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J. Enrique Ortega

Publications and source records attributed to J. Enrique Ortega.

At least 19 recordsLinked to original sources
arXiv2026

Plasmon-Enhanced Second-Harmonic Generation in Atomically Thin Crystalline Silver Nanostructures

The intrinsically weak nonlinear optical response of existing materials, further constrained by symmetry-forbidden second-order processes in centrosymmetric media, severely limits efficient frequency conversion in deeply subwavelength, ultrathin volumes. Addressing this challenge is crucial for the development of nonlinear nanophotonics. Here, we show that atomically thin, epitaxially grown crystalline silver films circumvent these restrictions through the interplay of vertical electronic quantum confinement and lateral plasmonic enhancement. We fabricate atomically thin films that exhibit an enhanced nonlinear response associated with electronic quantum wells, and subsequently pattern them into periodic nanoribbon and nanotriangle arrays sustaining infrared localized surface plasmon resonances. Strong near-field confinement in these structures further boosts second-harmonic generation compared to unpatterned films. Precise control over nanostructure geometry enables spectral tuning of the plasmonic resonance, and consequently, the enhanced harmonic frequency. Our findings establish an approach for activating robust second-order nonlinearities in quantum-confined metals, where intrinsic size effects and plasmonic resonances act synergistically. The compatibility of high-quality epitaxial growth with microchip fabrication technology offers a scalable route toward ultracompact nonlinear optical components for on-chip frequency conversion, sensing, and quantum photonic applications.

physics.optics↗
arXiv2026

Control of the MoTe$_2$ Fermi Surface by Nb Doping

Ab initio calculations and angle-resolved photoemission experiments show that the bulk and surface electronic structure of Weyl semimetal candidate MoTe$_2$ changes significantly by tuning the chemical potential by less than 0.4 eV. Calculations show that several Lifshitz transitions can occur among multiple electron and hole Fermi pockets of differing orbital character. Experiments show that 18% Nb-Mo substitution reduces the occupation of bulk and (001) surface bands, effectively producing a chemical potential shift of $\approx 0.3$ eV. Orbital character and dimensionality of the bulk bands is examined by soft X-ray angle resolved photoemission with control of the excitation light polarization. The band filling at the surface is shown to increase upon deposition of alkali atoms. The results indicate that multiple regimes of electronic properties can be easily accessed in this versatile, layered material.

cond-mat.mtrl-sci↗
arXiv2025

Atomically thin silver films for enhanced nanoscale nonlinear optics

The inherently weak nonlinear optical response of bulk materials remains a fundamental limitation in advancing photonic technologies. Nanophotonics addresses this challenge by tailoring the size and morphology of nanostructures to manipulate the optical near field, thus modulating the nonlinear response. Here, we explore a complementary strategy based on engineering the electronic band structure in the mesoscopic regime to enhance optical nonlinearities. Specifically, we demonstrate an increase in second-harmonic generation (SHG) from crystalline silver films as their thickness is reduced down to just a few atomic monolayers. Operating at the boundary between bulk and two-dimensional systems, these ultra-thin films exhibit a pronounced enhancement of SHG with decreasing thickness. This enhancement stems from quantum confinement effects that modify the interaction between electronic states and incident light, which we explain based on quantum-mechanical calculation. Our atomically-thin crystalline silver films provide a new means to overcome the small interaction volumes inherent to nanophotonic platforms, enabling efficient nanoscale nonlinear optics with potential applications in photonics, sensing, and quantum technologies.

physics.optics↗
arXiv2024

The role of rare-earth atoms in the anisotropy and antiferromagnetic exchange coupling at a hybrid metal-organic interface

Magnetic anisotropy and magnetic exchange interactions are crucial parameters that characterize the hybrid metal-organic interface, key component of an organic spintronic device. We show that the incorporation of 4$f$ RE atoms to hybrid metal-organic interfaces of CuPc/REAu$_2$ type (RE= Gd, Ho) constitutes a feasible approach towards on-demand magnetic properties and functionalities. The GdAu$_2$ and HoAu$_2$ substrates differ in their magnetic anisotropy behavior. Remarkably, the HoAu$_2$ surface boosts the inherent out-of-plane anisotropy of CuPc, owing to the match between the anisotropy axis of substrate and molecule. Furthermore, the presence of RE atoms leads to a spontaneous antiferromagnetic (AFM) exchange coupling at the interface, induced by the 3$d$-4$f$ superexchange interaction between the unpaired 3$d$ electron of CuPc and the 4$f$ electrons of the RE atoms. We show that 4$f$ RE atoms with unquenched quantum orbital momentum ($L$), as it is the case of Ho, induce an anisotropic interfacial exchange coupling.

cond-mat.mtrl-sci↗
arXiv2023

Simulating high-pressure surface reactions with molecular beams

Using a reactive molecular beam with high kinetic energy ($E_{kin}$) it is possible to speed gas-surface reactions involving high activation barriers ($E_{act}$), which would require elevated pressures ($P_0$) if a random gas with a Maxwell-Boltzmann distribution is used. By simply computing the number of molecules that overcome the activation barrier in a random gas at $P_0$ and in a molecular beam at $E_{kin}$=$E_{act}$, we establish an $E_{kin}$-$P_0$ equivalence curve, through which we postulate that molecular beams are ideal tools to investigate gas-surface reactions that involve high activation energies. In particular, we foresee the use of molecular beams to simulate gas surface reactions within the industrial-range ($>$ 10 bar) using surface-sensitive Ultra-High Vacuum (UHV) techniques, such as X-ray photoemission spectroscopy (XPS). To test this idea, we revisit the oxidation of the Cu(111) surface combining O$_2$ molecular beams and XPS experiments. By tuning the kinetic energy of the O$_2$ beam in the range 0.24-1 eV we achieve the same sequence of surface oxides obtained in Ambient Pressure Photoemission (AP-XPS) experiments, in which the Cu(111) surface was exposed to a random O$_2$ gas up to 1 mbar. We observe the same surface oxidation kinetics as in the random gas, but with a much lower dose, close to the expected value derived from the equivalence curve.

cond-mat.mtrl-sci↗
arXiv2023

A ferromagnetic Eu-Pt surface compound grown below hexagonal boron nitride

One of the fundamental applications for monolayer-thick 2D materials is their use as protective layers of metal surfaces and in-situ intercalated reactive materials in ambient conditions. Here we investigate the structural, electronic, and magnetic properties, as well as the chemical stability in air of a very reactive metal, Europium, after intercalation between a hexagonal boron nitride (hBN) layer and a Pt substrate. We demonstrate that Eu intercalation leads to a hBN-covered ferromagnetic EuPt$_2$ surface alloy with divalent Eu$^{2+}$ atoms at the interface. We expose the system to ambient conditions and find a partial conservation of the di-valent signal and hence the Eu-Pt interface. The use of a curved Pt substrate allows us to explore the changes in the Eu valence state and the ambient pressure protection at different substrate planes. The interfacial EuPt$_2$ surface alloy formation remains the same, but the resistance of the protecting hBN layer to ambient conditions is reduced, likely due to a rougher surface and a more discontinuous hBN coating.

cond-mat.mtrl-sci↗
arXiv2023

Ultraconfined plasmons in atomically thin crystalline silver nanostructures

The ability to confine light down to atomic scales is critical for the development of applications in optoelectronics and optical sensing as well as for the exploration of nanoscale quantum phenomena. Plasmons in metallic nanostructures can achieve this type of confinement, although fabrication imperfections down to the subnanometer scale hinder actual developments. Here, we demonstrate narrow plasmons in atomically thin crystalline silver nanostructures fabricated by prepatterning silicon substrates and epitaxially depositing silver films of just a few atomic layers in thickness. Combined with on-demand lateral shaping, this procedure allows for an unprecedented control over optical field confinement in the near-infrared spectral region. Specifically, we observe fundamental and higher-order plasmons featuring extreme spatial confinement and high-quality factors that reflect the crystallinity of the metal. Our approach holds potential for the design and exploitation of atomic-scale nanoplasmonic devices in optoelectronics, sensing, and quantum-physics applications.

cond-mat.mes-hall↗
arXiv2021

Engineering interfacial quantum states and electronic landscapes by molecular nanoarchitectures

Surfaces are at the frontier of every known solid. They provide versatile supports for functional nanostructures and mediate essential physicochemical processes. Being intimately related with 2D materials, interfaces and atomically thin films often feature distinct electronic states with respect to the bulk, which are key for many relevant properties, such as catalytic activity, interfacial charge-transfer, or crystal growth mechanisms. Of particular interest is reducing the surface electrons' dimensionality and spread with atomic precision, to induce novel quantum properties via lateral scattering and confinement. Both atomic manipulation and supramolecular principles provide access to custom-designed molecular superlattices, which tailor the surface electronic landscape and influence fundamental chemical and physical properties at the nanoscale. Herein, we review the confinement of surface state electrons focusing on their interaction with molecule-based scaffolds created by molecular manipulation and self-assembly protocols under ultrahigh vacuum conditions. Starting from the quasi-free 2D electron gas present at the (111)-terminated surface planes of noble metals, we illustrate the enhanced molecule-based structural complexity and versatility compared to simple atoms. We survey low-dimensional confining structures in the form of artificial lattices, molecular nanogratings or quantum dot arrays, which are constructed upon appropriate choice of their building constituents. Whenever the realized (metal-)organic networks exhibit long-range order, modified surface band structures with characteristic features emerge, revealing intriguing physical properties, such as discretization, quantum coupling or energy and effective mass renormalization. Such collective electronic states can be additionally modified by positioning guest species at the voids of open nanoarchitectures [...].

cond-mat.mes-hall↗
arXiv2020

Switching From Reactant to Substrate Engineering in the Selective Synthesis of Graphene Nanoribbons

The challenge of synthesizing graphene nanoribbons (GNRs) with atomic precision is currently being pursued along a one-way road, based on the synthesis of adequate molecular precursors that react in predefined ways through self-assembly processes. The synthetic options for GNR generation would multiply by adding a new direction to this readily successful approach, especially if both of them can be combined. We show here how GNR synthesis can be guided by an adequately nanotemplated substrate instead of by the traditionally designed reactants. The structural atomic precision, unachievable to date through top-down methods, is preserved by the self-assembly process. This new strategy s proof-of-concept compares experiments using 4,4 -dibromo-para-terphenyl as molecular precursor on flat Au(111) and stepped Au(322) substrates. As opposed to the former, the periodic steps of the latter drive the selective synthesis of 6 atom-wide armchair GNRs, whose electronic properties have been further characterized in detail by scanning tunneling spectroscopy, angle resolved photoemission and density functional theory calculations.

cond-mat.mtrl-sci↗
arXiv2020

Substrate-Independent Growth of Atomically Precise Chiral Graphene Nanoribbons

Contributing to the need of new graphene nanoribbon (GNR) structures that can be synthesized with atomic precision, we have designed a reactant that renders chiral (3,1) - GNRs after a multi-step reaction including Ullmann coupling and cyclodehydrogenation. The nanoribbon synthesis has been successfully proved on different coinage metals, and the formation process, together with the fingerprints associated to each reaction step, has been studied combining scanning tunnelling microscopy, core-level spectroscopy and density functional calculations. In addition to the GNR chiral edge structure, the substantial GNR lengths achieved and the low processing temperature required to complete the reaction grant this reactant extremely interesting properties for potential applications.

cond-mat.mtrl-sci↗
arXiv2020

Electronic structure tunability by periodic meta-ligand spacing in one-dimensional organic semiconductors

Designing molecular organic semiconductors with distinct frontier orbitals is key for the development of devices with desirable properties. Generating defined organic nanostructures with atomic precision can be accomplished by on-surface synthesis. We use this dry chemistry to introduce topological variations in a conjugated poly-para-phenylene chain in the form of meta-junctions. As evidenced by STM and LEED, we produce a macroscopically ordered, monolayer thin zigzag chain film on a vicinal silver crystal. These cross-conjugated nanostructures are expected to display altered electronic properties, which are now unravelled by highly complementary experimental techniques (ARPES and STS) and theoretical calculations (DFT and EPWE). We find that meta-junctions dominate the weakly dispersive band structure, while the bandgap is tunable by altering the linear segment's length. These periodic topology effects induce significant loss of the electronic coupling between neighboring linear segments leading to partial electron confinement in the form of weakly coupled Quantum Dots. Such periodic quantum interference effects determine the overall semiconducting character and functionality of the chains.

cond-mat.mtrl-sci↗
arXiv2019

Tunable energy and mass renormalization from homothetic Quantum dot arrays

Quantum dot arrays in the form of molecular nanoporous networks are renown for modifying the electronic surface properties through quantum confinement. Here we show that, compared to the pristine surface state, the fundamental energy of the confined states can exhibit downward shifts accompanied by a lowering of the effective masses simultaneous to the appearance of tiny gaps at the Brillouin zone boundaries. We observed these effects by angle resolved photoemission for two self-assembled homothetic (scalable) Co-coordinated metal-organic networks. Complementary scanning tunneling spectroscopy measurements confirmed these findings. Electron plane wave expansion simulations and density functional theory calculations provide insight into the nature of this phenomenon, which we assign to metal-organic overlayer-substrate interactions in the form of adatom-substrate hybridization. The absence to date of the experimental band structure resulting from single adatom metal-coordinated nanoporous networks has precluded the observation of the significant surface state renormalization reported here, which we infer are general of low interacting and well-defined adatom arrays.

physics.chem-ph↗
arXiv2019

Atomically precise step grids for the engineering of helical states

Conventional spin-degenerated surface electrons have been effectively manipulated by using organic and inorganic self-assembled nanoarrays as resonators. Step superlattices naturally assembled in vicinal surfaces are a particularly interesting case since they represent simple one-dimensional (1D) models for fundamental studies, and can imprint strong anisotropies in surface electron transport in real devices. Here we present the first realization of periodic resonator arrays on the BiAg2 atom-thick surface alloy with unprecedented atomic precision, and demonstrate their potential ability for tuning helical Rashba states. By employing curved crystals to select local vicinal planes we achieve tunable arrays of monoatomic steps with different morphology and orientation. Scanning the ultraviolet light beam on the curved surface during angle-resolved photoemission experiments allows one to unveil the scattering behavior of spin-textured helical states. In this way, we find coherent scattering of helical Rashba states from the step arrays, as well as step-density-dependent Rashba band shifts and spin-orbit splitting compared to the extended BiAg2 plane.

cond-mat.mtrl-sci↗
arXiv2018

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↗
arXiv2018

Symmetry, Shape and Energy Variations in Frontier Molecular Orbitals at Organic/Metal Interfaces: the Case of F$_4$TCNQ

Near Edge X-ray Absorption, Valence and Core-level Photoemission and Density Functional Theory calculations are used to study molecular levels of tetracyano-2,3,5,6-tetrafluoroquinodimethane (F$_4$TCNQ) deposited on Ag(111) and BiAg$_2$/Ag(111). The high electron affinity of F$_4$TCNQ triggers a large static charge transfer from the substrate, and, more interestingly, hybridization with the substrate leads to a radical change of symmetry, shape and energy of frontier molecular orbitals. The Lowest Unoccupied Molecular Orbital (LUMO) shifts below the Fermi energy, becoming the new Highest Occupied Molecular Orbital ($n$-HOMO), whereas the $n$-LUMO is defined by a hybrid band with mixed $π^*$ and $σ^*$ symmetries, localized at quinone rings and cyano groups, respectively. The presence of Bi influences the way the molecule contacts the substrate with the cyano group. The molecule/surface distance is closer and the bond more extended over substrate atoms in F$_4$TCNQ/Ag(111), whereas in F$_4$TCNQ/BiAg$_2$/Ag(111) the distance is larger and the contact more localized on top of Bi. This does not significantly alter molecular levels, but it causes the respective absence or presence of optical excitations in F$_4$TCNQ core-level spectra.

cond-mat.mtrl-sci↗
arXiv2017

Unraveling the electronic structure of narrow atomically-precise chiral graphene nanoribbons

Recent advances in graphene nanoribbon-based research have demonstrated the controlled synthesis of chiral graphene nanoribbons (cGNR) with atomic precision using strategies of on-surface chemistry. However their electronic characterization, including typical figures of merit like band gap or frontier bands effective masses, has not yet been reported. In this work, we provide a detailed characterization of (3,1)-cGNRs on Au(111). The structure and epitaxy, as well as the electronic band structure of the ribbons, are analyzed by means of scanning tunneling microscopy and spectroscopy, angle resolved photoemission and density functional theory.

cond-mat.mes-hall↗
arXiv2016

Tunable Band Alignment with Unperturbed Carrier Mobility of On-Surface Synthesized Organic Semiconducting Wires

The tunable properties of molecular materials place them among the favorites for a variety of future generation devices. In addition, to maintain the current trend of miniaturization of those devices, a departure from the present top-down production methods may soon be required and self-assembly appears among the most promising alternatives. On-surface synthesis unites the promises of molecular materials and of self-assembly, with the sturdiness of covalently bonded structures: an ideal scenario for future applications. Following this idea, we report the synthesis of functional extended nanowires by self-assembly. In particular, the products correspond to one-dimensional organic semiconductors. The uniaxial alignment provided by our substrate templates allows us to access with exquisite detail their electronic properties, including the full valence band dispersion, by combining local probes with spatial averaging techniques. We show how, by selectively doping the molecular precursors, the product's energy level alignment can be tuned without compromising the charge carrier's mobility.

cond-mat.mtrl-sci↗