| Literature DB >> 33352044 |
Ana Sánchez-Grande1, José I Urgel1, Libor Veis2, Shayan Edalatmanesh3,4, José Santos1,5, Koen Lauwaet1, Pingo Mutombo3, José M Gallego6, Jiri Brabec2, Pavel Beran2, Dana Nachtigallová4,7, Rodolfo Miranda1,8, Nazario Martín1,5, Pavel Jelínek3,4, David Écija1.
Abstract
Polycyclic aromatic hydrocarbons (PAHs) are a family of organic compounds comprising two or more fused aromatic rings which feature manifold applications in modern technology. Among these species, those presenting an open-shell magnetic ground state are of particular interest for organic electronic, spintronic, and non-linear optics and energy storage devices. Within PAHs, special attention has been devoted in recent years to the synthesis and study of the acene and fused acene (periacene) families, steered by their decreasing HOMO-LUMO gap with length and predicted open-shell character above some size. However, an experimental fingerprint of such magnetic ground state has remained elusive. Here, we report on the in-depth electronic characterization of isolated peripentacene molecules on a Au(111) surface. Scanning tunnelling spectroscopy, complemented by computational investigations, reveals an antiferromagnetic singlet ground state, characterized by singlet-triplet inelastic excitations with an experimental effective exchange coupling (Jeff) of 40.5 meV. Our results deepen the fundamental understanding of organic compounds with magnetic ground states, featuring perspectives in carbon-based spintronic devices.Entities:
Year: 2020 PMID: 33352044 DOI: 10.1021/acs.jpclett.0c02518
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475