Crossover from Kondo-assisted suppression to co-tunneling enhancement of tunneling magnetoresistance via ferromagnetic nanodots in MgO tunnel barriers

The dependence of the tunneling magnetoresistance (TMR) of planar magnetic tunnel junctions on the size of magnetic nanodots incorporated within MgO tunnel barriers is explored. At low temperatures, in the Coulomb blockade (CB) regime, for smaller nanodots the conductance of the junction is increased at low bias consistent with Kondo-assisted tunneling and the TMR is suppressed. For slightly larger nanodots but within the CB regime, the TMR is enhanced at low bias, consistent with co-tunneling. Magnetic tunnel junctions (MTJ) exhibit giant magnetoresistance in small magnetic fields that arises from the flow of spin-polarized current through an ultrathin tunnel barrier separating two magnetic electrodes. The current through an MTJ device depends on the magnetic orientation of the electrodes and is typically higher when the electrode moments are parallel than when they are antiparallel. It has recently been demonstrated that the spin polarization of the tunneling current can be greatly enhanced by using crystalline tunnel barriers formed from MgO as compared with conventional amorphous barriers formed from alumina, due to spin filtering across the MgO layer. The magneto-transport properties of magnetic granular alloys and magnetic tunnel junction devices with magnetic nanodots embedded in amorphous dielectric matrices, and tunnel barriers, respectively, have been studied by several groups, but no systematic studies of the dependence on these properties on the nanodot size have been made.     

Structural contributions to charge transport across Ni-octanedithiol multilayer junctions

We report the fabrication and characterization of multilayer thin films incorporating 1,8-octanedithiols and Ni atoms. Low-temperature charge transport measurements exhibit inelastic co-tunneling and resonant tunneling features that correspond energetically to vibrational excitations of the molecular multilayer. Several junctions exhibit changes in conductance features characteristic of charge defect-gating. Transport through our junctions is shown to be dominated by the intrinsic properties of the multilayer.     

Impedance Spectroscopy of Ionic Ligand‐Modulated Charge Transport of Gold Nanoparticle Films

Assembled monolayer‐protected nanoparticles (NPs) possess unique electrical properties that are determined by the coupled effects of their nano‐sized electroactive inorganic cores that are capable of donating and accepting electrons and the organic shells. Core and ligand engineering for NP conductance modulation has been extensively explored; however, most studies focus on electron transport and not the interplay between the ion and electron transport processes. It is demonstrated here that electronic‐ and ionic‐conducting properties of nanoparticle assemblies can be controlled by engineering the charge and flexibility of the ligand shell. By using impedance spectroscopy, the electronic, mixed ionic and electronic, and responsive conductance of the nanoparticle film and structure‐function correlation are systematically investigated, and this correlation is used to provide a prototype volatile gas sensor based on the combined ionic and electronic conductance behavior of ionic ligand‐functionalized gold NPs.     

Enhanced gas sensing by individual SnO2 nanowires and nanobelts functionalized with Pd catalyst particles

The sensing ability of individual SnO(2) nanowires and nanobelts configured as gas sensors was measured before and after functionalization with Pd catalyst particles. In situ deposition of Pd in the same reaction chamber in which the sensing measurements were carried out ensured that the observed modification in behavior was due to the Pd functionalization rather than the variation in properties from one nanowire to another. Changes in the conductance in the early stages of metal deposition (i.e., before metal percolation) indicated that the Pd nanoparticles on the nanowire surface created Schottky barrier-type junctions resulting in the formation of electron depletion regions within the nanowire, constricting the effective conduction channel and reducing the conductance. Pd-functionalized nanostructures exhibited a dramatic improvement in sensitivity toward oxygen and hydrogen due to the enhanced catalytic dissociation of the molecular adsorbate on the Pd nanoparticle surfaces and the subsequent diffusion of the resultant atomic species to the oxide surface.     

A molecular dynamics simulation study to investigate the effect of filler size on elastic properties of polymer nanocomposites

The influence of filler size on elastic properties of nanoparticle reinforced polymer composites is investigated using molecular dynamics (MD) simulations. Molecular models for a system of nanocomposites are developed by embedding a fullerene bucky-ball of various sizes into an amorphous polyethylene matrix. In all cases, bucky-balls are modeled as non-deformable solid inclusions and infused in the matrix with a fixed volume fraction. The interaction between polymer and the nanoparticle is prescribed by the Lennard-Jones non-bonded potential. The mechanical properties for neat polymer and nanocomposites are evaluated by simulating a series of unidirectional and hydrostatic tests, both in tension and compression. Simulation results show that the elastic properties of nanocomposites are significantly enhanced with the reduction of bucky-ball size. An examination at the atomic level reveals that densification of polymer matrix near the nanoparticle as well as the filler-matrix interaction energy play the major role in completing the size effect.     

The effect of process parameters on physical and mechanical properties of commercial low density polyethylene/ORG-MMT nanocomposites

Polyethylene/organo-montmorillonite clay (org-MMT) nanocomposites were prepared utilizing PP-g-MA as a compatibilizer by melt intercalation method. In order to increase the miscibility of polyethylene (PE) with nanoparticle surface at firs, a primary masterbatch consist of compatibilizer and org-MMT was prepared then, this compound was melt intercalated with PE to synthesis the PE/org-MMT nanocomposites. In this study, the presence of commercial low density polyethylene in Nanocomposites structure and also the effect of process parameters such as: amount of nanoparticles, mixing rate and mixing time on nanocomposite structure and properties have been investigated. The X-ray diffraction (XRD) and transmission electron microscopy (TEM) results showed that the interlayer distance of nanoparticle layers increased and a partially intercalated structure was prepared by melt intercalation method. Interaction between polyethylene chains and nanoparticle layers could be improved if the control of above parameters causes to penetrate the chains into nanoclay layers; by an optimization, this effect could improve the physical and mechanical properties. The DSC data revealed that melting temperature has slowly increased and crystalinity has lightly decreased. Consequently we can claim the thermal properties of LDPE/clay nanocomposite did not considerably change with clay content. A rise in the mechanical properties such as yield stress and modulus was observed by tension test; by addition of 5% clay content the tensile strength increased about 7%, the tensile modulus enhanced about 60% and the yield stress increased about 16% in comparison with the pure LDPE.     

Synergistic Modulation of Surface Interaction to Assemble Metal Nanoparticles into Two‐Dimensional Arrays with Tunable Plasmonic Properties

A simple strategy based on the synergistic modulation of inter‐particle and substrate‐particle interaction is applied for the large‐scale fabrication of two‐dimensional (2D) Au and Ag nanoparticle arrays. The surface charge of the substrate is used to redistribute the double layer electric charges on the particles and to modulate the inter‐particle distance within the 2D nanoparticle arrays on the substrate. The resultant arrays, with a wide range of inter‐particle distances, display tunable plasmonic properties. It can be foreseen that such 2D nanoparticle arrays possess potential applications as multiplexed colorimetric sensors, integrated devices and antennas. Herein, it is demonstrated that these arrays can be employed as wavelength‐selective substrates for multiplexed acquisition of surface‐enhanced Raman scattering (SERS) spectra. This simple one step process provides an attractive and low cost strategy to produce high quality and large area 2D ordered arrays with tunable properties.     

Ethylene glycol oxidation on Pt and Pt-Ru nanoparticle decorated polythiophene/multiwalled carbon nanotube composites for fuel cell applications

A novel supporting material containing polythiophene (PTh) and multiwalled carbon nanotubes (MWCNTs) (PTh-CNTs) is prepared by in?situ polymerization of thiophene on carbon nanotubes using FeCl(3) as oxidizing agent under sonication. The prepared polythiophene/CNT composites are further decorated with Pt and Pt-Ru nanoparticles by chemical reduction of the corresponding metal salts using HCHO as reducing agent at pH = 11 (Pt/PTh-CNT and Pt-Ru/PTh-CNT). The fabricated composite films decorated with nanoparticles were investigated towards the electrochemical oxidation of ethylene glycol (EG). The presence of carbon nanotubes in conjugation with a conducting polymer produces a good catalytic effect, which might be due to the higher electrochemically accessible surface areas, electronic conductivity and easier charge-transfer at polymer/electrolyte interfaces, which allows higher dispersion of Pt and Pt-Ru nanoparticles. Such nanoparticle modified PTh-CNT electrodes exhibit better catalytic behavior towards ethylene glycol oxidation. Results show that Pt/PTh-CNT and Pt-Ru/PTh-CNT modified electrodes show enhanced electrocatalytic activity and stability towards the electro-oxidation of ethylene glycol than the Pt/PTh electrodes, which shows that the composite film is more promising for applications in fuel cells.     

Electrochromic properties of N-doped tungsten oxide thin films prepared by reactive DC-pulsed sputtering

In depositing nitrogen doped tungsten oxide thin films by using reactive DC-pulsed magnetron sputtering process, nitrous oxide gas (N₂O) was employed instead of nitrogen (N₂) as the nitrogen dopant source. The nitrogen doping effect on the structural and electrochromic properties of WO₃ thin films was investigated. X-ray diffraction (XRD) results show that the films are amorphous. Morphological images reveal that the films are characterized by a hybrid structure comprising nanoparticles embedded in amorphous matrix and open channels between the agglomerated nanoparticles, which promotes rapid charge transport through the film. Increasing the nitrogen doping concentration is found to decrease the nanoparticle size and the band gap energy. The electrochromic properties were studied using cyclic voltammetric and spectroeletrochemical techniques. The film with N content of ~ 5 at.% exhibits higher optical modulation and coloration efficiency as well as faster ion transport kinetics. The results reveal that electrochromic and lithium ion transport properties are moderately enhanced relative to the un-doped tungsten oxide thin films by appropriate content of dopant, due to the effects of nitrogen doping.     

Plasmonic enhancement of fluorescence on silver nanoparticle films

The localized plasmon controlled fluorescence has been discussed by comparing the fluorescence enhancement of dyes on different shaped silver nanoparticle self-assembled films. A trilayer structure, composed of a silver nanoparticle monolayer, a proper thickness polyelectrolyte spacing layer and a dye-adsorbed layer, was constructed to study the plasmon enhanced fluorescence properties. The effective coupling of the plasmon band with the excitation or emission of dye resulted in different enhancement factors. Moreover, the plasmon enhanced fluorescence resonance energy transfer (FRET) of two dyes was observed. The FRET efficiency of the spherical silver nanoparticle self-assembled film had a 2.8-fold increase. The improvement of FRET efficiency via localized surface plasmons would increase the sensitivity of FRET-based bioassays.     

A nanoparticulate indium tin oxide field-effect transistor with solid electrolyte gating

Reversible tuning of the transport properties of metallic conducting systems is not reported widely in the literature. Here, we report a junction field-effect transistor (FET) based on a transparent conducting oxide (TCO) nanoparticle channel and a solid polymer electrolyte as a gate. The device principle is based on the variation of the drain current induced by the capacitive double layer charging at the electrolyte/nanoparticle interfaces. A device with a metallic conducting channel made of indium tin oxide (ITO) nanoparticles exhibits an on/off ratio of 2 × 10(3) even when the gate potential is limited within the electrochemical capacitive region to avoid redox reactions at the interface. An FET device with metal-like conductance is always favored for the low dimensions of the device and a high on-state current. The field-effect mobility is calculated to be 24.3?cm(2)?V(-1)?s(-1). A subthreshold swing between 230 and 425?mV?dec(-1) is observed.     

Three-dimensional assembly of nanoparticles from charged aerosols

The capability of assembling nanoparticles into a desired ordered pattern is a key to realize novel devices which are based not only on the unique properties of nanoparticles but also on the arrangements of nanoparticles. While two-dimensional arrays of nanoparticles have been successfully demonstrated by various techniques, a controlled way of building ordered arrays of three-dimensional (3D) nanoparticle structures remains challenging. We report that a variety of 3D nanoparticle structures can be formed in a controlled way based on the ion-induced focusing, electrical scaffold, and antenna effects from charged aerosols. Particle trajectory calculations successfully predict the whole process of 3D assembly. New surface enhanced Raman scattering substrates based on our 3D assembly were constructed as an example showing the viability of the present approach. This report extends the current capability of positioning nanoparticles on surface to another spatial dimension, which can serve as the foundation of future optical, magnetic, and electronic devices taking the advantage of multidimensions.     

Effect of filler types and calcination temperature on the microstructure and the nitric oxide photocatalytic activity of composite titanium dioxide films

The composite titanium dioxide (TiO(2)) films coating on the woven glass fabric were prepared by a modified sol-gel process, using pre-calcinated TiO(2) nanoparticle or silica gel as filler. The characterized physicochemical properties of the prepared catalyst films showed that the specific surface area, the microstructure and the crystal structure of the catalysts were greatly affected by the fillers and the calcination temperature. The physicochemical properties of composite films and the photocatalytic activity of nitric oxide (NO) show that the pre-calcinated TiO(2) nanoparticle is more favorable than silica gel as filler. The pre-calcinated TiO(2) nanoparticle filler can increase the photocatalytic activities of the catalysts by increasing the specific surface area, introducing a bimodal mesoporous structure, and creating a polymorphous crystal structure. And the TiO(2)-TiO(2) film calcinated at 400 degrees C exhibits the highest photocatalytic activity for NO oxidation and is more active than Degussa P25.     

Conductance oscillations in molecularly linked Au nanoparticle film-superconductor systems

Charge transport across a disordered normal-superconductor (DN-S) interface was studied using a macroscopic, molecularly linked Au nanoparticle film as the DN component. Low-temperature conductance versus voltage and magnetic field exhibit zero-bias and zero-field peaks, respectively. Importantly, the latter typically exhibit superimposed oscillations. Such oscillations are rarely seen in other DN-S systems and are remarkable given their robustness in these macroscopic films and interfaces. A number of observations indicate that conductance peaks and oscillations arise due to a 'reflectionless tunnelling' process. Scattering length scales extracted from the data using a reflectionless tunnelling picture are consistent with literature values. Factors resulting in the observation of oscillations in this system are discussed.     

Measurement of discrete charge in the systems of ultra-small tunnel junctions

The measurement of a charge of an almost isolated metal island gives discrete values. The non-equilibrium quantum effects on the shape of transition between these discrete values are studied here. They were shown to determine the width of transition in the limit of small temperatures and junction conductivities. Since any real measurement sets the system to non-equilibrium state the result of measurement is determined by properties of a measuring device. The most practical cases are discussed below: measurements by Fulton-Dolan electrometer as well as by co-tunneling electrometer and self-measurement of the charge by the SET transistor. The results obtained seem to be of general importance for non-equilibrium dissipative quantum dynamics.     

Convective assembly of linear gold nanoparticle arrays at the micron scale for surface enhanced Raman scattering

A convective assembly technique at the micron scale analogous to the writing action of a “pipette pen” has been developed for the linear assembly of gold nanoparticle strips with micron scale width and millimeter scale length for surface enhanced Raman scattering (SERS). The arrays with interparticle gaps smaller than 3 nm are hexagonally stacked in the vicinity of the pipette tip. Variable numbers of stacked layers and clean surfaces of the assembled nanoparticles are obtained by optimizing the velocity of the pipette tip. The SERS properties of the assembled nanoparticle arrays rely on their stacking number and surface cleanliness.      

Ru-Pt core-shell nanoparticles for preferential oxidation of carbon monoxide in hydrogen

Most of the world's hydrogen supply is currently obtained by reforming hydrocarbons. 'Reformate' hydrogen contains significant quantities of CO that poison current hydrogen fuel-cell devices. Catalysts are needed to remove CO from hydrogen through selective oxidation. Here, we report first-principles-guided synthesis of a nanoparticle catalyst comprising a Ru core covered with an approximately 1-2-monolayer-thick shell of Pt atoms. The distinct catalytic properties of these well-characterized core-shell nanoparticles were demonstrated for preferential CO oxidation in hydrogen feeds and subsequent hydrogen light-off. For H2 streams containing 1,000 p.p.m. CO, H2 light-off is complete by 30 (composite function)C, which is significantly better than for traditional PtRu nano-alloys (85 (composite function)C), monometallic mixtures of nanoparticles (93 (composite function)C) and pure Pt particles (170 ( composite function)C). Density functional theory studies suggest that the enhanced catalytic activity for the core-shell nanoparticle originates from a combination of an increased availability of CO-free Pt surface sites on the Ru@Pt nanoparticles and a hydrogen-mediated low-temperature CO oxidation process that is clearly distinct from the traditional bifunctional CO oxidation mechanism.     

Enhanced antimicrobial activity of silver nanoparticles‐Lonicera Japonica Thunb combo

Silver metals have long been known to possess antimicrobial properties. Recently, even the nanoparticle version of silver (AgNPs) has also been established as antimicrobials. In this study AgNPs were combined with extracts of the medicinal plant Chinese honeysuckle, Lonicera japonica Thunb. The antimicrobial activity of the AgNPs‐herb was tested against pathogenic Escherichia coli CMCC44113. Using different AgNPs or herb (honeysuckle water extract or HWE) ratios in the presence of a fixed concentration of E. coli CMCC44113, potencies were found to be proportional with concentrations. The antimicrobial activities of AgNPs‐HWE combo were significant enhanced, when compared with solely AgNPs or HWE. Thus, atomic force microscopic and propidium monoazide‐PCR were used to probe the damages caused by AgNPs‐HWE combo on the cell morphology and cell membrane integrity of E. coli. The mechanism of AgNPs‐HWE combo against E. coli may attribute to AgNPs leads to cell wall lysis and damages cell membrane integrity, and thus increases the penetration of HWE into the bacterium, which results in more serious damage to bacterial cells. These findings indicated that AgNPs‐herb was more potent than the AgNPs alone and holds promise for the development of nanoparticle enhanced herbal pharmaceuticals.Inspec keywords: microorganisms, cellular biophysics, silver, nanoparticles, nanomedicine, antibacterial activity, vegetation, biomembranes, biomedical materialsOther keywords: enhanced antimicrobial activity, silver nanoparticle‐Lonicera japonica Thunb combo, silver metals, antimicrobial properties, medicinal plant Chinese honeysuckle, AgNP‐herb, pathogenic Escherichia coli CMCC44113, E. coli CMCC44113 concentration, antimicrobial activity, AgNP‐HWE combo, atomic force microscopy, propidium monoazide‐PCR, cell morphology, E. coli, cell wall lysis, cell membrane integrity, HWE penetration, bacterial cells, nanoparticle enhanced herbal pharmaceuticals, Ag     

Conductivity and adhesion enhancement in low-temperature processed indium tin oxide/polymer nanocomposites

We report on the conductivity and adhesion enhancement of indium tin oxide (In₂O₃:Sn; ITO) nanoparticle films by the application of polymers as matrix material. We fabricated ITO layers at a maximum process temperature of 130 °C by modifying and spin-coating nanoparticulate ITO dispersions. Dispersions containing the organic film-forming agent polyvinylpyrrolidone (PVP) and the organofunctional coupling agent 3-methacryloxypropyltrimethoxysilane (MPTS) have been developed to obtain transparent and conducting coatings on substrates which do not withstand high process temperatures like polymers or already processed glasses. The layers were cured by UV-irradiation as well as by low-temperature heat treatment (T = 130 °C) in air and under forming gas atmosphere (N₂/H₂). The influence of the additives on the electrical, optical, morphological and mechanical layer properties is reported. Compared to best pure ITO layers (3.1 Ω^− 1 cm^− 1), the ITO-MPTS-PVP nanocomposite coatings exhibit a conductance of 9.8 Ω^− 1 cm^− 1. Stable sheet resistances of 750 Ω/□ at a coexistent transmittance of 86% at 550 nm for a layer thickness of about 1.3 µm were achieved. The conductance enhancement is a consequence of the consolidation of the ITO nanoparticle network due to the acting shrinkage forces caused either by drying in the case of PVP or UV-irradiation induced condensation and polymerization reactions in the case of MPTS.     

Chemically sensitive field-effect transistor with polyaniline-ionic liquid composite gate

A sensing layer for a chemically sensitive field-effect transistor (CHEMFET) based on a composite of camphorsulfonic acid (CSA)-doped polyaniline (PANI) and the room-temperature ionic liquid (IL) 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)-imide, BMI(Tf2N), has been developed and characterized for the sensing of ammonia gas. The work function responses of the cast films with and without IL were analyzed by "stepwise" changes of ammonia gas concentration from 0.5 to 694 ppm in air as a function of the mole fraction of IL to PANI. The PANI x CSA/BMI(Tf2N) layers showed enhanced sensitivities, lower detection limits, and shorter response times. There is experimental evidence that PANI forms a charge-transfer complex with imidazolium cation.