Lasers are increasingly used for a wide range of different applications for both civil and military purposes. Due to the distinct properties of laser light, use of lasers often comes with a risk of damage to the human eye and other optical sensors. Therefore, an effective laser protection is needed. 2D-materials is a relatively new class of materials, which have shown to possess many unique properties compared to its bulk counterparts. Some 2D-materials exhibit nonlinear optical (NLO) properties, and specifically optical power limiting (OPL) effects, and have therefore been researched for laser protection applications. In this work, two different 2D-materials, MXene Ti3C2 and graphene oxide (GO), have been combined with a hybrid organic-inorganic polymer, a so called melting gel (MG), to synthesise nanocomposites possessing OPL effects for laser protection applications. Different methods of incorporating the 2D-materials in the polymer matrix as well as the effect on optical properties of different concentrations of 2D-materials were investigated. The prepared nanocomposites were characterised using optical microscopy, spectroscopy and OPL measurements in order to investigate and quantify their linear and nonlinear optical properties. The MG was optically clear, mechanically stable and easy to synthesise, which makes it a suitable candidate as a matrix for a laser protection nanocomposite. Additionally, it was possible to dope the MG with the two different 2D-materials to create nanocomposites showing desirable optical properties in the visible spectrum. However, many samples showed signs of clustered 2D-particles indicating that the dispersion could be improved. Finally, OPL measurements, performed at 532 nm, showed that the MG itself exhibited OPL effects, both 2D-materials showed a stronger OPL effect than the non-doped MG and that GO-doped samples gave a better protection than the MXene samples.

Among emerging materials systems for thermoelectric applications, the early transition-metal nitrides based on ScN and CrN show unexpectedly promising properties. These properties are determined by high Seebeck coefficient, low thermal conductivity, and high electrical conductivity. There is, however, still a need to improve the thermoelectric properties. One idea is to introduce dopants or alloying elements to alter the concentration, mobility, and/or type of charge carriers, such as in (Cr1-xVx)N. Another is to focus on the different scattering mechanisms, such as to reduce the scattering of electrons and increase the scattering of phonons, thus increasing the electrical conductivity while lowering the thermal conductivity. Electrical conductivity can be altered by grain boundary modifications, such as larger grains as well as metallic inclusions, for a smoother interface for the electrons. Such nanoinclusions could potentially also act as phonon scattering centra. Phonon scattering can also occur by site substitution of isoelectronic but heavier atoms, which could reduce the phonon mean free path while retaining the electrical conductivity. For CrN, the obvious substitutions are Mo or W.This thesis investigates these effects for CrN-based materials, and how to control the growth of them in a DC-magnetron sputtering system.First, an optimization study for CrN was made, here the power was fixed while the temperature and nitrogen content were varied. Second, the effect of in-situ annealing at the deposition temperature was investigated. Here, both films with pure CrN and films with a mix of CrN and Cr2N were annealed. It was found that temperature, pressure, and ambient gas have a large effect on the decomposition of CrN to Cr2N. Third, alloying with V and Mo was implemented. It was found that Mo quickly breaks the rock-salt structure, and for further investigation of CrMoN and Cr(Mo,V)N systems, other deposition methods which allows for lower deposition rates need to be investigated.The sample deemed best was the CrVN-sample, showing a Seebeck coefficient of -141 μV/K, resistivity of 1520 μΩ∙cm and a power factor of 1.3 mW/mK2.

Absolicon is a pioneering solar technology development company specializing in the manufacturing and selling of advanced solar energy systems engineered to generate renewable energy for diverse use. Comprising essential components such as reflectors (mirrors) and a solar receiver tube, these solar energy systems are equipped to efficiently capture and convert solar irradiation into usable thermal energy. As an integral facet of an ongoing research, this project will contribute to optimize the reflection and absorption capacity in receiver tubes of Absolicon's solar collectors. The aim is to investigate optically selective plasmonic coatings intended as an undercoating in the solar selective surfaces. The main coating material that will be used and analysed is gold due to its plasmonic properties and inert nature as well as its low toxicity. The gold will be coated on stainless steel using physical vapor deposition (PVD) and then annealed at mid-to-high temperatures to produce a plasmonic surface. The effect of Au thicknesses, annealing times/temperature and will be investigated to optimize the coating with regards to optical properties based on a systematic method called Design of Experiments (DoE). The goal for the gold coating is to increase the reflectance in the infrared region while generating a plasmonic absorption peak in the visible region (the position and width will be optimized), making it a more beneficial surface to coat a solar selective surface than the original stainless steel (SS). It was found that the size and inter-particle distance of GNPs depend on the temperature and annealing time for different thickness. The surface analysis from SEM-images and AFM-topographs provided that samples with smaller grains are more likely to exhibit significant plasmonic effects compared to larger grains. According to the surface characterization, either thinner gold coating exposed to high temperature for short annealing time or thicker gold coating with longer annealing time provide plasmonic absorption peak in visible light region.

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Ion sensing represents a grand research challenge. It finds a vast variety of applications in, e.g., gas sensing for domestic gases and ion detection in electrolytes for chemical-biological-medical monitoring. Semiconductor genome sequencing exemplifies a revolutionary application of the latter. For such sensing applications, the signal mostly spans in the low frequency regime. Therefore, low-frequency noise (LFN) present in the same frequency domain places a limit on the minimum detectable variation of the sensing signal and constitutes a major research and development objective of ion sensing devices. This thesis focuses on understanding LFN in ion sensing based on both experimental and theoretical studies. The thesis starts with demonstrating a novel device concept, i.e., ion-gated bipolar amplifier (IGBA), aiming at boosting the signal for mitigating the interference by external noise. An IGBA device consists of a modified ion-sensitive field-effect transistors (ISFET) intimately integrated with a bipolar junction transistor as the internal current amplifier with an achieved internal amplification of 70. The efficacy of IGBA in suppressing the external interference is clearly demonstrated by comparing its noise performance to that of the ISFET counterpart. Among the various noise sources of an ISFET, the solid/liquid interfacial noise is poorly studied. A differential microelectrode cell is developed for characterizing this noise component by employing potentiometry and electrochemical impedance spectroscopy. With the cell, the measured noise of the TiN/electrolyte interface is found to be of thermal nature. The interfacial noise is further found to be comparable or larger than that of the state-of-the-art MOSFETs. Therefore, its influence cannot be overlooked for design of future ion sensors. To understand the solid/liquid interfacial noise, an electrochemical impedance model is developed based on the dynamic site-binding reactions of surface hydrogen ions with surface OH groups. The model incorporates both thermodynamic and kinetic properties of the binding reactions. By considering the distributed nature of the reaction energy barriers, the model can interpret the interfacial impedance with a constant-phase-element behavior. Since the model directly correlates the interfacial noise to the properties of the sensing surface, the dependencies of noise on the reaction rate constants and binding site density are systematically investigated.

Abstract The wood industries to this day use almost exclusively petroleum derived adhesives that are based mainly on the reaction of formaldehyde with urea, melamine or phenol. These adhesives have low cost and good adjustable properties which makes it hard for bio-based alternatives to compete. Phenol formaldehyde (PF), as an example of a synthetic adhesive, has been in use for over 100 years. In some parts of the world, legislation around formaldehyde is changing, and there is an increasingly voluntary awareness about the toxicity and unsustainability of formaldehyde. Industries realize that raw materials from oil is unstainable. The latter is currently a driving factor behind research on alternatives to amino based adhesives. Also, consumer interest in healthy and sustainable products, such as emitting less formaldehyde indoors, increases the need for bio based adhesives. Cellulose contained in plant cell walls is a renewable, abundant and nontoxic resource. During the last decades, many innovations have been achieved around cellulose and this trend does not seem to be slowing down. Cellulose shows excellent mechanical properties, high strength, high elastic modulus as well as having a low density. Research about cellulose reinforced adhesives has been increased the last years. This thesis studied the enhancement of phenol formaldehyde adhesive with Crystalline Nano Cellulose (CNC) at 5wt% and 10wt% loading levels for producing plywood boards. Indecisive results when using CNC higher than 3wt%, especially with PF resin, have been reported by other authors. In this thesis, European standards were applied. EN 314 was applied to test the panels shear strength. Three (3) treatment classes were selected, indoor room condition as well as pre-treatments 5.1.1 and 5.1.3. Other properties measured were modulus of elasticity, thickness swelling, formaldehyde emissions. Results showed a shear strength increase for all pre-treatment classes. 10wt% CNC mixture with phenol formaldehyde in water bath, pre-treatment (5.1.1) for 24h showed the highest increase in shear strength (+73,9%). The 10 wt% CNC mixture panels also showed the highest wood fibre failure of all panel types produced. A decrease in MOE has been observed with 10 wt% CNC compared to the 5 wt% CNC panels. Formaldehyde emissions tests were inconclusive, but since less PF was used, there was a general reduction in emissions. The 5 wt% CNC panels were superior in terms of modulus of elasticity and swelling and also showed improved shear strength.

Thermal nanoimprint lithography (T-NIL) is a cheap and fast technique to produce nanopatterns in polymeric materials. It creates these patterns by pressing a stamp down into a polymer film that has been heated above its glass transition temperature. These nanopatterned polymer films can be used in a wide variety of scientific fields, not the least the organic semiconductor industry. There the nanopatterned films have, among else, been used to improve the efficiency of organic light-emitting diodes (OLEDs). The light-emitting electrochemical cell (LEC), which is similar in structure to an OLED, also uses polymer films in their device structure but the light emitting layer also contains an electrolyte. However, it has not been shown if nanopatterns can improve LECs as well or if it is even possible to make an imprint in their polymer films that are mixed with an electrolyte. This thesis shows that T-NIL can be used to imprint nanopatterns in films made of poly(ethylene oxide) and the conjugated polymer Super Yellow. The best nanopatterns were produced by setting the imprint parameters to  85 °C, 10 bar, 1800 s for poly(ethylene oxide) and 115 °C, 20 bar, 1800 s for Super Yellow. Imprints were also performed on polystyrene but no nanopatterns could be produced. This was most likely because the stamp could not handle the high temperature that is required to make a nanopattern in polystyrene. The best imprint parameters of Super Yellow were then used to produce a pattern in a film made of Super Yellow mixed with the salt tetrahexylammonium tetrafluoroborate (THABF4) in order to be able to produce one imprinted and one reference LEC. The imprinted LEC had a luminosity of 139 cd/m2, an improvement of 20% compared to the reference’s 115 cd/m2 when operated under identical conditions.  The forward direction and the angular dependent electroluminescence spectrum of the imprinted LEC clearly showed an effect not observed in the reference. These findings show that the polymer films used in a LEC can be imprinted with a nanopattern by using T-NIL. The imprinted films can be used to create functional LECs that show different behavior and a higher luminosity compared to a non-imprinted reference. If these results can be repeated it might be the starting point of a brighter future.

Mesoscopic spin systems can be designed and fabricated using modern nano-fabrication techniques. These systems can contain large numbers of patterned ferromagnetic elements, for which the shape will generally determine their effective mesospin dimensionality. The lateral arrangement of these mesospins can be further used to tune the interactions between them. With an appropriate choice of material, it is possible to define a temperature range where thermal fluctuations of these mesospins are experimentally accessible. To actively define this range, we use δ-doped Palladium, a three-layer system of Palladium—Iron—Palladium, for which the Curie-temperature scales with the Iron layer thickness. The patterned mesoscopic elements used in this work have a stadium-like shape that promotes a single magnetic domain state, thus making these islands behave as one-dimensional Ising-like mesospins that can be observed using magnetic imaging techniques. We investigate the impact on the magnetic order resulting from modifications of the square spin ice geometry. By adding, removing and merging elements in the square artificial spin ice architecture, energy-landscape variations can be realized. Firstly, an added interaction modifier is used to equilibrate the interactions between the mesospins at the vertex level, which can restore the degenerate ground state of the square spin ice model. Secondly, the removal of elements can lead to topologically frustrated spin systems, as not all building blocks can simultaneously be in their lowest energy state. Furthermore, the merging results in multiple element sizes in the mesospin system. As the magnetization reversal barrier is dependent on the element size, these mesospin systems have different energy barriers. The thermal ordering process in such a system differs from a single-size element system with its unique energy barrier. Using reciprocal space analysis tools like the magnetic spin structure factor we show that systems with multiple element sizes achieve a higher short-range order then their single-size element references. The magnetic order in mesoscopic spin systems could successfully be tailored by modifications of the lattice geometry.

A new rising star in the carbon nanomaterial family is carbon dots. Carbon dots have received great attention due to their excellent luminescence and low toxicity. In this project, a new carbon dot derived from birch leaves is studied and characterized. The birch leaf carbon dot (BL-CD) exhibits narrow red photoluminescence (peak = 670 nm, full width at half maximum = 23 nm) with a photoluminescence quantum yield of 26% in dilute methanol solution.  The presence of the characteristic peaks of the pigment pheophytin-a in the absorption spectrum and the photoluminescence spectrum of the BL-CD and the absence of a crystal structure together with the narrow and excitation-independent photoluminescence indicate a carbon dot with a non-emissive amorphous structure with emissive molecular sites consisting of the pigment. The photoluminescence quenching of the BL-CDs in solid-state is reduced by the introduction of a hostmaterial. The use of a host enabled the employment of BL-CDs as the emitter in a light-emitting electrochemical cell (LEC). This project paves the way for further development of the environmentally friendly and sustainable BL-CD LEC.

During the past decades, emission of greenhouse gases has accelerated to unsustainable levels. This is a serious issue that can have a devastating impact on everything from global economy to the terrestrial or marine ecosystem. A method for reducing the emission is named carbon capture and storage, which this project is based on. In this study, different concentrations of citric acid (CA) is used (as an additive) for the enhancement and optimization of carbon dioxid sorption properties of amorphous calcium carbonate (ACC), mesoporous magnesium carbonate (MMC) and calcium magnesium carbonate composite (CMC). These materials were heat treated in a calcination and an alternating carbonation process in order to study the carbon dioxid sorption performance. During the calcination process, CA undergoes a pyrolysis reaction in order to increase the specific surface area of the individual nanoparticles, which is an important factor for the sorption capacity. In the case of CMC, different molar ratios of magnesium oxide and calcium oxide were used in order to alter the concentration of the resulting magnesium oxide prior to heating. All three materials consisted of aggregations of nanometer-sized particles. Thermogravimetric analysis, scanning electron microscopy, surface area and porosimetry and infrared spectroscopy analysis suggest that the carbon dioxid sorption properties and the sintering stability of ACC and MMC do not improve since CA evaporates due to pyrolysis. Sintering was a greater problem for the evaluated CA treated ACC sample. However, in the case of CMC, the sorption and sintering properties were enhanced due to the higher Tamman-temperature of magnesium oxide, specifically for the lower concentration of magnesium oxide. After 19 carbonation cycles, CMC-1:1-25% CA showed signs of improved sintering stability and sorption capacity, compared to ACC-75% CA. / <p>Presentationen genomfördes på distans.</p>