No Arabic abstract
Recent advances in nanotechnology have created tremendous excitement across different disciplines but in order to fully control and manipulate nano-scale objects, we must understand the forces at work at the nano-scale, which can be very different from those that dominate the macro-scale. We show that there is a new kind of curvature-induced force that acts between nano-corrugated electrically neutral plasmonic surfaces. Absent in flat surfaces, such a force owes its existence entirely to geometric curvature, and originates from the kinetic energy associated with the electron density which tends to make the profile of the electron density smoother than that of the ionic background and hence induces curvature-induced local charges. Such a force cannot be found using standard classical electromagnetic approaches, and we use a self-consistent hydrodynamics model as well as first principles density functional calculations to explore the character of such forces. These two methods give qualitative similar results. We found that the force can be attractive or repulsive, depending on the details of the nano-corrugation, and its magnitude is comparable to light induced forces acting on plasmonic nano-objects.
Lateral Casimir force near a laterally-inhomogeneous plate is first revealed by both rigorous simulations and proximity approximations. The inhomogeneity-induced lateral Casimir force provides a novel method to control the lateral motion of nano-objects above the plate, and makes source-free manipulations of them possible. When incorporated with the Casimir repulsion in a fluid, the lateral Casimir force is shown to dominate over Brownian motion and enables long-distance quantum propulsion and firm quantum trapping of nano-objects. Gratings of varying filling factors to mimic micro-scale inhomogeneity also confirm those effects. The idea to design asymmetric distributions of nano-structures paves the way to sophisticated tailoring of the lateral Casimir force.
We study the effects of the structural corrugation or rippling on the electronic properties of undoped armchair graphene nanoribbons (AGNR). First, reanalyzing the single corrugated graphene layer we find that the two inequivalent Dirac points (DP), move away one from the other. Otherwise, the Fermi velocity decrease by increasing rippling. Regarding the AGNRs, whose metallic behavior depends on their width, we analyze in particular the case of the zero gap band-structure AGNRs. By solving the Dirac equation with the adequate boundary condition we show that due to the shifting of the DP a gap opens in the spectra. This gap scale with the square of the rate between the high and the wavelength of the deformation. We confirm this prediction by exact numerical solution of the finite width rippled AGNR. Moreover, we find that the quantum conductance, calculated by the non equilibrium Greens function technique vanish when the gap open. The main conclusion of our results is that a conductance gap should appear for all undoped corrugated AGNR independent of their width.
Electrically-driven optical antennas can serve as compact sources of electromagnetic radiation operating at optical frequencies. In the most widely explored configurations, the radiation is generated by electrons tunneling between metallic parts of the structure when a bias voltage is applied across the tunneling gap. Rather than relying on an inherently inefficient inelastic light emission in the gap, we suggest to use a ballistic nanoconstriction as the feed element of an optical antenna supporting plasmonic modes. We discuss the underlying mechanisms responsible for the optical emission, and show that with such a nanoscale contact, one can reach quantum efficiency orders of magnitude larger than with standard light-emitting tunneling structures.
Achieving fully tunable quantum confinement of excitons has been a long-standing goal in optoelectronics and quantum photonics. We demonstrate electrically controlled 1D quantum confinement of neutral excitons by means of a lateral p-i-n junction in a monolayer transition metal dichalcogenide semiconductor. Exciton trapping in the i-region occurs due to the dc Stark effect induced by in-plane electric fields. Remarkably, we observe a new confinement mechanism arising from the repulsive polaronic dressing of excitons by electrons and holes in the surrounding regions. The overall confinement potential leads to quantization of excitonic motion, which manifests in the emergence of multiple spectrally narrow, voltage-dependent resonances in reflectance and photoluminescence measurements. Additionally, the photoluminescence from confined excitonic states exhibits high degree of linear polarization, highlighting the 1D nature of quantum confinement. Electrically tunable quantum confined excitons may provide a scalable platform for arrays of identical single photon sources and constitute building blocks of strongly correlated photonic many-body systems.
We predict plasmonic mediated nucleation of pancake shaped resonant nano-cavities in metallic layers that are penetrable to laser fields. The underlying physics is that the cavity provides a narrow plasmonic resonance that maximizes its polarizability in an external field. The resonance yields a significant energy gain making the formation of such cavities highly favorable. Possible implications include nano-optics and generation of the dielectric bits in conductive films that underlie the existing optical recording phase change technology.