Sharif Digital Repository

CdS nanoparticles were synthesized by a thermochemical method by using Na2S2O3 and CdSO4 as the precursors and thioglycerol as the capping agent. We have investigated the effect of different temperatures on the size and crystalline phase of the CdS nanoparticles. The results of the optical spectroscopy and XRD analyses clarified that increasing the synthesis temperature increased the final nanoparticles size and also changed the crystalline phase of the particles from hexagonal to cubic phase. The size of the synthesized particles was less than 4nm. TEOS was also used in cooperation with thioglycerol for better surface passivation. The results of the PL analysis showed that using this... 

CdS nanoparticles were grown using CdSO4 and Na 2S2O3 as the precursors and thioglycerol (TG) as the capping agent. TG was shown to exhibit a catalytic role in the reaction and also acted as a capping agent. It was demonstrated that size growth is linearly related to the temperature of the reaction, i.e.the sizes can be controllably adjusted by temperature. The crystalline phase of the nanocrystals was also dependent on the temperature of growth: higher temperature favours the cubic phase. The pH also plays an important role in nanoparticle growth, as lower pH leads to a higher release rate of sulfur species. At pH as high as 10, the growth rate remains slow even at boiling temperature. This... 

In this study, maghemite (γ-Fe2O3) nanoparticles were produced using gelatin protein as an effective mediator. Size, shape, surface morphology and magnetic properties of the prepared γ-Fe2O3 nanoparticles were characterized using XRD, FT-IR, TEM, SEM and VSM data. The effects of furnace temperature and time of heating together with the amount of gelatin on the produced gelatin-Fe3O4 nanocomposite were examined to prove the fundamental effect of gelatin; both as a capping agent in the nanoscale synthesis and as the director of the spinel γ-Fe2O3 synthesis among possible Fe 2O3 crystalline structures  

In the current study, γ-Fe2O3/SiO 2/PCA/Ag-NPs hybrid nanomaterials were successfully synthesized and characterized. At first, prepared γ-Fe2O3 core nanoparticles were modified by SiO2 layer. Then they were covered by poly citric acid (PCA) via melting esterification method as well. PCA shell acts as an effective linker, and provides vacancies for conveying drugs. Moreover, this shell as an effective capping agent directs synthesis of silver nanoparticles (Ag-NPs) via in situ photo-reduction of silver ions by sunlight-UV irradiation. This system has several benefits as a suitable cancer therapy nanomaterial. Magnetic nanoparticles (MNPs) can guide Ag-NPs and drugs to cancer cells and then... 

Silver nanostructures are very important agents in biomedical research, because of its unique activity against unfavorable processes in bioscience. In the current study, reagent-free facile preparation of silver nanoparticles (average diameter: 72 nm) and silver nanoparticles/ nanorods hybrid was reported via wet chemical synthesis method. Kappa-carrageenan (kC), a hydrophilic biopolymer with sulphate groups on its backbone, as capping agent was used in the reaction medium. Silver nanoparticles and silver nanoparticles/ nanorods formation was confirmed by SEM images. Further investigations were carried out using DLS data and GPC analysis  

A biocompatible ferrofluid have been prepared by coprecipitation of FeCl 2.4H 2O and FeCl 3.6H 2O under ultrasonic irradiation and with NaOH as alkaline agent. Cystein was also used as capping agent in the solution. Magnetic properties of the produced ferrofluid were then determined by VSM test and magnetite nanoparticles were characterized by XRD and TEM techniques. The effect of surfactant to Fe ion weight ratio was also studied during this project by using two different amount of Dextran. Results showed the presence of a biocompatible superparamagnetic ferrofluid including magnetite nanoparticles with particle size ranging under 20 nm. The increase in the surfactant content results in the... 

The optical and electrical properties of semiconductor nanoparticles are strongly dependent on their size. A flexible control of the size of the nanoparticles is of interest for tuning their properties for different applications. Here we use a coupled method to control the size of CdS nanoparticles. The method involves the photochemical growth of CdS nanoparticles together with the use of a capping agent as an inhibiting factor. CdS nanoparticles were formed through a photoinduced reaction of CdSO4 and Na2S2O3 in an aqueous solution. Mercaptoethanol (C2H6OS) was used as the capping agent, and we investigated the effect of illumination time, illumination intensity and the concentration of... 

Magnetite nanoparticles (mean particle size ranging from 10 to 20 nm) were prepared by a biomoleculeassisted solution-phase approach under ultrasonic irradiation. Cysteine was used as the capping agent in the solution. The results show that cysteine could be an efficient biocapping agent in producing Fe3O4 nanoparticles. The crystal structure and magnetic properties of the nanoparticles were characterized by XRD and VSM techniques, respectively. FT-IR was used to investigate the presence of cysteine on the nanoparticles surface. The influence of pH value of the solution on the size distribution and hydrodynamic size of nanoparticles were studied by TEM and DLS methods, respectively. The MTT... 

We have synthesized CdS NCs (NCs) by a thermochemical approach. CdSO 4 and Na2S2O3 were used as the precursors and thioglycolic acid (TGA) was used as capping agent molecule. The structure and optical property of the NCs were characterized by means of XRD, TEM, UV-visible optical spectroscopy and photoluminescence (PL). XRD and TEM analyses demonstrated hexagonal phase CdS NCs with an average size of around 2 nm. Synthesized NCs exhibited a band gap of about 3.21 eV and showed a broad band emission from 400 to 750 nm centered at 503 nm. This broad band emission is related to surface states of CdS and our results showed that the emission peak can be attributed to the interstitial sulfur. The... 

Linear-dendritic triblock copolymers of linear poly(ethylene glycol) and hyperbranched poly(citric acid) (PCA-PEG-PCA) were used as the reducing and capping agents to encapsulate gold and silver nanoparticles (AuNPs and AgNPs). PCA-PEG-PCA copolymers in four different molecular weights were synthesized using 2, 5, 10 and 20 citric acid/PEG molar ratios and were called A 1, A 2, A 3 and A 4, respectively. Nanoparticles were encapsulated simultaneously during the preparation process. AuNPs were simply synthesized and encapsulated by addition a boiling aqueous solution of HAuCl 4 to aqueous solutions of A 1, A 2, A 3 and A 4. In the case of silver, an aqueous solution of AgNO 3 was reduced... 

Linear-dendritic copolymers containing hyperbranched poly(citric acid) and linear poly(ethylene glycol) blocks (PCA-PEG-PCA) were used as reducing and capping agents to synthesize and support gold nanoparticles (AuNPs). PCA-PEG-PCA copolymers with 1758, 1889 and 3446 molecular weights, called A1, A2 and A3 through this work, respectively, were synthesized using 2, 5, and 10 citric acid/PEG molar ratios. The diameter of A1, A2 and A3 in a fresh water solution was investigated using dynamic light scattering (DLS) and it was between 1.8 and 2.8 nm. AuNPs were simply synthesized and supported by addition a boiling aqueous solution of HAuCl4 to aqueous solutions of A1, A2 and A3. Supported AuNPs... 

We have synthesized CdS nanocrystals (NCs) by a microwave activated method. CdSO4 and Na2S2O3 were used as the precursors and thioglycolic acid (TGA) was used as capping agent molecule. The aqueous synthesis was based on the heat sensitivity of Na2S 2O3. In this method, microwave irradiation creates the activation energy for dissociation of Na2S2O3 and leads to the CdS NCs formation. X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses demonstrated hexagonal phase CdS NCs with an average size around 3 nm for sample prepared at 5 min irradiation time. A band gap range of 3.38-2.89 eV was possible only by increasing the microwave irradiation time, corresponding to a... 

In this work we report a fast two-step microwave activated synthesis of the ZnS:Mn nanocrystals. Zn(NO3)2 and Na2S 2O3 were used as the precursors and Mn(NO 3)2 was employed as the source of the impurity. The aqueous synthesis was based on the heat sensitivity of Na2S 2O3, which releases some S species on heating. Consequently, the reaction was well activated under microwave irradiation resulting in formation of ZnS:Mn nanocrystals. Thioglycerol (TG) was also used as the capping agent and the catalyst of the reaction. The synthesis process was done in two steps, i.e. 1 min irradiation without TG and then injection of TG and continuation of irradiation. ZnS:Mn nanocrystals were quickly formed... 

In this work we report a new thermochemical method for the synthesis of ZnS:Mn nanocrystals. Zn(NO3)2 and Na2S 2O3 were used as the precursors and Mn(NO 3)2 was the source of impurity. Thioglycerol (TG,C 3H8O2S) was also used as the capping agent and the catalyst of the reaction. Na2S2O3 is a heat sensitive material which releases S species upon heating. Consequently, the reaction proceeds in temperatures higher than room temperature. The reaction was done in two steps. In the first step, the precursors were heated at 96 °C for an hour without TG. In the second step, TG was injected to the solution and the heating process was continued for longer heating durations. A fast growth occurred in...