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Jose Ignacio Pascual

Publications and source records attributed to Jose Ignacio Pascual.

35 records · Page 2Linked to original sources

Aza-Triangulene: On-Surface Synthesis, Electronic and Magnetic Properties

Nitrogen heteroatom doping into a triangulene molecule allows tuning its magnetic state. However, the synthesis of the nitrogen-doped triangulene (aza-triangulene) has been challenging. Herein, we report the successful synthesis of aza-triangulene on the Au(111) and Ag(111) surfaces, along with their characterizations by scanning tunneling microscopy and spectroscopy in combination with density functional theory (DFT) calculations. Aza-triangulenes were obtained by reducing ketone-substituted precursors. Exposure to atomic hydrogen followed by thermal annealing and, when necessary, manipulations with the scanning probe, afforded the target product. We demonstrate that on Au(111) aza-triangulene donates an electron to the substrate and exhibits an open-shell triplet ground state. This is derived from the different Kondo resonances of the final aza-triangulene product and a series of intermediates on Au(111). Experimentally mapped molecular orbitals match perfectly with DFT calculated counterparts for a positively charged aza-triangulene. In contrast, aza-triangulene on Ag(111) receives an extra electron from the substrate and displays a closed-shell character. Our study reveals the electronic properties of aza-triangulene on different metal surfaces and offers an efficient approach for the fabrication of new hydrocarbon structures, including reactive open-shell molecules.

cond-mat.mtrl-sci↗

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↗

Topological phase transition in chiral graphene nanoribbons: from edge bands to end states

Precise control over the size and shape of graphene nanostructures allows engineering spin-polarized edge and topological states, representing a novel source of non-conventional $π$-magnetism with promising applications in quantum spintronics. A prerequisite for their emergence is the existence of robust gapped phases, which are difficult to find in extended graphene systems: only armchair graphene nanoribbons (GNRs) show a band gap that, however, closes for any other GNR orientation. Here we show that semi-metallic chiral GNRs (chGNRs) narrowed down to nanometer widths undergoes a topological phase transition, becoming first topological insulators, and transforming then into trivial band insulators for the narrowest chGNRs. We fabricated atomically precise chGNRs of different chirality and size by on surface synthesis using predesigned molecular precursors. Combining scanning tunnelling microscopy (STM) measurements and theory simulations, we follow the evolution of topological properties and bulk band gap depending on the width, length, and chirality of chGNRs. The first emerging gapped phases are topological, protected by a chiral interaction pattern between edges. For narrower ribbons, the symmetry of the interaction pattern changes, and the topological gap closes and re-opens again as a trivial band insulator. Our findings represent a new platform for producing topologically protected spin states and demonstrates the potential of connecting chiral edge and defect structure with band engineering.

cond-mat.mes-hall↗

Coupled Yu-Shiba-Rusinov states induced by a many-body molecular spin on a superconductor

A magnetic impurity on a superconductor induces Yu-Shiba-Rusinov (YSR) bound states, detected by tunneling spectroscopy as long-lived quasiparticle excitations inside the superconducting gap. Coupled YSR states constitute basic elements to engineer artificial superconducting states, but their substrate-mediated interactions are generally weak. In this paper, we report that intramolecular (Hund's like) exchange interactions produce coupled YSR states across a molecular platform. We measured YSR spectra along a magnetic iron-porphyrin on Pb(111) and found evidences of two orbital interaction channels, which invert their particle-hole asymmetry across the molecule. Numerical calculations show that the identical YSR asymmetry pattern of the two channels is caused by two spin-hosting orbitals with opposite potential scattering and coupled strongly. Both channels can be similarly excited by tunneling electrons into each orbital, depicting a new scenario for entangled superconducting bound states using molecular platforms.

cond-mat.mes-hall↗

Band Depopulation of Graphene Nanoribbons Induced by Chemical Gating with Amino Groups

The electronic properties of graphene nanoribbons (GNRs) can be precisely tuned by chemical doping. Here we demonstrate that amino (NH$_2$) functional groups attached at the edges of chiral GNRs (chGNRs) can efficiently gate the chGNRs and lead to the valence band (VB) depopulation on a metallic surface. The NH$_2$-doped chGNRs are grown by on-surface synthesis on Au(111) using functionalized bianthracene precursors. Scanning tunneling spectroscopy resolves that the NH$_2$ groups significantly up-shift the bands of chGNRs, causing the Fermi level crossing of the VB onset of chGNRs. Through density functional theory simulations we confirm that the hole-doping behavior is due to an upward shift of the bands induced by the edge NH$_2$ groups.

cond-mat.mes-hall↗

Uncovering the Triplet Ground State of Triangular Graphene Nanoflakes Engineered with Atomic Precision on a Metal Surface

Graphene can develop large magnetic moments in custom crafted open-shell nanostructures such as triangulene, a triangular piece of graphene with zigzag edges. Current methods of engineering graphene nano-systems on surfaces succeeded in producing atomically precise open-shell structures, but demonstration of their net spin remains elusive to date. Here, we fabricate triangulene-like graphene systems and demonstrate that they possess a spin $S=1$ ground state. Scanning tunnelling spectroscopy identifies the fingerprint of an underscreened $S=1$ Kondo state on \rev{these} flakes at low temperatures, signaling the dominant ferromagnetic interactions between two spins. Combined with simulations based on the meanfield Hubbard model, we show that this $S=1$ $π$-paramagnetism is robust, and can be manipulated to a $S=1/2$ state by adding additional H-atoms to the radical sites. \rev{Our results demonstrate that $π$-paramagnetism of high-spin graphene flakes can survive on surfaces, opening the door to study the quantum behaviour of interacting $π$-spins in graphene systems.

cond-mat.mes-hall↗

Electrically addressing the spin of a magnetic porphyrin through covalently connected graphene electrodes

We report on the fabrication and transport characterization of atomically-precise single molecule devices consisting of a magnetic porphyrin covalently wired by graphene nanoribbon electrodes. The tip of a scanning tunneling microscope was utilized to contact the end of a GNR-porphyrin-GNR hybrid system and create a molecular bridge between tip and sample for transport measurements. Electrons tunneling through the suspended molecular heterostructure excited the spin multiplet of the magnetic porphyrin. The detachment of certain spin-centers from the surface shifted their spin-carrying orbitals away from an on-surface mixed-valence configuration, recovering its original spin state. The existence of spin-polarized resonances in the free-standing systems and their electrical addressability is the fundamental step for utilization of carbon-based materials as functional molecular spintronics systems.

cond-mat.mes-hall↗

Single Spin Localization and Manipulation in Graphene Open-Shell Nanostructures

Predictions state that graphene can spontaneously develop magnetism from the Coulomb repulsion of its $π$-electrons, but its experimental verification has been a challenge. Here, we report on the observation and manipulation of individual magnetic moments localized in graphene nanostructures on a Au(111) surface. Using scanning tunneling spectroscopy, we detected the presence of single electron spins localized around certain zigzag sites of the carbon backbone via the Kondo effect. Two near-by spins were found coupled into a singlet ground state, and the strength of their exchange interaction was measured via singlet-triplet inelastic tunnel electron excitations. Theoretical simulations demonstrate that electron correlations result in spin-polarized radical states with the experimentally observed spatial distributions. Hydrogen atoms bound to these radical sites quench their magnetic moment, permitting us to switch the spin of the nanostructure using the tip of the microscope.

cond-mat.mes-hall↗

Electronic Properties of Substitutionally Boron-doped Graphene Nanoribbons on a Au(111) Surface

High quality graphene nanoribbons (GNRs) grown by on-surface synthesis strategies with atomic precision can be controllably doped by inserting heteroatoms or chemical groups in the molecular precursors. Here, we study the electronic structure of armchair GNRs substitutionally doped with di-boron moieties at the center, through a combination of scanning tunneling spectroscopy, angle-resolved photoemission, and density functional theory simulations. Boron atoms appear with a small displacement towards the surface signaling their stronger interaction with the metal. We find two boron-rich flat bands emerging as impurity states inside the GNR band gap, one of them particularly broadened after its hybridization with the gold surface states. In addition, the boron atoms shift the conduction and valence bands of the pristine GNR away from the gap edge, and leave unaffected the bands above and below, which become the new frontier bands and have negligible boron character. This is due to the selective mixing of boron states with GNR bands according to their symmetry. Our results depict that the GNRs band structure can be tuned by modifying the separation between di-boron moieties.

cond-mat.mes-hall↗

On-surface route for producing planar nanographenes with azulene moieties

Large aromatic carbon nanostructures are cornerstone materials due to their increasingly active role in functional devices, but their synthesis in solution encounters size and shape limitations. New on-surface strategies facilitate the synthesis of large and insoluble planar systems with atomic-scale precision. While dehydrogenation is usually the chemical zipping reaction building up large aromatic carbon structures, mostly benzenoid structures are being produced. Here, we report on a new cyclodehydrogenation reaction transforming a sterically stressed precursor with conjoined cove regions into planar carbon platform by incorporating azulene moieties in their interior. Submolecular resolution STM is used to characterize this exotic large polycyclic aromatic compound on Au(111) yielding unprecedented insight into a dehydrogenative intramolecular aryl-aryl coupling reaction. The resulting polycyclic aromatic carbon structure shows a [18]annulene core hosting peculiar pore states confined at the carbon cavity.

cond-mat.mes-hall↗

Probing magnetic interactions between Cr adatoms on the $β$-Bi$_2$Pd superconductor

We show that the magnetic ordering of coupled atomic dimers on a superconductor is revealed by their intra-gap spectral features. Chromium atoms on the superconductor $β$-Bi$_2$Pd surface display Yu-Shiba-Rusinov bound states, detected as pairs of intra-gap excitations in the tunneling spectra. We formed Cr dimers by atomic manipulation and found that their intra-gap features appear either shifted or split with respect to single atoms. The spectral variations reveal that the magnetic coupling of the dimer changes between ferromagnetic and antiferromagnetic depending on its disposition on the surface, in good agreement with density functional theory simulations. These results prove that superconducting intra-gap state spectroscopy is an accurate tool to detect the magnetic ordering of atomic scale structures.

cond-mat.mes-hall↗

Doping of Graphene Nanoribbons via Functional Group Edge Modification

We report on the on-surface synthesis of 7 armchair graphene nanoribbons (7-AGNRs) substituted with nitrile (CN) functional groups. The CN groups are attached to the GNR backbone by modifying the 7-AGNR precursor. While many of these groups survive the on-surface synthesis, the reaction process causes the cleavage of some CN from the ribbon backbone and the on-surface cycloisomerization of few nitriles onto pyridine rings. Scanning Tunneling Spectroscopy and Density Functional Theory reveal that CN groups behave as very efficient n-dopants, significantly downshifting the bands of the ribbon, and introducing deep impurity levels associated to the nitrogen electron lone pairs.

cond-mat.mes-hall↗

Mapping the orbital structure of impurity bound states in a superconductor

A magnetic atomic impurity inside a superconductor locally distorts superconductivity. They scatter Cooper pairs as a potential with broken time-reversal symmetry, what leads to localized bound states with subgap excitation energies, named hereon Shiba states. Most conventional approaches to study Shiba states treat magnetic impurities as point scatterers with an isotropic exchange interaction, while the complex internal structure of magnetic impurities is usually neglected. Here, we show that the number and the shape of Shiba states are correlated to the spin-polarized atomic orbitals of the impurity, hybridized with the superconducting host, as supported by Density Functional Theory simulations. Using high-resolution scanning tunneling spectroscopy, we spatially map the five Shiba excitations found on sub-surface chromium atoms in Pb(111), resolving both their particle and hole components. While the maps of particle components resemble the \textit{d} orbitals of embedded Cr atoms, the hole components differ strongly from them. The orbital fingerprints of Shiba states thus unveil the magnetic ground state of the impurity, and identify scattering channels and interactions, all valuable tools for designing atomic-scale superconducting devices.

cond-mat.supr-con↗

Gating the charge state of a single molecule by local electric fields

The electron acceptor molecule TCNQ is found in either of two distinct integer charge states when embedded into a monolayer of a charge transfer-complex on a gold surface. Scanning tun- neling spectroscopy measurements identify these states through the presence/absence of a zero-bias Kondo resonance. Increasing the (tip-induced) electric field allows us to reversibly induce the ox- idation/reduction of TCNQ species from their anionic or neutral ground state, respectively. We show that the different ground states arise from slight variations in the underlying surface potential, pictured here as the gate of a three-terminal device.

cond-mat.mes-hall↗

Induction of a photostationary ring-opening/closing state of spiropyran monolayers on the semi-metallic Bi(110) surface

Molecular switches on metal surfaces typically show very little photoreactivity. Using scanning tunneling microscopy we show that the ring-opening/-closing switch nitrospiropyran thermally and optically isomerizes to the open merocyanine form on a Bi(110) surface. Irradiation by blue light of a monolayer spiropyran molecules leads to mixed domains of the two isomers. At large illumination intensities a photostationary state is established, indicating the bidirectional ring-opening and closing reaction of these molecules on the bismuth surface. The enhanced photoactivity contrasts with the case of adsorption on other metal surfaces, probably due to the low density of states at the Fermi level of the semi-metallic Bi(110) surface.

cond-mat.mtrl-sci↗

Surface states on a topologically non-trivial semimetal: The case of Sb(110)

The electronic structure of Sb(110) is studied by angle-resolved photoemission spectroscopy and first-principle calculations, revealing several electronic surface states in the projected bulk band gaps around the Fermi energy. The dispersion of the states can be interpreted in terms of a strong spin-orbit splitting. The bulk band structure of Sb has the characteristics of a strong topological insulator with a Z2 invariant nu0=1. This puts constraints on the existence of metallic surface states and the expected topology of the surface Fermi contour. However, bulk Sb is a semimetal, not an insulator and these constraints are therefore partly relaxed. This relation of bulk topology and expected surface state dispersion for semimetals is discussed.

cond-mat.str-el↗

Resonant heating and substrate-mediated cooling of a single C60 molecule in a tunnel junction

We study the influence of different metallic substrates on the electron induced heating and heat dissipation of single C60 molecules in the junction of a low temperature scanning tunneling microscope. The electron current passing through the molecule produces a large amount of heat due to electron-phonon coupling, eventually leading to thermal decomposition of the fullerene cage. The power for decomposition varies with electron energy and reflects the resonance structure participating in the transport. The average value for thermal decomposition of C60 on Cu(110) amounts to 21 $μ$W, while it is much lower on Pb(111) (2.9 $μ$W) and on Au(111) (1.0 $μ$W). We ascribe this difference to the amount of charge transfer into C60 upon adsorption on the different surfaces, which facilitates molecular vibron quenching by electron-hole pair creation.

cond-mat.mtrl-sci↗