Controlled ZnO nanostructures were grown on a flexible substrate for the future development of smart sensing tags. Thermolysis-assisted chemical solution deposition was used to grow ZnO nanorods at 85°C from 0.01mol of Zinc nitrate hexahydrate and HMT (Hexamethyltetramine) solution. To promote and modulate the ZnO nanorods, R.F. sputtered ZnO seed layers were deposited on polyimide substrates at various film thicknesses in the range of 8 to 160 nm. The optimum processing conditions to fabricate ZnO nanostructures have been investigated to examine the growth behaviors and to correlate the process parameters with the morphological characteristics. When the ethanol gas sensitivities were measured at different thickness of ZnO seed layers before growing ZnO nanorods, the highest sensitivity was obtained at 40 nm thick ZnO film at 300°C where the film thickness is similar to the Debye length. When ZnO nanorods were grown on such a ZnO seed layer, the sensitivities were more heavily influenced by the ZnO nanostructures rather than the thickness of the seed layer probably due to the dominant proportion of carrier density involved with the gas absorption.

We report white light emission from ZnO nanostructures in powder form, prepared by microwave irradiation-assisted chemical synthesis, in the presence of a structure directing agent. Determination of their crystallinity, actual shape, and orientation was made using X-ray diffraction, scanning electron microscopy (SEM) and transmission electron microscopy (TEM), and optical properties have been studied through photoluminescence (PL), measured using He-Cd laser (325 nm) as the excitation source. There is a noticeable variation in the luminescence correlated with variation of process parameters, such as microwave power, duration of irradiation, and the type/concentration of surfactants. The CIE (Commission Internationale l’Eclairage) diagram shows that the luminescence lies in yellow region of the color space. As the luminescence from the powder of ZnO lies in the yellow region, it is possible to produce white light from the powder of ZnO by using a blue laser as the excitation source.

Carbon nanotube (CNT)-based piezoresistive strain sensors have the potential to outperform traditional silicon-based piezoresistors in MEMS devices due to their high strain sensitivity. However, the resolution of CNT-based piezoresistive sensors is currently limited by excessive 1/f or flicker noise. In this paper we will demonstrate several noise mitigation techniques that can be used to decrease noise in the CNT-based sensor system without reducing the sensor’s strain sensitivity. First, the CNTs were placed in a parallel resistor network to increase the total number of charge carriers in the sensor system. By carefully selecting the types of CNTs used in the sensor system and by correctly designing the system it is possible to reduce the noise in the sensor system without reducing sensitivity. The CNTs were also coated with aluminum oxide to help protect the CNTs from environmental variations. Finally, the CNTs were annealed to improve contact resistance and to remove adsorbates from the CNT sidewall. Overall, using these noise mitigation techniques it is possible to reduce the total noise in the sensor system by almost two orders of magnitude and increase the dynamic range of the sensors by 29 dB.

We describe a near perfect broad band absorber based on a laterally nanostructured multilayer material. We present calculations of the structure that demonstrates over 99% absorption of the 500 K black body spectrum. We also show the ability to manufacture an anti-reflective layer using a nanostructured metamaterial which allows us to tailor the index of refraction using effective medium theory. The absorber can be adapted for use in any frequency range and any source type. These materials may have applications in energy harvesting and scattered light control.

Graphene and its derivatives have attracted much attention for potential applications in biological sensing systems because of their unique 2D structural, surface and electronic properties. Reports on graphene - based electrochemical impedance biosensors are emerging rapidly. In this research, we have explored the RF (radio frequency) impedance –based sensing feasibility of graphene and graphene derivative materials on the coplanar waveguide (CPW) device. The transmission line based sensing experiments demonstrated clear and significant blueshifts of resonance frequencies and decrease of the resistance at and beyond resonance frequencies after graphene oxide is absorbed with DNA. The results may lead to an alternative approach in developing graphene based chemical and biosensors.

Increasing solar cell efficiency by using spectral conversion is addressed in this article. To that purpose rare-earth doped YAG nanoparticles exhibiting down-conversion and quantum cutting properties have been prepared. These nanoparticles have been synthesized with different concentrations of dopants in order to optimize the luminescence and the quantum cutting efficiency. Results on the incorporation of selected material into the encapsulating layer of c-Si based PV-modules are also presented. The effect of down-conversion has been demonstrated through the increase of photocurrent of encapsulated silicon solar cells.

Integration of nanomaterials into composite systems is the next evolutionary step in nanoscale science. Until recently nanocomposites are formed by embedding nanomaterial components into matrices, through chemical bonding or with various wrapping agents. We seek to show that through directed self assembly nanomaterials can be coupled with photosensitizing ruthenium complexes while avoiding chemical augmentation and insulating effects from polymer, surfactant or DNA wrapping. We have synthesized dinuclear ruthenium complexes (dimers) possessing rigid conjugated π-electron systems that form a nanoscale pocket. The pocket is dimensionally suited to interact strongly with nanomaterials forming an architecture that could facilitate photon collection and charge transfer across the interaction. This study explores the binding interaction of our ruthenium dimers with SWNTs. The binding strength varies relative to the magnitude of formal charge which trends with DFT simulations that predict SWNT dimer interactions. SWNT surface saturation by ruthenium dimers can be observed using UV-visible spectroscopy and characterized with adsorption isotherms. We also explore a new technique to measure nanomaterial interactions, isothermal titration calorimetry (ITC). We show that ITC can be used to directly measure the binding enthalpy of nano material surface interactions in solution.

Organic photovoltaic devices offer a potentially cheap source of electrical power due to the relative ease of processing compared to silicon devices. Over the last decade the efficiency of these devices has improved significantly and the best devices are currently have >6% power conversion efficiency and ~100% quantum efficiency.

A novel blend of ferroelectric nanostructures, poly(3-hexylthiophene) (P3HT) and [6, 6]-phenyl-C61-butyric acid methyl ester (PCBM) has been used to fabricate hybrid organic and inorganic photovoltaic devices. These devices comprise a glass substrate coated with indium tin oxide (ITO) and an layer of PEDOT:PSS to form the first electrode. The active layer was deposited by spin coating and finally metallic top contacts have been added by thermal evaporation. The devices were characterized using standard current-voltage (IV) measurements under illuminated and dark conditions using an AM1.5 solar simulator and a source-voltage device and the results indicate a difference in efficiency compared to similar devices fabricated at the same time without the novel nanostructures. Additional UV-Vis measurements were used to determine the absorption characteristics of the active layers. The initial results suggest an improvement in the absorption of light in the visible region and higher open circuit voltages and short circuit currents compared to P3HT/PCBM alone.

Poly(3-hexylthiophene) (P3HT) nanofibers were fabricated with an association of poly(vinyl pyrrolidone) (PVP) by electrospinning. A mixture of P3HT/PVP in a mixed solvent of chlorobenzene and methanol was electrospun to form composite fibers with 60 nm - 2 μm in diameter, followed by getting rid of PVP by selective extraction. After extraction, pure P3HT nanofibers were obtained as a spindle-like structure with wrinkled surface. The nanofibers obtained exhibit specific features of strong interchain contribution as investigated by UV-vis, fluorescence spectroscopic, X-ray diffraction (XRD), and photo-electron investigations. Bulk heterojunction P3HT:PCBM nanofibers with ~200 nm in diameters were also successfully fabricated by using the same technique. The preliminary results from the study of P3HT:PCBM nanofiber-based photovoltaic cells with conversion efficiency over 0.2% could be achieved.