Long-range surface plasmon polariton （LRSPP） modes in an asymmetrical system, in which the thin metal film is sandwiched between a semi-infinite substrate and a high permittivity polymer film with a finite thickness, are theoret~ ically calculated and analyzed. Due to the high permittivity of the polymer film, at proper polymer film thicknesses, the index-matching condition of the dielectrics at both sides of the metal can be satisfied for supporting LRSPP modes, and the electromagnetic field above the metal can be localized well. It is found that these LRSPP modes have both long propagation lengths and subwavelength mode expansion above the metal at the optimal polymer film thickncsses. Furthermore, the requirements on the refractive index and the thickness of the polymer film to support LRSPP modes at the optimal thicknesses are found to be not critical.
With the development of nanotechnology,many new optical phenomena in nanoscale have been demonstrated.Through the coupling of optical waves and collective oscillations of free electrons in metallic nanostructures,surface plasmon polaritons can be excited accompanying a strong near field enhancement that decays in a subwavelength scale,which have potential applications in the surface-enhanced Raman scattering,biosensor,optical communication,solar cells,and nonlinear optical frequency mixing.In the present article,we review the Green's matrix method for solving the surface plasmon resonances and near field in arbitrarily shaped nanostructures and in binary metallic nanostructures.Using this method,we design the plasmonic nanostructures whose resonances are tunable from the visible to near-infrared,study the interplay of plasmon resonances,and propose a new way to control plasmonic resonances in binary metallic nanostructures.
Femtoscience offers a unique way to understand the dynamics in physics, chemistry and biology. This subject focuses on the process happening at femto-to pico-second time scale by femtosecond optical methods. Widely used in chemistry it reveals chemical reactions, including bond breaking, forming, and stretching, which happens at an ultrafast time scale. Femtoscience is also important in the biological system, for example, light harvesting system and vision system. Femtoscience in physics is also widely used, but it is not studied in this paper. Instead, we report new advances in femtochemistry and femtobiology, including structural dynamics, coherent control, enzyme function dynamics and hydration in the protein system. We also introduce attosecond science, focusing on electron dynamics at an extreme short time scale.
We present an experimental investigation of a filamentation-assisted fourth-order nonlinear optical process in KTP crystals pumped by intense 1.53 eV （807 nm） femtosecond laser pulses. Femtosecond light pulses at 2.58 eV （480 nm） are generated by the fourth-order nonlinear polarization （p（4） （ω2） = X（4） （ω2, ω, ω, ω, -ω1）E3 （ω）E＊ （ω1）, where E（w） corresponds to the pump frequency and E（wl） to the supercontinuum generated through filamentation）. If the system is seeded by a laser beam at ω1 or ω2 and there are spatial and temporal overlaps with the pump beam, E（ω1） and E（ω2） are simultaneously amplified. When the intensity of the seed laser beam exceeds a certain intensity threshold, the contribution of p（4） （ω） = X（4） （ω, ω1, ω2, -ω, -ω）E（ω1）E（ω2）（E＊ （ω））2 becomes non-negligible, and the amplification weakens. The conversion efficiency from the pump to the signal at 2.58 eV （480 nm） attains to 0.1%.
Through theoretical analysis,we show how aligning pulse durations affect the degree and the time-rate slope of nitrogen field-free alignment at a fixed pulse intensity.It is found that both the degree and the slope first increase,then saturate,and finally decrease with the increasing pump duration.The optimal durations for the maximum degree and the maximum slope of the alignment are found to be different.Additionally,they are found to mainly depend on the molecular rotational period,and are affected by the temperature and the aligning pump intensities.The mechanism of molecular alignment is also discussed.
