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Probing the mechanism for graphene nanoribbon formation on gold surfaces through X-ray spectroscopy

机译:通过X射线光谱探究金表面石墨烯纳米带的形成机理

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摘要

We studied the formation of graphene nanoribbons (GNRs) via the self-assembly of 10,10'-dibromo-9,9'-bianthryl precursor molecules on gold surfaces with different synchrotron spectroscopies. Through X-ray photoemission spectroscopy core-level shifts, we followed each step of the synthetic process, and could show that the Br-C bonds of the precursors cleave at temperatures as low as 100 °C on both Au(lll) and Au(llO). We established that the resulting radicals bind to Au, forming Au-C and Au-Br bonds. We show that the polymerization of the precursors follows Br desorption from Au, suggesting that the presence of halogens is the limiting factor in this step. Finally, with angle-resolved ultraviolet photoemission spectroscopy and density functional theory we show that the GNR/Au interaction results in an upshift of the Shockley surface state of Au(lll) by ~0.14 eV, together with an increased electron effective mass.
机译:我们研究了通过10,10'-dibromo-9,9'-bianthryl前体分子在金表面上具有不同的同步加速器光谱的自组装而形成的石墨烯纳米带(GNR)。通过X射线光电子能谱核心水平的变化,我们遵循了合成过程的每个步骤,并且可以证明前体的Br-C键在低至100°C的温度下在Au(III)和Au( 11)。我们确定所得的自由基与Au结合,形成Au-C和Au-Br键。我们表明,前驱体的聚合反应是随着Au从Br解吸而来的,这表明卤素的存在是该步骤中的限制因素。最后,利用角度分辨紫外光发射光谱法和密度泛函理论,我们表明,GNR / Au相互作用导致Au(III)的Shockley表面态上移约0.14 eV,同时电子有效质量增加。

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