Institute of Applied Physics, University of Hamburg, Germany.
Nano Lett. 2012 Jun 13;12(6):3174-9. doi: 10.1021/nl301149d. Epub 2012 May 14.
An important development in recent synthesis strategies is the formation of electronically coupled one and two-dimensional organic systems for potential applications in nanoscale molecule-based devices. Here, we assemble one-dimensional spin chains by covalently linking basic molecular building blocks on a Au(111) surface. Their structural properties are studied by scanning tunneling microscopy and the Kondo effect of the basic molecular blocks inside the chains is probed by scanning tunneling spectroscopy. Tunneling spectroscopic images reveal the existence of separate Kondo regions within the chains while density functional theory calculations unveil antiferromagnetic coupling between the spin centers.
近年来,在合成策略方面的一个重要发展是形成电子耦合的一维和二维有机体系,以应用于纳米级基于分子的器件。在这里,我们通过在 Au(111)表面上共价连接基本的分子构建块来组装一维自旋链。通过扫描隧道显微镜研究它们的结构性质,并通过扫描隧道光谱法探测链内基本分子块的 Kondo 效应。隧道光谱图像揭示了链内存在单独的 Kondo 区域,而密度泛函理论计算则揭示了自旋中心之间的反铁磁耦合。