Magnetic Interactions in Substitutional Core-Doped Graphene Nanoribbons.
Ethan Chi Ho WenPeter H JacobseJingwei JiangZiyi WangPeter H JacobseSteven G LouieMichael F CrommieFelix R FischerPublished in: Journal of the American Chemical Society (2022)
The design of a spin imbalance within the crystallographic unit cell of bottom-up engineered 1D graphene nanoribbons (GNRs) gives rise to nonzero magnetic moments within each cell. Here, we demonstrate the bottom-up assembly and spectroscopic characterization of a one-dimensional Kondo spin chain formed by a chevron-type GNR (cGNR) physisorbed on Au(111). Substitutional nitrogen core doping introduces a pair of low-lying occupied states per monomer within the semiconducting gap of cGNRs. Charging resulting from the interaction with the gold substrate quenches one electronic state for each monomer, leaving behind a 1D chain of radical cations commensurate with the unit cell of the ribbon. Scanning tunneling microscopy (STM) and spectroscopy (STS) reveal the signature of a Kondo resonance emerging from the interaction of S = 1/2 spin centers in each monomer core with itinerant electrons in the Au substrate. STM tip lift-off experiments locally reduce the effective screening of the unpaired radical cation being lifted, revealing a robust exchange coupling between neighboring spin centers. First-principles DFT-LSDA calculations support the presence of magnetic moments in the core of this GNR when it is placed on Au.
Keyphrases
- room temperature
- density functional theory
- molecularly imprinted
- single molecule
- single cell
- high resolution
- cell therapy
- ionic liquid
- sensitive detection
- molecular docking
- molecular dynamics
- stem cells
- reduced graphene oxide
- mesenchymal stem cells
- gene expression
- high throughput
- gold nanoparticles
- carbon nanotubes
- amino acid
- solid state