Defect-induced π-magnetism into non-benzenoid nanographenes

The synthesis of nanographenes (NGs) with open-shell ground states have recently attained increasing attention in view of their interesting physicochemical properties and great prospects in manifold applications as suitable materials within the rising field of carbon-based magnetism. A potential rou...

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Detalhes bibliográficos
Autores: Biswas, Kalyan, Yang, Lin, Ma, Ji, Sánchez Grande, Ana, Chen, Qifan, Lauwaet, Koen, Gallego, José M., Miranda Soriano, Rodolfo, Écija, David, Jelínek, Pavel, Feng, Xinliang, Urgel, José I.
Tipo de documento: artigo
Data de publicação:2022
País:España
Recursos:Universidad Autónoma de Madrid
Repositório:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglês
OAI Identifier:oai:repositorio.uam.es:10486/714002
Acesso em linha:http://hdl.handle.net/10486/714002
https://dx.doi.org/10.3390/nano12020224
Access Level:Acceso aberto
Palavra-chave:Nanographenes
Nanomagnetism
Nc-AFM
On-surface synthesis
Open-shell character
Polycyclic aromatic hydrocarbons
STM
Física
Descrição
Resumo:The synthesis of nanographenes (NGs) with open-shell ground states have recently attained increasing attention in view of their interesting physicochemical properties and great prospects in manifold applications as suitable materials within the rising field of carbon-based magnetism. A potential route to induce magnetism in NGs is the introduction of structural defects, for instance non-benzenoid rings, in their honeycomb lattice. Here, we report the on-surface synthesis of three open-shell non-benzenoid NGs (A1, A2 and A3 ) on the Au(111) surface. A1 and A2 contain two five-and one seven-membered rings within their benzenoid backbone, while A3 incorporates one five-membered ring. Their structures and electronic properties have been investigated by means of scanning tunneling microscopy, noncontact atomic force microscopy and scanning tunneling spectroscopy complemented with theoretical calculations. Our results provide access to openshell NGs with a combination of non-benzenoid topologies previously precluded by conventional synthetic procedures