Gold Nanostar Synthesis with a Silver Seed Mediated Growth Method

The physical, chemical and optical properties of nano-scale colloids depend on their material composition, size and shape ^1-5. There is a great interest in using nano-colloids for photo-thermal ablation, drug delivery and many other biomedical applications ⁶. Gold is particularly used because of its low toxicity ^7-9. A property of metal nano-colloids is that they can have a strong surface plasmon resonance ¹⁰. The peak of the surface plasmon resonance mode depends on the structure and composition of the metal nano-colloids. Since the surface plasmon resonance mode is stimulated with light there is a need to have the peak absorbance in the near infrared where biological tissue transmissivity is maximal ^{11, 12}.We present a method to synthesize star shaped colloidal gold, also known as star shaped nanoparticles ^13-15 or nanostars ¹⁶. This method is based on a solution containing silver seeds that are used as the nucleating agent for anisotropic growth of gold colloids ^17-22. Scanning electron microscopy (SEM) analysis of the resulting gold colloid showed that 70 % of the nanostructures were nanostars. The other 30 % of the particles were amorphous clusters of decahedra and rhomboids. The absorbance peak of the nanostars was detected to be in the near infrared (840 nm). Thus, our method produces gold nanostars suitable for biomedical applications, particularly for photo-thermal ablation.     

Pt nanoflower/polyaniline composite nanofibers based urea biosensor

Hybrid materials with special structures are of great interest because of their superior properties compared with their pure counterparts. Hybrid polyaniline (PANi) nanofibers with integrated Pt nanoflowers are studied in this research. PANi is prepared by in situ polymerization of aniline on an electrospun nanofiber template in an acidic solution with ammonium persulfate (APS) as the oxidant. Pt nanoflowers are further electrodeposited onto the PANi nanofibers backbone by cyclic voltammetry (CV), resulting in novel functionalized hybrid nanofibers. The coverage of Pt nanoflowers on PANi nanofibers can be facilely controlled by adjusting the electrodeposition conditions. The factors affecting Pt nanoflowers formation are further investigated. As a demonstration, urease is immobilized onto the Pt/PANi hybrid nanofibers and the composite was employed as the sensing platform for urea detection in a flow-injection-analysis (FIA) system. The detection of urea shows a wide linear range (up to 20 mM), a good limit of detection of 10 μM (S/N=3), and an excellent anti-interference property against chloride ion. In addition, it was found that the response to urea was attributed not only to the conductivity change of PANi due to the interaction between PANi and ammonia (liberated from the enzymatic reaction), but also to the interaction between Pt nanoflowers and amine groups in urea. The strategy developed in this study can be extended to synthesize other composite nanofibers consisting of conducting polymer and metal nanoparticles for a wide range of sensing applications.     

Improve the Plasmonic Spectral Detection of Alpha-Fetoprotein: the Effect of Branch Length on the Coagulation of Gold Nanostars

Plasmonics - A sensitive spectral sensing method for detection of alpha-fetoprotein (AFP) was proposed based on the intense aggregation of colloidal gold nanostars. It has been found that the...     

Hemin-incorporated nanoflowers as enzyme mimics for colorimetric detection of foodborne pathogenic bacteria

Rapid, sensitive and point-of-care detection of foodborne pathogenic bacteria is essential for food safety. In this study, we found that hemin-concanavalin A hybrid nanoflowers (HCH nanoflowers), as solid mimic peroxidase, could catalyze oxidation of 2,2′-azino-bis (3-ethylbenzthiazoline-6-sulfonic acid) diammonium salt (ABTS) in the presence of H₂O₂ to a green-colored product. HCH nanoflowers, integrating the essential functions of both biological recognition and signal amplification, meet the requirements of signal labels for colorimetric immunoassay of bacteria. In view of the excellent peroxidase mimetic catalytic activity of HCH nanoflowers, a colorimetric biosensing platform was newly constructed and applied for sensitive detection of foodborne Escherichia coli O157:H7 (E. coli O157:H7). The corresponding detection limits was as low as 4.1?CFU/mL with wide linear ranges (10¹–10⁶?CFU/mL).     

Hydroxyl-proton resonance shifts for a range of aqueous sugar solutions

At low temperature and in a narrow pH-range, the hydroxyl-proton resonance spectra of a range of mono-, di- and oligo-saccharides in dilute aqueous solutions have been resolved. The signals rapidly broaden on raising the temperature and on changing the pH of the solutions. Optimum conditions for obtaining maximum resolution are described and attempts are made to assign the resonances to specific hydroxyl groups. In all cases the resonances for the anomeric hydroxyl-proton occurred at lowest field and the pH value for optimum resolution of these resonances was always lower than that for the other hydroxyl resonances.     

One‐Step Synthesis of 2‐Ethylhexylamine Pillared Vanadium Disulfide Nanoflowers with Ultralarge Interlayer Spacing for High‐Performance Magnesium Storage

Rechargeable magnesium batteries (RMBs) are attractive candidates for large‐scale energy storage owing to the high theoretical specific capacity, rich earth abundance, and good safety characteristics. However, the development of desirable cathode materials for RMBs is constrained by the high polarity and slow intercalation kinetics of Mg²⁺ ions. Herein, it is demonstrated that 2‐ethylhexylamine pillared vanadium disulfide nanoflowers (expanded VS₂) with enlarged interlayer distances exhibit greatly boosted electrochemical performance as a cathode material in RMBs. Through a one‐step solution‐phase synthesis and in situ 2‐ethylhexylamine intercalation process, VS₂ nanoflowers with ultralarge interlayer spacing are prepared. A series of ex situ characterizations verify that the cathode of expanded VS₂ nanoflowers undergoes a reversible intercalation reaction mechanism, followed by a conversion reaction mechanism. Electrochemical kinetics analysis reveal a relatively fast Mg‐ion diffusivity of expanded VS₂ nanoflowers in the order of 10^?11–10^?12 cm² s^?1, and the pseudocapacitive contribution is up to 64% for the total capacity at 1 mV s^?1. The expanded VS₂ nanoflowers show highly reversible discharge capacity (245 mAh g^?1 at 100 mA g^?1), good rate capability (103 mAh g^?1 at 2000 mA g^?1), and stable cycling performance (90 mAh g^?1 after 600 cycles at 1000 mA g^?1).     

Vibrational resonances in biological systems at microwave frequencies

Many biological systems can be expected to exhibit resonance behavior involving the mechanical vibration of system elements. The natural frequencies of such resonances will, generally, be in the microwave frequency range. Some of these systems will be coupled to the electromagnetic field by the charge distributions they carry, thus admitting the possibility that microwave exposures may generate physiological effects in man and other species. However, such microwave excitable resonances are expected to be strongly damped by interaction with their aqueous biological environment. Although those dissipation mechanisms have been studied, the limitations on energy transfers that follow from the limited coupling of these resonances to the electromagnetic field have not generally been considered. We show that this coupling must generally be very small and thus the absorbed energy is so strongly limited that such resonances cannot affect biology significantly even if the systems are much less strongly damped than expected from basic dissipation models.     

Plasmonic Fano Resonances in Single-Layer Gold Conical Nanoshells

Plasmonic Fano resonances arise in symmetric single-layer conical nanoshells, which can be switched on and off by changing the polarization of the incident electric field. By breaking the symmetry, higher-order dark hybridized modes emerge in the spectrum, which couple to the superradiant bright mode and induce higher-order plasmonic Fano resonances. From a comparison with spherical nanostructures, it comes out that single-layer conical nanoshells are found to be highly capable in the generation of higher-order Fano resonances with larger modulation depths in the optical spectra. Such nanostructures are also found to offer high values of figure of merit and contrast ratio due to which they are highly suitable for biological sensors.     

5,6,7,8-Tetrahydrofolic acid. Conformation of the tetrahydropyrazine ring

It is suggested from analysis of proton spin-spin coupling constants that the tetrahydropyrazine ring of tetrahydrofolate is a roughly equal mixture of two half-chair conformations, one with the C-6 proton axial and the other with the C-6 proton equatorial. The chemical shifts and spin-spin coupling constants for the carbon-bound protons of (+/-)-L-, (-)-L-, and (-)-L-[6-2H] 5,6,7,8-tetrahydrofolate were measured at 25 degrees and at 300 MHZ. The resonances corresponding to the two C-7 protons in the deuterated compound constituted an AB quartet with JAB of 12 Hz and chemical shift difference of 92 Hz or 0.307 ppm; the C-7 protons are proposed to be a geminally coupled axial-equatorial pair whose rapid equilibration does not result in equivalence due to the adjacent chiral center at C-6. The spin-spin splitting in the C-7 resonances were 3.0 and 6.6 Hz for the low field and high field resonances, respectively, reflecting coupling to the C-6 proton. These coupling constants reflect the conformational equilibrium. The resonances assignable to C-9 protons are nearly equivalent in the 6-2H compound, but exhibit the resonances corresponding to a complex spin system in the 6-H compound.     

Surface Plasmon Resonances of an Axially Magnetized Plasma Column in the Presence of Collisional Loss

Surface plasmon resonances arising in the course of scattering of an H-polarized plane electromagnetic wave by an axially magnetized plasma column are analyzed. Main attention is paid to the behavior of these resonances in the presence of collisional loss in the magnetoplasma filling the scatterer. The frequencies, Q factors, and amplitude coefficients of the electromagnetic field of multipole surface plasmon resonances of different orders are found, and conditions under which the collisional loss in the plasma completely suppresses a given resonance are determined.     

A new generation approach in enzyme immobilization: Organic-inorganic hybrid nanoflowers with enhanced catalytic activity and stability

Many different micro and nano sized materials have been used for enzymes immobilization in order to increase their catalytic activity and stability. Generally, immobilized enzymes with conventional immobilization techniques exhibit improved stability while their activity is lowered compared to free enzymes. Recently, an elegant immobilization approach was discovered in synthesis of flower-like organic-inorganic hybrid nanostructures with extraordinary catalytic activity and stability. In this novel immobilization strategy, proteins (enzymes) and metal ions acted as organic and inorganic components, respectively to form hybrid nanoflowers (hNFs). It is demonstrated that the hNFs highly enhanced catalytic activities and stability in a wide range of experimental conditions (pHs, temperatures and salt concentration, etc.) compared to free and conventionally immobilized enzymes. This review mainly discussed the synthesis, characterization, development and applications of organic-inorganic hybrid nanoflowers formed of various enzymes and metal ions and explained potential mechanism underlying enhanced catalytic activity and stability.     

Higher Order Tunable Fano Resonances in Multilayer Nanocones

We present a computational study of the plasmonic response of a gold–silica–gold multilayered nanostructure based on truncated nanocones. Symmetry breaking is introduced by rotating the nanostructure and by offsetting the layers. Nanocones with coaxial multilayers show dipole–dipole Fano resonances with resonance frequencies depending on the polarization of the incident light, which can be changed by rotating the nanostructure. By breaking the axial symmetry, plasmonic modes of distinct angular momenta are strongly mixed, which provide a set of unique and higher order tunable Fano resonances. The plasmonic response of the multilayered nanocones is compared to that of multishell nanostructures with the same volume and the former are discovered to render visible high-order dark modes and to provide sharp tunable Fano resonances. In particular, higher order tunable Fano resonances arising in non-coaxial multilayer nanocones can vary the plasmon lines at various spectral regions simultaneously, which makes these nanostructures greatly suitable for plasmon line shaping both in the extinction and near field spectra.     

Enhanced Electron Photoemission by Collective Lattice Resonances in Plasmonic Nanoparticle-Array Photodetectors and Solar Cells

We propose to use collective lattice resonances in plasmonic nanoparticle arrays to enhance and tailor photoelectron emission in Schottky barrier photodetectors and solar cells. We show that the interaction between narrow-band lattice resonances (the Rayleigh anomaly) and broader-band individual-particle excitations (localized surface plasmon resonances) leads to stronger local field enhancement. In turn, this causes a significant increase of the photocurrent compared to the case when only individual-particle excitations are present. The results can be used to design new photodetectors with highly selective, tunable spectral response, which are able to detect photons with the energy below the semiconductor bandgap. The findings can also be used to develop solar cells with increased efficiency.     

Tunable Properties of Surface Plasmon Resonance of Metal Nanospheroid: Graphene Plasmon Interaction

Plasmonics - Graphene plasmonic resonances play a significant role for enhancing the photon absorption inside thin film solar devices. We investigate the field rising at the intersection of...     

NMR study of the modified base resonances of tRNA tyr- coli

220MHz NMR spectra at 28° show several resolved resonances in the high field region for D₂O solutions of tyrosine specific tRNA from E. coli. These resonances are tentatively identified as arising from protons of the modified nucleoside, 2-methylthio-N⁶-(Δ²-isopentenyl)-adenosine and from the modified guanosine of unknown structure in the “wobble position” of the anti codon loop. Assignment of resonances was aided by comparison with spectra of tRNA_su⁺III^tyr, Form II, whose sequence is closely homologous to tRNA_coli^tyr, except for changes in some modified bases. Line widths of resolved resonances indicate that, at 28°, the methyl groups of modified nucleosides are not completely restricted in their motion relative to the overall motion of the macromolecule.     

Rotational motions in myoglobin assessed by carbon 13 relaxation measurements at two magnetic field strengths.

Proton-decoupled Fourier transform nuclear magnetic resonance spectroscopy of natural abundance 13C was used to obtain spectra of cyanoferrimyoglobin of sperm whale (Physeter catadon) at 14.1 and 23.5 kG. Comparison of the spin lattice relaxation times at these two field strengths allowed the unambiguous assignment of a rotational correlation time of 22 plus or minus 5 ns for the alpha carbon resonances. The spin lattice relaxation time value for a major band attributable to aromatic carbon atoms also corresponded to a single correlation time, attributable to over-all tumbling of the molecule. Certain narrower resonances reflect other modes of rotational motion in addition to the over-all tumbling. Observations of nuclear Overhauser enhancement and line widths accord with these conslusions.     

Glycolic acid-g-chitosan-gold nanoflower nanocomposite scaffolds for drug delivery and tissue engineering

This paper reports a simple novel method for the synthesis of flower like gold nanoparticle (three dimensional branched nanoparticle) with >30 tips, under controlled temperature condition. Formation of flower like Au nanoparticle was confirmed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Next step of this paper reveals the potential use of novel hybrids of chitosan-g-glycolic acid and gold nanoflower (AuNF) in controlled drug delivery and tissue engineering applications. The drug loaded novel nanohybrid scaffold is prepared by freeze drying of grafted polymer solution. Grafting of glycolic acid to the chitosan and incorporation of drug were evaluated by Fourier transform infrared spectroscopy (FTIR). The nanohybrid scaffolds were found to be stable towards the pH of the medium. The cell viability study shows that prepared nanohybrid scaffolds are biocompatible. Gold nanoflowers were found to control the drug release rate in the buffer solution (pH 7.4). Therefore, for the glycolic acid grafted chitosan based system, gold nanoflowers are the viable additive for drug delivery.     

Sequential assignment of the 1H and 31P resonances of the double stranded deoxynucleotide d (ATGCAT)2 by 2D-NMR correlation spectroscopy

31p-1H and 1H-1H chemical shift correlation spectroscopy are jointly used for providing a complete assignment of sugar proton (except H5' and H5") and phosphorus resonances in the double stranded oligonucleotide d (ATGCAT)2. In contrast to previous methods the specific assignment of overcrowded H5' H5" proton resonances is not required. Using the H3'-P coupling and also the long range H4'-P coupling, this quite general method can be easily implemented on intermediate field spectrometer. The present results pave the way to the 1H and 31P resonance assignment of longer double-stranded oligonucleotides.     

Magnetic-Based Fano Resonance by a Trimer with Y-shaped Gap

We introduce a Y-shaped gap into a silver disk to break the structure symmetry which can be looked as a loop-linked structure. Magnetic resonances are excited by incident light when incident electric field is parallel to the trimer plane. Fano resonance is generated by the coupling between bright electric mode and dark magnetic mode. These resonances can be adjusted by tuning the gap size, the radius of trimer, and the position of Y-shaped gap. The extinction cross section of the structure is calculated with the finite element method (FEM). The maximum figure of merit (FOM) is 37.8. Both the magnetic and electric field are greatly enhanced at the Fano dip and the magnetic resonance peak.