A tunable infrared plasmonic polarization filter with asymmetrical cross resonator

A tunable infrared plasmonic polarization filter is proposed and investigated in this paper. The filter is based on the sandwich absorption structure which consists of three layers. The top layer is an array of asymmetrical cross resonator. The middle and bottom layers are dielectric spacer and metal film respectively. By absorbing specific wavelength of the incident light perfectly, the reflection spectrum of the structure shows filter performance. The calculated results show that the absorption wavelength is strongly dependent on the length of branch of the asymmetrical cross resonator which is parallel to the light polarization and independent of the length of the vertical one. Therefore, the asymmetrical cross resonator filter structure opens the way for freely tuning the filtering wavelength for a different light polarization. We can fix a resonant wavelength （absorption wavelength） corresponding to one polarization and change the resonant wavelength for the other polarization by adjusting the corresponding branch length of the asymmetrical cross resonator, or change the two resonant wavelengths of both two polarizations at the same time.

Differential cross sections of positron-hydrogen collisions

We make a detailed study on the angular differential cross sections of positron–hydrogen collisions by using the momentum-space coupled-channels optical（CCO） method for incident energies below the H ionization threshold. The target continuum and the positronium（Ps） formation channels are included in the coupled-channels calculations via a complex equivalent-local optical potential. The critical points, which show minima in the differential cross sections, as a function of the scattering angle and the incident energy are investigated. The resonances in the angular differential cross sections are reported for the first time in this energy range. The effects of the target continuum and the Ps formation channels on the different cross sections are discussed.

Nitrogen Forms of Maillard Polymers Derived from Xylose and ^(15)N-Labelled Glycine

Water-soluble, nondialyzable Maillard polymers were prepared by reacting D-xylose with 15N-glycine (and/or glycine) at 68 ℃ and pH 8.0 at equimolar concentrations of 1, 0.5 and 0.1 mol L-1, respectively,for 13 days and partitioned into acid-insoluble (MHA) and acid-soluble (MFA) fractions. The nitrogen forms in these polymers were studied by using the 15N cross polarization-magic angle spinning nuclear magnetic resonance (CPMAS NMR) technique in combination with chemical methods. The 15N nuclear magnetic resonance (NMR) data showed that while the yield, especially the MHA/MFA ratio, varied considerably with the concentrations of the reactants, the nitrogen distribution patterns of these polymers were quite similar.From 65% to 70% of nitrogen in them was in the secondary amide and/or indole form with 24%~25% present as aliphatic and/or aromatic ammes and 5% to 11% as pyrrole and/or pyrrole-like nitrogen. More than half (50%~77%) of the N in these polymers were nonhydrolyzable. The role of Maillard reaction in the formation of nonhydrolyzable nitrogen in soil organic matter is discussed.

Improvement of the chirality near avoided resonance crossing in optical microcavity

Chirality is one of the important phenomena at the vicinity of exceptional point(EP). The conventional understanding is that the chirality is determined by asymmetrical scattering efficiency(?), which reaches to zero only when the resonance approaches EP. Here we study the possibility to enhance the chirality in open systems with a more robust mechanism. By combining chirality with avoided resonance crossing, we show that the chirality and ? can be dramatically modified. Taking a spiral shaped annular cavity as an example, we show that the chirality of optical resonances can be significantly improved when two sets of chiral states approach each other. The imbalance between counterclockwise(CCW) components and clockwise(CW) components has been enhanced by more than an order of magnitude. Our research provides a new route to tailor and control the chirality in open systems.

Complete crossing of Fano resonances in an optical microcavity via nonlinear tuning

We report on the modeling, simulation, and experimental demonstration of complete mode crossings of Fano resonances within chip-integrated microresonators. The continuous reshaping of resonant line shapes is achieved via nonlinear thermo-optical tuning when the cavity-coupled optical pump is partially absorbed by the material.The locally generated heat then produces a thermal field, which influences the spatially overlapping optical modes, allowing us to alter the relative spectral separation of resonances. Furthermore, we exploit such tunability to continuously probe the coupling between different families of quasi-degenerate modes that exhibit asymmetric Fano interactions. As a particular case, we demonstrate a complete disappearance of one of the modal features in the transmission spectrum as predicted by Fano [Phys. Rev. 124, 1866(1961)]. The phenomenon is modeled as a third-order nonlinearity with a spatial distribution that depends on the stored optical field and thermal diffusion within the resonator. The performed nonlinear numerical simulations are in excellent agreement with the experimental results, which confirm the validity of the developed theory.