Photocatalytic processes over semiconducting oxide surfaces have attracted worldwide attention aspotentially efficient, environmentally friendly and low cost methods for water/air purification as well as forrenewable hydrogen production. However, some limitations to achieve high photocatalytic efficiencies havebeen found due to the fast recombination of the charge carriers. Development of heterostucture photocatalystsby depositing metals on the surface of semiconductors or by coupling two semiconductors with suitable bandedge position can reduce recombination phenomena by vectorial transfer of charge carriers. To draw newprospects in this domain, three different kinds of heterostructures such as n-type/n-type semiconductor(SnO2/ZnO), metal/n-type semiconductor (RuO2/TiO2 and RuO2/ZnO) and p-type/n-type semiconductor(NiO/TiO2) heterojunction nanomaterials were successfully prepared by solution process. Their composition,texture, structure and morphology were thoroughly characterized by FTIR, X-ray diffraction (XRD), Ramanspectroscopy, transmission electron microscopy (TEM) and N2 sorption measurements. On the other hand, asuitable combination of UV-visible diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy(XPS) and ultraviolet photoemission spectroscopy (UPS) data provided the energy band diagram for eachsystem. The as-prepared heterojunction photocatalysts showed higher photocatalytic efficiency than P25 TiO2for the degradation of organic dyes (i.e. methylene blue and methyl orange) and the production of hydrogen.Particularly, heterostructure RuO2/TiO2 and NiO/TiO2 nanocomposites with optimum loading of RuO2 (5 wt %)and NiO (1 wt %), respectively, yielded the highest photocatalytic activities for the production of hydrogen.These enhanced performances were rationalized in terms of suitable band alignment as evidenced by XPS/UPSmeasurements along with their good textural and structural properties. This concept of semiconductingheterojunction nanocatalysts with high photocatlytic activity should find industrial application in the future toremove undesirable organics from the environment and to produce renewable hydrogen.

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L’alimentation en énergie des réseaux de capteurs miniaturisés pose une question fondamentale, dans la mesure où leur autonomie est un critère de qualité de plus en plus important pour l’utilisateur. C’est même une question cruciale lorsque ces réseaux visent à assurer une surveillance d’infrastructure (avionique, machines, bâtiments…) ou une surveillance médicale ou environnementale. Les matériaux piézoélectriques permettent d’exploiter l’énergie mécanique inutilisée présente en abondance dans l’environnement (vibrations, déformations liées à des mouvements ou à des flux d’air…). Ils peuvent ainsi contribuer à rendre ces capteurs autonomes en énergie. Sous la forme de nanofils (NF), les matériaux piézoélectriques offrent une sensibilité qui permet d’exploiter des sollicitations mécaniques très faibles. Ils sont également intégrables, éventuellement sur substrat souple.Dans cette thèse nous nous intéressons au potentiel des nanofils de matériaux semi-conducteurs piézoélectriques, tels que ZnO ou les composés III-V, pour la conversion d’énergie mécanique en énergie électrique. Depuis peu, ceux-ci ont fait l’objet d’études relativement nombreuses, avec la réalisation de nanogénérateurs (NG) prometteurs. De nombreuses questions subsistent toutefois avec, par exemple, des contradictions notables entre prédictions théoriques et observations expérimentales.Notre objectif est d’approfondir la compréhension des mécanismes physiques qui définissent la réponse piézoélectrique des NF semi-conducteurs et des NG associés. Le travail expérimental s’appuie sur la fabrication de générateurs de type VING (Vertical Integrated Nano Generators) et sur leur caractérisation. Pour cela, un système de caractérisation électromécanique a été construit pour évaluer les performances des NG réalisés et les effets thermiques sous une force compressive contrôlée. Le module d’Young et les coefficients piézoélectriques effectifs de NF de GaN; GaAs et ZnO et de NF à structure cœur/coquille à base de ZnO ont été évalués également dans un microscope à force atomique (AFM). Les nanofils de ZnO sont obtenus par croissance chimique en milieu liquide sur des substrats rigides (Si) ou flexibles (inox) puis sont intégrés pour former un générateur. La conception du dispositif VING s’est appuyée sur des simulations négligeant l’influence des porteurs libres, comme dans la plupart des études publiées. Nous avons ensuite approfondi le travail théorique en simulant le couplage complet entre les effets mécaniques, piézoélectriques et semi-conducteurs, et en tenant compte cette fois des porteurs libres. La prise en compte du piégeage du niveau de Fermi en surface nous permet de réconcilier observations théoriques et expérimentales. Nous proposons notamment une explication au fait que des effets de taille apparaissent expérimentalement pour des diamètres au moins 10 fois plus grands que les valeurs prévues par simulation ab-initio ou au fait que la réponse du VING est dissymétrique selon que le substrat sur lequel il est intégré est en flexion convexe ou concave. / Energy autonomy in small sensors networks is one of the key quality parameter for end-users. It’s even critical when addressing applications in structures health monitoring (avionics, machines, building…), or in medical or environmental monitoring applications. Piezoelectric materials make it possible to exploit the otherwise wasted mechanical energy which is abundant in our environment (e. g. from vibrations, deformations related to movements or air fluxes). Thus, they can contribute to the energy autonomy of those small sensors. In the form of nanowires (NWs), piezoelectric materials offer a high sensibility allowing very small mechanical deformations to be exploited. They are also easy to integrate, even on flexible substrates.In this PhD thesis, we studied the potential of semiconducting piezoelectric NWs, of ZnO or III-V compounds, for the conversion from mechanical to electrical energy. An increasing number of publications have recently bloomed about these nanostructures and promising nanogenerators (NGs) have been reported. However, many questions are still open with, for instance, contradictions that remain between theoretical predictions and experimental observations.Our objective is to better understand the physical mechanisms which rule the piezoelectric response of semiconducting NWs and of the associated NGs. The experimental work was based on the fabrication of VING (Vertical Integrated Nano Generators) devices and their characterization. An electromechanical characterization set-up was built to evaluate the performance and thermal effects of the fabricated NGs under controlled compressive forces. Atomic Force Microscopy (AFM) was also used to evaluate the Young modulus and the effective piezoelectric coefficients of GaN, GaAs and ZnO NWs, as well as of ZnO-based core/shell NWs. Among them, ZnO NWs were grown using chemical bath deposition over rigid (Si) or flexible (stainless steel) substrates and further integrated to build VING piezoelectric generators. The VING design was based on simulations which neglected the effect of free carriers, as done in most publications to date. This theoretical work was further improved by considering the complete coupling between mechanical, piezoelectric and semiconducting effects, including free carriers. By taking into account the surface Fermi level pinning, we were able to reconcile theoretical and experimental observations. In particular, we propose an explanation to the fact that size effects are experimentally observed for NWs with diameters 10 times higher than expected from ab-initio simulations, or the fact that VING response is non-symmetrical according to whether the substrate on which it is integrated is actuated with a convex or concave bending.

Esta tese de doutorado é o resultado de um estudo dos mecanismos de operação de dispositivos poliméricos emissores de luz, com um particular enfoque nos processos de injeção e transporte de portadores de carga em polímeros derivados do poli(p-fenileno vinileno), PPV. Para tanto, se fez necessário o domínio de todas as etapas de produção e caracterização, desde a síntese química dos polímeros até a fabricação propriamente dita dos dispositivos, as quais são brevemente descritas neste trabalho. Basicamente, dois tipos diferentes de dispositivos foram caracterizados: diodos poliméricos emissores de luz (PLEDs), nos quais a camada ativa é composta por um filme fino (100-500 nm de espessura) do polímero eletroluminescente puro, e células eletroquímicas emissoras de luz (LECs), compostas por blendas do polímero conjugado com um eletrólito polimérico condutor iônico. As propriedades ópticas dos dispositivos foram analisadas através dos espectros de absorção óptica na região do ultravioleta/visível e de emissão (foto e eletroluminescência) enquanto as propriedades de injeção e de transporte de carga foram exploradas através de medidas elétricas de corrente-voltagem (I-V), espectroscopia de impedância no domínio da freqüência (condutividade ac), espectroscopia de fotocorrente e ressonância magnética detectada eletricamente (EDMR). A influência de parâmetros como a estrutura dos dispositivos, os metais utilizados como eletrodos e a temperatura permitiram uma análise mais detalhada de alguns modelos teóricos utilizados na interpretação dos resultados experimentais, fornecendo, dessa forma, um maior conhecimento das propriedades físicas dos materiais estudados. / This PhD thesis is an extensive study of the operation mechanisms of polymeric light-emitting devices, with a particular focus on the injection and transport properties of charge-carriers in poly(p-phenylene vinylene), PPV, derivatives. Therefore, it was necessary to dominate all the processes of fabrication and characterization of such devices, from the chemical synthesis of the polymers to the device fabrication, which are briefly described along this work. Two different kinds of devices were studied: polymeric ligh-emitting diodes (PLEDs) composed by a single thin layer (100-500 nm thick) of the pure electroluminescent polymer, and light-emitting electrochemical cells (LECs), which active layers are formed by a blend of the conjugated polymer and an ionic conductive polymeric electrolyte. The optical properties of the devices were analyzed by optical absorption in the ultraviolet-visible range and emission (photo- and electroluminescence) spectra. The charge injection and transport properties were studied by electrical measurements like current-voltage (I-V) curves, impedance spectroscopy in the frequency domain (ac conductivity), photocurrent spectroscopy and electrically detected magnetic resonance (EDMR). The influence of parameters like the device structure, the electrodes work function and the temperature allowed a detailed analysis of some theoretical models commonly used in the interpretation of the experimental results, providing more information about the physical properties of the studied conjugated polymers.

The constant trend of device miniaturization along with ever-growing list of unusual behaviour of nanoscale materials has fuelled the recent research in fabrication and applications of ultrathin (~2 nm diameter) nanowires. Although semiconductor nanowires of this dimension is well-researched, molecular-scale single-crystalline metal nanowires have not been addressed in details. Such single crystalline Au nanowires are formed by oriented attachment of Au nanoparticles along [111] direction. A very low concentration of extended defects in these wires result in a high electrical conductivity, making them ideal for nanoscale interconnects. Other metal nanowires, e.g. Ag and Cu, have very low absorption co-efficient useful for fabrication of transparent conducting films. On the other hand, because of the reduced dimensions, there exists a tantalizing possibility of dominating quantum effects leading to their application in sensing and actuation. Also, speaking in terms of atomic structure, these systems suffer from intense surface stress, and the atomistic picture can be drastically different from bulk. Thus, although a myriad of applications are possible with ultrathin metal nanowires, a rigorous systematic knowledge of their atomic and electronic structure is not yet available. This thesis is the first one to model such computationally demanding systems with emphasis on their possible applications. In this thesis, we have explored various structural and electronic aspects of one-dimensional ultrathin nanowires with ab initio density functional theory coupled with experiments. The merit of Au nanowires has been tested as nanoscale interconnects. From atomistic point of view, these FCC Au nanowires exhibit an intriguing relaxation mechanism, which has been explored by both theory and experiment. The primary factor governing the relaxation mechanism was found to be the anisotropic surface stress of the bounding facets, and it is extended to explain the relaxation of other metallic nanowires. Our studies suggest that AuNWs of this dimension show semiconductor-like sensitivity towards small chemical analytes and can be used as nanoscale sensors. Also, we have found that further reducing the diameter of the Au-nanowires leads to opening of a band gap.

Les spectroscopies de diffusion inélastique de la lumière (Raman/Brillouin) sont un outil versatile qui permet d'étudier les phonons thermiques de la matière à différentes échelles. Dans les milieux nano-granulaires, l'étude des phonons acoustiques dont la longueur d'onde est grande devant le diamètre D des grains (?/D >> 1) permet de caractériser l'élasticité macroscopique gouvernée par la loi du contact de Hertz. La validité de la loi de contact est étudiée pour des poudres d'oxyde constituées de nanoparticules sphériques d'une taille de quelques nanomètres. Lorsque la demi-longueur d'onde des phonons acoustiques devient égale à la dimension du confinement (diamètre D pour les sphères, épaisseur e pour une plaquette), la propagation n'est plus possible et un phénomène de résonance mécanique apparaît. La spectroscopie Raman basse fréquence a été utilisée pour caractériser les modes de vibration acoustique de nanoplaquettes semiconductrices habillées d'un « manteau » organique. Lorsque l'épaisseur est suffisamment faible (e ~1 nm) une forte déviation de la fréquence de résonance est observée par rapport au modèle de la plaquette libre, attribuée à la présence des molécules organiques et est interprétée par un effet nano-balance. Lorsque l'objet confinant est un nano-dimère métallique, une hybridation plasmonique et acoustique des nanoparticules ont lieu conjointement. L'excitation résonante du plasmon dimèrique permet d'observer à l'échelle d'un dimère unique la diffusion par les modes de vibration dipolaire hybridé l=1 ainsi que les modes non hybridés de moment angulaire l >2, interdits par les règles de sélection précédemment établies pour ce régime de taille / Inelastic light scattering spectroscopies (Raman/Brillouin) are a versatile tool to study thermal phonons at various scales. In nano-granular media, the study of acoustic phonons with a wavelength much greater than the grain diameter D (?/D >> 1) allows one to characterize the macroscopic elasticity governed by Hertz law of the contact. The validity of Hertz law is studied for powders made of oxide nanoparticles a few nanometers in diameter. When the phonon half-wavelength reaches the confinement dimension (diameter D for spheres, thickness e for plates) propagation is forbidden and mechanical resonances occur. Low frequency Raman spectroscopy has been used to characterize the acoustic resonances of semiconducting nanoplatelets “dressed” with an organic surfactant layer. When the thickness becomes thin enough (e ~ 1 nm), the resonance frequency is significantly downshifted compared to a free platelet, attributed to a mass load effect due to the organic molecules. When the confining object is a metallic nano-dimer, both plasmonic and acoustic hybridization occur at the same time. The resonant excitation of the dimeric plasmon allows one to observe down to single nano-object scale the inelastic scattering by dimer hybridized dipolar vibration modes l=1 as well as non-hybridized modes with higher angular momentum l >2, known to be Raman inactive in this size range according to previously established selection rules. Possibilities for a new plasmon-vibration coupling mechanism are discussed

Structures semi-conductrices à base de NiTiO3, et l'étude de leurs propriétés dans le but de les appliquer en photocatalyse. Une étude théorique et des simulations numériques ont été effectuées pour analyser les propriétés électroniques, vibrationnelles et optiques de NiTiO3 massif ou sous forme de clusters nanométriques. Les poudres NiTiO3 ont été synthétisées par sol-gel par réaction en phase solide, tandis que les films minces ont été obtenus par pulvérisation cathodique rf-magnétron. Les caractérisations de leurs propriétés physiques confirment l'obtention de NiTiO3 polycristallin dans sa phase ilménite. La détermination du gap électronique à 2,25 eV suggère la faisabilité de mise en oeuvre des matériaux synthétisés comme photocatalyseurs actifs sous irradiation en lumière visible. Cette fonctionnalité a été testée par la dégradation du bleu de méthylène en solution aqueuse en utilisant les couches minces de NiTiO3 sous irradiation visible, atteignant la dégradation de 60% de la concentration initiale du colorant en 300 minutes. En outre, l'électro-oxydation du méthanol a été réalisée en appliquant une tension externe sur une électrode contenant des poudres NiTiO3 dans des milieux alcalins. Les ions de Ni présents dans le catalyseur ont été identifiés comme des espèces actives et que l'oxydation des molécules organiques se produit sur la surface des sites de Ni3+. En résumé, NiTiO3 a été synthétisé sous forme de poudres et de films minces ayant des caractéristiques appropriées pour la photocatalyse hétérogène efficace et les capacités catalytiques de NiTiO3 ont été démontrées sur la photodégradation du bleu de méthylène et l'électrooxydation de méthanol. / The thesis work is devoted to the synthesis of NiTiO3-based semiconductive structures, i.e. powders and thin films, and the investigation of their related properties with the aim of their applications in photocatalysis. Theoretical approach and numerical simulations of the electronic, vibrational and optical properties of bulk and nanosized NiTiO3 structures have been carried out in order to deepen the understanding of the experimental results. The synthesis of NiTiO3 powders has been achieved by sol-gel and solid state reaction, while NiTiO3 thin films have been grown by rf-sputtering.Characterizations on their structural, vibrational and optical properties confirm the stabilization of polycrystalline NiTiO3 in its ilmenite phase in both powders and thin films as well. The determination of a band gap at 2.25 eV suggests the feasibility to implement the synthesized materials as visible-light-active photocatalysts. This feature has been tested in thedegradation of methylene blue in aqueous solution using rf-sputtered NiTiO3 thin films irradiated with visible light,achieving the degradation of 60% of the initial concentration of the colorant in 300 minutes. In addition, the electro-oxidation of methanol has been accomplished by applying an external voltage on an electrode containing NiTiO3 powders in alkaline media. The Ni ions present in the catalyst have been identified as the active species with the oxidation of the organic molecules on the surface of Ni3+ sites. As a main achievement, NiTiO3 has been synthesized as powders and thin films with suitable characteristics for efficient heterogeneous photocatalysis and the catalytic capabilities of NiTiO3 have beendemonstrated on the photodegradation of Methylene Blue and the electro-oxidation of methanol.

L’utilisation de semi-conducteurs organiques dans les dispositifs électroniques offre d’intéressantes perspectives. En effet, ils permettent d’alléger le poids de ces dispositifs en plus de diminuer grandement le coût de leur fabrication. Cependant, une des principales problématiques associées à ces semi-conducteurs organiques est leur procédé de fabrication qui requiert des solvants organiques toxiques et de multiples étapes de synthèse. Dans ce travail, un nouveau procédé de synthèse respectueux de l’environnement a été mis au point. Une seule étape était nécessaire à la préparation des semi-conducteurs, en utilisant la réaction de polycondensation entre une diamine et un dialdéhyde. Cette réaction a été réalisée à température ambiante, dans un solvant vert, l’éthanol, et sans utilisation de catalyseurs, minimisant ainsi la consommation énergétique et utilisant un milieu réactionnel de source renouvelable et peu toxique. Après leur dopage, ces polymères ont présentés des propriétés de conduction comparables à celles des principaux semi-conducteurs organiques. La deuxième partie de cette thèse a été consacrée à l’étude de l’utilisation du papier comme support pour les dispositifs d’électronique organique; s’affranchissant ainsi de l’utilisation de substrats généralement non biodégradables et/ou de sources non renouvelables (plastique ou verre). Deux stratégies ont été utilisées à cette fin. La première consistait en un dépôt direct des polymères semi-conducteurs à la surface de filaments de cellulose. La deuxième est basée sur la création d’un lien covalent entre les semi-conducteurs et la pâte Kraft, en utilisant la réaction de cycloaddition 1,3-dipolaire de Huisgen catalysée par le cuivre (CuAAc). / The use of organic semiconductors in electronic devices offers interesting prospects. Indeed, they make it possible to lighten the weight of these devices in addition to greatly reducing the cost of their manufacture. However, one of the main problems associated with these organic semiconductors is their manufacturing process, which requires toxic organic solvents and multiple synthesis steps. In this work, a new environmentally friendly synthesis process has been developed. A single step was necessary for the preparation of the semiconductors, using the polycondensation reaction between a diamine and a dialdehyde.This reaction was carried out at room temperature in ethanol, a green solvent and without the use of catalysts, thus minimizing energy consumption and using a reaction medium from a renewable and low-toxicity source. After their doping, these polymers exhibited conduction properties comparable to those observed for conventional organic semiconductors.The second part of this thesis was devoted to the study of the use of paper as a support for organic electronics devices; hus avoiding the use of generally non-biodegradable and/or non-renewable substrates (plastic or glass). Two strategies have been used to this end. The first consisted of a direct deposit of the semiconducting polymers to the surface of cellulose filaments.The second is based on the creation of a covalent bond between the semiconductors and the Kraft pulp, using the copper-catalyzed Huisgen 1,3-dipolar cycloaddition reaction (CuAAc).

The main motivation in this thesis is to compare the conformation and charge transport in conducting polymers and carbon nanotubes (CNTs) and to investigate those physical properties in their combined form of nanocomposites. It is known that both conducting polymers and carbon nanotubes are intrinsically 1-dimensional systems which consist of delocalized π-electrons. However, the main difference between these is the fact that flexibility of conducting polymers can be varied depending on the extent of conjugation while CNTs are rigid. Hence a comparison of electronic properties as correlated to their morphology has been carried out and their individual role in nanocomposites is further studied. The thesis consists of 6 chapters and appendix. Chapter 1 consists of brief introduction of general properties of both conducting polymers, CNTs and their nanocomposites. Chapter 2 deals with the sample preparation and experimental techniques used for the work. Chapter 3 elaborates on the conformational / structural studies on the systems. Chapter 4 focuses on the transport measurements to study the electronic properties of the samples. Chapter 5 reveals the magnetic properties of these systems which can be applied in technological devices. And chapter 6 gives the conclusion and future directions of the work being done. Chapter 1: Nanocomposites represent a guest-host matrix consisting of easily processible functionalized conjugated polymer as host, incorporating carbon nanotubes as fillers with versatile electronic and magnetic properties, which provide a wide range of technological applications. The conformation, charge dynamics as well as magnetic properties of these conducting polymers and carbon nanotubes, and various aspects of transport mechanism and spin dynamics present in the nanocomposite matrix are studied and presented in a consistent framework. Chapter 2: The multiwall carbon nanotubes (MWNTs) are grown by thermal chemical vapor deposition (CVD). The MWNTs are dispersed in solution of conducting polymers by ultrasonication and then the suspension is cast on glass substrate and slowly dried by moderate heating. Once dried completely, the free-standing films of thickness 15-25 μm are peeled off the substrate for measurements. The MWNTs, above a certain concentration, form an interconnected network in the 3-dimensional polymer matrix, following percolation mechanism. The disorder is brought into the system mainly by bundling of tubes and bundle intersections. The morphology and conformation of the samples are studied by SEM, TEM and small angle X-ray scattering (SAXS) techniques. Chapter 3: Small angle X-ray scattering (SAXS) studies in polymeric systems are carried out to probe local nanoscale morphology at various length scales to show the correlation among conformation and assembly of chains. Small angle X-ray scattering (SAXS) studies are carried out in poly [2-methoxy5-(2’–ethyl-hexyloxy)-1,4-phenylene vinylene] (MEH-PPV) solution of varying conjugation lengths as well as different solvents. By increasing the extent of πconjugation from 30 to 100 %, the persistence length increases by a factor of three. Moreover, a pronounced second peak in the pair distribution function is observed in fully conjugated chain, at larger length scales which indicates that the chain segments tend to self-assemble as the conjugation along the chain increases. The chain assembly and aggregation are further studied for suspensions of MWNTs in polyethylene dioxythiophene-polystyrene (PEDOT-PSS) with aqueous medium and DMSO (dimethyl sulphoxide). The SAXS profile of MWNT dispersion in aqueous PEDOT-PSS clearly show rigid-rod feature of the individual nanotubes evident by the q-1 behavior at short ranges. The crossover from q-1 to q-2 in the longer range further suggest that the suspension consists of individual nanotubes, nanotubes bundles and aggregates that give rise to a 3-dimensonal meshwork of intersecting tubes and ropes. For the MWNT dispersion in PEDOT-PSS with DMSO, however, such q-1 behavior is absent; which evidently shows that the rods are not isolated in the solution and are rather agglomerated. How these conformations affect the electrical and magnetic properties of these systems are studied further in Chapter 4. Chapter 4: Transport mechanism in single wall carbon nanotubes (SWNT), MWNT pellets, and nanocomposite films of MWNT and PEDOT-PSS is studied. The positive and negative magnetoresistance (MR) data in various SWNT samples are analyzed by taking into account the electron-electron interaction (EEI) contribution, in addition to the weak localization (WL) regime. The contribution from EEI to the total MR is confirmed from the universal scaling of MC relation showing that EEI plays a significant role at higher fields and lower temperatures. Intrinsic parameters like inelastic scattering length extracted for barely metallic sample follows the T-3/4 dependence due to inelastic electron-electron scattering in the dirty limit. Conductivity and magnetoresistance (MR) measurements on nanocomposite films with varying MWNT content (0.03 - 3 %) are performed at a field range 0-11 Tesla, and temperature range 1.3–300 K. The temperature dependence of resistance above 4 K suggests a Coulomb-gap variable range hopping (CG-VRH) transport in the network. Alhough solely negative MR (~ 5-6 %) is observed for pristine MWNT pellets; the nanocomposite films show a combination of large negative MR (~ 80 %) at T < 4 K, and a comparatively weaker positive MR (~ 30 %) for T > 4 K. This suggest that there are two mechanism interplaying and dominant at different temperature regimes which can be explained by the mechanism of transport of the charge carriers of MWNT intervened by that of the polymer matrix. In conclusion how the individual properties of conducting polymer and carbon nanotubes contribute to the unique electronic and conformational properties in their nanocomposites is framed in this investigation. Chapter 5: Magnetic properties of the pristine MWNTs as well as metal nanowires of nickel, nickel-iron (NiFe), nickel-iron-cobalt (NiFeCo) encapsulated in the MWNTs are studied using superconducting quantum interference device (SQUID) magnetometer. A typical example of Ni nanowires encapsulated in MWNT (Ni-MWNT) is taken and the results are compared to other forms of nickel (bulk, nanorod cluster, nanowire) to see the effect of size, shape and environment on the magnetic kproperties. The saturation magnetization and coercivity for Ni-MWNTs are 1.0 emu/gm and 230 Oe. The temperature dependence of magnetization indicates superparamagnetic which is supported by the field-cooled and zero-field-cooled plots determining a blocking temperature ~ 300 K. These altered magnetic properties of Ni-MWNTs are mainly due to the contribution from carbon nanotube encapsulation. Both the shape and environment enhance the total magnetic anisotropy of encapsulated nanowires at least by a factor of four. The encapsulation of metal nanowires in MWNTs tunes the magnetic properties of the system widely, e.g. from diamagnetic (pristine MWNTs) to paramagnetic (Ni-MWNT) to ferromagnetic (NiFe-MWNT) and a combination of para and ferro (NiFeCo-MWNT). Chapter 6: The conclusions of the different works presented in the thesis are coherently summarized in this chapter. Thoughts for future directions are also summed up. Appendix A: Spin dynamics in conducting polymer PEDOT-PSS in its pristine, processed with DMSO and nanocomposite form (with carbon nanotubes) is studied using solid state nuclear magnetic resonance (NMR). Plots of proton spin lattice relaxation times vs. temperature at a fixed frequency 23.4 MHz are compared to study the effect of the external agents on the polymer dynamics.

This diploma thesis focuses on the syhnthesis of multicomponent ceramic system based on Ca-(Mn,Co)-O. The thesis is devided in theoretical and experimental part. The theoretical part is describing ceramic materials for thermoelectric application, preparation and synthesis of these materials and their processing. The experimental part is dealing with synthesis of ceramic powder which is processed to the porous ceramics. The properties of prepared porous ceramics are observed.