In the past decade, the use of nanotechnology as a tool to develop and fabricate new structures and devices for biological sensing and energy applications has become increasingly widespread. In this work, a systematic study has been performed on one-dimensional nanomaterials, with a focus on the development of miniaturized devices with a "bottom up" approach. First, members of the nano - carbon family are utilized for biosensing applications; in particular, carbon nanotubes as well as nitrogen - doped and boron - doped nanocrystalline diamond (NCD) films. These carbon - based materials possess several unique electrochemical properties over other conductive materials which make them suitable for biosensing applications. Single walled carbon nanotubes were deposited on a glass carbon electrode and modified for the detection of Salmonella DNA hybridization. Electrochemical impedance spectroscopy (EIS) was used as the method of detection and a detection limit of 10-9 M was achieved. Nanocrystalline diamond was grown using a microwave enhanced plasma chemical vapor deposition method. The diamond electrodes were doped with either boron or nitrogen to provide substrates and characterization was performed using scanning electron microscopy, atomic force microscopy, Raman spectroscopy, Fourier transform infrared spectroscopy, UV-vis spectroscopy, as well as by electrochemical methods. Modified boron - doped NCD was able to detect Salmonella DNA hybridization via EIS and fluorescent microscopy. The detection limit for these genosensors was found to be 0.4 micrometer complementary DNA. Boron - doped and nitrogen - incorporated nanocrystalline diamond also served as functionalized electrodes for lactic acid detection. It was found that the boron - doped electrodes could detect 0.5 mM lactic acid in a phosphate buffer solution. Second, bismuth antimony nanowires were grown in an anodized alumina template for the fabrication of a thermoelectric cooling device. Bismuth antimony nanowires were chosen due to their high thermoelectric efficiency compared to their bulk material counterpart. The development of a successful anodized template was achieved and EIS was used to diagnose the optimal etch parameters of the barrier oxide layer for nanowire growth. Bismuth antimony nanowires were grown directly on a silicon substrate and a thermoelectric cooling device was fabricated. The nanowires exhibited a thermoelectric efficiency of 0.18 at room temperature.

With the development of modern industrial engineering technology, increasing demands of multifunctional materials drive the exploration of new applications of electrical conductive polymer nanocomposites (CPNCs). Toward applications of smart materials, sensing performance of CPNCs has gained immense attention in the last decade. Among them, strain sensors, based on piezoresistive behavior of CPNCs, are of high potential to carry out structural health monitoring (SHM) tasks. Poly(vinylidene fluoride) (PVDF) is highly thought to be potential for SHM applications in civil infrastructures like bridges and railway systems, mechanical systems, automobiles, windgenetors and airplanes, etc. because of its combination of flexibility, low weight, low thermal conductivity, high chemical corrosion resistance, and heat resistance, etc. This work aimed to achieve high piezoresistive sensitivity and wide measurable strain ranges in carbon nanotube based poly(vinylidene fluoride) (PVDF) nanocomposites. Four strategies were introduced to tune the sensitivity of the relative electrical resistance change (ΔR/R0) versus the applied tensile strain for such nanocomposites. Issues like the influence of dispersion of multi-walled carbon nanotubes (MWCNTs) on initial resistivity of PVDF nanocomposites and conductive network structure of MWCNTs, as well as piezoresistive properties of the nanocomposites, were addressed when using differently functionalized MWCNTs (strategy 1). In addition, the effects of crystalline phases of PVDF, mechanical ductility of its nanocomposites and interfacial interactions between PVDF and fillers on piezoresistive properties of PVDF nanocomposites were studied. Using hybrid fillers, to combine MWCNTs with conductive carbon black (strategy 2) or isolating organoclay (strategy 3), piezoresistive sensitivity and sensing strain ranges of PVDF nanocomposites could be tuned. Besides, both higher sensitivity and larger measurable strain ranges are achieved simultaneously in PVDF/MWCNT nanocomposites when using the ionic liquid (IL) BMIM+PF6- as interface linker/modifier (strategy 4). The detailed results and highlights are summarized as following: 1. The surface functionalization of MWCNTs influences their dispersion in the PVDF matrix, the PVDF-nanotube interactions and crystalline phases of PVDF, which finally results in different ΔR/R0 and the strain at the yield point (possibly the upper limit of sensing strain ranges). As a whole, regarding to the fabrication of strain sensors based on PVDF/MWCNT nanocomposite, in contrast to pristine CNTs, CNTs-COOH and CNTs-OH, CNT-NH2 filled PVDF nanocomposites possess not only high piezoresistive sensitivity but also wide measurable strain ranges. Gauge factor, i.e. GF, is ca.14 at 10% strain (strain at the yield point) for the nanocomposites containing 0.75% CNTs-NH2. 2. Using hybrid fillers of CNTs and CB to construct strain-susceptible network structure (conductive pathway consisting of string-like array of CNTs and CB particles) enhances the piezoresistive sensitivity of PVDF nanocomposites, which is tightly associated with the CNT content in hybrid fillers and mCNTs/mCB. The best piezoresistive effect is achieved in PVDF nanocomposites with fixed CNT content lower than the ΦC (0.53 wt. %) of PVDF/CNT nanocomposites. 3. ΔR/R0 and possible sensing strain ranges of PVDF nanocomposites were tailored by changing crystalline phases of PVDF and PVDF-MWCNT interactions. Besides, the increase of the strain at yield point in PVDF nanocomposites filled by CNTs-OH is more obvious than that in the nanocomposites containing the same amount of clay and CNTs. The nanocomposite consisting of 0.25% clay and 0.75% CNTs-OH have ca. 70% increase of the strain at the yield point (17%) and the GF at this strain is ca. 14, while GF for the nanocomposite filled by only 0.75% CNTs-OH is ca. 5 at 10% strain. 4. IL BMIM+PF6- served as interface linker for PVDF and MWCNTs, which significantly increased the values of ΔR/R0 and strain at the yield point of PVDF nanocomposites simultaneously. Besides, this increases with increasing IL content. With the aid of IL, the dispersion of nanotube and toughness of the nanocomposites are greatly improved, but the electrical conductivity of the nanocomposites is decreased with the incorporation of IL, which is related to the IL modified PVDF-MWCNT interface connection or bonding. GF reaches ca. 60 at 21% strain (the strain at the yield point) for PVDF nanocomposites filled by 10% IL premixed 2%CNTs-COOH.

Water splitting through photoelectrochemical reaction is widely regarded as a major method to generate H2 , a promising source of renewable energy to deal with the energy crisis faced up to human being. Efficient exploitation of visible light in practice of water splitting with pure TiO2 material, one of the most popular semiconductor material used for photoelectrochemical water splitting, is still challenging. One dimensional TiO2 nanotubes is highly desired with its less recombination with the short distance for charge carrier diffusion and light-scattering properties. This work is based on TiO2 NTPC electrode by the optimized two-step anodization method from our group. A highly crystalized p-type Cu2O layer was deposited by optimized pulse potentiostatic electrochemical deposition onto TiO2 nanotubes to enhance the visible light absorption of a pure p-type TiO2 substrate and to build a p-n junction at the interface to improve the PEC performance. However, because of the real photocurrent of Cu2O is far away from its theoretical limit and also poor stability in the aqueous environment, a design of rGO medium layer was added between TiO2 nanotube and Cu2O layer to enhance the photogenerated electrons and holes separation, extend charge carrier diffusion length (in comparison with those of conventional pure TiO2 or Cu2O materials) which could significantly increase photocurrent to 0.65 mA/cm2 under visible light illumination (>420 nm) and also largely improve the stability of Cu2O layer, finally lead to an enhancement of water splitting performance.

In this work, carbon nanotubes were deposited onto the insulative glass fibre surface to form a semiconductive network. Utilizing the unique properties of CNTs network, a multifunctional composite interphase could be achieved. The interfacial adhesion strength was improved by CNTs distributed in the interphase. The semiconductive interphase have been used as a chemical/phaysical sensor, strain sensor and microswitch.

The thesis "Anlre resolved dielectric response in carbon nanotubes" is dedicated to expounding the the anisotropy in the fundamental dielectric response of carbon nanotubes. While nanotubes are along their axis essentially planar graphene, the rolled up topology gives rise to entirely new features for perpendicular polarizations.

Carbon nanotubes (CNT) have gained interest for wide use as both support and catalyst due to the ease of uniquely tunable surface chemistry. Increasingly severe greenhouse effects have attracted attention to novel materials and technologies capable of capturing carbon dioxide (CO2). In this context, we develop a CNT based solid state amine for the CO2 capture. CNT are functionalized under various methods as a support for polymeric amines. Polyethyleneimine are physically adsorbed on CNT and are further characterized and studied for reversible CO2 capture. We obtain a high CO2 capture capacity (6.78 mmol∙g-1) for linear polyethyleneimine (LPEI) and 6.18 mmol∙g-1 for branched polyethyleneimine (BPEI). Based on the study of pore structure, we also demonstrate that in a steam post-combustion environment, supported polymeric amines on CNT show higher stability than traditional metal oxides. Besides the increased stability of the support in steam, we also improve the stability of amines under steam conditions by developing a covalent modification method. The CO2 capture capacity of the covalent bonded materials under steam conditions improved by 14% compared to dry conditions. In addition, the loading, chemical properties of PEI, and the surface chemistry of CNT remained stable under steam conditions compared to physically adsorbed PEI on CNT. These results suggest that covalent bonded PEI on CNT can be more suitable for CO2 capture in post-combustion processes. A different CNT application is as a catalyst for oxidative dehydrogenation (ODH) of ethane, and herein we develop a new processing technique for tuning the surface chemistry of the CNT-based catalyst. A one-step, gas-phase hydrogen (H2) surface modification is used to reduce carboxylic groups to phenolic groups on carbon nanotube (CNT) materials. This technique is greener and more facile for large-scale industrial catalysts than what has previously been reported. This method uses fundamental principles of CNT surface chemistry to efficiently reduce the unselective oxidation sites and enhances the active sites used for alkane oxidative dehydrogenation. The resulting catalyst improves the ethylene selectivity and yield by at most 81% and 28% respectively compared to the non-modified catalyst. A clear linear correlation between the functional groups and catalytic activity reveals the effect of specific oxygen species on performance. As the catalyst surface area increases, pretreatments generate more selective active sites instead of over-oxidation sites, providing a guideline for catalyst optimization. We suggest that the gas-phase H2 method is general for reducing carbon catalysts to increase selective oxidation sites for gas phase reactions.

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Carbon nanotube forests are vertically grown tubular formations of graphene. Samples were grown with an injection chemical vapor deposition method on substrates of silicon with various deposited layers and bare fused silica. The morphology of the forest is characterized by the height, density, and presence of defects. Total diffuse reflectance and transmittance measurements were taken in the 2-16 �m spectral range and correlated to the forest’s specific morphology. From these correlations, the conditions necessary to maximize the absorption of the forest were found and exploited to cater sample growth for specific substrates to make ideal absorbers. From the transmittance data, the absorption coefficient is found via Beer-Lambert’s Law and also correlated to sample morphology, giving us an indication of the height of the forest needed for ideal absorption. Two models were used to attempt to reproduce the experimental absorption coefficient: an effective medium theory using a Maxwell Garnett approximation and by treating the carbon nanotube forest as an effective cylindrical waveguide with walls of graphite. Each model leads to a set of fitting parameters providing a better physical understanding of the forests. It was found that the effective medium theory gave results loosely corroborated with electron microscopy, but had trouble fitting the experimental data, and the index of refraction it provides does not behave like a unified medium. The waveguide model fits the data well, but it requires more experimental evidence to be more conclusive. The theoretical models need more work, but fabrication of ideal absorbers has been achieved on various substrates providing framework for their usage in radiometry and spectroscopy.

Thermal interface materials (TIMs) are used as an aid in transporting heat away from a circuit or electronic module. Composite materials are a popular research area for TIMs because they allow the desired properties from the individual constituents to be combined. The composite selected for this study uses carbon nanotubes (CNT) as the filler and an elastomeric polymer for the matrix, specifically a multiwalled carbon nanotube (MWCNT) / polydimethylsiloxane (PDMS) composite. Additionally, functionalization of the CNT may affect the composites’ thermal conductivity because of its effect on the CNT dispersion in the polymer matrix and its effect on the CNT-polymer interface. The objective of this study was to determine the effect CNT functionalization has on the effective thermal conductivity of a MWCNT/PDMS composite. The three functionalization’s used in this study are unfunctionalized, functionalized with a carboxyl group, and functionalized with a hydroxyl group. Secondary objectives were to develop the initial stages of a carbon-polymer composite database and to perform an uncertainty analysis on the stepped bar apparatus used in this study. The database is to be used for visualization of data found in literature to promote data driven research. The uncertainty analysis on the stepped bar apparatus is to qualify the instrument for thermal measurements in this study Initial results showed some increase in thermal properties of the composite, but there was little difference between the thermal conductivity of the three functionalization’s because of the high level of uncertainty used early on in this study. Later results showed an increase in mechanical properties of the composite which offset any thermal advantage with use as a TIM. A stronger composite means less compression under a similar load, resulting in a thicker TIM and higher resistance. However, the mechanical and thermal properties compound to show that -OH functionalized MWCNT present better properties for a TIM than unfunctionalized and -COOH functionalized; none show better results than the polymer by itself.

No description available.