Electrical properties and photoconductivity of polyaniline/sulfonated poly(arylene ether sulfone) composite films

Temperature dependent electrical conductivity of the polyaniline-sulfonated poly(arylene ether sulfone) with 35 mol percent sulfonation (PANI-BPS35) composite films were investigated in the temperature range of 80–380 K. These composite films showed semiconductor behavior with the exponential variation of inverse temperature dependence of electrical conductivity. Calculated Mott’s parameters showed that variable range hopping mechanism is the dominant transport mechanism for the carriers in low temperature region. Photoconductivity of the PANI-BPS35 composite films having 10, 20, and 40 weight percent conductive filler under various illumination intensities was also studied. Photocurrent of the composite films increased with increasing both polyaniline weight fraction and temperature. Finally, the effect of doping on both electrical conductivity and the photoconductivity of the composite films was investigated.     

Characterization and ammonia sensing properties of pure and?modified ZnO films

Zinc oxide (ZnO) films have been prepared by thermal oxidation of pre-deposited zinc films on the glass substrate kept at room temperature. These films were surface modified by dipping them into an aqueous solution (0.1 M) of lithium chloride (LiCl) and aluminium chloride (AlCl₃) followed by firing at 500°C. Based on X-ray diffraction results it is observed that modification of pure ZnO by lithium and aluminium precursor results a change in the lattice parameters. Li and Al ions appear to enhance the a-axis orientation and c-axis orientation of pure ZnO films, respectively. Field emission scanning electron micrographs of lithium-modified ZnO film indicate the presence of nanoneedles, while nanorods are observed in case of aluminium-modified ZnO film. The electrical resistance measurements of modified ZnO films also show variation in resistance as compared to pure ZnO film. Pure and Al-modified films of ZnO are sensitive to ammonia at room temperature, while Al-modified ZnO film is found to be more sensitive with 99% of response at 250 ppm.     

Enhancement in electrochemical properties of ionic liquid-based nanocomposite polymer electrolytes by 100 MeV Si9+ swift heavy ion irradiation

Swift heavy ion (SHI) irradiation has been used as a tool to enhance the electrochemical properties of ionic liquid-based nanocomposite polymer electrolytes dispersed with dedoped polyaniline (PAni) nanorods; 100 MeV Si⁹⁺ ions with four different fluences of 5?×?10¹⁰, 1?×?10¹¹, 5?×?10¹¹, and 1?×?10¹² ions cm^?2 have been used as SHI. XRD results depict that with increasing ion fluence, crystallinity decreases due to chain scission up to fluence of 5?×?10¹¹ ions cm^?2, and at higher fluence, crystallinity increases due to cross-linking of polymer chains. Ionic conductivity, electrochemical stability, and dielectric properties are enhanced with increasing ion fluence attaining maximum value at the fluence of 5?×?10¹¹ ions cm^?2 and subsequently decrease. Optimum ionic conductivity of 1.5?×?10^?2 S cm^?1 and electrochemical stability up to 6.3 V have been obtained at the fluence of 5?×?10¹¹ ions cm^?2. Ac conductivity studies show that ion conduction takes place through hopping of ions from one coordination site to the other. On SHI irradiation, amorphicity of the polymer matrix increases resulting in increased segmental motion which facilitates ion hopping leading to an increase in ionic conductivity. Thermogravimetric analysis (TGA) measurements show that SHI-irradiated nanocomposite polymer electrolytes are thermally stable up to 240–260 °C.     

Evaluation of ammonia–nitrogen removal efficiency from aqueous solutions by ultrasonic irradiation in short sonication periods

In this study, mechanisms and efficiency of ammonia–nitrogen removal from aqueous solutions by ultrasonic irradiation were investigated. Depending on the factors affecting the sonication (initial concentration, initial pH, ultrasonic power density and sonication period), sonication tests were carried out and ammonium–nitrogen removal efficiency by ultrasonic irradiation was determined. In these experiments, ammonia–nitrogen removal efficiency was achieved in the range of 8–64%. In short sonication periods, the best ammonia–nitrogen removal efficiency was achieved at pH 8.2–11. Lower ammonia–nitrogen removal efficiency was observed in high initial ammonia–nitrogen concentration of solutions. It was observed that high initial ammonia–nitrogen concentrations may led to decreased ammonia–nitrogen removal efficiency however quantity of ammonia–nitrogen removal was higher. Because high initial concentration had a negative impact on the sonochemical reactions the heat of cavitation bubbles was reduced. Ammonia–nitrogen removal efficiency was increased with ultrasonic density and sonication period. This study showed that effective ammonia–nitrogen removal could be achieved by the ultrasonic irradiation in short sonication periods (as 60–600 s). Specific cost of ammonia–nitrogen removal by the ultrasonic irradiation from simulated ground water, surface water, wastewater and landfill leachate was also calculated. The specific removal cost was varied between 0.01 and 0.25 $/g ammonia–nitrogen.     

Improvement of microstructure and magnetic properties of Nd–Fe–B alloys by Nb and Co additions

In order to establish the role of niobium on the hydrogenation, disproportionation, desorption and recombination (HDDR) behavior of near-stoichiometric alloys, two alloys: NdI3Fe8OB7 and Nd13Fe78Nb1Co1B7 (at%) were investigated before, during and after the HDDR process. The microstructure of the as-cast Nb-free alloy before employing the HDDR process was found to consist of three phases, the matrix Nd₂Fe₁₄B (φ) phase, Nd-rich phase and a significant amount of free iron; whereas, the microstructure of the Nb-containing alloy consisted of only the first two phases.     

Dating study of two rock crystal carvings by surface microtopography and by ion beam analyses of hydrogen

Two artefacts made of rock crystal (quartz) from the collection of the Musée du quai Branly in Paris, France, a skull approximately half of the size of a real cranium and a smaller anthropomorphic head, purportedly attributed to pre-Columbian Mesoamerican cultures, were studied to assess their authenticity. The surface of the artefacts were examined by means of optical microscopy and scanning electron microscopy (SEM) and were analyzed nondestructively by ERDA (Elastic Recoil Detection Analysis), an ion beam analytical method that can measure hydrogen concentration profiles in depth. Optical and SEM imaging of tool marks indicates that the skull has been cut from a rock crystal block using machine lapidary techniques unavailable to pre-Columbian artisans, whereas the anthropomorphic head has more likely been carved and polished with manual techniques comparable to ancient ones. Hydrogen depth profiles in the first micron below the surface of the artefacts have been measured by ERDA with a 3-MeV He beam in a controlled helium atmosphere. Recently the progressive penetration of water at the surface of a quartz sample exposed to the natural environment has been proposed as a dating method (labeled quartz hydration dating or QHD) applicable to archaeological artefacts made of this material. The shallower penetration of H clearly indicates that the rock crystal skull was manufactured more recently than the reference quartz sample cut in 1740. As for the anthropomorphic head, the deep penetration profiles indicate an older artefact. Thus the converging micro-topographical examinations and hydrogen profiles of the samples surfaces indicate that the skull is probably not a pre-Columbian artefact but has been carved in the 18th or 19th century. The anthropomorphic head, on the other hand, could have been carved in the pre-Columbian period. In addition, the ERDA method carried out with an external beam presented here provides a new and simple approach for the nondestructive authentication of quartz-based archaeological artefacts by QHD.     

Polarization switching properties of spray deposited CsNO3: PVA composite films

The ferroelectric and switching properties of spray deposited cesium nitrate: poly (vinyl alcohol) composite films at different substrate temperatures (T _s ) have been studied. The optimum value of remanent polarization was obtained in the film deposited at T _s =200°C, which may be due to larger structural distortion (c/a ratio) and less porosity as revealed by x-ray diffraction and field emission scanning electron microscope (FESEM) analysis. The switching current transients have been analyzed by nucleation limited switching model (NLS) with the Lorentzian distribution function. This model gives excellent agreement with the experimental polarization current throughout the whole time range. The switching parameters were determined in the composite films deposited at different T _s and found to be optimum at T _s =200°C. The effect of pulse amplitude on the domain switching properties has also been studied and analyzed. The peak value of polarization current exhibits an exponential dependence on the external applied field.     

The impact of point thermal absorbers in ablation of poly(methyl methacrylate)

Molecular dynamics (MD) simulations are used to study the interactions of photons with a poly(methyl methacrylate), or PMMA, substrate and point thermal absorbers. The point thermal absorbers are embedded within the polymer matrix which can be excited and transfer energy to the surrounding particles through an internal vibrational mode. Using a fluence above the ablation threshold, two excitation channels are studied—one includes a direct heating of the polymer and the other includes the excitation of the thermal absorbers. Although the yield of ejected particles is similar for both simulations, the plume composition differs. For the simulation of the excitation of the point thermal absorbers, the plume consists of a greater number of smaller substrate fragments due to local high temperature regions.     

Charge state effect on K-shell ionization of aluminum by 600–3400 keV xenonq+ (12 < q < 29) ion collisions

K-shell X-ray spectra of Al were measured by the interaction of 600–3400 keV Xe ^q+ (q = 12–29) ions with Al surface. The X-ray yields per incident ion were deduced and the K-shell ionization cross-sections were obtained from the experimental yield data. With the same incident energy, the K-shell ionization cross-sections of Al excited by Xe ^q+ (q < 26) ions were of the same order of magnitude, while for q = 26 and 29 Xe ion collisions, they were, respectively, about two and ten times larger. Taking into account the binding-energy-modification and the recoil effect of target atoms, the binary encounter approximation (BEA) theory was consistent with the experimental data for q < 26 Xe ion collisions, but it underestimated those excited by q = 26 and 29 Xe ions. This indicates that the K-shell ionization of target induced by Xe ^q+(q < 26) ions was mainly due to the direct Coulomb excitation. However for q = 26 and 29 Xe ions collisions, the transfer of 3d vacancies of projectile to the 1s orbital of target via rotational coupling of the 3dπ, δ-3dσ molecular orbitals, which were formed in the ion-atom quasi-molecule, may cause a considerable contribution to the enhancement of ionization. In addition to the well known Auger and X-ray transition, our experiments proved that the molecular orbital transition (“side-feeding”) mechanism is also a significant channel for de-excitation of hollow atoms formed below the surface.     

Synthesis,characterization and mechanical properties of nylon–silver composite nanofibers prepared by electrospinning

Silver (Ag) nanoparticles (∼3 nm) were synthesized using silver nitrate as the starting precursor, ethylene glycol as solvent and poly (N-vinylpyrrolidone) (PVP) introduced as a capping agent. These nano-Ag particles were reinforced in nylon matrix by electrospinning of nylon-6/Ag solution in 2,2,2-trifluoroethanol and composite nanofibrous membranes were synthesized. The effects of solution concentration and relative humidity (RH) on the resultant fibrous membranes were studied. Scanning electron microscopy and Transmission electron microscopy was used to study the size and morphology of the fibers. It was observed that concentration and RH could be used to modulate the fiber diameter. Tensile test was used to evaluate the mechanical property of these electrospun composite membranes. The composite membranes showed higher strength (approx. 2–3 times increase in strength) compare to as synthesized nylon fibers.     

Effect of 100 MeV O7+ ion beam irradiation on structural,optical and electronic properties of SnO2 thin films

In this paper, we present the impact of swift heavy ion beam irradiation on the structural, optical and electronic properties of SnO₂ thin films. Thin films were deposited using the pulsed laser deposition technique on Al₂O₃ substrates. Atomic force microscopy, X-ray diffraction, UV–visible absorption and temperature-dependent resistivity measurements were performed to explore the morphological, structural, optical and electronic properties of the as-deposited and irradiated samples. The peak intensity of the (200) peak was found to decrease monotonously with increasing irradiation fluence. The band gap energy of the 1×10¹¹ ion/cm² irradiated sample was found to increase. The electrical resistivity of the samples showed a continuous increase with the irradiation fluence.     

Enhancement of thermoelectric properties of SrTiO_3/LaNb–SrTiO_3 composite by different doping levels

Strontium titanate(STO)is an n-type oxide thermoelectric material,which has shown great prospects in recent years.The doping of La and Nb into STO can improve its power factor,whereas its thermal conductivity is still very high.Thus,in order to obtain a high thermoelectric figure-of-merit z T,it is very important to reduce its thermal conductivity.In this paper,using a combination of a hydrothermal method and a high-efficiency sintering method,we succeed in preparing a composite of pure STO and La Nb-doped STO,which simultaneously realizes lower thermal conductivity and higherSeebeck coefficient,therefore,the thermoelectric properties of STO are significantly improved.In the SrTiO_3/La Nb–SrTiO_3 bulk samples,the lowest thermal conductivity is 2.57 W·m~(-1)·K~(-1)and the highest z T is 0.35 at 1000 K for the STO/La_(10)Nb_(20)–STO sample.     

Photoluminescence properties of Er-doped β-FeSi2 grown by ion implantation

Photoluminescence (PL) properties of Er-doped β-FeSi₂ (β-FeSi₂:Er) and Er-doped Si (Si:Er) grown by ion implantation were investigated. In PL measurements at 4.2 K, the β-FeSi₂:Er showed the 1.54 μm PL due to the intra-4f shell transition of ⁴I_13/2→⁴I_15/2 in Er³⁺ ions without a defect-related PL observed in Si:Er. In the dependence of the PL intensity on excitation photon flux density, the obtained optical excitation cross-section σ in β-FeSi₂:Er (σ=7×10⁻¹⁷ cm²) is smaller than that in Si:Er (σ=1×10^-15 cm²). In the time-resolved PL and the temperature dependence of the PL intensity, the 1.54 μm PL in β-FeSi₂:Er showed a longer lifetime and larger activation energies for non-radiative recombination (NR) processes than Si:Er. These results revealed that NR centers induced by ion implantation damage were suppressed in β-FeSi₂:Er, but the energy back transfer from Er³⁺ to β-FeSi₂ was larger than Si:Er.     

Electrical properties, structure, and surface morphology of poly(p-xylylene)–silver nanocomposites synthesized by low-temperature vapor deposition polymerization

The crystalline structure, surface morphology, electrical, and optical properties of thin films of nanocomposites consisting of silver nanoparticles embedded in poly(p-xylylene) matrix prepared by low-temperature vapor deposition polymerization were studied. Depending on the filler content, the average size of silver nanoparticles varied from 2 to 5 nm for nanocomposites with 2 and 12 vol.% of silver, correspondingly. The optical adsorption in the visible region due to surface plasmon resonance also exhibited a clear correlation from silver content, revealing a red shift of the adsorption peak with the increase of the metal concentration. The temperature dependences of the dc resistance of pure p-xylylene condensate and p-xylylene–silver cocondensates during polymerization as well as temperature dependences of the formed poly(p-xylylene)–silver nanocomposites were examined. The observed variation of the temperature dependences of electrical resistance as a function of silver concentration are attributed to different conduction mechanisms and correlated with the structure of the composites. The wide-angle X-ray scattering and AFM measurements consistently show a strong effect of silver content on the nanocomposite structure. The evolution of the size of silver nanoparticles by thermal annealing was demonstrated.     

Improved mechanical properties of hydroxyapatite/poly(?-caprolactone) scaffolds by surface modification of hydroxyapatite

Scaffolds comprising hydroxyapatite (HAP) or poly(?-caprolactone)-grafted hydroxyapatite (g-HAP) and poly(?-caprolactone) (PCL) were prepared using the thermally induced phase separation/salt leaching technique. The g-HAP nanoparticles were evaluated by Fourier Transformation Infrared Spectroscopy (FTIR) and thermal gravimetric analysis (TGA). Power X-ray Diffraction (XRD) patterns confirmed the successful grafting on the surface of HAP. The effects on mechanical strength, porosity and thermal property of scaffolds by the introduction of nanoparticles were extensively investigated. The compressive modulus of the scaffold was greatly improved by the addition of g-HAP nanoparticles. Especially the compressive modulus of the g-HAP/PCL scaffold containing 20 wt% of g-HAP was 59.4% higher than that of the corresponding HAP/PCL scaffold.     

Influence of photoexcitation pathways on the initiation of ablation in poly (methyl methacrylate)

Experimental and theoretical studies of laser ablation of polymers, under various processing conditions, have identified many possible photoexcitation pathways and consequently many likely processes responsible for the onset of ablation. We investigate the role of these processes—namely the thermal, mechanical and chemical processes—occurring in a polymeric substrate during UV irradiation. Molecular dynamics simulations with an embedded Monte Carlo-based reaction scheme were used to study ablation of Poly (methyl methacrylate) at 157 nm. Laser-induced heating and chemical decomposition of the polymeric substrate are considered as ablation pathways. For the heating case, the mechanism of ejection is thermally driven limited by the critical number of bonds broken. This fragmentation process is well reproduced by the existing bulk photothermal ablation model. Alternatively, if the photon energy goes toward direct bond breaking, it initiates chemical reactions, polymer unzipping, and formation of gaseous products leading to near complete decomposition, loss of strength and cohesiveness of the top layers of the polymeric substrate. The ejection of small gaseous molecules weakens and hollows out the substrate, facilitating liftoff of larger fragments of material. These larger clusters are thermally ejected and the photochemical ablation process can be described by the two-step model proposed by Kalontarov.     

Effects of neutron irradiation on superconducting properties of orthorhombic Y–Ba–Cu oxides

Abstract

We have studied the effects of fast neutron (E>0.1 MeV) irradiation at reactor (～ 360 K) and low (～ 20 K) temperatures on the superconducting properties of polycrystalline orthorhombic YBa₂Cu₃O_7?y . Measurements were made on the superconducting critical temperature T_c , critical current J_c , Meissner effect and magnetic field dependence of J_c . The T_c drops by an irradiation at reactor temperature and J_c increases with increasing fluence. On the other hand with the irradiation at low temperature, T_c rises and J_c increases. Results of observation of Meissner effect and the magnetic field dependence of J_c are consistent with the behavior of T_c and J_c .     

In situ processing and properties of nanostructured hydroxyapatite/alginate composite

A series of hydroxyapatite/alginate (HA/Alg) nanocomposites with alginate amounts varying from 10 to 40 wt% were prepared through in situ hybridization technique. The inorganic phase in the composites was carbonate-substituted HA with low crystallinity. The crystallinity of HA decreased with the increase of alginate content. HA crystallites were needle-like in shape with a typical size of 20 to 50 nm in length and 5 nm in width. FT-IR spectroscopy indicated that the chemical interaction occurred between the mineral phase and the polymer matrix. As compared to pure HA without alginate, the composites showed more homogeneous microstructures, where HA nanocrystals were well embedded in alginate matrix. Among all the samples, the composite containing 30 wt% alginate exhibited a highly ordered three-dimensional network, similar to natural bone’s microstructure.