Department of Applied Physics, Aalto University School of Science, PO Box 15100, 00076, Aalto, Finland.
Chemphyschem. 2019 Sep 17;20(18):2297-2300. doi: 10.1002/cphc.201900255. Epub 2019 May 28.
On-surface metal-organic coordination provides a promising way for synthesizing different two-dimensional lattice structures that have been predicted to possess exotic electronic properties. Using scanning tunneling microscopy (STM) and spectroscopy (STS), we studied the supramolecular self-assembly of 9,10-dicyanoanthracene (DCA) molecules on the Au(111) surface. Close-packed islands of DCA molecules and Au-DCA metal-organic coordination structures coexist on the Au(111) surface. Ordered DCA Au metal-organic networks have a structure combining a honeycomb lattice of Au atoms with a kagome lattice of DCA molecules. Low-temperature STS experiments demonstrate the presence of a delocalized electronic state containing contributions from both the gold atom states and the lowest unoccupied molecular orbital of the DCA molecules. These findings are important for the future search of topological phases in metal-organic networks combining honeycomb and kagome lattices with strong spin-orbit coupling in heavy metal atoms.
表面金属有机配位为合成具有奇异电子性质的不同二维晶格结构提供了一种很有前途的方法。我们使用扫描隧道显微镜(STM)和光谱(STS)研究了 9,10-二氰基蒽(DCA)分子在 Au(111)表面上的超分子自组装。在 Au(111)表面上,DCA 分子的密堆积岛和 Au-DCA 金属有机配位结构共存。有序的 DCA-Au 金属有机网络具有一种结构,它结合了金原子的蜂窝晶格和 DCA 分子的 kagome 晶格。低温 STS 实验表明存在一个离域电子态,其中包含来自金原子态和 DCA 分子的最低未占据分子轨道的贡献。这些发现对于未来在具有强自旋轨道耦合的重原子的蜂窝和 kagome 晶格的金属有机网络中寻找拓扑相具有重要意义。