Controlling directional emission of nanophotonic radiation sources is fundamental to tailor radiation-matter interaction and to conceive highly efficient nanophotonic devices for on-chip wireless communication and information processing. Nanoantennas coupled to quantum emitters have proven to be very efficient radiation routers, while electrical control of unidirectional emission has been achieved through inelastic tunneling of electrons. Here we prove that the radiation emitted from the interaction of a high-energy electron beam with a graphene-nanoparticle composite has beaming directions which can be made to continuously span the full circle even through small variations of the graphene Fermi energy. Emission directionality stems from the interference between the double cone shaped electron transition radiation and the nanoparticle dipolar diffraction radiation. Tunability is enabled since the interference is ruled by the nanoparticle dipole moment whose amplitude and phase are driven by the hybrid plasmonic resonances of the composite and the absolute phase of the graphene plasmonic polariton launched by the electron, respectively. The flexibility of our method provides a way to exploit graphene plasmon physics to conceive improved nanosources with ultrafast reconfigurable radiation patterns.
Ciattoni, Conti, Marini in https://arxiv.org/abs/2010.09017
With an exact recursive approach, we study photonic crystal fibers and resonators with topological features induced by Aubry–Andre–Harper cladding modulation. We find nontrivial gaps and edge states at the interface between regions with different topological invariants. These structures show topological protection against symmetry-preserving local perturbations that do not close the gap and sustain strong field localization and energy concentration at a given radial distance. As topological light guiding and trapping devices, they may bring about many opportunities for both fundamentals and applications unachievable with conventional devices.
Spin and angular momenta of light are important degrees of freedom in nanophotonics which control light propagation, optical forces and information encoding. Typically, optical angular momentum is generated using q-plates or spatial light modulators. Here, we show that graphene-supported plasmonic nanostructures with broken rotational symmetry provide a surprising spin to orbital angular momentum conversion, which can be continuously controlled by changing the electrochemical potential of graphene. Upon resonant illumination by a circularly polarized plane wave, a polygonal array of indium-tin-oxide nanoparticles on a graphene sheet generates scattered field carrying electrically-tunable orbital angular momentum. This unique photonic spin-orbit coupling occurs due to the strong coupling of graphene plasmon polaritons and localised surface plasmons of the nanoparticles and leads to the controlled directional excitation of graphene plasmons. The tuneable spin-orbit conversion pave the way to high-rate information encoding in optical communications, electric steering functionalities in optical tweezers, and nanorouting of higher-dimensional entangled photon states.
We show that quantum fluids enable experimental analogs of relativistic orbital precession in the presence of non-paraxial effects. The analysis is performed by the hydrodynamic limit of the Schroedinger equation. The non-commutating variables in the phase-space produce a precession and an acceleration of the orbital motion. The precession of the orbit is formally identical to the famous orbital precession of the perihelion of Mercury used by Einstein to validate the corrections of general relativity to Newton’s theory. In our case, the corrections are due to the modified uncertainty principle. The results may enable novel relativistic analogs in the laboratory, also including sub Planckian phenomenology.