9 research outputs found

    Spin-Orbit Dirac Fermions in 2D Systems

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    We propose a novel model for including spin-orbit interactions in buckled two dimensional systems. Our results show that in such systems, intrinsic spin-orbit coupling leads to a formation of Dirac cones, similar to Rashba model. We explore the microscopic origins of this behaviour and confirm our results using DFT calculations

    Electronic properties of low-dimensional systems

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    This work deals with transport and general electronic phenomena in low-dimensional systems. The first chapter is dedicated to Variable Range Hopping. It starts with a brief review of the general hopping formalism, based on previous work. Next, new methods and results are presented and discussed. In particular, studies of both Ohmic and non-Ohmic regime are performed and the stark differences between the two are elucidated. In addition, apparent power law dependence of current on voltage in disordered one-dimensional materials is analyzed. The results obtained compare favorably with the experiments. Finally, the behavior of the conducting network in d dimensions is discussed using the percolation approach. The second chapter deals with plasmonic effects in graphene. After giving a short introduction to graphene and plasmonic behavior, current work is presented. Charge oscillations in graphene half-plane are discussed and compared with experimental results obtained from near-field microscopy. In addition, plasmonic oscillations in a "narrow-flake" geometry are analyzed analytically and numerically, showing good agreement between the two method

    Colossal Ultraviolet Photoresponsivity of Few-Layer Black Phosphorus

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    Black phosphorus has an orthorhombic layered structure with a layer-dependent direct band gap from monolayer to bulk, making this material an emerging material for photodetection. Inspired by this and the recent excitement over this material, we studied the optoelectronics characteristics of high-quality, few-layer black phosphorus-based photodetectors over a wide spectrum ranging from near-ultraviolet (UV) to near-infrared (NIR). It is demonstrated for the first time that black phosphorus can be configured as an excellent UV photodetector with a specific detectivity ∼3 × 10<sup>13</sup> Jones. More critically, we found that the UV photoresponsivity can be significantly enhanced to ∼9 × 10<sup>4</sup> A W<sup>–1</sup> by applying a source-drain bias (<i>V</i><sub>SD</sub>) of 3 V, which is the highest ever measured in any 2D material and 10<sup>7</sup> times higher than the previously reported value for black phosphorus. We attribute such a colossal UV photoresponsivity to the resonant-interband transition between two specially nested valence and conduction bands. These nested bands provide an unusually high density of states for highly efficient UV absorption due to the singularity of their nature

    Tuning and Persistent Switching of Graphene Plasmons on a Ferroelectric Substrate

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    We characterized plasmon propagation in graphene on thin films of the high-κ dielectric PbZr<sub>0.3</sub>Ti<sub>0.7</sub>O<sub>3</sub> (PZT). Significant modulation (up to ±75%) of the plasmon wavelength was achieved with application of ultrasmall voltages (< ±1 V) across PZT. Analysis of the observed plasmonic fringes at the graphene edge indicates that carriers in graphene on PZT behave as noninteracting Dirac Fermions approximated by a semiclassical Drude response, which may be attributed to strong dielectric screening at the graphene/PZT interface. Additionally, significant plasmon scattering occurs at the grain boundaries of PZT from topographic and/or polarization induced graphene conductivity variation in the interior of graphene, reducing the overall plasmon propagation length. Lastly, through application of 2 V across PZT, we demonstrate the capability to persistently modify the plasmonic response of graphene through transient voltage application

    Ultrafast and Nanoscale Plasmonic Phenomena in Exfoliated Graphene Revealed by Infrared Pump–Probe Nanoscopy

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    Pump–probe spectroscopy is central for exploring ultrafast dynamics of fundamental excitations, collective modes, and energy transfer processes. Typically carried out using conventional diffraction-limited optics, pump–probe experiments inherently average over local chemical, compositional, and electronic inhomogeneities. Here, we circumvent this deficiency and introduce pump–probe infrared spectroscopy with ∼20 nm spatial resolution, far below the diffraction limit, which is accomplished using a scattering scanning near-field optical microscope (s-SNOM). This technique allows us to investigate exfoliated graphene single-layers on SiO<sub>2</sub> at technologically significant mid-infrared (MIR) frequencies where the local optical conductivity becomes experimentally accessible through the excitation of surface plasmons via the s-SNOM tip. Optical pumping at near-infrared (NIR) frequencies prompts distinct changes in the plasmonic behavior on 200 fs time scales. The origin of the pump-induced, enhanced plasmonic response is identified as an increase in the effective electron temperature up to several thousand Kelvin, as deduced directly from the Drude weight associated with the plasmonic resonances
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