Li Hui, Felix Levi C, Li Qiucheng, Ruan Qiyuan, Yakobson Boris I, Hersam Mark C
Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States.
Department of Materials Science and NanoEngineering, Rice University, Houston, Texas 77005, United States.
Nano Lett. 2024 Aug 28;24(34):10674-10680. doi: 10.1021/acs.nanolett.4c03224. Epub 2024 Aug 14.
The successful synthesis of borophene beyond the monolayer limit has expanded the family of two-dimensional boron nanomaterials. While atomic-resolution topographic imaging has been previously reported, vibrational mapping has the potential to reveal deeper insight into the chemical bonding and electronic properties of bilayer borophene. Herein, inelastic electron tunneling spectroscopy (IETS) is used to resolve the low-energy vibrational and electronic properties of bilayer-α (BL-α) borophene on Ag(111) at the atomic scale. Using a carbon monoxide (CO)-functionalized scanning tunneling microscopy tip, the BL-α borophene IETS spectra reveal unique features compared to single-layer borophene and typical CO vibrations on metal surfaces. Distinct vibrational spectra are further observed for hollow and filled boron hexagons within the BL-α borophene unit cell, providing evidence for interlayer bonding between the constituent borophene layers. These experimental results are compared with density functional theory calculations to elucidate the interplay between the vibrational modes and electronic states in bilayer borophene.
超越单层极限成功合成硼烯,扩展了二维硼纳米材料家族。虽然此前已有原子分辨率形貌成像的报道,但振动图谱有潜力更深入地揭示双层硼烯的化学键合和电子性质。在此,非弹性电子隧穿光谱(IETS)被用于在原子尺度上解析Ag(111)上双层-α(BL-α)硼烯的低能振动和电子性质。使用一氧化碳(CO)功能化的扫描隧道显微镜针尖,BL-α硼烯的IETS光谱显示出与单层硼烯以及金属表面典型CO振动相比的独特特征。在BL-α硼烯晶胞内的空心和填充硼六边形中进一步观察到不同的振动光谱,为构成硼烯层之间的层间键合提供了证据。将这些实验结果与密度泛函理论计算进行比较,以阐明双层硼烯中振动模式与电子态之间的相互作用。