Nature develops several materials with remarkable functional properties composed of comparatively simple base substances. Biological materials are often composites, which optime the conformation to their function. On the other hand, synthetic materials are designed a priori, structuring them according to the performance to be achieved. 3D printing manufacturing is the most direct method for specific component production and earmarks the sample with material and geometry designed ad-hoc for a defined purpose, starting from a biomimetic approach to functional structures. The technique has the advantage of being quick, accurate, and with a limited waste of materials. The sample printing occurs through the deposition of material layer by layer. Furthermore, the material is often a composite, which matches the characteristics of components with different geometry and properties, achieving better mechanical and physical performances. This thesis analyses the mechanics of natural and custom-made composites: the spider body and the manufacturing of metallic and non-metallic graphene composites. The spider body is investigated in different sections of the exoskeleton and specifically the fangs. The study involves the mechanical characterization of the single components by the nanoindentation technique, with a special focus on the hardness and Young's modulus. The experimental results were mapped, purposing to present an accurate comparison of the mechanical properties of the spider body. The different stiffness of components is due to the tuning of the same basic material (the cuticle, i.e. mainly composed of chitin) for achieving different mechanical functions, which have improved the animal adaptation to specific evolutive requirements. The synthetic composites, suitable for 3D printing fabrication, are metallic and non-metallic matrices combined with carbon-based fillers. Non-metallic graphene composites are multiscale compounds. Specifically, the material is a blend of acrylonitrile-butadiene-styrene (ABS) matrix and different percentages of micro-carbon fibers (MCF). In the second step, nanoscale filler of carbon nanotubes (CNT) or graphene nanoplatelets (GNP) are added to the base mixture. The production process of composite materials followed a specific protocol for the optimal procedure and the machine parameters, as also foreseen in the literature. This method allowed the control over the percentages of the different materials to be adopted and ensured a homogeneous distribution of fillers in the plastic matrix. Multiscale compounds provide the basic materials for the extrusion of fused filaments, suitable for 3D printing of the samples. The composites were tested in the configuration of compression moulded sheets, as reference tests, and also in the corresponding 3D printed specimens. The addition of the micro-filler inside the ABS matrix caused a notable increment in stiffness and a slight increase in strength, with a significant reduction in deformation at the break. Concurrently, the addition of nanofillers was very effective in improving electrical conductivity compared to pure ABS and micro-composites, even at the lowest filler content. Composites with GNP as a nano-filler had a good impact on the stiffness of the materials, while the electrical conductivity of the composites is favoured by the presence of CNTs. Moreover, the extrusion of the filament and the print of fused filament fabrication led to the creation of voids within the structure, causing a significant loss of mechanical properties and a slight improvement in the electrical conductivity of the multiscale moulded composites. The final aim of this work is the identification of 3D-printed multiscale composites capable of the best matching of mechanical and electrical properties among the different compounds proposed. Since structures with metallic matrix and high mechanical performances are suitable for aerospace and automotive industry applications, metallic graphene composites are studied in the additive manufacturing sector. A comprehensive study of the mechanical and electrical properties of an innovative copper-graphene oxide composite (Cu-GO) was developed in collaboration with Fondazione E. Amaldi, in Rome. An extensive survey campaign on the working conditions was developed, leading to the definition of an optimal protocol of printing parameters for obtaining the samples with the highest density. The composite powders were prepared following two different routes to disperse the nanofiller into Cu matrix and, afterward, were processed by selective laser melting (SLM) technique. Analyses of the morphology, macroscopic and microscopic structure, and degree of oxidation of the printed samples were performed. Samples prepared followed the mechanical mixing procedure showed a better response to the 3D printing process in all tests. The mechanical characterization has instead provided a clear increase in the resistance of the material prepared with the ultrasonicated bath method, despite the greater porosity of specimens. The interesting comparison obtained between samples from different routes highlights the influence of powder preparation and working conditions on the printing results. We hope that the research could be useful to investigate in detail the potential applications suitable for composites in different technological fields and stimulate further comparative analysis.

Within the framework of this thesis, the electron beam melting of pure copper for the purpose of producing electrical windings was examined. The conventional manufacturing process of copper windings was investigated, and the potential advantages offered by the design freedom inherent in the electron beam melting process were explored. A comprehensive parameter study was conducted to optimize the existing production parameters for the electron beam melting of pure copper, with a specific focus on achieving the desired material properties suitable for electric motor windings. Moreover, according to additive manufacturing possibilities, conceptual winding models were developed and subsequently were fabricated in a laboratory setting using electron beam melting. The investigation revealed a notable correlation between the achievable wall thickness and the focus offset. A focused electron beam, which was achieved with a focus offset of 17 mA, allowed for the production of thinner walls with reduced surface roughness. Additionally, the study highlighted that the density of the manufactured parts decreased as the hatch offset increased, particularly posing a more critical impact on smaller cross-sectional areas than larger ones. Furthermore, implementing a double-scanned contour for the hatch contributed to diminishing roughness while simultaneously increasing the maximum density to 99.6 %. Influencing the electrical conductivity of printed copper samples through heat treatment was successfully demonstrated, resulting in a conductivity of 91.7% ± 1.8% IACS post-heat treatment. / Inom ramen för denna avhandling undersöktes elektronstrålesmältningen av ren koppar i syfte att producera elektriska lindningar. Den konventionella tillverkningsprocessen av kopparlindningar undersöktes, och de potentiella fördelarna som erbjuds av designfriheten som är inneboende i elektronstrålesmältningsprocessen undersöktes. En omfattande parameterstudie genomfördes för att optimera befintliga produktionsparametrar för elektronstrålesmältning av ren koppar, med särskilt fokus på att uppnå önskade materialegenskaper lämpliga för elmotorlindningar. Dessutom, i enlighet med additiva tillverkningsmöjligheter, utvecklades konceptuella lindningsmodeller och tillverkades därefter i laboratoriemiljö med användning av elektronstrålesmältning. Undersökningen avslöjade en anmärkningsvärd korrelation mellan den möjliga väggtjockleken och fokusförskjutningen. En fokuserad elektronstråle, som uppnåddes med en fokusförskjutning på 17 mA, möjliggjorde produktion av tunnare väggar med minskad ytjämnhet. Dessutom visade studien att densiteten hos de tillverkade delarna minskade när avståndet mellan smältlinjerna ökade, vilket i synnerhet innebar en mer kritisk påverkan på mindre tvärsnittsareor än större. Dessutom bidrog implementeringen av en dubbelskannad kontur för luckan till att minska grovheten samtidigt som den maximala densiteten ökade till 99,6 %. Att påverka den elektriska ledningsförmågan hos tryckta kopparprover genom värmebehandling demonstrerades framgångsrikt, vilket resulterade i en ledningsförmåga på 91,7 % ± 1,8 % IACS efter värmebehandling.

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Thesis (M.Sc. Agriculture (Horticultrure)) -- University of Limpopo, 2017 / The current South African ‘Hass’ type avocado cultivars are inadequate to enhance competitiveness, cultivar diversity and profitability. In an effort to ensure competitiveness and maintain sustainability, the Agricultural Research CouncilInstitute for Tropical and Subtropical Crops (ARC-ITSC) as one the South African Avocado Industry’s (SAAI) main stakeholder, has bred and selected new superior ‘Hass’ type avocado selections. However, the cold storage potential and associated physico-chemical ripening properties of these selections (‘Jalna’, ‘OA 184’ and ‘Balboa’) have not been documented. Therefore, the objective of this study was to evaluate the effect of cold storage on internal and external physico-chemical ripening variables of the new ‘Hass’ type avocado selections. New ‘Hass’ type avocado fruit maturity was evaluated using moisture content, thereafter, harvested, sorted, graded and stored under two temperature regimes (2.0°C and 5.5°C) for 28 days to simulate export conditions. The experiment was a completely randomised factorial design with three treatment factors; temperature regimes (2.0°C and 5.5°C), days to ripening and ‘Hass’ type avocado selections fruit and control (commercial ‘Hass’) replicated three times. After withdrawal from cold storage, fruit were ripened at ambient temperature and evaluated for electrical conductivity, external chilling injury, fruit water loss, skin colour change, ripening percentage, firmness, respiration rate and seed:fruit weight ratio. Results indicated that treatment factors had no significant effect on moisture content (P=0.733) and chilling injury (P=0.776). Treatment factors had a significant effect on electrical conductivity (P=0.004), skin colour parameters; eye colour (P<0.001), hue angle (P<0.001), lightness (P=0.011) and chroma (P=0.042). Selection ‘Jalna’ fruit started changing colour whilst in storage (2.0°C and 5.5°C). Furthermore, ‘Hass’ type avocado selection fruit followed a declining pattern for lightness, chroma and hue angle in agreement with commercial ‘Hass’. Moreover, results indicated that treatment factors had a significant effect (P<0.001) on respiration rate, fruit firmness, ripening percentage and seed:fruit weight ratio. Selection ‘Jalna’ and ‘OA 184’ desynchronised mesocarp softening with exocarp due to genetically non-softening exocarp. Treatment factors had no significant effect (P=0.998) on fruit water loss during ripening. Selection ‘OA 184’ fruit showed export potential due to its good storage, ripening physico-chemical and shelf-life properties. Studies on cold sterilisation would add more value on generated scientific information, as such would enable the SAAI to gain access to high paying export markets. In addition, the selections should be planted and evaluated in other avocado producing region

Pine tree substrate (PTS) is a relatively new substrate for container crop production. There are no detailed studies that elucidate how storage time impacts PTS chemical, physical, and biological aspects. The objective of this research was to determine how PTS storage time influenced PTS chemical and physical properties, nitrification, and plant growth. Pine tree substrate was manufactured by hammer-milling chips of loblolly pine trees (Pinus taeda L.) through two screen sizes, 4.76 mm (PTS) and 15.9 mm amended with peat (PTSP). PTS and PTSP were amended with lime at five rates. A peat-perlite mix (PL) served as a control treatment. Prepared substrates were placed in storage bags and stored in an open shed in Blacksburg, Virginia. Subsamples were taken at 1, 42, 84, 168, 270, and 365 days. At each subsampling day, twelve 1-L containers were filled with each substrate. Six containers were left fallow and six were planted with marigold (Tagetes erecta L. "Inca Gold") seedlings. Substrate was also collected from select treatments for Most Probable Number assays to estimate density of nitrifying microorganisms, and for chemical and physical property analyses. Pour-through extracts were collected from fallow containers at 0, 2, and 4 weeks, and from marigold containers at harvest for determination of pH, electrical conductivity, ammonium-N and nitrate-N. At harvest, marigold height, width, and dry weight were measured. At least 1 kg·m-3 lime for PTS, and 2 to 4 kg·m-3 lime for PTSP were needed to maintain pH values ≥ 5.5 for 365 days. Bound acidity of unlimed PTS increased but cation exchange capacity for unlimed PTS and PTSP decreased over 365 days. Carbon to nitrogen ratio and bulk density values were unchanged over time in all treatments. There were minor changes in particle size distribution for limed PTS and unlimed and limed PTSP. Marigold growth in PTS and PTSP was ≥ PL in all limed treatments, except at day 1. Nitrite-oxidizing microorganisms were present and nitrification occurred in PTS and PTSP at all subsampling days. Pine tree substrate is relatively stable in storage, but pH decreases, and lime addition may be necessary to offset this decrease. / Ph. D.

A highly effective electrocatalyst is the central component of advanced electrochemical energy conversion. Recently, two-dimensional conjugated metal-organic frameworks (2D c-MOFs) have emerged as a class of promising electrocatalysts due to their advantages including 2D layered structure with high in-plane conjugation, intrinsic electrical conductivity, permanent pores, large surface area, chemical stability, and structural diversity. In this review, we summarize the recent advances of 2D c-MOF electrocatalysts for electrochemical energy conversion. Firstly, we introduce the chemical design principles and synthetic strategies of the reported 2D c-MOFs, as well as the functional design for the electrocatalysis. Subsequently, we present the representative 2D c-MOF electrocatalysts in various electrochemical reactions, such as hydrogen/oxygen evolution, and reduction reactions of oxygen, carbon dioxide and nitrogen. We highlight the strategies for the structural design and property tuning of 2D c-MOF electrocatalysts to boost the catalytic performance, and offer our perspectives in regard to the challenges to be overcome.

Geophysical methods are essential for exploration and monitoring of subsurface formations, e.g. in carbon dioxide sequestration or enhanced geothermal energy. One of the keys to their successful application is the knowledge of how the measured physical quantities are related to the desired reservoir parameters. The work presented in this thesis shows that the presence of carbon dioxide (CO2) in pore space gives rise to multiple processes all of which contribute to the electrical rock conductivity variation. Basically, three mechanisms take place: (1) CO2 partially replaces the pore water, which is equivalent to a decrease in water saturation. (2) CO2 chemically interacts with the pore water by dissolution and dissociation. These processes change both the chemical composition and the pH of the pore filling fluid. (3) The low-pH environment can give rise to mineral dissolution and/or precipitation processes and changes the properties of the grain-water interface. Investigations on the pore water phase show that the reactive nature of CO2 in all physical states significantly acts on the electrical conductivity of saline pore waters. The physico-chemical interaction appears in different manifestations depending mainly on the pore water composition (salinity, ion types) but also on both temperature and pressure. The complex behaviour includes a low- and a high-salinity regime originating from the conductivity increasing effect of CO2 dissociation, which is opposed by the conductivity decreasing effect of reduced ion activity caused by the enhanced mutual impediment of all solutes. These results are fundamental since the properties of the water phase significantly act on all conduction mechanisms in porous media. In order to predict the variation of pore water conductivity, both a semi-analytical formulation and an empirical relationship for correcting the pore water conductivity, which depends on salinity, pressure and temperature, are derived. The central part of the laboratory experiments covers the spectral complex conductivity of water-bearing sand during exposure to and flow-through by CO2 at pressures up to 30MPa and temperatures up to 80°C. It is shown that the impact of CO2 on the real part of conductivity of a clean quartz sand is dominated by the low- and high-salinity regime of the pore water. The obtained data further show that chemical interaction causes a reduction of interface conductivity, which could be related to the low pH in the acidic environment. This effect is described by a correction term, which is a constant value as a first approximation. When the impact of CO2 is taken into account, a correct reconstruction of fluid saturation from electrical measurements is possible. In addition, changes of the inner surface area, which are related to mineral dissolution or precipitation processes, can be quantified. Both the knowledge gained from the laboratory experiments and a new workflow for the description and incorporation of geological geometry models enable realistic finite element simulations. Those were conducted for three different electromagnetic methods applied in the geological scenario of a fictitious carbon dioxide sequestration site. The results show that electromagnetic methods can play an important role in monitoring CO2 sequestration. Compared to other geophysical methods, electromagnetic techniques are generally very sensitive to pore fluids. The proper configuration of sources and receivers for a suitable electromagnetic method that generates the appropriate current systems is essential. Its reactive nature causes CO2 to interact with a water-bearing porous rock in a much more complex manner than non-reactive gases. Without knowledge of the specific interactions between CO2 and rock, a determination of saturation and, consequently, a successful monitoring are possible only to a limited extend. The presented work provides fundamental laboratory investigations for the understanding of the electrical properties of rocks when the reactive gas CO2 enters the rock-water system. All laboratory results are put in the context of potential monitoring applications. The transfer from petrophysical investigations to the planning of an operational monitoring design by means of close-to-reality 3D FE simulations is accomplished.

As interessantes propriedades eletrônicas, mecânicas e óticas dos materiais orgânicos conjugados fizeram emergir diversas aplicações tecnológicas e comerciais em dispositivos baseados nesses materiais, tais como sensores, memórias, células solares e diodos emissores de luz poliméricos (LEDs). Neste sentido, o tema central desta tese é o estudo das propriedades elétricas e morfológicas e os mecanismos de transporte eletrônico de cargas no PEDOT:PSS, uma blenda polimérica que consiste de um policátion condutivo, o poli(3,4- etilenodioxitiofeno) (PEDOT) e do poliânion poli(estirenosulfonado) (PSS). PEDOT:PSS é amplamente usado como material de eletrodo em aplicações na área de eletrônica plástica, como mencionado anteriormente. Apesar da condutividade elétrica dos filmes finos de PEDOT:PSS possa variar várias ordens de grandeza, dependendo do método pela qual é processado e transformado em filme fino, as razões para este comportamento é essencialmente desconhecido. Esta tese descreve um estudo detalhado do transporte eletrônico de cargas anisotrópico e sua correlação com a morfologia, as condições e as dimensões da separação de fase entre os dois materiais, PEDOT e PSS. Antes de abordar as propriedades do PEDOT:PSS, uma camada de filme fino inorgânica usada para aumentar o tempo de vida de dispositivos orgânicos é descrita no Capítulo 2. Um importante mecanismo de degradação em LEDs poliméricos é a fotooxidação da camada ativa. Assim, isolar a camada ativa da água, oxigênio e luz, torna-se crucial para o aumento do tempo de vida. Um sistema de deposição química a partir da fase de vapor estimulada por plasma (PECVD) é usado para depositar filmes finos de nitreto de carbono em baixas temperaturas, menores que 100 °C, sobre PLEDs com a intenção de aumentar o tempo de vida destes dipositivos e diminuir a fotodegradação do poli[2-metoxi-5- (2-etil-hexiloxi)-p-fenileno vinileno] (MEH-PPV) em ambiente atmosférico. O filme fino de nitreto de carbono possui as características de um material que pode bloquear a umidade e que tem espessura e flexibilidade adequados para a nova geração de PLEDs flexíveis. As características dos filmes finos de nitreto de carbono e MEH-PPV foram investigadas usando-se técnicas de espectroscopia ótica, com particular ênfase no processo de degradação do MEHPPV sob iluminação. Os resultados mostraram que o filme fino de nitreto de carbono protege o filme polimérico e diminui consideravelmente a fotooxidação. Para avaliar o efeito do encapsulamento em dispositivos reais, LEDs poliméricos foram fabricados e pelas curvas de corrente-tensão um aumento no tempo de vida é confirmado quando a camada de nitreto de carbono é presente. O tempo de vida desejado, maior que 10.000 horas, para aplicações comerciais não foi atingido, entretanto, o encapsulamento pode ser melhorado otimizando as propriedades da camada de nitreto de carbono e combinando-as com camadas de outros materiais orgânicos e inorgânicos. Os capítulos seguintes deste trabalho aborda os estudos realizados com o PEDOT:PSS, uma vez que é amplamente usado em eletrônica orgânica, mas relativamente tem recebido pouca atenção com respeito ao transporte eletrônico de cargas, bem como sua correlação com a morfologia. No Capítulo 3, experimentos com microscopia de varredura por sonda (SPM, Scanning Probe Microscopy) e medidas de condutividade macroscópica são utilizados para estudar e obter um modelo 3D morfológico completo que explica, qualitativamente, a condutividade anisotrópica observada nos filmes finos de PEDOT:PSS depositados pela técnica de spin coating. Imagens topográficas de microscopia de varredura por tunelamento (STM) e imagens da seção transversal observadas com o microscópio de forca atômica (X-AFM) revelaram que o filme fino polimérico é organizado em camadas horizontais de partículas planas ricas em PEDOT, separadas por lamelas quasi-contínuas de PSS. Na direção vertical, lamelas horizontais do isolante PSS reduzem a condutividade e impõe o transporte eletrônico a ser realizado por saltos em sítios vizinhos próximos (nn-H, nearest-neighbor hopping) nas lamellas de PSS. Na direção lateral, o transporte eletrônico via saltos 3D em sítios a longas distâncias (3D-VRH, variable range hopping) ocorre entre as ilhas ricas em PEDOT que são separadas por barreiras muito mais finas de PSS, causando um aumento da condutividade nesta direção. Esta discussão é estendida ao Capítulo 4 com uma descrição quantitativa do transporte eletrônico de cargas predominantes. Particularmente, é demonstrado que o transporte de cargas via saltos 3D em sítios a longas distâncias ocorre entre ilhas ricas em PEDOT e não entre segmentos isolados de PEDOT ou dopantes na direção lateral, enquanto que na direção vertical o transporte de cargas via saltos em sítios vizinhos próximos ocorre dentro das lamelas do quasi-isolante PSS. Em algumas aplicações, faz-se necessário usar PEDOT:PSS com alta condutividade elétrica. Isso pode ser feito adicionando-se sorbitol à solução aquosa de PEDOT:PSS. Após um tratamento térmico, e dependendo da quantidade de sorbitol adicionado, a condutividade aumenta várias ordens de grandeza e as causas e consequências de tal comportamento foram investigadas neste trabalho. O Capítulo 5 investiga as várias propriedades tecnológicas do PEDOT:PSS altamente condutivo tratado com sorbitol, tais como a própria condutividade, os efeitos dos tratamentos térmicos e exposição à umidade. É observado que o aumento da condutividade elétrica, devido à adição de sorbitol na solução aquosa, é acompanhado por uma melhoria na estabilidade da condutividade elétrica em condições atmosféricas. Surpreendentemente, a condutividade elétrica do PEDOT:PSS, sem tratamento com sorbitol (~ 10-3 S/cm), aumenta mais de uma ordem de grandeza sob ambiente úmido de 30-35 % umidade relativa. Este efeito é atribuido a uma contribuição iônica à condutividade total. Análise Temogravimetrica (TGA), espectrometria de massa com sonda de inserção direta (DIP-MS) e análise calorimétrica diferencialmodulada (MDSC) foram usadas como técnicas adicionais para o entendimento dos estudos deste Capítulo. No Capítulo 6, microscopia de varredura por sonda-Kelvin (SKPM) foi empregada para medir o potencial de superfície dos filmes finos de PEDOT:PSS tratados com diferentes concentrações de sorbitol. Mostra-se que a mudança no potencial de superfície é consistente com uma redução de PSS na superfície do filme fino. Para estudar o transporte eletrônico nos filmes finos de PEDOT:PSS altamente condutivos tratados com sorbitol, o Capítulo 7 usa medidas de temperatura e campo elétrico em função da conduvitidade correlacionados com analises morfológicas realizadas por STM. É observado que o transporte eletrônico por saltos, na direção lateral, muda de 3D-VRH para 1D-VRH quando o PEDOT:PSS é tratado com sorbitol. Esta transição é explicada por uma auto-organização das ilhas ricas em PEDOT em agregados 1D, devido ao tratamento com sorbitol, tornando-se alinhadas em domínios micrométricos, como observado pelas imagens de STM. / Employing the unique mechanical, electronic, and optical properties of the conjugated organic and polymer materials several technological and commercial applications have been developed, such as sensors, memories, solar cells and light-emitting diodes (LEDs). In this respect, the central theme of this thesis is the electrical conductivity and mechanisms of charge transport in PEDOT:PSS, a polymer blend that consists of a conducting poly(3,4-ethylenedioxythiophene) polycation (PEDOT) and a poly(styrenesulfonate) polyanion (PSS). PEDOT:PSS is omnipresent as electrode material in plastic electronics applications mentioned above. Although the conductivity of PEDOT:PSS can vary by several orders of magnitude, depending on the method by which it is processed into a thin film, the reason for this behavior is essentially unknown. This thesis describes a detailed study of the anisotropic charge transport of PEDOT:PSS and its correlation with the morphology, the shape, and the dimension of the phase separation between the two components, PEDOT and PSS. Before addressing the properties of PEDOT:PSS, a new barrier layer is described in Chapter 2 that enhances the lifetime of organic devices. An important degradation mechanism in polymer LEDs is photo-oxidation of the active layer. Hence, isolating the active layer from water and oxygen is crucial to the lifetime. Plasma-enhanced chemical vapor deposition (PECVD) is used to deposit a thin layer of carbon nitride at low deposition temperatures, below 100 °C, on a polymer LED that uses poly[2-methoxy-5-(2´-ethylhexyloxy)-1,4- phenylene vinylene] (MEH-PPV) as active layer. A thin layer of carbon nitride acts as barrier for humidity, but is still sufficiently bendable to be used in flexible polymer LEDs. The characteristics of carbon nitride and MEH-PPV films have been investigated using optical spectroscopy, with particular emphasis on the degradation process of MEH-PPV under illumination. The measurements show that the carbon nitride coating indeed protects the polymer film and diminishes the photo-oxidation considerably. To study the effect of the encapsulation in real devices, polymer LEDs were made and their current-voltage characteristics confirm the enhanced lifetime in the presence of a carbon nitride barrier layer. However, the target, a lifetime of more than 10,000 hours for commercial applications, was not achieved. The remaining chapters of this thesis describe the investigations of PEDOT:PSS. PEDOT:PSS is widely used in organic electronics. So far, relatively little attention has, been paid to the mechanisms of charge transport in this material and the correlation of those properties to the morphology. In Chapter 3, scanning probe microscopy (SPM) and macroscopic conductivity measurements are used to obtain a full 3D morphological model that explains, qualitatively, the observed anisotropic conductivity of spin coated PEDOT:PSS thin films. Topographic scanning probe microscopy (STM) and cross-sectional atomic force microscopy images (X-AFM) reveal that the thin film is organized in horizontal layers of flattened PEDOT-rich particles that are separated by quasi-continuous PSS lamella. In the vertical direction, the horizontal PSS insulator lamellas lead to a reduced conductivity and impose nearest-neighbor hopping (nn-H) transport. In the lateral direction, 3D variable-range hopping (3D-VRH) transport takes place between PEDOT-rich clusters which are separated by much thinner barriers, leading to an enhanced conductivity in this direction. This discussion is extended in Chapter 4, where a quantitative description of the length scales of the predominant transport is obtained. Particularly, it is demonstrated that the hopping process takes place between PEDOT-rich islands and not between single PEDOT segments or dopants in the lateral direction, whilst in the vertical direction the current limiting hopping transport occurs between dilute states inside the quasi-insulating PSS lamellas. By a post-treatment it is possible to modify PEDOT:PSS to raise its conductivity, by orders of magnitude. Typically, the addition of sorbitol to the aqueous dispersion of PEDOT:PSS that is used to deposit thin films via spin coating leads to an enhancement of the conductivity after thermal annealing. The causes and consequences of such behavior were investigated in detail. Chapter 5 describes the various properties of the highly conductive sorbitol-treated PEDOT:PSS, such as the conductivity itself, and the effects of thermal annealing and exposure to moisture. It is found that the conductivity enhancement upon addition of sorbitol is accompanied by a better environmental stability. Surprisingly, the electrical conductivity of PEDOT:PSS thin films without sorbitol treatment is increased by more than one order of magnitude in an environment with more than 30-35 % relative humidity. This effect is attributed to an ionic contribution to the overall conductivity. Thermal gravimetric analysis (TGA), direct insert probe-mass spectrometry (DIP-MS) and modulation differential scanning calorimetry (MDSC) were used as additional tools to demonstrate that, after thermal treatment, the concentration of sorbitol in the final PEDOT:PSS layer is negligibly small. In Chapter 6, scanning Kelvin probe microscopy (SKPM) is employed to measure the surface potential and work function of this PEDOT:PSS films that were deposited from water with different sorbitol concentrations. It is shown that work function of PEDOT:PSS is reduced with increasing sorbitol concentration. This shift can be explained by and is in agreement with- a reduction in the surface enrichment with PSS of the film. To study the charge transport properties of the highly conductive sorbitoltreated PEDOT:PSS films, temperature dependent and electric field dependent measurements are correlated with morphological analysis by STM in Chapter 7. It is found that by sorbitol treatment the hopping transport changes from 3DVRH to 1D-VRH. This transition is explained by a sorbitol-induced selforganization of the PEDOT-rich grains into 1D aggregates that are aligned within micrometer sized domains, as observed in STM images.

Diese Arbeit demonstriert die vollständige thermoelektrische Charakterisierung einzelner einkristalliner Bismuttellurid- und Silbernanodrähte und deren anschließende lokale strukturelle und chemische Charakterisierung mittels analytischer Transmissionselektronenmikroskopie. Die lokale strukturelle, chemische und morphologische Charakterisierung entlang der Nanodrähte trägt essentiell zum Verständnis des thermoelektrischen Transportes bei und bestätigt die Korrelation zwischen Oberflächen- und den thermoelektrischen Eigenschaften. Für durchmesservariierte Bismuttelluridnanodrähte wird der Einfluss der Morphologie auf die Wärmeleitfähigkeit bei Raumtemperatur quantifiziert. Im Vergleich zu einem glatten Referenznanodraht zeigt der durchmesservariierte Nanodraht gleicher Zusammensetzung und Kristallorientierung eine Reduktion der Wärmeleitfähigkeit um 55 %. Diese Reduktion kann durch Phononenrückstreuung an der eingekerbten Oberfläche erklärt werden. Die elektrische Leitfähigkeit und der Seebeckkoeffizient der Bismuttelluridnanodrähte deuten auf einen topologischen Oberflächenzustand hin. Für Silbernanodrähte werden die elektrische Leitfähigkeit und die Wärmeleitfähigkeit im Temperaturbereich von 1,4 K bis 300 K gemessen. Mit fallender Temperatur steigt die relative Reduktion der Wärmeleitfähigkeit im Verhältnis zur elektrischen Leitfähigkeit stärker, sodass die Lorenzzahl die klassische Wiedemann-Franz-Relation nicht erfüllt und eine Funktion der Temperatur darstellt. Der Temperaturverlauf der Lorenzzahl der Silbernanodrähte entspricht der 1938 von Makinson aufgestellten Theorie für hochreine Metalle und ist im Tieftemperaturbereich um bis zu zwei Größenordnungen zum Sommerfeldwert reduziert. / This work demonstrates the full thermoelectric characterisation of individual single crystalline bismuth telluride and silver nanowires and their subsequent local structural and chemical characterisation via analytical transmission electron microscopy along the whole nanowires. Therefore, the correlation between the structure, in particular the surface morphology, and the thermoelectric transport properties is unambiguously shown. For diameter varied bismuth telluride nanowires the influence of the morphology on the thermal conductivity is quantified at room temperature. The diameter varied nanowire shows a reduction of 55 % with respect to the smooth nanowire of the same chemical composition and structural orientation. This reduction can be explained by phonon backscattering at the indents. The electrical conductivity and the Seebeck coefficient indicate the presence of a topological surface state. For silver nanowires the electrical and thermal conductivity are determined in the temperature range between 1.4 K and 300 K. With decreasing temperature the relative reduction of the thermal conductivity is higher than the reduction of the electrical conductivity resulting in a temperature-dependent Lorenz number, so that the classical Wiedemann-Franz relation is not fulfilled. The temperature characteristic of the silver nanowires'' Lorenz number is in agreement with the theory Makinson established for highly pure metals in 1938 and is reduced by two orders of magnitude with respect to the Sommerfeld value in the low temperature regime.