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تسجيل مستخدم جديدInvestigation of Nanostructures with X-ray Scattering Techniques
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The structural investigations of nanomaterials motivated by their large variety and diverse set of applications have attracted considerable attention. In particular, the ever-improving machinery, both in laboratory and at large scale facilities, together with the methodical improvements available for studying nanostructures ranging from epitaxial nanomaterials, nanocrystalline thin films and coatings, to nanoparticles and colloidal nanocrystals allows us to gain a more detailed understanding of their structural properties. As the structure essentially determines the physical properties of the materials, this advances the possibilities of structural studies and also enables a deeper understanding of the structure to property relationships. In this special issue entitled Investigation of Nanostructures with X-ray Scattering Techniques five contributions show the recent progress in various research fields. Contributions cover topics as diverse as neutron scattering on magnetic multilayer films, epitaxial orientation of organic thin films, nanoparticle ordering and chemical composition analysis, and the combination of nanofocused X-ray beams with electrical measurements.
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We report the near-edge x-ray absorption fine structure (NEXAFS) spectrum of a single layer of graphite (graphene) obtained by micromechanical cleavage of Highly Ordered Pyrolytic Graphite (HOPG) on a SiO2 substrate. We utilized a PhotoEmission Elect
ron Microscope (PEEM) to separately study single- double- and few-layers graphene (FLG) samples. In single-layer graphene we observe a splitting of the pi* resonance and a clear signature of the predicted interlayer state. The NEXAFS data illustrate the rapid evolution of the electronic structure with the increased number of layers.
The Zeeman spatial splitting of a neutron beam takes place during a neutron spin-flip in magnetically non-collinear systems at grazing incidence geometry. We apply the neutron beam-splitting method for the investigation of magnetically non-collinear
clusters of submicron size in a thin film. The experimental results are compared with ones obtained by other methods.
Resonance anomalous surface x-ray scattering (RASXS) technique was applied to electrochemical interface studies. It was used to determine the chemical states of electrochemically formed anodic oxide monolayers on platinum surface. It is shown that RA
SXS exhibits strong polarization dependence when the surface is significantly modified. The polarization dependence is demonstrated for three examples; anodic oxide formation, sulfate adsorption, and CO adsorption on platinum surfaces. s- and p- polarization RASXS data were simulated with the latest version of ab initio multiple scattering calculations (FEFF8.2). Elementary theoretical considerations are also presented for the origin of the polarization dependence in RASXS.
We report that the lowest energy transverse-optic phonon in metallic SnTe softens to near zero energy at the structural transition at $T_C=75 text{~K}$ and importantly show that the energy of this mode below $T_C$ increases as the temperature decreas
es. Since the mode is a polar displacement this proves unambiguously that SnTe undergoes a ferroelectric displacement below $T_C$. Concentration gradients and imperfect stoichiometry in large crystals may explain why this was not seen in previous inelastic neutron scattering studies. Despite SnTe being metallic we find that the ferroelectric transition is similar to that in ferroelectric insulators, unmodified by the presence of conduction electrons: we find that (i) the damping of the polar mode is dominated by coupling to acoustic phonons rather than electron-phonon coupling (ii) the transition is almost an ideal continuous transition (iii) comparison with density functional calculations identifies the importance of dipolar-dipolar screening for understanding this behaviour.
We have performed a resonant x-ray scattering (RXS) study near the Co K edge on a single crystal of Ca3Co2O6. In the magnetically ordered phase a new class of weak reflections appears at the magnetic propagation vector tau (1/3,1/3,1/3). These new re
flections allow direct access to the dipolar-quadrupolar E1E2 scattering channel. The theoretical possibility of observing isolated E1E2 electromagnetic multipoles has attracted a lot of interest in the recent years. Unfortunately in many system of interest, parity even and parity odd tensor contributions occur at the same positions in reciprocal space. We demonstrate that in Ca3Co2O6 it is possible to completely separate the parity even from the parity odd terms. The possibility of observing such terms even in globally centrosymmetric systems using RXS has been investigated theoretically; Ca3Co2O6 allows a symmetry based separation of this contribution.
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