Optical guided dispersions and subwavelength transmissions in dispersive plasmonic circular holes

The light transmission through a dispersive plasmonic circular hole is numerically investigated with an emphasis on its subwavelength guidance. For a better understanding of the effect of the hole diameter on the guided dispersion characteristics, the guided modes, including both the surface plasmon polariton mode and the circular waveguide mode, are studied for several hole diameters, especially when the metal cladding has a plasmonic frequency dependency. A brief comparison is also made with the guided dispersion characteristics of a dispersive plasmonic gap [K.Y. Kim, et al., Opt. Express 14, 320–330 (2006)], which is a planar version of the present structure, and a circular waveguide with perfect electric conductor cladding. Finally, the modal behaviour of the first three TM-like principal modes with varied hole diameters is examined for the same operating mode.     

Targeted destruction of murine macrophage cells with bioconjugated gold nanorods

Gold nanorods manifest a readily tunable longitudinal plasmon resonance with light and consequently have potential for use in photothermal therapeutics. Recent work by others has shown how gold nanoshells and rods can be used to target cancer cells, which can then be destroyed using relatively high power laser radiation (∼1×10⁵ to 1×10¹⁰ W/m²). Here we extend this concept to demonstrate how gold nanorods can be modified to bind to target macrophage cells, and show that high intensity laser radiation is not necessary, with even 5×10² W/m² being sufficient, provided that a total fluence of ∼30 J/cm² is delivered. We used the murine cell line RAW 264.7 and the monoclonal antibody CD11b, raised against murine macrophages, as our model system and a 5 mW solid state diode laser as our energy source. Exposure of the cells labeled with gold nanorods to a laser fluence of 30 J/cm² resulted in 81% cell death compared to only 0.9% in the control, non-labeled cells.     

Gold/monolayer graphitic carbon nitride plasmonic photocatalyst for ultrafast electron transfer in solar-to-hydrogen energy conversion

Gold (Au) plasmonic nanoparticles were grown evenly on monolayer graphitic carbon nitride (g-C₃N₄) nanosheets via a facile oil-bath method. The photocatalytic activity of the Au/monolayer g-C₃N₄ composites under visible light was evaluated by photocatalytic hydrogen evolution and environmental treatment. All of the Au/monolayer g-C₃N₄ composites showed better photocatalytic performance than that of monolayer g-C₃N₄ and the 1% Au/monolayer g-C₃N₄ composite displayed the highest photocatalytic hydrogen evolution rate of the samples. The remarkable photocatalytic activity was attributed largely to the successful introduction of Au plasmonic nanoparticles, which led to the surface plasmon resonance (SPR) effect. The SPR effect enhanced the efficiency of light harvesting and induced an efficient hot electron transfer process. The hot electrons were injected from the Au plasmonic nanoparticles into the conduction band of monolayer g-C₃N₄. Thus, the Au/monolayer g-C₃N₄ composites possessed higher migration and separation efficiencies and lower recombination probability of photogenerated electron-hole pairs than those of monolayer g-C₃N₄. A photocatalytic mechanism for the composites was also proposed.     

Light-Assisted Ullmann Coupling of Phenols and Aryl Halides: The Synergetic Effect Between Plasmonic Copper Nanoparticles and Carbon Nanotubes from Various Sources

Utilizing light and plastic wastes as resources to turn the wasted phenols and hazardous aryl halides into value added chemicals seems to be an attractive idea for alleviating the energy crisis and environmental problems. In this work, plasmonic copper nanoparticles (Cu NPs) were loaded onto carbon nanotubes (CNTs) from various sources including commercial CNTs and those derived from plastic wastes. Under visible-light irradiation, the catalyst could efficiently convert phenols and aryl halides to diaryl ethers. Similar with commercial CNTs, excellent activity is also achieved when utilizing CNTs derived from different kinds of plastic wastes as support for the system. Further investigation shows that the visible-light irradiation and light-excited plasmonic Cu NPs are necessary to inhibit the phenol degradation on CNTs and in turn promote the cross-coupling of phenol and aryl halides. Compared with metal oxides and other carbon materials, the excellent capability of CNTs to absorb light, to convert light to heat, and to adsorb both two reactants simultaneously are critical to enhance the activity of Cu NPs, achieving high yields of diaryl ethers. This study could provide a novel strategy for catalyst design and generate a more economically sustainable process.     

DNA-Origami-Based Assembly of Au@Ag Nanostar Dimer Nanoantennas for Label-Free Sensing of Pyocyanin

Early-stage detection of diseases caused by pathogens is a prerequisite for expedient patient care. Due to the limited signal-to-noise ratio, molecular diagnostics needs molecular signal amplification after recognition of the target molecule. In this present study, we demonstrate the design of plasmonically coupled bimetallic Ag coated Au nanostar dimers with controlled nanogap using rectangular DNA origami. We further report the utility of the designed nanostar dimer structures as efficient SERS substrate for the ultrasensitive and label-free detection of the pyocyanin molecule, which is a biomarker of the opportunistic pathogenic bacteria, Pseudomonas aeruginosa. The experimental results showed that the detection limit of pyocyanin with such nanoantenna based biosensor was 335 pM, which is much lower than the clinical range of detection. Thus, fast, sensitive and label-free detection of pyocyanin at ultralow concentration in an infected human body can pave a facile route for early stage warning for severe bacterial infections.     

Flow Synthesis of Plasmonic Gold Nanoshells via a Microreactor

Gold nanoshells with tunable surface plasmon resonances are a promising material for optical and biomedical applications. They are produced through seed‐mediated growth, in which gold nanoparticles (AuNPs) are seeded on the core particle surface followed by growth of the gold seeds into a shell. However, synthetic gold nanoshell production is typically a multistep, time‐consuming batch‐type process, and a simple and scalable process remains a challenge. In the present study, a continuous flow process for the seed‐mediated growth of silica–gold nanoshells is established by exploiting the excellent mixing performance of a microreactor. In the AuNP‐seeding step, the reduction of gold ions in the presence of core particles in the microreactor enables the one‐step flow synthesis of gold‐decorated silica particles through heterogeneous nucleation. Flow shell growth is also realized using the microreactor by selecting an appropriate reducing agent. Because self‐nucleation in the bulk solution phase is suppressed in the microreactor system, no washing is needed after each step, thus enabling the connection of the microreactors for the seeding and shell growth steps into a sequential flow process to synthesize gold nanoshells. The established system is simple and robust, thus making it a promising technology for producing gold nanoshells in an industrial setting.     

平面金属等离激元美特材料对光学Tamm态及相关激射行为的增强作用

本文对具有类EIR色散特性的平面金属等离激元美特材料(planar plasmonic metamaterials, PPM)对光学Tamm态及相关激射行为的增强作用进行了研究. 我们首先运用传输矩阵方法分析了利用PPM结构的色散来增强光学Tamm态对应模式电磁局域密度的可能性. 其次, 我们将具有类EIR特性的PPM与一维光子晶体(photonic crystal, PC)合在一起设计了一种平面等离激元美特材料-光子晶体(PPM-PC)异质结构. 研究发现, 通过在电磁局域密度最高的PPM结构中(或附近)加入增益介质, 可观察到比通常光学Tamm态更强的激射增强效应及更明显的单色性响应. 这些特性使得这种PPM-PC结构有望被应用于低阈值激光器、荧光增强等方面.