Synthesis of nearly monodispersive gold nanoparticles by a sodium diphenylamine sulfonate reduction process

Au nanoparticles have been prepared by the reaction of HAuCl₄ and sodium diphenylamine sulfonate in the presence/absence of poly(vinylpyrrolidone)(PVP) at room temperature. The nanoparticles were characterized by Transmission electron microscopy (TEM), UV-Vis absorption spectrum. The research showed that the molar ratio of PVP/ HAuCl₄ has effect on the size and the morphology of Au nanoparticles.     

金纳米粒子的制备及自组装

金纳米粒子以它独特的光学、电学和催化性质以及在纳米级电子线路中的应用潜力,受到人们越来越多的关注.本文主要评述了金纳米粒子的合成方法和自组装技术,即对各种制备方法和自组装的特点、纳米粒子的生长机理和自组装机理进行了介绍.展望了金纳米材料未来的研究方向和发展趋势.     

Wafer-scale fabrication of nanofluidic arrays and networks using nanoimprint lithography and lithographically patterned nanowire electrodeposition gold nanowire masters

Wafer scale (cm(2)) arrays and networks of nanochannels were created in polydimethylsiloxane (PDMS) from a surface pattern of electrodeposited gold nanowires in a master-replica process and characterized with scanning electron microscopy (SEM), atomic force microscopy (AFM), and fluorescence imaging measurements. Patterns of gold nanowires with cross-sectional dimensions as small as 50 nm in height and 100 nm in width were prepared on silica substrates using the process of lithographically patterned nanowire electrodeposition (LPNE). These nanowire patterns were then employed as masters for the fabrication of inverse replica nanochannels in a special formulation of PDMS. SEM and AFM measurements verified a linear correlation between the widths and heights of the nanowires and nanochannels over a range of 50 to 500 nm. The PDMS replica was then oxygen plasma-bonded to a glass substrate in order to create a linear array of nanofluidic channels (up to 1 mm in length) filled with solutions of either fluorescent dye or 20 nm diameter fluorescent polymer nanoparticles. Nanochannel continuity and a 99% fill success rate was determined from the fluorescence imaging measurements, and the electrophoretic injection of both dye and nanoparticles in the nanochannel arrays was also demonstrated. Employing a double LPNE fabrication method, this master-replica process was also used to create a large two-dimensional network of crossed nanofluidic channels.     

Raman spectroscopy of indium phosphide nanowire networks coated with gold clusters

Enhanced Raman signal of the longitudinal optical phonon mode in indium phosphide nanowire networks with gold coating of up to 5 nm thickness was observed experimentally to further study the phonon spectrum of nanowire networks. Indium phosphide nanowire networks coated with different nominal thicknesses of gold were prepared and optically studied. Scanning electron microscopy, photoluminescence spectroscopy and Raman spectroscopy were used to study the dependence of surface morphology and phonon modes of the nanowire networks on the nominal thickness of the gold coating. The Raman peak of longitudinal optical phonon mode for as grown sample was negligible, while the peak intensity for 1 and 5 nm gold coated sample reached to 1,379 and 792 a.u. respectively. Electromagnetic enhancement and extinction coefficient are discussed to qualitatively assess the role of the gold coating on indium phosphide nanowire networks.     

Synthesis of platinum nanowire networks using a soft template

Platinum nanowire networks have been synthesized by chemical reduction of a platinum complex using sodium borohydride in the presence of a soft template formed by cetyltrimethylammonium bromide in a two-phase water-chloroform system. The interconnected polycrystalline nanowires possess the highest surface area (53 +/- 1 m2/g) and electroactive surface area (32.4 +/- 3.6 m2/g) reported for unsupported platinum nanomaterials; the high surface area results from the small average diameter of the nanowires (2.2 nm) and the 2-10 nm pores determined by nitrogen adsorption measurements. Synthetic control over the network was achieved simply by varying the stirring rate and reagent concentrations, in some cases leading to other types of nanostructures including wormlike platinum nanoparticles. Similarly, substitution of a palladium complex for platinum gives palladium nanowire networks. A mechanism of formation of the metal nanowire networks is proposed based on confined metal growth within a soft template consisting of a network of swollen inverse wormlike micelles.     

Synthesis of PVP capped gold nanoparticles by the UV-irradiation technique

Multi twinned gold nanoparticles have been synthesized by an ultraviolet irradiation technique involving the reduction of a gold salt in the presence of polyvinyl pyrrolidone (PVP).     

Peptide synthesis of gold nanoparticles: the early steps of gold reduction investigated by density functional theory

Gold nanoparticles can be synthesized by reducing chloroaurate(III) ions in the presence of peptides. Here, such reduction for serine and tyrosine is studied by density functional theory including solvent effects. We find that the formation of chloroaurate complexes of these amino acids is thermodynamically viable and facilitates the reduction of Au(III), to a greater degree for tyrosine as found in experiments. Our results also suggest a rationale for the behavior of tyrosine-intercalated peptides.     

Synthesis of oxidation-resistant cupronickel nanowires for transparent conducting nanowire networks

Nanowires of copper can be coated from liquids to create flexible, transparent conducting films that can potentially replace the dominant transparent conductor, indium tin oxide, in displays, solar cells, organic light-emitting diodes, and electrochromic windows. One issue with these nanowire films is that copper is prone to oxidation. It was hypothesized that the resistance to oxidation could be improved by coating copper nanowires with nickel. This work demonstrates a method for synthesizing copper nanowires with nickel shells as well as the properties of cupronickel nanowires in transparent conducting films. Time- and temperature-dependent sheet resistance measurements indicate that the sheet resistance of copper and silver nanowire films will double after 3 and 36 months at room temperature, respectively. In contrast, the sheet resistance of cupronickel nanowires containing 20 mol % nickel will double in about 400 years. Coating copper nanowires to a ratio of 2:1 Cu:Ni gave them a neutral gray color, making them more suitable for use in displays and electrochromic windows. These properties, and the fact that copper and nickel are 1000 times more abundant than indium or silver, make cupronickel nanowires a promising alternative for the sustainable, efficient production of transparent conductors.     

超声化学制备单分散金纳米粒子

以乙二醇为溶剂和还原荆,氯金酸为反应前体物,聚乙烯吡咯烷酮为分散剂和保护剂.在水的参与下,室温中用超声方法成功制备单分散的纳米金粒子.纳米金粒子尺寸大小约为10nm,颗粒形状均匀.并进一步探讨了制备纳米金粒子的影响因素.     

Synthesis and agglomeration of gold nanoparticles in reverse micelles

Reverse micelles prepared in the system water, sodium bis-(2-ethylhexyl) sulfoccinate (AOT), and isooctane were investigated as a templating system for the production of gold nanoparticles from Au(III) and the reducing agent sulfite. A core-shell Mie model was used to describe the optical properties of gold nanoparticles in the reverse micelles. Dynamic light scattering of gold colloids in aqueous media and in reverse micelle solution indicated agglomeration of micelles containing particles. This was verified theoretically with an analysis of the total interaction energy between pairs of particles as a function of particle size. The analysis indicated that particles larger than about 8?nm in diameter should reversibly flocculate. Transmission electron microscopy measurements of gold nanoparticles produced in our reverse micelles showed diameters of 8-10?nm. Evidence of cluster formation was also observed. Time-correlated UV-vis absorption measurements showed a red shift for the peak wavelength. This was interpreted as the result of multiple scattering and plasmon interaction between particles due to agglomeration of micelles with particles larger than 8?nm.     

Surface-enhanced Raman scattering of rhodamine 6G on nanowire arrays decorated with gold nanoparticles

We investigate the surface-enhanced Raman scattering (SERS) of rhodamine 6G (R6G) adsorbed on Au nanoparticles attached to InP nanowires. We find that nanowire arrays act as frameworks for effective SERS substrates with a significantly higher Raman signal sensitivity than a planar framework of Au nanoparticles adsorbed two-dimensionally on a flat surface. The SERS signal displays a clear polarization-dependent effect when the nanowires are arranged in a row. We also find that the SERS signal increases with time during continuous laser illumination. The plasmon-enhanced optical forces between Au nanoparticles may either move pairs of nanoparticles closer together or attract adsorbed molecules by moving them to the junctions of Au nanoparticle aggregates. Such effects by plasmon optical forces may cause the observed increase of the SERS signal with continuous laser illumination.     

Synthesis process of gold nanoparticles in solution plasma

We describe the dynamics of the synthesis of gold nanoparticles by a glow discharge in aqueous solutions. A pulsed power supply was used to generate discharges in the aqueous solutions. The initial [AuCl₄]⁻ ion concentration and the voltage applied between the electrodes were varied. The [AuCl₄]⁻ ion was reduced by the H radicals generated in the discharge. The reduction rates were calculated from the changes in the [AuCl₄]⁻ ion concentration during the discharge time. Dendrite-shaped nanoparticles of about 150 nm size were formed in discharge during 1 min. The pH of the solution decreased gradually with the increase of the discharge time. The decrease in pH led to the dissolution of gold nanoparticles. The reduction and the dissolution rates increased proportionately with the applied voltage. The size of the gold nanoparticles decreased at 20 nm after running the discharge during 45 min. Moreover gold nanoparticles with exotic shapes, such as triangle, pentagon, and hexagon were also observed. The particles were confirmed to be as polycrystalline gold nanoparticles by electron diffraction patterns. In summary, when the reduction rate lowered as a result of dissolution, anisotropic nanoparticles were formed and continued to grow in size in the solution.     

Microtubule-based gold nanowires and nanowire arrays

Biological structures are attractive as templates to form nanoscale architectures for electronics because of their dimensions and the ability to interact with inorganic materials. In this study, we report the fabrication and electrical properties of microtubule (MT)-templated Au nanowires, and methods for assembling Au nanowire arrays based on these templates. The adsorption of MTs on silicon substrates is an effective means for preserving the conformation of the MT and provides a convenient platform for electrical measurements. To improve the metallization of MTs, a photochemical route for gold reduction is adapted, which leads to continuous coverage. The conductivity values measured on micrometer-long nanowires are similar to those reported for other biotemplated gold nanowires. A protocol for fabricating arrays of MT-templated gold nanowires is demonstrated.     

Synthesis, characterization and electrocatalytic activity of fused gold nanoparticles

This paper describes the synthesis of fused spherical gold nanoparticles (AuNPs) and their electrocatalytic activity towards the oxidation of hydroxylamine (HA). Fused AuNPs were prepared by one-pot synthesis using 2-mercapto-4-methyl-5-thiazoleacetic acid (TAA) as a stabilizing agent and sodium borohydride (NaBH4) as a reducing agent. The HR-TEM images showed that two individual AuNP were joined via on its surface with a size range of approximately 7 nm and a length of approximately 15 nm diameter. The pH studies showed that the synthesized fused AuNPs was stable at pH > 8. This indicated that the carboxylate ion present on the TAA molecule stabilized the AuNPs from aggregation. Further, the fused AuNPs were utilized for the electrocatalytic oxidation of hydroxylamine (HA) after immobilized them on (3-mercaptopropyl)-trimethoxysilane (MPTS) sol-gel film modified Au electrode. The AuNPs modified electrode showed an excellent electrocatalytic activity towards the oxidation of HA in 0.2 M phosphate buffer solution (pH 7.2) by shifting its oxidation potential to 100 mV less positive and enhancing its oxidation current for more than three times when compared to bare Au electrode. Further, it was found that the fused AuNPs modified electrode showed greater electrocatalytic activity towards HA than the spherical AuNPs modified electrodes.     

Synthesis and characterisation of liposomal doxorubicin with loaded gold nanoparticles

Developing nanostructures for cancer treatment is growing significantly. Liposomal doxorubicin is a drug that is used in the clinic and represents a lot of benefits over doxorubicin. The development of multifunctional liposomes with different cancer treatment capability enables broader applications of doxorubicin chemotherapy. Many efforts were carried to prepare more effective liposomal formulation through loading gold nanoparticles (GNPs) in the formulation. Here, GNPs with an average size of 6 nm were loaded in liposomal formulation alongside doxorubicin. The hydrodynamic diameter of final formulation was 177.3 ± 33.9 nm that in comparison with liposomes without GNPs (112.5 ± 10.3 nm), GNPs‐loaded liposomes showed the bigger hydrodynamic diameter. GNPs‐loaded liposomes are slightly positively charged (4.4 ± 1.1 mV), while liposomes without loading the GNPs were negatively charged (−18.5 ± 1.6 mV). Doxorubicin was loaded in this formulation through active loading technique. Doxorubicin loading efficiency in gold‐loaded liposomes is slightly lesser than liposomes without GNPs, but still considerably high in comparison to passive loading techniques.Inspec keywords: nanofabrication, drugs, nanomedicine, gold, cancer, lipid bilayers, drug delivery systems, nanoparticles, crystal growth from solutionOther keywords: liposomal doxorubicin, multifunctional liposomes, doxorubicin chemotherapy, active loading technique, doxorubicin loading efficiency, gold‐loaded liposomes, passive loading techniques, gold nanoparticles, cancer treatment, liposomal formulation, GNP‐loaded liposomes, hydrodynamic diameter     

Synthesis of L-phenylalanine stabilized gold nanoparticles and their thermal stability

Here we described the two synthesis methods of L-phenylalanine (L-phe) coated gold nanoparticles through a reduction of aqueous chloroaurate ions directly by L-phe, and also the borohydride reduction of chloroauric acid followed by capping with L-phe molecules. Phenylalanine reduced gold nanoparticles and the phenylalanine capped gold nanoparticles were evaluated by transmission electron microscope and UV-vis spectroscopy, and then their thermal stabilities were compared. We found that the phenylalanine reduced gold nanoparticles were unstable and form linearly arranged aggregates on aging, while as the phenylalanine capped gold nanoparticles were stable for months in ambient condition.     

Ultra-fast catalytic reduction of dyes by ionic liquid recoverable and reusable mefenamic acid derived gold nanoparticles

We synthesized mefenamic acid (MA) derived gold nanoparticles (MA-AuNps) in aqueous solution (MA-Au sol). Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) of the sol at 1, 5, 15 and 60 min showed changes in size and shape of formed AuNps. Fourier Transform Infrared (FTIR) Spectroscopy revealed the interaction between AuNps and MA. Each Au sol exhibited exceptional catalytic activity for the reduction of Methylene Blue (MB), Rose Bengal (RB) and Eosin B (EB) dye individually as well as collectively. However, complete reduction of dye(s) was accomplished by Au sol of 5 min in just 15s. The catalytic performance of Ma-Au sol was far superior to that adsorbed on glass. AuNps were recovered with the help of water insoluble room temperature ionic liquid and reused with enhanced catalytic potential. This finding is a novel, rapid and highly economical alternative for environmental safety against pollution by dyes and extendable for control of other reducible contaminants as well.     

Wavy PtCu alloy nanowire networks with abundant surface defects enhanced oxygen reduction reaction

Nano Research - Bimetallic platinum-copper (Pt-Cu) alloy nanowires have emerged as a novel class of fuel cell electrocatalysts for oxygen reduction reaction (ORR) due to their intrinsic high...     

化学还原法制备Fe3O4纳米颗粒及其性能研究

采用化学还原法制备得到了Fe3O4纳米颗粒,并用XRD对制备条件:分散剂种类、分散剂用量、煅烧温度、煅烧时间进行了研究。研究结果表明,当选用PEG(6000)做分散剂,PEG用量为50g/L,煅烧温度为700℃,煅烧时间为120min时,制备得到的Fe3O4纳米颗粒已经具有晶型完整的反尖晶石结构。将该样品做VSM分析,分析结果表明样品饱和磁化强度可达85A.m2/kg,并且矫顽力趋近于0,呈现出良好的顺磁性。