Modulation of Main Lobe for Superfocusing Using Subwavelength Metallic Heterostructures

A subwavelength metallic heterostructure is put forth for the purpose of suppressing sidelobes and improving superfocusing at a quasi-far field region. Improvement has been made by means of optimization of the heterostructure composed of structured Au and Ag thin films. By tuning thicknesses of both the structured Au and Ag films, we can modulate propagation distance of the plasmonic lens and beam width of main lobe for the superfocusing. A finite-difference and time-domain (FDTD) algorithm-based computational numerical calculation was carried out for analyzing the focusing performance and tuning ability of the metal films. Our computational calculation results show that the sidelobes which play negative role for the focusing can be suppressed significantly in the case of the metal film thicknesses of h _Au = 50 nm and h _Ag = 10 nm. Theoretically, the metallic structure with smaller thicknesses of the structured Au and Ag films is helpful for improving the focusing performance. This heterostructure-based device is possible to be used as a superlens or nanoprobe in data storage, nanometrology/inspection, and biosensing etc.     

Tuning Plasmonic Properties of Truncated Gold Nanospheres by Coating

The influence of TiO₂ coating on resonant properties of gold nanoisland films deposited on silica substrates was studied numerically and in experiments. The model describing plasmonic properties of a metal truncated nanosphere placed on a substrate and covered by a thin dielectric layer has been developed. The model allows calculating a particle polarizability spectrum and, respectively, its surface plasmon resonance (SPR) wavelength for any given cover thickness, particle radius and truncation parameter, and dielectric functions of the particle, the substrate, the coating layer, and the surrounding medium. Dependence of the SPR position calculated for truncated gold nanospheres has coincided with the measured one for the gold nanoisland films covered with titania of different thicknesses. In the experiments, gold films with thickness of 5 nm were deposited on a silica glass substrate, annealed at 500 °C to form nanoislands of 20 nm in diameter, and covered with amorphous titania layers using atomic layer deposition technique. The resulting structures were characterized with scanning electron microscopy and optical absorption spectroscopy. The measured dependence of the SPR position on titania film thickness corresponded to the one calculated for truncated sphere-shaped nanoparticles with the truncation angle of ~50°. We demonstrated the possibility of tuning the SPR position within ~100 nm range by depositing to 30 nm thick titania layer.

     

Behavior of Freezable Bound Water in the Bacterial Cellulose Produced by Acetobacter xylinum: An Approach Using Thermoporosimetry

The aim of the study is to examine thermal behavior of water within reticulated structure of bacterial cellulose (BC) films by sub-ambient differential scanning calorimetry (DSC). BC films with different carbon source, either manitol (BC (a)) or glycerol (BC (b)), were produced by Acetobacter xylinum using Hestrin and Shramm culture medium under static condition at 30 ± 0.2°C for 3 days. BC samples were characterized by electron scanning microscopy and X-ray diffraction spectroscopy. The pore analysis was done by B.H.J. nitrogen adsorption. The pre-treated with 100% relative humidity, at 30.0 ± 0.2°C for 7 days samples were subjected to a between 25 and −150°C-cooling–heating cycle of DSC at 5.00°C/min rate. The pre-treated samples were also hydrated by adding 1 μl of water and thermally run with identical conditions. It is observed that cellulose fibrils of BC (a) were thinner and reticulated to form slightly smaller porosity than those of BC (b). They exhibited slightly but non-significantly different crystalline features. The freezable bound water behaved as a water confinement within pores rather than a solvent of polymer which is possible to use thermoporosimetry based on Gibb–Thomson equation to approach pore structure of BC. In comparison with nitrogen adsorption, it was found that thermoporosimetry underestimated the BC porosity, i.e., the mean diameters of 23.0 nm vs. 27.8 nm and 27.9 nm vs. 33.9 nm for BC (a) and BC (b), respectively, by thermoporosimetry vs. B.H.J. nitrogen adsorption. It may be due to large non-freezable water fraction interacting with cellulose, and the validity of pore range based on thermodynamic assumptions of Gibb–Thomson theory.     

Heterologous expression of polyhydroxyalkanoate depolymerase from <Emphasis Type="Italic">Thermobifida</Emphasis> sp. in <Emphasis Type="Italic">Pichia pastoris</Emphasis> and catalytic analysis by surface plasmon resonance

A polyhydroxyalkanote depolymerase gene from Thermobifida sp. isolate BCC23166 was cloned and expressed as a C-terminal His₆-tagged fusion in Pichia pastoris. Primary structure analysis revealed that the enzyme PhaZ-Th is a member of a proposed new subgroup of SCL-PHA depolymerase containing a proline–serine repeat linker. PhaZ-Th was expressed as two glycosylated forms with apparent molecular weights of 61 and 70 kDa, respectively. The enzyme showed esterase activity toward p-nitrophenyl alkanotes with V _max and K _m of 3.63 ± 0.16 μmol min⁻¹ mg⁻¹ and 0.79 ± 0.12 mM, respectively, on p-nitrophenyl butyrate with optimal activity at 50–55°C and pH 7–8. Surface plasmon resonance (SPR) analysis demonstrated that PhaZ-Th catalyzed the degradation of poly-[(R)-3-hydroxybutyrate] (PHB) films, which was accelerated in (R)-3-hydroxyvalerate copolymers with a maximum degradation rate of 882 ng cm⁻² h⁻¹ for poly[(R)-3-hydroxybutyrate-co-3-hydroxyvalerate] (12 mol% V). Surface deterioration, especially on the amorphous regions of PHB films was observed after exposure to PhaZ-Th by atomic force microscopy. The use of P. pastoris as an alternative recombinant system for bioplastic degrading enzymes in secreted form and a sensitive SPR analytical technique will be of utility for further study of bioplastic degradation.     

Investigating Fluorescence Quenching of ZnS Quantum Dots by Silver Nanoparticles

Water dispersible zinc sulfide quantum dots (ZnS QDs) with an average diameter of 2.9 nm were synthesized in an environment friendly method using chitosan as stabilizing agent. These nanocrystals displayed characteristic absorption and emission spectra having an absorbance edge at 300 nm and emission maxima (λ _emission) at 427 nm. Citrate-capped silver nanoparticles (Ag NPs) of ca. 37-nm diameter were prepared by modified Turkevich process. The fluorescence of ZnS QDs was significantly quenched in presence of Ag NPs in a concentration-dependent manner with K _sv value of 9 × 10⁹ M⁻¹. The quenching mechanism was analyzed using Stern–Volmer plot which indicated mixed nature of quenching. Static mechanism was evident from the formation of electrostatic complex between positively charged ZnS QDs and negatively charged Ag NPs as confirmed by absorbance study. Due to excellent overlap between ZnS QDs emission and surface plasmon resonance band of Ag NPs, the role of energy transfer process as an additional quenching mechanism was investigated by time-resolved fluorescence measurements. Time-correlated single-photon counting study demonstrated decrease in average lifetime of ZnS QDs fluorescence in presence of Ag NPs. The corresponding F?rster distance for the present QD–NP pair was calculated to be 18.4 nm.     

Generation of <Emphasis Type="Italic">Vibrio anguillarum</Emphasis> Ghost by Coexpression of PhiX 174 Lysis <Emphasis Type="Italic">E</Emphasis> gene and Staphylococcal Nuclease <Emphasis Type="Italic">A</Emphasis> Gene

Vibrio anguillarum ghosts (VAG) were generated, for the first time, using a conjugation vector containing a ghost bacteria inducing cassette, pRK-λP_R-cI-Elysis, in which the expression of PhiX174 lysis gene E was controlled by the P _R /cI regulatory system of lambda phage. By scanning electron microscopy, holes ranging 80–200 nm in diameter were observed in the VAG. To avoid the presence of bacterial genomic DNA and an antibiotic resistance gene in the final VAG product, we constructed a new dual vector, pRK-λP_R-cI-E-SNA, containing the E-mediated lysis cassette and the staphylococcal nuclease A (SNA)-mediated DNA degradation cassette, and generated safety-enhanced VAG for use as a fish vaccine.     

Single-Step Synthesis and Surface Plasmons of Bismuth-Coated Spherical to Hexagonal Silver Nanoparticles in Dichroic Ag:Bismuth Glass Nanocomposites

Here, we report for the first time the synthesis of bismuth-coated silver nanoparticles in dichroic bismuth glass nanocomposites by a novel and simple one-step melt quench technique without using any external reducing agent. The metallic silver nanoparticles (Ag NPs) were generated first, and subsequently, metallic bismuth was deposited on the Ag NPs and formed a thick layer. The reduction of Bi³⁺ to Bi^o and subsequently its deposition on the Ag NPs (which were formed earlier than Bi^o) in the K₂O–Bi₂O₃–B₂O₃ (KBB) glass system have been explained by their standard reduction potentials. The UV–vis absorption spectra show a prominent surface plasmon resonance (SPR) absorption band at 575 nm at lower concentrations (up to 0.01 wt%); three bands at 569, 624 and 780 nm at medium concentration (0.02–0.03 wt%); and two weak bands at 619 and 817 nm at highest concentration (0.06 wt%) of silver. They have been explained by the electrodynamics theories. TEM images reveal the conversion of spheroidal (5–15 nm) to hexagonal (10–35 nm) shaped Ag NPs with the increase in concentration of silver (up to 0.06 wt%). SAED pattern confirms the crystalline planes of rhombohedral bismuth and cubic silver. Thermal treatment at 360 °C, which is the glass transformation temperature (T _g) of the sample containing lower concentration of silver (0.007 wt%), shows red-shifted SPR band due to increase in size of NPs. Whereas the sample containing higher concentration (0.06 wt%) of silver under similar treatment exhibited changes in SPR spectral profile happened due to conversion to spherical NPs from hexagonal shape and reduction in size (10–20 nm) of NPs after heat treatment for 65 h. HRTEM images corroborate the different orientations of the NPs. FESEM images reveal hexagonal disk like structure having different orientations. Dichroic nature of the nanocomposites has been explained with the size and shape of Ag nanoparticles. We believe that this work will create new avenues in the area of nanometal–glass hybrid nanocomposites and the materials have significant applications in the field of optoelectronics and nanophotonics.     

Solution-Deposited Thin Silver Films on Plastic Surfaces for Low-Cost Applications in Plasmon-Coupled Emission Sensors

We report the deposition of highly uniform thin silver films on plastic materials using a wet-chemistry method, suitable for surface plasmon-coupled emission (SPCE). This approach is reproducible for diverse low-cost applications and versatile to generate silver surfaces on various plastics substrates. An oxygen plasma pretreatment of the plastic provides for rapid silvering, leading to a 47-nm-thick continuous film for SPCE applications. The surface smoothness and thickness of the films have been estimated using atomic force microscope. The higher refractive index of polycarbonate, resulted in an SPCE angle of θ _F = 47⁰ for Rhodamine B, compared to glass (θ _F = 50⁰). The current study presents details on film deposition conditions, appropriate choice of index matching fluids, substrates, and light sources that play a vital role to augment SPCE emission intensity.     

Novel biosynthesis of (R)-ethyl-3-hydroxyglutarate with (R)-enantioselective hydrolysis of racemic ethyl 4-cyano-3-hydroxybutyate by Rhodococcus erythropolis

(R)-ethyl-3-hydroxyglutarate with highly optical purity (≥99%) can be used as a novel precursor for synthesis of chiral side chain of rosuvastatin. In this study, a novel synthesis route of (R)-ethyl-3-hydroxyglutarate by whole microorganism cells from racemic ethyl 4-cyano-3-hydroxybutyate was created. A strain ZJB-0910 capable of transforming racemic β-hydroxy aliphatic nitrile was isolated by employing a screening method based on a colorimetric reaction of Co²⁺ ion with ammonia, and identified as Rhodococcus erythropolis based on its morphology, physiological tests, Biolog, and the 16S rDNA sequence. After cultivation in a sterilized medium with composition of 20 g glucose, 5 g yeast extract, 0.5 g KH₂PO₄, 0.5 g K₂HPO₄, 0.2 g MgSO₄·7H₂O per liter at 30°C and 150 rpm for 48 h, the whole cells of R. erythropolis ZJB-0910 were prepared as a catalyst in (R)-enantioselective hydrolysis of racemic ethyl 4-cyano-3-hydroxybutyate for synthesis of (R)-ethyl-3-hydroxyglutarate, without bearing hydrolase activity for the ester bond of ethyl 4-cyano-3-hydroxybutyate. Under the optimized biotransformation conditions of pH 7.5, 30°C, and 20 mM substrate concentration, (R)-ethyl-3-hydroxyglutarate with 46.2% yield (ee > 99%) was afforded, and its chemical structure was determined by ESI-MS, NMR, and IR. The apparent Michaelis constant K _m and maximum rate V _max for this biocatalytic reaction were 0.01 M and 85.6 μmol min⁻¹ g⁻¹, respectively.     

Fabrication and characterization of silver nanoparticle and its potential antibacterial activity

In the present research silver nanoparticle was fabricated by chemical reduction of silver salt (Silver nitrate, AgNO₃) solution. Sodium citrate was used as a reducer. The formation of silver nanoparticle was observed visually by color change (greenish yellow). The surface plasmon resonance peak in absorption spectra of silver nanoparticle showed an absorption maximum at 420 nm in UV-VIS spectrometry. The X-ray diffraction pattern showed the presence of sharp reflections at 111, 200, 220, and 311. This would indicate the presence of silver nanoparticle. The scanning electron micrograph revealed that the average size of silver nanoparticle was 21.22 ± 5.17 nm. Silver nanoparticle exhibited better antimicrobial activity against Staphylococcus aureus than the other bacterial pathogens. The correlation coefficient between silver nanoparticles and selected bacterial pathogens revealed that there is a strong negative correlation with Escherichia coli, S. aureus and Klebsiella pneumonia (r = −0.975, −0.993, and −0.998, respectively).     

Detecting <Emphasis Type="Italic">Suaeda salsa</Emphasis> L<Emphasis Type="Italic">.</Emphasis> chlorophyll fluorescence response to salinity stress by using hyperspectral reflectance

Measurements of chlorophyll fluorescence and hyperspectral reflectance were used to detect salinity stress in Suaeda salsa L., beach of Dongtai, Jiangsu Province, China. Three experimental sites were used in our study, which belong to low salinity, middle salinity and high salinity. The results showed that leaf chlorophyll fluorescence changed along salinity gradient. To select the sensitive hyperspectral ranges of leaf chlorophyll fluorescence, the correlationship between leaf chlorophyll fluorescence and hyperspectral reflectance was regressed and analyzed. Statistical results indicated that the 680 and 935 nm were the most sensitive hyperspectral bands for estimating leaf chlorophyll fluorescence. Then, 11 relative hyperspectral indices were selected based on the sensitive bands and previous literature. (R ₆₈₀ − R ₉₃₅)/(R ₆₈₀ + R ₉₃₅) and R ₆₈₀/R ₉₃₅ have higher correlationship coefficient (R) and lower root mean square error, may be used for detecting chlorophyll fluorescence, such as F _o, F _m, F _v/F _m, qP, and ΦPSII, while NPQ may be detected by (R ₇₈₀ − R ₇₁₀)/(R ₇₈₀ − R ₆₈₀). These results suggest that chlorophyll fluorescence of halophyte response to salinity stress could be identified by remote sensing.     

Type 1 copper site synthetic model complexes with increased redox potentials

Reactions of NaSCPh₃ with (R₃tacn)Cu(OTf)₂ (R is Me, iPr; tacn is 1,4,7-triazacyclononane; OTf is CF₃SO₃ ⁻) yield blue complexes identified as ((R₃tacn)CuSCPh₃)(OTf) on the basis of UV–vis, resonance Raman, and electron paramagnetic resonance (EPR) spectroscopy and electrospray ionization mass spectrometry. These complexes exhibit spectroscopic properties typical of type 1 copper sites in proteins, including diagnostic Sπ → Cu(d_{x² - y²} ) (d_{{x^{2} - y^{2} }} ) ligand-to-metal charge transfer transitions at approximately 610–630 nm and small A _|| values in EPR spectra of less than 100 × 10⁻⁴ cm⁻¹. Cyclic voltammetry experiments revealed redox potentials for the complexes similar to those of several low-potential type 1 copper proteins (e.g., azurin, stellacyanin) and approximately 0.5 V higher than those of previously reported model compounds. Thus, the new complexes mimic key aspects of both the structure and the function of type 1 copper sites.     

Predicting vegetation water content in wheat using normalized difference water indices derived from ground measurements

Vegetation water content (VWC) is an important variable for both agriculture and forest fire management. Remote sensing technology offers an instantaneous and non-destructive method for VWC assessment provided we can relate in situ measurements of VWC to spectral reflectance in a reliable way. In this paper, based on radiative transfer models, three new normalized difference water indices (NDWI) are proposed for VWC [fuel moisture content (FMC), and equivalent water thickness (EWT)] estimation, taking both leaf internal structure and dry matter content into account. Reflectance at 1,200, 1,450 and 1,940 nm were selected and normalized with reflectance at 860 nm to establish three water indices, NDWI₁₂₀₀, NDWI₁₄₅₀ and NDWI₁₉₄₀. Good correlations were observed between FMC (R ² = 0.65–0.80) and EWT (both at the leaf scale, R ² = 0.75–0.81 for EWT_L and at the canopy scale, R ² = 0.80–0.83 for EWT_C) at various stages of wheat crop development.     

Scanning force microscopy studies of X-ray-induced double-strand breaks in plasmid DNA

We present an analysis of X-ray-induced damage in ΦX174 plasmid DNA, applying doses between D = 250 and 1,500 Gy. To analyse this damage in detail, the distribution of plasmid fragments after irradiation have been determined by scanning force microscopy. The results show that even for the lowest dose of D = 250 Gy, a significant amount of double-strand breaks are observed. For increasing dose, the percentage of small fragments increases and is accompanied by a shortening of the average fragment length from < L> = 1,400 nm for a dose of D = 250 Gy to < L> = 1,080 nm after irradiation with D = 1,500 Gy. The most crucial parameter, the average number of double-strand breaks per broken plasmid (<DSB_b> ) has been determined for the first time for the applied doses. The results show that the average number of DSBs per broken plasmid <DSB_b> increases almost linearly from a value of <DSB_b> = 1.3 after irradiation with D = 250 Gy to <DSB_b> = 1.7 after exposure to D = 1,500 Gy. The presented results show that the amount of DSBs induced by X-ray radiation in plasmid DNA can be calculated with high accuracy by means of scanning force microscopy, providing relevant information regarding the interaction of X-rays with DNA molecules.

Low Temperature Spectrophotometry on Phototransformation of PR in Pelletable Phytochrome of Pea

Phototransformation of P_R to P_FR in a 1,000–7,000 x gpelletable fraction (1–7 KP), which was extracted fromdark-grown pea shoots that had been irradiated by red then far-redlight, was studied by low temperature spectrophotometry. Redlight irradiation of P_R in 1–7 KP at –160°Cinduced an absorption increase at 695–696 nm with a concomitant,small decrease of P_R absorption at 670 nm. These changes werepartially photoreversed when the sample was irradiated subsequentlywith 700-nm light. At –55°C, red light irradiationof P_R resulted mainly in bleaching and consequently in a reductionof the P_R peak, accompanied by minor absorbance increases around695 nm. The intermediates formed at –165°C by 660-nmlight irradiation partly reverted back to P_R or formed a bleachedintermediate (probably the same bleached intermediate describedabove) in the dark, when the pellets were warmed to –60°C.The bleached intermediate was transformed to P_FR in the darkat –10°C or above. These characteristics of P_R transformation observed in the pelletablephytochrome were essentially the same as those observed in invivo or soluble phytochrome. (Received December 24, 1982; Accepted July 28, 1983)     

Glucose biosensor based on titanium dioxide-multiwall carbon nanotubes-chitosan composite and functionalized gold nanoparticles

In this paper, a new glucose biosensor was prepared. At first, Prussian blue (PB) was electrodeposited on a glassy carbon electrode (GCE) modified by titanium dioxide-multiwall carbon nanotubes-chitosan (TiO₂-MWNTs-CS) composite, and then gold nanoparticles functionalized by poly(diallyldimethylammonium chloride) (PDDA-Au) were adsorbed on the PB film. Finally, the negatively charged glucose oxidase (GOD) was self-assembled on to the positively charged PDDA-Au. The electrochemical performances of the modified electrodes had been studied by cyclic voltammetry (CV) and amperometric methods, respectively. In addition, the stepwise fabrication process of the as-prepared biosensor was characterized by scanning electron microscopy. PDDA-Au nanoparticles were characterized by ultraviolet–vis absorption spectroscopy and transmission electron microscopy. Under the optimal conditions, the as-prepared biosensor exhibited a good response performance to glucose with a linear range from 6 μM to 1.2 mM with a detection limit of 0.1 μM glucose (S/N = 3). In addition, this work indicated that TiO₂-MWNTs-CS composite and PDDA-Au nanoparticles held great potential for constructing biosensors.     

Species and material considerations in the formation and development of microalgal biofilms

The development of microalgal biofilms has received very limited study despite its relevance in the design of photobioreactors where film growth may be advantageous for biomass separation or disadvantageous in fouling surfaces. Here, the effects of species selection, species control, and substrate properties on biofilms of Scenedesmus obliquus and Chlorella vulgaris were investigated. Experiments were conducted in batch culture and in continuous culture modes in a flow cell. Cell growth was monitored using confocal laser scanning microscopy and gravimetrically. Species selection and species control had significant effects on biofilm development. On non-sterile wastewater, C. vulgaris shifted from primarily planktonic (23.7% attachment) to primarily sessile (79.8% attachment) growth. The biofilms that developed in non-sterile conditions were thicker (52 ± 19 μm) than those grown in sterile conditions (7 ± 6 μm). By contrast, S. obliquus attained similar thicknesses (54 ± 31 and 53 ± 38 μm) in both sterile and non-sterile conditions. Neither species was able to dominate a non-sterile biofilm. The effect of substrate surface properties was minimal. Both species grew films of similar thickness (∼30 μm for S. obliquus, <10 μm for C. vulgaris) on materials ranging from hydrophilic (glass) to hydrophobic (polytetrafluoroethylene). Surface roughness created by micropatterning the surface with 10 μm grooves did not translate into long-term increases in biofilm thickness. The results indicate that species selection and control are more important than surface properties in the development of microalgal biofilms.     

Autotrophic and heterotrophic respiration in needle fir and Quercus-dominated stands in a cool-temperate forest, central Korea

To investigate annual variation in soil respiration (R _S) and its components [autotrophic (R _A) and heterotrophic (R _H)] in relation to seasonal changes in soil temperature (ST) and soil water content (SWC) in an Abies holophylla stand (stand A) and a Quercus-dominated stand (stand Q), we set up trenched plots and measured R _S, ST and SWC for 2 years. The mean annual rate of R _S was 436 mg CO₂ m⁻² h⁻¹, ranging from 76 to 1,170 mg CO₂ m⁻² h⁻¹, in stand A and 376 mg CO₂ m⁻² h⁻¹, ranging from 82 to 1,133 mg CO₂ m⁻² h⁻¹, in stand Q. A significant relationship between R _S and its components and ST was observed over the 2 years in both stands, whereas a significant correlation between R _A and SWC was detected only in stand Q. On average over the 2 years, R _A accounted for approximately 34% (range 17–67%) and 31% (15–82%) of the variation in R _S in stands A and Q, respectively. Our results suggested that vegetation type did not significantly affect the annual mean contributions of R _A or R _H, but did affect the pattern of seasonal change in the contribution of R _A to R _S.     

Regulation of inorganic carbon acquisition by nitrogen and phosphorus levels in the Nannochloropsis sp.

Nannochloropsis sp. was grown to the exponential phase and transferred to the high CO₂ (2,800 μl l⁻¹) and irradiance (100 μmol photons m⁻² s⁻¹) condition with different levels of nitrate and phosphate for 72 h, then the photosynthetic activity and inorganic carbon acquisition of the alga were measured. The apparent photosynthetic efficiency (α) of Nannochloropsis sp. decreased with increasing NO₃ ⁻ concentration from 150 to 3,000 μM, and the high nitrate-grown cells showed the lowest levels of light-saturated photosynthetic rate (P _m), while the low nitrate-grown cells showed the highest levels of dark respiration rate (R _d). The maximal light-saturated photosynthetic rate and the minimal dark respiration rate were seen under the middle nitrate condition. When the nitrate concentration ranged from 150 to 3,000 μM, the affinity for inorganic carbons of Nannochloropsis sp. increased sharply with the increasing NO₃ ⁻ concentration to 300 μM and then decreased significantly. The middle phosphate-grown cells exhibited the highest light-saturated photosynthetic rate and apparent photosynthetic efficiency, however, the affinity for inorganic carbons of Nannochloropsis sp. was the maximum under the low phosphate condition. It was shown that the appropriate nitrogen and phosphorus levels were of vital importance to the photosynthesis of cells.     

Hybrid Dielectric-Loaded Plasmonic Waveguide-Based Power Splitter and Ring Resonator: Compact Size and High Optical Performance for Nanophotonic Circuits

The key challenge of the plasmonic waveguide is to achieve simultaneously both the long propagation length and high confinement. The hybrid dielectric-loaded plasmonic waveguide consists of a SiO₂ stripe sandwiched between a Si-nanowire and a silver film and thus promises as a best candidate to overcome this challenge. We propose to exploit this unique property of this structure to design different high-efficient silicon-based plasmonic components including waveguide, power splitter, and wavelength-selective ring resonator. As a result, the proposed power splitter with a waveguide cross section (λ ²/60) and a strong mode confinement area (~λ ²/240) features a low power transmission loss (<0.4 dB) at the optimal arm length of 4 μm with respect to different separation distances of output arms. Moreover, we also demonstrate that a plasmonic ring resonator with a compact ring radius of 2 μm may achieve high optical performance such as high-extinction ratio of 30 dB, large free spectral range of 67 nm, and small bandwidth of 0.6 nm. These superior performances make them promising building blocks for integrated nanophotonic circuits.