Doping-Induced Second-Harmonic Generation in Centrosymmetric Graphene from Quadrupole Response.

For centrosymmetric materials such as monolayer graphene, no optical second-harmonic generation (SHG) is generally expected, because it is forbidden under the electric-dipole approximation. Yet we observe a strong, doping-induced SHG from graphene, with its highest strength comparable to the electric-dipole-allowed SHG in noncentrosymmetric 2D materials. This novel SHG has the nature of an electric-quadrupole response, arising from the effective breaking of inversion symmetry by optical dressing with an in-plane photon wave vector. More remarkably, the SHG is widely tuned by carrier doping or chemical potential, being sharply enhanced at Fermi-edge resonances but vanishing at the charge neutral point that manifests the electron-hole symmetry of massless Dirac fermions. This striking behavior in graphene, which should also arise in graphenelike Dirac materials, expands the scope of nonlinear optics and holds the promise of novel optoelectronic and photonic applications.

Coherent control of ballistic photocurrents in multilayer epitaxial graphene using quantum interference.

We report generation of ballistic electric currents in unbiased epitaxial graphene at 300 K via quantum interference between phase-controlled cross-polarized fundamental and second harmonic 220 fs pulses. The transient currents are detected via the emitted terahertz radiation. Because of graphene's special structure symmetry, the injected current direction can be well controlled by the polarization of the pump beam in epitaxial graphene. This all optical injection of current provides not only a noncontact way of injecting directional current in graphene but also new insight into optical and transport process in epitaxial graphene.

Nanoscale porous silicon waveguide for label-free DNA sensing.

Porous silicon (PSi) is an excellent material for biosensing due to its large surface area and its capability for molecular size selectivity. In this work, we report the experimental demonstration of a label-free nanoscale PSi resonant waveguide biosensor. The PSi waveguide consists of pores with an average diameter of 20nm. DNA is attached inside the pores using standard amino-silane and glutaraldehyde chemistry. Molecular binding in the PSi is detected optically based on a shift of the waveguide resonance angle. The magnitude of the resonance shift is directly related to the quantity of biomolecules attached to the pore walls. The PSi waveguide sensor can selectively discriminate between complementary and non-complementary DNA. The advantages of the PSi waveguide biosensor include strong field confinement and a sharp resonance feature, which allow for high sensitivity measurements with a low detection limit. Simulations indicate that the sensor has a detection limit of 50nM DNA concentration or equivalently, 5pg/mm2.