State-of-the-art Li-ion cathode materials are based on LiMO2 (M=Ni, Mn, Co) layered transition metal oxides (denoted NMC) with Ni-rich composition because of their high specific capacity. Yet, these materials suffer from poor capacity retention due to crack formation during de-/lithiation cycling. Particle cracking leads to exposure of new electrode surface which leads to Li-inventory loss, increased side reactions, and electric disconnection. Quantification of the extent of cracking is therefore desirable, especially during in situ whilst cycling of the Li-ion cell. Herein, we evaluate and improve an analytical methodology based on electrochemical impedance spectroscopy (EIS) in order to estimate the changes in electrochemically active surface area of both poly- and single-crystalline Ni0.8Mn0.1Co0.1(NMC811) active materials. A transmission-line model (TLM) applied to both non-blocking and blocking electrode condition was utilized in order to deconvolute and interpret the acquired experimental data. Fits of the complex TLM equivalent-circuits to the impedance spectra was facilitated by developing a global stochastic iterative function based on local multivariate optimization. Impedance analysis during short- term cycling showed that the single-crystalline NMC811 suffered from less particle cracking and side reactions compared to polycrystalline NMC811, which was also confirmed from post-mortem gas adsorption analysis. A novel approach to estimate the extent of particle cracking in commercial Li-ion cells by utilizing an empirically strong positive correlation between the charge-transfer capacitance and resistance was proposed. The work presented herein demonstrates the unique prospects of the EIS methodology in the development and research of future rechargeable batteries

The application of different analytical techniques is fundamental in forensic drug analysis. In the wake of the occurrence of large numbers of new psychoactive substances possessing similar chemical structures as already known ones, focus has been placed on applied criteria for their univocal identification. These criteria vary, obviously, depending on the applied technique and analytical approach. However, when two or more substances are proven to have similar analytical properties, these criteria no longer apply, which imply that complementary techniques have to be used in their differentiation. This work describes the synthesis of some structural analogues to synthetic cannabinoids and cathinones based on the evolving patterns in the illicit drug market. Six synthetic cannabinoids and six synthetic cathinones were synthesized, that, at the time for this study, were not as yet found in drug seizures. Further, a selection of their spectroscopic data is compared to those of already existing analogues; mainly isomers and homologues. The applied techniques were mass spectrometry (MS), Fourier transformed infrared (FTIR, gas phase) spectroscopy and nuclear magnetic resonance (NMR) spectroscopy. In total, 59 different compounds were analyzed with the  selected techniques. The results from comparison of spectroscopic data showed that isomeric substances may in some cases be difficult to unambiguously identify based only on their GC-MS EI spectra. On the other hand, GC-FTIR demonstrated more distinguishable spectra. The spectra for the homologous compounds showed however, that the GC-FTIR technique was less successful compared to GC-MS. Also a pronounced fragmentation pattern for some of the cathinones was found. In conclusion, this thesis highlights the importance of using complementary techniques for the univocal identification of synthetic cannabinoids and cathinones. By increasing the number of analogues investigated, the more may be learnt about the capabilities of different techniques for structural differentiations, and thereby providing important identification criteria leading to trustworthy forensic evidence.

This thesis covers fundamental aspects of process control when growing titanium oxide nanoparticles in a reactive sputtering process. It covers the influence of oxygen containing gas on the oxidation state of the cathode from which the growth material is ejected, as well as its influence on the particles oxidation state and their nucleation. It was found that a low degree of reactive gases was necessary for nanoparticles of titanium to nucleate. When the oxygen gas was slightly increased, the nanoparticle yield and particle oxygen content increased. A further increase caused a decrease in particle yield which was attributed to a slight oxidation of the cathode. By varying the oxygen flow to the process, it was possible to control the oxygen content of the nanoparticles without fully oxidizing the cathode. Because oxygen containing gases such as residual water vapour has a profound influence on nanoparticle yield and composition, the deposition source was re-engineered to allow for cleaner and thus more stable synthesis conditions. The size of the nanoparticles has been controlled by two means. The first is to change electrical potentials around the growth zone, which allows for nanoparticle size control in the order of 25-75 nm. This size control does not influence the oxygen content of the nanoparticles. The second means of size control investigated was by increasing the pressure. By doing this, the particle size can be increased from 50 – 250 nm, however the oxygen content also increases with pressure. Different particle morphologies were found by changing the pressure. At low pressures, mostly spherical particles with weak facets were produced. As the pressure increased, the particles got a cubic shape. At higher pressures the cubic particles started to get a fractured surface. At the highest pressure investigated, the fractured surface became poly-crystalline, giving a cauliflower shaped morphology.

Superkondensatorer är energilagringsenheter som har uppmärksammats mer under det senaste decenniet. Några av de fördelar som dessa enheter har varit är lagring av hög effekttäthet, förlängda livscykler och snabba laddnings- och urladdningstider. Dock är superkondensatorer fortfarande begränsade i energitäthet i jämförelse med batterier. För att få högre effekt och energitäthet är en asymmetrisk hybrid superkondensator ett bra alternativ. Denna enhet består av en kolbaserad elektrod för icke-faradaiska reaktioner och en kolelektrod kombinerad med metalloxider för redoxreaktioner. Materialvalet spelar en avgörande roll för förmågan en hybrid asymmetrisk superkondensator ska ha. I denna studie undersöks fyra olika kommersiella kol. Den specifika ytan, porstorlekarna och morfologin jämförs. Dessutom syntetiseras metalloxidernanopartiklar MnO2 och kristallstrukturen undersöks. Därtill beläggs MnO2-partiklarna på de fyra kolen och tillväxten av dessa undersöks. Slutligen analyseras interaktionen mellan jonvätskan 1-butyl-3-metylimidazoliumtetrafluorborat (BMIM[BF4]) som en elektrolyt och de olika kolen. / Supercapacitors are energy storage devices that have drawn attention for the past decade. Some of the advantages of these devices are higher power density storage, extended life cycles, and fast charge and discharge times. However, supercapacitors are still limited in energy density compared to batteries. To obtain higher power and energy densities, a hybrid asymmetric supercapacitor is a good alternative. This device consists of one carbon-based electrode for non-faradaic reactions, and one carbon electrode combined with metal oxides for redox reactions. The material choice is important for the capability of a hybrid asymmetric supercapacitor. In this study, four different commercial carbons are investigated. The specific surface area, pore sizes, and morphology are compared. In addition, metal oxide nanoparticles MnO2 are synthesised, and crystal structure is investigated. Furthermore, the MnO2 particles are deposited on the four carbons and the growth of those is studied. Finally, the interaction between ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM[BF4]) as an electrolyte and the different carbons is studied.

Modified nanocellulose have distinctive qualities and have drawn a lot of interest from a variety of fields. It is a natural, sustainable product that is manufactured from plant-based materials like wood and other renewable resources. It is also biodegradable. It is a possible material for battery separators because of its great mechanical strength, flexibility, and ability to create a stable and consistent membrane. Due to the cost of using it as a membrane, it has been investigated in this work to see if it can be coated onto a substrate and used as battery separator. In this work sulfonated cellulose nanofibrils (SCNF) has been used to be coated on kraft paper and inkjet paper using a rod coater. Parameters like concentration, thickness and substrates have been varied in this experiment. Viscosity was measured using Brookfield instrument to measure the viscosity for 0,5% SCNF and 1,5% SCNF. The coating was carried out using a rod coater and varying between two rods to influence the thickness, the coating used concentrations of 0,5% SCNF and 1,5% SCNF and two different substrates, kraft paper and inkjet paper. Thickness was determined to study the effect of the variation in rod. The mechanical strength was tested on the coated paper substrates and compared the results to the noncoated substrates as reference, the mechanical strength showed an improvement with the coated SCNF substrates. Permeance through the Gurley method was studied in order to understand how the coated substrates behaves compared to the noncoated. Contact angle was determined as well to understand the wettability of the coated substrates and how they would behave as separators in zinc ion batteries. The contact angle decreased with increasing concentration of the SCNF which is a result of the sulfonate groups. Cross sections were analyzed using SEM to study the influence of the coating to the substrates. Ionic conductivity was also tested to evaluate the possibility of the coated substrates as separators.

Fuel cells play a key role in implementing hydrogen as alternative fuel to eliminate CO2-emissions and their performance is largely dependent on the contact resistance of the surface of bipolar plates. For stainless steel bipolar plates titanium carbonitride coatings were suggested for modifying surface properties and thereby reducing contact resistance while maintaining mechanical strength. This study analysed Ti(C,N) coatings with different carbon content in terms of composition, microstructure chemical bonding and contact resistance. The films were deposited either by reactive co-sputtering from a titanium and a graphite target under nitrogen flow or by co-reactive sputtering from a titanium target under flow of nitrogen and methane. It was found that an increase in carbon content results in a nanocomposite of Ti(C,N) and an amorphous carbon (a-C) matrix leading to nanocrystalline films with a smooth surface. Analysing the amount of a-C as a functions of overall carbon content, it is observed that carbon is more effectively incorporated into carbonitride grains when using methane gas as a carbon source. Furthermore, the contact resistance of the titanium carbonitride coatings was found to be lowest (below 10 mΩ) for a small amount of a-C phase and overall lower than that of carbide and nitride reference samples. Therefore, titanium carbonitrides are a promising coating material for electrical contact applications such as fuel cells.

The pursuit of sustainable and high-performance materials is of utmost significance in driving the progress of battery technologies. Solid-state technology represents a promising avenue for the development of batteries with improved sustainability and performance. In this context, the present study delves into the examination of composition and the substitution of oxygen with nitrogen within the 50Li2O-xSiO2-(50-x)P2O5 glass system, specifically as applied to Solid-State electrolytes. The objective is to evaluate the influence of these factors on the electrical properties of the glass and their potential implications for Solid-State battery technology. The glass matrix was obtained through the melt-quenching technique, followed by comprehensive characterization using electrochemical impedance spectroscopy. The influence of varying silica content on the conductivity of the glass was investigated. This led to the selection of the glass system with the highest conductivity for further experiments involving nitridation. Subsequent experiments on nitridation aimed to explore the impact of nitrogen incorporation on the conductivity of the glass. By systematically varying the nitrogen content at different temperatures, the study sought to elucidate the relationship between nitrogen content and the resulting increase in glass conductivity.    The study reveals a noteworthy finding regarding the impact of nitrogen content on the conductivity of the glass. Specifically, when the nitrogen content was increased, the conductivity increased. In the case of a similar glass composition in pellet form, the conductivity at room temperature increased from Log σ = -8,009 (for glass without nitrogen) to Log σ = -6,951 (for nitrided glass). Additionally, the introduction of nitrogen into the glass resulted in a decrease in activation energy, being reduced from 0,66 eV (for oxide glass) to 0,60 eV (for oxynitride glass). These results indicate a clear correlation between increased nitrogen content and enhanced electrical properties of the investigated glasses; although obtaining a homogeneous bulk glass after nitridation was not feasible. Therefore, the nitrided samples were pelletized and sintered under different thermal conditions to obtain characterizable samples. The findings suggest that nitrogen substitution could be a promising approach for enhancing the electrical properties of the glasses of the title system of composition. Further investigation is required to optimize the process and achieve homogeneous bulk oxynitride glass.

Forskningsområdet för bärbar elektronik är fortfarande relativt ungt och det finns ett stort behov av utveckling av nya material inom området. Olika typer av kompositer är mycket intressanta och de ska uppvisa såväl hög hållfasthet som goda ledande egenskaper. I detta avseende är silkes fibroin och MXene mycket intressanta utgångsmaterial eftersom silkestrådarna kan ge en struktur med god jonledningsförmåga och god flexibilitet och MXene kan bidra med hög styvhet och god elektrisk ledningsförmåga. Med detta som bakgrund beslöts att undersöka om kompositer av silkestrådar och MXene kan användas i kompositer som kan användas i bärbar elektronik. 3 olika typer av hydrogeler studerades och de innehöll silkes fibroin med 0, 1 och 5% MXene. De egenskaper som utvärderades var struktur, mekaniska egenskaper, stabilitet i vatten, bionedbrytbarhet och både statisk och dynamisk ledningsförmåga. Resultaten visar att de tillverkade nanokompositerna har lovande förutsättningar inom området eftersom en kombination av silkes fibroin med 5 % MXene har god stabilitet, konduktivitet och en hög och stabil Gauge-faktor. / As the research area of wearable electronics is still relatively new, material science with this focus opens plenty of unexplored fields. That is why a study characterizing the unexplored composite system of silk fibroin and MXene (Silk/MXene) was conducted. These two biocompatible materials are complementary with regard to the requirements for wearable electronics materials. Silk fibroin dispose an ionic conductivity and solid flexibility, while MXene brings mechanical strength and significant increase of electrical conductivity. The reinforced hydrogel materials were studied at two concentrations of fillers, 1% and 5% and compared to pristine silk fibroin. All three materials were studied from the point of view of their structure, mechanical properties, behaviour in aqueous environment, biodegradability and electrical conductivity, both static and dynamic. Nanocomposite systems of silk fibroin and MXene have shown a potential for being used in the intended application area, as Silk/MXene 5% film displays good stability, conductivity with high andstable Gauge factor.

With the growing impact of climate change on both political decisions and how companies develop their products, it is increasingly important to find environmentally friendly alternatives to fossil-based materials. One of the more interesting materials in this respect is cellulose, which is the world's most naturally occurring polymer and can be used in a variety of applications. One way to modify the fibers and to change their properties is to use a method called Layer-by-Layer (LbL) treatment where two polymers of opposite charge are alternately adsorbed to the fiber surface. Another possibility is to oxidize the cellulose in the fibers to obtain a higher charge. This means that the fibers can adsorb a higher amount of cationic additives and that the fibers swell more which means that they are plasticized and can create stronger joints between the fiber surfaces in the dry state, which results in stronger dry fiber networks. However, wood-based fibers are small and inhomogeneous, both chemically and morphologically, which means that it is necessary to use model systems to be able to clarify, in detail, how treated and untreated surfaces interact with each other at a molecular level. One model system that can be used to investigate how cellulose fibers are affected by coating using the LbL method is to use spherical beads made from regenerated cellulose. In the present work, these beads were treated with polyallylamine hydrochloride (PAH) and hylauronic acid (HA) as well as with PAH and alginate (Alg) before being allowed to dry together and then subjected to tensile testing to clarify the adhesion between the surfaces. The beads were treated with five and ten bi-layers of these polymers, respectively, and then dried together on an AKD-coated surface, to avoid adhesion to the underlying surface, to examine the adhesion between the beads. The adhesion increased when treated with LbL and became higher upon adsorption of multiple layers of polyelectrolytes and the Alg / PAH system showed the greatest increase. Ten-layer samples of Alg / PAH were also tested after a solution of calcium chloride was added during drying, resulting in poorer adhesion between the beads. / Med klimatfrågans växande inverkan på både politiska beslut och hur företagen utvecklar sina produkter så läggs det allt större vikt vid att hitta miljövänliga alternativ till fossilbaserade material. Ett av de mer intressanta materialen är cellulosa vilket är världens mest naturligt förekommande polymer och som kan användas i en rad olika tillämpningar. Ett sätt att modifiera fibrerna och att ändra deras egenskaper är att använda sig av en metod som kalls Layer-by-layer (LbL) behandling där två polymerer mot motsatt laddning växelvis adsorberas till fiberytan. En annan möjlighet är att oxidera cellulosan i fibrerna så att de erhåller de en högre laddning. Detta innebär dels att fibrerna kan adsorbera en högre mängd katjoniska tillsatskemikalier samt att fibrerna sväller mera vilket innebär att de plasticeras och kan skapa starkare fogar mellan fiberytorna i torrt tillstånd vilket resulterar i starkare torra fibernätverk. Vedbaserade fibrer är dock små och inhomogena såväl kemiskt som morfologiskt vilket innebär att det är nödvändigt att använda modellsystem för att kunna klarlägga, i detalj, hur behandlade och icke behandlade ytor växelverkar med varandra på en molekylär nivå. Ett modellsystem som kan användas för att undersöka hur cellulosafibrer påverkas av att beläggas med hjälp av LbL metoden är att använda sig av sfäriska kulor tillverkade från regenererad cellulosa. I föreliggande arbete behandlades dessa kulor med polyallylaminhydroklorid (PAH) och hylauronsyra (HA) samt med PAH och alginat (Alg) innan de tilläts torka ihop och därefter utsattes för dragprovning för att klarlägga adhesionen mellan ytorna. Kulorna behandlades med fem respektive tio bilager av dessa polymerer och torkades sedan ihop på en AKD-belagd yta, för att undvika adhesion till den underliggande ytan, för att undersöka adhesionen mellan kulorna. Adhesionen ökade när de behandlades med LbL och blev högre vid adsorption av flera lager polyelektrolyter och systemet med Alg/PAH resulterade i den största ökningen. Prover med tio lager av Alg/PAH testades även efter att en lösning av kalciumklorid tillsattes under torkningen vilket resulterade i en sämre adhesion mellan kulorna.

In recent years, nanostructured materials incorporated with inorganic particles and polymers have attracted attention for simultaneous multifunctional biomedical applications. This thesis summarized three works, which are preparation of mesoporous silica coated superparamagnetic iron oxide (Fe3O4@mSiO2) nanoparticles (NPs) as magnetic resonance imaging T2 contrast agents, polymer grafted Fe3O4@mSiO2 NPs response to temperature change, synthesis and biocompatibility evaluation of high aspect ratio (AR) gold nanorods. Monodisperse Fe3O4@mSiO2 NPs have been prepared through a sol-gel process. The coating thickness and particle sizes can be precisely controlled by varying the synthesis parameters. Impact of surface coatings on magnetometric and relaxometric properties of Fe3O4 NPs is studied. The efficiency of these contrast agents, evaluated by MR relaxivities ratio (r2/r1), is much higher than that of the commercial ones. This coating-thickness dependent relaxation behavior is explained due to the effects of mSiO2 coatings on water exclusion. Multifunctional core-shell composite NPs have been developed by growing thermo-sensitive poly(N-isopropylacrylamide-co-acrylamide) (P(NIPAAm-co-AAm)) on Fe3O4@mSiO2 NPs through free radical polymerization. Their phase transition behavior is studied, and their lower critical solution temperature (LCST) can be subtly tuned from ca. 34 to ca. 42 °C, suitable for further in vivo applications. A seedless surfactant-mediated protocol has been applied for synthesis of high AR gold nanorods with the additive of HNO3. A growth mechanism based on the effect of nitrate ions on surfactant micelle elongation and Ostwald ripening process is proposed. The biocompatibility of high AR nanorods was evaluated on primary human monocyte derived dendritic cells (MDDCs). Their minor effects on viability and immune regulatory markers support further development for medical applications. / QC 20110701