Search

One of the most captivating properties of polaritons is their capacity to confine light at the nanoscale. This confinement is even more extreme in two-dimensional (2D) materials. 2D polaritons have been investigated by optical measurements using an external photodetector. However, their effective spectrally resolved electrical detection via far-field excitation remains unexplored. This fact hinders their potential exploitation in crucial applications such as sensing molecules and gases, hyperspectral imaging and optical spectrometry, banking on their potential for integration with silicon technologies. Herein, we present the first electrical spectroscopy of polaritonic nanoresonators based on a high-quality 2D-material heterostructure, which serves at the same time as the photodetector and the polaritonic platform. We employ metallic nanorods to create hybrid nanoresonators within the hybrid plasmon-phonon polaritonic medium in the mid and long-wave infrared ranges. Subsequently, we electrically detect these resonators by near-field coupling to a graphene pn-junction. The nanoresonators simultaneously present a record of lateral confinement and high-quality factors of up to 200, exhibiting prominent peaks in the photocurrent spectrum, particularly at the underexplored lower reststrahlen band of hBN. We exploit the geometrical and gate tunability of these nanoresonators to investigate their impact on the photocurrent spectrum and the polaritonic's waveguided modes. This work opens a venue for studying this highly tunable and complex hybrid system, as well as for using it in compact platforms for sensing and photodetection applications., Comment: 34 pages, 4 main figures and 22 supplementary figures

Magnetized ferromagnetic disks or wires support strong inhomogeneous fields in their borders. Such magnetic fields create an effective potential, due to Zeeman and diamagnetic contributions, that can localize charge carriers. For the case of two-dimensional transition metal dichalcogenides, this potential can valley-localize excitons due to the Zeeman term, which breaks the valley symmetry. We show that the diamagnetic term is negligible when compared to the Zeeman term for monolayers of transition metal dichalcogenides. The latter is responsible for trapping excitons near the magnetized structure border with valley-dependent characteristics, in which, for one of the valleys, the exciton is confined inside the disk, while for the other, it is outside. This spatial valley separation of exciton can be probed by circularly polarized light, and moreover, we show that the inhomogeneous magnetic field magnitude, the dielectric environment, and the magnetized structure parameters can tailor the spatial separation of the exciton wavefunctions., Comment: 10 pages, 5 figures

We construct a one-dimensional (1D) topological SSH-like model with chiral symmetry and a superimposed hopping modulation, which we call the chiral Aubry-Andr\'e model. We show that its topological properties can be described in terms of a pair (C,W) of a two-dimensional (2D) Chern number C, stemming from a superspace description of the model, and a 1D winding number W, originating in its chiral symmetric nature. Thus, we showcase for the first time explicit coexistence of 1D and 2D topology in a model existing in 1D physical space. We detail the superspace description by showcasing how our model can be mapped to a Harper-Hofstadter model, familiar from the description of the integer quantum Hall effect, and analyze the vanishing field limit analytically. An extension of the method used for vanishing fields is provided in order to handle any finite fields, corresponding to hopping modulations both commensurate and incommensurate with the lattice. In addition, this formalism allows us to obtain certain features of the 2D superspace model, such as its number of massless Dirac nodes, purely in terms of topological quantities, computed without the need to go into momentum space.

We show that hexagonal boron nitride (hBN), a two-dimensional insulator, when subjected to an external superlattice potential forms a new paradigm for electrostatically tunable excitons in the near- and mid-ultraviolet (UV). The imposed potential has three consequences: (i) it renormalizes the effective mass tensor, leading to anisotropic effective masses; (ii) it renormalizes the band gap, eventually reducing it; (iii) it reduces the exciton binding energies. All these consequences depend on a single dimensionless parameter, which includes the product of strength of the external potential with its period. In addition to the excitonic energy levels, we compute the optical conductivity along two orthogonal directions, and from it the absorption spectrum. The results for the latter show that our system is able to mimic a grid polarizer. These characteristics make one-dimensional hBN superlattices a viable and unexplored platform for fine-tuned polaritonics in the UV to visible spectral range.

Beyond the extensively studied microcavity polaritons, which are coupled modes of semiconductor excitons and microcavity photons, nearly 2D semiconductors placed in a suitable environment can support spatially localized exciton-polariton modes. We demonstrate theoretically that two distinct types of such modes can exist in a photonic crystal with an embedded transition metal dichalcogenide (TMD) monolayer and derive an equation that determines their dispersion relations. The localized modes of two types occur in the zeroth- and first-order stop-bands of the crystal, respectively, and have substantially different properties. The latter type of the localized modes, which appear inside the light cone, can be described as a result of coupling of the TMD exciton and an optical Tamm state of the TMD-intercalated photonic crystal. We suggest an experiment for detecting these modes and simulate it numerically., Comment: 2021 Optica Publishing Group. One print or electronic copy may be made for personal use only. Systematic reproduction and distribution, duplication of any material in this paper for a fee or for commercial purposes, or modifications of the content of this paper are prohibited

The use of graphene in surface plasmon resonance sensors, covering a metallic (plasmonic) film, has a number of demonstrated advantages, such protecting the film against corrosion/oxidation and facilitating the introduction of functional groups for selective sensing. Recently, a number of works have claimed that few-layer graphene can also increase the sensitivity of the sensor. However, graphene was treated as an isotropic thin film, with an out-of-plane refractive index that is identical to the in-plane index. Here, we critically examine the role of single and few layers of graphene in the sensitivity enhancement of surface plasmon resonance sensors. Graphene is introduced over the metallic film via three different descriptions: as an atomic-thick two-dimensional sheet, as a thin effective isotropic material (same conductivity in the three coordinate directions), and as an non-isotropic layer (different conductivity in the perpendicular direction to the two-dimensional plane). We find that only the isotropic layer model, which is known to be incorrect for the optically modelling of graphene, provides sizeable sensitivity increases, while the other, more accurate, models lead to negligible contribution to the sensitivity.

Graphene plasmons have attracted significant attention due to their tunability, potentially long propagation lengths and ultracompact wavelengths. However, the latter characteristic imposes challenges to light-plasmon coupling in practical applications, generally requiring sophisticated coupling setups, extremely high doping levels and/or graphene nanostructuting close to the resolution limit of current lithography techniques. Here, we propose and theoretically demonstrate a method for alleviating such a technological strain through the use of a practical substrate whose low and negative dielectric function naturally enlarges the graphene polariton wavelength to more manageable levels. We consider silicon carbide (SiC), as it exhibits a dielectric function whose real part is between -1 and 0, while its imaginary part remains lower than 0.05, in the 951 to 970 cm$^{-1}$ mid-infrared spectral range. Our calculations show hybridization with the substrate's phonon polariton, resulting in a polariton wavelenth that is an order of magnitude longer than obtained with a silicon dioxide substrate, while the propagation length increases by the same amount.

The field of 2D materials-based nanophotonics has been growing at a rapid pace, triggered by the ability to design nanophotonic systems with in situ control, unprecedented degrees of freedom, and to build material heterostructures from bottom up with atomic precision. A wide palette of polaritonic classes have been identified, comprising ultra confined optical fields, even approaching characteristic length scales of a single atom. These advances have been a real boost for the emerging field of quantum nanophotonics, where the quantum mechanical nature of the electrons and-or polaritons and their interactions become relevant. Examples include, quantum nonlocal effects, ultrastrong light matter interactions, Cherenkov radiation, access to forbidden transitions, hydrodynamic effects, single plasmon nonlinearities, polaritonic quantization, topological effects etc. In addition to these intrinsic quantum nanophotonic phenomena, the 2D material system can also be used as a sensitive probe for the quantum properties of the material that carries the nanophotonics modes, or quantum materials in its vicinity. Here, polaritons act as a probe for otherwise invisible excitations, e.g. in superconductors, or as a new tool to monitor the existence of Berry curvature in topological materials and superlattice effects in twisted 2D materials., Comment: 27 pages, 7 figures

Graphene hybrids, made of thin insulators, graphene, and metals can support propagating acoustic plasmons (AGPs). The metal screening modifies the dispersion relation of usual graphene plasmons leading to slowly propagating plasmons, with record confinement of electromagnetic radiation. Here, we show that a graphene monolayer, covered by a thin dielectric material and an array of metallic nanorods can be used as a robust platform to emulate the Su-Schrieffer-Heeger model. We calculate the Zak's phase of the different plasmonic bands to characterise their topology. The system shows bulk-edge correspondence: strongly localized interface states are generated in the domain walls separating arrays in different topological phases. We find signatures of the nontrivial phase which can directly be probed by far-field mid-IR radiation, hence allowing a direct experimental confirmation of graphene topological plasmons. The robust field enhancement, highly localized nature of the interface states, and their gate-tuned frequencies expand the capabilities of AGP-based devices., Comment: 5 pages, 4 figures

Terahertz polarizers are essential for advanced spectroscopic systems but face challenges like low transmission, short bandwidths and low extinction ratios. This study demonstrates the development of ultrabroadband THz polarizers using nanoimprint lithography, achieving high performance through double-wire-grid polarizer (DWGP) structures on cyclic olefin copolymer (COC) substrates. Compared to silicon-based alternatives, the polymer DWGPs demonstrated over twice the TM-polarized transmittance across the 0.1 - 25 THz range. The degree of polarization exceeded 98% in a 0.1-16 THz range, with a maximum extinction ratio above 65.4 dB at 4.2 THz. Simultaneous characterization of materials using THz time-domain spectroscopy (THz-TDS) and Fourier-transform infrared spectroscopy (FTIR) covered extended frequency ranges of 0.1 - 40 THz and 0.9 - 20 THz, respectively. Nanofabricated polymer DWGP revealed the superior optical properties, including enhanced TM transmittance and reduced TE leakage when compared to Si DWGP. Additionally, the fabricated polymer polarizers showcased cost-effectiveness, scalability, and durability, offering a sustainable alternative to conventional Si-based polarizers. The significant developments demonstrated in this study position polymer-based DWGPs as significant components for THz imaging, sensing, and wireless communication systems, paving the way for next-generation technologies., Comment: 19 pages, 9 figures

2D materials support unique excitations of quasi-particles that consist of a material excitation and photons called polaritons. Especially interesting are in-plane propagating polaritons which can be confined to a single monolayer and carry large momentum. In this work, we report the existence of a new type of in-plane propagating polariton, supported on monolayer transition-metal-dicalcogonide (TMD) in the visible spectrum, which has not yet been observed. This 2D in-plane exciton-polariton (2DEP) is described by the coupling of an electromagnetic light field with the collective oscillations of the excitons supported by monolayer TMDs. We expose the specific experimental conditions required for the excitation of the 2DEP and show that these can be created if the TMD is encapsulated with hexagonal-boron-nitride (hBN) and cooled to cryogenic temperatures. In addition, we compare the properties of the 2DEPs with those of surface-plasmons-polaritons (SPPs) at the same spectral range, and find that the 2DEP exhibit over two orders-of-magnitude larger wavelength confinement. Finally, we propose two configurations for the possible experimental observation of 2DEPs.

We compute binding energies, Stark shifts, electric-field-induced dissociation rates, and the Franz-Keldysh effect for excitons in phosphorene in various dielectric surroundings. All three effects show a pronounced dependence on the direction of the in-plane electric field, with the dissociation rates in particular decreasing by several orders of magnitude upon rotating the electric field from the armchair to the zigzag axis. To better understand the numerical dissociation rates, we derive an analytical approximation to the anisotropic rates induced by weak electric fields, thereby generalizing the previously obtained result for isotropic two-dimensional semiconductors. This approximation is shown to be valid in the weak-field limit by comparing it to the exact rates. The anisotropy is also apparent in the large difference between armchair and zigzag components of the exciton polarizability tensor, which we compute for the five lowest lying states. As expected, we also find much more pronounced Stark shifts in either the armchair or zigzag direction, depending on the symmetry of the state in question. Finally, an isotropic interaction potential is shown to be an excellent approximation to a more accurate anisotropic interaction derived from the Poisson equation, confirming that the anisotropy of phosphorene is largely due to the direction dependence of the effective masses.

Plasmonic excitations such as surface-plasmon-polaritons (SPPs) and graphene-plasmons (GPs), carry large momenta and are thus able to confine electromagnetic fields to small dimensions. This property makes them ideal platforms for subwavelength optical control and manipulation at the nanoscale. The momenta of these plasmons are even further increased if a scheme of metal-insulator-metal and graphene-insulator-metal are used for SPPs and GPs, respectively. However, with such large momenta, their far-field excitation becomes challenging. In this work, we consider hybrids of graphene and metallic nanostructures and study the physical mechanisms behind the interaction of far-field light with the supported high momenta plasmon modes. While there are some similarities in the properties of GPs and SPPs, since both are of the plasmon-polariton type, their physical properties are also distinctly different. For GPs we find two different physical mechanism related to either GPs confined to isolated cavities, or large area collective grating couplers. Strikingly, we find that although the two systems are conceptually different, under specific conditions they can behave similarly. By applying the same study to SPPs, we find a different physical behavior, which fundamentally stems from the different dispersion relations of SPPs as compared to GPs. Furthermore, these hybrids produce large field enhancements that can also be electrically tuned and modulated making them the ideal candidates for a variety of plasmonic devices., Comment: 9 pages, 4 figures

Acoustic-graphene-plasmons (AGPs) are highly confined electromagnetic modes, carrying large momentum and low loss in the mid-infrared/Terahertz spectra. Owing to their ability to confine light to extremely small dimensions, they bear great potential for ultra-strong light-matter interactions in this long wavelength regime, where molecular fingerprints reside. However, until now AGPs have been restricted to micron-scale areas, reducing their confinement potential by several orders-of-magnitude. Here, by utilizing a new type of graphene-based magnetic-resonance, we realize single, nanometric-scale AGP cavities, reaching record-breaking mode-volume confinement factors of $\thicksim5\cdot10^{-10}$. This AGP cavity acts as a mid-infrared nanoantenna, which is efficiently excited from the far-field, and electrically tuneble over an ultra-broadband spectrum. Our approach provides a new platform for studying ultra-strong-coupling phenomena, such as chemical manipulation via vibrational-strong-coupling, and a path to efficient detectors and sensors, in this challenging spectral range.

We revisit the classical problem of electromagnetic wave refraction from a lossless dielectric to a lossy conductor, where both media are considered to be non-magnetic, linear, isotropic and homogeneous. We derive the Fresnel coefficients of the system and the Poynting vectors at the interface, in order to compute the reflectance and transmittance of the system. We use a particular parametrisation of the referred Fresnel coefficients so as to make a connection with the ones obtained for refraction by an interface between two lossless media. This analysis allows the discussion of an actual application, namely the Fresnel polarisation of infra-red radiation by elemental bismuth, based on the concept of pseudo Brewster's angle., Comment: Version accepted by The European Physical Journal B

We describe exciton-polariton modes formed by the interaction between excitons in a 2D layer of a transition metal dichalcogenide embedded in a cylindrical microcavity and the microcavity photons. For this, an expression for the excitonic susceptibility of a semiconductor disk placed in the symmetry plane perpendicular to the axis of the microcavity is derived. Semiclassical theory provides dispersion relations for the polariton modes, while the quantum-mechanical treatment of a simplified model yields the Hopfield coefficients, measuring the degree of exciton-photon mixing in the coupled modes. The density of states (DOS) and its projection onto the photonic and the excitonic subspaces are calculated taking monolayer MoS 2 embedded in a Si 3 N 4 cylinder as an example. The calculated results demonstrate a strong enhancement, for certain frequencies, of the total and local DOS (Purcell effect) caused by the presence of the 2D layer.

Excitons in monolayer transition-metal-dichalcogenides (TMDs) dominate their optical response and exhibit strong light-matter interactions with lifetime-limited emission. While various approaches have been applied to enhance light-exciton interactions in TMDs, the achieved strength have been far below unity, and a complete picture of its underlying physical mechanisms and fundamental limits has not been provided. Here, we introduce a TMD-based van der Waals heterostructure cavity that provides near-unity excitonic absorption, and emission of excitonic complexes that are observed at ultra-low excitation powers. Our results are in full agreement with a quantum theoretical framework introduced to describe the light-exciton-cavity interaction. We find that the subtle interplay between the radiative, non-radiative and dephasing decay rates plays a crucial role, and unveil a universal absorption law for excitons in 2D systems. This enhanced light-exciton interaction provides a platform for studying excitonic phase-transitions and quantum nonlinearities and enables new possibilities for 2D semiconductor-based optoelectronic devices.

In this paper we show that graphene surface plasmons can be excited when an electromagnetic wave packet impinges on a single metal slit covered with graphene. The excitation of the plasmons localized over the slit is revealed by characteristic peaks in the absorption spectrum. It is shown that the position of the peaks can be tuned either by the graphene doping level or by the dielectric function of the material filling the slit. The whole system forms the basis for a plasmonic sensor when the slit is filled with an analyte., Comment: 10 pages, 6 figures

The ability to confine light into tiny spatial dimensions is important for applications such as microscopy, sensing and nanoscale lasers. While plasmons offer an appealing avenue to confine light, Landau damping in metals imposes a trade-off between optical field confinement and losses. We show that a graphene-insulator-metal heterostructure can overcome that trade-off, and demonstrate plasmon confinement down to the ultimate limit of the lengthscale of one atom. This is achieved by far-field excitation of plasmon modes squeezed into an atomically thin hexagonal boron nitride dielectric h-BN spacer between graphene and metal rods. A theoretical model which takes into account the non-local optical response of both graphene and metal is used to describe the results. These ultra-confined plasmonic modes, addressed with far-field light excitation, enables a route to new regimes of ultra-strong light-matter interactions., Comment: 17 pages, 4 figures

We derive an integral equation describing surface-plasmon polaritons in graphene deposited on a substrate with a planar surface and a dielectric protrusion in the opposite surface of the dielectric slab. We show that the problem is mathematically equivalent to the solution of a Fredholm equation, which we solve exactly. In addition, we show that the dispersion relation of the localized surface plasmons is determined by the geometric parameters of the protrusion alone. We also show that such system supports both even and odd modes. We give the electrostatic potential and the stream plot of the electrostatic field, which clearly show the localized nature of the surface plasmons in a continuous and flat graphene sheet., Comment: 11 pages, 9 figures, Accepted for publication in Physical Review B

Exciton-polariton modes arising from interaction between bound excitons in monolayer thin semiconductor sheets and photons in a Fabry-Perot microcavity are considered theoretically. We calculate the dispersion curves, mode lifetimes, Rabi splitting, and Hopfield coefficients of these structures for two nearly 2D semiconductor materials, MoS2 and WS2, and suggest that they are interesting for studying the rich physics associated with the Bose-Einstein condensation of exciton-polaritons. The large exciton binding energy and dipole allowed exciton transitions, in addition to the relatively easily controllable distance between the semiconductor sheets are the advantages of this system in comparison with traditional GaAs or CdTe based semiconductor microcavities. In particular, in order to mimic the rich physical properties of the quantum degenerate mixture of two bosonic species of dilute atomic gases with tunable inter-species interaction , we put forward a structure containing two semiconductor sheets separated by some atomic-scale distance (l) using a nearly 2D dielectric (e.g. h-BN), which offers the possibility of tuning the interaction between two exciton-polariton Bose-Enstein condensates. We show that the dynamics of this novel structure are ruled by two coupled Gross-Pitaevskii equations with the coupling parameter proportional to 1/l.

We study nonlinear properties of multilayer metamaterials created by graphene sheets separated by dielectric layers. We demonstrate that such structures can support localized nonlinear modes described by the discrete nonlinear Schr\"{o}dinger equation and that its solutions are associated with stable discrete plasmon solitons. We also analyze the nonlinear surface modes in truncated graphene metamaterials being a nonlinear analog of surface Tamm states., Comment: 9 pages, 5 figures

The band structure and the optical conductivity of an ABA (Bernal-type) stacked graphene trilayer are calculated. It is shown that, under appropriate doping, a strong resonant peak develops in the optical conductivity, located at the frequency corresponding to approximately 1.4 times the interlayer hopping energy and caused by the 'nesting' of two nearly parabolic bands in the electronic spectrum. The intensity of this resonant absorption can be controlled by adjusting the gate voltage. The effect is robust with respect to increasing temperature.

The propagation of electromagnetic waves along the surface of a nonlinear dielectric covered by a graphene layer is investigated. The main result is that such a surface can support and stabilize nonlinear transverse electric (TE) plasmon polaritons. We demonstrated that these nonlinear TE modes have a subwavelength localization in the direction perpendicular to the surface, with the intensity much higher than that of the incident wave which excites the polariton., Comment: 6 pages, 5 figures

We study the interaction of electromagnetic (EM) radiation with single-layer graphene and a stack of parallel graphene sheets at arbitrary angles of incidence. It is found that the behavior is qualitatively different for transverse magnetic (or p-polarized) and transverse electric (or s-polarized) waves. In particular, the absorbance of single-layer graphene attains minimum (maximum) for p (s) polarization, at the angle of total internal reflection when the light comes from a medium with a higher dielectric constant. In the case of equal dielectric constants of the media above and beneath graphene, for grazing incidence graphene is almost 100% transparent to p-polarized waves and acts as a tunable mirror for the s-polarization. These effects are enhanced for the stack of graphene sheets, so the system can work as a broad band polarizer. It is shown further that a periodic stack of graphene layers has the properties of an one-dimensional photonic crystal, with gaps (or stop--bands) at certain frequencies. When an incident EM wave is reflected from this photonic crystal, the tunability of the graphene conductivity renders the possibility of controlling the gaps, and the structure can operate as a tunable spectral--selective mirror., Comment: 11 pages, 12 figures, accepted for Journal of Optics

We study graphene on a photonic crystal operating in the terahertz (THz) spectral range. We show that the absorption of graphene becomes a modulated function of frequency and can be enhanced by more than three times at specific frequency values, depending on the parameters of the system. The problem of a semi-infinite photonic crystal is also solved., Comment: 5 pages, 4 figures

It is shown that an attenuated total reflection structure containing a graphene layer can operate as a tunable polarizer of the electromagnetic radiation. The polarization angle is controlled by adjusting the voltage applied to graphene via external gate. The mechanism is based on the resonant coupling of $p-$polarized electromagnetic waves to the surface plasmon-polaritons in graphene. The presented calculations show that, at resonance, the reflected wave is almost 100% $s-$polarized., Comment: submitted to the Applied Physics Letters

It is shown that monolayer graphene deposited on a spatially-periodic gate behaves as a polaritonic crystal. Its band structure depending on the applied gate voltage is studied. The scattering of electromagnetic radiation from such a crystal is presented calculated and analyzed in terms of Fano-type resonances between the reflected continuum and plasmon-polariton modes forming narrow bands., Comment: submitted to Phys. Rev. Lett

We investigate the electronic properties of heterostructures based on ultrathin hexagonal boron nitride (h-BN) crystalline layers sandwiched between two layers of graphene as well as other conducting materials (graphite, gold). The tunnel conductance depends exponentially on the number of h-BN atomic layers, down to a monolayer thickness. Exponential behaviour of I-V characteristics for graphene/BN/graphene and graphite/BN/graphite devices is determined mainly by the changes in the density of states with bias voltage in the electrodes. Conductive atomic force microscopy scans across h-BN terraces of different thickness reveal a high level of uniformity in the tunnel current. Our results demonstrate that atomically thin h-BN acts as a defect-free dielectric with a high breakdown field; it offers great potential for applications in tunnel devices and in field-effect transistors with a high carrier density in the conducting channel., Comment: 7 pages, 5 figures

We perform a phenomenological analysis of the problem of the electronic doping of a graphene sheet by deposited transition metal atoms, which aggregate in clusters. The sample is placed in a capacitor device such that the electronic doping of graphene can be varied by the application of a gate voltage and such that transport measurements can be performed via the application of a (much smaller) voltage along the graphene sample, as reported in the work of Pi et al. [Phys. Rev. B 80, 075406 (2009)]. The analysis allows us to explain the thermodynamic properties of the device, such as the level of doping of graphene and the ionisation potential of the metal clusters in terms of the chemical interaction between graphene and the clusters. We are also able, by modelling the metallic clusters as perfect conducting spheres, to determine the scattering potential due to these clusters on the electronic carriers of graphene and hence the contribution of these clusters to the resistivity of the sample. The model presented is able to explain the measurements performed by Pi et al. on Pt-covered graphene samples at the lowest metallic coverages measured and we also present a theoretical argument based on the above model that explains why significant deviations from such a theory are observed at higher levels of coverage., Comment: 16 pages, 10 figures

We review the problem of adatoms in graphene under two complementary points of view, scattering theory and strong correlations. We show that in both cases impurity atoms on the graphene surface present effects that are absent in the physics of impurities in ordinary metals. We discuss how to observe these unusual effects with standard experimental probes such as scanning tunneling microscopes, and spin susceptibility., Comment: For the Proceedings of the "Graphene Week 2008" at the ICTP in Trieste, Italy. 8 pages, 8 figures

In this paper we study the charge and spin currents transported by the elementary excitations of the one-dimensional Hubbard model. The corresponding current spectra are obtained by both analytic methods and numerical solution of the Bethe-ansatz equations. For the case of half-filling, we find that the spin-triplet excitations carry spin but no charge, while charge $\eta$-spin triplet excitations carry charge but no spin, and both spin-singlet and charge $\eta$-spin-singlet excitations carry neither spin nor charge currents., Comment: 24 pages, 14 figures

We show that a generalized charge SU(2) symmetry of the one-dimensional (1D) Hubbard model in an infinitesimal flux $\phi$ generates half-filling states from metallic states which lead to a finite charge stiffness $D(T)$ at finite temperature $T$, whose $T$ dependence we study. Our results are of general nature for many integrable quantum lattice systems, reveal the microscopic mechanisms behind their exotic $T>0$ transport properties and the interplay with T=0 quantum-phase transitions, and contribute to the further understanding of the transport of charge in systems of interacting ultracold fermionic atoms in 1D optical lattices, quasi-1D compounds, and 1D nanostructures., Comment: 7 pages, 4 figures