Optical properties of metal nanoparticles synthesized in a polymer by ion implantation: A review

Polymer composite layers irradiated by 30-keV Ag⁺ ions with doses from 3.1×10¹⁵ to 7.5×10¹⁶ cm^?2 and an ion current of 4 µA/cm² are investigated. The composites were examined using Rutherford backscattering (RBS), transmission electron microscopy (TEM), and optical spectroscopy. As follows from electron microscopy and electron microdiffraction data, ion implantation is a promising tool for synthesizing silver nanoparticles in the surface region. The optical density spectra taken of these composites demonstrate that the silver nanoparticles exhibit unusually weak plasma resonance. The formation of silver nanoparticles in layers carbonized by ion implantation is considered. Based on the Mie theory, optical extinction spectra for silver particles in the polymer and carbon matrices are simulated and optical spectra for complex silver core-carbon sheath nanoparticles are calculated. The physics behind the experimental optical spectra of the composite is discussed.     

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.     

Preparation, characterization and surface morphology of novel optically active poly(ester-amide)/functionalized ZnO bionanocomposites via ultrasonication assisted process

Novel bionanocompoites (BNCs) were prepared using zinc oxide (ZnO) nanoparticles which functionalized by γ-methacryloxypropyltrimethoxysilane (KH570) as a coupling agent. Poly(ester-amide) (PEA) based on tyrosine natural amino acid was synthesized and used as a polymer matrix. PEA/ZnO BNCs were characterized by fourier transform infrared spectra (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM) and transmission electron microscopy (TEM). All the results confirmed that the surface of ZnO particle has sufficient compatibility with PEA through the link of the coupling agent between ZnO and polymer and also proved that the presence of ZnO nanoparticles appeared to be dispersed in nanosize in polymer composite matrix. In addition, thermogravimetric analysis (TGA) data indicated an enhancement of thermal stability of new BNC materials compared with the pure polymer.     

Deposition of silver nanoparticles on carbon nanotube by chemical reduction method: Evaluation of surface,thermal and optical properties

Silver was stabilized on multi-walled carbon nanotubes (MWCNTs) by chemical-reduction technique using N,N-dimethylformamide (DMF) as a reducing agent. The influence of silver on the performance of carbon nanotubes (CNTs) was investigated by employing Fourier-transform infrared spectra (FTIR), Raman spectroscopy (RAS), thermal gravimetric analysis (TGA), zeta potential measurement, scanning electron microscope (SEM), electron dispersive X-ray spectrometer (EDX), transmission electron microscopy (TEM), and reflectance spectroscopy (RS). FTIR as well as RS methods evidenced the synthesis procedure using chemical reduction method was successful. Performing TGA of the samples under oxygen atmosphere demonstrated that the silver nanoparticles (Ag NPs) generated on MWCNTs surface can decrease the thermal stability of the particles by the catalytic oxidation of CNTs. In contrary, the thermal stability of the MWCNTs has improved under nitrogen atmosphere. EDX results showed the presence of Ag, Au and Co on the surface of deposited sample. The synthesised silver multi-walled carbon nanotubes (Ag–MWCNTs) were found to have higher UV reflection activity compared with untreated particles. The Ag–CNTs can be used in producing anti-UV composites.     

氯离子对银胶的宽波段光吸收光谱的影响

本文借助紫外-可见-近红外吸收光谱、透射电子显微镜技术,研究灰银胶中加入氯离子后此体系的宽波段吸收光谱的变化,旨在探索氯离子对纳米银颗粒表面特性的影响。实验结果表明,氯离子的加入会引起胶体中银颗粒的凝聚和银纳米颗粒的聚集体形态的变化,造成银颗粒的本征吸收光谱的"蓝移"和近红外区新吸收带的出现。最后我们初步分析了此现象产生的机制。     

Synthesis and characterization of silver-polypyrrole film composite

In this work, we report the chemical polymerization of pyrrole to obtain thin film of polypyrrole (PPy) hydrochloride deposited onto the electrode of the quartz crystal microbalance (QCM). The film in the base form was exposed to a solution of AgNO₃. Electroless reduction for silver ions by the PPy film took place and silver particles were adsorbed onto the film surface. The silver particles content at the PPy films were analyzed by QCM and the results showed that the concentrations of silver uptakes increase as the original AgNO₃ solution increases. The morphology of the surface of the PPy film and the silver-PPy film composite were studied by the scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectrometry (EDX). They showed that the obtained silver particles have spherical, cubic and tetrahedral structures. X-ray diffraction (XRD) and Fourier transformed infra-red spectroscopy (FTIR) were used to characterize the structure of the powder composite. This work reveals the capability of PPy film coating on QCM in sensing and removing silver from several environmental samples.     

Supercritical fluid-assisted synthesis of a carbon nanotubes-grafted biocompatible polymer composite

A nanocomposite consisting of multi-wall nanotubes (MWNTs) grafted with a biocompatible polymer poly(2-hydroxyethyl methacrylate) was prepared by in situ polymerization in supercritical carbon dioxide. The surface of the MWNTs was first surface modified with hydroxyl groups in the solution of KMnO₄ and a phase-transfer catalyst. MWNT-OH was then functionalized with vinyl groups using a silane coupling agent, γ-methacryloxypropyltrimethoxysilane. The silane groups can improve the dipersion of MWNTs in supercritical carbon dioxide, while the terminal vinyl groups help fabricate polymer chains on the MWNT surface. The as-synthesized products were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and thermo-gravimetric analysis. The SEM and TEM images showed that the nanotubes were well coated with the polymer shell. The composite had higher thermal stability than the pure polymer and dispersed well in methanol. This biocompatible polymer composite was prepared using a green method and is expected to be useful as a biomaterial composite with potential applications in the biological field.     

Electron microscopy and EXAFS studies on oxide-supported gold-silver nanoparticles prepared by flame spray pyrolysis

Gold and gold-silver nanoparticles prepared by flame spray pyrolysis (FSP) were characterized by electron microscopy, in situ X-ray absorption spectroscopy (XANES and EXAFS), X-ray diffraction (XRD) and their catalytic activity in CO oxidation. Within this one-step flame-synthesis procedure, precursor solutions of dimethyl gold(III) acetylacetonate and silver(I) benzoate together with the corresponding precursor of the silica, iron oxide or titania support, were sprayed and combusted. In order to prepare small metal particles, a low noble metal loading was required. A loading of 0.1-1 wt.% of Au and Ag resulted in 1-6 nm particles. The size of the noble metal particles increased with higher loadings of gold and particularly silver. Both scanning transmission electron microscopy (STEM) combined with energy dispersive X-ray spectroscopy (EDXS) and X-ray absorption spectroscopy (XAS) studies proved the formation of mixed Au-Ag particles. In case of 1% Au-1% Ag/SiO₂, TEM combined with electron spectroscopic imaging (ESI) using an imaging filter could be used in addition to prove the presence of silver and gold in the same noble metal particle. CO oxidation in the presence of hydrogen was chosen as a test reaction sensitive to small gold particles. Both the influence of the particle size and the alloying of gold and silver were reflected in the CO oxidation activity.     

Self Assembly of the Metal Nanoparticles: Formation of the Highly Oriented,Core-Shell Type,Bimetallic Gold–Silver Film

A synthetic route is presented for the preparation of a bimetallic gold–silver film under UV-irradiation. Methoxy polyethylene glycol, a water soluble polymer, is used as the reducing agent for the gold and silver ions in the presence of a ultra-violet source that results in the formation of gold and silver bimetallic nanoparticles. During stirring a centrifugal force is generated at the center of the solution, which results in a coalescence of the nanoparticles and forms a self-assembly of small subunits that ultimately produces a film-like network. UV–vis spectra and scanning electron microscopy were used to determine, respectively, the configuration of the gold and the silver in the nanoparticles, a Au_core–Ag_shell structure, and the thickness of the film.     

Synthesis and characterisation of polypyrrole–indium phosphide composite film

Polypyrrole (PPy)–indium phosphide (InP) composite material was electrochemically prepared by the incorporation of InP into a PPy matrix during electrochemical synthesis (cycling) under magnetic stirring from the acetonitrile/LiClO4 electrolyte containing the Py and InP particles. The PPy–InP composite material was designed to explore new approaches to improve light-collection efficiency in polymer photovoltaic. The samples were characterised by cyclic voltammetry, impedance spectroscopy measurement, scanning electron microscopy, energy dispersive X-ray spectroscopy, UV–visible and photoelectrochemical measurements. It was observed that the photocurrent of the composites was higher than that of the single PPy films and increased with InP concentration. The study showed that the presence of InP particles in the polymeric film improves the optical and the photovoltaic properties of PPy and give information on the use possibility of these films for photovoltaic cells' application.     

Microphase separation in a cross-linked epoxy phenol polymer

The microphase separation on the surface of samples of a cross-liked epoxy phenol (EP) polymer produced by the curing of a composition containing an epoxy diane oligomer (EO) and a phenol formaldehyde oligomer (PO) has been investigated using electron microscopy with decoration by silver chloride. It has been shown that, in the cross-liked EP polymer, there is a quasi-lattice of mixed-type AgCl nanoparticles, which consists of two sublattices. The formation of simple lattices of particles is caused by the microphase separation according to the type of nucleation and growth of fractal clusters of the cross-liked EO; the spinodal decomposition in the binary system; and the formation of interpenetrating polymer networks represented by the superposition of two lattices of particles or two infinite phase clusters (cross-liked EO and PO, respectively).     

Field emission studies of silver nanoparticles synthesized by electron cyclotron resonance plasma

Field emission has been studied for silver nanoparticles (25-200 nm), deposited within a cylindrical silver target in an electron cyclotron resonance (ECR) plasma. Particle size distribution was controlled by optimum biasing voltages between the chamber and the target. Presence of non-oxidized silver was confirmed from the X-Ray diffraction analysis; however, thin protective layer of oxide was identified from the selective area electron diffraction pattern obtained with transmission electron microscopy. The silver nanoparticles were seen to exhibit hilly pointed like structures when viewed under the atomic force microscopy (AFM). The emissive properties of these particles were investigated by field emission microscopy. It is found that this technique of deposition is ideal for formation of nanoparticles films on different substrate geometries with size controllability as well as its application to emission devices.     

Ionic conductivity and interfacial interaction in penton/AgI composites

New nanostructured composite system (1???x)penton/xAgI (where 0?< x?<?1) was synthesized by a solution-based technique, which involves the process of modification of polymer surface. Samples of the composite system were characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, and electrical impedance spectroscopy. It was shown that AgI nanoparticles form a continuous layer at the surface of penton particles and consist mainly of cubic γ-phase with a small amount of hexagonal β-phase. Maximum conductivity enhancement at almost one order of magnitude higher compared to the pristine AgI has been observed for the sample with x?=?0.5. The overall activation energy for conduction varies from 0.23 to 0.38 eV, depending on the content of γ-phase of silver iodide in the samples. Two percolation thresholds has been also recorded at the points x?=?0.1 and x?=?0.3.     

Synthesis of Nanoscale Bimetallic Particles in Polyelectrolyte Membrane Matrix for Reductive Transformation of Halogenated Organic Compounds

Nanosized Fe/Ni and Fe/Pd particles were synthesized in the polyacrylic acid (PAA)/polyether sulfone (PES) composite membrane matrix for reductive transformation of halogenated organic compounds (HOCs). The advantages of using membrane to immobilize nanoparticles are the reduction of particles loss, prevention of particles agglomeration, and potential application of convective flow. Cross-linked PAA/PES composite membranes containing metal ions as particles precursor were prepared by heat treatment with ethylene glycol (EG) as a cross-linking agent. Nanoscale metal particles were formed and immobilized inside the membrane matrix after reduction with sodium borohydride. Membrane morphology and structure were observed by scanning electron microscopy (SEM). Particle size and distribution were characterized by SEM and transmission electron microscopy (TEM). Energy dispersive X-ray spectroscopy (EDS) was used to obtain the qualitative and quantitative element information of particles. A specimen-drift-free EDS line profile and EDS mapping system was performed in a scanning transmission electron microscopy (STEM) to determine the two-dimensional element distribution of iron and nickel in the nano domain. In the dechlorination study with trichloroethylene (TCE) as a representative HOCs, rapid and complete destruction of TCE was achieved by using nanosized bimetallic Fe/Ni or Fe/Pd in PAA/PES composite membranes. Typically more than 95% of 10 mg/l TCE was reduced within 1 h. Ethane was found in the headspace as the main product.     

Preparation of poly(styrene-glucidylmethacrylate)/Fe3O4 composite microspheres with high magnetite contents

Magnetic polymer composite microspheres with high magnetite contents were prepared by dispersion polymerization of styrene (St) and glucidylmethacrylate (GMA), in which Fe₃O₄ nanoparticles were co-stabilized by oleic acid and silane surfactants. The microstructure of the composite microspheres was characterized by Fourier transform infrared (FTIR) spectrometry, X-ray diffraction (XRD) and transmission electron microscopy (TEM). Results demonstrated the presence of a hybrid morphology with organic polymer-encapsulated inorganic particles. Subsequently, thermogravimetric analysis (TGA) and vibrating sample magnetometry (VSM) were used to evaluate the magnetite content of the microspheres. It was found that an accordant magnetite content of about 70 wt%, could be obtained for the magnetic polymer microspheres, a value significantly higher than those reported thus far. The possible mechanism for the formation of the microspheres was proposed.     

Study of nano-CdS prepared in methanolic solution and polymer electrolyte matrix

This present paper reports the study of cadmium sulphide (CdS) nanoparticles prepared under controlled condition in methanolic solution and also in polyethylene oxide polymer electrolyte matrix. The sulphurations of the cadmium salts were done in situ by a sodium sulphide solution. The concentration of the precursors has been controlled as detailed in the paper. All the preparation and characterization were carried out at room temperature. The nanoparticles were characterized by UV/Vis spectra in the range of 600 to 250 nm. The absence of bulk/micron size particles was noted in either of the system. The absorption edge near 510 nm indicates the presence of bulk CdS, whereas the presence of nanometer-sized particles is also reflected in low wavelength region. The sizes of the particles as well as particle distribution have been estimated using X-ray diffraction and scanning electron microscopy, respectively. A comparison in the spectra has been done for the sample prepared in either of the matrices. The particle size distribution in the polymeric matrix has been found to be more in comparison to that in the methanolic suspension. The polymer is reported to work as a binder, but not as a capping agent.     

Preparation of Si-PPy-Ag composites and their electrochemical performance as anode for lithium-ion batteries

The nanosilicon connected by polypyrrole (PPy) and silver (Ag) particles was simply synthesized by a chemical polymerization process in order to prepare Si-based anodes for Li-ion batteries. The phase structure, surface morphology, and electrochemical properties of the as-synthesized powders were analyzed by X-ray diffraction, FT-IR, scanning electron microscopy, and galvanostatic charge/discharge measurements. The cycle stability of the Si-PPy-Ag composites was greatly enhanced compared with the pure nanosilicon. A high capacity of more than 823 mA h g^?1 was maintained after 100 cycles. The improved electrochemical characteristics are attributed to the volume buffering effect as well as effective electronic conductivity of the polypyrrole and silver in the composite electrode.     

Chitosan loaded with silver nanoparticles,CS‐AgNPs,using thymus syriacus,wild mint,and rosemary essential oil extracts as reducing and capping agents

The present study describes the green method for the preparation of chitosan loaded with silver nanoparticles (CS‐AgNPs) in the presence of 3 different extracted essential oils. The essential oils play dual roles as reductant and capping agents. The reducing power and DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) assay for the 3 essential oils—Thymus syriacus (T), wild mint (M), and rosemary (R)—have been reported. The preparation of CS‐AgNPs was performed by 2 steps. The 3 previously extracted essential oils have been used as reducing and capping agent in the first step, while in the second step, silver nanoparticles were integrated in chitosan. The integration of AgNPs in the structure of chitosan was confirmed by ultraviolet‐visible, Fourier transform infrared spectroscopy, scanning electron microscopy techniques, and energy dispersive X‐ray. Surface plasmon resonance confirmed the formation of CS‐AgNPs with maximum absorbance at λ_max between 405 ‐ 410 and 410 ‐ 430 nm for colloidal and films of CS‐AgNPs, respectively. The intensity of bands at 3408 cm^?1 in the fourier transform infrared spectroscopy measurements was decreased substantially and shifted slightly to lower frequency (?υ = 43 cm^?1). Scanning electron microscopy shows a spherical morphology of AgNPs with size of 62 nm for both colloidal and film samples, and energy dispersive X‐ray analysis shows peaks confirming AgNPs formation.     

Structural Characteristics of Metal Nanoparticles in Glass Upon Irradiation-Assisted Processing

Irradiation-assisted processing, i.e. ion, electron and laser irradiation, have been applied to fabricate metal/glass nanocomposites. The particle configurations are studied by transmission electron microscopy to get some insight into the rather complex formation mechanisms. Special attention is given to spheroidally shaped particles surrounded by smaller secondary particles observed upon ion beam mixing of silica/silver/silica layer compounds as well as irradiating femtosecond laser pulses on sodium silicate glass containing spherical silver particles. Another unique type of structure are cavities observed in silver particles formed by high fluence ion implantation into silica as well as upon laser pulse irradiation of silver particles in glass. The experimental findings are discussed in terms of irradiation-induced defect formation and radiation-enhanced diffusion.     

PS/Ag核壳结构复合微球的制备与性能

以乳液聚合法制备的平均粒径1.2~1.5μm单分散聚苯乙烯(PS)微球为核,经过超声敏化、化学镀、还原等过程制备了PS/Ag核壳结构复合微球。采用透射电镜、X射线衍射、红外光谱、紫外可见光谱对其形貌、物相、结构与光学性质进行了表征与分析。结果表明:PS/Ag复合微球粒径相对均一;通过多次敏化、控制二次银氨溶液浓度(0.002~0.006 mol/L),可实现对纳米银壳层厚度的调控;纳米银壳层沉积生长过程中,随着PS微球表面银粒子的增多、增大,复合微球的光学等离子体共振吸收峰产生显著的展宽与红移。