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Detecting the spin-polarization of edge states in graphene nanoribbons

Low dimensional carbon-based materials can show intrinsic magnetism associated to p-electrons in open-shell π-conjugated systems. Chemical design provides atomically precise control of the π-electron cloud, which makes them promising for nanoscale magnetic devices. However, direct verification of th...

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Detalles Bibliográficos
Autores principales: Brede, Jens, Merino-Díez, Nestor, Berdonces-Layunta, Alejandro, Sanz, Sofía, Domínguez-Celorrio, Amelia, Lobo-Checa, Jorge, Vilas-Varela, Manuel, Peña, Diego, Frederiksen, Thomas, Pascual, José I., de Oteyza, Dimas G., Serrate, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590394/
https://www.ncbi.nlm.nih.gov/pubmed/37865684
http://dx.doi.org/10.1038/s41467-023-42436-7
Descripción
Sumario:Low dimensional carbon-based materials can show intrinsic magnetism associated to p-electrons in open-shell π-conjugated systems. Chemical design provides atomically precise control of the π-electron cloud, which makes them promising for nanoscale magnetic devices. However, direct verification of their spatially resolved spin-moment remains elusive. Here, we report the spin-polarization of chiral graphene nanoribbons (one-dimensional strips of graphene with alternating zig-zag and arm-chair boundaries), obtained by means of spin-polarized scanning tunnelling microscopy. We extract the energy-dependent spin-moment distribution of spatially extended edge states with π-orbital character, thus beyond localized magnetic moments at radical or defective carbon sites. Guided by mean-field Hubbard calculations, we demonstrate that electron correlations are responsible for the spin-splitting of the electronic structure. Our versatile platform utilizes a ferromagnetic substrate that stabilizes the organic magnetic moments against thermal and quantum fluctuations, while being fully compatible with on-surface synthesis of the rapidly growing class of nanographenes.