This thesis presents the study of organic layers covalently assembled onto carbon surfaces. As a result of their attachment, the properties of carbon surfaces were controllably adjusted so that these surfaces could be used for desired applications. In order that a wide range of properties were imparted onto the carbon surface, many different modifiers were attached and thoroughly characterised. Three applications that the modified carbon surfaces were used for were the subsequent coupling of molecular species, adsorption of protein and assembly of aldehyde/sulfate-functionalised polystyrene (PS) and citrate-capped gold nanoparticles (NPs). Finally, patterning of different organic layers at pre-determined spatially defined locations on the one carbon surface was also investigated. The carbon surfaces used in this work were glassy carbon (GC) and pyrolysed photoresist film (PPF) surfaces. For PPF, methods for the reproducible fabrication of electrochemically suitable surfaces were investigated. The properties of GC and PPF surfaces are very similar apart from the surface roughness. PPF has near atomic smoothness and has RMS roughness values that are approximately four times smaller than GC. The first series of modifier layers attached to the carbon surfaces was via the oxidation of seven different primary amines. The different layers allowed the modulation of the wettability of the surface. Both n-tridecylamine (TDA, monoamine) and 1,12-diaminododecane (DAD, diamine) are able to form multilayers. The stability of TDA and DAD layers were tested by scanning, soaking and sonicating the layers in different media. Changes in the layer were monitored by the probe response of ferrocene monocarboxylic acid (FCA). However, atomic force microscope (AFM) depth profiling experiments showed that changes in the probe response did not indicate cleavage of the covalently attached layer and mechanisms are proposed to account for the changes in the response of the probe. Surface concentrations of the amine modifiers were estimated by the coupling of an electrochemically active species, FCA and nitrobenzoyl chloride (NBC). The electrochemical reduction of the 4-nitrophenylethylamine (NPEA) layer in acid caused the layer to 'shrink'. Surface concentration estimates of NPEA from acid reduction of layers with different thicknesses suggested that only a limited fraction of the p-nitrophenyl groups were reduced in acid. However, in ACN (acetonitrile)/0.1 M [Bu4N]BF4 (tetrabutyl ammonium fluoroborate) the relationship between the concentration of electroactive surface groups and layer thickness was linear. The other series of modifiers that was attached to alter the surface properties was performed by the reduction of aryl diazonium salts. Subsequent coupling reactions of tetraethylene glycol diamine (TGD) to para methylene carboxylic acid phenyl (MCA) and NBC to electrochemically reduced para nitro phenyl (NPh) layers were carried out. Surface concentrations of NPh as estimated from reduction scans was higher when reduction was performed in ethanol/water compared to acid. Four peaks at N1s binding energies were observed in x-ray photoelectron spectroscopy (XPS) spectra for both acid and ethanol/water reduced layers. The ability of attached amine and aryl layers to modulate the adsorption of protein was investigated using fluorescently labelled protein, bovine serum albumin-fluorescein isothiocynate (BSA-FITC) and fluorescence microscopy. TGD, para methyl phenyl (MP), para hexyl phenyl (HP) and para polyethylene glycol phenyl (PEG)-modified GC surfaces promoted protein adsorption relative to as-prepared GC, whereas n-hexylamine (HA) and polyethylene glycol diamine (PGD) layers reduced protein adsorption. The assembly of two types of NPs, aldehyde/sulfate-functionalised PS and citrate-capped gold NPs, onto amine-containing modifiers layers was examined. Citrate-capped gold NPs were synthesised and characterised. The surface coverage of the gold NPs was controlled by using different modifiers of different chemical compositions, tuning the modification conditions and adjusting the immersion time, concentration and pH of gold NP solution. Approaches to creating patterns of modifiers in pre-determined spatially defined locations on GC and PPF surfaces using poly(dimethyl)siloxane (PDMS), poly(vinyl)alcohol (PVA) and thin metal films were investigated. With the "fill-in" approach using PDMS, the smallest pattern of modifiers was the parallel lines with a line width of 20 µm and straight edges and was created by performing electrochemistry in PDMS microchannels which has not been previously investigated. Visualisation techniques, based on optical and scanning electron microscopy, were demonstrated for the molecular patterns.

This thesis presents the study of organic layers covalently assembled onto carbon surfaces. As a result of their attachment, the properties of carbon surfaces were controllably adjusted so that these surfaces could be used for desired applications. In order that a wide range of properties were imparted onto the carbon surface, many different modifiers were attached and thoroughly characterised. Three applications that the modified carbon surfaces were used for were the subsequent coupling of molecular species, adsorption of protein and assembly of aldehyde/sulfate-functionalised polystyrene (PS) and citrate-capped gold nanoparticles (NPs). Finally, patterning of different organic layers at pre-determined spatially defined locations on the one carbon surface was also investigated. The carbon surfaces used in this work were glassy carbon (GC) and pyrolysed photoresist film (PPF) surfaces. For PPF, methods for the reproducible fabrication of electrochemically suitable surfaces were investigated. The properties of GC and PPF surfaces are very similar apart from the surface roughness. PPF has near atomic smoothness and has RMS roughness values that are approximately four times smaller than GC. The first series of modifier layers attached to the carbon surfaces was via the oxidation of seven different primary amines. The different layers allowed the modulation of the wettability of the surface. Both n-tridecylamine (TDA, monoamine) and 1,12-diaminododecane (DAD, diamine) are able to form multilayers. The stability of TDA and DAD layers were tested by scanning, soaking and sonicating the layers in different media. Changes in the layer were monitored by the probe response of ferrocene monocarboxylic acid (FCA). However, atomic force microscope (AFM) depth profiling experiments showed that changes in the probe response did not indicate cleavage of the covalently attached layer and mechanisms are proposed to account for the changes in the response of the probe. Surface concentrations of the amine modifiers were estimated by the coupling of an electrochemically active species, FCA and nitrobenzoyl chloride (NBC). The electrochemical reduction of the 4-nitrophenylethylamine (NPEA) layer in acid caused the layer to 'shrink'. Surface concentration estimates of NPEA from acid reduction of layers with different thicknesses suggested that only a limited fraction of the p-nitrophenyl groups were reduced in acid. However, in ACN (acetonitrile)/0.1 M [Bu4N]BF4 (tetrabutyl ammonium fluoroborate) the relationship between the concentration of electroactive surface groups and layer thickness was linear. The other series of modifiers that was attached to alter the surface properties was performed by the reduction of aryl diazonium salts. Subsequent coupling reactions of tetraethylene glycol diamine (TGD) to para methylene carboxylic acid phenyl (MCA) and NBC to electrochemically reduced para nitro phenyl (NPh) layers were carried out. Surface concentrations of NPh as estimated from reduction scans was higher when reduction was performed in ethanol/water compared to acid. Four peaks at N1s binding energies were observed in x-ray photoelectron spectroscopy (XPS) spectra for both acid and ethanol/water reduced layers. The ability of attached amine and aryl layers to modulate the adsorption of protein was investigated using fluorescently labelled protein, bovine serum albumin-fluorescein isothiocynate (BSA-FITC) and fluorescence microscopy. TGD, para methyl phenyl (MP), para hexyl phenyl (HP) and para polyethylene glycol phenyl (PEG)-modified GC surfaces promoted protein adsorption relative to as-prepared GC, whereas n-hexylamine (HA) and polyethylene glycol diamine (PGD) layers reduced protein adsorption. The assembly of two types of NPs, aldehyde/sulfate-functionalised PS and citrate-capped gold NPs, onto amine-containing modifiers layers was examined. Citrate-capped gold NPs were synthesised and characterised. The surface coverage of the gold NPs was controlled by using different modifiers of different chemical compositions, tuning the modification conditions and adjusting the immersion time, concentration and pH of gold NP solution. Approaches to creating patterns of modifiers in pre-determined spatially defined locations on GC and PPF surfaces using poly(dimethyl)siloxane (PDMS), poly(vinyl)alcohol (PVA) and thin metal films were investigated. With the "fill-in" approach using PDMS, the smallest pattern of modifiers was the parallel lines with a line width of 20 µm and straight edges and was created by performing electrochemistry in PDMS microchannels which has not been previously investigated. Visualisation techniques, based on optical and scanning electron microscopy, were demonstrated for the molecular patterns.

Le travail présenté dans cette thèse concerne la réalisation et l'étude d'un bio-hybride nanotubes/protéines photosynthétiques pour des applications en optoélectronique et potentiellement en photovoltaïque. En effet, les protéines photosynthétiques sont des supers colorants dont les propriétés optoélectroniques ont été optimisées par la nature. Nous avons donc décidé de vérifier la viabilité de l'intégration de ces protéines dans un dispositif électronique en utilisant les nanotubes de carbone comme nano-sonde des propriétés de la protéine. Au cours de nos travaux, le problème de la fabrication de transistors à effet de champ à base de nanotubes de carbone performants s'est posé. Pour résoudre ce problème, nous avons opté pour la fonctionnalisation chimique spécifique par un diazonium qui rassemble tous les pré-requis pour une potentielle application à grande échelle. En effet, la fonctionnalisation des nanotubes par un diazonium est sélective envers les nanotubes métalliques mais pas suffisamment pour pouvoir réaliser des séparations. Il était donc nécessaire d'augmenter cette sélectivité et pour cela, nous avons décidé d'étudier le mécanisme du couplage nanotube-diazonium qui était jusque là encore méconnu. A l'aide d'une étude cinétique complète, nous avons montré que la réaction passe par un mécanisme radicalaire en chaine. Parallèlement, nous avons identifié les intermédiaires radicalaires en les détectant soit directement par résonance de spin électronique soit indirectement par piégeage de radicaux. Et surtout, cette thèse détermine enfin l'origine précise de la sélectivité de cette réaction et donne les voies possibles d'amélioration. Grâce à l'expertise acquise lors de la compréhension du mécanisme, nous avons amélioré la sélectivité de cette réaction en utilisant une base de Lewis. En effet, l'ajout d'une base de Lewis permet de former un diazoester qui augmente significativement la sélectivité envers les nanotubes métalliques. Nous avons ensuite réalisé grâce à cette technique une grande quantité de transistors à effet de champ à base de nanotubes avec de bonnes modulations. De plus, cette méthode innovante a été protégée par un brevet. Enfin, concernant la photosensibilisation des nanotubes de carbone par une protéine photosynthétique, le photosystème I, des résultats prometteurs ont été obtenus. En effet, nous avons vu que la création photo-induite d'un moment dipolaire dans la protéine modifie les caractéristiques électriques du transistor à effet de champ. Les performances de la protéine, optimisées par la nature, permettent accroître la sensibilité optique d'un tel dispositif. Mais surtout, cette thèse montre que, malgré l'apparente fragilité de la protéine, il est possible d'intégrer une protéine photosynthétique à un dispositif électronique. En effet, même dans des conditions non optimales, l'effet optoélectronique c'est-à-dire l'activité de la protéine est un phénomène robuste dans le temps. Enfin, cette thèse ouvre la voie à l'intégration de protéines photosynthétiques dans des dispositifs électroniques ou photovoltaïques.

Le mercure est un élément reconnu pour sa toxicité pour les êtres humains, pouvant être notamment la cause de maladies neurologiques ou rénales une fois absorbé dans l'organisme. Il est rejeté dans l'environnement, et en particulier dans les eaux de surface, par des phénomènes naturels comme le volcanisme, mais également par le biais des activités humaines liées à l'industrie. Une fois rejeté, il est ingéré par la faune et la flore marine et bioaccumule tout le long de la chaîne alimentaire. Il est alors présent dans les espèces marines prédatrices dans des proportions importantes, mettant en danger la santé de ces espèces animales et exposant les êtres humains à des quantités importantes de mercure dans l'alimentation. La législation Européenne est très stricte en ce qui concerne les taux de mercure autorisés dans les eaux et se base sur des valeurs relevant de la trace voir de l'ultra trace. Les techniques actuelles permettant de détecter de si faibles doses sont efficaces mais possèdent de nombreux inconvénients tel que leur coût ou l'impossibilité de faire des mesures in situ. Les capteurs électrochimiques sont actuellement l'une des alternatives les plus prometteuses pour la détection de ce métal lourd en solution. L'objectif de ces travaux a donc été de mettre au point un capteur électrochimique basé sur la fonctionnalisation d'une électrode en carbone vitreux par des couches organiques et des nanoparticules d'or pour la détection du mercure. Deux types de couches organiques ont été utilisées et les interfaces ainsi développées caractérisées par voltammétrie cyclique et Microscopie Électronique à Balayage. Deux protocoles d'activation des nanoparticules ont été testés. Les performances des interfaces ont été évaluées au regard de la détection de traces de mercure, ainsi que leur stabilité au stockage. / Mercury is known for its toxicity on human beings, causing neurological and kidney diseases when absorbed in the body. It is rejected in the environment, and especially in surface waters, through natural processes like volcanism and human industrial activities. When present in water, it is ingested by marine plants and wildlife and bioaccumulates all along the food chain. It is then present in high proportions in marine predators, jeopardizing their health and exposing human beings to important mercury quantities in the food supply. The European legislation is very strict regarding to allowed mercury levels in waters, and is based on very low values, from traces to ultra traces. Current techniques able to detect such small doses are efficient but suffer from numerous drawbacks like their cost or the impossibility to use them for in situ measurements. Electrochemical sensors appear to be one of the most interesting alternatives for detection of this heavy metal in aqueous solution. The aim of this work was then to develop an electrochemical sensor based on the functionalization of a glassy carbon electrode with organic layers and gold nanoparticles for mercury detection. Two types of organic layers were used and the interfaces were characterised by using cyclic voltammetry and Scanning Electron Microscopy. Two different gold nanoparticles activation processes were tested. The interfaces performances were evaluated for detection of traces of mercury, as well as their storage stability.

Le développement de l'internet des objets au service des " Smart Cities " requière des sources d'énergie miniaturisées. Ces travaux concernent la préparation de micro- supercondensateurs à hautes performances par voies sèches. Des films minces de carbure de titane ont été déposés sur wafer de silicium par pulvérisation, puis convertis par chloration partielle en films de carbone dérivé de carbure microporeux adhérents. 205 mF.cm-2 / 410 F.cm-3 ont été délivrés en milieu 1M H2SO4, et 170 F.cm-3 dans un mélange de liquide ionique et d'acétonitrile en contrôlant la taille des micropores. Les micro-supercondensateurs préparés sur wafer par cette voie, compatible avec les techniques de microfabrication utilisées dans l'industrie des semi-conducteurs, surpassent les performances des micro-supercondensateurs sur puce rapportées jusqu'alors. Enfin, l'écriture laser d'oxydes commerciaux sur polyimide s'est avérée prometteuse pour la préparation de micro-supercondensateurs flexibles. / The development of the internet of things, serving the concept of Smart Cities, demands miniaturized energy storage devices. Electrochemical double layer capacitors (or so called EDLCs) are a good candidate as they can handle fast charge and discharge over 1,000,000 cycles. This work focuses on the preparation of high performance micro- supercapacitors using non wet processing routes. Titanium carbide (TiC) thin films were first deposited on silicon wafer by non-reactive DC magnetron sputtering. The deposition parameters, such as pressure and temperature, were optimized to prepare dense and thick TiC films. Then, microporous carbide-derived carbon (CDC) films with sub-nanometer pore diameters were obtained by removing the metallic atoms of the TiC films under chlorine atmosphere. Partial chlorination led to strongly adherent TiC-CDC films which could be used as electrode in aqueous electrolyte. Capacitance values of 205 mF.cm-2 / 410 F.cm-3 were delivered in 1M H2SO4, and were stable over 10,000 cycles. In order to increase the energy density of the on-chip electrodes, the pore sizes were increased to accommodate the larger ions of organic electrolytes, by performing chlorination at higher temperatures. The 700°C chlorinated TiC-CDC electrodes delivered up to 72 mF.cm-2 within a 3 V potential window in an ionic liquid / acetonitrile mixture. Another strategy consisted in the grafting of anthraquinone (AQ) molecules, which brought additional faradic contribution to the capacitive current. Electrochemical grafting by pulsed chronoamperometry allowed to double the TiC-CDC capacitance in aqueous electrolyte (1M KOH). On-chip CDC-based micro-supercapacitors were successfully prepared via reactive ion etching/ inductive coupled plasma procedure followed by chlorination. This non-wet processing route is fully compatible with the microfabrication techniques used in the semi-conductor industry, and the as-prepared micro-devices outperforms the current state of art of on-chip micro-supercapacitors. Aside, the preparation of flexible micro-supercapacitors was achieved via direct laser-writing, which provided a facile and scalable engineering with low cost. Ruthenium oxide (RuO2)-based interdigitated electrodes were obtained from laser-writing of a commercial RuO2.xH2O / cellulose acetate mixture spin-coated onto KaptonTM. Capacitance values of ~30 mF.cm-2 were recorded in 1M H2SO4 for the flexible device. This work open the way for the design of high performance micro-devices at a large scale.