arXiv subjects

F. Javier García de Abajo

Publications and source records attributed to F. Javier García de Abajo.

At least 127 records · Page 7Linked to original sources

arXiv2017

Continuous-Wave Multiphoton Photoemission from Plasmonic Nanostars

Highly nonlinear optical processes, such as multiphoton photoemission, require high intensities, typically achieved with ultrashort laser pulses and, hence, were first observed with the advent of picosecond laser technology. An alternative approach for reaching the required field intensities is offered by localized optical resonances such as plasmons. Here, we demonstrate localized multiphoton photoemission from plasmonic nanostructures under continuous-wave illumination. We use synthesized plasmonic gold nanostars, which exhibit sharp tips with structural features smaller than 5 nm, leading to near-field-intensity enhancements exceeding 1000. This large enhancement facilitates 3-photon photoemission driven by a simple continuous-wave laser diode. We characterize the intensity and polarization dependencies of the photoemission yield from both individual nanostars and ensembles. Numerical simulations of the plasmonic enhancement, the near-field distributions, and the photoemission intensities are in good agreement with experiment. Our results open a new avenue for the design of nanoscale electron sources.

physics.optics↗

arXiv2017

Strong plasmon-phonon splitting and hybridization in 2D materials revealed through a self-energy approach

We reveal new aspects of the interaction between plasmons and phonons in 2D materials that go beyond a mere shift and increase in plasmon width due to coupling to either intrinsic vibrational modes of the material or phonons in a supporting substrate. More precisely, we predict strong plasmon splitting due to this coupling, resulting in a characteristic avoided crossing scheme. We base our results on a computationally efficient approach consisting in including many-body interactions through the electron self-energy. We specify this formalism for a description of plasmons based upon a tight-binding electron Hamiltonian combined with the random-phase approximation. This approach is accurate provided vertex corrections can be neglected, as is is the case in conventional plasmon-supporting metals and Dirac-fermion systems. We illustrate our method by evaluating plasmonic spectra of doped graphene nanotriangles with varied size, where we predict remarkable peak splittings and other radical modifications in the spectra due to plasmons interactions with intrinsic optical phonons. Our method is equally applicable to other 2D materials and provides a simple approach for investigating coupling of plasmons to phonons, excitons, and other excitations in hybrid thin nanostructures.

cond-mat.mes-hall↗

arXiv2017

Topologically protected Dirac plasmons in graphene

Topological optical states exhibit unique immunity to defects and the ability to propagate without losses rendering them ideal for photonic applications.A powerful class of such states is based on time-reversal symmetry breaking of the optical response.However, existing proposals either involve sophisticated and bulky structural designs or can only operate in the microwave regime. Here, we propose and provide a theoretical proof-of-principle demonstration for highly confined topologically protected optical states to be realized at infrared frequencies in a simple 2D material structure-a periodically patterned graphene monolayer-subject to a magnetic field below 1 tesla. In our graphene honeycomb superlattice structures plasmons exhibit substantial nonreciprocal behavior at the superlattice junctions, leading to the emergence of topologically protected edge states and localized bulk modes enabled by the strong magneto-optical response of this material, which leads to time-reversal-symmetry breaking already at moderate static magnetic fields. The proposed approach is simple and robust for realizing topologically nontrivial 2D optical states, not only in graphene, but also in other 2D atomic layers, and could pave the way for realizing fast, nanoscale, defect-immune devices for integrated photonics applications.

physics.optics↗

arXiv2017

Quantum Effects in the Nonlinear Response of Graphene Plasmons

The ability of graphene to support long-lived, electrically tunable plasmons that interact strongly with light, combined with its highly nonlinear optical response, has generated great expectations for application of the atomically-thin material to nanophotonic devices. These expectations are mainly reinforced by classical analyses performed using the response derived from extended graphene, neglecting finite-size and nonlocal effects that become important when the carbon layer is structured on the nanometer scale in actual device designs. Here we show that finite-size effects produce large contributions that increase the nonlinear response of nanostructured graphene to significantly higher levels than those predicted by classical theories. We base our analysis on a quantum-mechanical description of graphene using tight-binding electronic states combined with the random-phase approximation. While classical and quantum descriptions agree well for the linear response when either the plasmon energy is below the Fermi energy or the size of the structure exceeds a few tens of nanometers, this is not always the case for the nonlinear response, and in particular, third-order Kerr-type nonlinearities are generally underestimated by the classical theory. Our results reveal the complex quantum nature of the optical response in nanostructured graphene, while further supporting the exceptional potential of this material for nonlinear nanophotonic devices.

cond-mat.mes-hall↗

arXiv2016

Lateral Casimir force on a rotating particle near a planar surface

We study the lateral Casimir force experienced by a particle that rotates near a planar surface. The origin of this force lies in the symmetry breaking induced by the particle rotation in the vacuum and thermal fluctuations of its dipole moment, and, therefore, in contrast to lateral Casimir forces previously described in the literature for corrugated surfaces, it exists despite the translational invariance of the planar surface. Working within the framework of fluctuational electrodynamics, we derive analytical expressions for the lateral force and analyze its dependence on the geometrical and material properties of the system. In particular, we show that the direction of the force can be controlled by adjusting the particle-surface distance, which may be exploited as a new mechanism to manipulate nanoscale objects.

cond-mat.other↗

arXiv2016

Plasmon-assisted high-harmonic generation in graphene

High-harmonic generation (HHG) in condensed-matter systems is both a source of fundamental insight into quantum electron motion and a promising candidate to realize compact ultraviolet and ultrafast light sources. Here we argue that the large light intensity required for this phenomenon to occur can be reached by exploiting localized plasmons in conducting nanostructures. In particular, we demonstrate that doped graphene nanostructures combine a strong plasmonic near-field enhancement and a pronounced intrinsic nonlinearity that result in efficient broadband HHG within a single material platform. We extract this conclusion from time-domain simulations using two complementary nonperturbative approaches based on atomistic one-electron density-matrix and massless Dirac-fermion Bloch-equation pictures. High harmonics are predicted to be emitted with unprecedentedly large intensity by tuning the incident light to the localized plasmons of ribbons and finite islands. In contrast to atomic systems, we observe no cutoff in harmonic order. Our results support the strong potential of nanostructured graphene as a robust, electrically tunable platform for HHG.

cond-mat.mes-hall↗

arXiv2016

Shaping, imaging and controlling plasmonic interference fields at buried interfaces

Filming and controlling plasmons at buried interfaces with nanometer (nm) and femtosecond (fs) resolution has yet to be achieved and is critical for next generation plasmonic/electronic devices. In this work, we use light to excite and shape a plasmonic interference pattern at a buried metal-dielectric interface in a nanostructured thin film. Plasmons are launched from a photoexcited array of nanocavities and their propagation is filmed via photon-induced near-field electron microscopy (PINEM). The resulting movie directly captures the plasmon dynamics, allowing quantification of their group velocity at approximately 0.3c, consistent with our theoretical predictions. Furthermore, we show that the light polarization and nanocavity design can be tailored to shape transient plasmonic gratings at the nanoscale. These results, demonstrating dynamical imaging with PINEM, pave the way for the fs/nm visualization and control of plasmonic fields in advanced heterostructures based on novel 2D materials such as graphene, MoS$_2$, and ultrathin metal films.

cond-mat.mes-hall↗

arXiv2016

Phonon-mediated mid-infrared photoresponse of graphene

The photoresponse of graphene at mid-infrared frequencies is of high technological interest and is governed by fundamentally different underlying physics than the photoresponse at visible frequencies, as the energy of the photons and substrate phonons involved have comparable energies. Here we perform a spectrally resolved study of the graphene photoresponse for mid-infrared light by measuring spatially resolved photocurrent over a broad frequency range (1000-1600 cm$^{-1}$). We unveil the different mechanisms that give rise to photocurrent generation in graphene on a polar substrate. In particular, we find an enhancement of the photoresponse when the light excites bulk or surface phonons of the SiO$_2$ substrate. This work paves the way for the development of graphene-based mid-infrared thermal sensing technology.

cond-mat.mes-hall↗

arXiv2015

Graphene random laser

Manipulating and controlling the optical energy flow inside random media is a research frontier of photonics and the basis of novel laser designs. In particular, light amplification in randomly dispersed active inclusions under external pumping has been extensively investigated, although it still lacks external tunability, reproducibility, and control over the beam spatial pattern, thus hindering its application in practical devices. Here we show that a graphene random metamaterial provides the means to overcome these limitations through its extraordinarily-low threshold for saturable absorption. The nonlinear properties of nano-graphene combined with an optically pumped gain medium allow us to controllably tune the system from chaotic to stable single-mode lasing. Our results hold great potential for the development of single-mode cavity-free lasers with engineered beam patterns in disordered media.

physics.optics↗

arXiv2015

Ultrafast broadband tuning of resonant optical nanostructures using phase change materials

The functionalities of a wide range of optical and opto-electronic devices are based on resonance effects and active tuning of the amplitude and wavelength response is often essential. Plasmonic nanostructures are an efficient way to create optical resonances, a prominent example is the extraordinary optical transmission (EOT) through arrays of nanoholes patterned in a metallic film. Tuning of resonances by heating, applying electrical or optical signals has proven to be more elusive, due to the lack of materials that can induce modulation over a broad spectral range and/or at high speeds. Here we show that nanopatterned metals combined with phase change materials (PCMs) can overcome this limitation due to the large change in optical constants which can be induced thermally or on an ultrafast timescale. We demonstrate resonance wavelength shifts as large as 385 nm - an order of magnitude higher than previously reported - by combining properly designed Au EOT nanostructures with Ge2Sb2Te5 (GST). Moreover, we show, through pump probe measurements, repeatable and reversible, large amplitude modulations in the resonances, especially at telecommunication wavelengths, over ps time scales and at powers far below those needed to produce a permanent phase transition. Our findings open a pathway to the design of hybrid metal PCM nanostructures with ultrafast and widely tuneable resonance responses, which hold potential impact on active nanophotonic devices such as tuneable optical filters, smart windows, biosensors and reconfigurable memories.

physics.optics↗

arXiv2015

Second-order quantum nonlinear optical processes in single graphene nanostructures and arrays

Intense efforts have been made in recent years to realize nonlinear optical interactions at the single-photon level. Much of this work has focused on achieving strong third-order nonlinearities, such as by using single atoms or other quantum emitters while the possibility of achieving strong second-order nonlinearities remains unexplored. Here, we describe a novel technique to realize such nonlinearities using graphene, exploiting the strong per-photon fields associated with tightly confined graphene plasmons in combination with spatially nonlocal nonlinear optical interactions. We show that in properly designed graphene nanostructures, these conditions enable extremely strong internal down-conversion between a single quantized plasmon and an entangled plasmon pair, or the reverse process of second harmonic generation. A separate issue is how such strong internal nonlinearities can be observed, given the nominally weak coupling between these plasmon resonances and free-space radiative fields. On one hand, by using the collective coupling to radiation of nanostructure arrays, we show that the internal nonlinearities can manifest themselves as efficient frequency conversion of radiative fields at extremely low input powers. On the other hand, the development of techniques to efficiently couple to single nanostructures would allow these nonlinear processes to occur at the level of single input photons.

cond-mat.mes-hall↗

arXiv2015

Mid-Infrared Plasmonic Biosensing with Graphene

Infrared spectroscopy is the technique of choice for chemical identification of biomolecules through their vibrational fingerprints. However, infrared light interacts poorly with nanometric size molecules. Here, we exploit the unique electro-optical properties of graphene to demonstrate a high-sensitivity tunable plasmonic biosensor for chemically-specific label-free detection of protein monolayers. The plasmon resonance of nanostructured graphene is dynamically tuned to selectively probe the protein at different frequencies and extract its complex refractive index. Additionally, the extreme spatial light confinement in graphene, up to two orders of magnitude higher than in metals, produces an unprecedentedly high overlap with nanometric biomolecules, enabling superior sensitivity in the detection of their refractive index and vibrational fingerprints. The combination of tunable spectral selectivity and enhanced sensitivity of graphene opens exciting prospects for biosensing.

physics.optics↗

arXiv2014

Graphene optical-to-thermal converter

Infrared plasmons in doped graphene nanostructures produce large optical absorption that can be used for narrow-band thermal light emission at tunable frequencies that strongly depend on the doping charge. By virtue of Kirchhoff's law, thermal light emission is proportional to the absorption, thus resulting in narrow emission lines associated with the electrically controlled plasmons of heated graphene. Here we show that realistic designs of graphene plasmonic structures can release over 90% of the emission through individual infrared lines with 1% bandwidth. We examine anisotropic graphene structures in which efficient heating can be produced upon optical pumping tuned to a plasmonic absorption resonance situated in the blue region relative to the thermal emission. An incoherent thermal light converter is thus achieved. Our results open a radically different approach for designing tunable nanoscale infrared light sources.

cond-mat.mes-hall↗

arXiv2014

Fast optical modulation of the fluorescence from a single NV centre

The much sought after optical transistor --the photonic counterpart of the electronic transistor-- is poised to become a central ingredient in the development of optical signal processing. The motivation for using photons rather than electrons not only comes from their faster dynamics but also from their lower crosstalk and minor environmental decoherence, which enable a high degree of integration and the realization of quantum operations. A single-molecule transistor has been recently demonstrated at cryogenic temperatures. Here, we demonstrate that a single NV centre at room temperature can operate as an optical switch under non-resonant CW illumination. We show optical modulation of more than 80% and time response faster than 100 ns in the green-laser-driven fluorescence signal, which we control through an independent near-infrared (NIR) gating laser. Our study indicates that the NIR laser triggers a fast-decay channel of the NV mediated by promotion of the excited state to a dark band. This simple concept opens a new approach towards the implementation of nanoscale optical switching devices.

physics.optics↗

arXiv2014

Extraordinary absorption of decorated undoped graphene

We theoretically study absorption by an undoped graphene layer decorated with arrays of small particles. We discuss periodic and random arrays within a common formalism, which predicts a maximum absorption of $50\%$ for suspended graphene in both cases. The limits of weak and strong scatterers are investigated and an unusual dependence on particle-graphene separation is found and explained in terms of the effective number of contributing evanescent diffraction orders of the array. Our results can be important to boost absorption by single layer graphene due to its simple setup with potential applications to light harvesting and photodetection based on energy (Förster) rather than charge transfer.

cond-mat.mes-hall↗

arXiv2013

Strong plasmon reflection at nanometer-size gaps in monolayer graphene on SiC

We employ tip-enhanced infrared near-field microscopy to study the plasmonic properties of epitaxial quasi-free-standing monolayer graphene on silicon carbide. The near-field images reveal propagating graphene plasmons, as well as a strong plasmon reflection at gaps in the graphene layer, which appear at the steps between the SiC terraces. When the step height is around 1.5 nm, which is two orders of magnitude smaller than the plasmon wavelength, the reflection signal reaches 20% of its value at graphene edges, and it approaches 50% for step heights as small as 5 nm. This intriguing observation is corroborated by numerical simulations, and explained by the accumulation of a line charge at the graphene termination. The associated electromagnetic fields at the graphene termination decay within a few nanometers, thus preventing efficient plasmon transmission across nanoscale gaps. Our work suggests that plasmon propagation in graphene-based circuits can be tailored using extremely compact nanostructures, such as ultra-narrow gaps. It also demonstrates that tip-enhanced near-field microscopy is a powerful contactless tool to examine nanoscale defects in graphene.

cond-mat.mes-hall↗

arXiv2012

Diffractive arrays of gold nanoparticles near an interface: critical role of the substrate

The optical properties of periodic arrays of plasmonic nanoantennas are strongly affected by coherent multiple scattering in the plane of the array, which leads to sharp spectral resonances in both transmission and reflection when the wavelength is commensurate with the period. We demonstrate that the presence of a substrate (i.e., an asymmetric refractive-index environment) can inhibit long-range coupling between the particles and suppress lattice resonances, in agreement with recent experimental results. We find the substrate-to-superstrate index contrast and the distance between the array and the interface to be critical parameters determining the strength of diffractive coupling. Our rigorous electromagnetic simulations are well reproduced by a simple analytical model. These findings are important in the design of periodic structures and in the assessment of their optical resonances for potential use in sensing and other photonic technologies.

physics.optics↗

arXiv2012

Rotational Quantum Friction

We investigate the frictional forces due to quantum fluctuations acting on a small sphere rotating near a surface. At zero temperature, we find the frictional force near a surface to be several orders of magnitude larger than that for the sphere rotating in vacuum. For metallic materials with typical conductivity, quantum friction is maximized by matching the frequency of rotation with the conductivity. Materials with poor conductivity are favored to obtain large quantum frictions. For semiconductor materials that are able to support surface plasmon polaritons, quantum friction can be further enhanced by several orders of magnitude due to the excitation of surface plasmon polaritons.

cond-mat.mtrl-sci↗