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    Energy and symmetry of dd excitations in undoped layered cuprates measured By Cu L3 resonant inelastic x-ray scattering
    (Bristol : IOP, 2011) Moretti Sala, M.; Bisogni, V.; Aruta, C.; Balestrino, G.; Berger, H.; Brookes, N.B.; De Luca, G.M.; Di Castro, D.; Grioni, M.; Guarise, M.; Medaglia, P.G.; Miletto, Granozio, F.; Minola, M.; Perna, P.; Radovic, M.; Salluzzo, M.; Schmitt, T.; Zhou, K.J.; Braicovich, L.; Ghiringhelli, G.
    We measured the high-resolution Cu L3 edge resonant inelastic x-ray scattering (RIXS) of undoped cuprates La2CuO4, Sr2CuO2Cl2, CaCuO2 and NdBa 2Cu3O6. The dominant spectral features were assigned to dd excitations and we extensively studied their polarization and scattering geometry dependence. In a pure ionic picture, we calculated the theoretical cross sections for those excitations and used these to fit the experimental data with excellent agreement. By doing so, we were able to determine the energy and symmetry of Cu-3d states for the four systems with unprecedented accuracy and confidence. The values of the effective parameters could be obtained for the singleion crystal field model but not for a simple two-dimensional cluster model. The firm experimental assessment of dd excitation energies carries important consequences for the physics of high-Tc superconductors. On the one hand, we found that the minimum energy of orbital excitation is always ≥ 1.4 eV, i.e. well above the mid-infrared spectral range, which leaves to magnetic excitations (up to 300 meV) a major role in Cooper pairing in cuprates. On the other hand, it has become possible to study quantitatively the effective influence of dd excitations on the superconducting gap in cuprates.
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    Studies towards synthesis, evolution and alignment characteristics of dense, millimeter long multiwalled carbon nanotube arrays
    (Frankfurt, M. : Beilstein-Institut zur Förderung der Chemischen Wissenschaften, 2011) Mahanandia, P.; Schneider, J.J.; Engel, M.; Stühn, B.; Subramanyam, S.V.; Nanda, K.K.
    We report the synthesis of aligned arrays of millimeter long carbon nanotubes (CNTs), from benzene and ferrocene as the molecular precursor and catalyst respectively, by a one-step chemical vapor deposition technique. The length of the grown CNTs depends on the reaction temperature and increases from ~85 μm to ~1.4 mm when the synthesis temperature is raised from 650 to 1100°C, while the tube diameter is almost independent of the preparation temperature and is ~80 nm. The parallel arrangement of the CNTs, as well as their tube diameter can be verified spectroscopically by small angle X-ray scattering (SAXS) studies. Based on electron diffraction scattering (EDS) studies of the top and the base of the CNT films, a root growth process can be deduced.