@inproceedings{MuessigDabrowskiSchmeisser, author = {M{\"u}ssig, Hans-Joachim and Dabrowski, Jarek Marek and Schmeißer, Dieter}, title = {Interface Characterization of the High-k Gate Dielectric Pr2O3}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {Pr2O3 is currently under consideration as a potential alternative gate dielectric candidate for sub-0.1 µm Complementary Metal Oxide Semiconductor (CMOS) technology. For all thin gate dielectrics, the interface with silicon plays a key role, and in most cases is a dominant factor in determining overall electrical properties. We studied the Pr2O3/Si(001) interface by a non-destructive depth profiling using synchrotron radiation photo-electron spectroscopy and ab initio calculations. Our results provide evidence that a chemical reactive interface exists consisting of a mixed Si-Pr oxide such as (Pr2O3)x(SiO2)1-x, typically in non-stoichiometric composition. There is no formation of neither an interfacial SiO2 nor interfacial silicide: all Si-Pr bonds are oxidized and all SiO4 units dissolve in the Pr oxide. Interfacial silicates like (Pr2O3)x(SiO2)1-x are promising high-k dielectric materials because they represent incremental modification of SiO2 films by Pr ions so that the interface characteristics can be similar to Si-SiO2 interface properties. Under ultrahigh vacuum conditions, silicide formation is observed when the silicate film is heated above 800∘C. The praseodymium silicate system observed at the interface between Si(001) and Pr2O3 offers greater flexibility towards integration of Pr2O3 into future CMOS technologies.}, language = {en} } @inproceedings{MuellerSchmeisser, author = {M{\"u}ller, Klaus and Schmeißer, Dieter}, title = {Carbon-plot-microstructuring for all-polymer-transistors}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {This contribution describes the use of a low-cost technology to form organic microstructures for electronical applications. We demonstrate the principle ability of this method through the fabrication of organic field effect- transistors. With a computer driven plotter, substrates like printing foil and colloidal graphite (diluted in water) for the electrodes, we realized channel lengths of 20+10 micrometers. Compared with transistor devices, fabricated using conventional photolithographic methods and the same semiconducting material, this technique is a hopefull approach to produce microelectronic structures that are low-cost and all-organic.}, language = {en} } @inproceedings{MuellerMilkoBurkovetal., author = {M{\"u}ller, Klaus and Milko, Sergey and Burkov, Yevgen and Schmeißer, Dieter}, title = {Mischkristalle des Systems ZnS-CuInS2 f{\"u}r multispektrale Solarzellen}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {Wir haben CuInS2 (CIS) unterschiedlicher Herstellung (Koverdampfung, Sputtern, Pulsed Laser Deposition, CIS auf Kupferband aufgebracht) untersucht. Neben Tiefenprofilen (durch Sputtern) der Elementverteilung dieser Proben wurden der Einfluss der Temperatur, von aufgedampftem Kupfer und Indium, ebenfalls bei verschiedenen Temperaturen, auf das Verhalten der St{\"o}chiometrie mit spektroskopischen Methoden (XPS, UPS) studiert. Parallel dazu wurde das Verhalten von im Vakuum aufgedampften ZnS und die entsprechenden Oberfl{\"a}chenreaktionen in Abh{\"a}ngigkeit von der Temperatur untersucht und charakterisiert, so dass Aussagen {\"u}ber die Optimierung und Anpassung von Pr{\"a}parationsbedingungen und Parametern zur Herstellung von erstens reinem CIS und zweitens von Mischkristallen des Typs Zn2-xCuxInxS2 m{\"o}glich werden. Zwischen den beiden Endgliedern ZnS und CuInS2 besteht bis auf einen Phasen{\"u}bergang bei etwa 80\% CIS l{\"u}ckenlose Mischbarkeit gem{\"a}ss Zn2-xCuxInxS2 (Bente: Chem.Erde (1991)). Die elektronische Bandl{\"u}cke dieser Mischkristalle l{\"a}sst sich im Vergleich zu reinem CuInS2 in einem Bereich von 3,67 eV (ZnS) bis 1,55 eV (CuInS2) variieren. Damit besteht die M{\"o}glichkeit, durch kontrollierte {\"A}nderung der Zusammensetzung der Schichten die Effizienz von Solarzellen aus diesem Material zu optimieren.}, language = {de} } @inproceedings{HoffmannMikaloSchmeisser, author = {Hoffmann, Patrick and Mikalo, Ricardo Pablo and Schmeißer, Dieter}, title = {Si(001) surface oxidation}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {A Si(001) surface is cleaned in UHV by heating (flashing) and is exposed to different pressures of N2O at altered temperatures. Oxynitride layers of different thicknesses and different properties are grown depending on the N2O-pressure and the Si- temperature. This is illustrated by a schematic diagram. The properties of the different Oxynitride layers were studied by a combined PEEM- and PES-investigation using highly monochromatised synchrotron radiation. The amount of Oxygen and Nitrogen incorporated in the Oxynitride layers is determined from the PES measurements. The typical surface morphology for different preparation conditions is shown in PEEM images. A model based on differently established dipole layers in the Oxynitride layers is proposed. This model is capable of interpreting the features appearing in the PE-spectra. This model can also be applied to the interface of Si/SiO2.}, language = {en} } @inproceedings{MikaloHoffmannSchmeisseretal., author = {Mikalo, Ricardo Pablo and Hoffmann, Patrick and Schmeißer, Dieter and Lloyd Spetz, Anita and Lundstr{\"o}m, Ingemar and Wawra, Herbert and Pressel, Klaus and Ourmazd, Abbas}, title = {Depth profiling using synchrotron radiation with high energetic resolution as demonstrated for Si-, SiC-, SiGe-, and SiGeC-samples}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {Photoelectron spectroscopy utilizing synchrotron radiation of high energetic resolution (more than E/ΔE=3000) was used to record the Si2p emission signal of Si, SiC, SiGe, and SiGeC samples. The spectra exhibit signals of the elemental silicon as well as of fully oxidised silicon. Upon variing the photon energy, and therefore the escape depth of the photoelectrons, we find an oxidic silicon signal which is only half oxidized. This half oxidized silicon is located to be at the interface of the bulk material with the oxide. We determine the thickness of the surface oxide from the total ratio of oxidic and elemental silicon. We find differences between the interface and bulk oxides regarding their elemental composition. The line width of the elemental Si2p-signal exhibits a broadening of approximately 200meV while variing the photoelectron escape depth. This behaviour is interpreted as caused by surface stress.}, language = {en} } @inproceedings{BatchelorHoffmannSchmeisseretal., author = {Batchelor, David R. and Hoffmann, Patrick and Schmeißer, Dieter and Hulea, Iulian and Brinza, Monica}, title = {The Al-Fe interface of friction-welded joints}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {The interface region of friction-welded joints Al-Fe samples is investigated by scanning Auger Spectroscopy, Electron Probe Micro-analysis (EPMA), X-ray Photoelectron spectroscopy, and Photoemission Electron Microscopy, performed at the synchrotron light source (BESSY). We investigated polished samples cut to obtain a cross-section of the Al-Fe joints. At the Al-Fe interface there is a small number of Fe teeth protuding into the adjacent Al-matrix. Beside this mechanical interlock mechanism we identify an Fe-Al alloy which is formed in an almost homogeneous interface layer of approximately 80 micron thickness. We determine the valence band spectra within that layer and notice that the alloying formation is limited to the interface region. In addition, the profile of both, the Fe and O distribution within the Al next to that interface is determined. A model of the friction-welding mechanism is derived and discussed in terms of the ability of achieving low temperature Fe-Al joints.}, language = {en} } @inproceedings{HellerBoehmeSchmeisser, author = {Heller, Thomas and B{\"o}hme, Oliver and Schmeißer, Dieter}, title = {Molecular Resonances in the Photoionization Cross Section (PIX) of Oxidic Semiconductors}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {Despite their fascinating physical applications in sensoric there is no clear view of the electronic structure of these class of oxidic semiconductor materials. We studied the photo ionization cross sections (PIX) in a CIS like experiment of the valence states as well as the defect state and compare these to the CFS data obtained from X-ray absorption spectroscopy. While the first technique contains only transitions from a defined initial state the latter covers all the possible optical channels. We show for WO3-films that a structural reorganization of the surface is induced by doping (Na exposure) which increases the O2p/W5d orbital mixing. Pristine TiO2 (110) single crystals show basically the same behavior but have an initially stronger hybridization of Ti3d derived states with the O2p valence states. Upon doping the defect intensity is increased as well as the orbital hybridization. Our data give evidence that valence band derived states have almost the same orbital parentage like the defect state. They offer that the wave functions of these states are localized on a molecular scale. This is in contrast to the common treatment of resonances in the PIX which are usually discussed in terms of the resonant photoemission model, which does not include the possibility of mixed valence/defect states.}, language = {en} } @inproceedings{HellerLopezBitzeretal., author = {Heller, Thomas and Lopez, Alberto and Bitzer, Thomas and Richardson, Neville V. and Schmeißer, Dieter}, title = {Isopropoxy induced stabilisation of the 2x1 reconstruction of Si(100)}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {Alcohols are successfully employed as an additive in the anisotropic etching of silicon. In this HREELS study, we modelled the silicon/etching interface by the adsorption of alcohols (ethanol, isopropanol, n-propanol, tert-butyl alcohol) on Si(100)-2x1 and post-exposure to H2O under ultra high vacuum conditions. The vibrational data show that the adsorption of the alcohol molecules involves the cleavage of the O-H bond and the formation of a Si-O-C linkage to the alkoxy species. The dissociated hydrogen saturates one of the neighbouring dangling Si bonds. The Si-Si dimer bonds are not involved in the adsorption process. We observe a considerable chemisorption of water on the ethoxy and tert-butoxy passivated Si(100)-2x1 surface. From the disappearance of the 2x1 LEED pattern it can be concluded that the chemisorption of water occurs through a cleavage of the Si-Si dimer bond. In contrast, isopropoxy species on Si(100)-2x1 reduces dramatically the reactivity of Si(100)-2x1 towards water. Even following extreme exposures to water (1012 Torr s), a 2x1 LEED pattern was observed indicating the presence of intact Si-Si dimer bonds at the isopropoxy/Si(100)-2x1 surface.}, language = {en} } @inproceedings{HellerLopezBitzeretal., author = {Heller, Thomas and Lopez, Alberto and Bitzer, Thomas and Richardson, Neville V. and Schmeißer, Dieter}, title = {The Adsorption of Maleic Anhydride on Si(100)-2x1: A Combined HREELS and NEXAFS Study}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {Due to the growing range of applications for organic materials considerable interest has been focused on the controlled growth of films on silicon substrates. Recently, it has been shown that ultra-thin oligimide films can be grown on Si(100)-2x1 with a direct Si-C linkage to the substrate. In this study, we have focused on the chemisorption of maleic anhydride (C4O3H2) on Si(100)-2x1. The combined HREELS data indicate that the adsorption of maleic anhydride on Si(100)-2x1 at low dosages occurs mainly through cycloaddition of the C=C bond to the dangling bonds of the Si-Si dimer analogous to the behaviour of ethene. The Si-Si dimer bonds are not involved in the chemisorption, as the continued observation of a 2x1 pattern in LEED shows. In the NEXAFS spectra, a π* resonance indicative of a C=C bond is absent upon exposure of the silicon substrate to maleic anhydride. At higher dosages, we observe chemisorbed maleic anhydride species, which are bonded to the Si surface atoms via a single Si-C linkage with preservation of the C=C double bond. In this case, the dissociated hydrogen bonds to one of the neighbouring Si atoms. Possible adsorption geometries will be discussed.}, language = {en} } @inproceedings{HoffmannMikaloSchmeisseretal., author = {Hoffmann, Patrick and Mikalo, Ricardo Pablo and Schmeißer, Dieter and Kittler, Martin}, title = {Spektro-Mikroskopie auf multikristallinem Silizium}, series = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, booktitle = {Verhandlungen der Deutschen Physikalischen Gesellschaft}, publisher = {Deutsche Physikalische Gesellschaft}, address = {Bad Honnef}, abstract = {Es werden spektro-mikroskopische Untersuchungen an multikristallinem Silizium (mc-Si) vorgestellt, einem aussichtsreichen Material f{\"u}r die Herstellung preiswerter Solarzellen. Dazu wird ein Photoemissions- Elektronenmikroskop (PEEM) ausgestattet mit einem zus{\"a}tzlichen Energieanalysator f{\"u}r Elektronen (µESCA) genutzt. Bei Verwendung eines Synchrotrons als Anregungsquelle ist es so m{\"o}glich, sowohl Absorbtions-Spektren (NEXAFS) als auch Photoelektronen-Spektren (PES) mit Ortsaufl{\"o}sung zu erhalten. Dabei wird gezeigt, dass das nat{\"u}rliche Oxid zur Untersuchung der morphologie-abh{\"a}ngigen Oberfl{\"a}chenpotentiale nicht entfernt werden muss. Des Weiteren wird die Verteilung von Ca- und Na-Ausscheidungen, die auf dem mc-Si gefunden wurden, durch ortsaufgel{\"o}stes NEXAFS bzw. PES dargestellt. F{\"u}r den Photoemissions-Prozess des mc-Si im PEEM wird ein Modell aufgestellt, welches Photoemission mit einer Quecksilberdampflampe (hνmax = 4,9 eV) erkl{\"a}rt.}, language = {de} }