La diminution de la taille des transistors actuellement utilisés en microélectronique ainsi que l’augmentation de leurs performances demeure encore au centre de toutes les attentions. Cette thèse propose d’étudier et de fabriquer des transistors à base de nanofils empilés. Cette architecture avec des grilles enrobantes est l’ultime solution pour concentrer toujours plus de courant électrique dans un encombrement minimal. Les simulations ont par ailleurs révélé le potentiel des nanofeuillets de silicium qui permettent à la fois d’optimiser l’espace occupé tout en proposant des performances supérieures aux dispositifs actuels. L’importance de l’ajout de certaines étapes de fabrication a également été soulignée. En ce sens, deux séries d’étapes de fabrication ont été proposées : la première option vise à minimiser le nombre de variations par rapport à ce qui est aujourd’hui en production tandis que la deuxième alternative offre potentiellement de meilleures performances au prix de développements plus importants. Les transistors ainsi fabriqués proposent des performances prometteuses supérieures à ce qui a pu être fabriqué dans le passé notamment grâce à l’introduction de contraintes mécaniques importantes favorables au transport du courant électrique. / The future of the transistors currently used in Microelectronics is still uncertain: shrinking these devices while increasing their performances always remains a challenge. In this thesis, stacked nanowire transistors are studied, fabricated and optimized. This architecture embeds gate all around which is the ultimate solution for concentrating always more current within a smaller device. Simulations have shown that silicon nanosheets provide an optimal utilization of the space with providing increased performances over the other technologies. Crucial process steps have also been identified. Subsequently, two process flows have been suggested for the fabrication of SNWFETs. The first approach consists in minimizing the number of variations from processes already in mass production. The second alternative has potentially better performances but its development is more challenging. Finally, the fabricated transistors have shown improved performances over state-of-the-art especially due to mechanical stress induced for improving electric transport.

Orientador: José Antônio Malmonge / Resumo: O uso de nanocargas de carbono tais como nanotubos de carbono e nanolâminas de grafite (NLG), e/ou polímeros condutores em uma matriz polimérica, tem atraído à atenção de inúmeros pesquisadores que buscam sintetizar elastômeros eletricamente condutivos com amplo potencial aplicacional como dissipadores eletrostáticos, blindagem eletromagnética, sensores piezorresistivos, etc. Nesse trabalho, foram obtidos: (1) nanocompósitos de polianilina (PAni)/NLG com razão mássica anilina (An)/NLG entre 0 e 250%, utilizando ácido clorídrico como dopante (nanocompósitos PHN), e com razão mássica anilina An/NLG entre 0 e 950%, utilizando ácido dodecilbenzeno sulfônico (DBSA) como dopante (nanocompósitos PDN); (2) Blendas de borracha natural (BN)/PAni com diferentes razões BN/An, utilizando BN in natura (blendas BNP) e borracha pré-vulcanizada (BV), blendas BVP; e (3) Nanocompósitos de BN/PAni-NLG (BNP/NLG) e BV/PAni-NLG (BVP/NLG) com diferentes razões BN/An e 15% de NLG em relação a An (relação m/m). Em todas as sínteses a polimerização da anilina foi realizada in situ. Nos nanocompósitos de PAni/NLG a polimerização da PAni ocorreu sobre a superfície lisa das NLG sendo sua morfologia e grau de intercalação nas NLG influenciados pelo tipo de dopante utilizado. A condutividade elétrica máxima obtida para os nanocompósitos foi de 627 S.cm-1 e 582 S.cm-1 para nanocompósitos PHN contendo 200% de NLG e para nanocompósitos PDN contendo 600% de NLG, respectivamente. O aumento na estabilidade térmic... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: The use of carbon nanofiller such as carbon nanotube and graphite nanosheet (GNS), and/or conductive polymers as filler to a polymer matrix, has attracted the attention of numerous researchers who seek to synthesize electrically conductive elastomers with broad application potential such as electrostatic dissipator, piezoresistive sensor and electromagnetic interference shielding . In this work were synthesized: (1) nanocomposites of polyaniline (PAni)/NLG with aniline (An)/NLG mass ratio between 0 and 250%, using hydrochloric acid as a dopant (PHN nanocomposites) and aniline An/NLG between 0 and 950%, using dodecylbenzene sulfonic acid (DBSA) as a dopant (PDN nanocomposites); (2) Natural rubber blends (BN)/PAni with different BN/An mass ratio, using BN in nature (BNP blends) and pre-vulcanized rubber BV, BVP blends; and (3) BN/PAni-NLG (BNP/NLG) and BV/PAni-NLG (BVP/NLG) nanocomposites with different BN/An mass ratios and 15% NLG with respect to An (m/m ratio). In all syntheses the polymerization of aniline was performed in situ. In the nanocomposites PAni/GNS the polymerization of PAni occurred on the GNS surface and their morphology and degree of intercalation in NLGs were influenced by the type of dopant. The higher electrical conductivity obtained for PHN and PDN composites were 627 S.cm-1 and 582 S.cm-1, respectively. The increase in the thermal stability of PAni in PAni/NLG nanocomposites was attributed to the intercalation of PAni among GNS and barrier properties pres... (Complete abstract click electronic access below) / Doutor

Charles University Faculty of Science Study programme: Inorganic Chemistry Mgr. Barbora Hyklová Layered Transition Metal Hydroxides: Delamination and Properties Extended abstract Supervisor: Ing. Kamil Lang CSc., DSc. Supervisor-Consultant: RNDr. Jan Demel PhD. Prague, 2017 Layered transition-metal hydroxides have attracted increasing attention as promising active electrode materials for electrochemical energy storage and conversion device due to facile preparation and modification, good tunability, high capacitance capability, fast reversible redox reactions, and cost effectiveness. Many reported hierarchical architectures based on nickel and cobalt hydroxides are composed of bulky nanoplatelet-like aggregates; however, the nanomorphology and behavior of the separated hydroxide nanosheets is much less known. Figure 1. Scheme of layered nickel or cobalt hydroxide delamination and subsequent restacking on conductive HOPG support. In this respect, the dissertation thesis reports characterization and electrochemical performance of nickel, nickel-cobalt, and cobalt hydroxide nanosheets, synthesized by an economical and environmentally friendly method based on delamination of corresponding layered hydroxides in water (Figure 1). For this purpose, lactate and nitrate layered hydroxides were prepared by two...

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Li-ion thin film battery technology has attracted much attention in recent years due to its highest need in portable electronic devices. Development of new materials for lithium ion battery (LIB) is very crucial for enhancement of the performance. LIB can supply higher energy density because Lithium is the most electropositive (-3.04V vs. standard hydrogen electrode) and lightest metal (M=6.94 g/mole). LIBs show many advantages over other kind of batteries such as, high energy density, high power density, long cycle life, no memory effect etc. The major work presented in this thesis is on the development of nanostructured materials for anode of Li-ion battery. It involves the synthesis and analysis of grapheme nanosheet (GNS) and its performance as anode material in Li ion battery. We studied the synthesis of GNS over different substrates and performed the anode studies. The morphology of GNS has great impact on Li storage capacity. Tin and Tin oxide nanostructures have been embedded in the GNS matrix and their electrochemical performance has been studied. Chapter 1 gives the brief introduction about the Li ion batteries (LIBs), working and background. Also the relative advantages and characterization of different electrode materials used in LIBs are discussed. Chapter 2 discusses various experimental techniques that are used to synthesize the electrode materials and characterize them. Chapter3 presents the detailed synthesis of graphene nanosheet (GNS) through electron cyclotron resonance (ECR) microwave plasma enhanced chemical vapor deposition (ECR PECVD) method. Various substrates such as metallic (copper, Ni and Pt coated copper) and insulating (Si, amorphous SiC and Quartz) were used for deposition of GNS. Morphology, structure and chemical bonding were analyzed using SEM, TEM, Raman, XRD and XPS techniques. GNS is a unique allotrope of carbon, which forms highly porous and vertically aligned graphene sheets, which consist of many layers of graphene. The morphology of GNS varies with substrate. Chapter 4 deals with the electrochemical studies of GNS films. The anode studies of GNS over various substrates for Li thin film batteries provides better discharge capacity. Conventional Li-ion batteries that rely on a graphite anode have a limitation in the capacity (372 mAh/g). We could show that the morphology of GNS has great effect in the electrochemical performance and exceeds the capacity limitation of graphite. Among the electrodes PtGNS shown as high discharge capacity of ~730 mAh/g compare to CuGNS (590 mAh/g) and NiGNS (508 mAh/g) for the first cycle at a current density of 23 µA/cm2. Electrochemical impedance spectroscopy provides the various cell parameters of the electrodes. Chapter 5 gives the anodic studies of Tin (Sn) nanoparticles decorated over GNS matrix. Sn nanoparticles of 20 to 100nm in size uniformly distributed over the GNS matrix provides a discharge capacity of ~1500 mAh/g mAh/g for as deposited and ~950 mAh/g for annealed Sn@GNS composites, respectively. The cyclic voltammogram (CV) also shows the lithiation and delithiation process on GNS and Sn particles. Chapter 6 discusses the synthesis of Tinoxide@GNS composite and the details of characterization of the electrode. SnO and SnO2 phases of Tin oxide nanostructures differing in morphologies were embedded in the GNS matrix. The anode studies of the electrode shows a discharge capacity of ~1400 mAh/g for SnO phase (platelet morphology) and ~950 mAh/g for SnO2 phase (nanoparticle morphology). The SnO phase also exhibits a good coulumbic efficiency of ~95%. Chapter 7 describes the use of SnO2 nanowire attached to the side walls of the GNS matrix. A discharge capacity of ~1340 mAh/g was obtained. The one dimensional wire attached to the side walls of GNS film and increases the surface area of active material for Li diffusion. Discharge capacity obtained was about 1335 mAhg-1 and the columbic efficiency of ~86% after the 50th cycle. The research work carried out as part of this thesis, and the results have summarized in chapter 8.

Superparamagnetic iron oxide (Fe3O4 and γ-Fe2O3) nanoparticles (IONPs) are of great in-terest as a diagnostic and/or therapeutic aid. Several IONPs with biocompatible polymer coatings have been approved for clinical use, as MRI contrast agents. IONPs conjugated to targeting ligands and therapeutic agents are being investigated for targeted drug deliv-ery applications. The superparamagnetic properties of IONPs are also helpful for magnetic field assisted localization to specific target sites and for in situ MRI applications. This thesis primarily focuses on the synthesis and surface modifications (with biocompatible polymers including dextran, poly(ethylene glycol) (PEG), dextran, poly(ethyl methacry-late) (PEMA), poly(hydroxyethyl methacrylate) (PHEMA), etc.) of IONPs. The IONPs were prepared following the classical co-precipitation method and a novel reduction-hydrolysis method. Initial studies used bovine serum albumin (BSA) to examine the ca-pabilities of polymer coated IONP to deliver a model protein therapeutic. Gel migration studies using BSA physisorbed onto polymer coated IONP under gradient magnetic field of an MRI showed that the IONPs had limited control in transporting the protein. Cova-lent linking of therapeutics to IONP core can improve the time window of formers con-trollability using magnetic field. To facilitate covalent conjugations, functional silane coated IONPs (with surface amino and carboxylic acid) were prepared as general precur-sors. The utility of silane coated IONPs for bioconjugations was demonstrated by cova-lently linking PEG diacid through surface amino groups and by linking of BSA through surface carboxylic acid groups. The biocompatibility of the IONPs synthesized following the novel reduction-hydrolysis method were assessed in vitro on cell culture models using toxicity assays. The versatile reduction-hydrolysis method was further extended, as a general method to prepare several early transition metal oxide NPs (manganese oxide (Mn3O4), cobalt oxide (Co3O4), nickel/nickel oxide (Ni/NiO), copper/copper oxide (Cu/Cu2O) and zinc oxide (ZnO) NPs), silica nanoparticles with surface IONPs, and iron/iron oxide nanosheets.

In the past decade, rechargeable batteries attracted the attention from the researchers in search for renewable and sustainable energy sources. Up to date, lithium-ion battery is the most commercialized and has been supplying power to electronic devices and hybrid and electric vehicles. Lithium-ion battery, however, does not satisfy the expectations of ever-increasing energy and power density, which of their limits owes to its intercalation chemistry and the safety.1-2 Therefore, metal-air battery drew much attention as an alternative for its high energy density and a simple cell configuration.1 There are several different types of metal-air batteries that convey different viable reaction mechanisms depending on the anode metals; such as Li, Al, Ca, Cd, and Zn. Redox reactions take place in a metal-air cell regardless of the anode metal; oxidation reaction at the anode and reduction reaction at the air electrode. Between the two reaction, the oxygen reduction reaction (ORR) at the air electrode is the relatively the limiting factor within the overall cell reactions. The sluggish ORR kinetics greatly affects the performance of the battery system in terms of power output, efficiency, and durability. Therefore, researchers have put tremendous efforts in developing highly efficient metal air batteries and fuel cells, especially for high capacity applications such as electric vehicles. Currently, the catalyst with platinum nanoparticles supported on carbon material (Pt-C) is considered to exhibit the best ORR activities. Despite of the admirable electrocatalytic performance, Pt-C suffers from its lack of practicality in commercialization due to their prohibitively high cost and scarcity as of being a precious metal. Thus, there is increasing demand for replacing Pt with more abundant metals due economic feasibility and sustainability of this noble metal.3-5 Two different attitudes are taken for solution. The first approach is by optimizing the platinum loading in the formulation, or the alternatively the platinum can be replaced with non-precious materials. The purpose of this work is to discover and synthesize alternative catalysts for metal-air battery applications through optimized method without addition of precious metals. Different non-precious metals are investigated as the replacement of the precious metal including transition metal alloys, transition metal or mixed metal oxides, and chalcogenides. These types of metals, alone, still exhibits unsatisfying, yet worse, kinetics in comparison to the precious metals. Nitrogen-doped carbon material is a recently well studied carbon based material that exhibits great potential towards the cathodic reaction.6 Nitrogen-doped carbon materials are found to exhibit higher catalytic activity compared to the mentioned types of metals for its improved conductivity. Benefits of the carbon based materials are in its abundance and minimal environmental footprints. However, the degradation of these materials has demonstrated loss of catalytic activity through destruction of active sites containing the transition metal centre, ultimately causing infeasible stability. To compensate for these drawbacks and other limits of the nitrogen-doped carbon based catalysts, nitrogen-doped carbon nanotubes (NCNT) are also investigated in the series of study. The first investigation focuses on a development of a simple method to thermally synthesize a non-precious metal based nitrogen-doped graphene (NG) electrocatalyst using exfoliated graphene (Ex-G) and urea with varying amounts of iron (Fe) precursor. The morphology and structural features of the synthesized electrocatalyst (Fe-NG) were characterized by SEM and TEM, revealing the existence of graphitic nanoshells that potentially contribute to the ORR activity by providing a higher degree of edge plane exposure. The surface elemental composition of the catalyst was analyzed through XPS, which showed high content of a total N species (~8 at.%) indicative of the effective N-doping, present mostly in the form of pyridinic nitrogen groups. The oxygen reduction reaction (ORR) performance of the catalyst was evaluated by rotating disk electrode voltammetry in alkaline electrolyte and in a zinc-air battery cell. Fe-NG demonstrated high onset and half-wave potentials of -0.023 V (vs. SCE) and -0.110 V (vs. SCE), respectively. This excellent ORR activity is translated into practical zinc-air battery performance capabilities approaching that of commercial platinum based catalyst. Another approach was made in the carbon materials to further improve the cost of the electrode. Popular carbon allotropes, CNT and graphene, are combined as a composite (GC) and heteroatoms, nitrogen and sulfur, are introduced in order to improve the charge distribution of the graphitic network. Dopants were doped through two step processes; nitrogen dopant was introduced into the graphitic framework followed by the sulfur dopant. The coexistence of the two heteroatoms as dopants demonstrated outstanding ORR performance to those of reported as metal free catalysts. Furthermore, effects of temperature were investigated through comparing ORR performances of the catalysts synthesized in two different temperatures (500 ??? and 900 ???) during the N-doping process (consistent temperature was used for S-doping). Through XPS analysis of the surface chemistry of catalysts produced with high temperature during the N-doping step showed absence of N-species after the subsequent S-doping process (GC-NHS). Thus, the synergetic effects of the two heteroatoms were not revealed during the half-cell testing. Meanwhile, the two heteroatoms were verified in the catalyst synthesized though using low temperature during the N-doping process followed by the S-doping step (GC-NLS). Consequently, ORR activity of the resulting material demonstrated promising onset and half-wave potentials of -0.117 V (vs. SCE) and -0.193 V (vs. SCE). In combination of these investigations, this document introduces thorough study of novel materials and their performance in its application as ORR catalyst in metal air batteries. Moreover, this report provides detailed fundamental insights of carbon allotropes, and their properties as potential elecrocatalysts and essential concepts in electrochemistry that lies behind zinc-air batteries. The outstanding performances of carbon based electrocatalyst are reviewed and used as the guides for further direction in the development of metal-air batteries as a promising sustainable energy resource in the future.

<div>In this work, we investigate the trade-off between scalability and reliability for next generation logic-transistors i.e. Gate-All-Around (GAA)-FET, Multi-Bridge-Channel (MBC)-FET. First, we analyze the electronic properties (i.e. bandgap and</div><div>quantum conductance) of ultra-thin silicon (Si) channel i.e. nano-wire and nano-sheet based on first principle simulation. In addition, we study the influence of interface</div><div>states (or dangling bonds) at Si-SiO₂ interface. Second, we investigate the impact of bandgap change and interface states on GAA-FETs and MBC-FETs characteristics by</div><div>employing Non-equilibrium Green's Function based device simulation. In addition to that, we calculate the activation energy of Si-H bond dissociation at Si-SiO₂ interface for different Si nano-wire/sheet thickness and different oxide electric-field. Utilizing these thickness dependent activation energies for corresponding oxide electric-field, in conjunction with reaction-diffusion model, we compute the characteristics shift and analyze the negative bias temperature instability in GAA-FET and MBC-FET. Based on our analysis, we estimate the operational voltage of these transistors for a life-time of 10 years and the ON current of the device at iso-OFF-current condition. For example, for channel length of 5 nm and thickness < 5 nm the safe operating voltage needs to be < 0.55V. Furthermore, our analysis suggests that the benefit of Si thickness scaling can potentially be suppressed for obtaining a desired life-time of GAA-FET and MBC-FET.</div>