No description available.

No description available.

Downscaling of the contact length Lc of a side-contacted carbon nanotube field-effect transistor (CNTFET) is challenging because of the rapidly increasing contact resistance as Lc falls below 20–50 nm. If in agreement with existing experimental results, theoretical work might answer the question, which metals yield the lowest CNT–metal contact resistance and what physical mechanisms govern the geometry dependence of the contact resistance. However, at the scale of 10 nm, parameter-free models of electron transport become computationally prohibitively expensive. In our work we used a dedicated combination of the Green function formalism and density functional theory to perform an overall ab initio simulation of extended CNT–metal contacts of an arbitrary length (including infinite), a previously not achievable level of simulations. We provide a systematic and comprehensive discussion of metal–CNT contact properties as a function of the metal type and the contact length. We have found and been able to explain very uncommon relations between chemical, physical and electrical properties observed in CNT–metal contacts. The calculated electrical characteristics are in reasonable quantitative agreement and exhibit similar trends as the latest experimental data in terms of: (i) contact resistance for Lc = ∞, (ii) scaling of contact resistance Rc(Lc); (iii) metal-defined polarity of a CNTFET. Our results can guide technology development and contact material selection for downscaling the length of side-contacts below 10 nm.

Abstract Carbon nanotubes (CNTs) are known for their excellent mechanical, electrical and thermal properties, that have fostered a vast number of applications during the last two decades, from composites, electrodes and nanoelectonics components, to sensors and biological scaffolds. Direct integration of CNTs into devices is not straightforward, as high growth temperatures (above 600 °C) challenge the chemical and thermal stability of substrates, catalysts and other nearby materials or components. However, by decreasing growth temperature and/or working out protocols that take into account the thermal stability of the materials involved, it is possible to create several new types of architectures and devices with functionalities not shown before. In this work, we show that, with selection of the appropriate substrate, diffusion barrier and catalyst materials, direct growth of functional CNT films and their micropatterns may be achieved, not only on Si chips, but also on other atypical surfaces, using chemical vapor deposition. This thesis explores low-temperature CNT synthesis over bi- and trimetallic catalysts, and investigates the effect of diffusion barrier layers on the electrical properties of substrate-to-CNT contacts. On one hand, the lowest achieved CNT synthesis temperature (400 °C) is compatible with most silicon technologies, thus enabling direct integration of CNTs with materials and devices with low thermal budgets. On the other hand, the results of diffusion barrier studies helped us in designing and demonstrating on-chip micropatterned CNT structures for super and pseudocapacitor electrodes. In addition, we also show a method for maskless growth of CNT micropatterns using laser-treated steel and superalloy surfaces, whose surface diffusion properties change as a result of barrier-type metal oxide formation. Furthermore, we present CNT growth on carbon materials and demonstrate entirely carbon-based hierarchical composites for electromagnetic interference shielding applications, exhibiting outstanding absorption-based shielding performance. The results presented in this thesis are expected to contribute to a further expansion of CNT-based technologies, in particular with potential for future advances in high-frequency devices (arrays, amplifiers and shielding materials), energy materials (electrodes and scaffolds), as well as in nanoelectromechanical systems (sensors and actuators). / Tiivistelmä Hiilinanoputket tunnetaan niiden erinomaisista mekaanisista, sähköisistä ja termisistä ominaisuuksista, joita on hyödynnetty lukuisissa sovelluksissa viimeisen kahden vuosikymmenen aikana alkaen komposiiteista, elektrodeista, nanoelektroniikkakomponenteista ja sensoreista aina biologisiin tukirakenteisiin. Nanoputkien synteesi suoraan laitteessa ei ole suoraviivaista, sillä korkeat, yli 600 °C synteesilämpötilat asettavat haasteita substraatin, katalyytin sekä muiden lähellä olevien materiaalien ja komponenttien kemialliselle ja termiselle vakaudelle. Alentamalla synteesilämpötilaa ja/tai kehittämällä termisen vakauden huomioivia menetelmiä on mahdollista luoda uudenlaisia arkkitehtuureja ja sovelluksia ennennäkemättömillä ominaisuuksilla. Tässä työssä osoitetaan, että sopivan substraatin, diffuusiosuojan ja katalyyttimateriaalin valitsemalla funktionaalisten hiilinanoputkien synteesi on mahdollista piin lisäksi myös muille, epätavallisille pinnoille käyttäen kemiallista kaasufaasipinnoitusta. Väitöstyössä käsitellään hiilinanoputkien matalan lämpötilan synteesiä hyödyntäen kaksi- ja kolmimetallisia katalyyttejä sekä tutkitaan diffuusiosuojakerroksen sähköistä vaikutusta substraatin ja hiilinanoputkien väliseen kontaktiin. Alin saavutettu synteesilämpötila (400 °C) on yhteensopiva useimpien piiteknologioiden kanssa, mikä mahdollistaa nanoputkien suoran integroinnin matalaa lämpötilaa edellyttäville materiaaleille. Työssä tutkitun diffuusiosuojakerroksen kehitys mahdollisti myös piisirun päälle toteutettujen hiilinanoputkipohjaisten super- ja pseudokondensaattorielektrodien demonstroinnin. Lisäksi työssä esitetään menetelmä, jossa laserkäsittelemällä teräs- ja supermetalliseospinta, jonka avulla mikrokuvioitu hiilinanoputkien kasvu ilman litografiaprosessia on mahdollista. Viimeisenä työssä esitetään hiilinanoputkien synteesi suoraan toiselle hiilimateriaalille ja demonstroidaan täysin hiilipohjainen, hierarkkinen komposiittimateriaali erinomaisella absorptioon perustuvalla suojauskyvyllä sähkömagneettisiin häiriösuojaussovelluksiin. Väitöstyössä esitettyjen tulosten odotetaan osaltaan edistävän hiilinanoputkipohjaisten teknologioiden kehitystä erityisesti korkean taajuuden laitteissa, energiamateriaaleissa sekä nanosähkömekaanisissa järjestelmissä.

CO2 is a waste product from a number of human activities such as fossil fuel power generation, industrial manufacturing processes, and transport. The rising concentration of CO2 in the atmosphere is heating the planet’s surface via the well-established greenhouse effect; a mechanism for many irreversible climate change impacts. Coupled to this is the ever-increasing global pressure over the availability and access to fossil fuel reserves; the foundations of modern society. In recognition of this CO2 is gaining renewed interest as a carbon feedstock, a changing of attitude viewing it as an asset rather than waste. Carbon capture and utilisation (CCU) technologies are attempting to make use of it. However, little quantitative assessment work has been done to assessand verify such potentials. This thesis applies the principles and framework of the life cycle assessment (LCA) - environmental management tool to early stage CO2 utilisation laboratory processes. All processes employ engineered nanomaterials (ENM) to perform this function, a material class leading the way in the challenges of efficient and feasible CO2 chemistry. The LCA contribution in this thesis acts as a measuring and a guiding tool for technology developers, in the first instance to document the cradle-to-gate impacts of a number of formed ENMs. Appreciating the net environmental benefits of ENM uptake within society has yet to be wholly established, and the unavailability of data is recognised as a major factor. The work of this thesis will thus contribute to knowledge gaps, and be informative to wider community seeking to quantify technical performance benefits of ENMs in the context of net life cycle impact burdens. Finally the actual CCU processes are assessed, initially within the confines of the laboratory but further expanded for consideration at more industrially relevant scales. The potential for sound CCU performance were found achievable under best case conditions, with net GHG impact reductions over the life cycle, and the potential for lower impact carbon products, even carbon negative. However other environmental impacts such as ozone depletion, toxic emissions and the consumption of precious metalores are impacts that require consideration in the use of such technologies.

Les propriétés électriques et physiques de structures à faible dimensionalité ont été étudiées pour des applications dans des domaines divers comme l'électronique, les capteurs. La mesure du bruit bruit à basse fréquence est un outil très utile pour obtenir des informations relatives à la dynamique des porteurs, au piègeage des charges ou aux mécanismes de collision. Dans cette thèse, le transport électronique et le bruit basse fréquence mesurés dans des structures à faible dimensionnalité comme les dispositifs multi-grilles (FinFET, JLT...), les nanofils 3D en Si/SiGe, les nanotubes de carbone ou à base de graphène sont présentés. Pour les approches " top-down " et " bottom-up ", l'impact du bruit est analysé en fonction de la dimensionalité, du type de conduction (volume vs surface), de la contrainte mécanique et de la présence de jonction metalsemiconducteur.

Carbon nanotube (CNT) forests are an important class of nanomaterials with many potential applications due to their unique properties such as mechanical compliance, thermal and electrical conductance, etc. Their deformation and failure in compression loading is critical in any application involving contact because the deformation changes the nature of the contact and thus impacts the transfer of load, heat, and charge carriers across the interface. The micro- and nano-structure of the CNT forest can vary along their height and from sample to sample due to different growth parameters. The morphology of CNTs and their interaction contribute to their mechanical behavior with change of load distribution in the CNT forest. However, the relationship is complicated due to involvement of many factors such as density, orientation, and entanglement of CNTs. None of these effects, however, are well understood. This dissertation aims to advance the knowledge of the structure-property relation in CNT forests and find methodologies for tuning their mechanical behavior. The mechanical behavior of CNT forests grown with different methodologies is studied. Furthermore, the effects of coating and wetting of CNT forests are investigated as methods to tailor the degree of interaction between CNTs. In situ micro-indentation of uncoated CNT forests with distinct growth-induced structures are performed to elucidate the effects of change of morphology along the height of CNT forests on their deformation mechanism. CNT aerial density and tortuosity are found to dictate the location of incipient deformation along height of CNT forests. Macro-compression testing of uncoated CNT forests reveals mechanical failure of CNT forests by delamination at the CNT-growth substrate. Tensile loading of CNT roots due to post-buckling bending of CNTs is proposed to be the cause of this failure and simple bending theory is shown to estimate the failure load to be on the same order of magnitude as experimental measurements. Furthermore, delamination is observed to occur in the in situ micro-indentation of CNT forests coated with aluminum on the top surface, which demonstrates the role of the mechanical constraints within the CNT forest in the occurrence of delamination at the CNT-substrate interface. In addition, this dissertation explores the mechanical behavior of CNT forests coated conformally (from top to bottom) with alumina by atomic layer deposition. In situ micro-indentation testing demonstrates that the deformation mechanism of CNT forests does not change with a thin coating (2 nm) but does change with a sufficiently thick coating (10 nm) that causes fracturing of the hybrid nanotubes. Ex situ flat punch and Berkovich indentations reveal an increase in stiffness of the CNT forests that are in range with those predicted by compression and bending theories. An increase in the recoverability of the CNTs is also detected. Finally, solvent infiltration is proposed as a method of decreasing stiffness of CNT forests and changing the deformation mechanism from local to global deformations (i.e., buckling in the entire height). Presence of solvents between CNTs decreases the van der Waals forces between them and produces CNT forests with lower stiffness. The results demonstrate the effect of interaction between CNTs on the mechanical behavior. This dissertation reveals important information on the mechanical behavior of CNT forests as it relates to CNT morphology and tube-to-tube interactions. In addition, it provides a framework for future systematic experimental and theoretical investigations of the structure-property relationship in CNT forests, as well as a framework for tuning the properties of CNT forests for diverse applications.

ABSTRACT SYNTHESIS AND CHARACTERIZATION OF ETHANOL ELECTRO-OXIDATION CATALYSIS Demir-Kivrak, Hilal Ph.D., Department of Chemical Engineering Supervisor : Prof. Dr. Deniz &Uuml / ner Co-supervisor : Dr. Sadig Kuliyev October 2010, 196 pages In this study, the role of defects, the role of Sn in relation to defects, and the role of oxide phase of tin in ethanol electro-oxidation reaction were investigated. Firstly, adsorption calorimetry measurements were conducted on monometallic (1%Pt, 2%Pt, and 5%Pt) and bi-metallic (5% Pt-Sn) &gamma / -Al2O3 supported Pt catalysts. It was observed that while saturation coverage values decreased, intermediate heats remained same for Pt-Sn catalysts by the increasing amount of tin. The effect of particle size was investigated on Pt/C (pH=5), Pt/C (pH=11) catalysts at different scan rates. At high scan rates (quite above diffusion limitations), current per site activities were nearly the same for 20% Pt/C (E-Tek), Pt/C (pH=11), and Pt/C (pH=5) catalysts, which explained as electro-oxidation reaction takes place at the defects sites. Furthermore, the effect of support on ethanol electro-oxidation was investigated on CNT supported Pt catalyst. Results indicate that only the metal v dispersions improved ethanol electro-oxidation reaction and support did not have any effect on ethanol electro-oxidation reaction. Results on the 20% Pt-Sn/C (15:1 to 1:1 Pt: Sn atomic ratios) and 20% Pt-SnO2/C (6:1 and 1:1) catalysts indicated that ethanol electro-oxidation activity increased by increasing tin amount. For 20% Pt-Sn/C catalysts, Pt-Sn (6:1)/C indicated best activity. On the other hand, 20% Pt-SnO2 (6:1)/C catalyst was better than Pt-Sn (6:1)/C in terms of ethanol electro-oxidation activity due to the fact that there was low contact between Pt and tin oxide particles.

This research was designed to fabricate and characterize novel polyhedral phase segregated microstructures of polystyrene (PS)-matrix composites filled with multi-walled carbon nanotubes (MWNT) and indium tin oxide (ITO) nanopowders. PS-composites were compression molded with MWNT and ITO separately first. The resulting composites were conducting, and remained optically transparent. Mixtures of MWNT and ITO were then used to form mixed ITO/MWNT PS-composites in order to optimize their transparency and conductivity. This was achieved by fabricating composites with varying concentrations of fillers. Impedance spectroscopy was used to characterize the electrical properties of the PS-composites. Optical properties were characterized by measuring the transmission of light through the PS-composite in the visible light spectrum using a spectrophotometer. The electrical properties and microstructural attributes of the fillers used were also characterized. The main objective of the project was to understand the relationships between the structural, electrical, and optical properties of the PS-composites. The resistivity of PS-composites filled with MWNT ranged from 105 to 1013 Ω cm for samples with 0.007 to 0.9 vol% MWNT. The resistivity of PS-composites filled with ITO ranged from 107 to 1013 Ω cm for PS-composites with 0.034 to 0.86 vol% ITO. PS/ITO composites had a percolation threshold of 0.15, 0.25, or 0.3 phr ITO, depending on the type of ITO used in the composite. The percolation threshold of PS/MWNT composites was found to be 0.01 phr MWNT. Mixed ITO/MWNT PS-composites were already percolated, the concentrations investigated in xv ii this study were already above the percolation threshold of these composites. A time dependence on impedance was found for PS-composites filled with MWNT. As time increases there is a decrease in impedance, and in some cases also a dependence on voltage. All PS-composites showed a dependence on the microstructure of the PS matrix and the filler material. The resistivity and percolation threshold were lower for PS/MWNT composites than PS/ITO composites due to the difference in filler size and aspect ratio, since MWNT have a smaller size. The orientation of PS grains with respect to neighboring grains was found to affect the resistivity of PS/MWNT. PS/MWNT composites with preferentially oriented PS grains were found to have a lower resistivity. Mixed ITO/MWNT PS-composites with the right filler concentrations were able to maintain transmission while decreasing resistivity. The fracture surface of fractured PS-composites prepared in this work indicated that there was bonding between adjacent PS-grains. From this work, it can be concluded that large grain hybrid ITO/MWNT PS-composites provide insight into the effect of combining nanometer sized filler materials together in a polymer matrix on the resultant structural, electrical, and optical properties of the composite. In the future, it is recommended that this study be used to aid research in flexible transparent conducting electrodes using a polymer matrix and hybrid/mixed nanometer sized conducting fillers.

Eine Reihe wichtiger Wachstums- und Integrationsaspekte von Kohlenstoff-Nanoröhren wurde im Rahmen dieser Arbeit untersucht. Der Schwerpunkt der experimentellen Arbeit lag dabei hauptsächlich bei einschaligen Kohlenstoffnanoröhren (SWCNT). Das große Potential dieser Nanoröhren für Transistor-Anwendungen wurde durch die Herstellung einer Vielzahl funktionierender Bauelemente aus diesen Kohlenstoffnanoröhren mittels relativ einfacher Herstellungsprozesse demonstriert. Ein fundiertes Verständnis für die Abhängigkeiten des Nanoröhrenwachstums von einer Vielzahl an Parametern wurde mit Hilfe mehrerer tausend Wachstumsexperimente gesammelt. Verschiedene Katalysatormetalle, Kohlenstoffquellen und Katalysatorunterlagen wurden detailliert untersucht. Ein Hauptaugenmerk wurde dabei auf eine Reduzierung der Wachstumstemperatur gerichtet. Die niedrige Wachstumstemperatur spielt eine große Rolle für eine möglichst hohe Kompatibilität mit konventionellen Herstellungsverfahren der Silizium-Halbleitertechnik. Ein einfaches phänomenologisches Wachstumsmodell wurde für die Synthese von Nanoröhren mittels katalytisch-chemischer Gasphasen-Abscheidung (CCVD) formuliert. Dieses Modell basiert hauptsächlich auf der Oberflächendiffusion von adsorbierten Kohlenstoffverbindungen entlang der Seitenwände der Nanoröhren sowie auf der Oberfläche der Katalysatorunterlage. Das Modell ist eine wichtige Ergänzung zu dem VLS-Mechanismus. Ein Wachstumsverfahren zur Herstellung von Nanoröhren für niedrigere Temperaturen bis zu 600 °C wurde entwickelt. Experimentell wurde nachgewiesen, dass der Durchmesser des Katalysatorteilchens fast ausschließlich bestimmt, wie viele Schalen eine wachsende Nanoröhre bei geeigneten Wachstumsbedingungen hat. Es wurde zum ersten Mal gezeigt, dass einschalige Kohlenstoffnanoröhren auf Metallelektroden wachsen werden können, insofern eine dünne Aluminiumschicht als Trennschicht verwendet wird. Dadurch können in-situ kontaktierte Nanoröhren einfach hergestellt werden, was deren elektrische Charakterisierung weitaus erleichtert. Mittels stromloser Abscheidung von Nickel oder Palladium aus einer Lösung konnte eine deutliche Verbesserung der Kontaktwiderstände der in-situ-kontaktierten Nanoröhren erreicht werden. Durch Einbettung von Nanoröhren in eine Tantaloxidschicht konnten Transistoren mit einem Dielektrikum mit hoher relativer Dielektrizitätskonstante hergestellt werden. Die Tantaloxidschicht wurde mit einem neu entwickelten Tauchprozess abgeschieden. Erstmalig wurden Transistoren basierend auf Kohlenstoffnanoröhren hergestellt, die relativ hohe Ströme (Milliampere) mit einer Modulation bis zu einem Faktor 500 schalten können. Diese Transistoren beruhen auf einer Parallelschaltung einer großen Anzahl an Nanoröhren. Mit Hilfe der hergestellten Transistoren konnten die Eigenschaften einer großen Zahl von Nanoröhren untersucht werden, wobei große Unterschiede in den elektronischen Eigenschaften von metallischen Nanoröhren, halbleitenden Nanoröhren und Nanoröhren mit einer kleinen Bandlücke beobachtet wurden. / A number of very important growth and integration aspects of carbon nanotubes have been investigated during the course of this thesis. The focus was mainly on single-walled carbon nanotubes. Their potential for transistor applications was demonstrated by the successful fabrication of a variety of devices using rather simple processes. A detailed understanding of the dependence of SWCNT growth on a variety of parameters was obtained as the result of several thousand growth experiments. Various catalyst materials, gaseous carbon sources, and catalyst supports have been investigated. Special attention was paid to a considerable reduction of the growth temperature. A simple phenomenological growth model could be derived for CCVD of SWCNTs taking into account a number of effects observed during the various growth experiments. The model presented is mainly based on the surface diffusion of carbon species along the sidewalls of the carbon nanotubes or on the catalyst support and is an addition to the vapor-liquid-solid (VLS) mechanism. Growth methods for the CCVD synthesis of SWCNTs were developed for temperatures as low as 600 °C. It has been found that the size of the catalyst particle alone determines whether a SWCNT, DWCNT, or MWCNT will nucleate from a specific particle under suitable growth conditions. It could be demonstrated for the first time that SWCNTs can be grown on a variety of conducting materials if the catalyst is separated from the electrode by a thin Al layer. In-situ contacted SWCNTs can be easily obtained that way, largely facilitating the electronic characterization of as-grown SWCNTs. A tremendous improvement of the contacts of in-situ contacted SWCNTs could be achieved by electroless deposition. SWCNT growth on appropriate electrodes allowed the encapsulation of the nanotubes by electroless deposition of Ni and Pd, yielding good and reliable contacts. SWCNT transistors with a high-k dielectric could be fabricated by encapsulation of the nanotube with a tantalum oxide layer. The tantalum oxide was deposited by a newly developed dip-coat process. High-current SWCNT transistors consisting of a large number of SWCNTs in parallel were demonstrated for the first time during this work. Finally, the properties of a large number of CCVD grown SWCNTs have been investigated by electronic transport measurement. Large differences in the electronic transport have been observed for metallic, small band gap semiconducting (SGS), and semiconducting SWCNTs with small diameters.