29 research outputs found

    Nucleation of Graphene Layers On Magnetic Oxides: Co_3O_4(111) and Cr_2O_3(0001) from Theory and Experiment

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    We report direct grown strongly adherent graphene on Co_3O_4(111) by Carbon molecular beam epitaxy (MBE) at 850 K and DFT findings that the first graphene layer is reconstructed to fit the Co_3O_4 surface, while subsequent layers retain normal graphene structure. This adherence to the Co_3O_4 structure results from partial bonding of half the carbons to top oxygen of the substrate. This structure is validated by X-ray photoelectron spectroscopy and low energy electron diffraction studies, showing layer-by-layer graphene growth with ~ 0.08 electrons/carbon atom transferred to the oxide from the first graphene layer, in agreement with DFT. In contrast, C MBE on Cr_2O_3(0001) yields only graphite formation at 700 K, with C desorption above 800 K. For Cr_2O_3 DFT finds no strong bonding to the surface, with charge transfer is away from the oxide. Thus strong graphene-to-oxide charge transfer aids nucleation of graphene on incommensurate oxide substrates

    Atomic layer deposition of BN as a novel capping barrier for B2O3

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    Article demonstrating in situ deposition of BN by sequential BCl₃/NH₃ reactions at 600 K on two different oxidized boron substrates: (a) B₂O₃ deposited using BCl₃/H₂O ALD on Si at 300 K (“B₂O₃/Si”) and (b) a boron-silicon oxide formed by sequential BCl₃/O₂ reactions at 650 K on SiO₂ followed by annealing to 1000 K (“B-Si-oxide”). The data presented demonstrates that ultrathin BN films deposited by BCl₃/NH₃ ALD are promising candidates for passivation of boron oxide used in shallow doping applications

    Ordered three-fold symmetric graphene oxide/buckled graphene/graphene heterostructures on MgO(111) by carbon molecular beam epitaxy

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    Theory and experiment demonstrate the direct growth of a graphene oxide/buckled graphene/graphene heterostructure on an incommensurate MgO(111) substrate. X-ray photoelectron spectroscopy, electron energy loss, Auger electron spectroscopy, low energy electron diffraction, Raman spectroscopy and first-principles density functional theory (DFT) calculations all demonstrate that carbon molecular beam epitaxy on either a hydroxylated MgO(111) single crystal or a heavily twinned thin film surface at 850 K yields an initial C layer of highly ordered graphene oxide with C_(3v) symmetry. A 5 × 5 unit cell of carbon, with one missing atom, forms on a 4 × 4 unit cell of MgO, with the three C atoms surrounding the C vacancy surface forming covalent C–O bonds to substrate oxide sites. This leads to a bowed graphene-oxide with slightly modified D and G Raman lines and a calculated band gap of 0.36 eV. Continued C growth results in the second layer of graphene that is stacked AB with respect to the first layer and buckled conformably with the first layer while maintaining C_(3v) symmetry, lattice spacing and azimuthal orientation with the first layer. Carbon growth beyond the second layer yields graphene in azimuthal registry with the first two C layers, but with graphene-characteristic lattice spacing and π → π* loss feature. This 3rd layer is also p-type, as indicated by the 5.6 eV energy loss feature. The significant sp^3 character and C_(3v) symmetry of such heterostructures suggest that spin–orbit coupling is enabled, with implications for spintronics and other device applications

    Possible Detection of Low Energy Solar Neutrons Using Boron Based Materials

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    Solar neutrons have been detected aboard the International Space Station (ISS), using lithium tetraborate and boron carbide detector elements. We find that evidence of a solar neutron flux, as detected in a neutron calorimeter following subtraction of the proton background, with an energy of about 2 to 4 MeV. This solar neutron flux is likely no more than 250 to 375 neutrons cm−2sec−1, with a lower bound of 50–75 neutrons cm−2sec−1 at one au
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