditions. SIMFUEL burnup did not have a major effect on the dissolution rate. Analysis of the solution chemistry shows that uranium is the dominant element dissolved in the posttest solutions, and the dissolution rates calculated from uranium (U) concentrations are consistent with the dissolution rates obtained from impedance measurements. Simulated-fission product elements (i.e., barium, molybdenum, strontium, and zirconium) dissolved from the SIMFUEL electrode at a relatively high rate. Sorption test results indicated significant sorption of U onto the oxide formed on stainless steel. Electrochemical methods were found to be effective for measuring the uranium dissolution rate in real time.

Material like PET {polyethylene terephthalate (C10H8O4)n} are usually thrown away present in glasses of refreshments, water bottles between others which are hard to be degraded. However, this material can be recycled and used to acquire nanostructures. During this investigation the objective was to obtain nanoparticles and carbon based nanostructures from the polymer type PET by means of microwave irradiation at the temperature of 260°C at normal pressure and at 600 psi in the presence of acids, ethylene glycol and by means of calcinations. The obtained nanoparticles of ultrananocrystalline diamonds were studied by means of scanning electron microscopy (SEM), high-resolution transmission electron microscopy (TEM), and Raman spectroscopy.

The capability of tuning the functional properties of nanosize TiO2 nanoparticles (NPs) by suitable control of surface chemistry, phase stability and crystal size plays a key role on their safe use and enhanced efficacy in actual and envisioned applications, including nanomedicine, environmental remediation, and food safety, among others. On this basis, any attempt to develop a size-controlled synthesis method and an efficient surface treatment protocol becomes indispensable. Accordingly, we have synthesized TiO2 NPs via a modified aqueous processing route using HNO3 as a catalyst and polyvinylpyrrolidone as particle size controller and a dispersing agent. The NPs surface was treated by using Ethylenediamine (EDA) as a source for amine species. Bare and amine-treated TiO2 NPs were characterized by X-ray diffraction (XRD) and FTIR spectroscopy. The photocatalytic activity of TiO2 NPs was assessed by irradiating an aqueous solution of Methylene Blue (MB) dye containing different amounts of the NPs. XRD analyses evidenced the formation of two phases of crystalline TiO2 with an average crystallite size estimated at 15.3 nm. Bare and amine-treated TiO2 NPs exhibited significant activity under UV light illumination (365 nm). Bare NPs exhibited a dye photo degradation capability of about 38.02% with particle concentration of 0.5 g/l while amine-treated NPs reported 66.18% dye photo degradation capability with particle concentration of 0.5 g/l.

The dye-sensitized solar cells (DSSC) are a technological and economical alternative to conventional p-n junction solar cells. The DSSC is composed of a transparent conducting electrode (SnO2:F) coated by a porous, nanocrystalline film of n-ZnO to which dye molecules are attached, an organic electrolyte containing a reduction-oxidation couple, and finally a counter-electrode (glass/SnO2:F) coated by a thin film of platinum. The most efficient dyes for DSSCs are based on Ruthenium polypyridyl complexes, related to the high absorption coefficient in the entire visible range and the efficient injection of electrons into the conduction band of ZnO. However, the ruthenium polypyridyl complex contains a heavy metal of relatively high cost, and synthetic routes are complicated with low yields. Moreover, natural dyes in addition to their availability, are cost-effective, non-toxic and biodegradable materials, and can be extracted by simple procedures. In this paper we report the extraction of natural dyes from the stems of mangrove (D1) and tinto (D2) trees as well as from walnut (D3) shell. First, it was necessary to dehydrate the materials, after which extraction was performed using ethanol, water and sodium hydroxide solution. The dyes were characterized using UV-visible and infrared spectroscopy. The analysis of the infrared spectra shows an intense and broad band related to OH bond stretching vibration at 3393, 3442 and 3390 cm-1 for the mangrove tree, tinto tree and walnut shell, respectively. At 1051, 1123 and 1050 cm-1, there was a very strong absorption due to the stretching vibration of CO group, for the mangrove tree, tinto tree and walnut shell, respectively. These results indicate that the functional group for bonding to the ZnO is -OH for these dyes. The results of the U-Vis spectroscopy show that the strongest absorption in the visible region is provided by dyes of the tinto and mangrove trees. The current - voltage curve of a preliminary ZnO-DSSC sensitized with the natural dye of the mangrove tree bark is presented.