Detta examensarbete initierades och handledes av Mellifiq, ett företag som arbetar med rening av luft och vatten, där en applikation är rening av köksfrånluft med ozon. Ozon förhindrar att fettpartiklar i frånluften ansamlas på väggarna i kanalen och värmeväxlaren, vilket leder till högre brandsäkerhet och mer effektiv användning av värmeväxlaren. Syftet med detta examensarbete var att öka förståelsen av reaktionen mellan ozon och ytan av fettpartiklarna. Tunna fettsyrafilmer ovanpå ett fast underlag användes som modellsystem för att representera ytan av en fettpartikel. Tre fettsyror undersöktes, en mättad fettsyra, fettsyra A, en enkelomättad fettsyra, fettsyra B, och en fleromättad fettsyra, fettsyra C. TIR Raman-spektroskopi användes för att analysera effekten på fettsyrafilmen vid exponering av torr luft, fuktig luft med en relativ fuktighet på 80 % och fuktig luft med en konstant ozonkoncentration. Effekten av ozon undersöktes även med kontaktvinkelmätningar på fettsyrafilmerna. Resultaten från TIR Raman visade att torr luft och fuktig luft (RH 80 %) inte hade någon effekt på fettsyrafilmen, oberoende av vilken typ av fettsyra som användes. När det gäller effekterna av exponering för ozon kunde inga effekter observeras på filmen av fettsyra A i vare sig TIR Raman eller kontaktvinkelmätningar. Därför kunde ingen reaktion mellan fettsyra A och ozon bekräftas vid den ozonkoncentration som användes och de exponeringstiderna som undersöktes. Däremot oxiderades de omättade fettsyrafilmerna av fettsyra B och C när de exponerades för ozon, vilket bekräftades av den snabba minskningen av C-C-dubbelbindningarna i TIR Raman-spektra. Oxidationen av dubbelbindningar i fettsyra B verkade visa en mer komplex kinetik, med en tvåstegsprocess kopplad till en förändring av antalet molekyler vid ytan. Filmerna bestående av fettsyra C visade sig förlora materia när de exponerades för ozon, vilket tyder på att korta flyktiga ämnen bildades under oxidationsprocessen. Denna effekt observerades inte för fettsyra B, där även om den spektrala formen i CH-sträckningsområdet ändrades, vilket bevisade närvaron av nya arter, förblev den totala mängden material i filmen ungefär konstant. Dessutom gav både fettsyra B och C upphov till nya karbonyl-C=O-sträckningstoppar i spektra efter ozonisering, vilket visar att aldehyder, estrar eller båda bildas under processen. Slutligen bekräftade kontaktvinkelmätningarna med en minskning av statiska vinklar att ytan på filmerna av fettsyra B och C förändrades efter ozonisering. / This master thesis project was initiated and managed by Mellifiq, a company that works with purification of air and water, where one application is purification of kitchen exhaust air with ozone. Ozone prevents fat particles in the exhaust air from accumulating on the walls in the duct and the heat exchanger, reducing fire safety concerns and making the use of the heat exchanger more effective. The aim of this master thesis project was to further understand the reaction between ozone and the surface of the fat particles. Thin fatty acid films on top of a solid support were used as model systems to represent the surface of a fat particle. Three fatty acids were investigated, a saturated fatty acid, fatty acid A, a monounsaturated fatty acid, fatty acid B, and a polyunsaturated fatty acid, fatty acid C. TIR Raman spectroscopy was used to analyze the effect on the fatty acid film as it was exposed to dry air, humid air with a relative humidity of 80 %, and humid air with a fixed ozone concentration. The effect of ozone was also investigated with contact angle measurements on the fatty acid films. The results from TIR Raman showed that dry air and humid air (RH 80 %) had no effect on the fatty acid film, independent of the type of fatty acid used. Regarding the effects of exposure to ozone, no effects could be observed on the fatty acid A field in either the TIR Raman or contact angle measurements. Therefore, no reaction between fatty acid A and ozone could be confirmed at the fixed ozone concentration used and exposure times investigated. In contrast, the unsaturated fatty acid films of fatty acid B and fatty acid C were oxidized when exposed to ozone, as confirmed by the rapid decrease of the C-C double bonds in the TIR Raman spectra. However, the oxidation of double bonds in oleic acid appeared to show more complex kinetics, with a two-step process linked to a change in the number density of molecules at the surface. Interestingly, the films consisting of fatty acid C were shown to lose matter when exposed to ozone, indicating that short volatile species were formed during the oxidation process. This effect was not observed for fatty acid B, where though the spectral shape in the C-H stretching region changed, proving the presence of new species, the overall amount of material in the film remained approximately constant. Moreover, both fatty acid B and C gave rise to new carbonyl C=O stretching peaks in the spectra after ozonation, showing that aldehydes, esters, or both are formed during the process. Finally, the contact angle measurements confirmed with a decrease in static angles that the surface of the fatty acid B and C films changed after ozonation.

Litiumjonbatterier (LIB) är viktiga komponenter i dagens teknologi och används för att driva en mängd olika elektroniska system, allt från datorer och mobiltelefoner till bilar och flygplan. Eftersom efterfrågan på effektiv energilagring fortsätter att växa finns ett fortsatt behov för forskning och utveckling inom området. Denna rapport undersöker hårt kol, ett lovande material för anoder i litiumjonbatterier och andra alkali-jon batterier. I likhet med grafit är hårt kol ett kolbaserat material som inte är en väldefinierad allotropp utan en komplex blandning med avseende på både hybridiseringstillstånd och långdistansordning.  Därför är den mycket dåligt definierat. Ändå är hårt kol ett önskvärt material eftersom det kan produceras från förnybara resurser samt på grund av dess kompatibilitet med natrium, vilket möjliggör natriumjonbatterier. I den här studien har elektroder av hårt kol syntetiserats och litierats i olika grader och sedan studerats med 7Li NMR-spektroskopi där både spektra och longitudinella relaxationshastigheter mättes. Vid lägre litieringsnivåer observerades tydliga smala 7Li toppar inom intervallet 4-16 ppm, vilket indikerar förekomsten av joniskt litium. Vid högre litieringsnivåer framträdde en bred topp vid 61 ppm. Utseendet av denna topp, tillsammans med en hög Knight-skift, indikerar närvaron av kvasi-metalliskt litium. Det är värt att notera att detta kvasi-metalliska litium finns i de oordnade och porösa områdena hos hård kol. 7Li longitudinella relaxationshastigheter, som rapporterar om jonisk dynamik, registrerades vid olika temperaturer och från det observerade temperaturberoendet beräknades den genomsnittliga aktiveringsenergin för de involverade joniska rörelserna. Intressant nog visade sig denna aktiveringsenergi vara lägre jämfört med den i PAN-baserade kolfibrer och grafit, som båda uppvisar en högre grad av ordning. Denna observation tyder på ett samband mellan lokal oordning och snabbare jondynamik. / Lithium-ion batteries (LIB) are vital components of modern technology, powering a wide range of devices from computers and cell phones to cars and aeroplanes. As the demand for efficient energy storage continues to grow, research and development in the field of lithium-ion batteries remain active. This report focuses on the investigation of hard carbon, a promising anode material for lithium-ion batteries and other alkali-ion batteries. Akin to graphite, hard carbon is a carbon-based material that is not a well-defined allotrope but a complex mixture with regard to both hybridization state and long-range order. Hence it is very poorly defined. Yet, hard carbon is a desirable material as it can be produced from renewable resources and because of its compatibility with sodium, allowing for sodium-ion batteries. In this study, hard carbon electrodes were synthesised and lithiated to various degrees and then studied with 7Li NMR spectroscopy where both spectra and longitudinal relaxation rates were measured.   At lower lithiation levels, distinct narrow 7Li peaks were observed within the 4-16 ppm range, indicating the presence of ionic lithium. At higher lithiation levels a broad peak at 61 ppm emerged. The appearance of this peak, along with a high Knight shift, signifies the presence of quasi-metallic lithium, presumably in the more disordered and more porous regions of hard carbon. The 7Li longitudinal relaxation rates, reporting on ionic dynamics, were recorded at different temperature and from the observed temperature dependence the average activation energy for the involved ionic motions was calculated. Interestingly, this activation energy was found to be lower compared to that for PAN-based carbon fibres and graphite, both of which exhibit a higher degree of order. This observation suggests a correlation between local disorder and faster ion dynamics.

<p>A new kind of lipid/polymer composite particle, consisting of a biodegradable polymer matrix with well-defined lipid domains, has been created. The lipid used is the water-swelling lipid monoolein (MO), which forms a reversed bicontinuous cubic diamond structure in aqueous solutions. The polymer is poly(d,l-lactide-co-glycolide) (PLG), which degrades into water-soluble monomers through hydrolysis. This new particle might be a good alternative for encapsulation of active substances intended to be released over a longer period of time, i.e. sustained/retained/controlled release.</p><p>To prepare such particles can be difficult. Suitable phase behaviour and a solvent with the right properties are needed. For this reason, the phase behaviours of several different lipid/polymer/solvent/water systems have been explored. From the phase behaviour of a suitable system (i.e. MO/PLG/ethyl acetate/water), a route for formation of lipid/polymer composite particles has been deduced. Particles have been formed and distinct, water-swelling, lipid domains have been confirmed by characterization by means of confocal laser scanning probe microscopy (CLSM). </p><p>The sample preparation process has been automated and a method based on using a robotic liquid handler has been developed. Phase diagrams have been determined by examination of macroscopic behaviours and the microstructures of the phases have been studied by small- and wide-angle X-ray scattering (L₃, V₂, L_α, L), nuclear magnetic resonance self-diffusion (L, L₃), viscosimetry (L) and rheology (L). Several different theoretical models have been applied for interpretation of the results. For example, the swelling of the reversed bicontinuous cubic phases and the sponge phase have been modelled by applying the theory of infinite periodical minimal surfaces, the sponge phase has been shown to be bicontinuous according to the theory of interconnected rods and the phase behaviour of the polymer has been described by the Flory-Huggins theory. The main focus of this work (4/5) concerns phase studies in multicomponent systems from a physical-chemical point of view.</p>

People suffering from certain types of arrhythmia may benefit from the implantation of a cardiac pacemaker. Pacemakers artificially stimulate the heart by applying short electrical pulses to the cardiac tissue to restore and maintain a steady heart rhythm. By adjusting the pulse delivery rate the heart is stimulated to beat at desired pace. The stimulation pulses are transferred from the pacemaker to the heart via an electrode, which is implanted into the cardiac tissue. Additionally, the electrode must also sense the cardiac response and transfer those signals back to the electronics in the pacemaker for processing. The communication between the electrode and the tissue takes place on the electrode/electrolyte (tissue) interface. This interface serves as the contact point where the electronic current in the electrode is converted to ionic currents capable to operate in the body. The stimulation/sensing signals are transferred across the interface via three electrochemical mechanisms: i) non-faradaic charging/discharging of the electrochemical double layer, ii) reversible and iii) irreversible faradaic reactions. It is necessary to study the contribution of each mechanism to the total charge transferred to evaluate the pacing/sensing performance of the pacemaker electrode. In this thesis, the electrochemical properties and performance of stimulation/sensing electrodes for pacemaker applications have been investigated by electrochemical impedance spectroscopy, cyclic voltammetry and transient electrochemical techniques. All measurements were performed in synthetic body fluid with buffer capacity. Complementary surface analysis was performed with scanning electron microscopy, energy dispersive spectroscopy and X-ray photoelectron spectroscopy. The results reveal different interfacial behaviour and stability for electrode materials such as Pt, TiN, porous carbon, conducting oxides (RuO2 and IrO2 and mixed oxides) and porous Nb2O5 oxide. The influence of the charge/discharge rate on the electrode characteristics also has been evaluated. Although the rough and porous electrodes provide a high interfacial capacitance, the maximum capacitance cannot be fully employed at high charge/discharge rates because only a small part of the effective surface area is accessible. The benefit of pseudo-capacitive material properties on charge delivery was observed. However, these materials suffer similar limitations at high charge/discharge rate and, hence, are only utilising the surface bound pseudo-capacitive sites. Porous Nb2O5 electrodes were investigated to study the performance of capacitor electrodes. These electrodes predominantly deliver the charge via reversible non-faradaic mechanisms and hence do not produce irreversible by-products. They can deliver very high potential pulses while maintaining high impedance and, thus, charge lost by faradaic currents are kept low. By producing Nb oxide by plasma electrolysis oxidation a porous surface structure is obtained which has the potential to provide a biocompatible interface for cell adherence and growth. This thesis covers a multidisciplinary area. In an attempt to connect diverse fields, such as electrophysiology, materials science and electrochemistry, the first chapters have been attributed to explaining fundamental aspects of the respective fields. This thesis also reviews the current opinion of pacing and sensing theory, with special focus on some areas where detailed explanation is needed for the fundamental nature of electrostimulation/sensing. / QC 20101014

A new kind of lipid/polymer composite particle, consisting of a biodegradable polymer matrix with well-defined lipid domains, has been created. The lipid used is the water-swelling lipid monoolein (MO), which forms a reversed bicontinuous cubic diamond structure in aqueous solutions. The polymer is poly(d,l-lactide-co-glycolide) (PLG), which degrades into water-soluble monomers through hydrolysis. This new particle might be a good alternative for encapsulation of active substances intended to be released over a longer period of time, i.e. sustained/retained/controlled release. To prepare such particles can be difficult. Suitable phase behaviour and a solvent with the right properties are needed. For this reason, the phase behaviours of several different lipid/polymer/solvent/water systems have been explored. From the phase behaviour of a suitable system (i.e. MO/PLG/ethyl acetate/water), a route for formation of lipid/polymer composite particles has been deduced. Particles have been formed and distinct, water-swelling, lipid domains have been confirmed by characterization by means of confocal laser scanning probe microscopy (CLSM). The sample preparation process has been automated and a method based on using a robotic liquid handler has been developed. Phase diagrams have been determined by examination of macroscopic behaviours and the microstructures of the phases have been studied by small- and wide-angle X-ray scattering (L3, V2, Lα, L), nuclear magnetic resonance self-diffusion (L, L3), viscosimetry (L) and rheology (L). Several different theoretical models have been applied for interpretation of the results. For example, the swelling of the reversed bicontinuous cubic phases and the sponge phase have been modelled by applying the theory of infinite periodical minimal surfaces, the sponge phase has been shown to be bicontinuous according to the theory of interconnected rods and the phase behaviour of the polymer has been described by the Flory-Huggins theory. The main focus of this work (4/5) concerns phase studies in multicomponent systems from a physical-chemical point of view.

<p>Methods for performing large-scale parallel Molecular Dynamics(MD) simulations are investigated. A perspective on the field of parallel MD simulations is given. Hardware and software aspects are characterized and the interplay between the two is briefly discussed. </p><p>A method for performing <i>ab initio </i>MD is described; the method essentially recomputes the interaction potential at each time-step. It has been tested on a system of liquid water by comparing results with other simulation methods and experimental results. Different strategies for parallelization are explored.</p><p>Furthermore, data-parallel methods for short-range and long-range interactions on massively parallel platforms are described and compared. </p><p>Next, a method for treating electrostatic interactions in MD simulations is developed. It combines the traditional Ewald summation technique with the nonuniform Fast Fourier transform---ENUF for short. The method scales as <i>N log N</i>, where <i>N </i>is the number of charges in the system. ENUF has a behavior very similar to Ewald summation and can be easily and efficiently implemented in existing simulation programs.</p><p>Finally, an outlook is given and some directions for further developments are suggested.</p>

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.

Methods for performing large-scale parallel Molecular Dynamics(MD) simulations are investigated. A perspective on the field of parallel MD simulations is given. Hardware and software aspects are characterized and the interplay between the two is briefly discussed. A method for performing ab initio MD is described; the method essentially recomputes the interaction potential at each time-step. It has been tested on a system of liquid water by comparing results with other simulation methods and experimental results. Different strategies for parallelization are explored. Furthermore, data-parallel methods for short-range and long-range interactions on massively parallel platforms are described and compared. Next, a method for treating electrostatic interactions in MD simulations is developed. It combines the traditional Ewald summation technique with the nonuniform Fast Fourier transform---ENUF for short. The method scales as N log N, where N is the number of charges in the system. ENUF has a behavior very similar to Ewald summation and can be easily and efficiently implemented in existing simulation programs. Finally, an outlook is given and some directions for further developments are suggested.

The dye-sensitized solar cell (DSC) is a promising efficient low-cost molecular photovoltaic device. One of the key components in DSCs is the dye, as it is responsible for the capture of sunlight. State-of-the-art DSC devices, based on ruthenium dyes, show record efficiencies of 10-12 %. During the last decade, metal-free organic dyes have been extensively explored as sensitizers for DSC application. The use of organic dyes is particularly attractive as it enables easy structural modifications, due to fairly short synthetic routes and reduced material cost. Novel dye should in addition to the light-harvesting properties also be compatible with the DSC components. In this thesis, a series of new organic dyes are investigated, both when integrated in the DSC device and as individual components. The evaluation methods consisted of different electrochemical and photoelectrochemical techniques. Whereas the light-harvesting properties of the dyes were fairly easily improved, the behavior of the dye integrated in the DSC showed less predictable photovoltaic results. The dye series studied in Papers II and IV revealed that their dye energetics limited vital electron-transfer processes, the dye regeneration (Paper II) and injection quantum yield (Paper IV). Further, in Papers III-VI, it was observed that different dye structures seemed to alter the interfacial electron recombination with the electrolyte. In addition to the dye structure sterics, some organic dyes appear to enhance the interfacial recombination, possibly due to specific dye-redox acceptor interaction (Paper V). The impact of dye sterical modifications versus the use of coadsorbent was explored in Paper VI. The dye layer properties in the presence and absence of various coadsorbents were further investigated in Paper VII. The core of this thesis is the identification of the processes and properties limiting the performance of the DSC device, aiming at an overall understanding of the compatibility between the DSC components and novel organic dyes. / QC 20100730

The thesis concerns polyelectrolyte gels in contact with oppositely charged proteins and surfactant micelles, and includes of four papers (I-IV). In paper I confocal Raman spectroscopy was introduced as a method to trace micelles and investigate the structure of gel-surfactant complexes, in phase separated gel spheres. In paper II, the binding of surfactants to microspheres (~50-100 µm) was investigated by means of a micromanipulator-assisted microscopy method. The two surfactants were found to display qualitative difference respect to degree of swelling, surfactant distribution in the gels, and the difference is discussed in terms of absence/presence of hydrophobic attraction to the polyelectrolyte gel network. Kinetics of volume change in gels were analyzed. Aggregation numbers of micelles in polystyrenesulfonate (PSS) solutions, obtained from fluorescence quenching measurements, are presented. In paper III, phase behaviour, protein assembly and diffusion, was studied in PSS gel microspheres. Interpretation of results was aided by measurements of osmotic swelling of individual gel networks, and by combining the results with studies of protein diffusion in macroscopic (cm-sized) gel spheres. Complexes formed were further analyzed with small angle x-ray spectroscopy. In paper IV phase behaviour of mixed ionic/nonionic surfactant micelles is investigated in cm-sized gel spheres. The coexistence of three phases, the formation of dense shells in the bulk of the gels and other phenomena are described for the first time, and the results are presented along with discussion on the charge-density of spherical micelles and of  network induced hysteresis effects in gels. The composition and microstructure of phases are investigated by confocal Raman spectroscopy and small-angle x-ray scattering respectively. The results are interpreted with aid of highly detailed theoretical model calculations.