Molecular Kondo Lattice with Pure π-Magnetism on a Superconductor
Artificial Kondo lattices with tailored functionalities are the key to elucidating correlated quantum states. Here, we report a Kondo lattice based on organic π-magnetism in a perylene diimide monolayer on superconducting Pb(111). Using spectroscopic imaging scanning tunneling microscopy, we resolve Kondo resonances with uniform resonance widths that propagate across the entire molecular film, including both molecular cores and interstitial sites, demonstrating a periodic Kondo lattice with signatures consistent with lattice coherence. First-principles calculations unveil that the π-magnetism is induced via charge transfer from the substrate to an extended molecular orbital, with the intermolecular spin interaction mediated via hydrogen-bonding and conduction electrons. Furthermore, Yu-Shiba-Rusinov bands are generated in the molecular Kondo lattice, as induced by its interaction with the substrate superconductivity. Our work not only expands the Kondo lattice system to π-magnetism with s/p orbital character but also lays the foundation for tailoring the correlated states in view of the chemical versatility of molecules.
Authors
- Guilin Zhu
- Rui Sun (ORCID: https://orcid.org/0000-0003-0389-7485)
- Chaofei Liu (ORCID: https://orcid.org/0000-0002-9662-6096)
- Wenhao Zhang (ORCID: https://orcid.org/0000-0003-3589-2910)
- Ting-Fei Guo
- Jian-Wang Zhou
- Guijing Duan (ORCID: https://orcid.org/0009-0009-2913-7581)
- Rong Yu
- Hao Tang
- Lian-zhi Yang
- Tianyou Zhai
- Ying-Shuang Fu
- Gang Chen
Institutions
- Beijing Institute of Optoelectronic Technology (CN)
- Advanced Processing Technology (United States) (US)
- Huazhong University of Science and Technology (CN)
- Renmin University of China (CN)
- Wuhan Institute of Technology (CN)
Publication Details
- Journal
- The Journal of Physical Chemistry Letters
- Published
- 2026-02-27
- DOI
- https://doi.org/10.1021/acs.jpclett.5c04091
- Primary Topic
- Molecular Junctions and Nanostructures
- Type
- article
- Field-Weighted Citation Impact
- 0.00