Cette thèse expérimentale est consacrée à l’optimisation d’une source de rayons X Kalpha générée par interaction laser femtoseconde à fort contraste temporel avec une cible épaisse en molybdène. Ce travail vise à explorer l’effet du contraste temporel sur l’émission Kalpha sur une gamme d’intensité combinant les deux régimes relativiste et non-relativiste. La première étude est consacrée à l’évolution de l’émission Kalpha en fonction du contraste temporel et de l’intensité. L’étude a révélé différents comportements de l’émission Kalpha suivant la valeur du contraste et d’intensité. L’étude a aussi montré une émission Kalpha indépendante du contraste dans le régime relativiste. Au regard des travaux de la littérature, nous avons proposé une première interprétation des résultats obtenus. Il s’agit d’établir un lien entre l’émission Kalpha et les mécanismes d’absorption de l’énergie laser. Certains mécanismes sont dépendants de l’angle d’incidence. Afin d’appuyer notre interprétation, une deuxième étude du rendement de la source Kalpha en fonction de l’angle d’incidence a été réalisée. Ainsi les résultats obtenus sont en accord avec certaines de nos conclusions. En outre, Nous nous sommes intéressés à l’effet de l’étirement temporel de l’impulsion. Nous avons observé une sensibilité de l’émission suivant le signe du chirp. Enfin, nous avons étudié l’effet du contraste et de l’intensité sur la taille de la source X. Celle-ci est d’autant plus réduite que le contraste est plus fort et devient très proche de la tache focale laser à faible intensité laser. Le rendement de production en photon Kalpha atteint est de 2 × 10^−4, similaire au meilleur rendement reporté à ce jour. / This thesis is focused on the optimization of a Kalpha x-ray source induced by high contrast femtosecond laser molybdenum thick target interaction. The objective of this work is to explore the effect of the temporal contrast ratio on Kalpha emission in an intensity range including the non relativistic and relativistic regimes. The first study consists of the measurement of Kalpha emission as a function of contrast ratio and intensity. The study shows different behaviors of the emission depending on the contrast ratio and intensity range. Furthermore, it was found that in the relativistic regime Kalpha production is independant of the contrast ratio. According to published work in litterature, we proposed a first intepretation of the obtained results. In particular, we discuss the absorption mechanism of laser pulse energy for each contrast ratio and intensity condition. Some of the mechanisms are dependant on the angle of incidence of the pulse on target. Thus, to verify the validity of our interpretation, we study the Kalpha effciency as a function of the angle of incidence. Most of the results agree with our first conclusions. Furthermore, we investigate the effect of the chirped pulse of the Kalpha emission. It is shown that Kalpha emission is sensitive to the sign of the chirp. Finally, we performed a study on the effect of contrast ratio and intensity on the x-ray source size. It was observed that high contrast ratio decreases strongly the x-ray source size which aproaches the focal spot size at low laser intensity. High Kalpha efficiency is reached 2 × 10^−4 which is similar to the highest effciency reported to date in litterature for a thick molybdenum target.

Cette thèse porte sur l’assemblage de verres par impulsions laser femtosecondes. Une source laser femtoseconde à haute fréquence de répétition a été utilisée pour souder des lames de borosilicate de haute qualité de surface. La technique d’assemblage mise en œuvre diffère de la littérature par le système de focalisation utilisé. Un plan d’expériences a été réalisé afin de déterminer l’influence des différents paramètres laser sur les performances des soudures obtenues, démontrant que l’augmentation de la quantité d’énergie déposée améliore les performances mécaniques et thermiques. Les assemblages soudés peuvent atteindre une haute résistance mécanique supérieure à 25 MPa et supporter des chocs thermiques supérieurs à 300 ° C. L’adaptation des paramètres laser en fonction de la distance entre les lames de verre permet de souder des verres hors contact optique. Cette méthode a également été implémentée avec succès à l’assemblage de verre sur du silicium. / This PhD thesis is about glass bonding by femtosecond laser pulses. A femtosecond laser source generating high repetition rate laser pulses has been used to weld borosilicate glass plates with high surface quality. The method presented in this work differs from the literature by the focusing system implemented. The influence of the laser parameters on the bonded samples performances has been studied implementing a design of experiments, demonstrating that the mechanical and thermal resistance of the samples can be improved by increasing the amount of deposited. Thebonded samples provide high mechanical resistance, higher than 25 MPa, can held high thermal shock above 300 °C and present high transparency above 90 %. Glass bonding with a distance between the glass plates has been performed by adapting the laser parameters. Bonding of glass on silicon has also been performed successfully.

A influência das variáveis associadas ao laser como a fluência, o comprimento de onda, e a duração do pulso, assim como as relacionadas às propriedades das amostras, como a distribuição do tamanho das partículas e as características químicas da matriz, foram avaliadas visando à determinação quantitativa de macro- (P, K, Ca, Mg) e micronutrientes (Cu, Fe, Mn, Zn, B) em pastilhas de materiais vegetais por espectrometria de emissão óptica com plasma induzido por laser (LIBS). Os efeitos da distribuição do tamanho das partículas e da fluência do laser foram investigados a partir da análise de amostras peneiradas (150-20 µm) empregando-se um sistema LIBS, em regime temporal de nanossegundos (ns-LIBS), montado com um laser de Nd:YAG a 1064 nm (pulsos de 5 ns e 360 mJ)e um espectrômetro com óptica Echelle e detector ICCD. Observou-se um aumento na sensibilidade e na precisão das medições com a diminuição do tamanho das partículas usadas no preparo das pastilhas, e uma diminuição dos efeitos de matriz causados por diferenças no tamanho das partículas, quando pastilhas preparadas com partículas < 75 µm foram analisadas com pulsos de 50 J cm-2. Verificou-se uma melhora significativa na exatidão das medições de Mg, Fe, Mn e Zn feitas em um conjunto de pastilhas de folhas de cana-de-açúcar (partículas < 75 µm) empregando-se esta fluência. Em uma segunda etapa, observou-se que variações no comprimento de onda do laser de Nd:YAG (1064, 532, 355 e 266 nm) não influenciaram de maneira significativa a precisão e exatidão das medições em pastilhas de folhas de cana-de-açúcar, obtendo-se correlações lineares entre as intensidades dos sinais de emissão e as correspondentes frações de massa dos analitos. Variações no comprimento de onda do laser de Nd:YAG não afetaram a análise de um conjunto heterogêneo de amostras, composto por pastilhas de folhas de plantas de diferentes espécies, como soja, cana-de-açúcar, milho, citros, café, por exemplo, por ns-LIBS. No entanto, diferentemente do observado para o conjunto de pastilhas de folhas de cana-de-açúcar, observou-se, uma baixa correlação (r cal < 0,90) entre as frações de massa de Ca, Mg, P, Cu, Fe, Mn e Zn determinadas por ns-LIBS e os valores de referência, o que demonstra a baixa robustez de ns-LIBS frente às variações na composição química das matrizes. Posteriormente, analisou-se este conjunto heterogêneo de amostras com sistema LIBS, em regime temporal de femtossegundos (fs-LIBS), montado com laser de Ti:Safira (pulsos de 60 fs e 1,65 mJ) e espectrômetro com óptica Czerny-Turner e ICCD. Demonstrou-se que o uso de pulsos em regime de fs proporcionou calibrações e validação menos dependentes da composição química das matrizes. As frações de massa de Ca, Mg, P, Fe e Mn previstas por fs-LIBS foram estatisticamente concordantes com os valores de referência, independentemente do modelo de calibração usado. Além disso, o uso de calibração multivariada melhorou a capacidade preditiva de ns-LIBS, assemelhando-se à de fs-LIBS. Concluiu-se que o emprego de fs-LIBS foi a estratégia mais robusta e que ofereceu maior flexibilidade à variabilidade matricial / The influence of laser properties, such as fluence, wavelength and pulse duration, as well as sample characteristics, such as particle size distribution and chemical matrix composition, was evaluated aiming at the quantitative determination of macro- (P, K, Ca, Mg) and micronutrients (Cu, Fe, Mn, Zn, B) in pellets of plant materials by laser-induced breakdown spectroscopy (LIBS). Firstly, the effects of particle size distribution and laser fluence on the analysis of pellets (test samples) prepared with sieved samples (from 150 to 20 µm apertures) were investigated. Experiments were carried out with a nanosecond LIBS (ns-LIBS) system by using a Q-switched Nd:YAG laser at 1064 nm (5 ns; 360 mJ) and a spectrometer with Echelle optics and intensified charge-coupled device (ICCD) detector. Results indicated that smaller particles yielded to sensitivities\' enhancement and attained better measurements\' precision. Moreover, matrix effects were reduced by analyzing pellets prepared from < 75 ?m sieved fractions and pulses of 50 J cm-2. In addition, there was a significant improvement on accuracy of Mg, Fe, Mn and Zn measurements in a set of test samples of sugarcane leaves by using this fluence. In a second experiment, variations in the Nd:YAG laser wavelength (1064, 532, 355 and 266 nm) did not affect the analysis of test samples of sugarcane leaves, and provided linear correlations between emission signal intensities and corresponding analytes mass fractions. In addition, variations within Nd:YAG laser wavelength did not affect the analysis of a heterogeneous sample set composed by pellets of leaves from different crops, such as soy, sugarcane, maize, citrus and coffee by ns-LIBS. However, in contrast to previous findings, the univariate calibration models for ns-LIBS presented lower linearity (r cal < 0.90) for Ca, Mg, P, Cu, Fe, Mn and Zn, no matter the laser wavelength used for the analysis. These circumstances reflect the low robustness of ns-LIBS to variations within matrix chemical composition among test samples. Afterwards, test samples from different crops were analyzed by a femtosecond LIBS (fs-LIBS) by using a Ti:Sapphire laser, including a mode-locked oscillator and an ultrafast amplifier (60 fs; 1.65 mJ per pulse), and a spectrometer with Czerny-Turner optics and ICCD. Findings indicated that the pulse duration was a decisive variable for providing accurate quantification of nutrients in different plant species, which present substantial differences in terms of matrix chemical composition. Close agreement between Ca, Mg, P, Fe and Mn mass fractions predicted by fs-LIBS and those determined by ICP OES was evidenced, whatever the modeling approach used. Contrarily, for ns-LIBS analysis of test samples from different crops, only the use of multivariate partial least squares (PLS) regression appears capable for resolving the non-linear transformations of the emission intensities according to the physical mechanisms governing this temporal regime of ablation. Thus, when using multivariate modeling, the figures-of merit reflecting the predictive capabilities of ns-LIBS resemble to those achieved by fs-LIBS. Either way, fs-LIBS is a more robust approach that better offers larger flexibility to the matrix variability

O poli (p-fenilenevinileno), ou PPV, é um polímero de grande relevância tecnológica devido a suas propriedades eletroluminescentes, que têm sido exploradas em diodos emissores de luz orgânicos, displays flexíveis e outros dispositivos optoeletrônicos. Embora o PPV seja um material de importância para muitas aplicações, a sua síntese na nano/microescala não pode ser obtida através do método padrão, o qual utiliza o aquecimento de um polímero precursor poli (cloreto de xileno tetrahidrotiofenio) (PTHT). Este trabalho mostra como a microestruturação com pulsos de femtosegundo pode ser empregada para a síntese de PPV em regiões pré-determinadas, empregando três diferentes abordagens, permitindo uma nova metodologia para a fabricação precisa de microcircuitos poliméricos complexos, (i) na primeira abordagem, o processo de conversão é obtido pela irradiação de filmes de PTHT com pulsos laser ultracurtos em regiões previamente determinadas, o que leva ao controle espacial da formação de PPV em microescala, (ii) na segunda abordagem, microestruturas tridimensionais dopadas com PTHT foram fotopolimerizadas por absorção de dois fótons. A conversão de PTHT para PPV nestas microestruturas dopadas foi obtida após um tratamento térmico, (iii) na terceira abordagem, a transferência direta induzida por laser (LIFT) com pulsos de femtossegundos permite a deposição controlada de PPV com alta resolução espacial, fornecendo micropadrões 2D, preservando sua estrutura e propriedades ópticas. As estruturas foram caracterizadas por microscopia eletrônica de varredura, microscopia óptica de transmissão, microscopia de fluorescência e microscopia confocal de fluorescência. Suas propriedades ópticas foram analisadas através de sistemas de micro-fotoluminescência e micro-absorção implementadas em um microscópio invertido. Medidas de espectroscopia Raman, microscopia de força atômica e medidas elétricas também foram realizadas. Este trabalho mostra como a microestruturação com laser de fs pode ser explorada para a síntese de PPV em regiões pré-determinadas para fabricar uma variedade de microdispositivos, abrindo novos caminhos na optoeletrônica baseada em polímeros. / Poly(p-phenylenevinylene), or PPV, is a polymer of great technological relevance due to its electroluminescent properties, which have been exploited in organic light emitting diodes, flexible displays and other optoelectronic devices. Although PPV is a material of foremost importance for many applications, its synthesis at the nano/micro scale cannot be achieved through the standard method that uses heating of a precursor polymer poly(xylene tetrahydrothiophenium chloride)(PTHT). This work demonstrates the use of direct laser writing with femtosecond pulses to obtain the synthesis of PPV in pre-determined regions, by applying three different approaches, allowing the precise fabrication of complex polymeric microcircuits, (i) in the first approach the conversion process is achieved by irradiating PTHT films with ultra-short laser pulses in previously determined regions, which leads to the spatial control of PPV formation at microscale, (ii) in the second approach, three-dimensional microstructures doped with PTHT were photopolymerized by two photons absorption. The conversion of PTHT to PPV in these doped microstructures was obtained by a subsequent thermal treatment, (iii) in the third approach, laser-induced forward transfer (LIFT) with femtosecond pulses enables the controlled deposition of PPV with high spatial resolution, providing 2D micropatterns, while preserving its structure and optical properties. The structures were characterized by scanning electron, fluorescence, transmission and confocal fluorescence microscopies. Their optical properties were analyzed by micro-photoluminescence and micro-absorption setups assembled on an inverted microscope. Raman spectroscopy, electrical measurements and atomic force microscopy were also performed. This thesis shows the use of fs-laser writing methods for the synthesis of PPV in pre-determined regions, to fabricate a variety of microdevices, thus opening new avenues in polymer-based optoelectronics.

Les lasers à électrons libres (LELs) à simple passage représentent actuellement la possibilité la plus prometteuse pour fournir des impulsions lumineuses de haute énergie (µJ à mJ) à des échelles de durée femtoseconde (1 fs = 10⁻¹⁵s) et des longueurs d’ondes ultra-courtes (résolution nanométrique i.e., jusqu’aux domaines de l’extrême-ultraviolet et des rayons X). Les LELs émettant dans l’extrême-ultraviolet sont une technologie encore jeune, si bien que de nombreuses questions restent ouvertes. Celles posées au sein de ce manuscrit concernent la configuration dite injectée, dans laquelle le processus est initié par une source externe cohérente (le “seed"). Nous nous concentrons particulièrement dans cette thèse sur les caractéristiques transverses et longitudinales de la lumière, sa cohérence, les propriétés de la phase temporelle et les liens directs entre le seed et l’émission LEL. La technique de génération dans un gaz noble d’harmoniques d’ordres élevés d’un laser femtoseconde (GHE) se montre à la fois complémentaire et en compétition avec les LELs. En compétition car les impulsions produites ont des qualités similaires à celles obtenues avec un LEL ; complémentaire car le rayonnement GHE peut être utilisé comme seed ou en combinaison avec la lumière LEL, par exemple pour effectuer des expériences mettant en jeu de multiples faisceaux. Bien que la GHE fournisse des impulsions moins puissantes, l’implémentation d’une telle source requiert un effort significativement moins important. Le taux de conversion harmonique, l’accordabilité et la qualité spatiale du faisceau généré, et la manière dont ces paramètres dépendent du laser générateur sont les problématiques traitées au sein de ce manuscrit. La volonté de la communauté scientifique d’effectuer des expériences novatrices demande des études profondes et l’optimisation des sources de GHE et des LELs. En particulier, sur la source LEL injectée FERMI@Elettra de Trieste, l’induction d’une dérive de fréquence dans le rayonnement a conduit à des résultats marquants. Entre autres, une méthode de génération d’impulsions scindées avec différentes longueurs d’ondes a été analysée et développée. Une telle possibilité ouvre la voie à l’utilisation des LELs injectés en tant que source autonome pour des installations de type pompe-sonde à deux couleurs. Plus généralement, l’étude des phénomènes mis en jeu dans les processus de GHE et du LEL ainsi que la caractérisation des propriétés de leur lumière sont des sujets intrinsèquement excitants, ayant des connexions directes avec de nombreux aspects fondamentaux de la physique. / Single-pass free-electron lasers (FELs) are currently the most promising facilities for providing light pulses with high energies (µJ to mJ) at femtosecond time scales (1 fs = 10⁻¹⁵s) and with ultrashort wavelengths (nanometer resolution i.e., down to extreme-ultraviolet and X-ray spectral regions). Extreme-ultraviolet FELs are still quite young so that many questions remain open. Those addressed within this manuscript concern the so-called seeded configuration, where an external coherent source (the “seed") initiates the process. In particular, we focus in this thesis on the transverse and longitudinal characteristics of the light, its coherence, the properties of the temporal phase and the direct correlations between the seed and the FEL emission. With regard to FELs, high-order harmonics of femtosecond laser pulses generated in noble gases (HHG technique) exhibit both competitive and complementary features. Competitive, because the produced pulses have similar assets as the ones provided by an FEL. Complementary, because the generated harmonics can be used as a seed or, in combination with FEL light, to perform multi-beam experiments. Even though less powerful pulses are produced by a HHG source, its implementation requires a significantly smaller effort. The efficiency of harmonic conversion, the tunability and spatial quality of the generated beam, and how these parameters depend on the driving laser are the issues discussed within this manuscript. The general will of the scientific community to perform novel experiments requires deep studies and optimization of FEL and HHG sources. In particular, on the seeded FEL facility FERMI@Elettra of Trieste, the induction of chirp in the radiation has led to remarkable results. Among others, a method of generation of split pulses with different wavelengths has been construed and developed. Such a possibility paves the way for the use of seeded FEL facilities as stand-alone sources for two-colour pump-probe setups. More generally, the study of phenomena involved in the FEL and HHG processes, together with the characterization of the light properties, are intrinsically exciting matters that have direct connections with fundamental aspects of physics. / Laser na proste elektrone (LPE, ang. free-electron laser - FEL) z enojnim prehodom je trenutno najbolj obetaven vir femtosekundnih (1 fs = 10⁻¹⁵ s) svetlobnih pulzov z visoko energijo (μJ do mJ) in ultra kratko valovno dolžino (nanometrska ločljivost, t.j., vse do spektralnega območja ekstremne ultravijolične in rentgenske svetlobe). LPE-ji, ki delujejo na področju ekstremne ultravijolične svetlobe, so razmeroma novi svetlobni viri, kar pomeni, da so glede njihovega delovanja odprta še mnoga vprašanja. V pričujočem doktorskem delu smo se ukvarjali predvsem z dvostopenjsko konfiguracijo, pri kateri LPE ojači zunanje (koherentno) elektromagnetno valovanje (seed). Osredotočili smo se na transverzalne in longitudinalne lastnosti proizvedene svetlobe, koherenco, lastnosti časovne faze ter na direktne korelacije med zunanjim virom (seed) in sevanjem LPE-ja. Poleg LPE-jev so v vzponu tudi svetlobni viri, ki temeljijo na generaciji visokih harmonikov (GVH, ang. high-order harmonic generation - HHG) v žlahtnih plinih. Ti svetlobni viri so zaradi podobnih lastnosti pulzov konkurenčni LPE-jem, po drugi strani pa predstavljajo komplementarne izvore svetlobe, ker jih je mogoče uporabiti v dvostopenjski LPE konfiguraciji kot vir zunanjega elektromagnetnega valovanja (seed) ali v kombinaciji z LPE-jem v eksperimentih z dvema ali več žarki. Kljub temu, da so ti svetlobni viri šibkejši v primerjavi z LPE-ji, je njihova izvedba bistveno lažja. V dizertaciji obravnavamo izkoristek harmonične pretvorbe virov, ki temeljijo na principu GVH, nastavljivost in prostorsko kakovost žarkov, ter odvisnost omenjenih parametrov od gonilnega laserja. Zaradi vse večje težnje po novih eksperimentih na vseh znanstvenih področjih sta ključna zelo natančno poznavanje delovanja in optimizacija LPE-jev in virov, ki temeljijo na GVH. Med bolj pomembne dosežke na LPE-ju FERMI@Elettra v Trstu spadajo možnost spreminjanja trenutne frekvence proizvedene svetlobe (ang. chirp) na podlagi katere je bila razvita metoda za generacijo razdeljenih pulzov z različnimi valovnimi dolžinami. S pomočjo te metode bo možno dvostopenjske LPE-je uporabljati kot samostojne vire svetlobe za poskuse v t.i. načinu « pump-probe ». V dizertaciji so predstavljene študije pojavov, ki so prisotni pri generaciji svetlobe v LPE-jih ter virih, ki temeljijo na GVH. Ti pojavi so, skupaj z metodami karakterizacije proizvedene svetlobe, tesno povezani s temeljnimi principi v fiziki.

Nous avons mis en place un dispositif permettant l’acquisition d'échos de photons stimulés infrarouges à l’échelle femtoseconde. Le but est d'examiner la dynamique vibrationnelle aux temps courts de métaux carbonyles (W(CO)₆ and Fe(CO)₅) piégés en matrice cryogénique (4-50 K). Cet environnement solide, issu de la condensation d'un mélange gazeux contenant une impureté et un gaz inerte (N₂, CH₄, Ar, etc.), est propice à l’étude de systèmes dans leur état fondamental. L’excitation d’une vibration moléculaire s’atténue toujours temporellement, ce qui correspond dans le domaine spectral à un élargissement des raies d’absorption. L’étude de la dynamique vibrationnelle vise à examiner les causes physiques à l’origine de cet élargissement spectral. Typiquement, elles sont de trois sortes : phénomènes intramoléculaires, interactions entre molécules piégées et interactions entre la molécule piégée et l’environnement. Les échos de photons permettent de distinguer les contributions homogènes et inhomogènes de l’élargissement spectral et de caractériser les processus de déphasage, de relaxation des populations et de diffusion spectrale. Parmi les résultats obtenus, nous avons mis en évidence l'influence des phonons spécifiques aux matrices moléculaires (ex : libration de N₂ et rotation de CH₄ ) sur le déphasage vibrationnel ainsi que l’influence de la transition de phase du méthane solide à 20 K sur la dynamique vibrationnelle. Nous avons également montré que la dynamique vibrationnelle était dépendante du site cristallographique dans lequel est piégée la molécule. Enfin, en excitant plusieurs modes de vibration simultanément, nous avons pu examiner les couplages intramoléculaires. / We built an experimental set-up in order to generate infrared stimulated photon echoes at the femtosecond timescale. The purpose is to examine the short time vibrational dynamics of metal carbonyls (W(CO)₆ and Fe(CO)₅) trapped in cryogenic matrices (4-50 K). This environment, resulting from the condensation of a gas mixture containing the impurity and an inert gas (N₂, CH₄, Ar, etc.), is well suited to study systems in their ground state. An excited molecular vibration is always damped in the time domain. It corresponds in the frequency domain to a broadening of the absorption line. The study of the vibrational dynamics aims at examining the physical causes of this spectral broadening. Typically, there are three kinds of causes: intramolecular phenomena, interactions between trapped molecules and interactions between the impurity and the environment. Photon echoes allow distinguishing between the homogeneous and the inhomogeneous contributions of the spectral broadening and characterizing dephasing process, population relaxation and spectral diffusion. Among the obtained results, we highlighted the influence of phonons that are specific to molecular matrices (ex: N₂ libration and CH₄ rotation) on the vibrational dephasing. Moreover, we observed the influence of the phase transition of solid methane at 20 K on the vibrational dynamics. We also showed that the vibrational dynamics depends on the site in which the molecule is trapped. Finally, when exciting several vibrational modes, we are also able to study intramolecular couplings.

La spectroscopie par transformation de Fourier par peignes de fréquences femtosecondes tire parti d’un interféromètre sans partie mobile. Il mesure les interférences entre deux peignes de fréquences, sources lasers à large bande spectrale constituée de raies fines et équidistantes. Il améliore significativement le temps de mesure et la limite de résolution spectrale des spectromètres de Fourier. Néanmoins, les conditions sur la stabilité à court terme des peignes ne peuvent pas être remplies par les techniques d’asservissement classique. Jusqu’à présent, aucun spectre de qualité n’a pu être mesuré avec un très faible temps d’acquisition. Cette thèse présente le développement d’une méthode de correction en temps réel capable de compenser les fluctuations résiduelles des peignes et de restituer des spectres sans artefacts. La méthode, analogique, ne nécessite aucun asservissement ou traitement informatique a posteriori. Ses performances sont démontrées dans le proche infrarouge (1,5 µm) et le visible (520 nm), à l’aide d’oscillateurs femtosecondes fibrés. Des spectres moléculaires couvrant 12 THz sont mesurés en 500 µs à limite de résolution Doppler. Ils sont en excellent accord avec les données de la littérature. Pour la première fois, le plein potentiel de la spectroscopie de Fourier par peignes de fréquences est démontré. Le domaine de l’infrarouge moyen est la région de prédilection de la spectroscopie moléculaire car la plupart des molécules y présentent des absorptions fortes et caractéristiques. Étendre la spectroscopie par peignes de fréquences à cette région est donc l’objectif suivant à atteindre. Dans cette optique, un peigne émettant autour de 3 µm est caractérisé. Il est basé sur la conversion non-linéaire par différence de fréquences d’un oscillateur à erbium élargi spectralement par une fibre fortement non-linéaire. / Dual-comb Fourier-transform spectroscopy takes advantage of an interferometer without moving parts. Interferences pattern between two femtosecond frequency combs, broadband laser sources whose spectra consist of evenly-spaced narrow lines, is measured. The measurement time and the spectral resolution are significantly improved compared to traditional Fourier spectrometers. However, the required short-term stability of the combs cannot be achieved by classic locking methods. Until now, no high-quality spectra could be recorded within a very short acquisition time. This thesis reports on the development of a real-time correction method able to compensate for the combs’ residual fluctuations and to restore non-distorted spectra. This analog technique does not require any locking system or a posteriori calculation. Its performance is demonstrated in the near-infrared (1.5 µm) and in the visible (520 nm) with fiber-based femtosecond lasers. Doppler-limited molecular spectra spanning 12 THz are measured within 500 µs. They are in excellent agreement with databases. For the first time, the full potential of dual-comb spectroscopy is demonstrated. The mid-infrared region is an attractive spectral range for molecular spectroscopy due to the molecules’ strong and characteristic absorptions. Therefore, extending dual-comb spectroscopy to this region is the next goal to achieve. Toward this goal, a comb emitting around 3 µm is characterized. It is based on the non-linear difference frequency generation from an erbium oscillator spectrally broadened with a highly non-linear fiber.

Les verres de phosphates de zinc et gallium contenant de l’argent ont permis des développements originauxau travers de la structuration d’architectures photoniques multi-échelles innovantes en volume, en surfaceou sur fibre, et également à travers l’ingénierie de composition chimique du matériau. Un taux accru d’oxyded’argent permet de maximiser la quantité de paires au sein de la matrice vitreuse lors de la synthèse dumatériau. Ce dimère favorise les processus d’agrégation conduisant à la formation d’espèces lors del’interaction locale entre le verre et le laser femtoseconde infrarouge. Une étude par spectroscopie RPEmenée sur des échantillons irradiés par des sources ionisantes a permis de montrer que le débit de dose estprépondérant quant au contrôle des processus chimiques. Des centres à électron et à trou sont les espècesmajoritairement stabilisées à faible débit de dose, alors que la formation d’agrégats d’argent luminescentsintervient pour des puissances crête élevées typiques des lasers ultra-courts. Le caractère local de lastructuration par Direct Laser Writing a permis de créer des objets 3D originaux. L’analyse fine de ladistribution chimique au sein d’objets fluorescents a permis de montrer clairement une zone de déplétion enions argent au centre. Les effets de migration d’ions depuis le centre du faisceau laser vers le bord externea ainsi été mis en évidence. Le dopage des verres photosensibles par des ions europium a permis de montrerdes effets de synergie entre agrégats d’argent photo-inscrits et lanthanides trivalent. En effet, une exaltationde l’émission de luminescence de ces derniers à l’endroit des structurations laser a été mesurée. / The silver-containing phosphate glasses allowed original developments throughout the microstructuring ofarchitectures for innovative photonic in the volume, at the surface or in the fibered material. The chemicalengineering of the material plays an important role from this point of view. An increasing silver oxide ratioleads to an important quantity of pairs in the pristine glass matrix. This dimer in favor of the aggregationprocess bringing to the production of species during the interaction between the glass and the infraredfemtosecond laser. A study conducted by EPR spectroscopy on irradiated samples (ionizing sources)demonstrated that the dose rate is predominant for the control of the involved chemical process. Mainly,electron and holes are stabilized at low dose rate whereas the formation of luminescent silver clusters occursfor high peak power typical of ultra-short lasers. The Direct Laser Writing process allows local structuring ofthe matter and resulted in original tridimensional patterns. The fine chemical distribution analysis insideannular fluorescent objects clearly showed a depletion zone of the silver concentration in the center. Ionicmigration effects from the center towards the edges of the laser beam are then highlighted. The Eu3+-dopedphotosensitive glasses emphasized a synergy between photo-induced silver clusters and trivalentlanthanides. Indeed, a luminescence exaltation associated to the europium emission is measured.

La communauté de la chimie atmosphérique souffre d'un manque de mesures rapides, fiables résolues spatialement et temporellement pour un large éventail de molécules réactives (radicaux tels que NO2, OH, BrO, IO, etc). En raison de leur forte réactivité, ces molécules contrôlent largement la durée de vie et la concentration de nombreuses espèces clés dans l'atmosphère, et peuvent avoir un impact important sur le climat. Les concentrations de ces radicaux sont extrêmement faibles (ppbv ou moins) et très variable dans le temps et dans l'espace, ce qui impose un véritable défi lors de la détection. Dans la première partie de cette thèse, un spectromètre UV robuste, compacte et transportable est développé, exploitant la technique ML-CEAS pour mesurer à des niveaux très faibles (pptv et même en dessous) des molécules réactives d'importance atmosphérique, en particulier, les radicaux d'oxyde d'halogènes, afin de répondre aux besoins émergents. La technique ML-CEAS est basée sur le couplage d'un laser femtoseconde à blocage de modes à une cavité optique de haute finesse, qui agit comme un piège à photons pour augmenter l'interaction entre la lumière et l'échantillon de gaz intracavité. Cela permet d'améliorer fortement la sensibilité d'absorption. La limite de détection obtenue pour le radical IO est de 20 ppqv pour un temps d'acquisition de 5 minutes, ce qui est un résultat impressionnant. Dans la deuxième partie de cette thèse, une nouvelle technique spectroscopique est développée appelée effet Vernier, qui est également basé sur l'interaction entre un laser femtoseconde à blocage de mode et une cavité optique de haute finesse. Cette technique fournit une sensibilité de détection similaire à la technique ML-CEAS, mais l'avantage est que le nombre des éléments spectraux est donné par la finesse de la cavité optique et donc peut atteindre plusieurs dizaines de milliers. De plus, cette configuration simplifie le montage expérimental par la suppression du spectrographe qui est remplacé par une simple photodiode. Le temps d'acquisition d'un spectre peut être aussi réduit à moins d' 1 ms. / The atmospheric chemistry community suffers a lack of fast, reliable and space resolved measurements for a wide set of reactive molecules (e.g. radicals such as OH, NO3, BrO, IO, etc). Due to their high reactivity, these molecules largely control the lifetime and concentration of numerous key atmospheric species, and may have an important impact on the climate. The concentrations of such radicals are extremely low (ppbv or less) and highly variable in time and space, which imposes a real challenge during the detection. In the first part of this thesis, a compact, robust and transportable UV spectrometer is developed, exploiting the Mode-Locked Cavity Enhanced Absorption Spectroscopy (ML-CEAS) technique to measure pptv and sub-pptv levels of atmospherically important reactive molecules, in particular, halogen oxide radicals, to respond to the emerging needs. The ML-CEAS technique is based on coupling a Mode-Locked femtosecond laser to a high finesse optical cavity, which acts as a photon trap to increase the interaction between the light and the intracavity gas sample, which highly enhances the absorption sensitivity. The detection limit obtained for the IO radical is 20 ppqv (part per quadrillion), which is an impressive result. In the second part of this thesis, a new spectroscopic technique is developed, called Vernier effect, which is also based on the interaction between a mode-locked femtosecond laser with a high finesse optical cavity. This technique provides detection sensitivity similar to that of ML-CEAS technique, but the advantage is that the number of the spectral elements is given by the cavity finesse, so it can reach ten thousands, as well as this technique has a simple setup, where the spectrograph is replaced by a photodiode. Additionally, the time required to measure one output absorption spectrum can be less than 1 ms.

O poli (p-fenilenevinileno), ou PPV, é um polímero de grande relevância tecnológica devido a suas propriedades eletroluminescentes, que têm sido exploradas em diodos emissores de luz orgânicos, displays flexíveis e outros dispositivos optoeletrônicos. Embora o PPV seja um material de importância para muitas aplicações, a sua síntese na nano/microescala não pode ser obtida através do método padrão, o qual utiliza o aquecimento de um polímero precursor poli (cloreto de xileno tetrahidrotiofenio) (PTHT). Este trabalho mostra como a microestruturação com pulsos de femtosegundo pode ser empregada para a síntese de PPV em regiões pré-determinadas, empregando três diferentes abordagens, permitindo uma nova metodologia para a fabricação precisa de microcircuitos poliméricos complexos, (i) na primeira abordagem, o processo de conversão é obtido pela irradiação de filmes de PTHT com pulsos laser ultracurtos em regiões previamente determinadas, o que leva ao controle espacial da formação de PPV em microescala, (ii) na segunda abordagem, microestruturas tridimensionais dopadas com PTHT foram fotopolimerizadas por absorção de dois fótons. A conversão de PTHT para PPV nestas microestruturas dopadas foi obtida após um tratamento térmico, (iii) na terceira abordagem, a transferência direta induzida por laser (LIFT) com pulsos de femtossegundos permite a deposição controlada de PPV com alta resolução espacial, fornecendo micropadrões 2D, preservando sua estrutura e propriedades ópticas. As estruturas foram caracterizadas por microscopia eletrônica de varredura, microscopia óptica de transmissão, microscopia de fluorescência e microscopia confocal de fluorescência. Suas propriedades ópticas foram analisadas através de sistemas de micro-fotoluminescência e micro-absorção implementadas em um microscópio invertido. Medidas de espectroscopia Raman, microscopia de força atômica e medidas elétricas também foram realizadas. Este trabalho mostra como a microestruturação com laser de fs pode ser explorada para a síntese de PPV em regiões pré-determinadas para fabricar uma variedade de microdispositivos, abrindo novos caminhos na optoeletrônica baseada em polímeros. / Poly(p-phenylenevinylene), or PPV, is a polymer of great technological relevance due to its electroluminescent properties, which have been exploited in organic light emitting diodes, flexible displays and other optoelectronic devices. Although PPV is a material of foremost importance for many applications, its synthesis at the nano/micro scale cannot be achieved through the standard method that uses heating of a precursor polymer poly(xylene tetrahydrothiophenium chloride)(PTHT). This work demonstrates the use of direct laser writing with femtosecond pulses to obtain the synthesis of PPV in pre-determined regions, by applying three different approaches, allowing the precise fabrication of complex polymeric microcircuits, (i) in the first approach the conversion process is achieved by irradiating PTHT films with ultra-short laser pulses in previously determined regions, which leads to the spatial control of PPV formation at microscale, (ii) in the second approach, three-dimensional microstructures doped with PTHT were photopolymerized by two photons absorption. The conversion of PTHT to PPV in these doped microstructures was obtained by a subsequent thermal treatment, (iii) in the third approach, laser-induced forward transfer (LIFT) with femtosecond pulses enables the controlled deposition of PPV with high spatial resolution, providing 2D micropatterns, while preserving its structure and optical properties. The structures were characterized by scanning electron, fluorescence, transmission and confocal fluorescence microscopies. Their optical properties were analyzed by micro-photoluminescence and micro-absorption setups assembled on an inverted microscope. Raman spectroscopy, electrical measurements and atomic force microscopy were also performed. This thesis shows the use of fs-laser writing methods for the synthesis of PPV in pre-determined regions, to fabricate a variety of microdevices, thus opening new avenues in polymer-based optoelectronics.