TY - CHAP A1 - Henkel, Karsten A1 - Paloumpa, Ioanna A1 - Müller, Klaus A1 - Schmeißer, Dieter T1 - P(VDF/TrFE) as a ferroelectric dielectric for Organic Field effect Transistors in MFIS structure T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - MFIS structures consisting of metal, ferroelectric poly[vinylidene fluoride trifluoroethylene](P[VDF/TrFE]), insulator, semiconductor (Si) are fabricated and the influence of the polarization of the P(VDF/TrFE) on the CV characteristics of these structures is investigated. We find a characteristic ferroelectric hysteresis in the CV curves upon increasing the voltage scan window (e.g.-U...U,U=6...30V, |UP(VDF/TrFE)|≤15V, dP(VDF/TrFE)=300 nm). A writing process with adequate electric fields causes large shifts in the flatband voltage ( Δ UFB>4V for the quoted example before) which are stable over days. We report on our investigations which focus on the switching behavior by varying the parameters like polymer thickness, writing field strength and time, long time stability, reversing voltage and insulating material (SiO2, PMMA (Polymethylmetacrylate)). This material combination is favorable for transfer into our full organic concept of field effect transistors for application as a nondestructive readout memory (NDRO) cell. KW - P(VDF/TrFE) KW - Organic ferroelectric field effect transistor KW - capacitance voltage measurements Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/syoo/session/6/contribution/39?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Müller, Klaus A1 - Burkov, Yevgen A1 - Schmeißer, Dieter T1 - Surface potential profiling on organic thin film transistors by photoemission-electron-microscopy (PEEM) T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Surface potential imaging with Photoemission-electron-microskopy (PEEM) in high lateral resolution is introduced as a new tool for the characterisation of organic transistor structures. We use source-drain- electrode structures of different organic materials like carbon-black or graphite plotted on a printing foil. Semiconducting regioregular Poly(3-Hexylthiophene-2,5-diyl) (P3HT) was deposited by spin coating. For our measurements we used radiation of a standard high pressure Hg-lamp (4,9 eV) and synchrotron radiation at the BESSYII-U49/2 beam line. In contrast to Kelvin-AFM measurements of the surface potential, PEEM enables a simultaneous analysis of chemical composition by photoelectron spectroscopy. UPS, for example, at zero potential gives information on chemical homogeneity of the organic semiconductor in lateral resolution. PEEM images at applied voltages, compared with UPS-spectra, gives informations on doping profiles in the semiconductor, for example. In conclusion, PEEM should be a complementary method for characterisation of the surface potential with Kelvin-AFM. In addition, PEEM gives opportunities for measurements of chemical composition in the working state of the transistor (applied voltages). KW - organic field effect transistor KW - Photoemission-electron-microscopy (PEEM) KW - Kelvin-AFM KW - X-Ray photoelectron spectroscopy Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/syoo/session/6/contribution/41?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Müller, Klaus A1 - Paloumpa, Ioanna A1 - Henkel, Karsten A1 - Schmeißer, Dieter T1 - Organic Field Effect Transistors with polymer high-k dielectric insulator T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Organic field effect transistors consisting of the copolymer poly(vinylidene fluoridetrifluoroethylene) (P(VDF-TrFE)) and P3HT (poly(3-hexlythiophene)) as active layer have been fabricated. The influence of P(VDF-TrFE) on the transconductance of organic field effect transistors was investigated and enhanced gate effects are observed compared to similar transistors with PMMA (Polymethylmetacrylate) as gate dielectric. Due to the high dielectric constant of P(VDF-TrFE) (DK=12) an operation voltage smaller than for a conventional organic dielectric like PMMA (DK=3.3) was observed. The thickness of the spincoated dielectric layers is in the range of 2microns and in consequence, no significant hysteresis was found, a prerequisite for transistor operation. KW - organic field effect transistor KW - P(VDF/TrFE) KW - high-k organic Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/syoo/session/6/contribution/30?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Geuss, Markus A1 - Müller, Klaus A1 - Paloumpa, Ioanna A1 - Schmeißer, Dieter T1 - Surface Potential profiling on operating full organic thin film transistors by Kelvin probe force microscopy T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Kelvin-AFM is employed to study all polymer organic thin film transistors which are promising candidates for low cost - low performance applications like active matrix displays, sensors or single-serving devices. We use bottom contact source-drain- electrode structures of different organic materials like carbon-black or graphite plotted on a printing foil. Semiconducting regioregular Poly(3-Hexylthiophene-2,5-diyl) (P3HT) was subsequently deposited by spin coating. Surface potential profiles across the transistor channel were measured by Kelvin-AFM for various source-drain potential differences and signs. We found that contact resistances cause characteristic steps in the surface potential near the channel edges which vary with the electrode material. Furthermore, nonlinearities appear in the potential gradient which possibly give evidence for lateral inhomogeneities of the carrier mobilities. In summary, surface potential imaging with high lateral resolution ( approx. 100 nm) is introduced as a powerful tool for the characterisation of the transistor performance and the selection of suitable low cost electrode materials. KW - organic field effect transistor KW - Kelvin probe force microscopy Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/syoo/session/6/contribution/36?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Torche, Mohamed A1 - Schmeißer, Dieter T1 - The interaction of Al, Au, Ag, and Ti metal contacts with Pr2O3 thin films T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Pr2O3 is one of the promising high-k oxides desirable to replace SiO2 for the sub-100nm field-effect transistors (FETs) and dynamic random access memory (DRAM) capacitors. Here we focus on the metallic contacts used for the MOS and MIM based structures. With the thickness of Pr2O3 being around 3nm the metal interaction is crucial to avoid a reduction of the dielectric properties by metal percolation, crack filling or diffusion processes. We use XPS and SRPS to study the initial interaction as well as the thermal stability of metals (Al, Ag, Au, and Ti) on Pr2O3 films. We show that Al, Ag, Au form initial metallic layer which react already at temperatures around 300∘C. In contrast, Ti is found to be more stable than the other metals. We determine the formation of Ti-oxides at the Ti / Pr2O3 interface and its thermal stability. Ti is found to build a good diffusion barrier between the oxide and the metal. KW - high-k KW - Pr2O3 KW - X-ray photoelectron spectroscopy (XPS) KW - Al, Ag, Au, and Ti electrodes KW - metal dielectric interaction Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/ds/session/11/contribution/4?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Seifarth, Olaf A1 - Burkov, Yevgen A1 - Schmeißer, Dieter A1 - Sydorenko, Alexander A1 - Krenek, Radim A1 - Stamm, Manfred T1 - Photoelectron spectroscopy and microscopy on magnetic nano particles embedded into block copolymers T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - The formation of metallic nano particles stored in thin films of block copolymers has been investigated by means of synchrotron radiation based photoemission spectroscopy (PES) and microscopy (PEEM). Empty channels in poly(styrene-block-4-vinylpyridine) copolymer with diameters of tens of nanometers filled with CrO2, Cr2O3 and Ni provide ideal bases for performing electron spectroscopy with energy and lateral resolution on magnetic nano particles. We present UPS, XPS, NEXAFS spectra and PEEM images on and off the C 1s, Cr 2p, Ni 2p resonances and discuss the geometric and electronic structure of such compounds. The synchrotron radiation was delivered from the U49/2 beamline at BESSY II. KW - photoelectron emission microscopy (PEEM) KW - X-ray photoelectron spectroscopy KW - X-ray absorption spectroscopy KW - block copolymers KW - magnetic nano particles Y1 - 2005 UR - http://www.dpg-verhandlungen.de/year/2005/conference/berlin/part/cpp/session/29/contribution/27?lan=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Mikalo, Ricardo Pablo A1 - Appel, Günter A1 - Hoffmann, Patrick A1 - Schmeißer, Dieter T1 - Conducting Polypyrrole doped with Phthalocyaninesulfonates - new materials for chemical sensors T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Polypyrrole - a conducting polymer - is used as an active electrode of a quartz micro ballance and considered as a gate electrode in all-polymer field effect transistors used as chemical sensor. We use substituted phthalocyanines as dopants of polypyrrole as they offer the possibility to enhance the dopant concentration as well as to include functionalized groups. We studied these films by photoelectron spectroscopy, NEXAFS, PEEM, and TEM. These investigations revealed that the electronic structure as well as the morphology are highly dependent on the dopant’s structure. We suggest a new charge transport model for 5-ring heterocycle conductive polymers. Whereas in the standard model only the carbon backbone is considered for the charge transport, we found by NEXAFS investigations that the heteroatom has a considerable high participation in the gap states, which are responsible for the charge transport. The dopants π-interactions force the nitrogen lone pair wave functions to contribute to the conducting polymer π-system. This is a novel approach concerning the application as chemical sensors since the reversible interaction of the analyte modifies the dopant and not the matrix. KW - polypyrrole KW - conducting polymer KW - X-ray photoelectron spectroscopy (XPS) KW - X-Ray absorption spectroscopy (XAS) KW - photo emission electron spectroscopy (PEEM) KW - transmission electron microscopy (TEM) KW - quartz crystal micro ballance (QMB) KW - gas sensor Y1 - 2000 UR - http://www.dpg-verhandlungen.de/year/2000/conference/regensburg/part/o/session/15/contribution/1?lang=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Batchelor, David R. A1 - Follath, Rolf A1 - Schmeißer, Dieter T1 - Design of a PGM for the U49/2 Undulator at BESSY II T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - This poster describes the beamline proposed for the BESSY II U49/2 Undulator by the Collaborating Research Group of BTU Cottbus, HMI Berlin and the TU Darmstadt. The beamline is designed with both high resolution electron spectroscopy, valence band measurements and PEEM in mind and utilises the wide energy range of the U49 Undulator 40−1500eV. The design chosen is based on a Petersen PGM [1] but with the grating illuminated with parallel light [2]. This modification allows variation of the monochromator higher order content or resolution, spot size without changing the focus. The performance of the beamline was investigated using various programs available at BESSY. The Undulator character- istics were evaluated using both SMUT and WAVE, and the optical performance of the monochromator was checked using REFLEC and RAY. The calculations show a resolving power of 2×104 with a flux of the order 1013 photons s−1 over the energy range covered by the mono- chromator. The maximum nominal second order contributions are ≈ 2% at 300 eV for the first Undulator harmonic and ≈ 9% for the third harmonic at 500 eV, both of which can be reduced by increasing the grating incidence angle and, or decreasing the Undulator Pinhole size. KW - Bessy II KW - undulator beamline U49/2 KW - design Y1 - 1999 UR - http://www.dpg-verhandlungen.de/year/1999/conference/muenster/part/o/session/36/contribution/81?lang=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Heller, Thomas A1 - Schmeißer, Dieter T1 - Polaronen in SrTiO3(100) T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Vorgestellt werden Untersuchungen zur elektronischen Struktur von oxidischen Halbleitern wie SrTiO3(100)-Einkristallen und WO3-Filmen. Die Charakterisierung der Oberflächen erfolgt im Valenzbandbereich mittels Photoelektronenspektroskopie (TGM 7, Bessy I, hν=3D 15-100eV). Zustände entstehen in der Bandlücke dieser=20 Materialien durch Dotierung (Heizen oder Natrium-Belegung). Wir untersuchen den Wirkungsquerschnitt speziell für diese Gapzustände. Ohne Dotierung ist der Verlauf des Wirkungsquerschnittes unstrukturiert. Bei Dotierung bilden sich molekulare Resonanzen. Deren Auftreten zeigt, daß diese Gapzustände lokalisiert sind. Weiterhin beobachten wir ausgeprägte Feinstrukturen, die die charakteristische Anregung f=FCr Polaronen enthalten. KW - Polaron KW - Röntgen-Photoelektronenspektroskopie KW - Gapzustände Y1 - 1999 UR - http://www.dpg-verhandlungen.de/year/1999/conference/muenster/part/o/session/21/contribution/8?lang=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Hoffmann, Patrick A1 - Böhme, Oliver A1 - Schmeißer, Dieter A1 - Lloyd Spetz, Anita A1 - Mårtenson, Per T1 - Einfluß von Nanopartikeln auf die Funktion von Hochtemperatursensoren T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Es werden Untersuchungen an als Hochtemperatur-Sensoren arbeitenden Schottky-Dioden mit dem Aufbau Metall-Oxidschicht-Siliziumkarbid vorgestellt. Dazu wurden Tiefenprofile mit XPS durch abwechselndes Abtragen durch Sputtern und Messen erstellt. Die Messungen erfolgten an thermisch unterschiedlich vorbehandelten Proben. Dabei konnten dipol-bedingte Verschiebungen der Bindungsenergie von Rumpfniveaus beobachtet werden. Das dazu notwendige Dipol-Moment wird durch das Entstehen von mit einer Oxidschicht überzogenen Nanoteilchen erklärt. Die unterschiedlich ausgeprägten Dipol-Verschiebungen auf den einzelnen Proben erlaubten eine Erklärung der thermischen Vorbehandlung, die bei Weglassen zu „frischen“ und je nach Temperatur zu „aktivierten“ oder „toten“ Sensoren führte. KW - Hochtemperatursensoren KW - Röntgen-Photoelektronenspektroskopie (XPS) KW - Tiefenprofilierung Y1 - 1999 UR - http://www.dpg-verhandlungen.de/year/1999/conference/muenster/part/o/session/16/contribution/1?lang=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Mikalo, Ricardo Pablo A1 - Appel, Günter A1 - Hoffmann, Patrick A1 - Schmeißer, Dieter T1 - Leitfähiges Polypyrrol als Elektrodenmaterial: Wechselwirkungen mit Silber T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Untersuchungen des metallischen Kontaktes von Silber auf tosylat- und phthalocyanindotiertem Polypyrrol wurden mittels XPS- und µ-NEXAFS vorgenommen. Es wurde festgestellt, daß Silber mit dem Polypyrrol keine Verbindung eingeht. Daraus kann geschlossen werden, daß sowohl das leitfähige Polymer, als auch das Silber ihren Leitfähigkeitsmechanismus beibehalten. Es konnte gezeigt werden, daß bei steigender Silberbelegung die Intensität der Polaronenzustände des Polypyrrol in stärkerem Maße abnimmt, als die Intensität der unbesetzten Zustände. Das läßt darauf schließen, daß Silber die Grenzfläche stabilisiert. KW - Polypyrrol KW - leifähiges Polymer KW - Röntgen-Photoelektronenspektroskopie (XPS) KW - Röntgen-Absoprtionsspektroskopie (XAS, NEXAFS) Y1 - 1999 UR - http://www.dpg-verhandlungen.de/year/1999/conference/muenster/part/o/session/11/contribution/57?lang=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Oprea, Alexandru A1 - Schmeißer, Dieter A1 - Goldenblum, A. T1 - On the charge transfer process in ZnS based ac powder electroluminescent devices T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - The charge transfer process in ZnS based ac powder electroluminescent devices was experimentally and theoretically investigated. The time dependence of active currents and the voltage dependence of the brightness were measured in different operating conditions. This data allowed the hypothesis that each ZnS grain of the ac powder electroluminescent device (PWELD) behaves as a thin films electroluminescent device (TFELD) with metal-insulator-semiconductor-insulator-metal (MISIM) structure. The whole PWELD, itself, can be considered as a sum of many litle MISIM sandwiches electrically conected among them and having the quasi Fermi level of the semiconductor-insulator interface randomly distributed. On this basis, in the frame of a statistical Monte-Carlo like procedure, was developed a quantative semiclassical model, in good agreement with the experimental data. KW - ZnS KW - charge transfer process KW - ac powder electroluminescent device KW - time and brightness dependence KW - Monte Carlo simulation Y1 - 1999 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Heller, Thomas A1 - Böhme, Oliver A1 - Schmeißer, Dieter T1 - Gap - Zustände in Wolframoxid WO3 - relaxierten Oberflächen T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Vorgestellt werden Arbeiten an dünnen WO3-Schichten, die durch Verdampfen aus einer Knudsenzelle im UHV präpariert wurden. Diese Filme sind im Rahmen der XPS-Analysen stöchiometrisch, ohne Gap-Zustände. Definierte Gap-Zustände bilden sich durch Relaxierung der Oberfläche: nach einigen Stunden im UHV, nach Heizen in Argon-Atmosphäre und nach Belegung mit Natrium. Die Charakterisierung dieser definierten Wolframoxid-Schichten erfolgt durch: 1.)XPS-Intensitäten 2.)detailierte Analyse der W4f-Rumpfniveaus durch Synchrotronstrahlung (Bessy, TGM 7) 3.)die Variation der Austrittsarbeit beim Heizen und bei Natrium-Belegung 4.)das Auftreten von Gap-Zuständen in der Bandlücke KW - WO3 KW - Röntgen-Photoelektronenspektroskopie (XPS) KW - Gapzustände Y1 - 1998 UR - http://www.dpg-verhandlungen.de/year/1998/conference/regensburg/part/o/session/11/contribution/102?lang=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - CHAP A1 - Hoffmann, Patrick A1 - Mikalo, Ricardo Pablo A1 - Schmeißer, Dieter T1 - PEEM-Untersuchung an Spaltflächen von MoTe2-(0001) T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Molybdänditellurid (MoTe2) gehört zu den Schichtgitterverbindung und ist im allgemeinen durch den Herstellungsprozeß n-dotiert. Proben dieses MoTe2 wurden im Ultrahochvakuum gespalten und die so erhaltenen sauberen (0001)-Spaltflächen mit einem Photoemissions-Elektronenmikroskop (PEEM) untersucht. Diese Untersuchung erbrachte nebeneinander auf den Proben- oberflächen liegende stark kontrastierte helle und dunkle Bereiche. Da das PEEM Austrittsarbeitsunterschiede als Kontrast darstellt, können diese hellen und dunklen Bereiche auf lokale Unterschiede in der Austrittsarbeit zurückgeführt werden. Weiterhin wird über den Versuch berichtet, eine Zuordnung zwischen dem Kontrast und dem Unterschied in der Austrittsarbeit mit Hilfe eines Elektronenenergie-Analysators (micro-ESCA) zu treffen. KW - MoTe2 KW - Photoemissionselektronenspektroskopie (PEEM) KW - Austrittsarbeit Y1 - 1998 UR - http://www.dpg-verhandlungen.de/year/1998/conference/regensburg/part/o/session/5/contribution/5?lang=en PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - GEN A1 - Sowinska, Małgorzata A1 - Das, Chittaranjan A1 - Wojciechowski, Konrad A1 - Rouissi, Zied A1 - Snaith, Henry J. A1 - Schmeißer, Dieter T1 - Atomic layer deposition of Al2O3 on CH3NH3PbI3 for enhancement of perovskite solar cells stability T2 - Synchrotron Radiation in Natural Science : Bulletin of the Polish Synchrotron Radiation Society KW - atomic layer deposition KW - perovskite soloar cells KW - X-ray photoelectron spectroscopy (XPS) KW - Atomic foce microscopy (AFM) Y1 - 2016 SN - 1644-7190 VL - 15 IS - 1-2 SP - S. 33 ER - TY - GEN A1 - Schmeißer, Dieter A1 - Janowitz, Christoph T1 - The Cu2p-edge of superconducting BiSrCu-Oxides studed by resonant Photoelectron Spectroscopy T2 - Synchrotron Radiation in Natural Science : Bulletin of the Polish Synchrotron Radiation Society KW - synchrotron raidation KW - superconductor Y1 - 2016 SN - 1644-7190 VL - 15 IS - 1-2 SP - S. 35 ER - TY - CHAP A1 - Das, Chittaranjan A1 - Tallarida, Massimo A1 - Schmeißer, Dieter T1 - TiO2 laminated Silicon microstructures based stable photocathode for water splitting T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - The photoelectrochemical (PEC) water splitting is one of the most efficient ways to obtain hydrogen from water using solar power which can be used as carbon free fuel. The PEC device can bedesigned using semiconducting material that will convert solar radiation to H2. Silicon can be one of the best choices for PEC due to its success in solar cells technology. There are certain issues with Si such as stability in electrochemical medium [1] and higher surface reflectance (25%) which limits the Si as an ideal candidate for PEC technique [2]. In the present work we addressed these issues by surface structuring and laminating the surface with metal oxide. The microstructuring of Si was done by electrochemical method. The Si microstructure photocathode was stabilized by thin layer of ALD grown TiO2 film. The microstructuring and lamination of Si photocathode by ALD layer of TiO2 decreased the reflectance ofthe surface and shift the onset potential towards anodic direction by 350 mV with a prolonged stability over 60 hours[3]. [1] C. Levy-Clement, J. Electrochem. Soc 1991, 12, 69 [2] J. Oh, et al. Energy Environ. Sci., 2011, 4, 1690 [3] C. Das, et al. Nanoscale 2015,7, 7726 KW - water splitting KW - TiO2 KW - atomic layer deposition (ALD) KW - Si photoelectrodes Y1 - 2016 UR - http://www.dpg-verhandlungen.de/year/2016/conference/regensburg/part/ds/session/48/contribution/4?lang=en SP - S. 213 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER - TY - GEN A1 - Haeberle, Jörg A1 - Brizzi, Simone A1 - Gaspar, Diana A1 - Barquinha, Pedro A1 - Galazka, Zbigniew A1 - Schulz, Detlev A1 - Schmeißer, Dieter T1 - A spectroscopic comparison of IGZO thin film and the parent In2O3, Ga2O3, and ZnO single crystals T2 - Materials Research Express N2 - We use resonant photoelectron spectroscopy at the Zn 2p, Ga 2p, In 3d, and O 1s absorption edges to report on the electronic properties of indium–gallium–zinc-oxide thin films. We also compare the data with the respective data of the corresponding single crystals In2O3, Ga2O3, and ZnO. We focus on the elemental composition and, in particular, find no evidence for oxygen deficiency. The In, Ga, and Zn absorption data at resonance can be used to analyze the conduction band states in detail. We deduce that a configuration interaction between d10s0 and d9s1states is of importance. We provided a novel mechanism in which configuration interaction induced gap states create both, extended unoccupied states around E F as well as localized occupied states within the gap. KW - transparent conducting oxides (TCO) KW - resonant photoelectron spectroscopy KW - in-gapdefect states Y1 - 2016 U6 - https://doi.org/10.1088/2053-1591/3/10/106302 SN - 2053-1591 VL - 3 IS - 10 SP - 106302-1 EP - 106302-17 ER - TY - GEN A1 - Ghosh, Sujoy Kumar A1 - Biswas, Anirban A1 - Sen, Shrabanee A1 - Das, Chittaranjan A1 - Henkel, Karsten A1 - Schmeißer, Dieter A1 - Mandal, Dipankar T1 - Yb3+ Assisted Self-Polarized PVDF Based Ferroelectretic Nanogenerator: A Facile Strategy of Highly Efficient Mechanical Energy Harvester Fabrication T2 - Nano Energy N2 - Ytterbium (Yb3+) assisted porous poly(vinylidene fluoride) (PVDF) composite film comprising flexible ferroelectretic nanogenerator (FTNG) is highlighted where traditional poling treatment is completely avoided. The piezoelectric output of FTNG is realized by the co-operative activity of self-polarized -CH2/-CF2 dipoles with porous electret-like structure in the composite film. Owing to extraordinary ferroelectric and dielectric properties, FTNG is acting as a highly efficient mechanical energy harvester. It is capable to capture several forms of abundant mechanical energy arising from humanfinger movements, machine vibrations and sound waves. As a proof of concept, under compressive deformation, FTNG is enable to instantly powers up several consumer electronics and thus provides a promising strategy for achieving self-powered electronic devices. KW - PVDF KW - Yb 3+ KW - Porous ferroelectret material KW - Self-polarization KW - Ferroelectretic nanogenerator KW - Mechanical energy harvester KW - Self-powered electronics Y1 - 2016 U6 - https://doi.org/10.1016/j.nanoen.2016.10.042 SN - 2211-2855 VL - 2016 IS - 30 SP - 621 EP - 629 ER - TY - GEN A1 - Henkel, Karsten A1 - Kot, Małgorzata A1 - Schmeißer, Dieter T1 - Localized defect states and charge trapping in atomic layer deposited-Al₂O₃ films T2 - Journal of Vacuum Science and Technology, A : Vacuum, Surfaces, and Films N2 - In this study, the authors compared different Al₂O₃ films grown by atomic layer deposition (ALD) with the same aluminum precursor but on different substrates. The authors employed different process parameters such as thermal-ALD and plasma-enhanced-ALD using different substrate temperatures ranging from 280 °C down to room temperature. They characterized these films by resonant photoelectron spectroscopy and by electrical measurements. They established that generally the ALD-Al₂O₃ films show characteristic features of bulk Al₂O₃. For all films investigated, the authors found intrinsic defect states within the electronic band gap and identified excitonic, polaronic, and charge-transfer defect states. The authors gave an atomistic model to explain these intrinsic defects and found that their relative abundance is subject of the choice of ALD parameters and of the substrate used. They were able to relate the spectroscopic assigned in-gap defect states with the electronic charges as determined in our electrical measurements. KW - defect states KW - resonant photoelectron spectroscopy (resPES) KW - Al₂O₃ KW - atomic layer deposition (ALD) KW - excitons KW - polarons Y1 - 2017 U6 - https://doi.org/10.1116/1.4971991 SN - 0734-2101 SN - 1520-8559 VL - 35 IS - 1 SP - 01B125-1 EP - 01B125-18 ER - TY - GEN A1 - Kot, Małgorzata A1 - Das, Chittaranjan A1 - Wang, Zhiping A1 - Henkel, Karsten A1 - Rouissi, Zied A1 - Wojciechowski, Konrad A1 - Snaith, Henry J. A1 - Schmeißer, Dieter T1 - Room-Temperature Atomic Layer Deposition of Al₂O₃: Impact on Efficiency, Stability and Surface Properties in Perovskite Solar Cells T2 - ChemSusChem N2 - In this work, solar cells with a freshly made CH₃NH₃PbI₃ perovskite film showed a power conversion efficiency (PCE) of 15.4 % whereas the one with 50 days aged perovskite film only 6.1 %. However, when the aged perovskite was covered with a layer of Al₂O₃ deposited by atomic layer deposition (ALD) at room temperature (RT), the PCE value was clearly enhanced. X-ray photoelectron spectroscopy study showed that the ALD precursors are chemically active only at the perovskite surface and passivate it. Moreover, the RT-ALD-Al2O3-covered perovskite films showed enhanced ambient air stability. KW - Al₂O₃ KW - atomic layer deposition (ALD) KW - perovskite KW - solar cells KW - X-ray photoelectron spectroscopy (XPS) Y1 - 2016 U6 - https://doi.org/10.1002/cssc.201601186 SN - 1864-5631 SN - 1864-564X VL - 9 IS - 24 SP - 3401 EP - 3406 ER - TY - GEN A1 - Cuypers, Daniel A1 - Fleischmann, Claudia A1 - Dorp, Dennis H. von A1 - Brizzi, Simone A1 - Tallarida, Massimo A1 - Müller, Matthias A1 - Hönicke, Philipp A1 - Billen, Arne A1 - Chintala, Ravi A1 - Conard, Thierry A1 - Schmeißer, Dieter A1 - Vandervorst, Wilfried A1 - Elshocht, Sven van A1 - Armini, Silvia A1 - De Gendt, Stefan A1 - Adelmann, Christoph T1 - Sacrificial Self-Assembled Monolayers for the Passivation of GaAs(100) Surfaces and Interfaces T2 - Chemistry of Materials N2 - The use of sacrificial self-assembled monolayers (SAMs) to prepare clean n-type GaAs (100) surfaces without band bending in vacuo is demonstrated. GaAs surface passivation using octadecanethiol SAMs after HCl cleaning is shown to lead to an enhancement of the room-temperature photoluminescence intensity. Synchrotron-radiation photoelectron spectroscopy (SRPES) finds that the interfacial oxide between GaAs and the SAM remains below the detection limit. Evidence for both Ga–S and As–S bonds at the GaAs–thiolate interface is found. The limited thermal stability of the SAM allows the desorption of the alkyl chains by in situ thermal annealing at temperatures above 180 °C, leaving S bonded to Ga behind. The resulting surface contains only a very small amount of O (0.05 ML coverage) and C (about 3% of the SAM remaining) and shows no band bending with the surface Fermi level close to the conduction band. Atomic layer deposition of Al₂O₃ on this surface occurs via the formation of Al–S bonds without introducing any additional band bending. This indicates that the surface preparation of n-type GaAs (100) using sacrificial octadecanethiol SAMs followed by in situ thermal removal provides a route toward GaAs/oxide interfaces without interfacial oxides and without band bending. KW - GaAs KW - passivation KW - Al₂O₃ KW - atomic layer deposition (ALD) KW - Synchrotron-radiation photoelectron spectroscopy (SRPES) KW - self assembled monolayers (SAM) KW - interface engineering Y1 - 2016 U6 - https://doi.org/10.1021/acs.chemmater.6b01732 SN - 0897-4756 SN - 1520-5002 VL - 28 IS - 16 SP - 5689 EP - 5701 ER - TY - GEN A1 - Corrêa, Silma Alberton A1 - Brizzi, Simone A1 - Schmeißer, Dieter T1 - Depicting the Electronic Structure of HfO₂ Films by Spectroscopic Techniques T2 - ECS Transactions N2 - The electronic structure of HfO₂ films was investigated. The partial density of states for the valence and the conduction bands was determined by the detailed analysis of the O1s resonance profile by resonant photoelectron spectroscopy. The positions of valence band maximum and conduction band minimum, the excitation range for the polaronic states and the range of charge transfer band were found to be not influenced by the preparation conditions. The band gap was determined to be 6.2 eV and the energy of the charge neutrality level (referred to vacuum level) was determined as 4.7 eV. The Fermi level position was observed to vary about 1.2 eV depending on the preparation conditions, which indicates the presence of charges within the films. KW - HfO₂ KW - resonant photoelectron spectroscopy (resPES) KW - electronic structure KW - partial density of states KW - charge neutrality level Y1 - 2016 U6 - https://doi.org/10.1149/07506.0145ecst SN - 1938-6737 SN - 1938-5862 VL - 75 IS - 6 SP - 145 EP - 153 ER - TY - GEN A1 - Henkel, Karsten A1 - Das, Chittaranjan A1 - Kot, Małgorzata A1 - Schmeißer, Dieter A1 - Naumann, Franziska A1 - Kärkkänen, Irina A1 - Gargouri, Hassan T1 - In-gap states in titanium dioxide and oxynitride atomic layer deposited films T2 - Journal of Vacuum Science and Technology: A N2 - Valence band (VB) spectra of titanium dioxide (TiO2) and oxynitride (TiOxNy) films prepared by different atomic layer deposition (ALD) processes are compared and related to electrical characterization [current–voltage (JV) and capacitance–voltage (CV)] results. By increasing the nitrogen amount in the TiO2 film, band-gap narrowing is observed. The band-gap decrease is related to the contribution of the nitrogen density of states, which induces defects within the band-gap and thus reduces its optical band-gap. In-gap states are found in the VB spectra at 1 eV below the Fermi energy in all investigated ALD samples, i.e., in TiO2 as well as in TiOxNy films. An exponential correlation between leakage current density and in-gap state intensity is derived by the combination of JV measurements and VB spectra, whereas the in-gap states seem to have no influence on hysteresis and fixed oxide charges found in the CV data. It is argued that the in-gap states in TiO2 and TiOxNy have an excitonic or polaronic origin. Both, band-gap narrowing and in-gap state intensity can be tuned by the ALD process selection and the variation of its parameters. KW - Titanium dioxide (TiO2) KW - Titanium oxynitrdie (TiON) KW - valence band spectra KW - in-gap states KW - band-gap narrowing KW - electrical characterization Y1 - 2017 U6 - https://doi.org/10.1116/1.4972247 SN - 0734-2101 SN - 1520-8559 VL - 35 IS - 1 SP - 01B135-1 EP - 01B135-8 ER - TY - CHAP A1 - Garain, Samiran A1 - Adhikary, Prakriti A1 - Mandal, Dipankar A1 - Sen, Shrabanee A1 - Henkel, Karsten A1 - Schmeißer, Dieter T1 - Electro-active β-Phase Formation in Poly(vinylidene fluoride) Films by Hydrated Rare earth Metal Salt T2 - Proceeding of the International Conference on Nanotechnology 2013 (ICNT 2013) N2 - Polyvinylidene fluoride (PVDF) is a typical fluoro-polymer with complicated polymorphisms due to the semi-crystalline nature. Generally, four crystalline phases, α, β, γ and δ may exist in PVDF crystals. The nonpolar α- and δ-phase has a monoclinic lattice with trans-gauche conformation (TGTG⁄), which is thermodynamically most stable for PVDF. The polar β phase with all-trans (TTTT) planar zigzag conformation is attractive for its piezo-, pyro-, and ferroelectric properties. The polar β-Phase and also semi-polar γ-phase (TTTGTTTG⁄) have obtained wide device applications such as acoustic transducers, piezoelectric sensors, energy harvesting generators, pyroelectric sensors, non-volatile memories and energy storage capacitors. In this work, we explore the possibility to nucleate β-phase in PVDF hydrated salt composite films by addition of the hydrated Rare earth metal salt, (NH4)4 Ce (SO4)4, 2H2O) for the piezo- ferro and high dielectric based device applications. It has been found that the water molecules in (NH4)4 Ce (SO4)4, 2H2O could form hydrogen bonds with PVDF during the crystallization process and the hydrogen bonds promoted the electro-active crystalline β- phase in PVDF with all -trans conformations. In addition, the DMF (solvent used for films preparation) can also assist the rare-earth based nanoparticle preparation, as a result the electrostatic interaction of the surface charge of the nanoparticles and molecular dipoles in PVDF can resist the electroactive β- phase in PVDF. KW - PVDF KW - β-Phase KW - piezoelectric Y1 - 2013 SN - 978-81-927756-0-9 SP - S. 127 PB - Institute of Technology, Haldia, WB, India CY - Haldia ER - TY - CHAP A1 - Schmeißer, Dieter A1 - Müller, Sebastian A1 - Henkel, Karsten A1 - Müller, Klaus A1 - Wehner, Stefan T1 - In-situ analysis of moving reaction fronts for the bistable CO oxidation reaction on noble metal catalyst T2 - Extended Abstracts Book of First International Conference on Materials for Energy N2 - Experimental data on the reaction kinetics of catalytic processes are prerequisite for modeling of such reactions and their output. We investigate the CO oxidation on some noble metal catalysts, like Iridium(111) and Palladium(111) which is a bistable surface reaction. In a specific range of CO content in the feed gas islands of one or the other adsorbate nucleate and grow, which is recorded with photo electron emission microscopy (PEEM). During these transients the coverage on the surface changes from predominantly oxygen covered to predominantly CO covered resp. vice versa. But the resolution of PEEM and especially its unknown and nonlinear dependence of coverage of the two adsorbates (oxygen and CO) and image intensity make it impossible to extract the changes in coverage. On the other hand the reaction diffusion model based on the Langmuir-Hinshelwood-mechanism delivers the coverage of oxygen and carbon monoxide. The shapeand wall velocity of those islands has been connected perfectly to each other [CPL 423 (2006) 39], but not the absolute coverage and their variation during the reaction. Since the domain wall velocity is small on Iridium(111), this has opened the possibility for a detailed analysis of the changing coverage inside this domain wallutilizing synchrotron radiation and photo electron spectroscopy at BESSY II. The coverage profile of oxygen and CO inside a moving domain wall was measured for both cases using XPS spectra at O1s, C1s and the valence band during thereaction. Comparison with the reaction-diffusion-model and other catalytic surfaces, like Palladium(111) are done. KW - CO oxidation KW - Ir KW - Pd KW - photo electron emission microscopy (PEEM) Y1 - 2010 SN - 978-3-89746-117-8 SP - S. 932 PB - Dechema e.V. CY - Frankfurt ER - TY - GEN A1 - Menezes, Prashanth W. A1 - Indra, Arindam A1 - Das, Chittaranjan A1 - Walter, Carsten A1 - Göbel, Caren A1 - Gutkin, Vitaly A1 - Schmeißer, Dieter A1 - Driess, Matthias T1 - Uncovering the Nature of Active Species of Nickel Phosphide Catalysts in High-Performance Electrochemical Overall Water Splitting T2 - ACS Catalysis N2 - A systematic structural elucidation of the near-surface active species of the two remarkably active nickel phosphides Ni12P5 and Ni2P on the basis of extensive analytical, microscopic, and spectroscopic investigations is reported. The latter can serve as complementary efficient electrocatalysts in the hydrogen (HER) versus oxygen evolution reaction (OER) in alkaline media. In the OER Ni12P5 shows enhanced performance over Ni2P due to the higher concentration of nickel in this phase, which enables the formation of an amorphous NiOOH/Ni(OH)2 shell on a modified multiphase with a disordered phosphide/phosphite core. The situation is completely reversed in the HER, where Ni2P displayed a significant improvement in electrocatalytic activity over Ni12P5 owing to a larger concentration of phosphide/phosphate species in the shell. Moreover, the efficiently combined use of the two nickel phosphide phases deposited on nickel foam in overall electrocatalytic water splitting is demonstrated by a strikingly low cell voltage and high stability with pronounced current density, and these catalysts could be an apt choice for applications in commercial alkaline water electrolysis. KW - overall water splitting KW - electrocatalysis KW - nickel phosphide KW - structural rearrangement KW - surface structure Y1 - 2017 U6 - https://doi.org/10.1021/acscatal.6b02666 SN - 2155-5435 VL - 7 IS - 1 SP - 103 EP - 109 ER - TY - GEN A1 - Indra, Arindam A1 - Menezes, Prashanth W. A1 - Das, Chittaranjan A1 - Göbel, Caren A1 - Tallarida, Massimo A1 - Schmeißer, Dieter A1 - Driess, Matthias T1 - A facile corrosion approach to the synthesis of highly active CoOxwater oxidation catalysts T2 - Journal of Materials Chemistry A N2 - Ultra-small rock salt cobalt monoxide (CoO) nanoparticles were synthesized and subjected to partial oxidation (‘corrosion’) with ceric ammonium nitrate (CAN) to form mixed-valence CoOx(1 < x< 2) water oxidation catalysts. Spectroscopic, microscopic and analytical methods evidenced a structural reformation of cubic CoO to active CoOx with a spinel structure. The superior water oxidation activity of CoOx has been established in electrochemical water oxidation under alkaline conditions. Electrochemical water oxidation with CoOx was recorded at a considerably low overpotential of merely 325 mV at a current density of 10 mA cm-2 in comparison to 370 mV for CoO. Transformation of both octahedral CoII and CoIII sites into amorphous Co(OH)2–CoOOH is the key to high electrochemical activity while the presence of a higher amount of octahedral CoIII sites in CoOx is imperative for an efficient oxygen evolution process. KW - water splitting KW - water oxidation KW - cobalt oxide catalyst KW - transmission electron microscopy (TEM) KW - X-ray photoelectron spectroscopy (XPS) KW - X-ray absorption spectroscopy (XAS) KW - Cyclic voltammetry (CV) Y1 - 2017 U6 - https://doi.org/10.1039/c6ta10650a SN - 2050-7488 SN - 2050-7496 IS - 5 SP - 5171 EP - 5177 ER - TY - CHAP A1 - Łobaza, Justyna A1 - Kot, Małgorzata A1 - Schmeißer, Dieter T1 - Analysis of surface oxidation of TiON ALD films T2 - Verhandlungen der Deutschen Physikalischen Gesellschaft N2 - Titanium oxynitride (TiON) films are interesting due to their remarkable optical and electronic properties which strongly depend on the O/N ratio. However, it is known that films containing Ti are prone to oxidation in contact with the air [1]. In this work, we study the thickness of a surface oxidation layer which is inherently formed on the atomic layer deposition (ALD) grown TiON/TiN films on Si substrate. We use an Ar+ ion bombardment source and X-ray photoelectron spectroscopy (XPS) for this analysis. We calibrate the sputter rate by using substrate signal intensity decay (here Si 2p) in the XPS spectra of the 5 nm thick TiON sample accordingly. This rate is assumed to be constant when films with a larger thickness are analyzed. We find that the surface oxidation layer is about 1 nm thick, independent on the detailed ALD parameters of the films. The TiN films found underneath are close to the stoichiometric values and have a residual O content below 5%. Finally, we compare these data to our previous results collected with synchrotron-based radiation source [2,3]. References: [1] Sowinska et al., Applied Physics Letters 100, 233509 (2012). [2] M. Sowinska et al., Applied Surface Science 381, 42-47 (2016). [3] M. Sowińska et al., Journal of Vacuum Science and Tech- nology A, 01A12734 (2016). KW - titanium oxynitride KW - X-Rax photoelectron spectroscopy KW - depth profiling KW - sputtering Y1 - 2017 UR - http://www.dpg-verhandlungen.de/year/2017/conference/dresden/part/ds/session/21/contribution/7 SN - 0420-0195 SP - S. 202 PB - Deutsche Physikalische Gesellschaft CY - Bad Honnef ER -