Today, ceramic, polymer, and composite nanofibers are among the most charming materials for nanotechnology. Because of their small characteristic dimension, high surface area, and microstructural features, they provide unique mechanical, optical, electronic, magnetic, and chemical properties for an extensive variety of materials applications. Electrospinning provides an effective way of the nanofiber production in a nanometer scale. This technique utilizes a high voltage DC to create a strong electric field and a certain charge density in a viscous solution contained in a pipette. As a result, fibers with diameters ranging from the micrometer to nanometer are formed from this charged solution. This study deals with, the fabrication of alumina borosilicate ceramic nanofibers using electrospinning technique. Alumina borosilicates contain important components having intriguing characteristics for many applications and have been widely studied with different compositions. In this study, alumina borosilicate/PVA solution was prepared using the conventional sol-gel method. Polyvinyl alcohol (PVA) was added into this solution to increase the viscosity for electrospinning. After the alumina borosilicate/PVA solution was electrospun into fibers, high temperature sintering was carried to obtain ceramic alumina borosilicate fibers. The products were characterized by scanning electron microscopy (SEM), X-ray diffractometry (XRD), Fourier transform-infrared spectroscopy (FT-IR), and thermogravimetric/differential thermal analysis (TG-DTA) techniques.

Polymer-derived ceramics (PDCs) are exceptional ultra-high temperature and stable multifunctional class of materials that can be synthesized from a polymer precursor through thermal decomposition. The presented research focuses on 1-D nanofibers, 2-D films and 3-D bulk, carbon-rich silicon carbon nitride (SiCN) ceramics. 1-D nanofibers were prepared via electrospinning for light weight, flame retardant and conductive applications. The commercially available CerasetTM VL20, a liquid cyclosilazane pre-ceramic precursor, was mixed with polyacrylonitrile (PAN) in order to make the cyclosilazane electrospinnable. Carbon-rich PDC nanofibers were fabricated by electrospinning various ratios of PAN/cyclosilazane solutions followed by pyrolysis. Surface morphology of the electro spun nanofibers characterized by SEM show PDC nano?bers with diameters ranging from 100-300 nm. Also, thermal stability towards oxidation showed a 10% mass loss at 623°C. 2-D carbon/SiCN films were produced by drop-casting a mixture of PAN/cyclosilazane onto a glass slide followed by pyrolysis of the film. Samples ranging from 10:1 to 1:10 PAN:cyclosilazane were made by dissolving the solutes into DMF to produce solutions ranging from 1% to 12% by weight. Green, heat-stabilized, and pyrolyzed 8% films were examined with FTIR to monitor the change in chemical structure at each step of the ceramization. SEM shows that high PAN samples produced films with ceramic embedded spheroid components in a carbon matrix, while high cyclosilazane samples produced carbon embedded spheroid. Finally, this research focuses on the challenge of making fully dense, 3-D bulk PDCs materials. Here we present a composite of SiCN with reduced graphene oxide (rGO) aerogels as a route for fully dense bulk PDCs. Incorporation of the rGO aerogel matrix into the SiCN has its pros and cons. While it lowers the strength of the composite, it allows for fabrication of large bulk samples and an increase in the electrical conductivity of the PDC. The morphology, mechanical, electrical properties and thermal conductivity of graphene-SiCN composite with varying rGO aerogel loading (0.3-2.4%) is presented. The high temperature stability, high electrical conductivity and low thermal conductivity of these composites make them excellent candidates for thermoelectric applications. Generally, carbon-rich SiCN composites with improved thermal and electrical properties are of great importance to the aerospace and electronics industries due to their expected harsh operating environments.

This diploma thesis focuses on the fabrication of ceramic fibres by electrospinning. The theoretical part of the thesis summarizes the currently available information regarding ceramic fibres, their properties, applications and fabrication. The theoretical part also describes the process of electrospinning as one of the most frequently used methods of nanofibre fabrication, as well as the parametres influencing this process. The experimental part is aimed at the fabrication of ceramic fibres based on titania, pure non-doped zirconia and yttria-doped zirconia by electrospinning and at the characterization of thus fabricated fibres. Ceramic precursors based on propoxide and polyvinylpyrrolidone were subjected to electrospinning. The experimental part of this diploma thesis also describes the influence of precursor composition, process conditions and calcination temperature on the morphology and phase composition of the fibres. Precursors were characterized by viscosity measurements. Thermogravimetric analysis (TGA), Röntgen analysis (RTG) and scanning electron microscopy (SEM) were used to describe the fibres. By performing electrospinning of precursors based on titanium propoxide and subsequent calcination at 500-1300 °C, TiO2 fibres with thickness of 100-2500 nm were fabricated. The phase composition changed with calcination temperature from 500 °C from anatase phase through rutile blend to pure rutile at 900 °C. By performing electrospinning of precursors based on zirconium propoxide and subsequent calcination at 550-1100 °C, 0 – 8 mol% Y2O3 doped ZrO2 fibres with thickness of 50-1000 nm were fabricated. An analysis of fibres based on non-doped ZrO2, calcined at 550 °C showed a composition of predominantly monoclinic phase. An analysis of 3 or 8 mol% Y2O3 doped ZrO2 fibres calcined at 900 °C showed a composition of predominantly tetragonal phase or purely cubic phase, respectively. With the increasing calcination temperature, the morphology of the fibres changed from porous nanostructure to chain-like non-porous structure consisting of micrometer grains of TiO2 or ZrO2. The ZrO2 fibres calcined at 700 °C remained flexible as well as the spun ones, while their fragility increased with the increase in calcination temperature.

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