Organic conducting polymers are essential for the development of various electronic devices, including field-effect transistors, light-emitting diodes, solar cells, and thermoelectric devices. Understanding the charge transport mechanisms within these materials, particularly the roles of polarons and bipolarons as charge carriers, is crucial. Despite the recognized importance of these carriers, there are ongoing debates regarding the interpretation of their mid-IR absorption spectral signatures in the 0.3-0.7 eV range. This is mainly due to challenges in applying the conventional mid-gap state model, especially in the context of doped P3HT (poly(3-hexylthiophene)) films. The conventional model predicts a blueshift for the mid-IR P1 band of bipolarons compared to polarons, yet recent experiments reveal both blueshifted and redshifted bands, at elevated oxidation levels, leading to confusion about the true mid-IR spectral hallmark of spinless singlet bipolarons. This thesis aims to resolve these inconsistencies by proposing a Holstein-style model for singlet bipolarons in π-conjugated polymers with nondegenerate ground states. The model incorporates hole hopping, electron−vibration coupling involving the prominent aromatic-quinoidal mode, and Coulombic interactions between (hole) polarons and between polarons and dopant anions. In contrast to the conventional interpretation where bipolaron formation results from self-trapping, our findings indicate that it is primarily driven by attractive electrostatic interactions with dopant anions. Without these anions, two holes would not pair to form singlet bipolarons. More importantly, our results indicate that the observed blueshift at lower oxidation levels signifies the increased localization of Coulombically interacting polarons, whereas at higher oxidation levels, the simultaneous emergence of both redshifted and blueshifted bands is indeed the spectral signature of spinless singlet bipolarons formation. Furthermore, we find that the binding energy of bipolarons in π-stacks of P3HT chains is significantly higher, nearly threefold, than in a single chain, highlighting the profound influence of long-range order and chain stacking on bipolarons formation. This work contributes to resolving the theoretical ambiguities surrounding charge carrier dynamics in organic conjugated polymers and enhances our understanding of their optoelectronic properties. / Chemistry

O biodiesel tem sido amplamente utilizado como uma fonte de energia renovável, que contribui para a diminuição de demanda por diesel mineral. Portanto, existem várias propriedades que devem ser monitoradas, a fim de produzir e distribuir biodiesel com a qualidade exigida. Neste trabalho, as propriedades físicas do biodiesel, tais como massa específica, índice de refração e ponto de entupimento de filtro a frio foram medidas e associadas a espectrometria no infravermelho próximo (NIR) e espectrometria no infravermelho médio (Mid-IR) utilizando ferramentas quimiométricas. Os métodos de regressão por mínimos quadrados parciais (PLS), regressão de mínimos quadrados parciais por intervalos (iPLS), e regressão por máquinas de vetor de suporte (SVM) com seleção de variáveis por Algoritmo Genético (GA) foram utilizadas para modelar as propriedades mencionadas. As amostras de biodiesel foram sintetizadas a partir de diferentes fontes, tais como canola, girassol, milho e soja. Amostras adicionais de biodiesel foram adquiridas de um fornecedor da região sul do Brasil. Em primeiro lugar, o pré-processamento de correção de linha de base foi usado para normalizar os dados espectrais de NIR, seguidos de outros tipos de pré-processamentos que foram aplicados, tais como centralização dos dados na média, 1 derivada e variação de padrão normal. O melhor resultado para a previsão do ponto de entupimento de filtro a frio foi utilizando os espectros de Mid-IR e o método de regressão GA-SVM, com alto coeficiente de determinação da previsão, R2Pred=0,96 e baixo valor da Raiz Quadrada do Erro Médio Quadrático da previsão, RMSEP (C)= 0,6. Para o modelo de previsão da massa específica, o melhor resultado foi obtido utilizando os espectros de Mid-IR e regressão por PLS, com R2Pred=0,98 e RMSEP (g/cm3)= 0,0002. Quanto ao modelo de previsão para o índice de refração, o melhor resultado foi obtido utilizando os espectros de Mid-IR e regressão por PLS, com excelente R2Pred=0,98 e RMSEP= 0,0001. Para esses conjuntos de dados, o PLS e o SVM demonstraram sua robustez, apresentando-se como ferramentas úteis para a previsão das propriedades do biodiesel estudadas / Biodiesel has been widely used as a renewable energy source which contributes to the mineral diesel decrease demand. Therefore, there are several properties that must be monitored in order to produce and distribute biodiesel with the required quality. In this work, the biodiesel physical properties such as specific mass, refractive index and cold filter plugging point were measured and associated with near infrared spectroscopy (NIR) and mid-Infrared spectroscopy (mid-IR) spectra using chemometric tools. The Partial Least Squares Regression (PLS), Interval Partial Least Squares Regression (iPLS), and Support Vector Machines Regression (SVM) with variable selection by Genetic Algorithm (GA) methods were used to model the aforementioned properties. The biodiesel samples were synthesized from different sources such as canola, sunflower, corn, and soybean. Additional biodiesel samples were purchased from a Brazil South Region supplier. Firstly, the preprocessing baseline correction was used to normalize the NIR spectral data, following others preprocessing types were applied in such as the mean center, the first derivative and standard normal variate. The best result for predicting the cold filter plugging point was using Mid-IR spectra and GA-SVM regression method, with high coefficient determination of prediction, R2Pred = 0.94 and low value of the Root Mean Square Error of Prediction, RMSEP (C) = 0.7. For the specific mass prediction model, the best result was obtained using the Mid-IR spectrums and PLS regression, with the R2Pred = 0.98 and RMSEP (g/cm3) = 0.0002. As for a prediction model for the refractive index, the best result was obtained using the Mid-IR spectrums and PLS regression, with the R2Pred = 0.98 and RMSEP = 0.0001. For these datasets, the PLS and SVM models demonstrated theirs robustness, presenting themselves as useful tools for the biodiesel properties prediction studied

O biodiesel tem sido amplamente utilizado como uma fonte de energia renovável, que contribui para a diminuição de demanda por diesel mineral. Portanto, existem várias propriedades que devem ser monitoradas, a fim de produzir e distribuir biodiesel com a qualidade exigida. Neste trabalho, as propriedades físicas do biodiesel, tais como massa específica, índice de refração e ponto de entupimento de filtro a frio foram medidas e associadas a espectrometria no infravermelho próximo (NIR) e espectrometria no infravermelho médio (Mid-IR) utilizando ferramentas quimiométricas. Os métodos de regressão por mínimos quadrados parciais (PLS), regressão de mínimos quadrados parciais por intervalos (iPLS), e regressão por máquinas de vetor de suporte (SVM) com seleção de variáveis por Algoritmo Genético (GA) foram utilizadas para modelar as propriedades mencionadas. As amostras de biodiesel foram sintetizadas a partir de diferentes fontes, tais como canola, girassol, milho e soja. Amostras adicionais de biodiesel foram adquiridas de um fornecedor da região sul do Brasil. Em primeiro lugar, o pré-processamento de correção de linha de base foi usado para normalizar os dados espectrais de NIR, seguidos de outros tipos de pré-processamentos que foram aplicados, tais como centralização dos dados na média, 1 derivada e variação de padrão normal. O melhor resultado para a previsão do ponto de entupimento de filtro a frio foi utilizando os espectros de Mid-IR e o método de regressão GA-SVM, com alto coeficiente de determinação da previsão, R2Pred=0,96 e baixo valor da Raiz Quadrada do Erro Médio Quadrático da previsão, RMSEP (C)= 0,6. Para o modelo de previsão da massa específica, o melhor resultado foi obtido utilizando os espectros de Mid-IR e regressão por PLS, com R2Pred=0,98 e RMSEP (g/cm3)= 0,0002. Quanto ao modelo de previsão para o índice de refração, o melhor resultado foi obtido utilizando os espectros de Mid-IR e regressão por PLS, com excelente R2Pred=0,98 e RMSEP= 0,0001. Para esses conjuntos de dados, o PLS e o SVM demonstraram sua robustez, apresentando-se como ferramentas úteis para a previsão das propriedades do biodiesel estudadas / Biodiesel has been widely used as a renewable energy source which contributes to the mineral diesel decrease demand. Therefore, there are several properties that must be monitored in order to produce and distribute biodiesel with the required quality. In this work, the biodiesel physical properties such as specific mass, refractive index and cold filter plugging point were measured and associated with near infrared spectroscopy (NIR) and mid-Infrared spectroscopy (mid-IR) spectra using chemometric tools. The Partial Least Squares Regression (PLS), Interval Partial Least Squares Regression (iPLS), and Support Vector Machines Regression (SVM) with variable selection by Genetic Algorithm (GA) methods were used to model the aforementioned properties. The biodiesel samples were synthesized from different sources such as canola, sunflower, corn, and soybean. Additional biodiesel samples were purchased from a Brazil South Region supplier. Firstly, the preprocessing baseline correction was used to normalize the NIR spectral data, following others preprocessing types were applied in such as the mean center, the first derivative and standard normal variate. The best result for predicting the cold filter plugging point was using Mid-IR spectra and GA-SVM regression method, with high coefficient determination of prediction, R2Pred = 0.94 and low value of the Root Mean Square Error of Prediction, RMSEP (C) = 0.7. For the specific mass prediction model, the best result was obtained using the Mid-IR spectrums and PLS regression, with the R2Pred = 0.98 and RMSEP (g/cm3) = 0.0002. As for a prediction model for the refractive index, the best result was obtained using the Mid-IR spectrums and PLS regression, with the R2Pred = 0.98 and RMSEP = 0.0001. For these datasets, the PLS and SVM models demonstrated theirs robustness, presenting themselves as useful tools for the biodiesel properties prediction studied

Heterostructures of materials with dramatically different properties are exciting for a variety of devices. In particular, the epitaxial integration of metals with semiconductors is promising for low-loss tunnel junctions, embedded Ohmic contacts, high-conductivity spreading layers, as well as optical devices based on the surface plasmons at metal/semiconductor interfaces. This thesis investigates the structural, electrical, and optical properties of compound (III-V) semiconductors employing rare-earth monopnictide (RE-V) nanostructures. Tunnel junctions employing RE-V nanoparticles are developed to enhance current optical devices, and the epitaxial incorporation of RE-V films is discussed for embedded electrical and plasmonic devices. Leveraging the favorable band alignments of RE-V materials in GaAs and GaSb semiconductors, nanoparticle-enhanced tunnel junctions are investigated for applications of wide-bandgap tunnel junctions and lightly-doped tunnel junctions in optical devices. Through optimization of the growth space, ErAs nanoparticle-enhanced GaAs tunnel junctions exhibit conductivity similar to the best reports on the material system. Additionally, GaSb-based tunnel junctions are developed with low p-type doping that could reduce optical loss in the cladding of a 4 μm laser by ~75%. These tunnel junctions have several advantages over competing approaches, including improved thermal stability, precise control over nanoparticle location, and incorporation of a manifold of states at the tunnel junction interface. Investigating the integration of RE-V nanostructures into optical devices revealed important details of the RE-V growth, allowing for quantum wells to be grown within 15nm of an ErAs nanoparticle layer with minimal degradation (i.e. 95% of the peak photoluminescence intensity). This investigation into the MBE growth of ErAs provides the foundation for enhancing optical devices with RE-V nanostructures. Additionally, the improved understanding of ErAs growth leads to development of a method to grow full films of RE-V embedded in III-V materials. The growth method overcomes the mismatch in rotational symmetry of RE-V and III-V materials by seeding film growth with epitaxial nanoparticles, and growing the film through a thin III-V spacer. The growth of RE-V films is promising for both embedded electrical devices as well as a potential path towards realization of plasmonic devices with epitaxially integrated metallic films. / text

Quantum cascade lasers (QCLs) operate due to population inversion on intersubband in unipolar mutiple-quantum-well (MQW) heterostructure. QCLs are considered one of the most flexible and powerful light semiconductor sources in the mid- and far-infrared (IR) wavelength range, covering most of the critical spectral regions relevant to IR applications. InGaAs/InAlAs/InP QCLs are the only semiconductor lasers capable of continuous wave (CW) operation at room temperature (RT) in the spectral range 3.4-12 micron. This dissertation details the development of RT QCLs based on passive nonlinear coupled-quantum-well structures monolithically integrated into mid-IR QCLs to provide a giant nonlinear response for the pumping frequency. The primary focus of short-wavelength approach in this dissertation is to develop of RT InGaAs/InAlAs/InP QCLs for lamda=2.5-3.7 micron region, based on quasi-phase-matched intracavity second harmonic generation (SHG) associated with intersubband transition. Intersubband optical transition can be engineered by the choice of quantum well and barrier thicknesses to provide the appropriate energy levels, optical dipole matrix elements, and electron scattering rates amongst other parameters. Thus, aside from their linear optical properties, resonant intersubband transitions in coupled QW's can also be designed to produce nonlinear optical medium with giant nonlinear optical susceptibilities. In long-wavelength region, at high temperature, the population inversion is reduced between the upper and lower laser levels due to the longitudinal optical (LO) phonon scattering of thermal carriers in the upper laser state and the thermal backfilling of carriers into the lower laser level from the injector state. This dissertation aims to improve an alternative approach for THz QCL sources based on intra-cavity difference frequency generation (DFG) in dual-wavelength mid-IR QCLs with a passive nonlinear structure, designed for giant optical nonlinearity. Further studies describe that Cerenkov DFG scheme allows for extraction of THz radiation along the whole length of the laser waveguide and provides directional THz emission in 1.2-4.5 THz range. An important requirement for many applications, like chemical sensing and molecular spectroscopy, is single-mode emission. We demonstrate single-mode RT DFG THz QCLs operation in 1-5 THz region by employing devices as integrated dual-period DFB lasers, where efficient solid state RT sources do not exist. / text

In this thesis, we present our original theoretical investigations of SiC microstruc-tures for extreme light control in the Reststrahlen band of Silicon Carbide (SiC), that occurs in the Mid-IR spectral regime. In this frequency regime, most of the light will be reflected from bulk SiC, due to the extreme permittivity response of SiC. However, we demonstrate that it is possible to control light to be absorbed or ultra refracted within the microstructures constructed from SiC in the Reststrahlen band of SiC. In particular, we show that this high reflective behaviour of SiC can be over-come via different mechanisms: by achieving a Photonic Crystal (PC) band-edge reflectionless condition in a SiC terminated one-dimensional (1D)-PC, by tailoring the effective phonon-polariton gap in SiC-based effective metamaterials, or by cou-pling to cavity modes in SiC structures made of rectangular-cross-section pillars. Furthermore, we demonstrate that by varying the thickness of SiC layers and filling ratio throughout SiC 1D-PC structures or by using SiC pillars of different size in a pyramid arrangement, we can achieve a broad absorption bandwidth with the SiC microstructures. This absorption control provides insight for the design of efficient thermal emitters, which can be used in thermal conversion devices. Moreover, us-ing the concept of Bloch impedance, we find that translucent spectral regions can exist in SiC 1D-PCs. This possibility is highly desirable for constructing optical components in the Mid-IR spectrum where suitable bulk highly refractive materials are rare. In addition, we also present a complete theory of propagation in lossy 1D-PCs, by systematically extending the comprehensive theory for lossless 1D-PCs. Relying on this theory, we report superbending of light, beyond 90 0 in a judiciously designed superprism constructed with a SiC 1D-PC. Since, the findings reported in this thesis are in principle applicable to any polar material, we believe that our work will inspire the design of a variety of absorptive/emissive and ultra-refractive devices across the THz/Mid-IR spectrum.

Billions of people use biomass burning cookstoves in their homes and suffer serious health repercussions. Additionally, global warming is exacerbated by cookstove emissions containing greenhouse gases and particulate matter. Improved cookstoves (ICSs) mitigate the problem, but accurate and affordable emission gas measurements, particularly of Carbon Dioxide (CO2) and Carbon Monoxide (CO), are required in order to confidently declare ICSs cleaner burning than traditional cookstoves. The aim of this research is to assess the suitability of photoacoustic (PA) CO2 detection technology for cookstove emissions monitoring. The designs of several longitudinally resonant, photoacoustic, LED, CO2 sensors of varying levels of functionality are presented. Three aluminum cell designs allowed the detection of a photoacoustic signal: a 4cm long cylinder with a ~1cm diameter (Design 3), a 3.9cm long cylindrical resonator with ~1in diameter and quarter-acoustic-wavelength buffer volumes (Designs 4a,b), and a 3.7cm long cylinder with ~1in diameter (Design 5). All three cell designs operate in the longitudinal resonant mode via the irradiation of gases inside the PA cell with a 4.3um wavelength LED, driven at an on-off frequency in the kHz range by a square wave from an Arduino. A rudimentary lock-in amplifier (LIA) based on the AD630 was considered, but the SR830 LIA was actually used to extract the desired MEMS microphone signal from noise. Designs 3-4b produced PA signals dominated by wall-absorption, but the final design (Design 5) yielded a resonant PA signal proportional to CO2 concentration. It was discovered that photoacoustic gas detection is challenging to design and set up without extensive experience and equipment. Practical lessons learned are shared. Primary limitations with the presented designs are identified as the extremely low power of the 4.3um LEDs, wall absorption due to insufficient collimation of LED radiation, dependence on temperature, and reliance on an expensive, high performance, lock-in amplifier. Further testing and development of designs like Design 5 (short cylinder with large diameter-to-length ratio) is necessary to evaluate their potential for in-field, real-time CO2 concentration measurement. Though LED PA CO2 sensing was demonstrated to be possible, it is concluded that NDIR CO2 sensors are currently better suited for cookstove use. In addition to photoacoustic detection, a method of detecting CO2 concentration by measuring resonant frequency of the gas cell (The Acoustic Method) is presented.

Les plasmas d’air à pression atmosphérique ont de nombreuses applications. Nous pouvons par exemple citer les applications biomédicales, le traitement des matériaux, la bio-décontamination environnementale et la combustion assistée par plasma. La polyvalence des décharges plasma résulte de leur capacité à produire des densités élevées d’espèces actives, sans toutefois chauffer substantiellement le gaz. Les décharges nanosecondes répétitivement pulsées (NRP) ont particulièrement reçu une grande attention en raison de leur capacité à produire des densités électroniques élevées, qui conduisent à la création de fortes densités d’espèces actives telles que l’oxygène atomique (O). Par ailleurs, des mesures de spectroscopie d’émission ont montré que des états excités du monoxyde d’azote (NO) sont produits par les décharges NRP opérant dans l’air ou dans des mélanges combustibles. Bien que les décharges NRP aient déjà fait l’objet de plusieurs investigations, les mécanismes cinétiques conduisant à la production de NO sont toujours incertains. C’est la motivation première des travaux menés dans le cadre de cette thèse. En outre, les décharges NRP se sont avérées produire une grande quantité d’oxygène d’atomique, espèce de grande importance pour la combustion assistée par plasma. Il a été en particulier démontré que grâce à la production élevée d’espèces actives, les décharges NRP peuvent stabiliser efficacement des flammes pauvres, à pression atmosphérique. Cependant la production de NO par les décharges NRP et les flammes stabilisées à l’aide des décharges NRP reste à étudier. Cela constitue le second objectif de cette thèse. Les mesures in-situ de densités absolues de NO dans les décharges plasmas et/ou en combustion sont très difficiles. Les techniques de fluorescence telle que la fluorescence induite par laser (LIF) nécessitent de complexes méthodes de calibration. Ces techniques requièrent également la connaissance des taux de quenching des états excités (en particulier à pression atmosphérique). Or ces taux de quenching sont très fortement dépendants de la température, de la nature des espèces en présence et de leur densité, et peuvent donc énormément différer entre un plasma opérant dans l’air et en combustion. D’autres techniques telles que l’utilisation des sondes à chimiluminescence sont tout aussi sujettes aux problèmes de calibration et de quenching des états excités tandis que les mesures ex-situ à l’aide d’analyseurs à gaz réalisant de l’absorption dans l’UV et l’IR peuvent conduire à des erreurs, surtout lorsqu’il s’agit de mesurer des radicaux. Dans cette étude, nous avons développé la spectroscopie d’absorption par laser à cascade quantique (QCLAS), pour des mesures in-situ de densités de NO dans l’air et en combustion. Cette technique permet de surmonter les difficultés des autres méthodes par utilisation d’une spectroscopie rotationnelle-vibrationnelle de haute résolution spectrale (10-3 cm-1). La QCLAS a les avantages d’être spectralement sélective, d’avoir une grande sensibilité et de ne pas nécessiter de calibration. Deux dispositifs expérimentaux ont été développés pour mesurer des densités de NO et des températures (1) dans une décharge NRP dans l’air, avec une résolution spatiale de 300-µm, et (2) en aval de la décharge NRP opérant dans l’air et dans des flammes méthane/air assistée par plasma, par utilisation d’une cellule multi-passages. [...] / Atmospheric pressure plasmas have numerous potential applications. These applications include for instance biomedicine, material processing, environmental biodecontamination and plasma-assisted combustion. The versatility of plasma discharges results from their ability to produce high quantities of active species without increasing the temperature of the gas appreciably. Nanosecond Repetitively Pulsed discharges (NRP) have received great attention owing to their capacity to generate high electron densities, which lead to the creation of a high density of active species such as atomic oxygen. Optical Emission Spectroscopy (OES) showed that excited nitric oxide (NO) was released by NRP discharges in air or in air/fuel mixtures.Although NRP discharges have already been the object of several investigations, the kinetic mechanisms of NO production by NRP discharges at atmospheric pressure remain somewhat unclear. This is one of the motivations for the investigations conducted in this thesis. In addition, NRP discharges were found to produce large amounts of atomic oxygen, which is of great interest for applications such as plasma-assisted combustion. It was shown in particular that thanks to this high production of active species, NRP discharges can effectively stabilize lean flames at atmospheric pressure. However, the production of NO in NRP discharges and in plasma-stabilized flames remains to be investigated. This is the second purpose of this thesis.Absolute and in-situ NO density measurements in atmospheric pressure plasma or/and flame environments are very challenging. Fluorescence-based techniques such as Laser Induced Fluorescence (LIF) require complex calibration methods. These techniques also require the knowledge of the quenching rates of the excited states (particularly at atmospheric pressure), which strongly depend on the temperature, density and nature of the species and can be very different for plasma or/and flame environments. Other techniques, such as chemiluminescence probe sampling also have quenching and calibration issues, and ex-situ UV and IR absorption-based gas analyzers can lead to errors, in particular for radicals.In this study, we developed Quantum Cascade Laser Absorption Spectroscopy (QCLAS) for in-situ nitric oxide absolute density measurements in open-air and in combustion environments. This technique overcomes the difficulties of the previous ones by using high-resolution (10-3 cm-1) rotational-vibrational absorption spectroscopy. This technique presents the advantages of high spectral selectivity, no calibration requirement, and high sensitivity. Two experimental setups were developed to measure NO densities and temperature, (1) within a NRP discharge in air, with 300-µm spatial resolution, and (2) downstream of NRP discharges in air and in plasma-assisted methane/air flames, using multi pass cell. [...]

No description available.

Ce travail de thèse est centré sur l'étude expérimentale de deux types de transformations photo-induites observées dans différents complexes métalliques (Fe, Ru, ...) à ligand nitrosyle: (i) la photo-isomérisation au cours de laquelle le ligand NO passe d'un état lié par l'azote (M-NO, état stable GS) à un état lié par l'oxygène (M-ON, état métastable MSI). C'est un processus réversible et un second état métastable, 'side-on' MSII est observable au cours du processus inverse, MSI --> 'side-on' MSII --> GS; (ii) la libération photo-induite du radical NO°. La photo-isomérisation a été étudiée dans le système [Ru(py)_4Cl(NO)](PF_6)_2.1/2H_2O (sur monocristal) par la diffraction des RX, l'absorption visible statique et l'absorption UV-Vis résolue en temps. Nous avons pu mettre en évidence un processus d'absorption de photons (473 nm) en deux étapes, suivre la dynamique des transformations directes et inverses par l'évolution des paramètres de maille et des l'absorption optique visible, caractériser structuralement l'état 'side-on' MSII. La nature de l'état intermédiaire, MSII, lors du processus direct semble être différente de l'état 'side-on' mais la très faible population de cet intermédiaire n'a pas permis de trancher définitivement. Le rôle de la molécule d'eau dans la maille du complexe [Ru(py)_4Cl(NO)](PF_6)_2.1/2H_2O a été testé par diffraction des RX sur les échantillons hydratées, déshydratées et réhydratées. L'effet de déshydratation sur l'évolution des paramètres de maille et sur la génération d'espèces MSII au cours de la photo-commutation inverse, MSI --> MSII --> GS, est présenté. La libération photo-induite du radical NO° a été étudiée dans une solution d'acétonitrile du complexe trans-(Cl,Cl)[Ru^{II}(FT)Cl_2(NO)]PF_6 par spectroscopies d'absorption UV-Vis et Mi-IR, statiques et résolues en temps. En observant la dynamique ultra-rapide de la photo-transformation, nous avons mis en évidence un processus d'absorption de photons (406 nm) en deux étapes. La nature de l'état intermédiaire est discuté par rapport à de récents calculs théoriques et au processus de photo-isomérisation. / This Ph. D. thesis is focused on the experimental study of two photo-induced processes observed in various [ML_5NO] complexes, where M=Fe, Ru, ..., L=CN, Cl, ... : (i) photo-isomerization, where the system goes from N-bound state (M-NO, stable GS state) to O-bound state (M-ON, metastable MSI state) and a second metastable state, 'side-on' MSII is observed during the inverse photo-transformation, MSI --> 'side-on' MSII --> GS; (ii) photo-induced release of NO° radical. The photo-isomerization is investigated in single crystals of [Ru(py)_4Cl(NO)](PF_6)_2.1/2H_2O compound by means of X-Ray diffraction, steady state visible and time-resolved UV-visible absorption spectroscopies. During these experiments we observed the evidence of a two-step photon absorption process (473 nm), we followed the dynamics of direct and inverse photo-switching by the evolution of lattice parameters and absorption in the visible range and we caracterised the structure of 'side-on' MSII state. The nature of MSII in the direct photo-switching, GS --> MSI, seems to be different from the 'side-on' configuration, however, we do not have a direct access to this state due to its low population. The role of water molecule in the unit cell of [Ru(py)_4Cl(NO)](PF_6)_2.1/2H_2O complex was tested by X-Ray diffraction studies on hydrated, dehydrated and rehydrated samples. The effect of sample dehydration on the unit cell parameters evolution and MSII species generation during the MSI --> MSII --> GS inverse photo-switching is presented. The photo-induced NO° release in trans-(Cl,Cl)[Ru^{II}(FT)Cl_2(NO)]PF_6 system in acetonitrile solution is studied by the UV-visible and mid-IR absorption spectroscopies, both steady state and time-resolved. By observing the ultra-fast dynamics of photo-transformation we evidenced a two-step photon absorption process (406 nm). The nature of intermediate state is discussed within the recent theoretical calculations and the photo-isomerization process.