As the Internet-of-everything continues diversifying, wireless nods sensors, wearables, and smart-objects will require mature technologies to harvest energy from the environment in which they are installed. Out of the many energy forms, solar and artificial light are constantly present and the utilization solar technologies including organic photovoltaics can provide advantages including flexibility, semitransparency, and lightweight. Additionally, the incredibly low environmental footprint and reduced manufacturing costs associated with solution processing can provide an edge for entry into the industrial and consumer markets. While the utilization of conjugated polymers and nonfullerenes elevated the efficiencies of organic photovoltaic for commercialization, increasing the technological readiness level requires the development of protocols to translate lab performance of state-the-art-materials to scalable manufacturing techniques that can be adapted for roll-to-roll processing. This dissertation demonstrates the full fabrication of high-performance OPV devices through techniques such as inkjet printing and slot-die coating. The development of ink formulation frameworks based on solvent engineering, rheological and interface properties, and solubility parameters sets the base for standardized high-yield processes with reduced environmental footprint in line with circular carbon initiatives. Moreover, the utilization of engineering strategies involving intrinsic properties of materials, device architectures, and integration enables the development of complex energy harvesting and sensing devices for potential utilization in agrivoltaics and biosensing.

In this work the methodology is developed to study spreading and penetration of a custom ink-jet ink formulation, containing hydrophobic cationic crystal violet dye, ethoxylated surfactant, and ink solvent marked by lithium salt. With a new technique utilizing Time-of-Flight Secondary Ion Mass Spectrometry imaging, the ink component distribution and its effect on print quality of uncoated and coated papers are evaluated. High spatially resolved images obtained by ToF-SIMS illustrate differentiation of individual ink components, with ink solvent spreading more than the dye in all paper samples. Uncoated papers show greater and more irregular spreading leading to poor edge definition and poor print quality. Large separation of the dye from the solvent in the vertical direction of multipurpose and photo glossy ink-jet paper suggests a step-wise progression of ink penetration: ink flows through a more porous structure in the x-direction before advancing to the next sublayer in the z-direction of paper.

In this work the methodology is developed to study spreading and penetration of a custom ink-jet ink formulation, containing hydrophobic cationic crystal violet dye, ethoxylated surfactant, and ink solvent marked by lithium salt. With a new technique utilizing Time-of-Flight Secondary Ion Mass Spectrometry imaging, the ink component distribution and its effect on print quality of uncoated and coated papers are evaluated. High spatially resolved images obtained by ToF-SIMS illustrate differentiation of individual ink components, with ink solvent spreading more than the dye in all paper samples. Uncoated papers show greater and more irregular spreading leading to poor edge definition and poor print quality. Large separation of the dye from the solvent in the vertical direction of multipurpose and photo glossy ink-jet paper suggests a step-wise progression of ink penetration: ink flows through a more porous structure in the x-direction before advancing to the next sublayer in the z-direction of paper.

Capteur électrochimique basé sur des matériaux carbonés fonctionnalisés, pour la détection de deux micropolluants faisant partie des substances prioritaires de la Directive Cadre européenne sur l’Eau (DCE2000/60/CE) : le plomb et l’anthracène. Les capteurs électrochimiques permettent d’atteindre des limites de détection et une sélectivité adéquates pour l’analyse de micropolluants dont les concentrations sont de l’ordredu μg/L, et sont simples d’utilisation pour des analyses in situ à moindre coût comparés aux appareils d’analyses conventionnels. Leur robustesse est un paramètre important afin de permettre des mesures en continu ou semi-continu dans les eaux. Cette thèse propose tout d’abord le développement du capteur pour la détection du plomb. La formulation d’une encre conductrice de carbone est étudiée pour la sérigraphie de ’électrode réceptrice, permettant ainsi de contrôler la composition de l’encre et d’étudier l’influence de la phase carbonée sur les propriétés électrocatalytiques des électrodes. La fonctionnalisation des électrodes par greffage électrochimique d’un sel de diazonium est également étudiée afin de maîtriser la sensibilité et la reproductibilité des électrodes greffées, en contrôlant l’épaisseur et la qualité des couches. Avec cet objectif, la fonctionnalisation dans un liquide ionique protique qui permet le contrôle de la monocouche en modulant la viscosité de ce milieu a été étudiée. Les électrodes greffées montrent des performances analytiques améliorées notamment en termes de répétabilité et de reproductibilité. Enfin ce travail de thèse porte également sur le développement du capteur pour la détection électrochimique de l’anthracène, molécule sans fonctions chimiques. Les électrodes sont, dans ce cas, fonctionnalisées par un polymère à empreinte moléculaire, matériau connu pour sa très grande sélectivité. Les performances de ce capteur, dont la sélectivité est basée uniquement sur le facteur de forme de la molécule, pour la détection de l’anthracène sont alors mises en évidence. / Electrochemical sensor based on functionalized carbon materials, for the detection of two micropollutants, lead and anthracene, which are among of the priority substances of the European Framework Directive on Water(DCE 2000/60 / EC). Electrochemical sensors allow to achieve detection limits and selectivities for the analysis of micropollutants whose concentrations are of the order of μg/L. They are easy to use for in situ analyzes at lower costs compared to those of the conventional analysis equipment. Their robustness is an important parameter in order to allow continuous or semi-continuous measurements in water. First of all, this thesis proposes the development of a sensor for lead detection. The conductive carbon ink formulation is studied for the screen-printing of the receiving electrode, thus allowing to control the ink composition and to study the influence of the carbon phase on the electrocatalytic properties of electrodes. Functionalization of electrodes by electrochemical grafting of a diazonium salt is also studied in order to control the sensitivity and reproducibility of grafted electrodes, by controlling the thickness and the quality of the layers. With this aim it has been studied the functionalization in a protic ionic liquid in order to allow the control of the monolayer bymodulating the viscosity of this medium. The grafted electrodes show improved analytical performance especially in terms of repeatability and reproducibility. Finally, this work reports the development of a sensor for the electrochemical detection of anthracene, a molecule without chemical functions. In this case, a molecularly imprinted polymer, a material known for its very high selectivity, functionalizes the electrodes.Having a selectivity is only based on the form factor of the molecule, the performance of the sensor developed for the detection of anthracene is also highlighted.

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