No description available.

No description available.

<p>This master thesis in physics mainly treats Auger spectroscopy of interfaces that has been adhesively bond together with so called controlled delaminating materials (CDM). CDM is a new technology which involves adhesives with the distinctive property that they by the appliance of electricity can be released from a substrate. The reason for using Auger spectroscopy was that it gives a surface sensitive view of the chemical composition of the samples examined and this was believed to give hints of the mechanisms behind loss of adhesion. The samples were so called laminates which is an aluminium foil, CDM adhesive, aluminium foil structure. As expected Auger spectroscopy produced some promising results, especially regarding the breakdown of a certain anion contained into the examined CDM adhesive. This awoke new questions regarding how this anion was decomposed and the idea that it could be due to hydrolysis took form. The by far most important result within this work is that the anion breaks down. This could lead to the formation of hydrofluoric acid if this breakdown in fact is due to hydrolysis and the hydrofluoric acid could then react with the aluminium causing loss of adhesion. This could be the good starting point of a continuing work on CDM.</p>

This master thesis in physics mainly treats Auger spectroscopy of interfaces that has been adhesively bond together with so called controlled delaminating materials (CDM). CDM is a new technology which involves adhesives with the distinctive property that they by the appliance of electricity can be released from a substrate. The reason for using Auger spectroscopy was that it gives a surface sensitive view of the chemical composition of the samples examined and this was believed to give hints of the mechanisms behind loss of adhesion. The samples were so called laminates which is an aluminium foil, CDM adhesive, aluminium foil structure. As expected Auger spectroscopy produced some promising results, especially regarding the breakdown of a certain anion contained into the examined CDM adhesive. This awoke new questions regarding how this anion was decomposed and the idea that it could be due to hydrolysis took form. The by far most important result within this work is that the anion breaks down. This could lead to the formation of hydrofluoric acid if this breakdown in fact is due to hydrolysis and the hydrofluoric acid could then react with the aluminium causing loss of adhesion. This could be the good starting point of a continuing work on CDM.

No description available.

No description available.

No description available.

The filiform-like corrosion of Magnesium (Mg) alloys AZ31B and AM30 was investigated with electrochemical and microanalytical techniques. Potentiodynamic polarization testing and scanning vibrating electrode technique (SVET) measurements confirmed the “differential electrocatalytic” mechanism previously reported for filiform and filiform-like corrosion on pure Mg and AZ31B. Transmission electron microscopy (TEM) and Auger electron spectroscopy (AES) revealed that the MgO corrosion filaments on both alloys were likely a product of the direct reaction of Mg and water (H2O), responsible for the rapid hydrogen (H2) evolution observed at the propagating corrosion fronts. TEM analysis also revealed through-thickness cracks and noble intermetallic particles within the corrosion filaments and noble metal enrichment at the corrosion filament/metal interfaces, which were proposed to play significant roles in the cathodic activation of the corrosion filaments. The higher susceptibility of the AZ31B alloy to cathodic activation versus AM30 suggested that Zinc (Zn) has a detrimental effect on the resistance of Magnesium-Aluminum-Zinc (Mg-Al-Zn) alloys to filiform and filiform-like corrosion. / Thesis / Master of Applied Science (MASc)

This thesis is concerned with the chemistry and physics of C(100) surfaces of diamond. The polished and cleaned C(100) surface is examined by surface microscopy (Atomic-force Microscopy), electron diffraction (Low-energy Electron Diffraction) and photoemission (X-ray Photoelectron Spectroscopy and Ultra-violet Photoelectron Spectroscopy). Results are presented on the presence of oxygen, nitrogen and hydrogen/deuterium on the C(100) surface. Finally, the valence band structure of diamond is probed by angle-resolved photoemission. We have confirmed by AFM that the grooves from the soft polishing process are present on a polished C(100) surface and found sporadic traces of hard polish on a surface polished in the soft polishing direction. XPS studies have verified heating cycles by electron beam bombardment as a suitable cleaning procedure for pure reconstructed C(100) surfaces. By allowing the crystal to cool slowly, the first experimental evidence of quarter-order LEED spots have been found, which suggest that buckled dimerisation might have occurred similar to those on Si(100) and Ge(100). We present the first experimental electron spectroscopy results for a nitrogen impurity in diamond by showing the N KLL Auger spectrum. An attempt to smooth a C(100) surface of diamond by an atomic hydrogen plasma did not succeed. AFM studies showed no evidence for the surface smoothing reported in other studies, but the results enable us to explain the different plasma published in the literature. The valence band of diamond is investigated by off-normal ARUPS. The features observed are consistent with possible transitions, which are determined using bulk band structure calculations and comparison with the experimental binding energies.

<p>This thesis contains two parts. The first part concerns the research work on free molecules using synchrotron-radiation-related techniques. Auger electron spectra of two free open-shell molecules, O₂ and NO, were studied experimentally and theoretically. Photoionization experimental technique with tunable synchrotron radiation source was used to induce core-level electron ionization and obtain the <i>KVV</i> normal Auger electron spectra. A quantitative assignment of O₂ normal Auger spectrum was obtained by applying <i>ab initio</i> CI calculations and LVI Auger line shape simulations including the bond length dependence of Auger transition rates. The photon energy dependence of normal Auger electron spectra was focused on with photon energies in the vicinities of core-ionization threshold energies. Consequently, the MAPCI (Molecular Auger Post Collision Interaction) theory was developed. Taking the near-threshold O₂ normal Auger spectrum as an example, the two extreme cases of MAPCI effect, “atomic-like PCI” and “molecular PCI”, were discovered and discussed. The effect of shape resonance on near-threshold molecular normal Auger spectrum was discussed taking NO near threshold normal Auger spectra as example.</p><p>The second part deals with research work on the chemisorption of small epoxy organic molecules, ethylene oxide, methyl oxirane, on Si (100) surfaces. Synchrotron radiation related techniques, UPS, XPS and NEXAFS, were applied. Based on the valence photoemission spectra, C 1<i>s</i> and Si 2<i>p</i> XPS spectra, the epoxy ring opening reactions of these molecules in chemisorption process were proved. Further tentative search for the surface-adsorbate CDAD effect was performed, and no evident circular dichroism was confirmed.</p>