The armchair variety of single-wall carbon nanotubes (SWCNTs) is the only nanotube species that behaves as a metal with no electronic band gap and massless carriers, making them ideally suited to probe fundamental questions of many-body physics of one-dimensional conductors as well as to serve in applications such as high-current power transmission cables. However, current methods of nanotube synthesis produce bulk material comprising of a mixture of nanotube lengths, diameters, wrapping angles, and electronic types due to the inability to control the growth process at the nanometer level. As a result, measurements of as-grown SWCNTs produce a superposition of electrical and optical responses from multiple SWCNT species. This thesis demonstrates production of aqueous suspensions composed almost entirely of armchair SWCNTs using a post-synthesis separation method employing density gradient ultracentrifugation (DGU) to separate different SWCNT types based on their mass density and surfactant-specific interactions. Resonant Raman spectroscopy determines the relative abundances of each nanotube species, before and after DGU, by measuring the integrated intensity of the radial breathing mode, the diameter-dependent radial vibration of the SWCNT perpendicular to its main axis, and quantifies the degree of enrichment of bulk nanotube samples to exclusively armchair tubes. Raman spectroscopy of armchair-enriched samples of the G-band mode, which is composed of longitudinal (G-) and circumferential (G+) vibrations oscillating parallel and perpendicular to the tube axis, shows that the G- peak, long-held to be an indicator for the presence of metallic SWCNTs, appears only when electronic resonance with narrow-gap semiconducting SWCNTs occurs and shows only the G+ component in spectra containing only armchair species. Finally, by combining optical absorption measurements with nanotube composition as determined earlier via Raman scattering, peak fitting of absorption spectra indicates that interband transitions of armchair SWCNTs are strongly excitonic as shown by the highly symmetric peak lineshapes, a property normally attributed to semiconductors. Such lineshapes allow classification of armchair SWCNTs as a unique hybrid class of optical nanomaterial. Combining absorption and Raman scattering measurements establishes a distinct optical signature that describes the fundamental optical processes within armchair SWCNTs and lays the foundation for future studies of many-body photophysics and electrical applications.

Advancements in electronic performance lead to a decrease in device size and an increase in power density. Because of these changes, current cooling mechanisms for electronic devices are beginning to be ineffective. Microchannels, with their large heat transfer surface area to volume ratio, cooled with either gas or liquid coolant, have shown some potential in adequately maintaining a safe surface temperature. By modifying the walls of the microchannel with fins, the cooling performance can be improved. Using computational fluid dynamics software, microfins placed in a staggered array on the bottom surface of a rectangular minichannel are modeled in order to optimize microstructure geometry and maximize heat transfer dissipation through convection from a heated surface. Fin geometry, dimensions, spacing, height, and material are analyzed. Correlations describing the Nusselt number and the Darcy friction factor are obtained and compared to recent studies. These correlations only apply to short fins in the laminar regime. Triangular fins with larger fin height, smaller fin width, and spacing double the fin width maximizes the number of fins in each row and yields better thermal performance. Once the effects of microfins were found, an experiment with multi-walled carbon nanotubes (MWNTs) grown on the surface were tested using both water and Al2O3/H2O nanofluid as the working medium. Minichannel devices containing two different MWNT structures – one fully coated surface of MWNTs and the other with a circular staggered fin array of MWNTs - were tested and compared to a minichannel device with no MWNTs. It was observed that the sedimentation of Al2O3 nanoparticles on a channel surface with no MWNTs increases the surface roughness and the thermal performance. Finally, using the lattice Boltzmann method, a two dimensional channel with suspended particles is modeled in order to get an accurate characterization of the fluid/particle motion in nanofluid. Using the analysis based on an ideal fin, approximate results for nanofluids with increase surface roughness was obtained. Microchannels have proven to be effective cooling systems and understanding how to achieve the maximum performance is vital for the innovation of electronics. Implementation of these modified channel devices can allow for longer lasting electronic systems.

As pointed out more and more frequently in the literature, there is a pressing need for research into the health and environmental impact of nanoparticles. This work represents a joint effort between scientists in nanotechnology, chemistry and biology to answer this call and to investigate the environmental effects of carbon nantoubes (CNTs) from a brand new aspect. The results showed clearly the dose-dependent effects of single-walled carbon nanotubes (SWNTs) on the ingestion and digestion of bacteria by Tetrahymena thermophila, a ciliated protozoan, propagated to its prey bacteria, Escherichia coli. Investigated by confocal microscopy Tetrahymena were able to internalize large quantities of SWNTs and then excrete SWNTs and undigested bacteria in aggregates. Inhibition of ciliate bacterivory measured by Ciliate Bacterivory assay was evident at far below lethal concentrations. At high tube concentrations (above 6.8 μg∙ml-1), cell viability was affected. In addition, explored by fluorescence microscopy and scanning electron microscopy, SWNTs stimulated Tetrahymena to abnormally egest viable bacteria inside membrane protected structures, which enhanced bacterial survival during antimicrobial treatments, bacteriostatic or bacteriocidal. This phenomenon may have important implications to public health. In general, research on toxicity of nanoparticles is in a very early stage with most studies on direct fatality (kill or not to kill) of a single organism or certain type of cells. This work is believed to be among the first few investigating extrapolated effects. Hopefully, this wok will stimulate a line of research towards better understanding of the effects of nanomaterials on diverse organisms, and stimulate not only toxicology but also ecotoxicology studies.

The mounting concern for renewable energies from ecologically conscious alternatives is growing in parallel with the demand for portable energy storage devices, fuelling research in the fields of electrochemical energy storage technologies. The supercapacitor, also known as electrochemical capacitor, is an energy storage device possessing a near infinite life-cycle and high power density recognized to store energy in an electrostatic double-layer, or through a pseudocapacitance mechanism as a result of an applied potential. The power density of supercapacitors far exceeds that of batteries with an ability to charge and discharge stored energy within seconds. Supercapacitors compliment this characteristic very well with a cycle life in excess of 106 cycles of deep discharge within a wide operational temperature range, and generally require no further maintenance upon integration. Conscientious of environmental standards, these devices are also recyclable. Electrochemical capacitors are currently a promising candidate to assist in addressing energy storage concerns, particularly in hybridized energy storage systems where batteries and supercapacitors compliment each other’s strengths; however specific challenges must be addressed to realize their potential. In order to further build upon the range of supercapacitors for future market applications, advancements made in nanomaterial research and design are expected to continue the materials development trend with a goal to improve the energy density through the development of a cost-efficient and correspondingly plentiful material. However, it is important to note that the characteristic power performance and exceptional life-cycle should be preserved alongside these efforts to maintain their niche as a power device, and not simply develop an alternative to the average battery. It is with this clear objective that this thesis presents research on an emerging carbon material derived from an abundant precursor, where the investigations focus on its potential to achieve high energy and power density, stability and integration with other electroactive materials. Activated carbons have been the dominant carbon material used in electric double-layer capacitors since their inception in the early 1970s. Despite a wide range of carbon precursors and activation methods available for the generation of high surface area carbons, difficulties remain in controlling the pore size distribution, pore shape and an interconnected pore structure to achieve a high energy density. These factors have restricted the market growth for supercapacitors in terms of the price per unit of energy storage. Activation procedures and subsequent processes for these materials can also be energy intensive (i.e. high temperatures) or environmentally unfriendly, thus the challenge remains in fabricating an inexpensive high surface-area electroactive material with favourable physical properties from a source available in abundance. Double-layer capacitive materials researched to replace active carbons generally require properties that include: high, accessible surface-area; good electrical conductivity; a pore size distribution that includes mesopore and micropore; structural stability; and possibly functional groups that lend to energy storage through pseudocapacitive mechanisms. Templated, fibrous and aerogel carbons offer an alternative to activated carbons; however the drawbacks to these materials can include difficult preparation procedures or deficient physical properties with respect to those listed above. In recent years nanostructured carbon materials possessing favourable properties have also contributed to the field. Graphene nanoplatelet (GNP) and carbon nanotube (CNT) are nanostructured materials that are being progressively explored for suitable development as supercapacitor electrodes. As carbon lattice structured materials either in the form of a 2-dimensional sheet or rolled into a cylinder both of these materials possess unique properties desirable in for electrode development. In the proceeding report, GNPs are investigated as a primary material for the synthesis of electrodes in both a pure and composite form. Three projects are presented herein that emphasize the suitability of GNP as a singular carbon electrode material as well as a structural substrate for additional electroactive materials. Investigation in these projects focuses on the electrochemical activity of the materials for supercapacitor devices, and elucidation of the physical factors which contribute towards the observed capacitance. An initial study of the GNPs investigates their distinct capacitive ability as an electric double-layer material for thin-film applications. The high electrically conductivity and sheet-like structure of GNPs supported the fabrication of flexible and transparent films with a thickness ranging from 25 to 100 nm. The thinnest film fabricated (25 nm) yielded a high specific capacitance from preliminary evaluation with a notable high energy and power density. Furthermore, fast charging capabilities were observed from the GNP thin film electrodes. The second study examines the use of CNT entanglements dispersed between GNP to increase the active surface area and reduce contact resistances with thin-film electrodes. Through the use MWNT/GNP and SWNT/GNP composites it was determined that tube aspect ratio influences the resulting capacitive performance, with the formation of micropores in SWNT/GNP yielding favourable results as a composite EDLC. The third study utilizes electrically conducting polypyrrole (PPy) deposited onto a GNP film through pulse electrodeposition for use as a supercapacitor electrode. Total pulse deposition times were evaluated in terms of their corresponding improvements to the specific capacitance, where an optimal deposition time was discovered. A significant increase to the total specific capacitance was observed through the integration PPy, with the majority charge storage being developed via psuedocapacitive redox mechanisms. A summary of the studies presented here centers on the development of GNP electrodes for application in high power supercapacitor devices. The potential use for GNP in both pure and composite electrode films is explored for electrochemical activity and capacitive capabilities, with corresponding physical characterization techniques performed to examine influential factors which contribute to the final results. The work emphasizes the suitability of GNP material for future investigations into their application as carbon or carbon composite electrodes in supercapacitor devices.

Carbon nanotubes, and particularly single wall carbon nanotubes (SWNTs) have attracted much attention for their unique structure, as well as for their excellent mechanical, electrical and thermal properties. Most properties of carbon nanotubs are closely related with its anisotropic structure and geometry factor. Characterization of carbon nanotube length is critical for understanding their behavior in solutions as well as in polymer composites. Microscopy, particularly atomic force microscopy, has been used for their length measurement. Microscopy, though straightforward, is quite laborious, particularly for statistically meaningful sampling. Light scattering can be used to measure particle dimensions. In this study, light scattering has been used to study polyvinyl pyrrolidone (PVP) wrapped SWNTs surfactant assisted aqueous dispersion and SWNT dispersion in oleum. To determine the length of SWNTs, Stokes - Mueller formalism was used, which is a universal model for particles with any size and shape. The Mueller matrix for an ensemble of long, thin cylinders proposed by McClain et al. was used in this study. This Mueller matrix includes the information of size (length and radius) and optical constants (refractive index and extinction coefficient) of cylinders. In this matrix, extinction coefficient, radius and length of SWNTs are unknown. By normalizing scattering intensity I(theta) (theta from 30 to 155 degree) to that at 30degree , the effects of radius and extinction coefficient were cancelled out. Thus, the effect of SWNT length on scattering intensity could be studied independently. A series of curves of normalized scattering intensity of SWNTs (I(theta) /I(30degree)) with varied length as a function of wave vector were predicted. A curve of normalized scattering intensity of SWNT as a function of wave vector was also obtained experimentally. By comparing experimental and predicted curves, average SWNT length in the dispersion has been determined. Scattering intensity at a given angle initially increases with concentration, and then reaches a critical concentration(C*), above which the scattering intensity decreases. This phenomenon has been attributed to the competition between scattering and absorption of light by the presence of SWNT. By using Beer-Lambert law, this phenomenon has been used to determine the molar absorption coefficient of SWNTs.

Modern day engineering systems research presently lacks techniques to exploit the unique properties of many nanomaterials; coupled with this challenge exists the need to interface these nanomaterials with microscale and macroscale platforms. A nanomaterial of particular interest is the carbon nanotube (CNT), due to its enhanced physical properties. In addition to varied electrical properties, the CNT has demonstrated high thermal conductivity and tensile strength compared to conventional fiber materials. CNTs are beginning to see commercial applications in areas in which sufficient study has been dedicated. While a large part of the worldwide focus of CNT research has been in synthesis, an equally important area of research lies in CNT integration processes. The unique and useful properties of many nanostructured materials will never be realized in mainstream manufacturing processes and commercial applications without the proper exploration of integration methods such as those detailed in this thesis. The primary motivation for the research detailed in this thesis has been to develop CNT synthesis processing techniques that allow for novel interfacing methods between carbon nanotubes and eventual applications. In this study, an investigation was performed to look at several approaches to integrating CNTs into micro-electromechanical systems (MEMS). Synthesis of CNTs was studied in two different settings. Synthesis was first performed, directly on the microsystem, via a global scale chemical vapor deposition (CVD) process. Secondly, synthesis was performed directly onto a microsystem device via localized resistive heating. Following synthesis, the application of atomically layered, protective coatings was then investigated. Integration methods were then investigated to allow for CNT transfer to microsystem applications incapable of withstanding synthesis temperatures. The developed integration methods were evaluated by creating functional microscale electrical circuits in flexible substrates via hot emboss imprint lithography. Lastly, post synthesis processing methods were used to create micropatterned cell guidance substrates as well as neuronal stimulating substrates.

Current microfabrication materials include silicon, a wide variety of metals, dielectrics, and some polymers. Because of the low cost and high processing flexibility that polymers generally have, expanding the use of polymers in microfabrication would benefit the microfabrication community, enabling new routes towards goals such as low-cost 3D microfabrication. This work describes two main unconventional uses of polymers in microfabrication. The first unconventional use is as a carrier material in the self-assembly (SA) of millimeter-scale parts in which functional electronic components and electrical interconnects were cast into 5 mm cubes of Polymethylmethacrylate (PMMA). The second unconventional use is as a non-flat micromold for an alumina ceramic and as transfer material for multiple layers of micropatterned carbon nanotubes (CNTs). Both of these uses demonstrate 3D low-cost microfabrication routes. In the SA chapter, surface forces induced both gross and fine alignment of the PMMA cubes. The cubes were bonded using low-melting temperature solder, resulting in a self-assembled 3D circuit of LEDs and capacitors. The PMMA-encasulated parts were immersed in methyl methacrylate (MMA) to dissolve the PMMA, showing the possibility of using MEMS devices with moving parts such as mechanical actuators or resonators. This technique could be expanded for assembly of systems having more than 104 components. The ultimate goal is to combine a large number of diverse active components to allow the manufacture of systems having dense integrated functionality. The ceramic micromolding chapter explores micromolding fabrication of alumina ceramic microstructures on flat and curved surfaces, transfer of carbon nanotube (CNT) micropatterns into the ceramic, and oxidation inhibition of these CNTs through ceramic encapsulation. Microstructured master mold templates were fabricated from etched silicon, embossed thermally sacrificial polymer, and flexible polydimethylsiloxane (PDMS). The polymer templates were themselves made from silicon masters. Thus, once the master is produced, no further access to a microfabrication facility is required. Using the flexible PDMS molds, ceramic structures with mm-scale curvature were fabricated having microstructures on either the inside or outside of the curved macrostructure. It was possible to embed CNTs into the ceramic microstructures. To do this, micropatterned CNTs on silicon were transferred to ceramic via vacuum molding. Multilayered micropatterned CNT-ceramic devices were fabricated, and CNT electrical traces were encapsulated with ceramic to inhibit oxidation. During oxidation trials, encapsulated CNT traces showed an increase in resistance that was 62% less than those that were not encapsulated.

Drinkable water sources (mainly including rivers, reservoirs, and groundwater) are almost universally polluted by organic substances. In Taiwan, the majority of water treatment plants ensure high-quality drinking water by using chlorine to control the growth of algae and microorganisms, thereby removing odors, tastes, ferric and manganese irons. However, these processes produce disinfection by-products (DBPs), such as Trihalomethanes (THMs) and Haloacetic acids. These DBPs contained in drinking water increase the risk of cancer in human body. Thus commercial carbon nanotubes (CNTs) were employed as adsorbents to study adsorption of humic acid (HA) and dissolved organic matter (DOM) in raw water. Experiment results exhibited kinetic adsorption reached equilibrium about 120 minutes,the best selection in kinetic models evaluation, fitting models such as Modified Freundlich equation, Pseudo-1st-order equation and Pesudo-2nd-oder equation, is Modified Freundlch equation model. In addition, intraparticle diffusion equation model was fitted well and showed adsorption process was controlled with pore diffusion.The maximum adsorbed amounts of DOM onto SWCNTs was calculated by the Langmuir model at 25¢J, reaching 54.01 mg TOC / g which were much higher than that onto commercially available granular activated carbon (10.69 mg TOC / g).The maximum adsorbed amounts of HA onto CNTs was calculated by the Langmuir model at 25¢J, reaching 125.95 mg TOC / g which were much higher than that onto commercially availablepowdered activated carbon (42.37mg TOC / g).A favorable adsorption of single-wall carbon nanotubes was found when high initial concentration of DOM was adsorbed at low ion strength, low pH and low temperature .According to results of thermodynamic parameters indicated that the adsorption was spontaneously and an exothermic reaction. The short contact time needed to reach equilibrium as well as the high adsorption capacity of DOM suggests that CNTs possess highly potential applications for DOM removal from raw water.In the future, we can combine nanotube technology with disinfection technology and apply such technique on the end of processing unit for design of either the domestic treatment facilities or small simple water treatment in drinking water. Thus our results in this work will enhance the new treatment technology of drinking water and improve the safety of the public health. Another possibility will be to promote the opportunity of marketing development in drinking water.

A novel process which does not require the traditional Chemical Vapor Deposition (CVD) synthesis techniques and which works at temperatures lower than the conventional techniques was developed for synthesis of carbon nanotubes (CNT). The substrates used for this study involved MEMS (Micro Electrical Mechanical Systems) elements and passive elements. These were coated with Fullerene using Physical Vapor Deposition or through a solution in an organic solvent. Catalyst precursors were deposited on these Fullerene coated substrates using “wet processes”. These substrates were then heated using either the integrated microheaters or external heaters in an inert atmosphere to obtain CNT. Thus, in this process we tried to obviate the Chemical Vapor Deposition (CVD) process for synthesis of CNT (SWCNT and MWCNT). The synthesized CNT will be characterized using Scanning Electron Microscopy and Raman spectroscopy techniques. Also, conductivity measurements were carried out for the synthesized tubes using Dry (contact based) and Wet (electro-chemical) methods. This work also proves the concept for the feasibility for a portable hand held instrument for synthesis of CNT with tunable “on demand” chirality.

This research is focused on investigating the effect of carbon nanotubes on macroscale composite laminate properties, such as, interlaminar shear strength, interlaminar fracture toughness and electrical conductivity along with studying the micro and nano-scale interactions of carbon nanotubes with epoxy matrix via thermomechanical and electrical characterization of nanocomposites. First an introduction to the typical advanced composite laminates and multifunctional nanocomposites is provided followed by a literature review and a summary of recent status on the processing and the characterization work on nanocomposites and composite laminates. Experimental approach is presented for the development of processing techniques and appropriate characterization methods for carbon nanotubes reinforced epoxy resin based multi-functional nanocomposites and carbon fiber reinforced polymer composite laminates modified with carbon nanotubes. The proposed work section is divided into three sub-sections to describe the processing and the characterization of carbon nanotube reinforced epoxy matrix nanocomposites, woven-carbon fabric epoxy matrix composite laminates modified with selective placement of nanotubes and unidirectional carbon fiber epoxy matrix composite laminates modified with carbon nanotubes. Efforts are focused on comparing the effects of functionalized and unfunctionalized carbon nanotubes on the advanced composite laminates. Covalently functionalized carbon nanotubes are used for improved dispersion and fiber-matrix bonding characteristics and compared with unfunctionalized or pristine carbon nanotubes. The processing of woven carbon fabric reinforced epoxy matrix composite laminates is performed using a vacuum assisted resin transfer molding process with selective placement of carbon nanotubes using a spraying method. The uni-directional carbon fiber epoxy matrix pre-preg composites are processed using a hot press technique along with the spraying method for placement of nanotubes. These macroscale laminates are tested using short beam shear and double cantilever beam experiments for investigating the effect of nanotubes on the interlaminar shear stress and the interlaminar fracture toughness. Fractography is performed using optical microscopy and scanning electron microscopy to investigate the structure-property relationship. The micro and nano-scale interactions of carbon nanotubes and epoxy matrix are studied through the processing of unfunctionalized and functionalized single wall carbon nanotube reinforced epoxy matrix nanocomposites. The multifunctional nature of such nanocomposites is investigated through thermo-mechanical and electrical characterizations.