No Arabic abstract
Resonance diffraction in the periodic array of graphene micro-ribbons is theoretically studied following a recent experiment [L. Ju et al, Nature Nanotech. 6, 630 (2011)]. Systematic studies over a wide range of parameters are presented. It is shown that a much richer resonant picture would be observable for higher relaxation times of charge carriers: more resonances appear and transmission can be totally suppressed. The comparison with the absorption cross-section of a single ribbon shows that the resonant features of the periodic array are associated with leaky plasmonic modes. The longest-wavelength resonance provides the highest visibility of the transmission dip and has the strongest spectral shift and broadening with respect to the single-ribbon resonance, due to collective effects.
We show that a graphene sheet perforated with micro- or nano-size antidots have prominent absorption resonances in the microwave and terahertz regions. These resonances correspond to surface plasmons of a continuous sheet perturbed by a lattice. They are excited in different diffraction orders, in contrast to cavity surface plasmon modes existing in disconnected graphene structures. The resonant absorption by the antidot array can essentially exceed the absorption by a continuous graphene sheet, even for high antidot diameter-to-period aspect ratios. Surface plasmon-enhanced absorption and suppressed transmission is more efficient for higher relaxation times of the charge carriers.
We show that graphene possesses a strong nonlinear optical response in the form of multi-plasmon absorption, with exciting implications in classical and quantum nonlinear optics. Specifically, we predict that graphene nano-ribbons can be used as saturable absorbers with low saturation intensity in the far-infrared and terahertz spectrum. Moreover, we predict that two-plasmon absorption and extreme localization of plasmon fields in graphene nano-disks can lead to a plasmon blockade effect, in which a single quantized plasmon strongly suppresses the possibility of exciting a second plasmon.
Surface plasmon modes supported by graphene ribbon waveguides are studied and classified. The properties of both modes with the field concentration within the ribbon area (waveguiding modes) and on the edges (edge modes) are discussed. The waveguide and edge modes are shown to be separated from each other by a gap in wavenumbers. The even-parity hybridized edge mode results to be the fundamental electromagnetic mode of the ribbon, possessing also the lowest losses. All the plasmonic modes in the ribbons have an optimum frequency, at which the absorption losses are minimum, due to competition between the plasmon confinement and the frequency dependence of absorption in graphene.
When light is absorbed by a semiconductor, photoexcited charge carriers enhance the absorption of far-infrared radiation due to intraband transitions. We observe the opposite behavior in monolayer graphene, a zero-gap semiconductor with linear dispersion. By using time domain terahertz (THz) spectroscopy in conjunction with optical pump excitation, we observe a reduced absorption of THz radiation in photoexcited graphene. The measured spectral shape of the differential optical conductivity exhibits non-Drude behavior. We discuss several possible mechanisms that contribute to the observed low-frequency non-equilibrium optical response of graphene.
Plasmon and coupled plasmon-phonon modes in graphene are investigated the-oretically within the diagrammatic self-consistent field theory. It shows that two plasmon modes and four coupled plasmon-phonon modes can be excited via intra-and inter-band transition channels. It is found that with increasing q and carrier density, the plasmon modes couple strongly with the optic-phonon modes in graphene. The coupled plasmon-phonon modes exhibit some interesting features which can be utilized to realize the plasmonic devices. Our results suggest that the carrier-phonon interaction should be considered to understand and explain the properties of elementary electronic excitations in graphene.