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Sofía Sanz

Publications and source records attributed to Sofía Sanz.

3 recordsLinked to original sources

Systematic Modulation of Charge and Spin in Graphene Nanoribbons on MgO

Graphene nanostructures can be engineered with atomic precision to display customized electronic states with application in spintronics or quantum technologies. In order to take advantage of their full potential, their charge and spin state must be precisely controlled. Graphene systems exchange charge to reach thermodynamic equilibrium with their environment, requiring external gating potentials to tune their ground state. Alternative strategies like intrinsic doping or substrate modifications provided small variations of their equilibrium charge and poor control over their spin. Here, we show systematic manipulation of the electron occupation in graphene nanoribbons (GNRs) laying on MgO layers grown on Ag(001). Owing to the extraordinary decoupling properties of MgO, and the electropositive character of the substrate, GNRs are found to host an integer number of electron charges that depend on their length and shape. This results in the alternation between a non-magnetic closed-shell state and an open-shell paramagnetic system for even and odd electron occupations respectively. For the odd case, we found the spectral fingerprint of a narrow Coulomb correlation gap, which is the smoking gun of its spin 1/2 paramagnetic state. Comparisons of scanning tunnelling microscopy (STM) data with mean-field Hubbard (MFH) simulations confirm the practical discretization of the GNR electronic states and point to charge excess of up to 19 electrons in a single ribbon. We anticipate that GNRs supported by MgO ultra-thin insulating films can open the door to customized devices for quantum sensing and quantum processing applications..

cond-mat.mes-hall↗

Detecting the spin-polarization of edge states in graphene nanoribbons

Low dimensional carbon-based materials are interesting because they can show intrinsic $π$-magnetism associated to p-electrons residing in specific open-shell configurations. Consequently, during the last years there have been impressive advances in the field combining indirect experimental fingerprints of localized magnetic moments with theoretical models. In spite of that, a characterization of their spatial- and energy-resolved spin-moment has so far remained elusive. To obtain this information, we present an approach based on the stabilization of the magnetization of $π$-orbitals by virtue of a supporting substrate with ferromagnetic ground state. Remarkably, we go beyond localized magnetic moments in radical or faulty carbon sites: In our study, energy-dependent spin-moment distributions have been extracted from spatially extended one-dimensional edge states of chiral graphene nanoribbons. This method can be generalized to other nanographene structures, representing an essential validation of these materials for their use in spintronics and quantum technologies.

cond-mat.mes-hall↗

On-surface synthesis and collective spin excitations of a triangulene-based nanostar

Triangulene nanographenes are open-shell molecules with predicted high spin state due to the frustration of their conjugated network. Their long-sought synthesis became recently possible over a metal surface. Here, we present a macrocycle formed by six [3]triangulenes, which was obtained by combining the solution synthesis of a dimethylphenyl-anthracene cyclic hexamer and the on-surface cyclodehydrogenation of this precursor over a gold substrate. The resulting triangulene nanostar exhibits a collective spin state generated by the interaction of its 12 unpaired π-electrons along the conjugated lattice, corresponding to the antiferromagnetic ordering of six S = 1 sites (one per triangulene unit). Inelastic electron tunneling spectroscopy resolved three spin excitations connecting the singlet ground state with triplet states. The nanostar behaves close to predictions from the Heisenberg model of a S = 1 spin ring, representing a unique system to test collective spin modes in cyclic systems.

cond-mat.mes-hall↗