In this work we present the bases to perform investigation on the effects on the morphology and size of nanostructures of silver, owed to the modification of synthesis factors in a polyol process such as temperature, concentration, time of reaction, injection speed and time of injection. It is claimed that control over Ag nanostructures shape could be improved and significant information about the synthesis process can be obtained. The design of experiments was done aimed to obtain useful information about how to yield as much as possible specific structures of interest.

Medium scale integrated circuits with 108 CNT-TFTs have been fabricated using CNTs grown by plasma enhanced chemical vapor deposition (PECVD) which has the advantage of preferential growth of CNTs with semiconducting behavior in the FET current–voltage characteristics. High-speed operation with a switching time of 0.51 μs/gate, which is highest in the CNT-TFT integrated circuits to our knowledge, was demonstrated by a 53-stage ring oscillator. Characterization of CNT-TFTs using scanning probe microscopy has also been performed. The island-like structure in the electrical properties of the CNT network was observed even in a high-density CNT network in the subthreshold regime. This was explained by the decrease of the effective number of CNTs which contribute the electrical conduction.

Environmental, concerns regarding reducing CO2 emissions and the drive of having better fuel economy have already enthused the car manufacturer to use the weight materials having better mechanical properties. Automotive industry has shown a great interest in Dual Phase steels due to the possibility of reducing weight of vehicles and increasing the passenger safety at a very competitive cost. Automotive applications unavoidably entail welding and joining in the manufacturing process and the fatigue resistance of welded joints due to the integrity and safety requirements. The variation of welding parameters (voltage, current and speed of welding) affects weld performance, mechanical, and metallurgical properties.

The CMT (Cold Metal Transfer) braze welding is a relatively new technology that partially decouples the arc electrical transients from the filler wire feed rate. It allows reducing the heat required for welding and permits higher joining speeds.

The aim of this work is to study the interfacial microstructures and intermetallic compounds produced by cold metal transfer welding of two plates of galvanized DP600 dual phase steel with CuSi3 as filler metal. The study was performed by applying a CMT braze welding with three different joining speeds. The welded microstructures and microhardness were determined and related to the welding process conditions.

A small HAZ, constituted by martensite, bainite and coarse ferrite grains, has been highlighted. Furthermore, an intermetallic Fe-Si-Cu compound layer formed at the interface between steel and filler metal. The joining speed sways the size of ZTA since the heat input Q affects the phase transformation in the weld and heat affected zone

This parameter also affects the thickness of the compound layer and the size of precipitates in the filler metal, likewise the mechanical characteristics. The fracture starts at the interface steel-copper where intermetallic compounds formed.

In this paper the spore-crystal complex of Bacillus thuringiensis var. israelensis (Bti) was immobilized by the sol-gel process in a hybrid polymer using as precursors the inorganic tetraethyl orthosilicate (TEOS) and the organic Polydimethylsiloxane (PDMS); in order to combine the advantages of both materials in a hybrid matrix to improve aspects such as the thermal stability, the hydrophobic properties and the porosity. Bti produces different crystals during sporulation phase; these are of protein nature and are used as bio-insecticides. It is important to mention that the insecticide attack is specific to the mosquito larva that causes dengue and black flies. The samples were characterized to ensure viability by performing growth kinetics with fermentations immersed in a flask, this microbial growth was monitored by dry weight, glucose consumption and characterized by Fourier Transform Infrared Spectroscopy (FTIR) to observe the interaction of materials with spore-crystal complex.

Homoepitaxial layers were grown with very low surface roughness on 4", 4˚ off-axis substrates, but a new kind of large obtuse angled triangular defect that spanned 1000-2000 μm was observed. Process changes resulted in reduction of the size and concentration of these triangular defects from 3.5cm-2 to 0.13cm-2. Both large and small triangular defects were found to have a similar core structure. No degradation in the epitaxial morphology or quality was seen due to the process change. JBS diodes fabricated on wafers with large triangular defects had much higher leakage when the triangular defects were present in the active area of the diodes.

The relationship between tortuosity and porosity and its influence on effective transport properties in lithium-ion cells was analyzed. The variation in cell performance with changes in component thicknesses, porosities and tortuosities was investigated. Optimal, novel electrode designs are developed to improve their rate capability even at higher active material loadings.

Understanding factors affecting cell invasion influences the design ofengineered constructs for tissue regeneration. The objective of this workwas to investigate the effect of matrix stiffness on invasion of tumor cellsthrough a synthetic hydrogel with well-defined properties. A novel staracrylate-functionalized polyethylene glycol-co-lactide (SPELA) macromer wassynthesized to produce hydrogels with well-defined water content, elasticmodulus, degree of crosslinking and hydrophilicity. The hydrogel was formedby photo-polymerization of the macromer with or without integrin-bindingcell adhesive RGD peptide. Cell invasion experiments were carried out in atranswell with SPELA hydrogel as the invading matrix and 4T1 mouse breastcancer cells. The invading cells on the lower membrane side were countedwith an inverted fluorescent microscope. The concentration of SPELA macromerranged from 10-25 wt% and that of RGD ranged from 1x10-4 to 1x10-2 M. The shear modulus of the hydrogel varied from 200 Pato 25 kPa as the SPELA concentration increased from 10 to 25 wt%. Cellinvasion slightly increased with increasing RGD concentration. However, RGDconcentration >1% resulted in a significant decrease in cell migration.As the matrix stiffness increased from 0.15 to 0.4, 3, 5, 6, 14, and 25 kPathe invasion rate decreased from 18.0 to 5.5, 6, 5.7, 5.2, 1.5, and 1.0 cells/mm2/h, respectively. There was a sharp decrease ininvasion rate for matrix stiffness greater than 10 kPa. Results demonstratethat matrix stiffness plays a major role in invasion of tumor cell through agelatinous matrix.

This study consisted of the characterization of longitudinal cracking pattern observed in weld joint in the manufacture of 304L steel pipelines with thin wall thickness by GTAW process. These tubes are used in food and automotive industries. The cracks grown in the liquid-solid interdendritic zones at high temperatures. It was found that the cracks are associated with change on solidification mode and presence of the holes produced by shrinkage. The change in the solidification mode was associated with the presence of second phase particles. The results suggest that the formation of cracks is promoted by increasing current during the welding although the heat input is constant.

Charging of amorphous solid water (ASW) films has been characterized using high resolution, low energy positive ions (Ar+) and electrons at 1-50 eV energy range. This system responds to charging as a nano-capacitor and has been studied for its static electric field effect on electron-induced-desorption from top layers and internally trapped molecules within ASW film. In addition we have investigated the role of electron energy on chemical reactivity of trapped methyl chloride molecules as model for outer space surface chemistry.

Dynamic charging at inner pores of porous silicon (PSi) has been studied as the origin of highly efficient photo-induced desorption (PID) of adsorbates such as Xe, CO and N2O. Wavelength and laser power dependence suggest that cross sections for PID, 3 orders of magnitude larger than on non-porous surfaces, originate from dynamic charging of nanometer scale tips at inner pores. These have lead to transient negatively charged species that undergo an Antoniewitz-like PID mechanism.

PS-b-PEO block co-polymers have been reported to form cylindrical, lamellar, gyroidic, and supramolecular architectures due to several reasons: some of the reasons include the chemical incompatibility between the lipophilic and lipophobic covalently cross-linked blocks resulting in a high Flory-Huggins interaction parameter, the annealing solvent, and the interfacial boundary conditions between the substrate and the phase separating blocks. We report here for the first time on the spontaneous formation of nanopores and nanorings in PS-b-PEO block co-polymers. The mean size and depth of the pores are about 150nm and 40nm, respectively, while the pores occur randomly placed in clusters of about 2-5 pores. The pore clusters leave behind a breath-like architecture replicated by the phase separating block co-polymer. These breath architectures, in the shape of nanorings, are formed during the initial period of phase separation and do not disappear after phase separation has been achieved, leaving behind a PS-enriched circular framework. The diameter of the nanorings is in the 200-700nm range, as measured from AFM phase and height images. This range falls within the reported size of water droplets forming breath structures on polymer films. The resulting nanoarchitectured materials could find potential applications where biocompatibility and water permeability of the PEO block within the nanopores is desirable. In addition, the slightly elevated nanorings could also provide semi-enclosed barriers that can serve as micro/nano-enclosed cell and tissue cultures.

Oxide-metal-oxide structures are an alternative to single material transparent electrical contacts. Among other advantages, these multilayer systems provide good conductivity and transmittance, even when fabricated at room temperature. Low temperature processing is a requirement for silicon thin-film solar cells on various flexible substrates. The design and fabrication of oxide-metal-oxide structures based on ZnO:Al and Ag are investigated in this work. Further the integration of an optimized multilayer electrode into an amorphous silicon solar cell in substrate configuration was performed. Measurement results and possible loss mechanisms are discussed.

We used atomic force microscope (AFM) to acquire high-resolution images of collagen type I triple-helices under ambient conditions in tapping mode. Angles between consecutive fixed-length segments were measured and analyzed to yield persistence length and elastic constant. Changing the segment length allowed exploring the mechanics at various scales. Understanding the mechanical properties of collagen molecules could serve to elucidate mechanisms of complex mechanical properties of interest in nanomedicine and nanotechnology.

We report on our growth of superconducting SmFeAs(O,F) films by F diffusion. In our process, F-free SmFeAsO films were grown by molecular beam epitaxy (MBE) first, and subsequently F was introduced into the films via F diffusion from an overlayer of SmF3. We performed a detailed comparison of the growth conditions and also the properties of resultant films for fluoride and oxide substrates. The best films on CaF2 exhibited a high transition temperature, T c on (T c end) = 57.8 K (56.4 K) at highest, which may exceed the highest T c ever reported for bulk samples.Furthermore the films on CaF2 also showed high critical current density over 1 MA/cm2 in self-field at 5 K.

In the past two decades, the growing global demand for solar energy has spurred scientific interest in alternative technologies to conventional silicon. In particular, CuIn1-xGaxSe2 (CIGS) has emerged as a competitor. We have developed a scalable deposition technique using RF magnetron sputtering of quaternary CIGS. Notably, the resulting films do not require postselenization, reducing processing time and cost. We have fabricated devices above 10% efficiency using this approach, showing its promise as a production method for highperformance CIGS photovoltaics. However, the morphology of the sputtered CIGS layer is markedly different from conventional evaporated films; grain sizes vary through the thickness of the film, with numerous small grains dominating at the Mo/CIGS interface that then either terminate or grow in an inverted-pyramid fashion to form large, columnar grains at the CIGS/CdS interface.

To better understand the origin of this morphology, we have studied the growth behavior of the CIGS layer using a combination of atomic force microscopy and electron microscopy to observe initial nucleation and grain growth behavior of quaternary-sputtered CIGS. We also discuss the effects of interfacial layers at the Mo/CIGS interface, demonstrating a novel wetting layer that conformally coats the Mo surface.

We present the propagation properties of Dirac-electrons in multilayered Period-Doubling (MPDGS) and Silver-Mean (MSMGS) graphene structures. The multilayered graphene structures are built arranging breaking and non-breaking symmetry substrates such as SiC and SiO2 following a given quasirregular substitution rule locating on them a graphene sheet. We have implemented the Transfer Matrix technique to calculate the transmittance of these multilayered graphene structures. This technique allows us to analyze readily the main differences of the transmission properties between MPDGS and MSMGS.

Graphene, a two-dimensional carbon allotrope, has raised great interests as a material candidate for future electronics due to its superb carrier transport and unique physics. The demand for future-generation large-scale carbon-based electronics motivates assembly of large-area graphene and selection of ideal substrate material that best preserves the transport property of graphene. In this work, CVD-assembled large-area graphene on thin multilayer hexagonal boron nitride (h-BN) is employed to demonstrate the basic building block of digital circuit - inverter prototype made of two graphene-channel field-effect transistors (GFETs). The doping in the CVD-grown graphene, probed via electrical measurements, is implemented through non-uniform local surface chemistry. The full transfer response of the graphene logic inverter is demonstrated in the localized P/N doping region.

This work covers the design of stimuli-responsive membranes and their ever-expanding range of use. Stimuli-responsive membranes that change their physicochemical properties in response to changes in their environment were synthesized for biomedical application. Responsive cotton-g-[2-(dimethylamino) ethyl methacrylate] membranes were obtained using γ-rays by mutual irradiation (direct method). The effect of absorbed dose, dose rate, and monomer concentration on the grafting yield was determined. The grafted samples were verified by the FTIR-ATR, 1H and 13C HRMAS NMR and 13C CPMAS NMR spectroscopies; thermal properties were analyzed by TGA and DSC and the stimuli-responsive behavior was studied by DSC.

We studied the early stages of polymerization of CO under pressure. We performed DFT simulations of 128 and 432 atom models. Structures of random networks found at zero temperature were used for equilibration at 100 K by employing first principles MD. We found that the polymerization begins at 7 - 8 GPa and slightly depends on the size of the model. It turned out that there are several metastable phases of the extended CO solid, corresponding to different compression pressures from 7 - 8 GPa to 15-18 GPa with different numbers of CO fragments, not connected to the random network. We also found that the transition to the phases is irreversible which results in hysteresis loops. Random network structures obtained, say, under 18 GPa could exist at 3 GPa, whereas compression to 3 GPa results in the delta phase of CO crystal, with intact CO fragments and minor distortion of the cubic phase. To analyze the random structure fragments we calculated normal modes and IR intensities using the dipole approximation. Contributions from the main motifs of the random network are identified and compared with experimental IR measurements.

Modeling of free radical polymerizations of the liquid-crystalline monomer 6-[4-(4-heptyloxyphenylazo)phenoxy]hexylacrylate using the PREDICI software package is reported. The model accounts for all elemental reactions that were identified to be important for radical polymerizations of acrylate-type monomers. On the basis of butyl acrylate kinetic data a remarkable agreement between number average molar masses from modelling (M n,sim) and from experiments (M n,exp) is observed: M n,sim = 17800 g·mol−1 and M n,exp = 17400 g·mol−1. Similarly, dispersity values of 1.8 and 1.6 were determined via modelling and experiments, respectively. It is shown that the assumption of butyl acrylate kinetics provides a reasonable approximation even for acrylate-based monomers having mesogenic substituents.

Current energy demands and future energy needs are a growing industry which at present attracts a large amount of research and investment of which nuclear energy is an integral part. Eight new nuclear stations are proposed to be developed in the UK over the next ten years to meet this demand. In order for nuclear energy to sustain growth and development, nuclear decommissioning of first and second generation power stations needs to be addressed in the U.K. and worldwide. Presently the UK has 36 graphite moderated reactors as a result of the UK military and civil programs, which over the next twenty years will close. This will result in ∼99’000 tonnes of irradiated graphite waste for which no current national decommissioning strategy exists. The main issues associated with this waste are the large volume and activation products associated. By far the greatest inventory is from 3H and 14C. An EU Euroatom FP7 Program; CARBOWASTE was established in 2008 with the aim of developing treatment and disposal options for graphite.

This research is based within CARBOWASTE, the main objectives are to understand the mechanisms involved in the production, location and removal of radioisotopes from nuclear graphite. Computed X-ray Tomography (CT) will be used in order to quantify the initial porosity in conjunction with thermal treatment (ex situ) in order to eventually identify the location of 14C within the matrix of irradiated graphite, through the preferential chemically controlled oxidation of graphite. Unirradiated Pile Grade A graphite samples have been laser and manually marked in order align the samples prior to and post thermal treatment to determine the degree of porosity changes and weight loss under a range of thermal oxidation parameters.