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Atomic Structures of Silicene Layers Grown on Ag(111): Scanning Tunneling Microscopy and Noncontact Atomic Force Microscopy Observations

机译:Ag(111)上生长的硅层的原子结构:扫描隧道显微镜和非接触式原子力显微镜观察。

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摘要

Silicene, the considered equivalent of graphene for silicon, has been recently synthesized on Ag(111) surfaces. Following the tremendous success of graphene, silicene might further widen the horizon of two-dimensional materials with new allotropes artificially created. Due to stronger spin-orbit coupling, lower group symmetry and different chemistry compared to graphene, silicene presents many new interesting features. Here, we focus on very important aspects of silicene layers on Ag(111): First, we present scanning tunneling microscopy (STM) and non-contact Atomic Force Microscopy (nc-AFM) observations of the major structures of single layer and bi-layer silicene in epitaxy with Ag(111). For the (3 × 3) reconstructed first silicene layer nc-AFM represents the same lateral arrangement of silicene atoms as STM and therefore provides a timely experimental confirmation of the current picture of the atomic silicene structure. Furthermore, both nc-AFM and STM give a unifying interpretation of the second layer (√3 × √3)R ± 30° structure. Finally, we give support to the conjectured possible existence of less stable, ~2% stressed, (√7 × √7)R ± 19.1° rotated silicene domains in the first layer.
机译:近年来,人们已经在Ag(111)表面合成了被认为与石墨烯等效的硅碳硅。随着石墨烯的巨大成功,硅树脂可能会通过人工创造的新同素异形体进一步拓宽二维材料的视野。与石墨烯相比,由于更强的自旋-轨道耦合,较低的基团对称性和不同的化学性质,硅烯具有许多有趣的新特征。在这里,我们重点关注Ag(111)上硅层的非常重要的方面:首先,我们介绍了扫描隧道显微镜(STM)和非接触式原子力显微镜(nc-AFM)对单层和双分子层主要结构的观察结果。 Ag(111)外延生长的有机硅层。对于(3×3)重建的第一硅层nc-AFM表示与STM相同的硅原子横向排列,因此可以及时地对原子硅结构的当前图片进行实验确认。此外,nc-AFM和STM都统一解释了第二层(√3×√3)R±30°结构。最后,我们为第一层中可能存在的不稳定的,〜2%应力,(√7×√7)R±19.1°旋转的硅结构域提供了支持。

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