Preobrajenski Alexei, Vinogradov Nikolay, Duncan David A, Lee Tien-Lin, Tsitsvero Mikhail, Taketsugu Tetsuya, Lyalin Andrey
MAX IV Laboratory, Lund University, 221 00, Lund, Sweden.
Diamond Light Source, Didcot, OX11 0QX, UK.
Nat Commun. 2024 Dec 10;15(1):10518. doi: 10.1038/s41467-024-54464-y.
The synthesis of large, freestanding, single-atom-thick two-dimensional (2D) metallic materials remains challenging due to the isotropic nature of metallic bonding. Here, we present a bottom-up approach for fabricating macroscopically large, nearly freestanding 2D gold (Au) monolayers, consisting of nanostructured patches. By forming Au monolayers on an Ir(111) substrate and embedding boron (B) atoms at the Au/Ir interface, we achieve suspended monoatomic Au sheets with hexagonal structures and triangular nanoscale patterns. Alternative patterns of periodic nanodots are observed in Au bilayers on the B/Ir(111) substrate. Using scanning tunneling microscopy, X-ray spectroscopies, and theoretical calculations, we reveal the role of buried B species in forming the nanostructured Au layers. Changes in the Au monolayer's band structure upon substrate decoupling indicate a transition from 3D to 2D metal bonding. The resulting Au films exhibit remarkable thermal stability, making them practical for studying the catalytic activity of 2D gold.
由于金属键的各向同性,合成宏观尺寸、独立的、单原子厚度的二维(2D)金属材料仍然具有挑战性。在此,我们提出一种自下而上的方法来制备宏观尺寸、近乎独立的二维金(Au)单层,其由纳米结构的斑块组成。通过在Ir(111)衬底上形成Au单层并在Au/Ir界面嵌入硼(B)原子,我们获得了具有六边形结构和三角形纳米尺度图案的悬浮单原子Au片。在B/Ir(111)衬底上的Au双层中观察到周期性纳米点的交替图案。利用扫描隧道显微镜、X射线光谱学和理论计算,我们揭示了埋藏的B物种在形成纳米结构Au层中的作用。衬底去耦时Au单层能带结构的变化表明从三维到二维金属键的转变。所得的Au膜表现出显著的热稳定性,使其适用于研究二维金的催化活性。