Ultrasensitive terahertz metamaterial sensor based on vertical split ring resonators

An ultrasensitive metamaterial sensor based on double-slot vertical split ring resonators(DVSRRs) is designed and numerically calculated in the terahertz frequency. This DVSRR design produces a fundament LC resonance with a quality factor of about 20 when the incidence magnetic field component normal to the DVSRR array. The resonant characteristics and sensing performance of the DVSRR array design are systematically analyzed employing a contrast method among three similar vertical split ring resonator(SRRs) structures. The research results show that the elimination of bianisotropy, induced by the structural symmetry of the DVSRR design, helps to achieve LC resonance of a high quality factor. Lifting the SRRs up from the substrate sharply reduces the dielectric loss introduced by the substrate. All these factors jointly result in superior sensitivity of the DVSRR to the attributes of analytes. The maximum refractive index sensitivity is 788 GHz/RIU or 1.04 × 10~5 nm∕RIU.Also, the DVSRR sensor maintains its superior sensing performance for fabrication tolerance ranging from -4% to 4% and wide range incidence angles up to 50° under both TE and TM illuminations.

9.4 nm Tunable Vertically Coupled Microring Resonator Filter by Thermo-Optic Effect

A wide range (9.4nm) tuning of vertically coupled microring resonator filter was demonstrated utilizing a large TO coefficient of polymer. The power consumption was about 60m W and no degradation of filter response was observed.

Vertically Coupled Microring Resonator Filter :Versatile Building Block for VLSI Filter Circuits

In this review, the recent progress in the development of vertically coupled micro-ring resonator filters is summarized and the potential applications of the filters leading to the development of VLSI photonics are described.

Substituent Effect on N-Benzylideneanilines by DFT Energy Partition

To investigate the substituent effect on x-electron delocalization of the N-benzylideneaniline （NBA）, the vertical resonance energies △E^V（θ） of eleven substituted NBAs were separated into n and a parts at the B3LYP/6-311G（d） level of the Density Functional Theory （DFT）. When substituted with an electron-releasing group --OH, the calculated △E^V（θ） of NBA was increased, indicative of more resonance destabilization than the mother molecule. However, when substituted with an electron-withdrawing group -NO2, the calculated △E^V（θ） values indicated less resonance destabilization. The most destabilizing effect was observed especially when the -OH group located at the ortho-position of the aromatic ring in the fragment -N=CH-Ar. For most of the substituted NBA molecules, it was the destabilized a framework that determined the destabilizing feature of the vertical resonance energy, instead of the stabilized n system. When the -NO2 substituent at the para-position of the aromatic ring of the -N=CH-Ar group, the π system had the highest stabilizing effect while the σ framework exhibited the highest destabilizing effect. While the -NO2 substituent was at the para-position of the left aromatic ring （At-）, the NBA had the least vertical resonance energy value.