Nickel-based alloys are used in components such gas turbines within the aerospace industry and electric power generation due to its high tensile, rapture and creep strength. Increasing the efficiency of gas turbines are crucial to reduce emissions within the aerospace industry and increasing power gain for electric power generation. Innovation to increase the efficiency relies in part on the development of new nickel-based alloys with beneficial material properties. But also on stable and predictable material behavior during processing and post-processing of the components in the gas turbine. In two prominent material processing fields of precipitation hardened nickel-based alloys, additive manufacturing and welding, strain-age cracking (SAC) is a common phenomenon. SAC is a solid state phenomenon that generally occurs in alloys strengthened with 𝛾′, L12(Pm3m), or 𝛾′′, D022(I4/mmm), phase precipitates during post weld heat treatment or reheating where it manifests as intergranular cracking. Even though the existence of SAC has been known for several decades, its dominant mechanisms are still under considerable debate and the undertaken modeling efforts to gain insight on the phenomenon are virtually non-existent. This study aims to clarify the dominant mechanisms behind strain-age cracking. Breaching this gap would allow for new development for nickel-based alloys within both additive manufacturing and welding. To that extent the goal of this study is to provide tools to aid in clarifying the dominant mechanisms behind strain-age cracking. This is done by implementing the recently developed structural phase-field crystal (XPFC) model and examining the capabilities to model a precipitation event during reheating for a reference binary alloy in two dimensions. To evaluate the strain because of precipitation, a simple method based on the principles of neutron and synchrotron strain scanning is outlined and tested on the limited precipitation event achieved within the study. The XPFC model is capable of modeling precipitation with some restrictions that need further development with extended computational recourses. Lastly, the possibilities to extend the implemented XPFC model to cover nickel-based alloys is discussed.

In this master work, we investigated the feasibility of a magnetic resonance measurement technique using magnetic nanoparticle dispersions in both liquid and solid form. The implementation is realised as a coplanar waveguide operating in the frequency range of 0.5 - 20 GHz and an electromagnet producing a static magnetic field of strength up to 1.2 T. The Gilbert magnetic damping factor is determined for polymer composites of magnetic nanoparticles and the gyromagnetic ratio is determined for both nanoparticle dispersions in liquid form and polymer composites.

Metallic glasses produced with Selective Laser Melting (SLM) often contain internal mechanic stress. This internal stress can have an impact on the magnetic properties of the material due to its connection to the magnetic anisotropy of the material. Therefore the effect of different heat treatments aimed to reduce the effect of internal stress on the magnetic properties of an Fe-based Metallic Glass (MG) and how this relates to the crystallization of the material was examined in this project. The magnetic properties were measured with a Vibrating Sample Magnetometer (VSM) and the Longitudinal Magneto-Optic Kerr Effect (L-MOKE) and structural changes to the material from the heat treatments, such as crystallization, was examined with X-Ray powder Diffraction (XRD) before and after heat treatment. From the measurements we found that heat treatments close to and above the crystallization temperature Tx lead to crystallization and a decrease in magnetic saturation MS. Heat treatments below Tx around 430°C showed a smaller reduction in MS but did not show any crystallization. The measurements with L-MOKE showed no consistent change in coercivity so no conclusion could be drawn from these. / Metallglas som tillverkats med den additiva tillverkningstekniken Selective Laser Melting (SLM) innehåller ofta interna mekaniska spänningar. Dessa spänningar kan på grund av deras koppling till materialets magnetiska anisotropi ha en påverkan på materialets magnetiska egenskaper. I detta projekt har därför effekten av olika värmebehandlingar utförda för att minska de interna spänningarnas påverkan på de magnetiska egenskaperna av ett Fe-baserad metallglas och hur detta relaterar till kristalliseringen av materialet undersökts. De magnetiska egenskaperna av materialet mättes med en Vibrating Sample Magnetometer (VSM) och Longitudinal Magneto-Optic Kerr Effect (L-MOKE). Strukturella förändringar, så som kristallisering, hos materialet orsakade värmebehandlingarna undersöktes med X-Ray powder Diffraction (XRD). Samtliga mätningar genomfördes före och efter värmebehandling. Från mätningarna fann vi att värmebehandlingar nära kristalliseringstemperaturen Tx gav kristalltillväxt samt minskade mättnadsmagnetisering MS. Värmebehandlingar under Tx runt 430°C gav en lägre reducering av MS samt gav ej någon kristalltillväxt. L-MOKE-mätningarna gav ingen konsekvent förändring i materialets koercivitet och inga slutsatser kunde därmed dras från dessa.

The interplay of experiments and theory is essential to deepen our understanding of magnetization dynamics. This thesis aims to serve as a bridge between these two aspects by establishing a mathematical framework that enables the computation of optical observable quantities based on theoretical models. The equations are cast in a matrix representation that is well-suited for performing numerical simulations. Additionally, the generality of these methods enables their application to layered media with any geometry, regardless of whether they possess magnetic properties or not. Furthermore, it explores the various perspectives and physical mechanisms involved in magneto-optic measurements to provide the reader with a self consistent introduction to the subject matter. Numerical calculations are presented for bulk Fe, alternating layers of Fe/Au and Ni with a MgO coating and a SiO substrate for different energies, angle of incident and magnetization direction. The results demonstrate the effectiveness of the method in predicting measurable outcomes from theoretical considerations and enables the analysis of optimal experimental configurations. / Samverkan mellan experiment och teori är avgörande för fördjupa vår förståelse av magnetiska system och deras dynamik. Målet med denna uppsats är att etablera en koppling mellan dessa två aspekter genom att formulera ett matematiskt ramverk som möjliggör beräkningar av optiska observerbara storheter baserat på teoretiska modeller. Ekvationerna formuleras med matriser vilket är väl lämpat för att utföra numeriska simuleringar. Dessutom möjliggör metodens generella natur tillämpning på skiktade material av godtycklig geometri, oavsett om de har magnetiska egenskaper eller inte. Vidare utforskar uppsatsen olika perspektiv och fysikaliska mekanismer som är involverade i magneto-optiska mätningar för att ge läsaren en självständig introduktion till ämnet. Numeriska beräkningar presenteras för bulkjärn, växlande lager av Fe/Au och Ni med en MgO-beläggning och ett SiO-substrat för olika energier, infallsvinkel och magnetiseringsriktning. Resultaten visar på metodens förmåga att förutsäga mätbara resultat baserat på teoretiska överväganden och tillåter analys av optimala experimentella uppställningar.

Over the past 20 years’ researchers have tried to utilize the remarkable properties of single-walled carbon nanotubes (SWCNTs) to create new high-tech materials and devices, such as strong light-weight composites, efficient electrical wires and super-fast transistors. But the mass production of these materials and devices are still hampered by the poor uniformity of the produced SWCNTs. These are hollow cylindrical tubes of carbon where the atomic structure of the tube wall consists of just a single atomic layer of carbon atoms arranged in a hexagonal grid. For a SWCNT the orientation of the hexagonal grid making up the tube wall is what determines its properties, this orientation is known as the chirality of a SWCNT. As an example, tubes with certain chiralities will be electrically conductive while others having different chiralities will be semiconducting. Today’s large scale methods for producing SWCNTs, commonly known as growth of SWCNTs, gives products with a large spread of different chiralities. A mixture of chiralities will give products with a mixture of different properties. This is one of the major problems holding back the use of SWCNTs in future materials and devices. The ultimate goal is to achieve growth where the resulting product is uniform, meaning that all of the SWCNTs have the same chirality, a process termed chirality-specific growth. To achieve chirality-specific growth of SWCNTs requires us to obtain a better fundamental understanding about how they grow, both from an experimental and a theoretical point of view. This work focuses on theoretical studies of SWCNT properties and how they relate to the growth process, thereby giving us vital new information about how SWCNTs grow and taking us ever closer to achieving the ultimate goal of chirality-specific growth. In this thesis, an introduction to the field is given and the current state of the art experiments focusing on chirality-specific growth of SWCNTs are presented. A brief review of the current theoretical works and computer simulations related to growth of SWCNTs is also presented. The results presented in this thesis are obtained using first principle density functional theory. The first study shows a correlation between the stability of SWCNT-fragments and the observed products from experiments. Calculations confirm that in 84% of the investigated cases the chirality of experimental products matches the chirality of the most stable SWCNT-fragments (within 0.2 eV). Further theoretical calculations also reveal a previously unknown link between the stability of SWCNT-fragments and their length. The calculations show that at specific SWCNT-fragment lengths the most stable chirality changes. Thus, introducing the concept of a switching length for SWCNT stability. How these new results link to the existing understanding of SWCNT growth is discussed at the end of the thesis.

Ultra-thin solar cells that incorporate earth-abundant and non-toxic materials are promising candidates in the endeavor toward sustainable energy harvesting. Methods to counteract the inevitable low absorption of thinner semiconductor layers are of high interest and have raised considerable attention in the research society. In an attempt to increase the absorption of these types of assemblies, optical coupling effects between the localized surface plasmon resonances (LSPR) of disordered Au nanostructures and a Fabry-Pérot cavity were studied using a previously established absorber/spacer/reflector stack. The disordered Au array was fabricated by evaporating a thin Au film on a substrate with a 55 nm SiO2 dielectric spacer and a 100 nm Al reflecting film, followed by thermal annealing. Nominal Au film thicknesses in the range of 5-25 Å and annealing temperatures of 200-500 oC were investigated. In situ spectroscopic ellipsometry measurements during the subsequent atomic layer deposition (ALD) of tin monosulfide (SnS) allowed analysis of how the optical properties of the SnS/Au absorber layer changed as a function of the growing SnS layer thickness. By employing the Transfer Matrix Method with the estimated optical properties from the in situ analysis, the absorptance of the absorber/spacer/reflector stacks was simulated as a function of the spacer thickness, revealing any signs of the characteristic anti-crossing behavior. It was discovered that a nominal Au film thickness of 25 Å, annealed at 450 oC, and coated with a SnS film of ∼13 nm primed toward the π-phase, resulted in strong optical coupling between the cavity mode and the LSPR. The energy difference at the avoided crossing in the specular reflectance measurement gave an estimated Rabi-splitting energy of 537 meV. This corresponded to about 40% of the original LSPR energy, placing itself within the ultra-strong coupling regime. To evaluate the relevance of the thin-layered structure in photovoltaic applications, more advanced computational methods are required to estimate the useful absorption that occurs in the SnS layer. Nevertheless, these results elucidate the realization of strong optical coupling effects between disordered Au nanostructures and a Fabry-Pérot cavity, and further the possibility of using scalable fabrication methods for this type of ultra-thin absorber/spacer/reflector stack.

Semiconductors are used in many electronic applications, for example diodes, solar cells and transistors. Typically, semiconductors are inorganic materials, such as silicon and gallium arsenide, but lately more research and development has been devoted to organic semiconductors, for example semiconducting polymers. One of the reasons is that polymers can be customized, to a greater extent than inorganic semiconductors, to create a material with desired properties. Often, two polymers are blended to obtain the desired function, but two polymers do not usually result in an even blend. Instead they tend to separate from each other to varying degrees. The morphology of the blend affects the material properties, for example how efficiently it can convert electricity to light. In this project, thin films consisting of polymer blends were examined using microscopy techniques for the purpose of increasing our understanding of the morphology of such blends. One goal was to investigate whether a technique called correlative light and electron microscopy can be useful for examining the morphology of these films. In correlative light and electron microscopy, a light microscope and an electron microscope are used in the same location in order to be able to correlate the information from the two microscopes. The second goal was to learn about the morphology of the thin films using various microscopy techniques. The polymers used were Super Yellow and poly(ethylene oxide) with large molecular weight. Super Yellow is a semiconducting and light-emitting polymer while poly(ethylene oxide) is an isolating and non-emitting polymer that can crystallize. In the blend films, large, seemingly crystalline structures appeared. The structures could be up to 1 mm in the lateral direction, while the films were only approximately 170 nm thick. These structures could grow after the films had dried and their shapes were similar to those of poly(ethylene oxide) crystals. Consequently, there is reason to believe that it is the poly(ethylene oxide) that makes up the seemingly crystalline structures, but the structures also emitted more light than the rest of the film, and Raman spectroscopy showed that there was Super Yellow in the same location as the crystals. Among the microscopy techniques used, phase contrast microscopy was particularly interesting. This method visualizes differences in optical path length and was useful for studying polymer blends when the polymers have different indices of refraction. Correlating light and electron microscopy showed that there was a pronounced topographical difference between the seemingly crystalline regions and the rest of the thin film. Light microscopy has a limited resolution due to diffraction, but as long as the resolution of the light microscope is sufficient for seeing phase separation, correlative light and electron microscopy turned out to be a good method for studying the morphology of thin films of polymer blends. / Halvledare är viktiga för många elektroniska ändamål eftersom de kan användas till exempelvis dioder, solceller och transistorer. Traditionellt används inorganiska halvledande material som kisel eller galliumarsenid, men på senare tid har allt mer forskning och utveckling inriktat sig mot organiska (kolbaserade) halvledare, såsom halvledande polymerer, bland annat eftersom det i högre utsträckning går att skräddarsy de organiska materialen så att de får önskvärda egenskaper. Ofta blandas två polymerer med varandra för att skapa ett material med nya egenskaper som är önskvärda, men två polymerer brukar inte blandas jämnt utan tenderar att separera från varandra i olika utsträckning. Hur blandningen ser ut (morfologin) påverkar materialets egenskaper, till exempel hur effektivt det omvandlar ström till ljus. Med syfte att öka förståelsen för hur morfologin ser ut hos en blandning av två polymerer, har detta projekt gått ut på att undersöka tunna filmer av polymer-blandningar med hjälp av mikroskopiska tekniker. Ett delmål var att ta reda på om en teknik som heter korrelativ ljus- och elektronmikroskopi är en bra metod för att undersöka morfologin hos dessa filmer. Vid korrelativ ljus- och elektronmikroskopi används både ett ljusmikroskop och ett elektronmikroskop på samma plats för att kunna korrelera informationen som de båda mikroskopen ger. Det andra delmålet var att undersöka vad de olika mikroskopi-teknikerna kan säga om morfologin hos de tunna filmerna. De polymerer som använts är Super Yellow och poly(etylenoxid) med hög molekylmassa. Super Yellow är en oordnad halvledande och ljusemitterande polymer medan poly(etylenoxid) är en isolerande och icke-emitterande polymer som kan kristallisera. I de blandade filmerna uppstod stora kristall-liknande strukturer som kunde vara upp emot 1 mm breda trots att filmerna bara var ungefär 170 nm tunna. Dessa strukturer kunde växa fram efter det att filmerna redan hade torkat och påminde i form om kristaller som kan bildas av poly(etylenoxid). Det finns alltså skäl att tro att det är poly(etylenoxid) som kristalliserats, men de kristall-liknande strukturerna visade sig emittera mer ljus än vad resten av filmen gjorde, och Raman-spektroskopi visade att det även fanns Super Yellow på samma plats som kristallerna. Bland de mikroskopitekniker som testades utmärker sig faskontrastmikroskopi, som visar skillnader i den optiska vägskillnaden (det vill säga faktisk vägskillnad multiplicerat med brytningsindex). Det visade sig vara en intressant teknik för att studera polymerblandningar när de båda polymererna har olika brytningsindex. Genom att korrelera ljus- och elektronmikroskopi visade det sig att det fanns en tydlig skillnad i struktur mellan de kristall-liknande områdena och resten av den tunna filmen. Ljusmikroskopi har begränsad upplösning på grund av ett fenomen som heter diffraktion, men så länge som ljusmikroskopets upplösning är tillräcklig för att se fasseparation visade det sig att korrelativ ljus- och elektronmikroskopi är en bra metod för att studera morfologin hos tunna filmer av polymerblandningar.

Double perovskite materials exhibit alterations in magnetic order through manipulation oftheir crystal structure. Certain ultra thin metallic bilayers can create an exotic magnetic stateof confined spin textures called skyrmions. In both cases, new atomic arrangements leadto new electrical and magnetic properties. The following work comprises two studies, bothof which examine the magnetic properties of transition metals in either powder or thin filmsamples. The first part is dedicated to a series of muon spin rotation and relaxation (muSR)experiments on a LaSrNiReO6, double perovskite, powder sample. In the muSR technique, aspin polarized muon beam is focused onto a powder envelope in low pressure and temperatureconditions. The spins of the implanted muons evolve depending on the intrinsic or externallyapplied magnetic field according to Larmor precession. The measurement is based onthe detection of decay positrons that carry this precession information on their preferreddecay directions. Measurements that were realized in wTF, ZF and LF setups, reveal asecond transition to magnetic order at Tc ≃ 22K, below a transition that was observed at T =261K from magnetic susceptibility measurements. The experimental results point to threemagnetic phases, paramagnetic for T > 261K, dilute ferrimagnetic for 22 < T < 261K and amagnetically ordered state for T < 22K, that may implicate ferro- and antiferromagnetismfrom Ni sublattices and Ni-Re interactions. The second part follows an attempt to produce and characterize ultra thin bilayer filmsfor the observation of interfacial chiral structures and skyrmions. Co/Fe/MgO (100) andW/Ni/Cu (100) bilayers were grown with magnetron sputter deposition in various layerthicknesses and their structure was determined by X-ray reflectometry (XRR). The XRRscans presented a relatively thick-layered Co/Fe/MgO film, while extremely thin and roughW/Ni/Cu bilayers, for the purposes of studying films with broken interfacial inversionsymmetry. This study was concluded with indicative magneto-transport measurements thatalso point to the reconfiguration of the growth procedure.

Conductive polymers are also known as "organic metals" due to their semiconducting properties. They are found in a wide range of applications in the field of organic electronics. However, the growing number of experimental works is not widely supported with theoretical calculations. Hence, the field of conductive polymers is experiencing lack of understanding of mechanisms occurring in the polymers. In this PhD thesis, the aim is to increase understanding of conductive polymers by performing theoretical calculations.        The polymers poly(3,4-ethylenedioxythiophene) (PEDOT) together with its selenium (PEDOS) and tellurium (PEDOTe) derivatives, poly(p-phenylene) (PPP) and naphthobischalcogenadiazoles (NXz) were studied. Several computational methods were applied for analysis of mentioned structures, including density functional theory (DFT), tight-binding modelling (TB), and Car-Parrinello molecular dynamics (CPMD) calculations. The combination of CPMD and DFT calculations was applied to investigate the PEDOT, PEDOS and PEDOTe. The polymers were studied using four different functionals in order to investigate the full picture of structural changes, electronic and optical properties. Temperature effects were studied using molecular dynamics simulations. Wide statistics for structural and molecular orbitals analysis were collected.         The TB method was employed for PPP. The formation and motion of the excitations, polarons and bipolarons, along the polymer backbone was investigated in presence of electric and magnetic fields. The influence of non-magnetic and magnetic impurities was determined.        The extended π-conjugated structures of NXz were computed using B3LYP and ωB97XD functionals in combination with the 6-31+G(d) basis set. Here, the structural changes caused by polaron formation were analyzed. The combined analysis of densities of states and absorption spectra was used for understanding of the charge transition. / <p>QC 20170928</p>

Electrochemical systems, which rely on coupled phenomena of the chemical change and electricity, have been utilized for development an interface between biological systems and conventional electronics.  The development and detailed understanding of the operation mechanism of such interfaces have a great importance to many fields within life science and conventional electronics. Conducting polymer materials are extensively used as a building block in various applications due to their ability to transduce chemical signal to electrical one and vice versa. The mechanism of the coupling between the mass and charge transfer in electrochemical systems, and particularly in conductive polymer based system, is highly complex and depends on various physical and chemical properties of the materials composing the system of interest. The aims of this thesis have been to study electrochemical systems including conductive polymer based systems and provide knowledge for future development of the devices, which can operate with both chemical and electrical signals. Within the thesis, we studied the operation mechanism of ion bipolar junction transistor (IBJT), which have been previously utilized to modulate delivery of charged molecules. We analysed the different operation modes of IBJT and transition between them on the basis of detailed concentration and potential profiles provided by the model. We also performed investigation of capacitive charging in conductive PEDOT:PSS polymer electrode. We demonstrated that capacitive charging of PEDOT:PSS electrode at the cyclic voltammetry, can be understood within a modified Nernst-Planck-Poisson formalism for two phase system in terms of the coupled ion-electron diffusion and migration without invoking the assumption of any redox reactions. Further, we studied electronic structure and optical properties of a self-doped p-type conducting polymer, which can polymerize itself along the stem of the plants. We performed ab initio calculations for this system in undoped, polaron and bipolaron electronic states. Comparison with experimental data confirmed the formation of undoped or bipolaron states in polymer film depending on applied biases. Finally, we performed simulation of the reduction-oxidation reaction at microband array electrodes. We showed that faradaic current density at microband array electrodes increases due to non-linear mass transport on the microscale compared to the corresponding macroscale systems.  The studied microband array electrode was used for developing a laccase-based microband biosensor. The biosensor revealed improved analytical performance, and was utilized for in situ phenol detection.