By carefully manipulating and controlling the growth conditions, Ruthenium (Ru) and ruthenium oxide (RuO2) two-dimensional (2-D) nanostructure were self-assembled into a stack of plates on indium tin oxide coated glass substrate. The nanoplates were grown in a horizontal hot-wall metalorganic chemical vapor deposition (MOCVD) from ruthenocene. Each nanoplate has a thickness in the range of 25 - 60 nm and the average area is 1000 x 300 nm2. Each stack of nanoplates is approximately 1.2 m in height. A continuous layer of Ru and RuO2 thin film, which may serve as the growth template, is observed on the bottom of the nanoplate stacks. Field-emission scanning electron microscopy reveals that each stack of nanoplates was grown vertically aligned on the substrate and exhibited elongated shape. Structural properties which were examined by X-ray diffraction show that the nanoplates are polycrystalline.

We have explored the application of ion implantation as a tool for the enhancement of neural cell growth on glass surfaces. Glass substrates were ion implanted with gold and with carbon using a metal vapor vacuum arc (MEVVA) ion source-based implantation system at Ege University Surface Modification Laboratory. The implantation dose was varied over the range 1014 – 1017 ions/cm2 and the ion energy spanned the range 20 – 80 keV. B35 neural cells were seeded and incubated on the implanted substrates for 48h at 37°C. After 2-days in culture the cell attachment behavior was characterized using phase contrast microscopy. The adhesion and direct contact of neural cells on these ion implanted glass surfaces were observed

Ferromagnetic CrO2 nanoparticles embedded in a diamagnetic matrix of polyvinyl alcohol (PVA) presents an example of granular giant magnetoresistance (GMR) in a diluted magnetic composite structure. Usefully significant MR occurs at room temperature, viz. -6.8% in 3.0 wt% CrO2-PVA, at field as small as 1.1 kOe. We suggest that the system is a natural analogue to dilute ferro-fluid structures composed of nanoscale magnetic particles in a viscous organic fluid (diamagnetic as well as an electrical insulator), i.e., this material displays a GMR effect without an introduction of chemical interfaces. It has great potential in various applications and can also facilitate studies of magnetotransport properties in GMR materials.

The development of a multifunctional, micron-scaled, reticulated copper foam that reliably exhibits high intrinsic thermal conductivity, efficient capillary fluid and evaporative transport over a wide area presents a unique challenge. In this work, the relationship of critical foam processing variables such as sintering temperature and template size on the pore size distribution and pore neck/body ratio is investigated using image analysis. The resulting fluid permeability values of these foams are estimated by using the Kozeny Carman equation and the porosity, surface area per unit area and tortuosity obtained through image analysis. Estimating the fluid permeability of these foams is useful for predicting the mass and heat transfer within the porous network, and provides a metric for optimizing the foam’s structural characteristics for a particular application.

We present a method for performing nanoscale wet chemistry on single carbon nanotubes as well as spectroscopic characterization of the functionalized molecules using a coupled atomic force microscope (AFM) and optical microscope. An AFM probe was functionalized with a single multiwalled carbon nanotube and then locally oxidized by dipping it into nitric acid (HNO3) in situ using AFM manipulation. Raman scattering was collected from the carbon nanotube functionalized probe before and after the oxidation reaction. An increase in the Raman D band was observed after the acid treatment, demonstrating that oxidation had occurred. This is the first step towards developing a real-time technique for dynamic studies of chemical reactions on single nanoparticles/molecules.

This paper presents the experimental and numerical study of hydrophobic interaction forces at nanometer scale in the scope of engineering micron-sized building blocks for self-assembly in liquid. The hydrophobic force distance relation of carbon, Teflon and dodeca-thiols immersed in degassed and deionized water has been measured by atomic force microscopy. Carbon and dodeca-thiols showed comparable attractive and binding forces in the rage of pN/nm2. Teflon showed the weakest binding and no attractive force. Molecular dynamic simulations were performed to correlate the molecular arrangement of water molecules and the hydrophobic interactions measured by atomic force microscopy. The simulations showed a depletion zone of 2Å followed by a layered region of 8Å in the axis perpendicular to the hydrophobic surface.

High resolution far infrared absorption measurements were carried out for single walled and double walled carbon nanotubes samples (SWCNT and DWCNT) encased in a polyethylene matrix to investigate the temperature and bundling effects on the low frequency phonons associated with the low frequency circumferential vibrations. At a temperature where kBT is significantly lower than the phonon energy, the broad absorption features as observed at room temperature become well resolved phonon transitions. For a DWCNT sample whose inner tubes have a similar diameter distribution as the SWCNT sample studied, a series of sharp features were observed at room temperature at similar positions as for the SWCNT samples studied. The narrow linewidth is attributed to the fact that the inner tubes are isolated from the polyethylene matrix and the weak inter-tubule interactions. More systematic studies will be required to better understand the effects of inhomogeneous broadening and thermal-excitation on the detailed position and lineshape of the low frequency phonon features in carbon nanotubes.

In this study, aluminum nitride (AlN) and gallium nitride (GaN) thin films have been grown via metal organic vapor phase epitaxy (MOVPE) on silicon and sapphire substrates. Samples were annealed at temperatures ranging from 450 to 1000 °C in atmosphere. AlN and GaN thin film quality has been characterized before and after annealing using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and atomic force microscopy (AFM). Surface acoustic wave (SAW) devices with titanium/platinum interdigital transducers (IDTs) designed to operate at the characteristic frequency and fifth harmonic have been realized using traditional optical photolithographic processes. SAW devices on GaN were thermally cycled from 450 to 850 °C. The S21 scattering parameter of SAW devices was measured before and after thermal cycling by a vector network analyzer (VNA). An approach for the suppression of electromagnetic feedthrough (EF) to improve device performance is discussed. Feasibility of 5th harmonic excitation for GHz operation without sub-micron fabrication is also investigated. SAW devices have also been fabricated on the more traditional SAW substrate, lithium niobate (LiNbO3), and device response was compared with those on AlN and GaN at room temperature.

Atomistic simulations of nanoindentation tests were used to study the indenter radius size effect in the presence of vacancies in a (111) single crystal of nickel. For radii from 2 nm to 8 nm, the maximum shear stresses under the indenter at the onset of plastic deformation in crystals with vacancies were compared to those which cause yield in perfect crystals by placing a single vacancy in a position near the maximum shear stress underneath the indenter tip. The effect of the presence of vacancies is lowered by decreasing the indenter radius. Results obtained for several random distributions of vacancies, in the range 3.3e-4 to 0.0033, show that placing a single vacancy near a specific location produces similar results as using larger numbers of vacancies while simplifying the complexity of the simulation. Finally, visualizations of atomic configurations of a single crystal with vacancy concentration of 3.3e-4 for radii of 4 nm and 6nm show that the heterogeneous nucleation is a size dependent phenomenon.

Wide bandgap semiconductor films were obtained by spray pyrolysis, thermal evaporation and casting. These films were characterized under similar conditions in order to compare their structures, surface morphology and photocurrent properties. All films show either a crystalline or a polycrystalline structure. SEM pictures of sprayed films present holes and fissures and non-total covering of the substrate. The photoresponse was obtained for evaporated TlBr films, HgI2 casted with polystyrene (PS) scaffold, sprayed and evaporated PbI2 films. The photo to dark current ratio is discussed as well as the difference of photo to dark current at an electric field of 100 V/cm. The discussion also focuses on a future optimized material.

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The overarching goal of Dye Sensitized Solar Cells (DSSCs) is to improve photovoltaic performance and their long-term stability for use in practical applications because of their simple fabrication technology at a reasonable cost. The focus of this paper is to achieve cell stability and also to improve solar energy conversion efficiency experimenting with different electrolytes. The electrolyte’s role is critical to sustain the DSS cell performance over time to instill cell stability. Four different electrolytes, Iodolyte R-150, AN-50, PN-50 and MPN-100, are experimented in this work for fabricating the dye-sensitized solar cells for studying both the stability and efficiency of the DSSCs.

The electrolyte selection was made using the following key electrolyte parameters; lower viscosity for easier injection into the cell, lower vapor pressure and higher boiling point to minimize electrolyte evaporation, wide redox window to generate sufficient donating electrons to the dye, lower cost and non-toxicity. Electrolytes with higher concentration of Iodolyte were chosen for this study to widen redox potential window. These are Iodide based redox electrolytes and are made with 100 mM of tri-iodide in 3-methoxypropionitrile. The results of this investigation revealed that the cell with Iodolyte R-150 electrolyte achieved improved performance having an efficiency of 10.2% when compared to the reference cell efficiency of 8.4% with Iodolyte R-50. These cells were stabilized over a time of 4 weeks. The fill factor of the cell changed about 10% and the internal resistance decreased from 6.7 to 4.3 Ω. The results of this experiment demonstrated reduced internal resistance, and improved fill factor contributed to higher cell efficiency and stability. The results of the work presented in this paper support the argument that electrolytes with higher Iodolyte concentration can enhance the cell efficiency and stability along with scaling down of the cell size.

Nanocomposites formed by ferrimagnetic and ferroelectric materials are multiferroic material in which magnetoelectric coupling occurs via piezoelectricity and magnetostriction phenomena. These nanocomposites have a variety of applications in tunable microwave devices using electric control of spin wave propagation or new magnetic memories in which the magnetic response is controlled by electric field.

In this work, transparent and homogeneous thin films of barium titanate interleaved with cobalt ferrite were prepared by sol–gel method using dip-coating process. Films of pure barium titanate and cobalt ferrite were also prepared for comparison. The nanocomposite films were deposited onto clean quartz substrates, where a coating of each material was deposited interleaved, where the cobalt ferrite film formed the last layer. The films were dried in air after each dipping and heated at 900 o C for 1 hour to convert the amorphous films into crystalline ones. The samples were characterized by low angle X-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM) and UV-Vis spectroscopy.

Hafnium oxide-based resistive memory devices have been fabricated on copper bottom electrodes. The HfOx active layers in these devices were deposited by atomic layer deposition at 250 °C with tetrakis(dimethylamido)hafnium(IV) as the metal precursor and an O2 plasma as the reactant. Depth profiles of the HfOx by x-ray photoelectron spectroscopy and secondary ion mass spectroscopy revealed a copper concentration on the order of five atomic percent throughout the HfOx film. This phenomenon has not been previously reported in resistive switching literature and therefore may have gone unnoticed by other investigators. The MIM structures fabricated from the HfOx exhibited non-polar behavior, independent of the top metal electrode (Ni, Pt, Al, Au). These results are analogous to the non-polar switching behavior observed by Yang et al. [2] for intentionally Cu-doped HfOx resistive memory devices. The distinguishing characteristic of the material structure produced in this research is that the copper concentration increases to 60 % in a conducting surface copper oxide layer ~20 nm thick. Lastly, the results from both sweep- and pulse-mode current-voltage measurements are presented and preliminary work on fabricating sub-100 nm devices is summarized.

In this work, we present progress towards devices fabrication using all semiconducting nanotubes as the starting material. Individual nanotubes are known to have intrinsic mobility of more than 10,000 cm2/V-s but using a network of nanotubes will decrease this mobility because of tube-tube screening effect and junction resistance. Here we are using solution-based deposition of purified 99% semiconducting single-walled nanotubes as the channel in field effect transistors. DC analysis of devices’ characterization shows a high mobility, more than 50 cm2/Vs, and good on/off ratio in the range of more than 103 and 104. A critical issue is the ink formulation and dependence of electronic properties on the nanotube density after deposition. In addition, the channel length also plays an important role in controlling both mobility and on/off ratio.

Flash type electronic memories are the preferred format in code storage at complex programs running on fast processors and larger media files in portable electronics due to fast write/read operations, long rewrite life, high density and low cost of fabrication. Scaling limitations of top-down fabrication approaches can be overcome in next generation flash memories by replacing continuous floating gate with array of nanocrystals. Germanium (Ge) is a good candidate for nanocrystal based flash memories due its small band gap. In this work, we present effect of silicon dioxide (SiO2) host matrix density on Ge nanocrystals morphology. Low density Ge+SiO2 layers are deposited between high density SiO2 layers by using off-angle magnetron sputter deposition. After high temperature post-annealing, faceted and elongated Ge nanocrystals formation is observed in low density layers. Effects of Ge concentration and annealing temperature on nanocrystal morphology and mean size were investigated by using transmission electron microscopy. Positive correlation between stress development and nanocrystal size is observed at Raman spectroscopy measurements. We concluded that non-uniform stress distribution on nanocrystals during growth is responsible from faceted and elongated nanocrystal morphology.

Silicon-based films have gained much interest as protective coatings for transparent polymeric materials. In this study, SiOC(–H) thin films were deposited on polycarbonate (PC) or Si substrates from trimethylsilane (TrMS) gas diluted with He gas by atmospheric pressure plasma enhanced CVD (AP-PECVD) method with varying substrate temperature, and transparency and hardness of the films were investigated. The films exhibited a good optical transparency with an optical transmittance of about 90% irrespective of the substrate temperature, and the hardness increased from 0.6 to 1.3 GPa as the substrate temperature increased from 60 to 140°C. The results are discussed in terms of chemical structural changes in the films according to the substrate temperature.

A maskless method of employing polymer growth inhibitor layers is used to modulate the conflicting parameters of density and alignment of multi-junction nanowires via large-scale low temperature chemical route. This low temperature chemical route is shown to synthesize multi-junction nanostructures without compromising the crystal quality at the interfaces. The final morphology of an optimized multi-junctions nanowire arrays can be demonstrated on various substrates due to substrate independence and low temperature processing. Here, we also follow-up on device demonstrations whereby p-n junction are created by exposure of secondary nanowires to ammonia plasma, converting them to p-type characteristics and also the density modulated multi-junction nanowires were tuned to infiltrate nanoparticles to create a hybrid hierarchically-structured nanowire/nanoparticles solar cell. The fabrication of hierarchically-structured nanowire/nanoparticles composites presents an advantageous structure, one that allow nanoparticles to provide large surface areas for the dye adsorption, whilst the nanowires can enhance the light harvesting, electron transport rate, and also the mechanical properties of the films. This work can be of great scientific and commercial interest since the technique employed is of low temperature (< 90 °C) and economical for large-scale solution processing, much valued in today’s flexible display and photovoltaic industries. In addition, ZnO nanostructures for gas sensing will be presented.

Recent years, although silica aerogels are expected to be the promising material for energy savings, the lack of mechanical strength prevents from commercial applications such as to low-density thermal insulators. To improve mechanical properties, methyltrimethoxysilane (MTMS) and dimethyldimethoxysilane (DMDMS) are used in this study as the co-precursor of aerogels because the network becomes flexible due to the relatively low cross-linking density and to the unreacted methyl groups. Because of the strong hydrophobicity of MTMS/DMDMS-derived condensates, phase separation occurs in aqueous sol and must be suppressed to obtain uniform and monolithic gel. We employed surfactant n-hexadecyltrimethylammonium chloride (CTAC) in starting compositions to control phase separation during a 2-step acid/base sol-gel reaction. By changing the starting composition, various microstructures of pores are obtained. In the uniaxial compression test, the aerogel showed high flexibility and spring-back to the original shape after removing the stress.

This work shows the relationship between the morphology (studied by AFM) of an active bulk-heterojunction (BHJ) layer composed by MEH-PPV (poly(2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene) and PCBM ([6,6]-phenyl-C61-butyric acid methyl ester) and the respective photovoltaic figures of merit. It is observed that the most relevant parameter (influencing the efficiency) is the fill-factor (FF), as both the open circuit voltage and short circuit current are not significantly affected by the microscopic morphology. Different local conformation of the active films can change the FF from near 25% to more than 65%, having a strong impact in the efficiency. These results were modulated by an equivalent circuit. Serial and parallel resistances were related with the physical behavior of the organic cells. These were observed to have a direct relationship with the achieved morphology.