Having conducted the research described in this thesis I found that there exists a possibility to produce polyelectrolyte nanostructures on hydrophobic surfaces by application of the moving contact line approach. It was demonstrated that the morphology of nanostructures displays a range of structure variations from root-like to a single wire structure with a high anisotropy and aspect ratio (providing diameters of several nanometers and the length limited by the sample surface dimensions). Such nanostructures can be produced exactly on the spot of interest or can be transferred from the surface where they were produced to any other surfaces by the contact printing technique. A model describing the polymer deposition during the moving contact line processes on hydrophobic surfaces has been proposed. The application of this model provides the ground for an explanation of all the obtained experimental data. Utilizing moving contact line approach aligned one-dimensional polycation structures were fabricated and these structures were used as templates for assembling amphiphile molecules. Quasiperiodic aligned and oriented nanostructures of polyelectrolyte molecules formed in moving droplets were utilized for fabrication of electrically conductive one-dimensional nanowires.

A key to solar cells with lower environmental impact is higher efficiency and reduced material usages. Bifacial solar cells may have a higher efficiency as light can enter from two directions and tandem solar cells may use a larger part of the incoming solar spectrum, increasing the efficiency. However, both these applications require transparent and conducting contacts. This thesis aimed to investigate how suitable the transparent conductive oxides aluminum doped zinc oxide (AZO) and indium doped tin oxide (ITO) are as contacts in bifacial CIGS cells or CIGS/Silicon tandem cells. The contacts must remain stable when CIGS is deposited on top of it, meaning that they have to endure first 500°C and then 600°C in combination with copper, indium, gallium and selenium vapours. A thin layer of AZO topped with ITO and pure ITO films of different thicknesses were deposited by RF- and DC-sputtering, varying the oxygen flow. Opto-electrical characterization showed that the transparency in the infrared was balanced against high conductivity due to a shift in the plasmon peak's position. No great difference was seen between pure ITO samples and AZO/ITO samples, so only the first where further processed. The ITO films were annealed to 500°C in the CIGS deposition chamber, exposed to selenium vapour. The films' sheet resistances dropped drastically, which was mainly attributed to activation of tin donors. ITO produced with low oxygen flows also appeared more crystalline according to x-ray diffraction measurements. Photon absorption in the ITO was used to estimate the current loss in bifacial and tandem applications and graphs with current loss and sheet resistance can be used to select an ITO deposition process. Commercial ITO was exposed to 100s of the CIGS deposition process but only during selenium and gallium vapour. A layer of gallium selenide could be identified on the surface, but the ITO appeared to remain stable. Sodium fluoride pre deposition treatment lowered the samples absorption for all wavelengths compared to non-treated samples.

This master thesis is about to investigate what opportunities we have with a impedance varying probe on different material under test. This report begins with a theory part with the focus on; electromagnetic principles, material characterizations and the principle behind the measurement setup. The methods is describing the sensor probes affection on the specimen, the induced currents location and the method for crack detection and lift-off measurements. The result chapter shows the measured impedance created by our setup, as well as the potential and the weak points of the system. In the conclusion and discussion chapter we will go through what modifications can be done to increase the quality of the measurements.

Ink-jet printing (IJP) using conductive inks, has gained the attention of scientistsand researchers during the past decades. Solar Cells (SCs), Radio FrequencyIdentication (RFID), E-papers and antennas are only some of the applicationsfor which IJP is being applied. IJP facilitates printing complex antenna structureswith a good resolution. The use of the IJP process is compatible with devicefabrication on unusual substrates such as paper, polymer lms (Polyethylenenaphthalate (PEN), Polyethylene terephthalate (PET), Polyimide (PI)), textiles,etc at low temperature. The aim of this study is to design and fabricate antennason paper substrates capable of operating at 2.4 GHz via printing technique.Simulation and experimental studies have been presented for microstrip patchantenna and dipole antenna using Itoh's balun.

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Today, smart innovation has become an essential part of human life; thus, contemporary technologies are always looking for intelligent, responsive, and efficient materials to satisfy these demands. Consequently, synthetic "metals" or, more precisely, intrinsically conducting polymers (CPs) have begun to find a place as valuable and practical materials for a new generation of devices. Amongst all intrinsic conducting polymers, polyaniline (PANI) has attracted significant attention due to its outstanding air and moisture stability, simple preparation technique, and high electrical conductivity (chapter I). Chapter II represents the synthesis of a new PANI derivative that contains a phenoxazine unit co-polymerized with p-phenylenediamine derivatives by the Buchwald/Hartwig reaction. These polymers are soluble in many common organic solvents, which permit their full characterization and allow for solution processing. The polymers' optical properties mimicked PANI; however, they were more electrochemically stable and soluble compared to PANI. In addition, the analogous PANI emeraldine base forms a large bathochromic shift in the absorption spectra upon acidic doping to form analogues of PANI emeraldine salts. Chapter III describes our strategy to prepare economical, electrochemically stable, and processable PANI derivatives from carbazole and 1,4-aryldiamines for supercapacitor device. The polymers exhibit good solubility in various organic solvents, enabling a scalable spray-coating method to fabricate electrodes. The polymers were used to fabricate electrodes for supercapacitor devices and exhibit a maximum area capacitance of 64.8 mF cm−2 and specific capacitance of 319 F g−1 at a current density of 0.2 mA cm−2. Chapter IV MXene has been recently widely applied to energy storage devices due to its metallic conductivity and excellent electrochemical Activities. However, MXene sheets suffer from the restacking phenomena during cycling. Restacking restricts the ion diffusions and storage capability between the MXene layers, which lowers the accessible surface area. The restacking phenomena of MXene sheets was shown to be eliminated by the deposition of conductive polymers on the surface of MXene sheets.

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The new dihydrobis(4-cyano-3-tert-butylpyrazolylborate) ligand has been synthesized. Isolated crystals of the thallium complex were collected and structurally characterized by X-ray diffraction. Transition metal complexes of the ligand are currently under investigation.

Conductive polymer composite sensors have shown great potential in identifying gaseous analytes. To more thoroughly understand the physical and chemical mechanism of this type of sensors, a model was developed by combining two sub-models: a conductivity model and a thermodynamic model, which gives a relationship between the vapor concentration of analyte(s) and the change of the sensor signals. In this work, 64 chemiresistors representing eight different carbon concentrations (8–60 vol.% carbon) were constructed by depositing thin films of a carbon black–polyisobutylene composite onto concentric spiral platinum electrodes on a silicon chip. The responses of the sensors were measured in dry air and at various vapor pressures of toluene and trichloroethylene. Three parameters in the conductivity model were determined by fitting the experimental data. It was shown that by applying this model, the sensor responses can be predicted if the vapor pressure is known; furthermore the vapor concentration can be estimated based on the sensor responses. This model will guide the improvement of the design and fabrication of conductive polymer composite sensors for detecting and identifying organic vapors. A novel method was developed to optimize the selection of polymeric materials to be used within a chemiresistor array for anticipated samples without performing preliminary experiments. It is based on the theoretical predicted responses of chemiresistors and the criterion of minimizing the mean square error (MSE) of the chemiresistor array. After the number of chemiresistors to be used in an array and the anticipated sample chemistry are determined, the MSE values of all combinations of the candidate chemiresistors are calculated. The combination which has the minimum MSE value is the best choice. This can become computationally intensive for selection of polymers for large arrays from candidates in a large database. The number of combinations can be reduced by using the branch and bound method to save computation time. This method is suitable for samples at low concentrations where thermodynamic multi-component interactions are linear. To help users apply this polymer selection method for the sensors, a website including 10 solvents and 10 polymers was developed. Users can specify a target sample and obtain the best set of polymers for a sensor array to detect the sample. The activities of trichloroethylene and toluene in polyisobutylene were measured at very low concentrations. The activities for toluene are consistent with published values at higher concentrations. The values for trichloroethylene are a new contribution to the literature.