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Soft x-ray photoemission study of the Heusler-type Fe_2VAl_1-zGe_z alloysMIYAZAKI, Hidetoshi, SODA, Kazuo, KATO, Masahiko, YAGI, Shinya January 2007 (has links)
No description available.
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X-ray spectroscopy of electronic band structure in vanadium oxide nanoparticlesAnquillare, Emma L. B. 25 September 2021 (has links)
In order to elucidate the effects of nanostructuring on electron behavior in vanadium oxides, a suite of x-ray spectroscopy techniques was employed to comprehensively characterize the electronic structures of V2O5 and VO2 nanoparticles and compare them to their bulk counterparts. V2O5 and VO2 nanoparticle powders were characterized via PXRD, TEM, and HR-TEM to confirm size, purity, and crystallinity. Additionally, DSC and temperature-varied PXRD measurements on both VO2 samples confirmed the structural aspect of the monoclinic to rutile metal-insulator phase transition, and UV-Vis measurements allowed for Kubelka-Munk analysis on the V2O5 samples. XAS measurements enable the comparison of unoccupied conduction band states, while XES and RIXS measurements reveal occupied valence band states and the individual vanadium and oxygen PDOS below the Fermi level. XPS measurements of both core and valence band states both confirmed the valence band structure revealed by XES and also provide information on core-state energy levels. In the case of V2O5, the valence band O 2p states are upshifted in the nanoparticle sample, while the lowest V 3d conduction band states are unshifting but provide more available unoccupied states for excitation. These changes produce a shrunken bandgap in the V2O5 nanoparticles that is in line with much previous computational work, but unexpected from previous experimental results and defies the Moss-Burstein effect usually observed in V2O5. The resulting changes in band structure are attributed to a higher concentration of oxygen vacancy defects in the nanoparticle sample. Additionally, electron correlation effects in V2O5 nanoparticles are found to be enhanced relative to the bulk, likely due to added electron presence in the V 3d split-off band. In the case of VO2, dramatic changes in both the valence band and conduction band states are observed both below and above the structural phase transition temperature. These changes (lowered unoccupied conduction band states coupled with broadened and upshifted occupied valence band states) also lead to nanoparticle bandgap reduction and enhanced metallicity. The enhanced metallic nature of the VO2 nanoparticles is again attributed to the increased presence of surface oxygen vacancy defects, as well as a V2O3-like surface reconstruction. Additionally, electron correlation effects are found to be reduced in the VO2 nanoparticle samples relative to the bulk, unlike in the case of V2O5.
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Hybrid systems of molecular ruthenium catalyst anchored on oxide films for water oxidation: Functionality of the interfaceScholz, Julius 26 June 2017 (has links)
No description available.
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Study of the electronic structure of transition-metal oxides by synchrotron-based X-ray spectroscopiesChen, Bo 12 March 2016 (has links)
Transition-metal oxides (TMOs) display numerous fascinating and complex properties, such as mixed-valency, low dimensionality, lattice distortion, and phase transition, etc. These properties arise from the partially filled d- or f-electron shells of TM cations and are often accompanied by the intriguing interplay between degrees of freedom. To understand the complexity of d-electron TMOs, this thesis is primarily focused on studying their underlying electronic structure using X-ray absorption spectroscopy (XAS), X-ray emission spectroscopy (XES), X-ray photoemission spectroscopy (XPS), and resonant inelastic X-ray scattering (RIXS). The measurements at the O K- and TM L-edges are achieved by taking advantage of high-flux and high-resolution synchrotron radiation light with tunable monochromatic photon energy.
Four electronically and structurally distinctive oxides are selected as representative TMOs for investigation in this thesis. To begin with, through a comparative study of WO3 and Na0.67WO3 crystals, the narrowing of the conduction band is observed with Na doping and the core-hole energy shift in the O K-edge XAS process is experimentally determined. Indirect and direct band gaps of photoanode WO3 are measured from the resonant XES with polarization-dependent experimental geometry. The other sodium bronze studied is quasi-one-dimensional β-Na0.33V2O5 polycrystalline film. The film stoichiometry, preferential orientation, and orbital anisotropy are well characterized by a variety of photon and electron techniques and compared to density-functional theory (DFT) calculation. The V 3d orbital splitting of β-Na0.33V2O5 is surveyed by the V L-edge RIXS and compared with isoelectronic β-Sr0.17V2O5 regarding distortions to VO6 octahedra.
Furthermore, the complex electronic structure of Mott insulators La1-xLuxVO3 is investigated to understand their spin-orbital phase diagram. The effects of rare-earth size on the O 2p hybridization states and the local crystal field of VO6 octahedron are found to agree with the prediction of DFT calculation and the evolution of crystal structure. The changes of experimental spectra with temperature are associated with Jahn-Teller distortion and orbital ordering due to structural phase transition. Lastly, the band structure and low-energy excitations of spinel MnV2O4 are explored using soft x-ray spectroscopies and theoretical calculations. The presence of Hubbard bands and the mixing between V and Mn 3d states are suggested both experimentally and theoretically.
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DEFECT AND METAL OXIDE CONTROL OF SCHOTTKY BARRIERS AND CHARGE TRANSPORT AT ZINC OXIDE INTERFACESFoster, Geoffrey M. 18 September 2018 (has links)
No description available.
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Characterization of Self-Assembled Monolayers of Oligo(phenyleneethynylene) Derivatives on GoldWatcharinyanon, Somsakul January 2007 (has links)
<p>Oligo(phenyleneethynylene) (OPE) molecules are a class of fully conjugated aromatic molecules, that attract attention for their application as “molecular wires” in molecular electronic devices. In this thesis work, self-assembled monolayers (SAMs) formed from a variety of OPE derivatives have been studied. The chemical properties, structure, and packing density of the SAMs have been characterized utilizing techniques such as high-resolution X-ray photoemission spectroscopy (HRXPS), near-edge X-ray absorption fine structure spectroscopy (NEXAFS), Infrared reflection absorption spectroscopy (IRRAS), contact angle measurements, and atomic force microscopy (AFM).</p><p>In a first study, three OPE-derivatives, with benzene, naphthalene and anthracene, respectively, inserted into the backbone, and an acetyl-protected thiophenol binding group were found to form SAMs on Au(111) substrates with lower molecular surface densities and larger molecular inclination as the lateral π-system increases.</p><p>In a second study, porphyrin was introduced as the end group to a wire-like molecule such as OPE. The purpose was to obtain well-organized and functionalized surfaces with optical and redox properties. Three porphyrin-functionalized OPEs had different binding groups, an acetyl-protected thiophenol, a benzylic thiol, and a trimethylsilylethynylene group, and were found to form SAMs on gold surfaces with difference in structure and degree of order. The molecules with the acetyl-protected thiophenol binding group were found to form a high quality SAM compared to the other two. This SAM exhibits a well-ordered and densely packed layer.</p><p>This study gives rise to a better understanding of SAM formation of OPE derivatives, and will form a base for further investigations of charge transport properties of these molecular films, which is of interest for applications in molecular electronic devices.</p>
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Electrochemical modification of Si surfaces by methyl groups (CH 3, CD 3), ethynyl derivatives, pyrrole and thiopheneYang, Florent 30 November 2009 (has links)
Silizium (Si) wird für eine breite Palette von Anwendungen wie z.B. in Solarzellen, Mikroelektronik, Biochips und so weiter eingesetzt. In dieser Arbeit wurden neue Hybridsysteme aus Si und organischen Molekülen, bezüglich der Oberflächenpassivierung des Halbleiters und der resultierenden elektronischen Eigenschaften untersucht. Insbesondere wurden Methyl-Gruppen (CH3 und CD3), Ethynyl-Derivate (H−C≡C-, CH3−C≡C-, und C6H5−C≡C-), sowie Pyrrol und Thiophen aus Grignardlösungen untersucht. Bezüglich Stabilität und Defektkonzentration konnte gezeigt werden, dass organisch modifizierte Si-Oberflächen eine höhere Stabilität an Luft haben als Standard wasserstoffpassivierte Si-Oberflächen und dabei eine nur geringfügig höhere Defektkonzentration aufweisen. Untersuchungen mit Infrarot Spektroskopischer Ellipsometrie (IRSE) und Synchrotron Röntgen Photoemissions Spektroskopie (SXPS) zeigen, dass die Oxidationsrate für Oberflächen mit CH3-Terminierung stark reduziert ist. In der vorliegenden Arbeit gelang es erstmalig mittels IRSE die charakteristische „Umbrella“-Schwingungsmode zu beobachten und SXPS Messungen zeigten die Spin-Orbit-Aufspaltung der Si 2p Emission für CH3-passivierte Si-Oberflächen. Die CH3-Gruppen besitzen einen hohen Grad von Ordnung auf der Si(111)-Oberfläche. Das Aufbringen von Ethynyl-Derivaten führt zu extrem dünnen polymerisierten Schichten auf Si durch elektrochemische Radikaloxidation der C≡C Dreifachbindung. Diese Schichten sind homogen und haften sehr gut an der Si-Oberfläche. Weiterhin konnte gezeigt werden, dass die Abscheidung von Ethynyl-Derivaten vom Typ des Halogenatoms im Grignard-Precursor abhängig ist, wobei Br im Vergleich zu Cl zu geringeren Rekombinationsgeschwindigkeiten an der Polymer/Si-Grenzfläche führen. Eine Änderung der Austrittsarbeit von bis zu 0.5 eV und der Bandverbiegung von bis zu 0.24 eV wurde nach der Abscheidung dieser Moleküle gemessen. Diese elektronischen Eigenschaften hängen linear vom Oberflächendipol ab. / Organic functionalization of silicon (Si) surfaces has received a tremendous interest in the development of organic/semiconductor hetero-structures for plenty of potential applications from microelectronics, molecular electronics, photovoltaics to bio-applications. In this thesis, tailoring of the electronic properties and passivation properties of such organic hetero-structures have been investigated. Direct grafting of organic layers like methyl groups (CH3 and CD3), ethynyl derivatives (H−C≡C-, CH3−C≡C-, and C6H5−C≡C-), and heterocyclic molecules (pyrrole and thiophene) onto Si(111) surfaces have been performed in a one-step electrochemical process by anodic treatment in Grignard electrolytes. Organically modified Si surfaces show low interface recombination rates as measured by photoluminescence technique and reveal also a much better passivation with respect to stability in ambient air than H-terminated Si surfaces. Grafting of ethynyl derivatives and heterocyclic molecules lead to the formation of ultrathin polymeric layers, where the thickness depends on charge flow applied to the Si electrode, while methyl groups lead to a monolayer on Si(111) surfaces. Only a very small amount of oxidation states of Si has been observed by infrared spectroscopic ellipsometry (IRSE) and synchrotron X-ray photoemission spectroscopy (SXPS). For the first time, IRSE and SXPS measurements reveal the “umbrella” vibrational mode characteristic from methyl groups and a well-defined spin-orbit splitting of the Si 2p core level emission, respectively, in the case of methylated Si(111) surfaces. For all ethynyl derivatives, high-resolution SXPS investigations reveal the incorporation of halogen atoms in the organic layers obtained. Thereby, exchanging Br for Cl in the Grignard compound leads to lower interface recombination rates at the polymer/Si interface. A shift in work function and surface band bending of up to 0.5 and 0.24 eV has been observed, respectively. The electronic properties reveal a linear relation between the work function and the surface dipole.
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Characterization of Self-Assembled Monolayers of Oligo(phenyleneethynylene) Derivatives on GoldWatcharinyanon, Somsakul January 2007 (has links)
Oligo(phenyleneethynylene) (OPE) molecules are a class of fully conjugated aromatic molecules, that attract attention for their application as “molecular wires” in molecular electronic devices. In this thesis work, self-assembled monolayers (SAMs) formed from a variety of OPE derivatives have been studied. The chemical properties, structure, and packing density of the SAMs have been characterized utilizing techniques such as high-resolution X-ray photoemission spectroscopy (HRXPS), near-edge X-ray absorption fine structure spectroscopy (NEXAFS), Infrared reflection absorption spectroscopy (IRRAS), contact angle measurements, and atomic force microscopy (AFM). In a first study, three OPE-derivatives, with benzene, naphthalene and anthracene, respectively, inserted into the backbone, and an acetyl-protected thiophenol binding group were found to form SAMs on Au(111) substrates with lower molecular surface densities and larger molecular inclination as the lateral π-system increases. In a second study, porphyrin was introduced as the end group to a wire-like molecule such as OPE. The purpose was to obtain well-organized and functionalized surfaces with optical and redox properties. Three porphyrin-functionalized OPEs had different binding groups, an acetyl-protected thiophenol, a benzylic thiol, and a trimethylsilylethynylene group, and were found to form SAMs on gold surfaces with difference in structure and degree of order. The molecules with the acetyl-protected thiophenol binding group were found to form a high quality SAM compared to the other two. This SAM exhibits a well-ordered and densely packed layer. This study gives rise to a better understanding of SAM formation of OPE derivatives, and will form a base for further investigations of charge transport properties of these molecular films, which is of interest for applications in molecular electronic devices.
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Internal Structure and Self-Assembly of Low Dimensional MaterialsMukherjee, Sumanta January 2013 (has links) (PDF)
The properties of bulk 3D materials of metals or semiconductors are manifested with various length scales(e.g., Bohr excitonic radius, magnetic correlation length, mean free path etc.) and are important in controlling their properties. When the size of the material is smaller than these characteristics length scales, the confinement effects operate reflecting changes in their physical behavior. Materials with such confinement effects can be designated as low dimensional materials. There are exceedingly large numbers of low dimensional materials and the last half a century has probably seen the maximum evolution of such materials in terms of synthesis, characterization, understanding and modification of their properties and applications. The field of” nanoscience and nanotechnology”, have become a mature field within the last three decades where, for certain application, synthesis of materials of sizes in the nanometer range can be designed and controlled.
Interface plays a very important role in controlling properties of heterogeneous material of every dimensionality. For example, the interface forms in 2D thin films or interface of heterogeneous nanoparticles(0D). In recent times, a large number of remarkable phenomena have triggered understanding and controlling properties arises due to nature of certain interface. In the field of nanoparticles, it is well known that the photoluminescence property depends very strongly on the nature of interface in heterostructured nanoparticles. In the recent time a large variety of heterostructured nanoparticles starting from core-shell to quantum dot-quantum well kind has been synthesized to increase the photoluminescence efficiency up to 80%. Along with improvement of certain properties due to heterostructure formation inside the nanoparticles, the techniques to understand the nature of those interfaces have improved side by side. It has been recently shown that variable energy X-ray Photoemission Spectroscopy (XPS) can be employed to understand the nature of interfaces (internal structure) of such heterostructure nanoparticles in great detail with high accuracy. While most of the previous studies of variable energy XPS, uses photonenergies sensitive to smaller sized particle, we have extended the idea of such nondestructive approach of understanding the nature of buried interfaces to bigger sized nanoparticles by using photon energy as high as 8000eV, easily available in various 3rd generation synchrotron centers.
The nature of the interface also plays an important role in multilayer thin films. Major components of various electronic devices, like read head memory devices, field effect transistors etc., rely on interface properties of certain multilayer thin film materials. In recent time wide range of unusual phenomenon such as high mobility metallic behavior between two insulating oxide, superconductivity, interface ferroelectricity, unusual magnetism, multiferroicity etc. has been observed at oxide interface making it an interesting field of study. We have shown that variable energy photoemission spectroscopy with high photon energies, can be a useful tool to realize such interfaces and controlling the properties of multilayered devices, as well as to understand the origin of unusual phenomenon exists at several multilayer interfaces.
Chapter1 provides a brief description of low dimensional materials, overall perspective of interesting properties in materials with reduced dimensionality. We have emphasized on the importance of determining the internal structure of buried interface of different dimensionalities. We have given a brief overview and importance of different interfaces that we have studied in the subsequent chapters dealing with specific interfaces. Chapter 2 describes experimental and theoretical methods used for the study of interface and self-assembly reported in this thesis. These methods are divided into two categories. The first section deals with different experimental techniques, like, UV-Visible absorption and photoluminescence spectroscopy, X-Photoelectron Spectroscopy(XPS), X-Ray diffraction, Transmission Electron Microscopy(TEM) etc. This section also includes brief overview on synchrotron radiation and methods used for detail analysis of interface structure using variable energy XPS. In the second part of this chapter, we have discussed theoretical methods used in the present study. \
In Chapter 3A we have combined low energy XPS, useful to extract information of the surface of the nanoparticles, with high energy XPS, important to extract bulk information and have characterized the internal structure of nanoparticle system of different heterogeneity. We have chosen two important heterostructure systems namely, inverted core-shell(CdScore-CdSeshell) type nanoparticles and homogeneous alloy(CdSeS)type nanoparticles. Such internal structure study revealed that the actual internal structure of certain nanomaterial can be widely different from the aim of the synthesis and knowledge of internal structure is a prerequisite in understanding their property. We were able to extend the idea of variable energy XPS to higher energy limit. Many speculations have been made about the probable role of interface in controlling properties, like blinking behavior of bigger sized core-shell nanoparticles, but no conclusive support has yet been given about the nature of such interface. After successfully extending the technique to determine the internal structure of heterostructured nanoparticles to very high photon energy region, we took the opportunity to determine the internal structure of nanoparticles of sizes as large as 12nm with high energy photoemission spectroscopy for the first time.
In Chapter 3B we emphasize on the importance of interface structure in controlling the behavior of bigger sized nanoparticles systems, the unsettled issues regarding their internal structure, and described the usefulness of high energy XPS in elucidating the internal structure of such big particles with grate accuracy to solve such controversies.
The existence of high density storage media relies on the existence of highly sensitive magnetic sensors with large magnetoresistance. Today almost all sensor technologies used in modern hard disk drives rely on tunnel magnetoresistance (TMR)
CoFeB-MgO-CoFeB structures. Though device fabrication is refined to meet satisfactory quality assurance demands, fundamental understanding of the refinement in terms of its effect on the nature of the interfaces and the MgO tunnel barrier leading to improved TMR is still missing. Where, the annealing condition required to improve the TMR ratio is itself not confirmatory its effect on the interface structure is highly debatable. In particular, it has been anticipated that under the proposed exotic conditions highly mobile B will move into the MgO barrier and will form boron oxide. In Chapter 4 we are able to shed definite insights to heart of this problem. We have used high energy photoemission to investigate a series of TMR structures and able to provide a systematic understanding of the driving mechanisms of B diffusion in CoFeBTMR structures. We have solved the mix-up of annealing temperature required and have shown that boron diffusion is limited merely to a sub-nanometer thick layer at the interface and does not progress beyond this point under typical conditions required for device fabrication. We have given a brief overview on the evolution of magnetic storage device and have described various concepts relevant for the study of such systems.
The interface between two nonmagnetic insulators LaAlO3 and SrTiO3 has shown a variety of interface phenomena in the recent times. In spite of a large number of high profile studies on the interface LaAlO3 and SrTiO3 there is still a raging debate on the nature, origin and the distribution of the two dimensional electron gas that is supposed to be responsible for its exotic physical properties, ranging from unusual transport properties to its diverse ground states, such as metallic, magnetic and superconducting ones, depending on the specific synthesis. The polar discontinuity present across the SrTiO3-LaAlO3 interface is expected to result in half an electron transfer from the top of the LaAlO 3 layer to each TiofSrTiO3 at the interface, but, the extent of localization that can make it behave like delocalized with very high mobility as well as localized with magnetic moments is not yet clear. In Chapter 5 we have given a description of this highly interesting system as well as presented the outcome of our depth resolved XPS investigation on several such samples synthesized under different oxygen pressure. We were able to describe successfully the distribution of charge carriers.
While synthesizing and understanding properties of nanoparticles is one issue, using them for device fabrication is another. For example, to make a certain device often requires specific arrangements of nanoparticles in a suitable substrate. Self-assembly formation can be a potential tool in these regards. Just like atom or ions, both nano and colloidal particles also assemble by themselves in ordered or disordered structure under certain conditions, e.g., the drying of a drop of suspension containing the colloid particles over a TEM grid. This phenomenon is known as self-assembly. Though, the process of assembly formation can be a very easy and cost-effective technique to manipulate the properties in the nano region, than the existing ones like lithography but, the lack of systematic study and poor understanding of these phenomena at microscopic level has led to a situation that, there is no precise information available in literature to say about the nature of such assembly.
In Chapter 6 we have described experiments that eliminate the dependence of the self-assembly process on many complicating factors like substrate-particle interaction, substrate-solvent interaction etc., making the process of ordering governed by minimum numbers of experimental parameter that can be easily controlled. Under simplified conditions, our experiments unveil an interesting competition between ordering and jamming in drying colloid systems similar to glass transition phenomenon
Resulting in the typical phase behavior of the particles. We establish a re-entrant behavior in the order-disorder phase diagram as a function of particle density such that there is an optimal range of particle density to realize the long-range ordering. The results are explained with the help of simulations and phenomenological theory.
In summary, we were able to extend the idea of variable energy XPS to higher energy limit advantageous for investigating internal structure of nonmaterial of various dimensionalities and sizes. We were able to comprehend nature of buried interface indicating properties of heterostructures quantum dots and thin films. Our study revealed that depth resolved XPS combined with accessibility of high and variable energies at synchrotron centers can be a very general and effective tool for understanding buried interface. Finally, we have given insight to the mechanism of spontaneous ordering of nanoparticles over a suitable substrate.
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THE ROLE OF NATIVE POINT DEFECTS AND SURFACE CHEMICAL REACTIONS IN THE FORMATION OF SCHOTTKY BARRIERS AND HIGH N-TYPE DOPING IN ZINC OXIDEDoutt, Daniel R. 08 August 2013 (has links)
No description available.
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