Current strategies for designing biomaterials involve creating materials and interfaces that interact with biomolecules, cells and tissues.  This thesis aims to investigate several bioactive surfaces, such as nanocrystalline diamond (NCD), hydroxyapatite (HA) and single crystalline titanium dioxide, in terms of material synthesis, surface functionalization and characterization. Although cochlear implants (CIs) have been proven to be clinically successful, the efficiency of these implants still needs to be improved. A CI typically only has 12-20 electrodes while the ear has approximately 3400 inner hair cells. A type of micro-textured NCD surface that consists of micrometre-sized nail-head-shaped pillars was fabricated. Auditory neurons showed a strong affinity for the surface of the NCD pillars, and the technique could be used for neural guidance and to increase the number of stimulation points, leading to CIs with improved performance. Typical transparent ceramics are fabricated using pressure-assisted sintering techniques. However, the development of a simple energy-efficient production method remains a challenge. A simple approach to fabricating translucent nano-ceramics was developed by controlling the morphology of the starting ceramic particles. Translucent nano-ceramics, including HA and strontium substituted HA, could be produced via a simple filtration process followed by pressure-less sintering. Furthermore, the application of such materials as a window material was investigated. The results show that MC3T3 cells could be observed through the translucent HA ceramic for up to 7 days. The living fluorescent staining confirmed that the MC3T3 cells were visible throughout the culture period. Single crystalline rutile possesses in vitro bioactivity, and the crystalline direction affects HA formation. The HA growth on (001), (100) and (110) faces was investigated in a simulated body fluid in the presence of fibronectin (FN) via two different processes. The HA layers on each face were analysed using different characterization techniques, revealing that the interfacial energies could be altered by the pre-adsorbed FN, which influenced HA formation. In summary, micro textured NCD, and translucent HA and FN functionalized single crystalline rutile, and their interactions with cells and biomimetic HA were studied. The results showed that controlled surface properties are important for enhancing a material’s biological performance.

Micro- and nanostructured polymer brushes on diamond can be directly prepared by carbon templating and amplification of the latent structures by photografting of a broad variety of vinyl monomers such as styrenes, acrylates and methacrylates. Even template structures with lateral dimensions as small as 5 nm can be selectively amplified and defined polymer brush gradients of a variety of functional polymers are realizable by this technique. Furthermore, conjugation with a model protein (GFP) results in protein density gradients of high loading and improved chemical stability. The effective functionalization of chemically and biologically inert diamond surfaces with stable functional polymer brushes, the possibility of structuring by the carbon templating technique and the direct biofunctionalization are crucial steps for the development of diamond based biosensors. / Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.

Les travaux présentés dans ce mémoire ont pour but de mieux comprendre les relations entre la microstructure des revêtements métalliques nanocristallisés et leurs propriétés électrochimiques et mécaniques. Les dépôts de nickel sont élaborés par électrodéposition en courant continu et en courant pulsé dans un bain au sulfamate de nickel avec des sels de haute pureté, sans additif afin de minimiser les risques de contamination. Une caractérisation précise des états métallurgiques développés est réalisée au moyen de diverses techniques (MEB, MET, DRX, AFM, EBSD, SIMS, GDOES) afin d’évaluer la microstructure à différentes échelles (taille de grain, texture, contraintes internes, type de joints de grains) et d’identifier les contaminants. Trois types de texture ont été développés, associés à différentes tailles d’hétérogénéités structurales allant du micromètre à quelques dizaines de nanomètres. Une loi dite “d’échelle” a été mise en évidence, permettant de corréler les résultats obtenus par les diverses méthodes d’analyse. L’affinement de la taille de grain se traduit par une augmentation de la contamination dans les dépôts et entraîne une augmentation de la microdureté. La loi de Hall-Petch est influencée par l’orientation cristallographique ce qui a pu être relié à la nature des joints de grains et à la contamination des revêtements. Une étude préliminaire de la réactivité électrochimique en milieu acide a montré le rôle marqué des effets de surface (contamination et rugosité de surface). La réalisation d’un polissage électrolytique sur les revêtements a permis d’étudier l’influence des paramètres métallurgiques (taille de grain, contamination, nature des joints de grains) sur la réactivité. Les courbes de polarisation dans le domaine anodique et dans le domaine cathodique ont été simulées à l’aide de modèles cinétiques. Les résultats obtenus suggèrent que les joints de grains ont un effet qui peut être activant ou désactivant suivant l’étape considérée, ces effets pouvant être atténués par la présence d’impuretés. Les modifications de propriétés mécaniques et électrochimiques des revêtements ne peuvent être attribuées à une diminution de la taille de grain seule. / The purpose of the work presented in this manuscript is to better understand the relations between the microstructure of nanocrystallized metal coatings and their electrochemical and mechanical properties. Nickel deposits are elaborated by electrodeposition using direct current and pulse current in a nickel sulphamate bath with salts of high purity and without additive, in order to minimize the risks of contamination. A precise characterization of the developed metallurgical states is carried out by means of various techniques (SEM, TEM, XRD, AFM, EBSD, SIMS, GDOES) in order to evaluate the microstructure on various scales (grain sizes, textures, internal stresses, type of grain boundaries) and to identify contaminants. Three types of texture were developed associated with various sizes of structural heterogeneities from about one micrometer to a few dozens of nanometers. A “scale” law, allowing to correlating the results obtained by the various methods of analysis was shown. The grain size refinement results in an increase of contamination in the deposits and involves an increase of microhardness. The Hall-Petch law is influenced by the crystallographic orientation which could be connected to the nature of grain boundaries and the contamination of the coatings. A preliminary study of the electrochemical reactivity in acidic media showed the marked role of the surface effects (contamination and roughness of surface). Electrolytic polishing of the coatings highlights the influence of the metallurgical parameters (grain size, contamination, nature of grains boundaries) on the reactivity. The polarization curves in anodic domain and cathodic domains were simulated using kinetic models. The obtained results suggest that grain boundaries can either activate or deactivate the electrochemical kinetics according to the considered stage, these effects being able to be constrained by the presence of impurities. The modifications of mechanical and electrochemical properties of the coatings cannot be ascribed to a reduction of the grain size alone.

La complexité croissante des dispositifs en électronique de puissance nécessite l'intervention de la conception assistée par ordinateur. Le développement de systèmes électriques/électroniques est effectué à l'aide du prototypage virtuel dans lequel les logiciels de simulation sont utilisés pour prédire le comportement des composants. De ce fait, le prototypage virtuel permet une économie de temps et d'argent pour la réalisation de prototypes. La demande croissante d'appareils à faible puissance et à haut rendement a obligé les concepteurs à analyser précisément les pertes de chaque composant constituant du système. Les composants magnétiques constituent une partie importante des appareils en électronique, par conséquent la modélisation précise des matériaux magnétiques est nécessaire afin de prédire leur comportement réaliste dans des conditions de fonctionnement variables selon l'application. Notre travail s'inscrit dans ce contexte et propose un modèle dynamique non linéaire de composants magnétiques pour une utilisation dans des simulateurs de circuits électriques. Ce modèle de composant magnétique inclut le comportement d'hystérésis non linéaire du matériau et permet une modélisation précise des pertes fer et des pertes joule avec de plus la prise en considération des effets thermiques qui, généralement, ne sont pas pris en compte par les modèles existants. Le modèle est basé sur le principe de la séparation des contributions statiques et dynamiques des pertes fer et s'appuie sur la théorie de Bertotti. Le langage de programmation VHDL-AMS est utilisé en raison de sa fonctionnalité de modélisation multidomaines, permettant un couplage avec un modèle thermique. Le modèle de composant magnétique est mis en oeuvre dans le logiciel de simulation de circuit "Simplorer". Il est ensuite testé dans une application de convertisseur de puissance, le convertisseur abaisseur qui permet de fournir une excitation non-conventionnelle. Le modèle est validé pour différents noyaux d'inductances, différentes ondulations de courant et niveaux de charge, différentes températures et une large gamme de fréquence / The increasing complexity of power electronic devices requires the intervention of computer-aided design in electrical engineering. Development of electric/electronic systems nowadays is carried out by the help of virtual prototyping, in which simulation software are used to predict components behavior without investing time and money to build physical prototypes. The increasing demand of low power, high efficiency devices forced designers to precisely analyze losses in each component constituting the system. Magnetic components constitute a major part of electronics devices. Therefore accurate modeling of magnetic materials is mandatory in order to predict their realistic behavior under variable operating conditions. Our work takes place in this context by proposing a non-linear dynamic model of magnetic components for use in circuit simulators. It includes the material nonlinear hysteretic and dynamic behaviors with accurate modeling of winding and core losses in addition to thermal effects that are not taken into account by existing models. The model is based on the principle of separation of static and dynamic contributions as well as Bertotti’s theory. VHDL-AMS is used as a modeling language due to its multi-domain modeling feature, allowing coupling with a thermal model. The magnetic component model is implemented in circuit simulation software “Simplorer” It is then tested in a widely used power converter application, the buck converter, to ensure non conventional excitation. The model is validated for different core inductors, different current ripples, different loads, different temperatures and a wide frequency range

L'élaboration de nouveaux alliages maintient un fort intérêt pour le phénomène d’instabilité plastique, ou l'effet Portevin-Le Chatelier (PLC), provoqué par l'interaction des dislocations avec des atomes de soluté. Par ailleurs, l'effet PLC attire l'intérêt comme un exemple remarquable d'auto-organisation dans les systèmes dynamiques. Il est associé à des motifs complexes de séries de chutes de contrainte liées à la nucléation et au mouvement des bandes de déformation dans le matériau déformé, et nécessite une compréhension de l'auto-organisation des dislocations. La déformation plastique des alliages Al-Mg est sujette à l'instabilité dans une large gamme de conditions expérimentales. Pour cette raison, les alliages Al-Mg binaires ont longtemps servi d'objets modèles pour l'étude de l'effet PLC. En même temps, l'utilisation pratique des alliages binaires Al-Mg est limitée en raison d’une faible résistance mécanique. Une amélioration significative de leurs propriétés peut être atteinte en ajoutant des solutés supplémentaires, conduisant en particulier à la formation de précipités. En outre, une forte réduction de la taille de grains du polycristal pourrait être une technique clé pour produire des matériaux à haute résistance et ténacité. Cependant, il existe très peu d'information, souvent contradictoire, sur l'instabilité PLC dans les alliages Al-Mg à grains fins et contenant des précipités. Le but de l'étude de cette thèse a été d'étudier les caractéristiques spécifiques de l'effet PLC dans les alliages à base AlMg, avec et sans nanoparticules, à gros grains et à grains fins, ces derniers obtenus par une méthode de déformation plastique sévère. Grâce à l’application de méthodes d’extensométrie locale, notamment de la technique de corrélation d’images, ces études ont révélé une persistance non habituelle de la propagation des bandes de déformation dans les alliages comprenant des précipités et/ou des grains fins. Ce mode dynamique est observé dans un large intervalle de vitesses de déformation, tandis qu’il n’apparait qu’à haute vitesse dans des alliages modèles AlMg. Par ailleurs, l’analyse des distributions statistiques des amplitudes des chutes de contrainte a révélé une tendance vers une statistique en loi puissance, caractéristique du mode de propagation. Ce phénomène est attribué à une modification du couplage spatial entre les dislocations, due à la concentration de contraintes internes. La combinaison de ces études avec l’analyse de l’émission acoustique a mis en évidence une influence de la microstructure sur la compétition entre un facteur aléatoire et la synchronisation des dislocations. Enfin, l’étude par corrélation d’images a permis d’observer une interrelation entre l’instabilité PLC et la formation de la striction. / The elaboration of new alloys sustains a strong interest to the phenomenon of unstable plastic flow, or the Portevin–Le Chatelier (PLC) effect, caused by interaction of dislocations with solute atoms. Moreover, this effect attracts interest as a rich example of self-organization in dynamical systems. It is associated with complex patterns of stress serrations related to nucleation and motion of deformation bands in the deforming material, and requires understanding of self-organization of dislocations. Plastic deformation of Al-Mg alloys is prone to instability in a wide range of experimental conditions. For this reason, binary Al-Mg alloys served for a long time as model objects for investigation of the PLC effect. At the same time, the practical use of binary Al-Mg alloys is limited because of their low strength. A significant improvement of their properties can be achieved by additional alloying, in particular, leading to precipitation. Further, extensive grain refinement could be a key technique used to produce tough and high- strength materials. However, there exists very limited and often contradictory information on the PLC instability in fine-grained Al-Mg alloys containing precipitates. The objective of the present thesis was to investigate specific features of the PLC effect in AlMg-based alloys with and without nanoscale particles, both in coarse-grained and fine-grained states, the latter obtained by severe plastic deformation. Using local extensometry methods, particularly the image correlation technique, these studies revealed an unusual persistence of the propagation of deformation bands in alloys with precipitates and/or fine grains. This dynamic mode is observed in a wide range of strain rates, whereas it only appears at high strain rate in model Al-Mg alloys. Moreover, the analysis of statistical distributions of stress drop amplitudes revealed a tendency to power law statistics characteristic of the propagation mode. This phenomenon was attributed to a modification of the spatial coupling between dislocations due to the concentration of internal stresses. The combination of these studies with the acoustic emission analysis uncovered an influence of the microstructure on the competition between a random factor and the dislocation synchronization. Finally, the study by the image correlation made it possible to observe an interrelation between the PLC instability and the neck formation.

This work tries to show the significant competence and functionality of density functional theory (DFT) and time-dependent density functional theory (TD-DFT) as theoretical approaches, supporting experimental measurements in various fields of physics from astrophysics to surface science, to study the electronic structure and spectroscopic properties of molecules and clusters: Silicon nanocrystals: Due to their optical properties, silicon nanocrystals have attracted considerable attention in astrophysics. In this work, the optical properties of H-passivated silicon nanocrystals are determined by the energetics of the frontier orbitals and their dependence on the deformation in the relaxed excited state, using DFT and TD-DFT. The Jahn-Teller effect in the lowest excited state results in a distortion toward tetragonal symmetry, contributing significantly to the red shift of the photoluminescence (PL) spectra. Therefore, the deformation in the relaxed excited state consists of a symmetry conserving part and of a symmetry-breaking distortion from Td toward D2d. For nanocrystals up to a diameter of 1.5 nm, we project the deformations at the minima of the excited state potential surface onto the different symmetries, allowing for a discrimination of the respective contributions to the total Stokes shift. The results show a quantitative agreement between the TD-DFT calculations of PL gap and the observed PL energies better than 0.2 eV. It is also seen that the large PL linewidth is the fundamental property of each cluster, not of ensemble average over clusters of different size. 2,3-Benzofluorene: We have presented new theoretical results on the absorption spectroscopy of 2,3-benzofluorene (Bzf) for the transition from the ground state, S0, to the first electronically excited singlet state, S1, to support the measurements of S1(1A´) <- S0(1A´) absorption spectrum of jet-cooled Bzf. The potential energy surfaces (PESs) of the S(n=0,1,2) states of Bzf have been investigated with calculations based on DFT and TD-DFT. At the B3LYP/TZ level of theory, TD-DFT does not deliver a realistic difference between the excited S1 and S2 potential energy surfaces, a problem which can be avoided by introducing a reference geometry (q*) where this difference coincides with the observation. In this geometry, an expression for the Herzberg-Teller corrected intensities of the vibronic bands is proposed, allowing a straightforward assignment of the observed a′ modes below 900 cm−1, including realistic calculated intensities. In spite of the difficulties caused by the small energy difference between the S1 and S2 states, we have obtained a reasonable theoretical absorption spectrum based on a TD-DFT approach applied to the slightly modified molecular geometry. Although the agreement between the theoretical and observed spectra is very good only for vibrational modes with frequencies lower than 900 cm−1, we consider our calculations to be the best approach to an ab initio study realized for Bzf until now since only parametrized force fields had been used before. (Ni–, Pd–, Pt–) Phthalocyanine: We studied the HOMO–LUMO gap shrinking in order to investigate the tip-induced polarization in scanning tunneling spectroscopy (STS) of d8 (Ni, Pd, and Pt) phthalocyanines. By means of DFT, the electronic structure and vibronic properties of single neutral NiPc, PdPc, and PtPc and their singly and doubly ionized cations and anions have been calculated. Interestingly, the position of the HOMO decreases systematically with increasing the atomic number of the central metal atom. The first ionization energies of neutral molecules increase by changing the central metal atom, while the electron affinities remain constant. This causes an increase in the HOMO–LUMO gap. These results show a clear correlation to experimental observations. Furthermore, partitioning of the reorganization energy, corresponding to the photoelectron spectra of the first and second ionizations of studied molecules, into normal mode contributions shows that the major contributions are due to several vibrational modes with a1g symmetry and energies lower than 1600 cm−1. The results reveal that the reorganization energy due to the singly positive ionization in the studied molecules is about one order of magnitude less than other reorganization energies, which makes these metal–phthalocyanines more attractive as electron donor for intramolecular electron transfer in electron acceptor–donor systems.

Atomistic simulations are employed in this thesis to investigate defect nucleation and free volume of grain boundaries and nanocrystalline materials. Nanocrystalline materials are of particular interest due to their improved mechanical properties and alternative strain accommodation processes at the nanoscale. These processes, or deformation mechanisms, within nanocrystalline materials are strongly dictated by the larger volume fraction of grain boundaries and interfaces due to smaller average grain sizes. The behavior of grain boundaries within nanocrystalline materials is still largely unknown. One reason is that experimental investigation at this scale is often difficult, time consuming, expensive, or impossible with current resources. Atomistic simulations have shown the potential to probe fundamental behavior at these length scales and provide vital insight into material mechanisms. Therefore, work conducted in this thesis will utilize atomistic simulations to explore structure-property relationships of face-centered-cubic grain boundaries, and investigate the deformation of nanocrystalline copper as a function of average grain size. Volume-averaged kinematic metrics are formulated from continuum mechanics theory to estimate nonlocal deformation fields and probe the nanoscale features unique to strain accommodation mechanisms in nanocrystalline metals. The kinematic metrics are also leveraged to explore the tensile deformation of nanocrystalline copper at 10K. The distribution of different deformation mechanisms is calculated and we are able to partition the role of competing mechanisms in the overall strain of the nanocrystalline structure as a function of grain size. Grain boundaries are observed to be influential in smaller grained structures, while dislocation glide is more influential as grain size increases. Under compression, however, the resolved compressive normal stress on interfaces hinders grain boundary plasticity, leading to a tension-compression asymmetry in the strength of nanocrystalline copper. The mechanisms responsible for the asymmetry are probed with atomistic simulations and the volume-averaged metrics. Finally, the utility of the metrics in capturing nonlocal nanoscale deformation behavior and their potential to inform higher-scaled models is discussed.

Thin film nanostructures may be defined as assemblies, arrays, or randomly distributed nanoparticles, nanowires, or nanotubes, which together form a layer of materials supported on a substrate surface. Because such nanostructures are supported on a substrate surface, their potential applications cover a wide area in optical, magnetic, electrochemical, electromagnetic, and optoelectronic devices. The focus of the present thesis is the development of methodologies to grow certain thin film nanostructures of some transition metal oxides (TMOs), including copper oxides and LixCoO2, through CVD, sol-gel, and electromagnetic radiation-mediated approaches. The work towards this objective can be divided into three parts: first, the design, synthesis, and systematic identification of novel metalorganic precursors of copper (monometallic) and Li and Co (bimetallic); second, the growth of nanostructured oxides thin films using these precursors; and third, the application of electromagnetic radiation to control or tailor the growth of as grown nanostructures. The underlying growth mechanisms substantiated by appropriate evidence have been put forward, wherever found relevant and intriguing. It may be added that the principal objective of the work reported here has been to explore the several ideas noted above and examine possibilities, rather than to study any specific one of them in significant detail. It is hoped earnestly that this has been accomplished to a reasonable extent. Chapter 1 reviews briefly the reports available in the literature on three specific methods of growing thin films nanostructures, namely chemical vapour deposition, sol-gel processing and light-induced approach. The objective of this chapter has been to provide the background of the work done in the thesis, and is substantiated with a number of illustrative examples. Some of the fundamental concepts involved, viz., plasmons and excitons, have been defined with illustration wherever found relevant in the context of the work. Chapter 2 describes the various techniques used for synthesis and characterisation of the metalorganic complexes as well as of the thin films. This chapters covers mostly experimental details, with brief descriptions of the working principles of the analytical procedures adopted, namely, infrared spectroscopy, mass spectroscopy, elemental analysis, and thermal analysis for characterisation of the metalorganic complexes. This is followed by a similarly brief account of techniques employed to characterize the thin films prepared in this work, viz., glancing incidence X-ray diffraction (GIXRD), field-emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), electrostatic force microscopy (EFM), transmission electron microscopy (TEM), glancing incidence infra-red spectroscopy (GIIR) and, UV-visible spectroscopy. The metalorganic chemical vapour deposition (MOCVD) systems built in house and used for growth of films are described in detail. The topics in the different sections of the chapter are accompanied by pertinent diagrams. Chapter 3 deals with the design, synthesis and characterisation of novel polynuclear complexes of copper and cobalt. Keeping in mind the various advantages such as low toxicity, ease of synthesis, non-pyrophoricity, and low temperature volatility, of environmentally benign complexes based on biologically compatible such as triethanolamine, diethanolamine, the objective has been to synthesize complexes containing triethanolamine and diethanolamine of transition metals such as cobalt and copper, and to investigate their applicability in MOCVD processes as a novel class of precursors. With the notion of ‘better’ and efficient design of precursors, an attempt has been made, through a semi-empirical modeling, to understand the correlation between volatility and various intrinsic molecular parameters such as lattice energy, vibrational-rotational energy, and internal symmetry. Chapter 4 discusses the growth of nanoporous Cu4O3-C composite films through the MOCVD process employing Cu4(deaH)(dea)(oAc)5.(CH3)2CO as the precursor. The various characteristic aspects of as-grown films, such as their crystallinity, morphology, and composition have been covered elaborately in various sections of this chapter. The chapter describes the efficient guiding and confining of light exploiting the photonic band gap of these nanoporous films, which indicates the potential usefulness of these and similar films as optical waveguides. A model described in the literature on absorbing photonic crystals, wherein a periodically modulated absorption entails an inevitable spatial modulation of dispersion, i.e., of the index contrast to open a photonic band gap, has been used to calculate the indices of refraction of one of these nanoporous films. The chapter also reports briefly the preliminary electrochemical investigations carried out on a typical film, examining the notion of its application as the anode in a Li-ion rechargeable battery. Chapter 5 describes the synthesis of nanocrystalline LixCoO2 films by the sol-gel method. Reports available in literature indicate that the various phases of LixCoO2 are extremely sensitive to processing temperature, making it difficult to control dimensionality of a given phase using temperature as one of process parameters. We have investigated the possibility of using incoherent light to tailor the particle size/shape of this material. The as-grown and irradiated films were characterised by X-ray diffraction, and by microscopic and spectroscopic techniques.Optical spectroscopy was carried out in order to gain insight into the physico-chemical mechanism involved in such structural and morphological transformation. Chapter 6 deals with the synthesis of self-assembled nanostructures from the pre-synthesized nanocrystals building blocks, through optical means of exciton formation and dissociation. It has been demonstrated that, upon prolonged exposure to (incoherent) ultraviolet-visible radiation, LixCoO2 nanocrystals self-assemble into acicular architectures, through intermediate excitation of excitons. Furthermore, it has been shown that such self-assembly occurs in nanocrystals, which are initially anchored to the substrate surface such as that of fused quartz. This new type of process for the self-assembly of nanocrystals, which is driven by light has been investigated by available microscopic and spectroscopic techniques. Chapter 7 describes the stabilisation of chemically reactive metallic lithium in a carbonaceous nanostructure, viz., a carbon nanotube, achieved through the MOCVD process involving a lithium-alkyl moiety. This moiety is formed in situ during deposition through partial decomposition of a metalorganic precursor synthesized in house, which contains both lithium and cobalt. It is surmised that the stabilization of metallic Li in the nanostructure in situ occurs through the partial decomposition of the metalorganic precursor. Quantitative X-ray photoelectron spectroscopy carried out on such a film reveals that as much as 33.4% metallic lithium is trapped in carbon. Lastly, Chapter 8 briefly highlights the outlook for further investigations suggested by the work undertaken for this thesis. Novel precursors derived from biologically compatible ligands can open up possibility of growing new type of micro/nano-structures, and of unusual phases in the CVD grown films. Furthermore, it is proposed that the novel method of growth and alignment of nanocrystals through irradiation with incoherent light, employed for the specific material LixCoO2, may be employed for various other metallic and semiconducting materials.

The thesis consists of eight chapters of which the first chapter presents a brief overview of inorganic nanostructures. Synthesis and magnetic properties of MnO and NiO nanocrystals are described in Chapter 2, with emphasis on the low-temperature ferromagnetic interactions in these antiferromagnetic oxides. Chapter 3 deals with the synthesis and characterizations of nanocrystals of ReO3, RuO2 and IrO2 which are oxides with metallic properties. Pressure-induced phase transitions of ReO3 nanocrystals and the use of the nanocrystals for carrying out surface-enhanced Raman spectroscopy of the molecules form Chapter 4. Use of ionic liquids to synthesize different nanostructures of semiconducting metal sulfides and selenides is described in Chapter 5. Synthesis of Mn-doped GaN nanocrystals and their magnetic properties are described in Chapter 6. A detailed investigation has been carried out on the growth kinetics of nanostructures of a few inorganic materials by using small-angle X-ray scattering and other techniques (Chapter 7). The study includes the growth kinetics of nanocrystals of Au, CdS and CdSe as well as of nanorods of ZnO. Results of a synchrotron X-ray study of the formation of nanocrystalline gold films at the organic-aqueous interface are also included in this chapter. Chapter 8 discuses the use of the organic-aqueous interface to generate Janus nanocrystalline films of inorganic materials where one side of the film is hydrophobic and other side is hydrophilic. This chapter also includes the formation of nanostructured peptide fibrils at the organic-aqueous interface and their use as templates to prepare inorganic nanotubes.

Hochfeste Leitermaterialien werden für gepulste Hochfeld-Magnetspulen benötigt, um damit die sehr hohen Magnetfelder mit einer magnetischen Flussdichte von bis zu 100 T zerstörungsfrei erzeugen zu können. Cu-Nb-Legierungen besitzen ein hohes Potential, um die widersprüchlichen Anforderungen an das Leitermaterial, wie hohe Festigkeit, hohe Leitfähigkeit und gute Verformbarkeit, zu erfüllen. Die Herstellung von Cu-Nb-Legierungen ist jedoch auf dem konventionellen Weg der Schmelzmetallurgie aufgrund der vernachlässigbar kleinen gegenseitigen Randlöslichkeit der beiden Komponenten sehr kompliziert. Die hier vorliegende Arbeit befasst sich mit Untersuchengen zur Technologie für die Herstellung von hochfesten Cu-Nb-Leitermaterialien auf der Basis der Pulvermetallurgie. Gleichermaßen ist die Entwicklung der Legierung Kerninhalt der vorliegenden Arbeit. Hierfür wurden während der einzelnen Prozessschritte sowohl die Entwicklung des Gefüges als auch die für die Anwendung relevanten Eigenschaften der Legierung untersucht und die Beziehungen zwischen Gefüge und mechanischen wie auch elektrischen Eigenschaften ermittelt.