The effects of annealing and fatigue on the local structure of Zr50Cu40Al10 and Zr60Cu30Al10 bulk metallic glasses (BMG) were investigated using the pair density function (PDF) analysis of synchrotron X-ray and neutron diffraction data. Our results indicate that the two compositions respond differently to annealing. The first PDF peak becomes sharper after annealing in Zr50Cu40Al10 with its intensity increasing, indicating that short-range ordering may be induced after the heat treatment. On the other hand, in Zr60Cu30Al10, the effects due to the heat treatment on the local structure are more subtle. Separately, the as-quenched and annealed alloys with the composition Zr50Cu40Al10 were subjected to fatigue loading conditions with ~ 106 compression cycles. The room temperature measurements showed changes in the local structure with fatigue especially for the annealed sample, involving the Cu-Zr correlations. Our results suggest that the physical properties of BMGs upon fatigue loading conditions may become accentuated due to the structural relaxation brought upon by annealing, leading to observable structural changes at the atomic level from fatigue.

The ability to strongly attach biomolecules such as enzymes and antibodies to surfaces underpins a host of technologies that are rapidly growing in utility and importance. Such technologies include biosensors for medical and environmental applications and protein or antibody diagnostic arrays for early disease detection. Emerging new applications include continuous flow reactors for enzymatic chemical, textile or biofuels processing and implantable biomaterials that interact with their host via an interfacial layer of active biomolecules. In many of these applications it is desirable to maintain physical properties of an underlying material whilst engineering a surface suitable for attachment of proteins or peptide constructs. Nanoscale polymeric interlayers are attractive for this purpose.

We have developed interlayers[1] that form the basis of a new biomolecule binding technology with significant advantages over other currently available methods. The interlayers, created by the ion implantation of polymer like surfaces, achieve covalent immobilization on immersion of the surface in protein solution. The interlayers can be created on any underlying material and ion stitched into its surface. The covalent immobilization of biomolecules from solution is achieved through the action of highly reactive free radicals in the interlayer.

In this paper, we present characterisation of the structure and properties of the interlayers and describe a detailed kinetic model for the covalent attachment of protein molecules directly from solution.

We present the memory performance of devices with bistable electrical behavior based on MEH-PPV (Poly (1-methoxy-4-(2-ethylhexyloxy)-p-phenylenevinylene)) containing metal (Zn or Fe-Ni) particles. Another memory device based on aluminum phthalocyanine chloride (PcAlCl) added to the composite material reveals the photoinduced switching, in addition to the electrical one. Possible mechanisms for resistive switching are discussed.

The martensitic microstructure of shape memory alloys is an aggregate of self accommodating plate groups. The principal character of this aggregate is its demonstration of pseudoplasticity, wherein a macroscopic shape change is brought about by extensive rearrangement and reorientation of the self accommodating martensite variants, and that of microstructural reversibility, wherein the polyvariant microstructure transforms back to the original grain of the parent phase after pseudoplastic deformation. These aspects of the shape memory intermetallic alloys are intriguing and, to a great extent, unsolved. The aim of this paper is to show that the underlying crystallographic interrelationships of the self accommodating microstructure of intermetallic alloys are responsible for the observed effect. The paper will discuss the relation between autocatalytic nucleation and self accommodation, the relation between microstructural reversibility and intervariant interfaces of the martensitic microstructure and the manifestations of microstructural irreversibility using results from the microstructural examination of the self accommodating microstructures.

We consider a tight binding model for magnetic systems, in which we allow atoms to become charged and to interact via the long ranged Coulomb interaction to a published tight binding model; this is then applied to the study defects in ferromagnetic iron. We encounter several problems with achieving self consistency with existing schemes. To address the issue of instability and slow convergency we developed a robust, efficient scheme for charge and spin self consistency. This is based on minimizing an extended form of the Harris-Foulkes functional which includes spin, leading to a Newton-Raphson iterative procedure. We then apply this to both bulk and defect calculations for iron.

Classically, the limit for optical machining is on the order of the wavelength of the incident light. However, by taking advantage of precise, nonlinear damage mechanisms that occur for femtosecond laser pulses, damage can be achieved on a scale an order of magnitude lower, allowing precise removal of very small amounts of material to produce holes mere tens of nanometers wide. Femtosecond laser nanomachining can be carried out in a variety of dielectrics, and in transparent substrates machining can be sub-surface, in contrast to other nanomachining techniques such as using an electron beam or focused ion beam. We focus on the use of glass, as it is in many ways an ideal material for use in biological applications due to its chemical, optical, electrical and mechanical properties. By precisely placing laser pulses in glass, three dimensional nano and microfluidic channels and devices can be formed including nozzles, mixers, and separation columns. Recent advances in this technique allow the formation of high aspect ratio nanochannels from single pulses, thus helping address the fabrication speed limitations presented by serial processing. These nanochannels have a range of applications including the fabrication of nanoscale pores and nanowells that may serve as vias between fluidic channels, or from channels to a surface. These nanochannels have applications as a standalone technique for fabrication of nanopores and nanowells, but can also complement other fabrication techniques by allowing precisely placed jumpers that can connect channels that are out of plane. We discuss applications for diagnostic microfluidic devices, and basic cell biology research.

A new technique in microscopy is demonstrated in which the domain of Atomic Force Microscopy (AFM) is extended to optical spectroscopy at the nanometer scale. Molecular resonance of feature sizes down to the single molecular level were detected and imaged purely by mechanical detection of the force gradient between the interaction of the optically driven object molecular dipole and its mirror image in a Platinum coated scanning probe tip. We provide full experimental details including a basic theory for this new technique. The microscopy and spectroscopy technique is extendable to frequencies ranging from radio to infrared and the ultra violet.

An alternative high temperature structural alloy system based on the X-X3Si eutectic compositions of chromium and vanadium is put forward. These low-density (~6g/cm3) eutectics have a bcc solid-solution to increase alloy fracture toughness, and a A15 X3Si as the high temperature load-bearing phase. (½Cr,½V)-(½Cr,½V)3Si was used as the base alloy for further element additions, and is represented by the symbol 山 10at.% tantalum and aluminium were substituted for vanadium as quaternary and quinary alloy additions.

Microstructure, elemental phase partitioning, compression creep and oxidation results will be discussed. Cr-Cr3Si has a tidy, fine lamellar microstructure. Vanadium coarsens and destabilises the lamellae to a limited extent. Tantalum addition causes two distinct populations of eutectic to form; one population having finer lamellae than the other. Aluminium does not coarsen or destabilise the lamellar microstructure. High temperature compression tests at 1200°C and 1300°C show that 山 is stronger than the binary alloys, and of similar strength to the quaternary and quinary alloys.

Cluster Variation Method (CVM) has been recognized as one of the most reliable theoretical tools to incorporate wide range of atomic correlations into a free energy formula. By combining CVM with electronic structure total energy calculations, one can perform first-principles calculations of alloy phase equilibria. The author attempted such CVM-based first-principles calculations for various alloy systems including noble metal alloys, transition-noble alloys, III-V semiconductor alloys and Fe-based alloy systems. Furthermore, CVM can be extended to two kinds of kinetics calculations. One is Path Probability Method (PPM) which is the natural extension of the CVM to time domain and is quite powerful to investigate atomistic kinetic phenomena. The other one is Phase Field Method (PFM) with the CVM free energy as a homogeneous free energy density term in the PFM. The author’s group applied the latter procedure to study time evolution process of ordered domains associated with disorder-L10 transition in Fe-Pd and Fe-Pt systems. CVM has, therefore, a potential applicability for the systematic studies covering atomistic to microstructural scales. It has been, however, pointed out that the conventional CVM is not able to include local lattice relaxation effects and that the resulting order-disorder transition temperatures are overestimated. In order to circumvent such inconveniences, Continuous Displacement Cluster Variation Method (CDCVM) has been developed. Since first-principles CDCVM calculations are still beyond the scope at the present stage, preliminary results on the two dimensional square lattice and an fcc lattice with primitive Lennard-Jones type potentials are demonstrated in the last section.

In this paper, we report on the growth and fabrication of thin film Si photovoltaic devices on photonic structures which were fabricated on steel and PEN and Kapton substrates. Both amorphous Si and thin film nanocrystalline Si devices were fabricated. The 2 dimensional photonic reflector structures were designed using a scattering matrix theory and consisted of appropriately designed holes/pillars which were imprinted into a polymer layer coated onto PEN, Kapton and stainless steel substrates. The photonic structures were coated with a thin layer of Ag and ZnO. Both single junction and tandem junction (amorphous/amorphous and amorphous/nanocrystalline) cells were fabricated on the photonic layers. It was observed that the greatest increase in short circuit current and efficiency in these cells due to the use of photonic reflectors was in nanocrystalline Si cells, where an increase in current approaching 30% (compared to devices fabricated on flat substrates) was obtained for thin (∼ 1 micrometer thick i layers) films of nano Si deposited on steel structures. The photonic structures (which were nanoimprinted into a polymer) were shown to stand up to temperatures as large as 300 C, thereby making such structures practical when a steel (or glass) of kapton substrate is used. Detailed measurements and discussion of quantum efficiency and device performance for various photonic back reflector structures on steel, kapton and PEN substrates will be presented in the paper.

For successful implementation of the nanomaterial-based PV and Energy storage devices there is a need for well-structured nano films consisting of a strictly controlled sequence of nanoparticle layers. Most promising nano-films include a “built-in” gradient of a nanoparticle size and/or material composition across the part or entire thickness of the film. Such Gradient Multilayer (GML) nano films will be able to significantly improve a PV efficiency of the 3rd generation Solar Cells and Energy storage devices. The development of GML-based devices is presently limited by lack of simple, inexpensive, scalable, and production-worthy deposition methods that are capable of forming GML nano-film on PV-suitable substrates such as flexible materials.

The proposed concept describes novel principles of an advanced non-conventional deposition of the highly efficient GML nano films.

The proposed GML deposition method is based on the phenomena of Flying Particles (FP). According to the FP-methods a pre-selected mix of nanoparticles (NP) of various size and/or material composition is deposited on a flexible (or other) substrate in a pre-defined order of NP size and/or composition thus forming GML nano film. Deposited GML film comprises a sequence of size-tuned and/or composition-tuned NP layers, which has a potential for significant increase of PV efficiency.

The deposition process includes the NPs launch and flight through a resistant gas ambient. Due to the Stokes aerodynamic laws the FP times-to-target will be different for NP of a different size and/or density (material composition). Simulation is presented to confirm the separation of FP”s of a different size and/or density during their motion through the low-pressure gas. The calculations have been made for the initial stages of the FP process thus establishing the most efficient parameters of the process. Resultant GML nano films are expected to have superior qualities, particularly for building high efficiency / low cost PV panels. The FP-method allows for a fast development and easy implementation in PV manufacturing.

Composite Organic-Inorganic Nanoparticles (COINs) are a novel type of surface-enhanced Raman (SER) scattering nanoparticle formed by aggregating inorganic silver particles in the presence of a chosen organic molecule with a distinct Raman fingerprint. Binding between antibody-functionalized COINs and cells is detected primarily using Raman spectroscopy, which measures spectral shifts of the excitation light due to inelastic scattering. It has been suggested that the amount of antibody-conjugated COINs binding on cells will vary according to the antigen-expression levels in cells and will lead to changes in measured SERS intensities. COINs functionalized with antibodies CD54 and CD8 were conjugated to U937 and SupT1 cancer cells and investigated in this study. SERS intensity measurements were obtained from each of the four sample variants and normalized against control samples comprising non-antibody-functionalized COINs with cells. The amount of COINs binding on cells was determined using scanning electron microscopy (SEM) and correlated with the SER spectroscopy intensity. Although we found a positive correlation between the number of COINs binding to cells and their respective SERS intensity, this relationship is not one-to-one, nor does it appear to be linear. We demonstrated that SEM imaging and SER spectroscopy can complement each other to provide information about COINs binding onto cancer cells.

In a-Si:H, large concentrations of B or P (of order 1%) are required to dope the material, suggesting that doping mechanisms are very different than for the crystal for which much smaller concentrations are required. In this paper, we report simulations on B and P introduced into realistic models of a-Si:H and a-Si, with concentrations ranging from 1.6% to 12.5% of B or P in the amorphous host. The results indicate that tetrahedral B and P are effective doping configurations in a-Si, but high impurity concentrations introduce many defect states. For a-Si:H, we report that both B(3,1) and P(3,1) (B or P atom bonded with three Si atoms and one H atom) are effective doping configurations. We investigate H passivation in both cases. For both B and P, there exists a “hydrogen poison range” of order 6 Å for which H in a bond-center site can suppress doping. For B doping, nearby H prefers to stay at the bond-center of Si-Si, leaves B four-fold and neutralizes the doping configuration; for P doping, nearby H spoils the doping by inducing a reconstruction rendering initially tetrahedral P three-fold.

Ternary variations of the II-VI zincblende semiconductors have received little attention for thermoelectric applications. Here we present the first systematic doping study on Cu3SbSe4, a zincblende-like ternary semiconductor with a unit cell four times larger than the parent II-VI compounds. The large unit cell of Cu3SbSe4 results in a low room temperature thermal conductivity (~3.0 W/m*K) and its large hole effective mass produces a Seebeck coefficient approaching 500 μV/K in the undoped compound. Our results show that Ge is an effective p-type dopant in Cu3SbSe4, and the power factor reaches nearly 16 μW/cm*K2 at 630K when 3% Ge is added, rivaling that of state-of-the-art thermoelectric materials at this temperature.

Common igniters such as black powder, benite, and boron potassium nitrate (BKNO3) are routinely employed in all calibers of gun systems. Armament Research Development Engineering Center (ARDEC) has pursued efforts to improve the ignition of gun propellants which has been demonstrated to be the root cause of many tribulations for gun systems. We have developed several extrudable nitrocellulose-BKNO3 based igniter materials that are more energetic, and exhibit smaller ignition delay times than most traditional igniters. We have demonstrated this via static firing. High speed video during static testing has demonstrated significantly more consistent, intense, and rapid flame generation in comparison to Benite leading to improved ignition effectiveness of the propellant bed.

Effects of Ag content on microstructure, mechanical properties, and electrical conductivity in long time aged Cu-Ti-Ag alloys were investigated. In short time ageing condition, both electrical conductivity and mechanical properties were enhanced by Ag addition. On the other hand, in long time ageing condition, Ag addition showed a faster deterioration of mechanical properties than Ag free CuTi alloys.

This paper reports results on the use of a pi’n/pin a-SiC:H heterostructure as an active band-pass filter transfer function whose operation depends on the wavelength of the trigger light, on the applied voltage and on the wavelength of the additional optical bias.

Results show that the device combines the demultiplexing operation with the simultaneous photodetection and self amplification of the signal. Experimental and simulated results show that the output signal has a strong nonlinear dependence on the light absorption profile. The device, modeled by a simple circuit with variable capacitors and interconnected phototransistors through a resistor, is a current-controlled device. It uses a changing capacitance to control the power delivered to the load acting as a state variable filter circuit. It combines the properties of active high-pass and low-pass filter sections into a capacitive active band-pass filter.

Next-generation bioanalytical approaches for protein-level measurements are advanced by the integration capacity of microfluidic design strategies, as well as the fine fluid and material control possible. Photopatterning of polymers within fluidic volumes is a key tool in the suite of technologies available for seamless integration of assay measurement modalities, as well as rapid target detection. Here, we overview recent advances in heterogeneous and homogeneous immunoassays using functional polymers, electrophoretic transport, and microdevices.

Market demand for touch panel/lens has been exceptionally high for the recent years due to smartphones, tablet PCs, etc. Among the available technologies to envision touch functionality, capacitive touch screen has received the great attention due to the various superiorities over the competing ones. Capacitive touch screen features two transparent conductive electrodes, such as ITO (indium tin oxide). However, the difference in refractive indices of ITO, substrate, and air, ITO pattern is clearly visible if there is no proper countermeasure. Most of touch screen makers and ITO substrate supplier utilize “index-matching technology” to prevent this phenomenon.

Even though of the attempts to minimize visible ITO pattern in final product, there are many technical and process challenges. In this study, the causes around visible ITO pattern were investigated to understand and provide the proper countermeasures.

One of the possible causes for visible ITO pattern was improper annealing process in ITO especially for film substrate. According to XPS (X-ray photoelectron spectroscopy)/ESCA (electron spectroscopy for chemical analysis) and other analysis results, ITO, which is normally deposited through sputtering, is not fully transformed to oxidized state. After aligning and adjusting annealing condition, acknowledged visible ITO pattern was disappeared.

Other causes for visible patterns were also discussed in detail, and the relevant countermeasures were provided.