IBM Research, Zurich Research Laboratory, Ruschlikon, Switzerland.
Nano Lett. 2010 Jul 14;10(7):2475-9. doi: 10.1021/nl100834v.
We present scanning tunneling microscopy (STM)-based single-molecule synthesis of linear metal-ligand complexes starting from individual metal atoms (iron or nickel) and organic molecules (9,10-dicyanoanthracene) deposited on an ultrathin insulating film. We directly visualize the frontier molecular orbitals by STM orbital imaging, from which, in conjunction with detailed density functional theory calculations, the electronic structure of the complexes is inferred. Our studies show how the order of the molecular orbitals and the spin-state of the complex can be engineered through the choice of the metal atom. The high-spin iron complex has a singly occupied delocalized orbital with a large spin-splitting that points to the use of these engineered complexes as modular building blocks in molecular spintronics.
我们展示了基于扫描隧道显微镜(STM)的从单个金属原子(铁或镍)和沉积在超薄绝缘膜上的有机分子(9,10-二氰基蒽)开始的线性金属-配体复合物的单分子合成。我们通过 STM 轨道成像直接观察到前沿分子轨道,根据轨道成像,结合详细的密度泛函理论计算,推断出复合物的电子结构。我们的研究表明,通过选择金属原子,如何可以通过改变分子轨道的顺序和复合物的自旋态来实现对其的工程设计。高自旋铁复合物具有占据的离域轨道,其自旋分裂较大,这表明这些工程化复合物可用作分子自旋电子学中的模块化构建块。