[Truncated abstract] The sale of fraudulent South-East Asian ceramics constitutes a large proportion of the illegal artefact and antique trade and threatens to undermine the legitimate international market. The sophistication and skill of forgers has reached a level where, using traditional appraisal by eye and hand, even the most experienced specialist is often unable to distinguish between a genuine and fraudulent piece. In addition, the current scientific method of authentication used by the international antiques and art industry, thermoluminescence (TL) dating, carries severe limitations. The technique has an error margin of +/-20 % and requires the removal of a significant piece of the sample being tested, which decreases both the monetary and cultural value of the artefact. Of more concern, forgers have developed methods which produce false test results and which appear to corroborate false claims for the age of artefacts. Consequently, the use of TL dating for authentication of ancient ceramics, especially those of South-East Asian origin, has now come into serious question. The most suitable method for authenticating ceramics is through provenance establishment. Studies published in the literature have investigated the application of various analytical techniques to provide this information for ceramic wares and have highlighted their potential to be used for provenance establishment. However, the value of each of these techniques is limited rendering them generally unsuitable for practical use in the international antiques and art world to authenticate high-value South-East Asian artefacts. Consequently, there is a desperate need for the development of a robust, accurate and non-destructive method which can be practically applied in the industry to authenticate South-East Asian ceramics. ... Minor variations between spectral profiles of artefacts produced in the same country have also been used to further provenance artefacts to a specific production region or kiln site. The results of analyses have been compiled to form a unique reference database which can be added to in the future and used by experts internationally. Adaptation of the developed sampling and analytical methodologies to allow in-situ sampling of large artefacts using the

Cellular therapy is emerging as a clinically viable strategy in the field of solid organ transplantation, where it is expected to reduce the dependency on conventional immunosuppression. This has produced a demand for highly sensitive methods to monitor the persistence and tissue distribution of administered cells in vivo. However, tracking cells presents significant challenges. In many cases transplanted cells are autologous with the immune system of the transplant recipient, and hence are invisible to typical methods of detection. To enable their differentiation, the cells must be labelled with a suitable, non-toxic and long lifetime label, prior to their administration to patients. In addition, administered cells represent only a small fraction of the recipient's endogenous cells, which necessitates the use of an extremely sensitive detection method. Laser ablation – inductively coupled plasma – mass spectrometry (LA-ICP-MS) is an exquisitely sensitive analytical technique, capable of imaging trace elements in complex samples, at high spatial resolution.

[pt] Norfloxacina (NFX) é um antibiótico fluorescente de amplo espectro bacteriológico, membro da família das fluorquinolonas (FQs). A interação das FQs com íons metálicos pode incrementar a ação bactericida e agir contra a resistência das bactérias frente aos antibióticos. Diversos exemplos de complexos mistos de norfloxacina e Cu(II) podem ser encontrados na literatura. A compreensão dos mecanismos moleculares de interação desses antibióticos com os diferentes componentes das células e com nanopartículas de ouro, como transportadores do fármaco, é extremamente importante. Para entender essas interações, neste trabalho utilizamos diferentes técnicas espectroscópicas, como espectroscopia de fluorescência estacionária e resolvida no tempo, absorção de luz UV-Visível e ressonância paramagnética eletrônica (RPE). A interação de NFX e do complexo ternário Cu(II):L:NFX, onde o ligante L é a 1,10-fenantrolina (Phen) ou 2,2-bipiridina (Bipy), com micelas e lipossomas unilamelares pequenos de fosfatidilcolina de ovo (PC) foi estudada usando espectroscopia de fluorescência em estado estacionário e resolvida no tempo. Foi estudada a estabilidade dos complexos ternários formados em micelas. Foram obtidas constantes de estabilidade no interior de micelas de SDS, as quais mostraram valores muito maiores do que em tampão. Já os espectros de RPE deram maiores detalhes sobre a estrutura dos complexos e confirmaram a formação do complexo ternário dentro das micelas. Foram estudadas as interações de FQs e seus complexos de cobre com lipossomas de PC preparados com diferentes densidades superficiais de carga elétrica negativa. No estudo da interação de FQs com nanopartículas de ouro sintetizadas por ablação a laser (nanocompósitos, AuNCs), NFX mostrou maiores mudanças, tanto na absorbância como na fluorescência, do que as FQs ciprofloxacina (CFX) e levofloxacina (LFX). Os resultados sugerem mudanças no índice de refração na superfície dos AuNCs, por associação com o fármaco e/ou formação de aglomerados como resultado da interação. Observou-se também uma supressão lenta, porém significativa, na fluorescência da NFX, sem mudança na posição do pico, indicando que NFX mantém o seu estado inicial de protonação ligando-se à superfície dos AuNCs. Também foi observada a liberação de FQs ligadas à superfície de AuNPs mediante substituição por tióis, que ocasiona recuperação parcial da fluorescência da fluorquinolona. Por último, como o surfactante aniônico SDS se mostrou promissor na interação com NFX, em comparação com surfactantes catiônicos e neutros, e como os AuNCs são estáveis em SDS, estudamos a interação de NFX com AuNCs sintetizados em presença de SDS e, para comparação, com AuNCs colocados em solução de SDS após a síntese. / [en] Norfloxacin (NFX) is a fluorescent antibiotic of broad bacteriological spectrum, member of the fluoroquinolone (FQ) family. The interaction of FQs with metal ions can increase the bactericidal action and act against antibiotics bacterial resistance. Several examples of mixed-ligand norfloxacin Cu (II) complexes can be found in the literature. Understanding the molecular mechanisms of interaction of these antibiotics with different cell components and with gold nanoparticles as drug transporters is extremely important. To clarify these interactions, we used different spectroscopic techniques, such as steady-state and time-resolved fluorescence spectroscopy, UV-Visible light absorption, and electron paramagnetic resonance (EPR). The interaction of NFX and the ternary complex Cu(II):L:NFX, where the L is the ligand 1,10-phenanthroline (Phen) or 2,2-bipyridine (Bipy), with micelles and small unilamellar liposomes of egg phosphatidylcholine (PC) was studied using steady-state and time-resolved fluorescence spectroscopy. The stability of the ternary complexes formed in micelles was studied, and stability constants were obtained inside SDS micelles, which showed values much larger than in buffer. The EPR spectra gave further details on the structure of the complexes, and confirmed the formation of the ternary complex inside the micelles. The interactions of FQs and their copper complexes with PC liposomes prepared with different surface densities of negative electrical charge were studied. In the study of the interaction of FQs with gold nanoparticles synthesized by laser ablation (nanocomposites, AuNCs), NFX showed greater changes than FQs ciprofloxacin (CFX) and levofloxacin (LFX) in both absorbance and fluorescence. The results suggest changes in the surface refractive index of the AuNCs and/or cluster formation, as result of the interaction with the drug. A slow but significant quenching of NFX fluorescence was also observed, with no change in peak position, indicating that NFX maintains its initial state of protonation by binding to the surface of the AuNCs. Release of FQs attached to the surface of AuNCs by thiols has also been observed, which causes partial recovery of FQ fluorescence. Finally, as the anionic surfactant SDS showed to be promising in the interaction with NFX, compared to cationic and neutral surfactants, and because the AuNCs are stable in SDS, we studied the interaction of NFX with AuNCs synthesized in the presence of SDS and, for comparison, with AuNCs placed in SDS solution after synthesis.

Le cadmium (Cd) est un élément toxique. Les activités humaines ont contaminé un large éventail de sols agricoles. L'exposition de l'homme au Cd se fait majoritairement par voie alimentaire, notamment à travers les aliments de base tels que les céréales. Le blé dur accumule naturellement plus de Cd dans ses grains que les autres céréales. Une fraction significative de la production française de blé dur dépasse la limite réglementaire européenne fixée pour le Cd. Il est donc nécessaire de réduire l'accumulation de Cd dans les grains de blé dur. Cette thèse portant sur l'écophysiologie de l'allocation du Cd aux grains chez le blé dur a pour ambition d'aider au développement de stratégies agronomiques visant à réduire le niveau de contamination en Cd du blé dur et de ses dérivés.Dans un premier temps, nous avons étudié la relation entre la structure de la biomasse aérienne et l'allocation de Cd aux grains. Nous avons fait l'hypothèse que la répartition de la biomasse aérienne entre pailles et grains était un facteur déterminant de l'allocation du Cd aux grains. Huit cultivars Français de blé dur - de hauteur de paille contrastée - ont été cultivés en présence de Cd. Comme prévu, le principal facteur expliquant la différence d'accumulation de Cd dans le grain était la structure de la biomasse aérienne. Les cultivars allouant une plus grande proportion de leur biomasse aérienne aux pailles - autrement dit les cultivars à longue tige - avaient tendance à accumuler moins de Cd dans leurs grains, car les tiges et les feuilles sont des puits de Cd en concurrence avec les grains lors de leur remplissage.Les minéraux importés dans les grains proviennent soit de leur absorption directe par la racine après l'anthèse, soit de leur remobilisation depuis des réserves constituées avant l'anthèse. La deuxième partie de ce travail a été consacrée à déterminer l'importance quantitative de ces deux « sources » pour le Cd chez le blé dur, et de préciser comment leur contribution relative varie entre cultivars et avec le niveau d'azote (N). Le traçage isotopique a été utilisé pour suivre le flux de Cd absorbé après l'anthèse. L'impact du niveau d'azote a été testé en privant la moitié des plantes de N après l'anthèse, sur deux cultivars montrant une capacité contrastée à accumuler le Cd dans leurs grains. La contribution de la remobilisation a été estimé à 50%, ce qui signifie que la moitié du Cd accumulé dans les grains provenait du Cd prélevé après l'anthèse. Le Cd a été remobilisé à partir des tiges, peut-être des racines, mais pas à partir des feuilles. La contribution de la remobilisation n'a pas varié entre les deux cultivars, de sorte qu'aucune relation entre la « source » de Cd et son niveau d'accumulation dans le grain n'a été mise en évidence. La privation d'azote en phase de remplissage a stimulé la remobilisation de N sans affecter celle de Cd, ce qui suggère que la remobilisation de Cd est un processus indépendant de la sénescence.En troisième lieu, nous avons examiné comment les caractéristiques d'allocation de Cd aux grains étaient modulées par le niveau d'exposition au Cd. [...]Enfin, nous nous sommes intéressés à la localisation de Cd dans le grain. [...] Ce travail a fourni la première carte de localisation de Cd dans un grain de blé dur. La distribution de Cd s'est caractérisée par une forte accumulation de Cd dans le sillon et par une dissémination dans l'endosperme amylacé plus prononcée que celle de Fe et Zn. / Cadmium (Cd) is a toxic element. Human activities have contaminated a wide range of agricultural soils. Most of Cd entering human bodies is through the dietary intake, and especially through staple food like cereals. Durum wheat naturally accumulates more Cd in its grains than other cereals. A significant fraction of the French durum wheat production has been found to exceed the European regulatory limit set for Cd. There is thus a need to reduce the accumulation of Cd in durum wheat grains. This thesis is dedicated to a better understanding of the ecophysiology of Cd allocation to the grains in durum wheat, with the ambition of helping to find agronomic strategies to reduce the Cd contamination level of durum wheat products.In first, we investigated the relationship between the aboveground partitioning of Cd and the shoot allometry. We hypothesized that the partitioning of shoot biomass between grains and straws is a driver of the allocation of Cd to the grains. Eight French durum wheat cultivars differing in their stem height were grown in presence of Cd. As expected, the main factor explaining the difference in their grain Cd was the shoot biomass partitioning. Cultivars allocating a higher proportion of their aerial biomass to the straws, i.e. long-stem cultivars, tended to accumulate less Cd in their grains because stems and leaves are sinks for Cd in competition with developing grains.Minerals imported into cereal grains originate from either direct post-anthesis root uptake or from the remobilization of pre-anthesis stores. The second part of this work was dedicated to determine the quantitative importance of these two pathways for Cd in durum wheat, and how their relative contribution vary between cultivars and with the level of nitrogen (N) supply. Stable isotopic labelling was used to trace the flux of Cd taken up post-anthesis. The impact of N supply was tested by depriving half of the plants of N after anthesis, in two cultivars showing a contrasted ability to accumulate Cd in their grains. The contribution of Cd remobilization was around 50%, which means that half of Cd in grains originated from Cd taken up pre-anthesis. Cd was remobilized from stems, possibly from roots, but not from leaves. The contribution of remobilization did not vary between the two cultivars so that no relationship between the pathway and the level of accumulation of Cd in grain was evidenced. Post-anthesis N deprivation triggered the remobilization of N without affecting that of Cd, which suggests that Cd remobilization is a senescent-independent process.In third, we investigated how the characteristics of Cd allocation to the grains was affected by the level of Cd exposure. [...]In last, we focused on how Cd was distributed within durum wheat grains. [...] This work provided the first map of Cd localization in durum wheat grains. Cd distribution was characterized by a strong accumulation of Cd in the crease and by a non-negligible dissemination in the starchy endosperm, as compared to Fe and Zn.

Une cellule photovoltaïque organique (OPV) consiste en un empilement de couches minces et comporte une électrode transparente, constituée le plus souvent par une couche mince d’oxyde d’indium dopé à l’étain (ITO). Des matériaux alternatifs sans indium, déposables par voie liquide à l’air ambiant, et sur de grandes surfaces souples plus adaptées à la filière OPV, sont actuellement l’objet d’un grand nombre de recherches. Les nanofils d’argent (Ag NWs) représentent un sérieux candidat pour remplacer l’ITO et sont l’objet de ce travail de thèse. Une méthode de dépôt des Ag NWs par spray à air sur des substrats de PET a été développée en vue de réaliser des films conducteurs et transparents sur une grande surface souple. Puis ces électrodes transparentes ont été intégrées dans des cellules OPV sur substrat souple avec des rendements comparables à l’ITO. Les dépôts par voie liquide ont été privilégiés (spray-coating, Dr Blade), excepté pour l’électrode supérieure en argent, évaporée sous vide. Enfin les cellules ont été interconnectées en série pour former un module OPV, plus efficace en termes de puissance électrique délivrée. Une étude sur l’ablation sélective de couches de l’empilement OPV par laser est également présentée pour la fabrication de modules. / An organic photovoltaic (OPV) cell consists of a thin-layer stack which includes a transparent electrode, usually made of indium tin-doped oxide (ITO). Alternative, indium-free materials, deposited in air with a wet deposition process on large, flexible substrates that are more compatible with the OPV field are currently widely investigated. Silver nanowires (Ag NWs), which represent a serious candidate to replace ITO, are the subject of this thesis. In this work a method to deposit Ag NWs on PET substrates by air spray-coating has been developed : efficient patterned conductive and transparent coatings could be processed on a large, flexible substrate. This transparent electrode was then integrated in flexible and large area OPV cells, with efficiencies comparable to ITO. Wet deposition techniques were preferred except for the silver top electrode, evaporated under vacuum. OPV cells were eventually interconnected in series in order to make an OPV module, delivering a higher electrical output. A study on selective laser ablation of layers in the OPV stack is also shown towards module processing.

Les déchets solides générés par notre société sont nombreux. Les cendres volantes sont des déchets solides produits lors de la combustion de déchets domestiques ou industriels dans des incinérateurs. Les cendres volantes sont également produites par la combustion du charbon dans les centrales à charbon. Les cendres volantes sont des résultats de ces combustions et représentent importante quantité de déchets produits chaque année par notre société. Les possibilités de recyclage de ces déchets sont nombreuses : dans la construction, l'industrie routière. Elles sont également stockées pour une utilisation ultérieure. Les origines différentes des charbons et déchets incinérés conduisent à une minéralogie et une composition élémentaire complexe. En tant que sous-produit le devenir des cendres volantes est important à déterminer, aussi la détermination de la composition élémentaire de ces cendres volantes est-elle indispensable.Les méthodes classiques de préparation des échantillons solides sont la minéralisation acide ou la fusion alcaline. Ces procédures prennent du temps et supposent l’utilisation de réactif, de plus la digestion complète n'est pas toujours assurée. Le risque de contamination par les réactifs employés est important au cours de ces méthodes classiques de préparation. Au cours de la dernière décennie, le développement d’analyse directe d'échantillons solides en utilisant des méthodes d'ablation laser a été important en raison de la nécessité de réduire le temps d'analyse et de réduire aussi la consommation de réactifs. Dans ce travail, deux méthodes basées sur l'ablation par laser seront étudiées pour l'analyse des cendres: Laser Induced Breakdown Spectroscopy (LIBS) et Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS). La spectrométrie LIBS sera étudiée pour la détermination quantitative des éléments majeurs dans les échantillons de cendres alors que le couplage ablation laser ICP / MS sera employé pour détermination des éléments traces. L'optimisation de la sensibilité et les stratégies d'étalonnage sont les principaux problèmes traités dans ce travail. La préparation des échantillons et l’optimisation ont été effectuées pour déterminer les éléments tels que Al, As, Ba, Ca, Cr, Cu, Fe, Mg, Mn, Pb, Sr, V et Zn par les deux méthodes.Les performances analytiques telles que les limites de détection, justesse ont été obtenus à la suite d'optimisations appropriées des liants et de la sélection de l’étalon interne approprié. En conclusion, l’analyse directe de solides en utilisant les techniques basées sur l’ablation laser développées dans ce travail conduisent à une justesse acceptable pour la détermination des éléments majeurs et traces dans les cendres volantes / Solid waste generated by our society are numerous, fly ashes are produced during the combustion of domestic or industrial waste in incinerators. Fly ashes are also produced through coal combustion in coal fired power plants. Fly ashes are results of these combustions and represent important quantity of waste produced every year by our society. They have variable use – in construction, road industry, or they can be stocked for further use. As they are result of different origin, they have complex mineral and elemental composition. As a by-product or as a recycled product fly ashes fate is important to determine. In this view the determination of the elemental composition of fly ashes is the aim of this work.Conventional methods of sample preparation are acid digestion or alkali fusion. These procedures are time and reagent consuming and complete digestion is not assured. The potential contamination of the reagents employed is important during these classical sample preparation methods. During the past decade, development of direct solid sampling using laser ablation methods was important due to the need of reducing analysis time and also reducing reagent consumption. In this work, two methods based on laser ablation will be studied for fly ash analysis: Laser Induced Breakdown Spectroscopy (LIBS) and Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS). LIBS will be studied for quantitative determination of major elements in fly ash samples while Laser ablation / ICP MS will be employed for trace element determination.The sensitivity optimization and different calibration strategies are key problems of laser sampling methods. Sample preparation and condition optimisation were performed to determine major, minor and trace elements such as Al, As, Ba, Ca, Cr, Cu, Fe, Mg, Mn, Pb, Sr, V and Zn by both methods – LIBS for major elements and LA-ICP-MS for minor and trace elements.Analytical properties such as detection limits, accuracy and analytical working curves were obtained following suitable optimisation of binders and internal standards. Compromise binder and analytical conditions were selected to determine the elements in fly ash samples.In conclusion, direct solid sampling using laser ablation followed by LIBS or for solid introduction into ICP was found to determine major, minor and trace elements in fly ashes, improving pellets mechanical stability, high samples sensitivity and acceptable accuracy and detection limits.

Lorsqu'une impulsion laser est focalisée sur une cible solide immergée dans un liquide, de la matière est vaporisée. La nucléation et la croissance ont lieu dans le liquide et des nanoparticules sont ainsi synthétisées. La méthode est très polyvalente puisqu'une grande variété de matériaux peut être générée. De plus, les nanoparticules sont directement stabilisées dans le solvant. L'ajout d'agent complexant n'est pas nécessaire mais peut tout de même permettre de mieux contrôler la taille des nanoparticules. Cependant, de nombreux processus sont mis en jeu durant la synthèse et l'objectif de ce travail doctoral est de développer la compréhension de ces éléments. Dans la mesure où l'ablation laser déploie une multitude d'´échelle de temps, il a fallu employer différentes méthodes pour élucider ces mécanismes. Pour commencer, je définirai un état de l'art de l'utilisation de l'ablation laser en milieu liquide et nos résultats concernant la synthèse d'aluminium oxyde dopé chrome. Par la suite, je présenterai la spectroscopie des plasmas et les questions sous-jacentes à la notion d'´équilibre dans un plasma moléculaire. Ensuite, je décrirai notre approche atomistique de la nucléation basée sur les techniques de chimie quantique. Enfin, je montrerai l'apport de l'utilisation des méthodes d'ombrographie pour mieux comprendre la thermodynamique du système au temps plus long. Notre étude démontre que la bulle formée suite à l'ablation laser est constituée essentiellement de molécule du solvant dont la quantité n'évolue quasiment pas au cours du temps de vie de la bulle / When a pulsed-laser is focused into a solid target immersed in water, the material is evaporated. Nucleation and growth occur in the liquid and nanoparticles are synthesized. The method can be considered as versatile because one can try to synthesize any kinds of materials. Also, the nanoparticles are directly stabilized by the solvant so there is no need of complexing agents. The nanoparticles are described as ligand-free. However, various processes can occur during the synthesis and the aim of my work is to understand these different components. Since the laser ablation in liquid displays a wide range of timescales, we used numerous methods to address this problem. First, I will present the use of plasma spectroscopy and the questions it raises towards local thermodynamic equilibrium. Then, I will describe our microscopic approach of nucleation based on quantum chemistry techniques. Finally, I will illustrate the advantages of shadowgraphic measurements to reach an hydrodynamic understanding of the system

L’ablation laser dans l’air à la pression atmosphérique est souvent appliquée dans l’industrie, l’analyse chimique, la chirurgie, … Pour un développement plus approfondi des technologies laser basées sur l’effet d’ablation, il est nécessaire de mieux comprendre les phénomènes à l’origine de l’interaction laser-matière. Lors d’un impact du faisceau laser sur la surface d’un matériau, une plume plasma se forme au dessus de la cible. Ce plasma contient des électrons, des atomes et des ions du matériau évaporé, ainsi que du gaz ambiant, s’il est présent. Lors de l’impulsion laser, cette plume absorbe une grande partie d’énergie du faisceau laser, réduisant ainsi la quantité du rayonnement laser qui arrive à la surface de la cible. Les dimensions, ainsi que les paramètres de cette plume plasma évoluent très rapidement avec le temps. L’étude de la dynamique et des paramètres de cette plume est très importante, parce qu’ils influent sur tous les processus physiques ayant lieu à la surface du matériau traité. Nous avons étudié l’expansion de la plume plasma formée lors de l’ablation des échantillons métalliques (Al, Ti, Fe) par faisceau laser Nd :YAG nanoseconde (durée d’impulsion : 5.1 ns, longueur d’onde : 1064 nm, irradiance de l’ordre de grandeur de GW/cm2) dans l’air à la pression atmosphérique en utilisant la technique d’imagerie rapide. Cette technique nous a permis d’observer l’évolution spatio-temporelle de la plume au début de son expansion. Les résultats obtenus indiquent que la plume d’ablation laser a une structure : deux régions ont été distinguées – le cœur et la périphérie de la plume. La dynamique de ces deux régions de la plume a été étudiée et les vitesses de leur expansion ont été déterminées. En plus, nous avons examiné l’influence de l’irradiance laser, ainsi que l’influence de la composition de la cible sur la dynamique de la plume. D’autre part, nous avons développé des modèles numériques sous COMSOL Multiphysics pour simuler le processus d’ablation laser. Un modèle thermique a été utilisé pour simuler l’interaction laser – cible. Les résultats de ce modèle ont été employés comme conditions à la limite du modèle hydrodynamique, utilisé pour simuler l’expansion de la plume du plasma dans l’air ambiant. Deux approches ont été proposées : approche microscopique et macroscopique. Les résultats de simulation basée sur l’approche macroscopique donnent l’évolution temporelle et distribution spatiale (1D) des paramètres de la plume : masse volumique, vitesse, pression. / Laser ablation in the air at atmospheric pressure is nowadays frequently applied in industry, chemical analysis, surgery… For a further development of laser ablation based technologies, it is necessary to better understand the laser – matter interaction. During the impact of a laser pulse on the surface of the treated material, a plasma plume forms above the target surface. This plume contains particles (electrons, ions, atoms) of ablated matter, as well as of ambient gas, if present. During the laser pulse, this plume absorbs a large amount of the laser beam energy, thus reducing the quantity of the laser radiation arriving to the target surface. Dimensions, as well as parameters of this plasma plume evolve very quickly in time. Study of the plasma plume’s dynamics and parameters is very important, since they influence all the physical processes occurring at the surface of the treated material. In this work, we have investigated the expansion of the plasma plume formed during the laser ablation of metallic targets (Al, Ti, Fe) by a Nd:YAG laser beam (wavelength 1064 nm, pulse duration 5.1 ns and irradiance of the order of GW/cm2) in the air at atmospheric pressure using fast imaging technique. The obtained results show that laser ablation plume has a certain structure: two regions have been distinguished – the core and the periphery of the plume. Dynamics of these two plume regions has been studied and expansion velocities have been determined. In addition, we have examined the influence of the laser irradiance, as well as of the target composition on the plume dynamics. On the other hand, we have developed numerical models in COMSOL Multiphysics in order to simulate laser ablation process. A thermal model has been used to simulate the laser – target interaction. The results obtained from this model have been employed as boundary conditions in the hydrodynamic model, used to simulate plasma plume expansion in the ambient air. Two approaches have been proposed: microscopic and macroscopic approach. The results obtained by the simulation based on macroscopic approach give temporal evolution and spatial distribution (1D) of plume parameters: density, velocity and pressure.

Une technique d'ablation laser dite en champ proche a été développée pour l'analyse chimique d'échantillons solides à l'échelle sub-micrométrique. Cette technique combine un laser Nd:YAG nanoseconde, un microscope à force atomique AFM et un spectromètre de masse à plasma à couplage inductif (ICPMS). Afin d'améliorer la résolution spatiale de la technique d'ablation laser classique, l'effet de champ proche, consistant à amplifier l'énergie du laser très localement a été mis à profit. Cet effet est obtenu par illumination, par un faisceau laser, de la pointe conductrice de l'AFM placée à quelques nanomètres (5-30 nm) de la surface d'un échantillon. En appliquant cette technique d'ablation sur des échantillons conducteurs, l'or et le tantale, et un échantillon semi-conducteur, le silicium, une résolution latérale de 100 nm et des profondeurs de quelques nanomètres ont été obtenues. Deux codes numériques développés au laboratoire ont permis l'étude de deux phénomènes intervenant aux alentours de la pointe : l'amplification du champ électrique du laser par effet de pointe, et le chauffage induit par le laser à la surface de l'échantillon. L'influence des principaux paramètres opératoires sur ces deux phénomènes d'amplification et de chauffage a été étudiée. Une étude expérimentale multiparamétrique a été réalisée afin d'étudier l'influence des différents paramètres (fluence du laser, longueur d'onde du laser, nombre de tirs laser, distance pointe-échantillon, nature et dimensions de la pointe, nature de l'échantillon) sur l'efficacité d'ablation, sur les dimensions des cratères et sur la quantité de matière ablatée. / A near field laser ablation method was developed for chemical analysis of solid samples at sub-micrometric scale. This analytical technique combines a nanosecond laser Nd:YAG, an Atomic Force Microscope (AFM), and an inductively coupled plasma mass spectrometer (ICPMS). In order to improve the spatial resolution of the laser ablation process, the near-field enhancement effect was applied by illuminating, by the laser beam, the apex of the AFM conductive sharp tip maintained at a few nanometers (5 to 30 nm) above the sample surface. The interaction between the illuminated tip and the sample surface enhances locally the incident laser energy and leads to the ablation process. By applying this technique to conducting gold and tantalum samples, and semiconducting silicon sample, a lateral resolution of 100 nm and depths of a few nanometers were demonstrated. Two home-made numerical codes have enabled the study of two phenomena occurring around the tip: the enhancement of the laser electrical field by tip effect, and the induced laser heating at the sample surface. The influence of the main operating parameters on these two phenomena, amplification and heating, was studied. An experimental multi-parametric study was carried out in order to understand the effect of different experimental parameters (laser fluence, laser wavelength, number of laser pulses, tip-to-sample distance, sample and tip nature) on the near-field laser ablation efficiency, crater dimensions and amount of ablated material.

Due to their inherent BW capacity, optical interconnect (OI) offers a means of replacement to BW limited copper as bottlenecks begin to appear within the various interconnect levels of electronics systems. Low-cost optically enabled printed circuit boards are a key milestone on many electronics roadmaps, e.g. iNEMI. Current OI solutions found in industry are based upon optical fibres and are capable of providing a suitable platform for inter-board applications especially on the backplane. However, to allow component assembly onto high BW interconnects, an integral requirement for intra-board applications, optically enabled printed circuit boards containing waveguides are essential. Major barriers to the deployment of optical printed circuit boards include the compatibility of the technique, the cost of acquiring OI and the optical power budget. The purpose of this PhD research programme is to explore suitable techniques to address these barriers, primarily by means of laser material processing using UV and IR source lasers namely 248 nm KrF Excimer, 355 nm UV Nd:YAG and 10.6 μm IR CO2. The use of these three main lasers, the trio of which dominates most PCB production assembly, provides underpinning drive for the deployment of this technology into the industry at a very low cost without the need for any additional system or system modification. It further provides trade-offs among the suitable candidates in terms of processing speed, cost and quality of waveguides that could be achieved. This thesis presents the context of the research and the underlying governing science, i.e. theoretical analysis, involving laser-matter interactions. Experimental investigation of thermal (or pyrolitic) and bond-breaking (or photolytic) nature of laser ablation was studied in relation to each of the chosen lasers with regression analysis used to explain the experimental results. Optimal parameters necessary for achieving minimum Heat Affected Zone (HAZ) and surface/wall roughness were explored, both of which are key to achieving low loss waveguides. While photochemical dominance - a function of wavelength and pulse duration - is desired in laser ablation of photopolymers, the author has been able to find out that photothermallyprocessed materials, for example at 10.6 μm, can also provide desirable waveguides. Although there are literature information detailing the effect of certain parameters such as fluence, pulse repetition rate, pulse duration and wavelength among others, in relation to the etch rate of different materials, the machining of new materials requires new data to be obtained. In fact various models are available to try to explain the laser-matter interaction in a mathematical way, but these cannot be taken universally as they are deficient to general applications. For this reason, experimental optimisation appears to be the logical way forward at this stage of the research and thus requiring material-system characterisation to be conducted for each case thereby forming an integral achievement of this research. In this work, laser ablation of a single-layer optical polymer (Truemode™) multimode waveguides were successfully demonstrated using the aforementioned chosen lasers, thus providing opportunities for rapid deployment of OI to the PCB manufacturing industry. Truemode™ was chosen as it provides a very low absorption loss value < 0.04 dB/cm at 850 nm datacom wavelength used for VSR interconnections - a key to optical power budget - and its compatibility with current PCB fabrication processes. A wet-Truemode™ formulation was used which required that optical polymer layer on an FR4 substrate be formed using spin coating and then UV-cured in a nitrogen oxygen-free chamber. Layer thickness, chiefly influenced by spinning speed and duration, was studied in order to meet the optical layer thickness requirement for multimode (typically > 9 μm) waveguides. Two alternative polymers, namely polysiloxane-based photopolymer (OE4140 and OE 4141) from Dow Corning and PMMA, were sparingly utilized at some point in the research, mainly during laser machining using UV Nd:YAG and CO2 lasers. While Excimer laser was widely considered for polymer waveguide due to its high quality potential, the successful fabrication at 10.6 μm IR and 355 nm UV wavelengths and at relatively low propagation loss at datacom wavelength of 850 nm (estimated to be < 1.5 dB/cm) were unprecedented. The author considered further reduction in the optical loss by looking at the effect of fluence, power, pulse repetition rate, speed and optical density on the achievable propagation but found no direct relationship between these parameters; it is therefore concluded that process optimisation is the best practice. In addition, a novel in-plane 45-degree coupling mirror fabrication using Excimer laser ablation was demonstrated for the first time, which was considered to be vital for communication between chips (or other suitable components) at board-level.