Philosophiae Doctor - PhD / Supercapacitors are charge-storage devices. Compared to batteries, they have higher power density, more excellent reversibility and longer cycle life. Therefore, supercapacitors have played an increasingly important role in the fields of power source especially in automotive applications, such as electric and hybrid electric vehicles. The higher power density of supercapacitors offers improved vehicle acceleration and the ability to recover more energy from regenerative breaking, since they can be charged and discharged at high current. Generally, the key for supercapacitors to achieve high specific power depends on the inherent properties and the surface areas of their electrode materials. Therefore, current research in the field of supercapacitors has been carried out with increased emphasis on the development of new electrode materials. Optimal novel synthesis of electrode materials for supercapacitor application in hybrid vehicles was accomplished with polypyrrole nanowires, manganese oxide and its carbon composites, ruthenium oxide and its carbon composites being the products. A set of structural and chemical parameters influencing the performance of synthesized electrode materials were identified. Parameters included crystallinity, particle size, particle size distribution, surface area, electrochemical activity. A large range of analytical tools were employed in characterizing the electrode materials of interest. High accuracy and precision in the quantitative and qualitative structural characterization of electrode materials collected by x-ray diffractometry, transmission electron microscopy, scanning electron microscopy and Fourier transform infra-red spectroscopy was demonstrated. N₂-physisorption produced surface area and pore size distribution data of high quality. Cyclic voltammetry, charge and discharge cycling, electron impedance spectroscopy were employed in the electrochemical characterization of the synthesized electrode materials and both qualitative and quantitative information obtained. The techniques were able to discriminate between various synthesized electrode materials and identify the highly electroactive materials. Preparation variables could be critically evaluated for the synthesis of electrode materials. The techniques were deemed to be applicable in discriminating high and low activity electrode materials based on their structural and chemical properties.

Developing novel electrode materials is a substantial issue to improve the performance of lithium ion batteries. In the present study, single phase Ti–Sn alloys with different Sn contents of 1 to 10 at% were used to fabricate Ti–Sn–O nanotubes via a straight-forward anodic oxidation step in an ethylene glycol-based solution containing NH4F. Various characterization tools such as SEM, EDXS, TEM, XPS and Raman spectroscopy were used to characterize the grown nanotube films. Our results reveal the successful formation of mixed TiO2/SnO2 nanotubes in the applied voltage range of 10–40 V. The as-formed nanotubes are amorphous and their dimensions are precisely controlled by tuning the formation voltage which turns Ti–Sn–O nanotubes into highly attractive materials for various applications. As an example, the Ti–Sn–O nanotubes offer promising properties as anode materials in lithium ion batteries. The electrochemical performance of the grown nanotubes was evaluated against a Li/Li+ electrode at a current density of 504 μA cm−2. The results demonstrate that TiO2/SnO2 nanotubes prepared at 40 V on a TiSn1 alloy substrate display an average 1.4 fold increase in areal capacity with excellent cycling stability over more than 400 cycles compared to the pure TiO2 nanotubes fabricated and tested under identical conditions. This electrode was tested at current densities of 50, 100, 252, 504 and 1008 μA cm−2 exhibiting average capacities of 780, 660, 490, and 405 μA cm−2 (i.e. 410, 345, 305 and 212 mA h g−1), respectively. The remarkably improved electrochemical performance is attributed to enhanced lithium ion diffusion which originates from the presence of SnO2 nanotubes and the high surface area of the mixed oxide tubes. The TiO2/SnO2 electrodes retain their original tubular structure after electrochemical cycling with only slight changes in their morphology.

Les accumulateurs Li-ion sont des systèmes de stockage électrochimique de l’énergie composés de deux électrodes, dans lesquelles les ions Li+ vont venir s’insérer réversiblement lors des cycles de charge et de décharge. Afin d’intégrer le domaine des véhicules électriques, leur densité d’énergie doit être augmentée pour apporter l’autonomie demandée. Ceci peut être réalisé en augmentant la d.d.p. entre les deux électrodes. Nous visons ici la synthèse de nouveaux matériaux polyanioniques d’électrode positive dans lesquels le lithium pourrait venir s’insérer à haut potentiel en faisant intervenir le couple Cu3+/Cu2+ (5,3 V vs Li+/Li). Parmi les phosphates de cuivre synthétisés, Li2CuP2O7 présente une oxydation non réversible à haut potentiel (> 5 V). Sa synthèse à basse température permet d’exacerber les réactions, en raison de la faible taille des particules obtenues ainsi que de la présence de carbone conducteur à leur surface, mais la phase s’avère instable à haut potentiel.En ce qui concerne les composés de type sulfate, une nouvelle phase Li4Cu4O2(SO4)4 est isolée, montrant une insertion réversible du lithium à une valeur moyenne de 4,7 V. Cependant, la capacité de ce matériau est très faible (15 mAh.g-1) et plusieurs substitutions chimiques avec du fluor, du magnésium ou du sodium sont étudiées dans le but d’augmenter la mobilité du lithium. / Li-ion batteries (LIBs) are energy storing electrochemical devices composed of two electrodes, in which Li+ ions are reversibly inserted during charge and discharge cycles. Their use in electric vehicles relies on the increase of their energy density, to provide enough autonomy. This can be reached by increasing the cell d.d.p. We thus aim the synthesis of new positive electrode polyanionic materials, in which lithium could be inserted at high potential, using the Cu3+/Cu2+ couple’s activity (5,3 V vs Li+/Li). Among the synthesized copper phosphates, Li2CuP2O7 presents a non-reversible oxidation at high potential (>5 V). Its low temperature synthesis intensifies the reaction, due to the smaller particle size achieved as well as the presence of a conductive carbon coating, but the phase is instable at high potential. Concerning sulfate-type compounds, a new phase Li4Cu4O2(SO4)4 is isolated, showing a reversible lithium insertion at an average value of 4.7 V. Nevertheless, its capacity is very low (15 mAh.g-1) and various chemical substitutions with fluorine, magnesium or sodium are attempted to increase lithium’s mobility.

L’étude traite la réalisation et la validation d’un microréacteur destiné à l’électrosynthèse organique. Le système électrochimique modèle est l’oxydation du 4-méthylanisole en 4-méthoxy-benzaldéhyde-diméthylacétal. La simulation du comportement théorique d’un réacteur électrochimique travaillant à haute conversion pour l’oxydation du 4-méthylanisole a permis de déterminer les conditions pour lesquelles le réacteur apporte un meilleur rendement. Les essais expérimentaux effectués sur un microréacteur travaillant en continu et à haute conversion ont montré l’influence de la concentration de l’électrolyte support KF sur le rendement de la réaction. Pour un débit optimal de 0,2 ml min-1, une concentration initiale en réactif de 0,1 M et en appliquant un courant égal à 85% du courant théorique nécessaire à convertir totalement le réactif en une seule passe dans la cellule, la sélectivité atteint 86% (pour une conversion de 95%), alors qu’elle n’est que de 68% dans le procédé BASF. / This work concerns the realization and the validation of a microstructured reactor for organic electrosynthesis. The electrochemical reaction is the oxidation of 4-methylanisole to 4-methoxy-benzaldehyde-dimethylacetal. Theoretical behaviour simulations of high conversion thin-gap flow cell of the 4-methylanisole show conditions for which the reactor has best productivity. The experimental tests carried out on high conversion thin-gap flow reactor showed the influence of the supporting electrolyte (KF) concentration on the reaction yield. For an optimal flow rate of 0.2 ml min-1, an initial reagent concentration of 0.1 M and a current equal to 85% of the theoretical current necessary to convert all reagent, it is possible to reach selectivity of 86% with single pass high conversion (95%) , whereas selectivity on BASF process doesn’t exceed 68%.

Recent development in portable electronics and electric vehicles have increased the demand for high performance lithium ion batteries. However, it is still challenging to produce high energy and high power lithium ion batteries. The major objective of this research is to fabricate advanced electrode materials with enhanced power density and energy density. Porous Li4Ti5O12 (LTO) and its nanocomposites (with Si and reduced graphene oxide (rGO)) synthesized by electrostatic spray deposition (ESD) technique were mainly studied and promising electrochemical performance was achieved. In chapter 3, porous LTO thin film electrode was synthesized by ESD to solve the low energy density and low power density issues by providing good ionic and electronic conductivities. Electrochemical test results showed that it had a large specific capacity of 357 mAh g-1 at 0.15 A g-1, which was even higher than its theoretical capacity. It also exhibited very high rate capability of 98 mAh g-1 at 6 A g-1. The improved electrochemical performance was due to the advantage of ESD generated porous structures. In order to further enhance the power density of LTO, ESD derived LTO/rGO composite electrodes were studied in chapter 4. In chapter 5, high energy density component Si was introduced viii into LTO composite. The synergistic effect between commercial LTO and Si powder was studied. Then, ESD derived LTO/Si/rGO composite was prepared and evaluated. At 0.15 A g-1, a stable capacity of 624 mAh g-1 was observed, which was much higher than the capacities of LTO and LTO/rGO electrodes. In addition, effect of activation process on electrochemical performance of carbon nanofibers (ACNFs) and feasibility of ion intercalation into 2D MMT montmorillonite clay (MMT) were studied and discussed in chapter 6. In summary, we have successfully synthesized various LTO based electrodes by ESD. Both high energy and high power density were achieved as compared to commercial LTO electrode. Through electrochemical characterization and charge storage distribution analysis, origins of the high rate capability were proposed. This work demonstrates ESD as a powerful tool for fabricating high performance porous structures and nanocomposite electrode materials.

Lors d’infections, l'identification rapide des micro-organismes est cruciale pour améliorer la prise en charge du patient et mieux contrôler l'usage des antibiotiques. L’électrochimie présente plusieurs avantages pour les tests rapides : elle permet des analyses in situ, faciles et peu chères dans la plupart des liquides. Son utilisation pour l’identification bactérienne est récente et provient de la découverte de molécules donnant de forts signaux redox dans le surnageant de bactéries du genre Pseudomonas.Cette thèse s’intéresse à l’analyse de surnageants de la bactérie Pseudomonas aeruginosa, 4e cause de maladies nosocomiales en Europe. Tout d’abord, l’intérêt de l’analyse électrochimique de surnageants de culture dans une visée d’identification a été évalué. Pour cela, après l’étude de 4 potentiels biomarqueurs de la présence de cette bactérie en solutions modèles, l’analyse électrochimiques de surnageant de plusieurs souches P. aeruginosa a été effectuée. Les résultats obtenus sont prometteurs. Ils mettent en évidence une signature électrochimique complexe et souche-dépendante du surnageant.La suite de la thèse s’est intéressée à l’amplification de la détection électrochimique grâce à l’utilisation du polymère conducteur PEDOT:PSS. Il a été choisi pour ses bonnes propriétés électrochimiques, sa biocompatibilité et sa facilité de mise en forme. Il a tout d’abord été utilisé sous forme de films minces pour confirmer son pouvoir d’amplification. Une électrode 3D a ensuite été fabriquée par lyophilisation. L’utilisation de ce type d’électrode permet d’amplifier encore la détection en augmentant la surface d’échange mais aussi en confinant les bactéries dans l'électrode. / During infections, microorganisms fast identification is critical to improve patient treatment and to better manage antibiotics use. Electrochemistry exhibits several advantages for rapid diagnostic: it enables easy, cheap and in situ analysis in most liquids. Its use for bacterial identification is recent and comes from the discovery of molecules giving strong redox signals in the bacterial supernatant of the Pseudomonas genus.This thesis focuses on the supernatants analysis of the bacterium Pseudomonas aeruginosa. This bacteria is the fourth cause of nosocomial infections in Europe. First, the interest of supernatants electrochemical analysis for identification was evaluated. For this, after the study of four redox biomarkers of this bacterium in model solutions, supernatant electrochemical analysis of several strains of P. aeruginosa was performed. The results are promising. They highlight a complex strain-dependant electrochemical signature of the supernatant.Following, we focused in the amplification of the electrochemical detection through the use of the conductive polymer PEDOT: PSS. This polymer was chosen for its good electrochemical properties, its biocompatibility and its easy shaping. It was first used as a thin films to confirm its amplification power through biomarker adsorption. Then, a 3D electrode was made by freeze drying. The use of this type of electrode can further amplify the detection by increasing the exchange surface as well as confining the bacteria in the electrode.

There is an increasing need for tuneable spectrally pure semiconductor laser sources as well as broadband and polarization insensitive semiconductor optical amplifiers based on the InGaASP/InP material system, to be monolithically integrated with other active and passive components in a photonic integrated circuit. This thesis aims to contribute to finding a solution through modelling, experimental characterization and design improvements. In this thesis we have analyzed laterally-coupled distributed feedback (LC-DFB) lasers. These lasers have the gratings etched directly out of the ridge sidewalls thus lowering the cost associated with the re-growth process required if the gratings were otherwise embedded above the active region. The performance characteristics are analyzed for the LC-DFB lasers partitioned into 1-, 2-, and 3-, electrodes with individual bias control at various operating temperatures. The laser exhibits a stable single mode emission at 1560 nm with a current tuning rate of ~14 pm/mA for a tuning of 2.25 nm. The side modes are highly suppressed with a maximum side-mode suppression ratio of 58 dB. The light-current characteristics show a minimum 40 mA threshold current, and power saturation occurring at higher injection currents. The linewidth characteristics show a minimum Lorentzian linewidth of 210 kHz under free-running and further linewidth reduction under feedback operation. The multi-electrode LC-DFB laser devices under appropriate and selective driving conditions exhibit a flat frequency modulation response from 0 to above 300 MHz. The multi-electrode configuration can thus be further exploited for certain requirements. Simulation results and design improvements are also presented. The experimental characterization of semiconductor optical amplifier (SOA) and Fabry-Perot (FP) laser operating in the E-band are also presented. For the SOA, the linear vertical and horizontal states of polarization corresponding to the transverse electric (TE) and transverse magnetic (TM) modes were considered. For various input power and bias, performance characteristics shows a peak gain of 21 dBm at 1360 nm, gain bandwidth of 60 nm and polarization sensitivity of under 3 dB obtained for the entire wavelength range analyzed from 1340 to 1440 nm. The analysis presented in this thesis show good results with room for improvement in future designs.

Il existe un réel besoin de développer des matériaux et des technologies avancés pour améliorer l’interface avec le cerveau humain. De tels enregistrements électrophysiologiques sont nécessaires pour des fins diagnostiques ou dans des domaines innovants tels que l’interface homme/machine. Les dispositifs issus de l’électronique organique représentent des alternatives prometteuses grâce à leurs propriétés mécaniques et leur biocompatibilité. L’utilisation de polymères conducteurs ouvre la voie vers une nouvelle interface avec le milieu biologique. Ce travail présente un procédé de fabrication innovant permettant d’intégrer le polymère conducteur PEDOT:PSS sur des électrodes sèches pour une application à l’électroencéphalographie (EEG). L’étape suivante consiste en l’utilisation d’un dispositif actif tel que le transistor organique électrochimique (OECT) afin de profiter de l’amplification locale qu’il permet. Cette dernière est extrêmement importante dans le cas de la neurophysiologie, domaine dans lequel l’amplitude des signaux enregistrés est très basse. En ce sens, l’intégration d’OECTs à des dispositifs d’enregistrement de signaux neuronaux a montré un bien supérieur rapport signal / bruit (SNR) en comparaison à des électrodes conventionnelles. La bioélectronique est un domaine innovant à applications variées. Cette thèse présente la conception et la validation par l’application de dispositifs organiques dans le domaine des neurosciences. D’autres progrès dans les domaines du diagnostic, des biocapteurs, ou de la distribution de médicaments pavent la voie pour de nouvelles applications dans l’agroalimentaire ou encore la qualité de l’eau ou de l’air. / There is a tremendous need for developing advanced materials technologies for interfacing with brain and record neural activity. Such electrophysiological recordings are necessary for diagnostic purposes and brain/machine interfaces. Among the existing technologies, organic electronic devices constitute a promising candidate because of their mechanical flexibility and biocompatibility. The use of conducting polymers, which allow both ionic and electronic transport, allows new modes for interfacing with the biological milieu. This work presents an innovative process to incorporate the conducting polymer poly(3,4-Ethylenedioxythiophene: poly(styrene sulfonate) (PEDOT:PSS) onto electrodes for applications in electroencephalography (EEG). A step beyond conducting polymer electrodes is provided by the Organic Electrochemical Transistor (OECT). The primary advantage of using active devices is the local amplification they provide. This local amplification becomes extremely important in the case of electrophysiological signals, for which the amplitude is very low. The use of the OECT for various electrophysiological measurements is presented, done for clinical purposes like ECG or EEG, for new marketing studies like EOG, and for more fundamental neurological applications, like the recording in vitro of neuronal unitary activity. Bioelectronics is an inspiring field with broad scope. This thesis deals with applications of organic electronic devices in neuroscience. Other applications in diagnostics, biosensing, or drug delivery will offer huge opportunities for food safety, pollution control or even environmental applications.

The aim of this research is to explore the integration of ad hoc and mobile sensors into a conventional Electrical Resistance Tomography (ERT) system. This is motivated by the desire to improve the spatial resolution of 3D reconstructed images that are produced using ERT. The feasibility of two approaches, referred to as the Extended Electrical Tomography (EET) and Augmented Electrical Tomography (AET) are considered. The approaches are characterized according to the functionality of the sensors on the ad hoc 'pills'. This thesis utilizes spectral and numerical analysis techniques, with the goal of providing a better understanding of reconstruction limitations, including quality of measurements, sensitivity levels and spatial resolution. These techniques are applied such that an objective evaluation can be made, without having to depend heavily on visual inspection of a selection of reconstructed images when evaluating the performance of different set-ups. In EET, the sensors on the pills are used as part of the ERT electrode system. Localized voltage differences are measured on a pair of electrodes that are located on an ad hoc pill. This extends the number of measurements per data set and provides information that was previously unobtainable using conventional electrode arrangements. A standalone voltage measurement system is used to acquire measurements that are taken using the internal electrodes. The system mimics the situation that is envisaged for a wireless pill, specifically that it has a floating ground and is battery-powered. For the present exploratory purposes, the electronic hardware is located remotely and the measured signal is transmitted to the PC through a cable. The instrumentation and data acquisition circuits are separated through opto-isolators which essentially isolates both systems. Using a single pill located in the centre of a vessel furnished with 16 electrodes arranged in a single plane, spectral analysis indicates that 15 of the 16 extended measurements acquired using the adjacent current injection strategy are unique. Improvement is observed for both the sensitivity and spatial resolution for the voxels in the vicinity of the ad hoc pill when comparing the EET approach with the conventional ERT approach. This shows the benefit of the EET approach. However, visual inspection of reconstructed images reveals no apparent difference between images produced using a regular and extended dataset. Similar studies are conducted for cases considering the opposite strategy, different position and orientation of the pill, and the effect of using multiple pills. In AET, the sensors on the ad hoc pills are used as conductivity probes. Localized conductivity measurements provide conductivity values of the voxels in a discretized mesh of the vessel, which reduces the number of unknowns to be solved during reconstruction. The measurements are incorporated into the inverse solver as prior information. The Gauss-Newton algorithm is chosen for implementation of this approach because of its non-linear nature. Little improvement is seen with the inclusion of one localized conductivity measurement. The effect on the neighbouring voxels is insignificant and there is a lack of control over how the augmented measurement influences the solution of its neighbouring voxels. This is the first time that measurements using ad hoc and 'wireless' sensors within the region of interest have been incorporated into an electrical tomography system.

The focus of this project was to investigate the use of interdigitated electrodes (IDEs) as impedimetric ion-selective chemical sensors for the determination of several important analytes found within a freshwater aquarium. The overall aim of this research was to work towards a prototype sensing device that could eventually be developed into a commercial product for sale to aquarium owners. Polyvinyl chloride and sol-gels containing commercially-available ionophores for four aquarium-significant ions (NH4+, NO2-, NO3- and pH) were prepared and investigated for use within polymeric ion-selective membranes. Three separate IDE transducers were produced using either photolithography or screen-printing microfabrication techniques. A sinusoidal voltage was applied to the IDEs and an LCR meter was used to measure changes in the conductance and capacitance of the ion-selective membrane layer deposited over the electrode digits. Each ionophore, when tested within potentiometric ion-selective electrodes (ISEs), was found to be suitable for further investigation within IDE devices. Sol-gels were investigated as a potential membrane material for a coated wire electrode; however, poor response characteristics were observed. An IDE sensor fabricated in-house using lift-off photolithography and spin-coated with a polymeric membrane was found to produce non-selective responses caused by changes in the conductivity of the test solution. IDE devices with reduced geometric parameters were purchased and coated with a selective polymeric membrane. When the membrane was spin-coated, non-selective responses were observed; therefore, drop-coating of the membrane material was investigated. This initially resulted in an unacceptably long response time; however, this effect was reduced by decreasing the membrane solution viscosity prior to drop-coating. A fully-screen printed carbon IDE device was fabricated by incorporating the ionophore into a support matrix based on a commercial dielectric paste. Matrix interferences to the sensor response were reduced by printing ‘build-up’ layers over the sensing area prior to the ion-selective membrane. Two novel routes for monitoring the water quality of an aquarium, using IDE sensors fabricated by either photolithography or screen-printing, have been demonstrated. Due to the commercial aspect of this project, it is important to consider the final cost of producing these sensors. Both of the techniques used to produce ion-selective sensors require further experimentation to optimise the sensor response, prior to integration within a multi-analyte sensing prototype.