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Conversion of multilayer graphene into continuous ultrathin sp 3-bonded carbon films on metal surfaces

机译:将多层石墨烯转化为金属表面上连续的超薄sp 3键碳膜

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摘要

The conversion of multilayer graphenes into sp 3-bonded carbon films on metal surfaces (through hydrogenation or fluorination of the outer surface of the top graphene layer) is indicated through first-principles computations. The main driving force for this conversion is the hybridization between sp 3 orbitals and metal surface d z 2 orbitals. The induced electronic gap states and spin moments in the carbon layers are confined in a region within 0.5â.nm of the metal surface. Whether the conversion occurs depend on the fraction of hydrogenated (fluorinated) C atoms at the outer surface and on the number of stacked graphene layers. In the analysis of the Eliashberg spectral functions for the sp 3 carbon films on a metal surface that is diamagnetic, the strong covalent metal-sp 3 carbon bonds induce soft phonon modes that predominantly contribute to large electron-phonon couplings, suggesting the possibility of phonon-mediated superconductivity. Our computational results suggest a route to experimental realization of large-area ultrathin sp 3-bonded carbon films on metal surfaces.
机译:通过第一性原理计算表明了多层石墨烯在金属表面上通过sp 3键合碳膜的转化(通过顶层石墨烯层外表面的氢化或氟化)。该转换的主要驱动力是sp 3轨道与金属表面d z 2轨道之间的杂化。碳层中的感应电子间隙状态和自旋矩被限制在金属表面0.5nm范围内。转换是否发生取决于外表面氢化(氟化)碳原子的比例以及堆叠的石墨烯层的数量。在抗磁性金属表面上的sp 3碳膜的Eliashberg光谱函数的分析中,强共价金属sp 3碳键会诱导软声子模式,这主要有助于大的电子-声子耦合,这表明存在声子介导的超导性。我们的计算结果表明了在金属表面上实验实现大面积超薄sp 3键碳膜的途径。

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