Aix-Marseille Université, CNRS, CINaM UMR 7325, 13288 Marseille, France.
Sci Rep. 2013;3:2399. doi: 10.1038/srep02399.
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.
硅烯被认为是硅的类石墨烯体,最近已在 Ag(111) 表面合成。继石墨烯取得巨大成功之后,硅烯可能会通过人为创造新的同素异形体进一步拓宽二维材料的视野。由于与石墨烯相比,硅烯具有更强的自旋轨道耦合、更低的群对称性和不同的化学性质,因此呈现出许多新的有趣特性。在这里,我们重点关注硅烯在 Ag(111) 上的层的几个非常重要的方面:首先,我们展示了单层和双层硅烯在与 Ag(111)外延生长过程中的主要结构的扫描隧道显微镜 (STM) 和非接触原子力显微镜 (nc-AFM) 观测结果。对于 (3 × 3)重构的第一层硅烯,nc-AFM 代表了与 STM 相同的硅烯原子的横向排列,因此及时为当前的原子硅烯结构图像提供了实验确认。此外,nc-AFM 和 STM 都对第二层 (√3 × √3)R ± 30°结构给出了统一的解释。最后,我们支持第一层中可能存在较少稳定、约 2%应变的 (√7 × √7)R ± 19.1°旋转硅烯畴的推测。