On étudie le comportement thermomécanique de colis de déchets vitrifiés par modélisation multi- physiques. Les colis sont réalisés avec un conteneur en acier inoxydable dans lequel est coulé un verre borosilicaté. Pour le verre, la méthode des éléments finis est employée pour les calculs thermiques, la relaxation structurale du volume massique, le comportement viscoélastique et l’endommagement. Ces lois consécutives modélisent l’influence de la sollicitation thermique initiale. La relaxation structurale du verre, issue du modèle TNM-KAHR, permet la prise en compte d’effets fondamentaux quant à la transition vitreuse, en fonction des traitements thermiques expérimentaux et simulés. Lorsque le verre dépasse localement une criticité du champ de contrainte, on procède au couplage du calcul de structure viscoélastique, pour le verre solide en relaxation,avec la mécanique de l’endommagement qui réactualise la rigidité et les contraintes en mode I et en mode II. On applique cette méthodologie complète de simulation à l’issue des adaptations nécessaires au cas de blocs de verre massifs en solidification. Ces modèles permettent alors l’obtention de surfaces de fracturation quantifiées, dans le verre, à partir de l’énergie dissipée par le modèle d’endommagement. / We study the thermomechanical behavior of vitrified waste packages by multiphysics modeling. The packages are manufactured by the cast of borosilicate glass into stainless steel canisters. The finite element method is used for the thermal computations.In the glass, the finite element analysis is also used to compute the specific volume evolution and the viscoelastic behavior, due to the structural relaxation of glass, as well as the simulation of the damage behavior. These consecutive behavior laws model theinfluence of the initial thermal response. Glass structural relaxation is computed using the TNM-KAHRmodel, which allows us to take into account fundamental phenomena of the glass transition, depending on the results of experimental and simulated thermal treatments. For the solid glass within this relaxation process, the stress may locally increase beyond critical values. The viscoelastic structure simulation is then coupled with continuum damage mechanics where stresses and stiffness are updated in mode I and mode II. We apply this simulation protocol after adopting conditions relative to the case of these manufactured bulky solidifying glass casts. The models then allow us to quantify the cracking surfaces inside the glass fromthe energy dissipated within the damagemodel.

Ce projet est consacré à l'étude des propriétés optiques des films minces en nitrure d'aluminium dopé par des terres rares. Plus particulièrement, le travail est orienté pour étudier les mécanismes de luminescence des éléments RE sélectionnés incorporés dans des films minces AlN pour être utilisés comme candidats aux dispositifs d'éclairage. Au cours de cette thèse, la technique de pulvérisation de magnétron réactif est utilisée pour synthétiser les films minces AlN non dopés et dopés. La technique et le traitement des films sont discutés en détail. L'effet des conditions de pulvérisation sur la structure et les propriétés optiques des films préparés est étudié. La corrélation entre les conditions de pulvérisation cathodique, l'orientation cristallographique, la morphologie, la microstructure et les propriétés optiques sont établies. Les analyses de structure et de composition des échantillons préparés ont été étudiées par plusieurs moyens, tels que la microscopie électronique à transmission, la spectroscopie à rayons X à énergie dispersive et la spectrométrie de rétrodiffusion Rutherford. Les propriétés optiques des films sont caractérisées par une transmission UV-Visible, une spectroscopie d'Ellipsometry et une spectroscopie de photoluminescence / This project is dedicated to study the optical properties of rare earth-doped aluminum nitride thin films. More particularly, the work is oriented to investigate the luminescence mechanisms of selected RE elements incorporated in AlN thin films to be used as a candidate for lighting devices. During this thesis, reactive magnetron sputtering (RMS) technique is used to synthesize the undoped and doped AlN thin films. The technique and films processing are discussed in details. The effect of sputtering conditions on the structure and optical properties of the prepared films are investigated. The correlation between the sputtering conditions, the crystallographic orientation, the morphology, the microstructure and the optical properties are established. The structure and composition analyses of the prepared samples have been investigated by several means, such as transmission electron microscopy (TEM), Energy-dispersive X-ray spectroscopy (EDS), and Rutherford backscattering spectrometry (RBS). The optical properties of the films are characterized by UV-Visible transmission, Ellipsometry spectroscopy, and Photoluminescence spectroscopy

Στην παρούσα Ειδική Ερευνητική Εργασία μελετόνται οι φωτοφυσικές ιδιότητες γνωστών χρωμοφόρων μορίων. Συγκεκριμένα μελετάται η Coumarin 30, η Fluorescein Isothiocyanate και η Dichlorofluorescein, τόσο με φασματοσκοπία σταθερής κατάστασης όσο και με φασματοσκοπία χρονικής ανάλυσης μέσω της τεχνικής Time Correlated Single Photon Counting. Η διερεύνηση γίνεται με τα μόρια αυτά να βρίσκονται σε μορφή διαλυμάτων με στόχο τον προσδιορισμό της συμπεριφοράς τους όταν αυτά βρισκονται σε διαφορετικά περιβάλλοντα (διαλύτες). Επιπλέον ερευνώνται οι αλληλεπιδράσεις των μορίων αυτών μέσω της φασματοσκοπίας σταθερής κατάστασης και χρονικής ανάλυσης όταν βρίσκονται σε μορφή μειγμάτων. / In this Master Thesis, the phophysical properties of chromophrores are investigated. Specifically, Coumarin 30, Fluorescein Isothiocyanate and Dichlorofluorescein are studied with steady – state spectroscopy as well as with time – resolved spectroscopy via the technique of Time Correlated Single Photon Counting. The study of these molecules focuses also on solvent – solute effects. Finally, interactions between them are also studied through steady – state spectroscopy and time resolved spectroscopy.

In this work, alkaline earth aluminate phosphors doped with rare-earth ions and manganese were synthesized using combustion method. Several characterization techniques were used to study the structural and luminescent properties of the as-synthesized phosphors, namely X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray energy Dispersive Spectroscopy (EDS), Ultraviolet-Visible (UV-Vis) Spectroscopy, Photoluminescence (PL), and Thermoluminescence (TL). The structural properties were studied by collecting the XRD patterns of the samples using an X'Pert PRO PANalytical diffractometer with CuKα at λ = 0.15405 nm. The particle morphologies of the as-synthesized powder phosphors were investigated using a JEOL JSM-7500F field-emission scanning electron microscope (FE-SEM). The optical properties of the phosphors were studied using Perkin-Elmer Lambda 750s UV-Vis spectrometer, Jobin Yvon/SPEX FluoroLog spectrofluorometer (Model FL-1040) and Riso TL/OSL reader (Model DA-20). The as-prepared SrAl2O4:Eu 2+ ; SrAl2O4:Dy 3+; SrAl2O4:Mn 2+; phosphors were synthesized at an initiating temperature of 600 oC. The XRD patterns were consistent with the low temperature monoclinic structure of SrAl2O4 for all the as-synthesized phosphor powders. SEM measurements showed nano-rod like particles. The SrAl2O4:Eu 2+ ; SrAl2O4:Dy 3+; SrAl2O4:Mn 2+ samples were excited using a 450 W Xenon light source at 364 nm, 390 nm, and 426 nm respectively. A broad blue emission peak at 500 nm shown by the SrAl2O4:Eu 2+ sample is attributed to the 6 1 7 4f 5d 4f transition of the Eu 2+ ion. Also, the red sharp emission lines due to the 4f-4f transition of the Eu 3+ were observed. SrAl2O4:Dy3+ samples exhibited blue, green, and red emissions which can be atributed to the 4 6 9/2 15/2 F  H ,4 6 9/2 13/2 F  H , and 4 6 9 11 2 2 F  H transitions of Dy 3+ ions respectively. The two broad emissions (green at 513 nm and red at 650 nm) shown by 2+ 0.98 2 4 0.02 Sr Al O :Mn sample can be atributed to the 4 4 6 6 1 1 T ( G)  A ( S) transition of the Mn 2+ ion in the sample. The SrAl2O4:Eu 2+ , Dy 3+ ; SrAl2O4:Eu 2+, Mn 2+ ; SrAl2O4:Dy 3+, Mn 2+; and SrAl2O4:Eu 2+ ,Mn 2+, Dy 3+ phosphors were synthesized by combustion method at an initiating temperature of 600 oC. The blue emissions were observed in all the samples except SrAl2O4:Eu 2+ ,Mn 2+, Dy 3+ sample. The SrAl2O4:Eu 2+ ,Mn 2+, Dy 3+ phosphor showed the longest afterglow intensity. The BaAl2O4 doped with Eu 2+ , Mn 2+ and Dy 3+ phosphors synthesized at an initiating temperature of 600 oC using combustion method. The XRD patterns confirmed the hexagonal structure of BaAl2O4 in all the as-synthesized samples. A broad blue emission of the BaAl2O4:Eu 2+ sample at 490 nm is attributed to the 6 1 7 4f 5d 4f transition of the Eu 2+ ion in the sample. A red emission peak observed at 611 nm is due to the 4f - 4f transition of un-reduced Eu 3+ ions during the combustion reaction. A blue emission at 482 nm, a green emission at 575 nm, and a red emission at 663 nm of the BaAl2O4:Dy 3+ sample can be associated with 4 6 9/2 15/2 F  H ,4 6 9/2 13/2 F  H , and 4 6 9 11 2 2 F  H transitions of the Dy 3+ ions respectively. The green emission peaks exhibited by BaAl2O4:Mn 2+ sample at 512 nm is due to the 4 4 6 6 1 1 T ( G)  A ( S) transitions of the Mn 2+ ions. Barium aluminate phosphors doped with different concentrations of Dy 3+ ion were synthesized by combustion method at an initiating temperature of 600 oC. The XRD patterns confirmed the hexagonal structure of BaAl2O4. The emission peaks observed at 482 nm, 575 nm, and 663 nm are due to4 6 9/2 15/2 F  H ,4 6 9/2 13/2 F  H and 4 6 9 11 2 2 F  H transitions of Dy 3+ ion respectively. The PL measurements also confirmed the quenching of luminescence at higher concentrations of the Dy 3+ ion. The UV-Vis measurements has confirmed the increase in the band-gap of the BaAl2O4 sample followed by a decrease and an increase again as doping concentration of the Dy 3+ increased. The X-ray diffraction patterns of the Ca0.97M0.3Al2O4:Eu 2+ , Dy 3+ (M = Ba, Mg, and Sr) powder samples prepared by combustion method confirms the monoclinic structure of CaAl2O4 in all samples. A broad emission peak at 490 nm for both Ba 2+ and Mg 2+ substituted samples and the one for Sr 2+ substituted sample at 485nm are attributed to the 6 1 7 4f 5d 4f transition of the Eu 2+ . The decay curves confirmed that the Mg 2+ substituted sample has a longer persistence (phosphorescence) than all the other samples. / Physics / M. Sc. (Physics)

Un-doped, Tb3+ as well as Yb3+ doped ZnO nanocrystals with different concentrations of RE3+ (Tb3+, Yb3+) ions were successfully synthesized via sol-gel method to produce rare earth activated zinc oxide nanophosphors. The phosphor powders were produced by drying the precursor gels at 200˚C in ambient air. Based on the X-ray diffraction results, it was found that the pure and RE3+ doped ZnO nanophosphors were highly polycrystalline in nature regardless of the incorporation of Tb3+ or Yb3+ ions. Moreover, the diffraction patterns were all indexed to the ZnO Hexagonal wurtzite structure and belong to P63mc symmetry group. The Raman spectroscopy confirmed the wurtzitic structure of the prepared samples. Elemental mapping conducted on the as prepared samples using Scanning electron microscope (SEM) equipped with energy dispersive X-ray spectrometer (EDX) revealed homogeneous distribution of Zn, O, and RE3+ ions. The high resolution transmission electron microscope (HR-TEM) analyses indicated that the un-doped and RE3+ doped samples were composed of hexagonal homogeneously dispersed particles of high crystallinity with an average size ranging from 4 to 7 nm in diameter, which was in agreement with X-ray diffraction (XRD) analyses. ZnO:Tb3+ PL study showed that among different Tb3+ concentrations, 0.5 mol% Tb3+ doped ZnO nanoparticles showed clear emission from the dopant originating from the 4f-4f intra-ionic transitions of Tb3+ while the broad defects emission was dominating in the 0.15 and 1 mol% Tb3+doped ZnO. Optical band-gap was extrapolated from the Ultraviolet Visible spectroscopy (UV-Vis) absorption spectra using TAUC‟s method and the widening of the optical band-gap for the doped samples as compared to the un-doped sample was observed. The PL study of ZnO:Yb3+ samples was studied using a 325 nm He-Cd laser line. It was observed that the ZnO exciton peak was enhanced as Yb3+ions were incorporated in ZnO matrix. Furthermore, UV-VIS absorption spectroscopic study revealed the widening of the band-gap in Tb3+ doped ZnO and a narrowing in the case of Yb3+ doped ZnO system. X-ray photoelectron spectroscopy demonstrated that the dopant was present in the doped samples and the result was found to be consistent with PL data from which an energy transfer was evidenced. Energy transfer mechanism was evidenced between RE3+ and ZnO nanocrystals and was discussed in detail. / Physics / M.Sc. (Physics)

Ce travail de thèse est dédié à l'étude des transitions radiatives dans les matériaux de nitrure et d'oxyde de silicium dopés aux ions de terres rares (Er3+, Nd3+). La caractérisation optique des films minces élaborés par évaporation thermique est basée sur la spectroscopie de photoluminescence. Les études menées s'inscrivent dans la recherche de processus d'excitation indirecte des ions Er3+ et Nd3+ dans des matrices à base de silicium. Dans les nitrures et oxynitrures de silicium, un processus de transfert d'énergie permettant l'excitation indirecte des ions Er3+ est mis en évidence. Pour les couches minces amorphes, le couplage est attribué à des états électroniques localisés dans la bande interdite de la matrice. Pour les films recuits à haute température, les nanocristaux de silicium (nc-Si) jouent un rôle majeur dans l'excitation indirecte de l'erbium. Dans les matrices d'oxyde de silicium, l'existence de processus d'excitations directe et indirecte des ions Nd3+ est démontrée. Pour les films amorphes, l'excitation indirecte du Nd se fait via des états électroniques localisés dans la bande interdite de la matrice. Pour les films recuits au-delà de 1000 °C, les nc-Si jouent le rôle de sensibilisateurs pour les ions Nd3+. Les résultats suggèrent que l'excitation indirecte des ions Nd3+ grâce aux états localisés dans la bande interdite de la matrice pourrait être plus efficace que l'excitation via les nc-Si / This thesis is devoted to the study of radiative transitions in rare-earth (Er, Nd) doped silicon oxide and silicon nitride thin films. The optical characterization of thin films prepared by thermal evaporation is based on photoluminescence spectroscopy. In this work, we investigate indirect excitation processes of Er3+ and Nd3+ ions in silicon based materials. In silicon nitride and silicon oxinitride, an energy transfer leading to the indirect excitation of Er3+ ions is demonstrated. For amorphous samples, the sensitization of Er3+ ions is attributed to localized electronic states in the matrix bandgap. For samples annealed at high temperature, silicon nanocrystals play a major role in the indirect excitation of erbium. In silicon oxide thin films, we evidences that both direct and indirect excitation processes of Nd3+ ions occur. For amorphous samples, indirect excitation occurs thanks to localized electronic states in the matrix bandgap. For samples annealed at temperatures above 1000 °C, silicon nanocrystals are sensitizers of Nd3+ ions. Results suggest that indirect excitation thank to localized states in the matrix bandgap could be more efficient than indirect excitation thanks to silicon nanocrystals

The aim of the present thesis is to evaluate fast scintillator materials, in both single-crystal and powder form, for possible usage in dedicated gamma ray imaging applications as well as in X-ray imaging techniques, requiring high frame rates. Powder scintillators are traditionally used in conventional X-ray imaging due to their property to produce high resolution images. This is because laterally directed optical photons, originating from the point of X-ray interaction, are strongly attenuated by light scattering effects on powder grains. This property however is their principal drawback for routine Nuclear Medicine applications. In these applications, photon counting accuracy rather than spatial resolution is required and to this aim high transparency crystals are used. In the present study we have tried to estimate whether the use of powder phosphors can improve the image quality in a dedicated gamma-ray system where spatial resolution than sensitivity is of primary significance. Evaluation was performed in thin and thick phosphor layers easily produced in the laboratory. In addition we present a low cost solution – consisting of a thick continuous powder scintillator screen – for use in dedicated high resolution small gamma imager. The advantages and disadvantages of proposed powder detector performance were compared to two standard 3 x 3 x 5mm3 and 2 x 2 x 3mm3 pixellated CsI:Tl scintillator detector configurations. System performance in terms of system sensitivity, system spatial resolution, energy resolution and linear energy response were measured at energy of 140 keV for close-proximity nuclear emission imaging. All measurements were carried out in photon counting mode in planar imaging configuration. The investigation was divided into two parts: Fast powder scintillators: In this part, powder scintillator screens of LSO:Ce, YAG:Ce and GOS:Pr were prepared in various coating thicknesses. Measurements concerning determination of emission spectra and absolute luminescence efficiency were carried out under X-ray excitation from 22 to 140 kV. Related parameters giving informations on luminescence and intrinsic properties of the phosphors such as X-ray luminescence efficiency, quantum detection efficiency, energy absorption efficiency and intrinsic conversion efficiency were also examined. Low cost and high resolution detector module: The goal of this part was to propose and evaluate a low cost solution for detector module – consisting of a thick continuous powder scintillator screen – for use in dedicated high resolution small gamma imagers. For the latter purpose, we examined the performance of the aforementioned fast powder scintillators in the form of thick screens easily produced in the laboratory. System performance in terms of system sensitivity, system spatial resolution, energy resolution and linear energy response were measured and compared for two standard 3 x 3 x 5mm3 and 2 x 2 x 3mm3 pixellated CsI:Tl. / Ο σκοπός της παρούσας διατριβής είναι η αποτίμηση φθοριζόντων υλικών υψηλής απόκρισης, τόσο σε κρυσταλλική όσο και σε κοκκώδη μορφή για πιθανή χρησιμοποίησή τους σε συγκεκριμένους τύπους ανιχνευτικών συστημάτων Πυρηνικής Ιατρικής όπως επίσης σε συστήματα απεικόνισης με ακτίνες Χ που απαιτούν πολύ γρήγορες λήψεις ιατρικής εικόνας. Τα φθορίζοντα υλικά κοκκώδους μορφής χρησιμοποιούνται ευρύτατα στην απεικόνιση με ακτίνες-Χ λόγω της υψηλής διακριτικής ικανότητας που μπορεί να επιτευχθεί. Στην παρούσα διατριβή μελετήθηκε κατά πόσο η χρήση νέων, γρήγορων φθοριζόντων υλικών κοκκώδους μορφής μπορεί να βελτιώσει την απόδοση συγκεκριμένων τύπων ανιχνευτικών συστημάτων Πυρηνικής Ιατρικής (π.χ. dedicated small nuclear imagers), στα οποία η διακριτική ικανότητα του συστήματος είναι πιο σημαντική από την ευαισθησία. Η αποτίμηση έγινε σε φθορίζοντα μεγάλου πάχους που παρασκευάστηκαν στο εργαστήριο. Επιπρόσθετα στην παρούσα διατριβή παρουσιάζεται η εφαρμογή ενός χαμηλού κόστους συμπαγούς ανιχνευτικού υλικού κοκκώδους μορφής σε ένα εξειδικευμένο σύστημα Πυρηνικής Ιατρικής. Γίνεται συστηματική μελέτη και εκτενής αναφορά στα πλεονεκτήματα και τα μειονεκτήματα αυτού του συστήματος. Τα αποτελέσματα συγκρίνονται με αντίστοιχα αποτελέσματα που ελήφθησαν με χρήση διακριτοποιημένων σπινθηριστών τύπου CsI:Tl, μεγέθους 3 x 3 x 5mm3 και 2 x 2 x 3 mm3. Η απόδοση του συστήματος ως προς την ευαισθησία (sensitivity), τη χωρική διακριτική ικανότητα (spatial resolution) και την ενεργειακή διακριτική ικανότητα (energy resolution) αποτιμήθηκε για ενέργεια 140 keV, που αντιστοιχεί στην ενέργεια του ισοτόπου 99mTc που χρησιμοποιείται ευρύτατα σε εξετάσεις Πυρηνικής Ιατρικής. Η πειραματική μελέτη χωρίστηκε σε δύο μέρη: Φθορίζοντα υλικά κοκκώδους μορφής: Στο πρώτο μέρος της παρούσας διδακτορικής διατριβής μελετήθηκαν τα φθορίζοντα υλικά κοκκώδους μορφής LSO:Ce, YAG:Ce και GOS:Pr σε διάφορα πάχη και για μεγάλη κλίμακα ενεργειών (Υψηλή τάση λυχνίας ακτίνων-Χ από 22 kV έως 140 kV). Ανιχνευτής χαμηλού κόστους και υψηλής διακριτικής ικανότητας: Ο τελικός στόχος της παρούσας διατριβής ήταν η κατασκευή ενός ενιαίου ανιχνευτή, βασισμένου σε σπινθηριστή κοκκώδους μορφής, χαμηλού κόστους και υψηλής διακριτικής ικανότητας, κατάλληλου για χρήση σε εξειδικευμένα συστήματα Πυρηνικής Ιατρικής. Για το σκοπό αυτό μελετήθηκε η συμπεριφορά των υλικών κοκκώδους μορφής LSO:Ce, YAG:Ce και GOS:Pr υπό διέγερση ακτίνων γάμμα με ισότοπο Τεχνητίου (99mTc), ενέργειας 140 keV, που χρησιμοποιείται ευρύτατα στην Πυρηνική Ιατρική. Τα υλικά αυτά υπό την μορφή ενιαίου, μεγάλου πάχους ( ≥2mm) και διαμέτρου (9 cm), συμπαγούς ανιχνευτή αξιολογήθηκαν με τεχνικές απεικόνισης μονού φωτονίου (single photon counting mode).