Simple synthesis of ZnS nanoparticles in alkaline medium

ZnS nanoparticles were successfully synthesized by reflux under an alkaline medium. The nanoparticles were characterized by using X-Ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The optical properties of ZnS nanoparticles were examined by photoluminescence (PL) spectrum. The result shows that the as-synthesized ZnS nanoparticles had a cubic phase. SEM image shows that ZnS nanoparticles are basically in spherical shape and are homogeneous. The particle size was found to be in the range of 18 nm.     

Comparative Nanoparticle Size Characterization of EEW Alumina Using Various Measurement Techniques

Modern material science is paying more attention on the development of nanomaterials for superior properties in various fields of applications like mechanical, thermal, electronic, bio-medical etc. For such applications, determination of nanoparticle sizes along with their distribution is important for attaining the desired properties. Particle sizes along with the crystallite sizes of oxides, non-oxides and metallic nanopowders produced by different processes can be determined by different techniques which includes x-ray diffraction/neutron diffraction (XRD/ND), transmission electron microscopy/field emission scanning electron microscopy (TEM/FESEM), Brunauer-Emmett-Teller (BET) surface area method, small angle neutron scattering (SNAS), dynamic light scattering (DLS), static light scattering (SLS), etc. For average nano-metric particle size determination, DLS is the most frequently used technique that gives a distribution that approximates the exact binomial distribution of large numbers of nanoparticulates with varying particle size under investigation (Gaussian distribution). However, the other techniques mainly give either localized distribution of the particles under observation or the distribution derived from type II isotherm. In this investigation, nano-alumina powder produced by the electrical explosion of wire technique (EEW) is used for comparative evaluation of particle size analysis by DLS measurement technique for nanoparticles vis-à-vis to other techniques like XRD (for crystallite size), FESEM, BET, and TEM. The superiority of the DLS technique has been discussed in details with respect to the unique features of its Gaussian distribution nature.     

PEI-conjugated AuNPs as a sensing platform for arsenic (AS-III)

We have developed a simple method for synthesis of spherical gold nanoparticles (AuNPs) with enhanced surface properties. The polyethyleneimine (PEI) has good potential to minimise the size of the precursor. The UV–vis spectra of synthesised AuNPs with reducing agents (PEI) have been characterised with a peak at 530?nm. The size and shape measurement of AuNPs was confirmed by transmission electron microscopy (TEM) which shows that the mean diameter is 3.9?nm. The optimal concentration of reducing agents was found to be 1% for synthesis of AuNPs. PEI-conjugated AuNP shows binding with arsenic III (0.1?ppm) as confirmed by scanning electron microscope (SEM)/energy dispersive X-rays mapping. TEM revealed the particle shape and size. Zeta potential, zeta deviation, effective particle size, Z-average diameter, polydispersity index and electrophoretic mobility have been observed in order to understand the stability of AuNPs. The image of SEM confirmed that As (III) particles were eventually distributed in PEI-conjugated AuNPs matrix. Further, this study demonstrated that PEI-conjugated AuNPs is a sensing platform of As (III).     

Synthesis of wurtzite ZnS nanocrystals at low temperature

Nanocrystallites of wurtzite hexagonal ZnS have been successfully synthesized without using any capping agent by simple chemical precipitation method at a low calcination temperature of 150 °C. It has been found that the size of the synthesized ZnS nanocrystallites decreases as Zn²⁺:S^2? ratio is decreased. The synthesized nanoparticles have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–vis absorption spectroscopy and M–H characteristics. The XRD patterns have confirmed that the prepared ZnS nanoparticles are of wurtzite hexagonal phase. XRD, SEM and TEM studies have shown the decrease in the particle size with the increase in S^2? source. TEM images have clearly shown that size distribution of the particles lie in the range of 5–30 nm. The optical absorption bandgap of the synthesized nanocrystals has been found to be in the range of 3.69–3.74 eV. Magnetization study has shown the ‘diamagnetic’ behavior of synthesized ZnS nanocrystallites with a weak ferromagnetic behavior in the low field regime. The observed weak ferromagnetism has been understood due to the presence of defects in the synthesized ZnS nanoparticles.     

Hydrothermal synthesis,characterization and luminescent properties of lanthanide-doped NaLaF<Subscript>4</Subscript> nanoparticles

Nanoparticles of sodium lanthanum (III) fluoride-doped and co-doped with Eu³⁺/Tb³⁺ were prepared by the hydrothermal method using citric acid as structure-directing agent. Structural aspects and optical properties of synthesized nanoparticles were studied by powder X-ray diffraction (XRPD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED), energy-dispersive X-ray spectra (EDS), particle size by dynamic light scattering (DLS), Fourier transform infrared (FTIR) spectrum and photoluminescence (PL) techniques. Nanoparticles consist of well-crystallized hexagonal phase and the average crystallite size for undoped and doped-NaLaF₄ nanoparticles are in the range of 20–22 nm. TEM images show that nanoparticles have cylindrical shape and crystalline nature of nanoparticles was confirmed by SAED patterns. Down- conversion (DC) luminescent properties of doped NaLaF₄ were also investigated and impact of co-doping has been explored.     

Photocatalytic mineralization of carboxylic acids over Fe-loaded ZnS nanoparticles

Zinc sulfide (ZnS) nanoparticles prepared by hydrothermal synthesis were subsequentially impregnated with different iron amounts (0.5−5.0 at%) to obtain Fe-loaded ZnS nanoparticles. Phase composition, crystallinity, crystal size, and morphology of 0.5–5.0 at% Fe-loaded ZnS nanoparticles were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDXS), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma (ICP). Specific surface area determined by the Brunauer, Emmett and Teller (BET) method was found to be in the range of 85–197 m²/g. The average particle size obtained from TEM analysis of pure ZnS and 2.0 at% Fe-loaded ZnS nanoparticles was 5–20 nm. The optical absorption properties of the samples measured by UV–vis diffuse reflectance spectroscopy (UV–vis DRS) clearly indicated the bathochromic shift upon loading ZnS with Fe. Photocatalytic activities of pure ZnS and Fe-loaded ZnS nanoparticles were examined by studying the mineralization of oxalic acid and formic acid under UVA illumination. It was found that 2.0 at% Fe-loaded ZnS sample exhibited the highest degradation activity possibly due to the presence of Fe in an optimum amount and the increases of surface area and light absorption in UVA region.     

Amine-terminated TEG-derived PAMAM dendrimer as template for preparation of gold nanoparticles in water

Nano-sized monodisperse gold particles (AuNPs) have received significant attention in the past decade, due to their unique physical properties and good chemical stability, which can lead to a wide variety of potential applications. In this work, TEG-derived PAMAM dendrimers with amine-terminating groups were synthesized and characterized by ¹H NMR and FT-IR. These dendrimers were investigated as the templates for preparation of gold nanoparticles through the reduction of HAuCl₄ by NaBH₄ in water. Stable gold nanoparticles with diameters around 10 nm were obtained in the presence of G2.0 – G5.0 dendrimers and characterized by UV-Vis spectroscopy, transmission electron microscopy (TEM) and dynamic light scattering (DLS). The particle size of the produced AuNPs decreased with increasing dendrimer generations. A dendrimer of higher generation has a rigid structure with many end groups on the surface and may play a powerful role in the growth of the AuNPs, as well as having a solid stabilization effect on the AuNPs.     

Effect of pH on Size of ZnS Nanoparticles and Its Application for Dye Degradation

This paper presents the results from a study related to the effect of solution pH on particle size and photocatalytic properties of ZnS nanoparticles (NPs). ZnS NPs capped with 2-Mercaptoethanol (2-ME) have been synthesized via chemical precipitation route at different pH values, i.e., 8, 10, and 12. Effect of solution pH on particle size of NPs has been studied by the Dynamic Light Scattering (DLS) technique. A comparison of the results obtained from the DLS technique for ZnS NPs synthesized at different pH values showed narrower particle size distribution as we go from higher pH value, i.e., 12, to lower pH value, i.e., 8. Fourier Transform Infrared Spectroscopy (FTIR) has been carried out to study the presence of hydroxyl groups and 2-ME on the surface of NPs. Comparative photocatalytic study of these NPs has also been carried out using Ponceau S dye.     

Facile method for the preparation of the WS2 nanoparticles

A facile and simple synthetic route was proposed for the synthesis of WS2 nanoparticles. The as-prepared WS2 nanoparticles can be characterized with X-ray diffraction spectrum (XRD), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). The average particle size of the product is about 85 nm that was calculated from XRD pattern by the Debye-Scherrer formula.     

Facile synthesis of chondroitin sulfate-stabilized gold nanoparticles

A facile and simple method for the synthesis of biocompatible gold nanoparticles (AuNPs) at room temperature has been developed by using sodium borohydride as the reducing agent and employing an inexpensive water-soluble chondroitin sulfate (CS) biopolymer as the stabilizing agent. The as-prepared AuNPs were characterized with ultraviolet–visible (UV–vis) spectroscopy and transmission electron microscopy (TEM). Additionally, the stability of AuNPs in aqueous solution was investigated as a function of the electrolyte sodium chloride concentration. The experimental results showed that even high sodium chloride concentration (1 M) also did not destabilize the colloidal gold solution. So it could be speculated that the high stability of AuNPs should be attributed to the electrostatic repulsion and steric hindrance between the AuNPs stabilized by CS molecules, which wrapped around the surface of as-prepared AuNPs and prevented their agglomeration, and simultaneously improve biocompatibility of AuNPs as well.     

Amine-terminated TEG-derived PAMAM dendrimer as template for preparation of gold nanoparticles in water

Nano-sized monodisperse gold particles (AuNPs) have received significant attention in the past decade, due to their unique physical properties and good chemical stability, which can lead to a wide variety of potential applications. In this work, TEG-derived PAMAM dendrimers with amine-terminating groups were synthesized and characterized by ¹H NMR and FT-IR. These dendrimers were investigated as the templates for preparation of gold nanoparticles through the reduction of HAuCl₄ by NaBH₄ in water. Stable gold nanoparticles with diameters around 10 nm were obtained in the presence of G2.0–G5.0 dendrimers and characterized by UV-Vis spectroscopy, transmission electron microscopy (TEM) and dynamic light scattering (DLS). The particle size of the produced AuNPs decreased with increasing dendrimer generations. A dendrimer of higher generation has a rigid structure with many end groups on the surface and may play a powerful role in the growth of the AuNPs, as well as having a solid stabilization effect on the AuNPs.     

Determination of mean diameter and particle size distribution of acrylate latex using flow field-flow fractionation, photon correlation spectroscopy, and electron microscopy

Flow field-flow fractionation (flow FFF) was employed to determine the mean diameter and the size distribution of acrylate latex materials having diameters ranging from 0.05 to 1 μm. Mean diameters of the samples determined by flow FFF are in good agreement with those obtained from photon correlation spectroscopy (PCS). Scanning electron microscopy (SEM) yielded a mean diameter that is about 20% lower than those obtained from flow FFF or PCS, probably due to the shrinkage of particles during sample drying and high-vacuum measurements. It was found that flow FFF is particularly useful for the determination of particle size distributions of latex materials having broad size distributions. Flow FFF separates particles according to their sizes and yields an elution curve that directly represents the particle size distribution of the sample. In PCS, measurements had to be repeated at more than one scattering angle to obtain an accurate mean diameter for the latex having a broad size distribution. Flow FFF was fast (less than 12 min of run time) and showed an excellent repeatability in measuring the mean diameter with ±5% relative error.     

Biosynthesis,characterisation and antimicrobial activity of silver and gold nanoparticles by Dolichos biflorus Linn seed extract

The bioreduction method employed for the synthesis of colloidal AgNPs and AuNPs is reported here. Methanolic and aqueous extracts of Dolichos biflorus Linn seed was used as the bio-reducing agent. The structural and morphological aspects of the synthesised metal nanoparticles were investigated using X-ray diffraction (XRD), energy-dispersive spectroscopy (EDX), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). XRD, revealed crystalline nature of the synthesised particles, UV–vis spectrophotometric analysis showed characteristic absorption peak for both AgNPs and AuNPs. EDX analysis confirmed the presence of elemental silver and gold particles and the average size and morphology were determined by SEM and TEM. The synthesised AgNPs exhibited good antibacterial potential whereas AuNPs showed poor activity against human pathogenic, gram-positive bacteria such as Staphylococcus aureus, Bacillus subtilis and gram-negative bacteria, such as Escherichia coli, Pseudomonas aeruginosa.     

Biosynthesis of silver nanoparticles using Azadirachta indica leaves: characterisation and impact on Staphylococcus aureus growth and glutathione‐S‐transferase activity

Silver nanoparticles (AgNPs) are toxic to various microbes, but the mechanism of action is not fully understood. The present report explores Azadirachta indica leaf extract as a reducing agent for the rapid biosynthesis of AgNPs. The effects of AgNPs on the growth, glutathione‐S‐transferase (GST) activity, and total protein concentration in Staphylococcus aureus were investigated, as was its antibacterial activity against seven other bacterial strains. Nanoparticle synthesis was confirmed by the UV‐Vis spectrum and colour change of the solution. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential analysis, and infrared spectroscopy were used to characterise the synthesised nanoparticles. The UV‐Visible spectrograph showed an absorbance peak at 420 nm. DLS analysis showed an average AgNP size of 159 nm and a Polydispersity Index of 0.373. SEM analysis showed spherical particle shapes, while TEM established an average AgNP size of 7.5 nm. The element analysis profile showed small peaks for calcium, potassium, zinc, chlorine, with the presence of oxygen and silver. AgNPs markedly affected the growth curves and GST activity in treated bacteria, and produced moderate antibacterial activity. Thus AgNPs synthesised from A. indica leaves can interrupt the growth curve and total protein concentration in bacterial cells.Inspec keywords: ultraviolet spectra, microorganisms, nanomedicine, visible spectra, nanoparticles, electrokinetic effects, antibacterial activity, scanning electron microscopy, infrared spectra, transmission electron microscopy, light scattering, nanofabrication, particle size, silver, enzymes, biochemistry, molecular biophysics, cellular biophysicsOther keywords: silver nanoparticles, glutathione‐S‐transferase activity, green leaves, rapid biosynthesis, total protein concentration, nanoparticle synthesis, colour change, zeta potential analysis, UV‐Visible spectrograph, DLS analysis, SEM analysis, element analysis profile, growth curve, GST activity, bacterial strains, antibacterial activity, staphylococcus aureus growth, microbes, Azadirachta azadirachta indica leaf, reducing agent, scanning electron microscopy, transmission electron microscopy, dynamic light scattering, infrared spectroscopy, absorbance peak, polydispersity index, spherical particle shapes, TEM, bacterial cells, Ag     

Systematic study of bimodal suspensions of latex nanoparticles using dynamic light scattering

Determining the size of nanoparticles accurately, quickly and easily is becoming more and more important as the use of such particles increases. One of the common techniques for measuring the size of particles in suspension is dynamic light scattering (DLS). In principle, DLS is able to estimate the hydrodynamic particle diameter and its intensity-weighted distribution. However, the measured correlation function or power spectrum must be inverted to obtain this size distribution. The inversion is an ill-posed mathematical problem, and only under certain assumptions can the distribution be determined reliably. Suspensions containing bimodal (or multi-modal) particle size distributions are particularly challenging. This study reports on DLS measurements on a range of bimodal distributions of latex spheres with varying ratios of particle sizes. To determine the efficacy of different inversion techniques, the data has been analyzed both with the algorithms implemented in the DLS instrument’s proprietary analysis software and with other inversion routines based on simple analytical models of the particle size distribution. In addition, the results of the DLS analysis have been compared to scanning and transmission electron microscopy (SEM and TEM) measurements.     

Morphology control in synthesis of nickel nanoparticles in the presence of polyvinylpyrrolidone (PVPK30)

Nickel nanoparticles with different morphologies have been synthesized with polyvinylpyrrolidone (PVPK30) as structure-directing agent through a chemical reduction process. SEM, TEM and selected-area electron diffraction (SAED) were employed in the analysis of morphological characteristics of nickel nanoparticles. It was found that nickel nanoparticles are formed by the aggregation of nanoscale nickel crystallites, and particle morphology was strongly dependent on the PVPK30 concentration. In addition, crystallite size and formation time of nickel nanoparticles increased with the increasing PVPK30 concentration. PVPK30 additive seems to influence the three steps of nickel particle precipitation: nucleation, crystal growth and aggregation. The resultant spherical nickel nanoparticles showed high coercivity.     

Photoluminescent, transparent and flexible di-ureasil hybrids containing CdSe/ZnS quantum dots

We describe, in this paper, the sol-gel synthesis of di-ureasil based nanocomposites prepared in situ in the presence of organically capped CdSe quantum dots (QDs) or CdSe QDs which have been coated with a ZnS shell. For the latter a new chemical route to coat the CdSe QDs with ZnS shells was investigated and is now reported. The QDs became well dispersed in the final nanocomposites, whose microstructural homogeneity was evaluated by atomic force microscopy (AFM) and transmission electron microscopy (TEM) analyses. In order to understand the optical behaviour of di-ureasil containing QDs, a detailed photoluminescent study was undertaken for a selected particle size distribution of ZnS coated CdSe QDs (d～4.5?nm). Emission quantum yields up to 0.11 were measured in the final nanocomposites that present a huge (between 3 and 6 orders of magnitude) increase in the lifetime of the QDs (relative to that of isolated ones), as a result of energy transfer occurring between the intimately mixed di-ureasil host and the QDs.     

Structural characterization of CdSe/ZnS core–shell quantum dots (QDs) using TEM/STEM observation

CdSe/ZnS core–shell structured nano-crystal quantum dots (QDs) are ideal candidates for light-emission applications due to their high quantum efficiency, narrow-band, and particle-size-tunable photoluminescence. In particular, their small size results in the quantum confinement of semiconductor nano-crystals, which widens their energy gaps. In general, structural analyses of QDs using a transmission electron microscope (TEM) are very important due to the significantly small size of QDs. We were able to obtain structural information of CdSe/ZnS core–shell QDs using nano-beam diffraction by controlling the nano-probe of the dark field scanning TEM (DF-STEM) mode and strain analysis with high-resolution TEM (HRTEM)/STEM images. Furthermore, we could clearly distinguish the interface between the CdSe core and the ZnS shell from the strain analysis with the HRTEM/STEM images.     

Luminescence of er doped ZnS quantum dots excited by infrared lasers

ZnS:Er quantum dots were prepared in aqueous medium from readily available precursors. The construction, morphology and luminescence properties of the ZnS:Er quantum dots were evaluated by X-ray diffraction (XRD), transmission electron microscopy (TEM), and photoluminescence spectra. The average particle size was calculated using the Scherrer formula to be 4 nm, which is also observed from high resolution transmission electron microscopy (HRTEM) image. Different laser wavelengths at 976 +/- 2 nm and 1480 nm were utilized as the excitation source. ZnS:Er quantum dots had a fluorescence spectrum in 1550 nm region through the 4I13/2 --> 4I15/2 transition. Furthermore, intensity increased with increasing excitation intensity and dopant concentration. The reason for the photoluminescence spectra broadening is discussed. It is because the energy levels of Er3+ are split by a coulombic interaction between electrons, including spin correction and spin-orbit coupling, and eventually by the Stark effect due to ZnS QDs crystal field and local coordination.     

Optical encoding of microbeads based on silica particle encapsulated quantum dots and its applications

A novel method concerning the coding technology of polystyrene beads with Si encapsulated quantum dot (QD) particles (Si@QDs particles) is studied in this paper. In the reverse microemulsion system containing tetraethoxysilane (TEOS), water-soluble QDs (emission peak at 600?nm) were enveloped within the silica shell, forming Si@QDs particles. The Si@QDs particles were characterized by TEM, showing good uniform size, with an average diameter of about 167.0?nm. In comparison with the pure water-soluble QDs, the encapsulation of water-soluble QDs in the silica shell led to an enhancement in anti-photobleaching by providing inert barriers for the QDs. Images presented by SEM and confocal laser scanning microscopy demonstrated that the Si@QDs particles were equably coated on the surface of carboxyl functionalized polystyrene (PS) beads. Then, with the assistance of ethyl-3-(dimethyl aminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS), human IgG could be successfully crosslinked to Si@QDs particle coated PS-COOH beads. Furthermore, the Si@QDs coated PS-COOH beads with human IgG were examined in immunoassay experiments, and the results indicated that these beads could be applied in the specific recognition of goat-anti-human IgG in solution. This investigation is expected to provide a new route to bead coding in the field of suspension microarrays, based on the use of QDs.