Ce mémoire traite des propriétés du La2CuO4 dopé en trous, le premier supraconducteur à haute température critique ayant été découvert. Les différentes phases électroniques du cristal y seront présentées, ainsi que le diagramme de phases en dopage de ce matériau. Les trois structures dans lesquelles on peut retrouver ce cristal seront décrites en détail, et leurs liens présumés avec les phases électroniques seront présentés. Il s’en suivra une étude utilisant la théorie de la fonctionnelle de la densité combinée au modèle de Hubbard (DFT+U) des différentes phases structurales, en plus des phases antiferromagnétiques et paramagnétiques. L’effet de la corrélation électronique sur la structure cristalline sera également étudié par l’intermédiaire du paramètre de Hubbard. Le but sera de vérifier si la DFT+U reproduit bien le diagramme de phases expérimentales, et sous quelles conditions. Une étude des effets de l’inclinaison des octaèdres d’oxygène sur la structure électronique sera également présentée. / Presented here is a study on the hole doped La2CuO4, the first discovered high-­‐Tc superconductor of the cuprate family. The different electronic phases of this crystal are briefly reviewed. The three crystal structures present in this material are described, and the link between those phases and the electronic structure are discussed. The relationship of those structural phases with the magnetic phases is investigated with the help of calculations based on the density functional theory where an additional Hubbard term has been added (DFT+U). With the help of the Hubbard parameter, the effect of the electronic correlation’s strength on the structural parameters of the crystal is also studied. The idea here is to verify how well the DFT+U is able to reproduce the experimental phase diagram of this material. The effect of the tilting of the oxygen octahedras on the electronic structure is also addressed.

Ce mémoire traite des propriétés du La2CuO4 dopé en trous, le premier supraconducteur à haute température critique ayant été découvert. Les différentes phases électroniques du cristal y seront présentées, ainsi que le diagramme de phases en dopage de ce matériau. Les trois structures dans lesquelles on peut retrouver ce cristal seront décrites en détail, et leurs liens présumés avec les phases électroniques seront présentés. Il s’en suivra une étude utilisant la théorie de la fonctionnelle de la densité combinée au modèle de Hubbard (DFT+U) des différentes phases structurales, en plus des phases antiferromagnétiques et paramagnétiques. L’effet de la corrélation électronique sur la structure cristalline sera également étudié par l’intermédiaire du paramètre de Hubbard. Le but sera de vérifier si la DFT+U reproduit bien le diagramme de phases expérimentales, et sous quelles conditions. Une étude des effets de l’inclinaison des octaèdres d’oxygène sur la structure électronique sera également présentée. / Presented here is a study on the hole doped La2CuO4, the first discovered high-­‐Tc superconductor of the cuprate family. The different electronic phases of this crystal are briefly reviewed. The three crystal structures present in this material are described, and the link between those phases and the electronic structure are discussed. The relationship of those structural phases with the magnetic phases is investigated with the help of calculations based on the density functional theory where an additional Hubbard term has been added (DFT+U). With the help of the Hubbard parameter, the effect of the electronic correlation’s strength on the structural parameters of the crystal is also studied. The idea here is to verify how well the DFT+U is able to reproduce the experimental phase diagram of this material. The effect of the tilting of the oxygen octahedras on the electronic structure is also addressed.

Le coût de fabrication des modules photovoltaïques est un point critique pour implanter l’énergie solaire dans le mix énergétique. L’un des moyens d’abaisser ce coût est la réduction de l’épaisseur de silicium utilisé pour la fabrication des cellules photovoltaïques. Il est techniquement possible de produire des cellules photovoltaïques en silicium cristallin d’une épaisseur de quelques dizaines de micromètres d’épaisseur seulement, bien que cela représente un défi à la fois pour le procédé de fabrication de telles cellules et pour leur optimisation. Celle-ci est différente des cellules d’épaisseur conventionnelle notamment par le besoin d’un piégeage optique et d’une passivation de surface de haut niveau. Cet aspect sera étudié au travers de deux structures : un réflecteur en face arrière de la cellule, et un procédé de texturisation innovant pour limiter la gravure du silicium de la cellule, déjà mince. Enfin, l’implantation du réflecteur dans des cellules photovoltaïques sera traitée. L’optimisation du réflecteur considéré pour des cellules minces en silicium cristallin a montré de très bonnes propriétés réfléchissantes et de passivation de surface, ainsi qu’une compatibilité avec l’ensemble des étapes du procédé de fabrication. Ensuite, la texturisation avancée développée dans ce travail a montré un gain potentiel important en photogénération pour des cellules de faible épaisseur. La caractérisation de ces structures a montré des performances optiques et électriques comparables à l’état-de-l’art. Enfin, la fabrication de cellules photovoltaïques d’épaisseur standard utilisant le procédé développé pour les cellules minces a montré le gain du réflecteur développé pour la face arrière par rapport à une structure classique de cellule. De plus, la réalisation de ces cellules avec le procédé destiné aux cellules minces a permis d’établir que les étapes non-standard du procédé sont compatibles avec l’obtention de cellules photovoltaïques performantes. / The cost of fabrication of photovoltaic modules is a critical figure for settling solar power into the energy mix. One way to lower this cost is to decrease silicon use in photovoltaic cells. It is technically possible to produce crystalline silicon solar cells only a few dozens of microns thick, although this represents a challenge both for their fabrication process and their optimization. This last one is different from cells of standard thickness, especially by the need of high level light trapping and surface passivation. Two structures will be studied in order to fulfill these aspects : a reflector on the rear side of the cell, and an innovative texturing process used to limit the etching of the already thin silicon absorber. Eventually, the implementation of the rear side reflector into photovoltaic cells will be discussed. The rear side reflector optimized for thin-film crystalline silicon solar cells has shown very good passivating and reflecting properties, as well as compatibility with the overall fabrication process. Moreover, the advanced texturation process developped in this work has shown a large potential gain in photogeneration for thin solar cells. These structures have been characterized and have shown a reflectivity and a passivation level coherent with the state-of-the-art. Finally, solar cells of standard thickness have been fabricated with the thin solar cells process, and have shown an improvement from the rear side reflector in comparison with a standard cell structure. Moreover, making these cells with the thin cells process has shown that the non-standard steps of this process are compatible with high-performance solar cells fabrication.

Les verres métalliques ont commencé à être produit dans les années 1960 et sous forme massive dans les années 1980. De nombreuses études se sont intéressées à ces matériaux sous leur forme amorphe et ont conclu qu’ils avaient une forte résistance mécanique mais présentaient un comportement très fragile. Dans le cadre du projet EDDAM débuté en 2011, ces matériaux ont été introduits sous forme de petites sphères dans une matrice d’aluminium. Le premier objectif de notre étude est de voir si le verre métallique sous cette forme permet de le rendre peu fragile. Le second objectif est de trouver une alternative aux renforts céramique dans les composites à matrice métallique qui présentent une faible cohésion à l’interface matrice/inclusion. Dans le but de caractériser l’endommagement dans des nouveaux composites amorphe-cristallins métalliques, la tomographie aux rayons X a été utilisée. Cette technique permet de caractériser de manière non destructive l’endommagement des matériaux et de le visualiser en 3D. Cela apporte une contribution à l’étude des matériaux composites par rapport aux techniques classiques utilisées. L’objectif général de cette thèse a été d’étudier l’endommagement en termes d’amorçage, de croissance et de coales- cence des matériaux composites amorphe-cristallins métallique par tomographie aux rayons X lors d’essais de traction monotone in situ. Les matériaux sélectionnés sont constitués d’une matrice aluminium ("molle" de type 1070A ou "dure" de type 5083) et de renforts en verre métallique Zr57Cu20Al10Ni8Ti5 de taille peu dispersée et répartis de manière homogène, avec différentes fractions volumiques (1%, 4% et 10%). Les matériaux composites ont été élaborés par la voie de la métallurgie des poudres au Spark Plasma Sintering (SPS) suivi d’une étape d’extrusion à chaud. Une attention particulière a été portée sur la caractérisation microstructurale des constituants de base. L’analyse qualitative a permis de comparer l’ensemble des composites fabriqués au SPS et ceux extrudés à chaud après SPS. Les différents modes d’amorçage de l’endommagement ont été observés ainsi que la croissance et la coa- lescence amenant la rupture des composites. L’analyse quantitative a été essentiellement consacrée au premier stade de l’endommagement. La croissance et la coalescence étant très rapide, il a été difficile de les suivre lors des essais interrompus. La modélisation d’un composite amorphe-cristallin métallique à matrice molle a été introduite dans le but de reproduire l’endommagement observé lors des analyses expérimentales. Cette première approche nécessite d’être approfondie dans le but de prédire, compte tenu des propriétés mécaniques des différentes phases et de la fraction volumique des renforts, le mode d’endommagement préférentiel apparaissant dans les composites étudiés. Elle montre cependant les prémices d’une modélisation innovante basée sur la microstructure expérimentale. / Metallic glasses have been produced in the 1960s and bulk metallic glasses in the 1980s. Many studies, focused on these materials in their amorphous state, concluded that they had high mechanical strength but shown low ductility. As part of EDDAM project that started in 2011, these materials were introduced as small particles in an aluminum matrix. The first objective of this study is to see if the metallic glass is less brittle in this form. The second objective is to find an alternative of ceramic reinforcements in metal matrix composites. These materials have low cohesion at the matrix/inclusion interface. In order to characterize the damage in new amorphous-crystalline composite, X-ray tomography was used. This allows to characterize damage in materials and to obtain a 3D viewing. The main objective of this thesis was to study damage (nucleation, growth and coalescence) in composite materials using X-ray tomography during tensile tests. Selected materials are constituted of an aluminum matrix and small metallic glass reinforcements (Zr57Cu20Al_10Ni8Ti5). Composites with different volume fractions (from 1vol.% to 10vol.%) were prepared by Spark Plasma Sintering (SPS) and hot extrusion. A particular attention was paid to the microstructural characterization of the basic constituents. Qualitative analysis was used to compare SPS composites with SPS plus hot extrusion composites. Damage nucleation, growth and coalescence were observed. Quantitative analysis was mainly devoted to the first damage step. Growth and coalescence were difficult to follow due to fast rupture and interrupted tensile tests. The modeling of an amorphous-crystalline composite has been introduced in order to reproduce experimental damage analyses. The first approach requires further investigation to predict damage with different volume fractions. However, this part shows the beginning of an innovative model based on the experimental microstructure.

The thesis entitled "Phase Behaviour in Crystalline Solids: Exploring the Structure Guiding Factors via Polymorphism, Phase Transitions and Charge Density Studies" consists of five chapters divided into two parts. A basic introductory section describes the topics relevant to the work and the methods and techniques utilized. Part A contains two chapters that discuss the structural aspects related to polymorphism, solvatomorphism, conformational preferences and phase transitions exhibited by active pharmaceutical ingredients (APIs). It also discusses the structure-property correlations in API crystal forms and the possible utility of second harmonic generation (SHG) for their bulk characterization. Part B has three chapters that discuss experimental and theoretical charge density analyses of intra-and intermolecular interactions that play structure guiding roles in some of the APIs discussed in Part A. The main focus of the present work is to characterize the interaction patterns devoid of strong classical hydrogen bonds. The case studies include multifurcated C - H …O hydrogen bonds, the “carbon bonding” and chalcogen interactions involving Se and S atoms. In addition to charge density studies, in situcryocrystallography and molecular complexation experiments have been employed to examine structural consequences of chalcogen bonding. Further, Appendices 1 and 2 describe phase transition studies on the inorganic mineral kröhnkite and its high temperature phase transitions leading to novel inorganic structural types. Part A: Polymorphism and phase behaviour in Active Pharmaceutical Ingredients (APIs) Chapter 1 discusses case studies of polymorphism, supramolecular preference sand phase transitions exhibited by active pharmaceutical ingredients (APIs). Section 1.1 deals with the polymorphism of an anti-oxidant drug candidate ebselen and its hydroxyl derivative. The potential of organoselenium compounds to form a Se…O chalcogen bonded supramolecular recognition unit (synthon) has been established in these polymorphs and its generality is substantiated with the help of a Cambridge Structural Database (CSD) analysis. Section 1.2 demonstrates the utility of the ‘chalcogen bonded supramolecularsynthon’ in generating molecular complexes of APIs. A series of salts and co-crystals of the amyotrophic lateral sclerosis drug Riluzole have been synthesized in order to evaluate the structure directing role of S…O chalcogen bonded synthon in their crystal structures. Section 1.3adescribes the generation of polymorphs and solvatomorphs of the antidepressant drug candidate fenobamand associated phase transitions. The tautomeric preference in this molecule has been rationalized from the crystal structure analysis and abinitioenergy calculations. Further, section 1.3b utilizes chemical derivatization as a means to experimentally simulate thetautomeric preference and molecular conformations in several derivatives of fenobam and thiofenobam. Section 1.4 describes the issue of solvatomorphism and the generation of the fifth solvatomorph of gallic acid, its structural complexity and temperature induced phase transitions. The ability of solvent water molecules to drive structural diversity, by forming ‘hydration synthons’,is demonstrated in this case. Chapter 2 presents a novel methodology for the detection of polymorphic impurities in APIs based on second harmonic generation (SHG).The SHG based method has been employed to polymorphic mixtures of fenobam, hydrochlorothiazide, pyrazinamide, tolbutamide, curcumin, febuxostat and nimesulide.The conventional methods such as powder X-ray diffraction (profile fitting analysis), FT-IR, Raman spectroscopy and thermal analysesto detect the presence of polymorphic impuritiesin bulk API samples are employed on the mixtures of these API samples and the impurity detection limits are compared with the proposed SHG methodology. The APIs used in these case studies were screened for their SHG efficiency using quantum chemical calculations of hyperpolarizability and HOMO-LUMO charge redistribution behaviour. Further, a correlation with the crystal symmetry, relative packing arrangement of molecules and the observed SHG efficiency have been discussed in of some of these cases. Part B: Exploring the nature and structural consequences of nonbonding interactions in molecular crystals Chapter 3 discusses the electron density features of quasi-trifurcated CH…Cl/CH…O interaction motifs leading to ‘carbon bonding’ and a trifurcated CH…O hydrogen bond motif. Section 3.1 describes the experimental and theoretical charge density analyses of quasi-trifurcated CH…Cl and CH…O motifsand investigates the existence of “carbon bonding” in solid state. The experimental charge density evidence for “carbon bonding” have been analyzed in cases of fenobam and dimethylamine: 4-hydroxybenzoic acid complex. The existence of this unconventional interaction, which roughly mimics the transition state geometry of SN2 (bimolecular nucleophilic substitution) reaction, is further established by a CSD analysis. Section 3.2 describes the experimental and theoretical charge density analyses of ferulic acid and compares the topological features associated with a trifurcated CH…O hydrogen bond motif, with corresponding strong classical OH…O hydrogen bonds. The study demonstrates the “Gulliver effect” of weak interactions in charge density terms. Charge density based interaction energy calculations via EPMM and EML methods have been utilized in this context to evaluate the relative strength of such interactions. Chapter 4 discusses the charge density features of intermolecular chalcogen bonding interactions involving selenium and sulphur atoms.Section 4.1 describes the experimental and theoretical charge density analyses of ebselen and its hydroxyl derivative. The charge density characterization of the conserved chalcogen bond synthon (discussed in chapter 1, section 1.1) has been carried out and electronic nature and geometric dependence of Se…O interactions have been explored. The mechanism of drug action of ebselen has been correlated with the experimentally observed charge density distribution around the intramolecular SeC and SeN bonds. Section 4.2 explores the homochalcogen interactions such as S…SandSe…Se in phenol analogues. In situ cryocrystallographic studies on thiophenol, selenophenol and their solid solutions are described. Veggard’s law-like behaviour observed in these solid solutions have been rationalized and the S…S and Se…Sehomochalcogen interactions have been evaluated in these liquid systems which are devoid of any other packing forces such as strong hydrogen bonds. Chapter 5 discusses the conformation locking potential of intramolecular S…O chalcogen bonding in sulfadrugs. Section 5.1 discusses conformation locking in the antibioticdrugsulfamethizole. A two pronged approach has been adopted in the study; a) generation of cocrystals and salts of sulfamethizole for the ‘experimental simulation’ of the molecular conformation, b) evaluation of charge density distribution around the intramolecular S…O interaction region in sulfamethizole. Section 5.2 describes the effect of ‘simple hybridized orbital geometry’ in the formation of intramolecular S…O chalcogen bonding. The experimental charge density analysis of the carbonic anhydrase inhibitor drug acetazolamide has been carried out and the two different intramolecular S…O geometries have been compared in terms of the charge density topology. The analysis highlights the advantage of “orbital geometry” consideration over the conventional distance-angle criteria in assessing nonbonded interactions.

MENVSC / Department of Ecology and Resource Management / Mine tailings (MT) have been a global problem due to the environmental impacts the waste generates such as air, soil and water pollution. The detrimental impacts include a global problem such as acid mine drainage (AMD) which has been difficult to cleanup. Several studies have been conducted to find alternative measures in reducing or mitigating impacts such as AMD and air pollution. Several studies have revealed how alumino-silicate mineral waste can be used as raw material to produce construction materials. This study aimed at evaluating the potential of synthesizing a geopolymer material from Musina copper mine tailings. Tailings were characterized for their physicochemical and mineralogical compositions using standard laboratory techniques in order to evaluate suitability in geopolymerization. First section of the results presented physicochemical and mineralogical characterization of the Musina copper tailings together with the bioavailability of the chemical species. It was observed that the tailings are mainly composed of SiO2 and Al2O3 as the major oxides indicating that they are aluminosilicate material. Mineralogical analysis revealed dominance of quartz, epidote and chlorite as the major minerals. The bioavailability assessment showed that largely Cu and Ca are bioavailable and highly soluble in an aqueous solution while Al, Mg, Ni, Co, Cr and Fe have a high proportion in non-labile phase. Second section presented the preliminary results wherein the potential application of Musina copper tailings in geopolymerization was evaluated. The results showed that Musina copper tailings can be used to synthesize a geopolymer material. However, it was recommended that several parameters influencing geopolymerization need to be evaluated. The third section presented the evaluation of optimum parameters that influence the geopolymerization process, which include type of alkali activators, alkali activator concentration, curing temperature, liquid-solid (L/S) ratio and curing regime. It was observed that a mixture of NaOH:Na2SiO3.5H20 at a ratio of 70:30 yields a better geopolymer material. The concentration of 10 M NaOH:Na2SiO3.5H20 at a ratio of 70:30 was observed to be the best that yielded the UCS that is acceptable according to SANS1215 standards. When evaluating curing regime, it was found that the material cured using greenhouse has lower UCS as compared to the material cured using oven. The v effect of temperature showed that the UCS decreases with increasing curing temperature. An admixture of river sand and cement was introduced which resulted in a high UCS of 21.16 MPa when using an admixture of cement. The mineralogical composition of the geopolymer bricks showed formation of secondary minerals such as phlogopite, fluorapatite, diopside and actinolite. Batch leaching conducted on the geopolymer bricks detected high leaching of Na from the bricks. Based on the findings of the study of the raw MT potential to produce geopolymer bricks, it was concluded that the material can be used to produce bricks that are within the SANS 1215 requirements. The study further recommended that the study a focus on using cylindrical moulds, other alkali activators and a mechanical mixer. It was also recommended that the greenhouse be restructured to contain heat within the greenhouse during the evening so as to allow constant temperature within / NRF