296 research outputs found

    Diamond nanowires and the insulator-metal transition in ultrananocrystalline diamond films

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    Further progress in the development of the remarkable electrochemical, electron field emission, high-temperature diode, and optical properties of n-type ultrananocrystalline diamond films requires a better understanding of electron transport in this material. Of particular interest is the origin of the transition to the metallic regime observed when about 10% by volume of nitrogen has been added to the synthesis gas. Here, we present data showing that the transition to the metallic state is due to the formation of partially oriented diamond nanowires surrounded by an sp2-bonded carbon sheath. These have been characterized by scanning electron microscopy, transmission electron microscopy techniques (high-resolution mode, selected area electron diffraction, and electron-energy-loss spectroscopy), Raman spectroscopy, and small-angle neutron scattering. The nanowires are 80–100nm in length and consist of ~5nm wide and 6–10nm long segments of diamond crystallites exhibiting atomically sharp interfaces. Each nanowire is enveloped in a sheath of sp2-bonded carbon that provides the conductive path for electrons. Raman spectroscopy on the films coupled with a consideration of plasma chemical and physical processes reveals that the sheath is likely composed of a nanocarbon material resembling in some respects a polymer-like mixture of polyacetylene and polynitrile. The complex interactions governing the simultaneous growth of the diamond core and the sp2 sheath responsible for electrical conductivity are discussed as are attempts at a better theoretical understanding of the transport mechanism

    Level densities and thermodynamical properties of Pt and Au isotopes

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    The nuclear level densities of 194−196^{194-196}Pt and 197,198^{197,198}Au below the neutron separation energy have been measured using transfer and scattering reactions. All the level density distributions follow the constant-temperature description. Each group of isotopes is characterized by the same temperature above the energy threshold corresponding to the breaking of the first Cooper pair. A constant entropy excess ΔS=1.9\Delta S=1.9 and 1.11.1 kBk_B is observed in 195^{195}Pt and 198^{198}Au with respect to 196^{196}Pt and 197^{197}Au, respectively, giving information on the available single-particle level space for the last unpaired valence neutron. The breaking of nucleon Cooper pairs is revealed by sequential peaks in the microcanonical caloric curve

    Enhanced low-energy γ\gamma-decay strength of 70^{70}Ni and its robustness within the shell model

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    Neutron-capture reactions on very neutron-rich nuclei are essential for heavy-element nucleosynthesis through the rapid neutron-capture process, now shown to take place in neutron-star merger events. For these exotic nuclei, radiative neutron capture is extremely sensitive to their γ\gamma-emission probability at very low γ\gamma energies. In this work, we present measurements of the γ\gamma-decay strength of 70^{70}Ni over the wide range 1.3≤Eγ≤81.3 \leq E_{\gamma} \leq 8 MeV. A significant enhancement is found in the γ\gamma-decay strength for transitions with Eγ<3E_\gamma < 3 MeV. At present, this is the most neutron-rich nucleus displaying this feature, proving that this phenomenon is not restricted to stable nuclei. We have performed E1E1-strength calculations within the quasiparticle time-blocking approximation, which describe our data above Eγ≃5E_\gamma \simeq 5 MeV very well. Moreover, large-scale shell-model calculations indicate an M1M1 nature of the low-energy γ\gamma strength. This turns out to be remarkably robust with respect to the choice of interaction, truncation and model space, and we predict its presence in the whole isotopic chain, in particular the neutron-rich 72,74,76Ni^{72,74,76}\mathrm{Ni}.Comment: 9 pages, 9 figure
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