As of 21st September 2017, industrial use of hexavalent chromium (Cr(VI)) will, due to its environmental toxicity and carcinogenicity, be restricted by REACH regulations. Saab Aeronautics is therefore shifting anticorrosion surface treatment of aluminum alloys from hexavalent chromium conversion to trivalent chromium (Cr(III)) passivation. The purpose of this thesis is to investigate the characteristics of conversion coatings formed with the passivation chemical SurTec 650V, in order to facilitate transfer to the more environmental friendly alternative. Process parameters, such as pH and immersion time in SurTec 650V passivation baths, have been investigated for passivation of three different aluminum alloys; 2024, 6061 and 7075. The characteristics of the Cr(III) conversion coatings achieved at laboratory scale in the thesis work have been compared with SurTec 650V process in production scale and with Cr(VI) containing Alodine 1200 and Alodine 1500 processes. The impact of varying process parameters have been investigated with goniometry, x-ray photoelectron spectroscopy (XPS), auger electron spectroscopy (AES), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) to analyse characteristics of the conversion coatings. Differences in chemical composition on the surface and in depth profile was detected with XPS and AES, respectively and topology of coatings was found to differ for different aluminium alloys and parameter combinations. With TEM, the thickness of the conversion coating was found to be approximately 30-50 nm, which is thinner than the coatings formed with Cr(VI) passivation. Characteristics of coatings formed with Cr(III) passivation is concluded to be very dependent on parameter variation, especially for alloy 2024. Differences also occur between passivation at laboratory and production scale. Further evaluation of the production scale SurTec 650V process and corrosion testing should be performed, and an elaboration of a process control is required before the shift to an environmental friendly passivation process can be completely successful at Saab.

A crescente preocupação com o desenvolvimento sustentável, aliada com uma maior conscientização com relação à preservação do meio ambiente, tem incentivado pesquisas com a finalidade de encontrar substitutos ambientalmente amigáveis para os eficientes sistemas à base de cromo hexavalente (Cr6+), que são empregados como pré-tratamento em ligas de alumínio de alta resistência utilizadas na indústria aeronáutica. Neste trabalho, o desempenho do silano BTSE (Bis-1,2-(trietoxisilil) etano) como método de proteção contra a corrosão da liga de alumínio 2024-T3 foi investigado utilizando técnicas de caracterização eletroquímicas, microestruturais e químicas. Para melhorar as propriedades anticorrosivas do sistema, a camada de silano foi modificada pela introdução de aditivos, tendo sido estudados também sistemas em bi-camada. Efeitos das condições de cura (tempo e temperatura) do BTSE e da quantidade de modificantes sobre as propriedades dos substratos revestidos também foram avaliados. Para os estudos eletroquímicos, realizados em solução de NaCl 0,1 M, foram empregadas a espectroscopia de impedância eletroquímica (EIS) e curvas de polarização potenciodinâmica anódica e catódica. As técnicas de caracterização morfológica e microestrutural foram microscopia de força atômica (AFM), microscopia eletrônica de varredura (SEM) e medidas de ângulo de contato. A caracterização da composição e do estado químico da camada foi realizada usando as espectroscopias por energia dispersiva de Raios-X (EDS), de infravermelho (IR) e de fotoelétrons excitados (XPS). Os resultados dos ensaios de corrosão mostraram que a adição dos modificantes à camada de BTSE melhora o desempenho anticorrosivo do sistema, o qual também teve seu comportamento melhorado quando utilizado em forma de bi-camada. Verificou-se que um excesso de aditivos tende a deteriorar as propriedades protetoras do silano, e que o aumento do tempo e da temperatura de cura é benéfico para as propriedades anticorrosivas dos diferentes sistemas. Os resultados dos ensaios de caracterização química e microestrutural também detectaram que os modificantes contribuem para uma melhor cobertura do substrato pela camada de silano, assim como para uma maior reticulação da mesma, sem, no entanto, modificar sua estrutura química e física. / The increasing concern with sustainable development, allied with a stronger awareness with environmental preservation, has stimulated researches in order to find environmentally friendly substitutes to replace the efficient hexavalent chromium-based pre-treatment systems (Cr6+) used to protect high-strength aluminium alloys employed in the aircraft industry. In this work, the performance of BTSE (bis-1, 2-(triethoxysilyl) ethane) as a protection method against corrosion of aluminium alloy 2024-T3 was investigated using electrochemical, microstructural and chemical characterization techniques. In order to improve the system anticorrosion properties, modifiers were added to the silane layer, and bi-layers systems were also tested. The effects of the silane curing conditions (time and temperature) and of the modifiers amounts on the properties of the layers were also evaluated. Electrochemical impedance spectroscopy (EIS) and anodic and cathodic potentiodynamic polarization curves were employed for the electrochemical studies, which were performed in 0.1 M NaCl solution. For microstructural and morphological characterization, atomic force microscopy (AFM), scanning electron microscopy (SEM) and contact angle measurements were used. The chemical state and the composition of the different layers were evaluated using X-ray photoelectrons (XPS), infrared (IR) and X-ray dispersive energy (EDS) spectroscopy. The results of the corrosion studies have shown that the addition of modifiers to the BTSE layer improves its anticorrosion performance, which was also improved in the bi-layers systems. It was also verified that addition of modifiers excess hinders the performance of the layers, as well as that increasing curing time and temperature are beneficial to the anticorrosion properties of the systems. The results of the different chemical and microstructural analyses showed that the modifiers contribute to better substrate coverage by the silane layer, as well as to a more complete reticulation. However, this does not imply in modifications of the chemical and physical structure of the layer.

My dissertation focuses on (i) the development of new analysis tools and methodologies for analyzing X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) data, and (ii) the comprehensive characterization of materials (nanodiamonds) using a multi-instrument approach. Chapter 1 contains (i) a discussion of the two techniques I focused on most in my work: XPS and ToF-SIMS, (ii) a discussion of the common chemometrics techniques used to analyze data from these methods, and (iii) the advantages/rationale behind the multi-instrument characterization of materials. Chapter 2 describes various good practices for obtaining reasonable peak fits in XPS, which can also be applied to peak fitting data from different techniques. To address the issue of user subjectivity/bias in XPS peak fitting, I introduce two less biased mathematical functions for characterizing XPS narrow scans, namely the equivalent width (EW) and the autocorrelation width (AW). These functions are discussed in Chapters 3 and 4. In Chapter 5, I then introduce uniqueness plots as simple and straightforward graphical tools for assessing the quality of XPS peak fits and for determining whether fit parameters are correlated. This tool is extensively used in spectroscopic ellipsometry, and the mathematics behind it is known in XPS. However, to the best of my knowledge, this graphical tool has never been applied to XPS. ToF-SIMS data analysis is somewhat challenging due to the enormous amounts of data that are collected, and also the matrix effect in SIMS. This amount of information is significantly increased when depth profiles are performed on samples. Chapter 6 discusses a new chemometrics tool that I introduce for analysis of complex data sets, with emphasis on XPS and ToF-SIMS depth profiling data. The new approach is called the Information Content (IC) or entropy, which is adapted from Claude Shannon's work on Information Theory. Chapter 7 then contains a presentation of the comprehensive characterization of five nanodiamond samples used to manufacture particles for liquid chromatography. The advantages of a multi-instrument approach for material characterization and the lack of comprehensive material characterization in the literature are emphasized. To the best of my knowledge this is the most comprehensive characterization of nanodiamonds that has been reported in the literature. Chapter 8 presents conclusions of my work and future work. This thesis also contains six appendices. Appendix 1 contains an article from a scientific magazine that I wrote to highlight the importance and applications of the EW and AW to characterize XPS narrow scans. Appendices 2-5 are application notes I wrote on separations I performed on a nanodiamond based HPLC column. Finally, Appendix 6 describes the ToF-SIMS analysis of the tungsten species in the nanodiamond samples characterized in Chapter 7.

Les mémoires flash non volatiles - utilisées dans les ordinateurs, téléphones portables ou clés USB - peuvent être constituées de nanocristaux semiconducteurs (SC) insérées dans une matrice isolante. Elles nécessitent l'élaboration d'hétérostructures de type "oxyde/SC/oxyde/Si(00l)" et la maîtrise de chaque interface. Dans ce cadre, nous avons étudié les mécanismes de croissance initiale du Si et du Ge (SC) sur des substrats d'oxyde cristallins LaA1O3(001) à forte permittivité (high-k). Les propriétés chimiques et structurales ont été déterminées in-situ par photoémission X (XPS et XPD) et par diffraction d'électrons (RHEED et LEED) puis ex-situ par microscopies en champ proche (AFM) et en transmission (HRTEM). Le substrat LaAlO3(001) propre présente une reconstruction de surface c(2x2) attribuée à des lacunes d'O en surface. Les croissances de Si et Ge ont été réalisées par épitaxie par jet moléculaire (MBE), soit à température ambiante suivies de recuits, soit à haute température. L'épitaxie requiert des températures de dépôt supérieures à 550°C. Le mode de croissance est de type Volmer Weber caractérisé par la formation d'îlots cristallins de dimensions nanométriques et de forte densité. Ces îlots sont relaxés et présentent une interface abrupte avec le substrat. Quant aux îlots de Ge, ils ont majoritairement des orientations aléatoires avec néanmoins une relation d'épitaxie privilégiée, la même que celle du Si. / Non-volatile flash memory used in computers, mobile phones and USB-keys can be made up of nanocrystals (SC) inserted in an insulating matrix. It requires development of "Oxide/SC/oxide/Si (001)" type hetero-structures and the control of each interface. Within this framework, we studied the initial growth mechanisms of Si and Ge (SC) on LaA1O3(001) crystal oxide substrates with high permittivity (high-k). Chemical and structural properties have been studied in-situ by X-Ray photoemission (XPS and XPD) and electron diffraction (RHEED and LEED) technics and ex­ situ by atomic force microscopy (AFM) and high resolution tunneling electron microscopy (HRTEM). Clean LaA1O3(001) substrate contains a c(2x2) surface reconstruction which attributed to gaps of oxygen (O) on the surface. Si and Ge have been deposited by molecular bearn epitaxy (MBE), at room temperature followed by series of annealings at high temperatures. Epitaxy requires temperature more than 550°C for the deposition. Volmer Weber growth mode was characterized by the formation of nanometric densely packed islands. These islands are relaxed and have an abrupt interface with the substrate. Islands of Ge have mostly random orientations with nevertheless epitaxy privileged relationship, same as that of the Si.

The objective of this master s thesis is the preparation and characterization of ribonucleic acid (RNA)/inorganic material interfaces by electrospray deposition and photoemission spectroscopy. This was done through investigation of the chemical and electronic structure of the surface of Highly Ordered Pyrolytic Graphite (HOPG) and gold before and after multiple steps of RNA thin film deposition by electrospray. Great interest has been shown by researchers into RNA due to its self-assembling ability. A series of experiments was conducted depositing RNA Poly adenosine, RNA Poly cytidine, and (for control purposes) DI water on HOPG. RNA Poly adenosine was also deposited on Gold. Gold is a more practical surface for use with RNA, but HOPG is useful for this study because it allows the precise determination of the density of states (DOS) of RNA. X-ray photoemission spectroscopy (XPS) and ultraviolet photoemission spectroscopy (UPS) were used to characterize the RNA-interfaces. The work function, high binding energy cutoff, and HOMO energies were determined. The clean, in-vacuum deposition of RNA was carried out using an electrospray thin film deposition device. The HOPG and gold substrates were prepared by in-situ cleavage and sputtering respectively. The electrospray method can be used for many different types of molecules including Polymers, metal-organics, crystals, and biological materials including RNA or DNA. These measurements provided data that will be helpful in determining the electronic properties of biological and substrate interfaces.

Throughout the last half century of materials science, significant motivations came from, and still do, the industrial applications of these materials. Whether it is electronic, thermal, tribological or chemical in nature, the study of metals, semiconductors and insulators eventually reveals that the surface plays a significant part in the properties of these materials. Understanding metal terminations reveals often that an oxide is the stable state of the metallic surface in an ambient atmosphere and the ability to predict and control these oxides has led to significant strides forward in not just the metallic bulk but the oxide as well. Here we add to the understanding of the class of materials known as transition metal oxides by focusing on the structural and chemical nature of their surfaces. Vanadia, chromia and a new mixed metal oxide, VTiO3, all of which form the corundum structure and have physical properties that need further study. Specifically, Cr2O3 has been at the center of much debate over how oxygen chemical potential influences surface terminations and top layer relaxation. Chromia is a wide band gap (~3.4eV) insulator with substantial ligand field interaction and measurements of the 3d states reveal these states split to t2g and eg– consistent with the distorted octahedral. V2O3 is known to be a Mott insulator and paramagnetic, properties that can be modified through dopants, stoichiometry and strain. In this work, solid solutions of V2O3 and Ti2O3 are studied. VTiO3, has been synthesized in a corundum – like structure by epitaxial growth on an isostructural α-Al2O3 substrate. Section I offers a review of corundum like transition metal oxides and their surface properties and motivations of continued research. In section II we describe in detail, the critical components of PLD thin film growth and in the next section a review of the pertinent characterization techniques utilized in the process. Finally, the results are presented of the study of two transition metal oxide structures namely: 1) Novel VTiO3 in a corundum structure has been grown via Pulsed Laser Deposition – Molecular Beam Epitaxy on a single crystal Al2O3(0001) substrate. The sapphire substrate with modest lattice mismatch was utilized in an effort to compel heteroepitaxial growth of the VTiO3 film. Confirmation of the films structure & chemical state were performed by X-Ray diffraction, Transmission Electron Microscopy (HR), X-Ray Photo-electron Diffraction, Ultra-Violet Photo-Electron Diffraction and Reflection High Energy Electron expected that the metal ions exist in a 3+ charge state. While XPS clearly points to a V3+ charge state and this suggests that Ti should as well, however there is also a strong Ti4+ component present. EELS spectra support the existence of a mixed state Ti3+ & 4+. Broadening of the valance band edge as revealed by UPS spectra indicate that the 3d orbitals are occupied and that the a1g molecular states are occupied. The conflict in diffraction data supporting corundum and PES/EELS data suggesting a mixed state implies that additional final state effects are present and/or an oxygen rich structure. 2) Additionally, corundum like Chromium(III) Oxide is formed on a Cr(110) surface and characterized with X-Ray Photoelectron Diffraction, Low Energy Electron Diffraction and XPS for the purpose of characterizing surface termination and terminating layer relaxation. Comparison of the XPD diffraction data with known and previously discussed terminations reveal the as grown film does not conform. Consequently, we propose a new, stoichiometric termination with oxygen termination and 1st layer chromium interstitials. Atop this structure was grown an ultra-thin film of V2O3 by vanadium e-beam evaporation in background oxygen. This final structure supports the previously proposed vanadyl structured surface

The presented study investigated the Induced Density of Interface States (IDIS) model at different polymer interfaces by using photoemission spectroscopy in combination with electrospray deposition. In recent years, organic electronics have attracted considerable attention due to their advantages of low-cost and easy-fabrication. The performance of such devices crucially depends on the energy barrier that controls the interface charge transfer. A significant effort has been made to explore the mechanisms that determine the direction and magnitude of charge transfer barriers in these devices. As a result of this effort, the IDIS model was developed to predict the energy alignment at metal/organic and organic/organic interfaces. The validity of the IDIS model on molecular interfaces was confirmed by the results of a series of experiments with small molecular materials, which are in good agreement with the theoretical calculations from the IDIS model. The charge neutrality level (CNL) and screening factor for various organic materials can be determined from the linear correlation between the hole injection barrier at metal/organic interface and the work function of its corresponding metal substrate, which stands as one of the most important features of the IDIS model. The study presented here explores whether the IDIS model is also valid for polymer interfaces. Two prototypical polymer materials: poly(3-hexylthiophene) (P3HT) and poly[2-methoxy-5-(2'-ethylhexyloxy)-p-phenylene vinylene] (MEH-PPV) were selected for the investigation. In the first part of this study, a series of metal/polymer interfaces were prepared using electrospray and investigated with photoemission spectroscopy. The linear relationship between the hole barriers extracted from the metal/polymer interface and the work function of its respective metal substrate suggests that the IDIS model is also valid for metal/polymer interfaces. The CNLs and the screening factors of P3HT and MEH-PPV are determined respectively. The experiment results are also discussed with regard to the Integer Charge Transfer (ICT) model. The comparison between the two models suggests that the IDIS model should be applied to interfaces prepared in vacuum while the ICT model works on interfaces with an ambient contamination layer present. The second part of the dissertation discusses the photoemission results of the MEH-PPV/P3HT heterojunction from the perspectives of the two models. The results indicate that the IDIS model is valid for polymer/polymer heterojunctions. The IDIS model more accurately predicted the measured orbital line up by using its principles for organic/organic heterojunction than the ICT model.

L'objectif de ce travail était d'étudier les interactions entre une protéine modèle, l'albumine de sérum bovin (BSA), et la surface d'un acier inoxydable ferritique, le Fe-17Cr, lors des toutes premières étapes de formation de la couche d'oxyde en solution aqueuse. Différents paramètres ont été testés : potentiel (potentiel de corrosion Ecor et potentiel passif), pH (compris entre 1,3 et 10) et absence/présence d'ions chlorures en solution. Pour atteindre cet objectif, des méthodes électrochimiques (courbes de polarisation, spectroscopie d'impédance électrochimique (SIE)) et la spectroscopie de photoélectrons induits par rayons X (XPS) ont été couplées. En absence de chlorures, les mesures d'impédance révèlent une inhibition de la corrosion par la BSA, à pH 1,3 et Ecor. Les analyses XPS montrent que la couche de BSA adsorbée sur la surface d'acier inoxydable (molécules chimiquement intactes ; épaisseur d'environ 4 nm) n'a d'effet ni sur la composition chimique ni sur l'épaisseur des couches d'oxyde et d'hydroxyde. Par conséquent, l'inhibition de la corrosion mise en évidence à pH 1,3 et Ecor est due à la protéine elle-même et non pas à un changement de composition chimique et/ou d'épaisseur des couches de surface. En présence de chlorures (NaCl 0,5M), la protéine accélèrerait la corrosion localisée du Fe-17Cr passivé à pH 5,5 ; de plus, le potentiel de piqûration Ep est plus faible quand la passivation et l'exposition à la BSA sont simultanées. Le potentiel de piqûration est d'autant plus cathodique que la quantité de protéine adsorbée est importante.

Des couches minces d'oxynitrure de titane, TiNxOy, ont été élaborées sur Si(100) par MOCVD (dépôt chimique en phase vapeur) à partir d'isopropoxyde de titane Ti(OCH(CH3)2)4 et d'ammoniac NH3. En modifiant la température de croissance, il est possible de contrôler le rapport N/O et d'obtenir ainsi des composés de conductivité variable.<br /><br />L'objectif de ce travail était la détermination de la composition et de la structure des couches minces de TiNxOy de façon à en comprendre les propriétés électriques. Cependant, cette étude s'est rapidement avérée plus complexe que prévue, les techniques de caractérisation classiques (MEB, DRX, Raman, XPS...) étant insuffisantes pour décrire le système TiNxOy dans sa totalité. En effet, une seule phase cristallisée, isomorphe de TiN, a pu être mise en évidence dans les échantillons élaborés à haute température (T > 550 °C) tandis que des analyses quantitatives ont révélé des proportions d'oxygène relativement importantes dans tous les échantillons. Aussi, cette étude a été élargie à des films de TiN afin de comprendre l'importance de l'oxygène dans cette structure.<br /><br />Des méthodes de caractérisation originales, basées sur le fait qu'il est possible de relier la structure d'un matériau à sa réactivité, ont alors été mises en œuvre afin de compléter les analyses précédentes. Notamment, l'étude de la réactivité des couches minces vis-à-vis d'une irradiation ionique ou lors de traitements thermiques a permis de qualifier et quantifier les différentes phases des films minces de TiNxOy en réalité constitués d'une phase Ti(N,O) conductrice et d'une phase TiO2 isolante. Un modèle de percolation permettant la simulation des variations de conductivité des films à partir des proportions relatives de chacune de ces deux phases a alors pu être proposé.

Les phénomènes de sorption aux interfaces solide-liquide jouent un rôle important dans le transport des éléments toxiques ou radioactifs et pour la prévision de la sûreté des sites de stockage de déchets. Notre étude a consisté à déterminer les mécanismes de fixation du sélénium (élément toxique à forte concentration mais également radionucléide à vie longue présent parmi les déchets de la fission nucléaire) et à sélectionner les matériaux sorbants les plus efficaces. Deux types de matériaux ont été choisis pour cette étude : une hydroxyapatite et une fluoroapatite Ca10 (PO4)6 (OH, F)2 ainsi que des oxy-hydroxydes de fer (goethite FeOOH et hématite Fe2O3). Après avoir comparé les propriétés d'acido-basicité de surface de la goethite et de l'hématite avec celles de l'alumine g-Al2O3 et de la bayerite Al (OH)3 grâce à des mesures de zétamétrie et des titrages potentiométriques (mise en évidence de l'influence de la cinétique, de l'évolution du solide au cours de la phase d'hydratation, de la solubilité du matériau et des impuretés présentes en surface), nous avons étudié la sorption des espèces sélénites (SeIV) et sélénates (SeVI). Sur la goethite et l'hématite, SeIV se sorbe en plus grande quantité que SeVI, la sorption augmentant fortement en milieu acide. De plus, les courbes de sorption peuvent être ajustées à l'aide de modèles de complexation de surface : dans le cas de SeIV, on identifie un complexe de sphère interne (monodentate ou bidentate) alors que SeVI formerait plutôt un complexe de sphère externe. Dans le cas des apatites, la sorption de SeIV se produit par échange d'ions entre les PO4 de l'apatite et SeO32-. Grâce à un modèle mathématique et des mesures par XPS et ICP/OES, la profondeur de pénétration des ions dans la matrice apatitique a pu être déterminée. En comparaison, le cadmium, dont on étudie également la sorption, diffuse plus profondément dans le solide.