This thesis reports new gold nanoparticle-based methods to treat chemotherapy-resistant and metastatic tumors that frequently evade conventional cancer therapies. Gold nanoparticles represent an innovative generation of diagnostic and treatment agents due to the ease with which they can be tuned to scatter or absorb a chosen wavelength of light. One area of intensive investigation in recent years is gold nanoparticle photothermal therapy (PTT), in which gold nanoparticles are used to heat and destroy cancer. This work demonstrates the utility of gold nanoparticle PTT against two categories of cancer that are currently a clinical challenge: trastuzumab-resistant breast cancer and metastatic cancer. In addition, this thesis presents a new method of gold nanoparticle delivery using T cells that increases gold nanoparticle tumor accumulation efficiency, a current challenge in the field of PTT. I ablated trastuzumab-resistant breast cancer in vitro for the first time using anti-HER2 labeled silica-gold nanoshells, demonstrating the potential utility of PTT against chemotherapy-resistant cancers. I next established for the first time the use of T cells as gold nanoparticle vehicles in vivo. When incubated with gold nanoparticles in culture, T cells can internalize up to 15000 nanoparticles per cell with no detrimental effects to T cell viability or function (e.g. migration and cytokine secretion). These AuNP-T cells can be systemically administered to tumor-bearing mice and deliver gold nanoparticles four times more efficiently than by injecting free nanoparticles. In addition, the biodistribution of AuNP-T cells correlates with the normal biodistribution of T cell carrier, suggesting the gold nanoparticle biodistribution can be modulated through the choice of nanoparticle vehicle. Finally, I apply gold nanoparticle PTT as an adjuvant treatment for T cell adoptive transfer immunotherapy (Hyperthermia-Enhanced Immunotherapy or HIT) of distant tumors in a melanoma mouse model. The results presented in this thesis expand the potential of gold nanoparticle PTT from only chemotherapy-sensitive or localized cancers to chemotherapy-resistant non-localized cancers that currently defy conventional therapies.

The electromagnetic absorption properties of plasmonic nanostructures were utilized to develop mesoscopic sites for highly efficient photothermal generation steam, SERS biosensing, and light-triggered cellular delivery uptake. Plasmonic nanostructures embedded in common thermal solutions produces vapor without the requirement of heating the fluid volume. When particles are dispersed in water at ambient temperature, energy is directed primarily to vaporization of water into steam, with a much smaller fraction resulting in heating of the fluid. Solar illuminated aqueous nanoparticle solution can drive water-ethanol distillation, yielding fractions significantly richer in ethanol content than simple thermal distillation and also produced saturated steam destroying Geobacillus stearothermophilus bacteria in a compact solar powered autoclave. Subwavelength biosensing sites were developed using the plasmonic properties of gold nanoshells to investigate the properties of aptamer (DNA) target complexes. Nanoshells are tunable core-shell nanoparticles whose resonant absorption and scattering properties are dependent on core/shell thickness ratio. Nanoshells were used to develop a label free detection method using SERS to monitor conformational change induced by aptamer target binding. The conformational changes to the aptamers induced by target binding were probed by monitoring the aptamer SERS spectra reproducibility. Furthermore, nanoshells can serve as a nonviral light-controlled delivery vector for the precise temporal and spatial control of molecular delivery in vitro. The drug delivery concept using plasmonic vectors was shown using a monolayer of ds-DNA attached to the nanoshell surface and the small molecular “parcel” intercalated inside ds-DNA loops. DAPI, a fluorescent dye, was used as the molecular parcel to visualize the release process in living cells. Upon laser illumination at the absorption resonance the nanoshell converts photon energy into heat producing a local temperature gradient that induces DNA dehybridization, releasing the intercalated molecules.

There has been growing interest in developing colloidal metal and semiconductor nanocrystals as biomedical imaging contrast agents and therapeutics, since light excitation can cause the nanocrystals to fluoresce or heat up. Recent advances in synthetic chemistry produced fluorescent 2-4 nm diameter silicon and 1-2 nm diaemeter CuInSSe nanocrystals, as well as 16 nm diameter copper selenide (Cu₂₋[subscript x]Se) nanocrystals exhibiting strong absorbance of near infrared light suitable for biomedical applications. However, the syntheses yield nanocrystals that are stabilized by an adsorbed layer of hydrocarbons, making the nanocrystals hydrophobic and non-dispersible in aqueous solution. Encapsulating these nanocrystals in amphiphilic polymer micelles enables the nanocrystals to disperse in water. Subsequently, the Si nanocrystals were injected into tissue to demonstrate fluorescence imaging, the photothermal transduction efficiency of copper selenide nanocrystals was characterized in water, and the copper selenide nanocrystals were used enhance the photothermal destruction of cancer cells in vitro. The polymer-encapsulated copper selenide nanocrystals were found to have higher photothermal transduction efficiency than 140 nm diameter Au nanoshells, which have been widely investigated for photothermal therapy. Combining the optical properties of metal and semiconductor nanocrystals with the drug-carrying capability of lipid vesicles has received attention lately since it may create a nanomaterial capable of performing simultaneous drug delivery, optical contrast enhancement, and photo-induced therapy. Hydrophobic, dodecanethiol-coated Au nanocrystals were dispersed in water with phosphatidylcholine lipids and characterized using cryo transmission electron microscopy. 1.8 nm diameter Au nanocrystals completely load the bilayer of unsaturated lipid vesicles when the vesicles contain residual chloroform, and without chloroform the nanocrystals do not incorporate into the vesicle bilayer. 1.8 nm Au nanocrystals dispersed in water with saturated lipids to form lipid-coated nanocrystal agglomerates, which sometimes adhered to vesicles, and the shape of the agglomerates varied from linear nanocrystal chains, to flat sheets, to spherical clusters as the lipid fatty acid length was increased from 12 to 18 carbons. Including squalene formed lipid-stabilized emulsion droplets which were fully loaded with the Au nanocrystals. Results with 4.1 nm Au and 2-3 nm diameter Si nanocrystals were similar, but these nanocrystals could not completely load the bilayers of unsaturated lipids. / text

Primarily, newly developed, high sensitive and accurate methods for thermal characterization of liquids using photothermal radiometry are presented. Two experimental configurations are suggested, tested and validated with usual liquid materials. These methods are used to study polymer dispersed liquid crystal samples. Dynamic thermal properties of samples are analysed verses amplitude varying applied electric field with constant frequency as well as versus frequency varying electric field with constant amplitude. Our results clearly show the thermal properties of the samples are prone to depolarizing field effects at the lower frequencies of the applied electric field. The experimental results are modeled against existing theories to predict electric properties of the sample composites. Second part of the manuscript describes the development of a novel photothermal technique based on thermoelectric effect. This technique is particularly useful for thermally characterizing thermoelectric materials without using a separate sensor for measuring induced temperature changes. A theoretical and experimental study is presented. The experiments are done on polyaniline - carbon nanotube composite pellets by measuring Seebeck voltage generated by the samples upon heating by a modulated laser beam. Additional infrared radiometry experiments are done on the same samples and the results are in good agreement with those previously found. Later on, the possibility of photothermoelectric materials to be used as sensors for finding thermal transport properties of materials with a thermal wave resonant cavity is suggested.

This dissertation is focused on the interaction between femtosecond laser and patterned two-dimensional gold nanostructures. The sample was prepared by two different lithographic techniques, the nanosphere lithography and the electron beam lithography. Characterization was carried out with scanning electron microscopy, transmission electron microscopy, atomic force microscopy, and UV-vis absorption spectroscopy. Femtosecond transient absorption spectroscopy was used to answer a number of fundamental questions regarding the laser-nanostructure interaction. Under a low density irradiation of a femtosecond laser, we examined the effect of the lattice crystallinity on the electron-phonon relaxation in monolayer periodic array nanoparticles prepared with nanosphere lithography. We found that the electron-phonon relaxation rate was faster in polycrystalline nanoparticles and decreases greatly in single crystalline nanospheres, which is explained by the presence of high density grain boundaries. The ultrafast laser-induced coherent phonon oscillations in patterned gold nanoparticles are also fully characterized. We studied the effect of size, shape, thickness, monitoring wavelength, and materials of the prismatic array nanoparticles on the period of their coherent phonon oscillations. In a gold nanodisk pair system, we found that the fractional change in the vibration frequency increases exponentially with decreasing the ratio of the interparticle separation to the particle diameter, which is explained by the coupling of the induced electric field in one nanodisk by the strong surface plasmon field of its pair partner. Based on the coherent phonon oscillation of gold caps on a polystyrene sphere monolayer array, a new all-optical gigahertz modulation technique is developed. Under a high density irradiation of a femtosecond laser, the melting and ablation processes can be induced in gold nanoparticles. We studied femtosecond laser induced shape and localized surface plasmon resonance band changes of gold prismatic array nanoparticles. We also observed that the femtosecond laser irradiation of the nanoprisms at the surface plasmon resonance absorption maximum can cause them to detach from the substrate and 'fly away'. Atomic force microscopy and scanning electron microscopy measurements revealed that the displaced nanoparticles are thinner and smaller than the undisplaced ones, which supports an atomic ablation mechanism.

Ce travail s'inscrit dans le contexte du retraitement du combustible irradié dans l'industrie nucléaire. La gestion du combustible usé fait partie des enjeux majeurs de l'industrie nucléaire aujourd'hui. Ses vastes implications sont de nature économique, politique et écologique. Puisque le combustible irradié contient 97 % des matières valorisables, de nombreux pays ont choisi de retraiter le combustible, non tant pour des raisons économiques que pour le besoin de réduire la quantité en déchets radiotoxiques. Le procédé de séparation le plus répandu est connu sous le nom PUREX et consiste à diluer le combustible dans une solution d'acide nitrique afn d'en extraire les matières valorisables, comme notamment l'uranium et le plutonium. Le procédé est soumis à des strictes contrôles qui s'effectuent au présent par prélèvement et analyse manuel des flux radiotoxiques. Il n'existe cependant peu d'outils pour la supervision du procédé en ligne. Ces travaux visent alors à développer un capteur adapté à cet environnement de mesure à la fois acide et ionisant. Les verres borosilicates étant répandus pour leur inertie chimique, nous proposons l'étude d'un capteur optique fondé sur le substrat de verre Borofloat 33 de Schott. Le capteur étudié et réalisé a été fabriqué grâce à deux technologies différentes : l'optique intégrée sur verre par échange d'ions pour la fabrication de fonction de guidage optique, et la microfluidique pour la gestion des flux acides au sein du capteur. L'approche optique permet de répondre aux besoins de polyvalence, de sensibilité et d'immunité au rayonnement électromagnétique. La microfluidique permet, quant à elle, de travailler sur des très faibles volumes d'échantillon, réduisant ainsi la radiotoxicité des flux d'analyse. Le principe de mesure du capteur repose sur l'effet photothermique, induit dans le fluide par absorption optique d'un faisceau laser d'excitation. L'absorption entraîne un changement de l'indice de réfraction du fluide qui est sondé par un interféromètre de Young, intégré sur la puce. Le volume sondé au sein du canal était de (33,5 ± 3,5) pl. Le changement d'indice de réfraction à la limite de détection était de ∆n_min = 1,2 × 10−6 , nous permettant de détecter une concentration minimale de cobalt(II) dans de l'éthanol de c_min = 6 × 10−4 mol/l, équivalent à un coefficient d'absorption de alpha_min = 1,2 × 10−2 cm−1. À la limite de détection du capteur, une quantité de N_min = (20 ± 2) fmol de cobalt(II) peut être détectée. La longueur d'interaction était de li = 14,9 µm et par conséquent l'absorbance minimale détectable égal K_min = (1,56±0,12)×10−5. / This work has been done in the context of fuel reprocessing in the nuclear industry. In fact, the handling of nuclear waste is one of the major issues in the nuclear industry. Its implications reach from economical to political to ecological dimensions. Since used nuclear fuel consists of 97 % of recyclable substances, many countries have chosen to reprocess used fuel, not only for economical reasons but also to limit the quantity of nuclear waste. The most widely employed extraction technique is the PUREX process, where the used fuel is diluted in nitric acid. The recyclable compounds can then be extracted by solvent techniques. Such processes need to be monitored crucially. However, nowadays, the process supervision is carried out by manually sampling the radioactive fluents and analyzing them in external laboratories. Not only prone to potential risks, this approach is little responsive and produces radiotoxic samples that cannot be reintroduced in the nuclear fuel cycle. In this study, we therefore present the development of a microfluidic glass sensor, based on the detection of a photothermal effect induced in the sample fluid. Microfluidics allows fluid handling on a microliter-scale and can therefore significantly reduce the sample volume and thereby the radiotoxcicity of the analyzed fluids. Photothermal spectrometry is well suited for small-scale sample analysis, since its sensitivity does not rely on the length of optical interaction with the analyte. The photothermal effect is a local refractive index variation due to the absorption of photons by the analyte species which are contained in the sample. On the sensor chip, the index refraction change is being sensed by an integrated Young interferometer, made by ion-exchange in glass. The probed volume in the channel was (33.5 ± 3.5) pl. The interferometric system can sense refractive index changes as low as ∆n_min = 1.2 × 10−6 , allowing to detect a minimum concentration of cobalt(II) in ethanol c_min = 6 × 10−4 mol/l, which is equivalent to an absorption coefficient of alpha_min = 1.2 × 10−2 cm−1 . At the detection limit, we could sense an absolute quantity of cobalt(II) of N_min = (20 ± 2) fmol. The interaction length between the excitation light and the sensing zone was li = 14.9 µm leading to a minimum detectable absorbance of K_min = (1.56 ± 0.12) × 10−5 .

Le développement d'outils numériques de prédiction de la durée de vie des polymères constitue un levier prometteur pour réduire les durées des processus de certification de ces matériaux dans le domaine automobile sans sacrifier leur fiabilité. Cette thèse s'applique à la modélisation de la photo-thermo-oxydation du polypropylène isotactique (iPP), laquelle est responsable de l'altération de ses propriétés mécaniques et d'aspect. L'approche adoptée consiste à coupler la cinétique des réactions de photo- et thermo-oxydation avec des phénomènes physiques, comme le transport du dioxygène et l'atténuation de la lumière UV dans l'épaisseur du matériau, pour décrire l'ensemble des évolutions physico-chimiques. Les propriétés aux échelles supérieures, sur lesquelles seront définis les critères de fin de vie, seront calculées a posteriori en appliquant les relations structure-propriété adéquates. Le principal enjeu était d'étendre le modèle cinétique de vieillissement thermique préexistant au vieillissement photo-thermique en prenant en compte les réactions d'amorçage photolytique. De lourdes campagnes d'essais de vieillissement et de caractérisation menées sur un iPP de référence, ainsi qu'une capitalisation exhaustive des données de la littérature d'autres iPPs, ont permis de mettre au point un modèle cinétique de photo-thermo-oxydation et de le généraliser à l'ensemble de la famille des iPPs dans de larges domaines de pression partielle d'oxygène (de 0.2 à 50 bars), de température (de 40 à 230°C) et d'exposition à la lumière UV (intensités et sources lumineuses variables) décrivant des conditions de vieillissements naturels et accélérés. La validation expérimentale du modèle a permis d'étayer l'approche cinétique et de montrer ses limites, mais aussi de révéler un certain nombre d'enjeux numériques. Le modèle a été conçu pour être un outil numérique évolutif qui permettra, à terme, d'optimiser la représentativité des méthodes d'essais de vieillissement et la performance des formulations commerciales d'iPP. L'ensemble de ces développements théoriques et numériques peut être appliqué à la photo-thermo-dégradation d'autres types de polymères, mais aussi dans d'autres champs d'application de la photochimie macromoléculaire telle que la photo-polymérisation UV.Mots-Clés : Polypropylène, photo-thermo-oxydation, contrôle par la diffusion d'oxygène, effet d'écran, modélisation cinétique, prédiction de durée de vie. / Developing numerical tools for polymer lifetime prediction constitutes a promising opportunity for shortening the duration of material certification procedures in the automotive industry without decreasing their reliability. This PhD thesis aims at modeling the photothermal oxidation of isotactic polypropylene (iPP), which is responsible for the alteration of both its mechanical and aspect properties. The adopted approach consists in coupling the kinetics of photo- and thermo-oxidation reactions with physical phenomena, such as oxygen transport and UV-light attenuation in the material thickness, in order to describe all the physico-chemical changes. Upper-scale properties, from which will be defined the end-of-life criteria, will be calculated afterwards by applying the suitable structure-property relationships. The main challenge was to extend the pre-existing kinetic model of thermal ageing to photothermal ageing by taking into account initiation reactions of photolysis. Heavy campaigns of ageing and characterization tests made on a reference iPP, as well as an exhaustive capitalization of literature data of other iPPs, have allowed elaborating a kinetic model of photothermal oxidation and to generalize it to the whole iPP family in large domains of oxygen partial pressure (from 0.2 to 50 bars), temperature (from 40 to 230°C) and UV-light exposure (variable intensities and light sources) describing both natural and accelerated ageing conditions. The experimental validation of the model has allowed substantiating the kinetic approach and showing its limitations, as well as highlighting some numerical issues. The model has been designed in order to be an upgradable numerical tool which will allow, at term, optimizing the representativeness of the ageing testing devices and the performance of commercial iPP formulations. All these theoretical and numerical developments are prone to be applied to the photothermal degradation of other types of polymer substrates, but also in other application fields of the macromolecular photochemistry such as UV-photopolymerization.Keywords: Polypropylene, photothermal oxidation, oxygen diffusion control, screen effect, kinetic modeling, lifetime prediction.

L’effet photothermique permet de détecter efficacement des nanoparticules d’or avec un microscope en champ lointain grâce à leur forte absorption de la lumière. L’absence de problème photophysique fait des nanoparticules d’or une alternative au marquage de biomolécules par des sondes fluorescentes. La méthode PhACS (Photothermal Absorption Correlation Spectroscopy) utilise les fluctuations de signal photothermique dues au passage de nanoparticules dans le volume de détection pour étudier leur diffusion. Cette méthode permet également la mesure précise de diamètres hydrodynamiques de nanoparticules fonctionnalisées. La méthode SNaPT (Single Nano-Particle Tracking) réalise le suivi bidimensionnel de nanoparticules individuelles grâce à une localisation effectuée par triangulation. Nous avons appliqué cette méthode pour étudier la diffusion des intégrines alphaV-beta3 marquées par des nanoparticules d’or de 5 nm dans les adhérences focales, points d’ancrage entre le cytosquelette de la cellule et la matrice extracellulaire. Nous observons que ces intégrines ont tendance à former des agrégats qui alternent entre un mouvement diffusif et un mouvement confiné. Ce résultat appelle maintenant à un nouveau modèle où nous aurions une redistribution continue des intégrines au sein des adhérences focales. / Gold nanoparticles may be detected with optical far-field microscopy by use of the photothermal effect due to their strong light absorbance. With no photophysic issues, gold nanoparticles are an alternative to fluorescent probes for use in biological systems. The PhACS method (Photothermal Absorption Correlation Spectroscopy) is used to study diffusion by measuring the autocorrelation of photothermal signal fluctuations due to nanoparticles passing through the detection volume. This method is sensitive enough to mesure the precise hydrodynamic diameter of functionalised nanoparticles. The SnaPT method (Single Nano-Particle Tracking) can track 2-dimensional motion of individual nanoparticles by pinpointing the localization with a triangulation method. The SNaPT method was used to study motion of alphaV-beta3 integrins that were bound to a 5 nm gold nanoparticle inside focal adhesion, where the cell cytoskeleton is linked to the extracullular matrix. The integrin was found to organize into clusters oscillating between the bound and diffuse states. These observations require new working models where integrins would be constantly redistributed.

Durant cette thèse, les difficultés rencontrées pour la mesure de température de surface des composants métalliques face au plasma dans les tokamaks sont présentés. Les méthodes de thermographie infrarouge nécessitent de connaitre l'émissivité du matériau et la contribution de l'environnent pour les matériaux de faible émissivité. Des méthodes ont été développées afin de s'affranchir de ces difficultés mais elles répondent à des configurations particulières et aucune n'est adaptée pour une mesure de température de surface de matériaux métalliques dans un tokamak.La méthode de pyrométrie active présentée dans cette étude réalise des mesures de température de surface indépendamment du flux réfléchi et de l'émissivité en utilisant l'effet photothermique. La validation de cette technique en laboratoire sur des matériaux métalliques avec un flux réfléchi pour les régimes impulsionnel et modulé s'est accompagnée d'une modélisation de la variation de température induite par l'effet photothermique et de l'évolution temporelle des signaux obtenus pour optimiser les paramètres de la source et de la chaine d'acquisition. Les résultats expérimentaux ont déterminé les domaines d'application en température et en longueur d'onde de détection.Le dimensionnement d'une installation de pyrométrie active sur tokamak avec une caméra infrarouge bicolore a été réalisé pour une mesure de température sans contact.La méthode de pyrométrie active est une technique complémentaire des méthodes classiques utilisées dans le cadre de la thermographie en environnement tokamak qui permet de réaliser des mesures de température de surface locale et 2D indépendantes du flux réfléchi et de l'émissivité. / During this PhD, the challenges on the non-intrusive surface temperature measurements of metallic plasma facing components in tokamaks are reported. Indeed, a precise material emissivity value is needed for classical infrared methods and the environment contribution has to be known particularly for low emissivities materials. Although methods have been developed to overcome these issues, they have been implemented solely for dedicated experiments. In any case, none of these methods are suitable for surface temperature measurement in tokamaks.The active pyrometry introduced in this study allows surface temperature measurements independently of reflected flux and emissivities using pulsed and modulated photothermal effect. This method has been validated in laboratory on metallic materials with reflected fluxes for pulsed and modulated modes. This experimental validation is coupled with a surface temperature variation induced by photothermal effect and temporal signal evolvement modelling in order to optimize both the heating source characteristics and the data acquisition and treatment. The experimental results have been used to determine the application range in temperature and detection wavelengths.In this context, the design of an active pyrometry system on tokamak has been completed, based on a bicolor camera for a thermography application in metallic (or low emissivity) environment.The active pyrometry method introduced in this study is a complementary technique of classical infrared methods used for thermography in tokamak environment which allows performing local and 2D surface temperature measurements independently of reflected fluxes and emissivities.

Ce mémoire de thèse porte sur l'exploitation de l'effet Seebeck pour la caractérisation thermo-physique des matériaux thermoélectriques (TE) solides et liquides. Lors de travaux récents au sein du laboratoire, la technique photothermoélectrique (PTE) a été développée pour la caractérisation thermique de matériaux TE solides de faibles conductivités électriques. Dans ce travail, l'utilisation de cette technique a été généralisée à tous les matériaux TE solides (de faibles ou de hautes conductivités électriques). Cela est rendu possible par la prise en compte de la nature gaussienne de l'excitation thermique modulée à laquelle le matériau est soumis ainsi que par la compréhension des effets de couplage des mécanismes de transport thermique et électrique dans les matériaux TE. Dans cette thèse, plusieurs matériaux thermoélectriques solides ont été étudiés : le trisulfure de titane (TiS₃), les oxydes types Bi₂Ca₂Co₁,₇Oₓ, le séléniure du tellurure de bismuth (Bi₂Te₂,₄Se₀,₆). La tension auto-induite par effet Seebeck a été aussi exploitée pour la détection des transitions de phases que présentent certains matériaux thermoélectriques, ici le cas du séléniure de cuivre a été étudié. Une nouvelle procédure qui permet de déterminer l'évolution de la diffusivité thermique d'un matériau TE en fonction de la température est présentée. En plus des matériaux TE solides, la technique PTE a été étendue à l'étude des matériaux thermoélectriques liquides (LTE). Un modèle théorique qui décrit le signal délivré par un matériau LTE soumis à une excitation thermique périodique a été développé. Ensuite, une étude de l'évolution des propriétés thermiques d'un matériau LTE en fonction de la concentration d'un soluté a été réalisée. Enfin, l'approche dite de cavité résonnante d'ondes thermiques (TWRC) a été utilisée pour investiguer thermiquement des matériaux LTE. À notre connaissance, c'est la première fois que l'approche TWRC est utilisée pour l'analyse du signal généré par un liquide thermoélectrique. L'utilisation des LTE comme capteurs thermiques a été aussi abordée dans ce travail. / The use of the self-induced Seebeck effect in thermophysical characterization of solid and liquid thermoelectric (TE) materials is described in this manuscript. In previous works, the photothermoelectric technique (PTE) has been developed in our laboratory for the thermal characterization of solid TE materials having low electrical conductivities. In this work, we first generalized the use of the PTE technique to all solid thermoelectric materials (with high or low electrical conductivities). This is achieved by taking into account the Gaussian shape of the thermal source exciting the material as well as by the understanding of the coupling effects between thermal and electrical transport mechanisms when a TE material is submitted to a modulated thermal excitation. In this thesis, several solid thermoelectric materials were studied : Titanium trisulfide (TiS₃),Bi₂Ca₂Co₁,₇Oₓ oxydes and Bismuth Selenido-telluride (Bi₂Te₂,₄Se₀,₆). Then, the self-induced Seebeck voltage was used for the detection of phase transitions exhibited by certain thermoelectric materials. The case of the copper selenide (Cu₂Se) was studied. A new procedure allowing to follow the temperature dependance of the thermal diffusivity of solid TE materials is also presented. In this work, the PTE technique was extended to liquid thermoelectric (LTE) materials. Indeed, a theoretical model describing the signal delivered by a LTE material subject to a periodic thermal excitation has been developed. Then, a study of the evolution of the thermal properties of an electrolyte as function of a solute concentration was performed. Finally, the thermal-wave resonator cavity (TWRC) approach was used to characterize thermally LTE materials. As far as we know, this is the first method proposing a TWRC approach applied directly to the sensor itself. The use of LTE such as heat sensors was also addressed here.