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Silver Particles (silver + particle)
Selected AbstractsA green process for preparing silver nanoparticles using spinning disk reactorAICHE JOURNAL, Issue 2 2008Clifford Y. Tai Abstract The main theme of this research was to synthesize nanoparticles using green materials in a spinning disk reactor (SDR), which is a type of Higee equipment. The reducing agent and protecting agent were glucose and starch, respectively, either of which is an inexpensive and nontoxic material. Silver particles were prepared by continuously pumping two solutions, which were a mixture of AgNO3 aqueous solution containing protecting agent and another mixture of NaOH aqueous solution containing the reducing agent, into the chamber of the SDR, where a liquid,liquid reaction took place. The reaction time was less than 10 min, which was much shorter than the traditional methods. After washing and redispersing, silver particles of 10 nm or smaller were obtained, and the redispersed aqueous suspensions were stable for more than 40 days with or without the addition of a dispersing agent. A high-gravity process that combines economic benefit with environmental benignancy was successfully developed to produce silver nanoparticles. © 2007 American Institute of Chemical Engineers AIChE J, 2008 [source] Surface-enhanced resonance Raman scattering using pulsed and continuous-wave laser excitationJOURNAL OF RAMAN SPECTROSCOPY, Issue 6-7 2005Rachael E. Littleford Abstract Pulsed and continuous-wave (CW) lasers were compared as excitation sources for surface-enhanced resonance Raman scattering (SERRS). CW excitation provided SERRS spectra with a greater signal-to-noise ratio and more sensitive detection by a factor of ,50 compared with the high peak power, low repetition rate pulsed configuration used. The SERRS intensity using a pulsed laser produced a non-linear response with respect to changes in power of the laser. At powers of less than ,0.012 mW, the absolute intensity under the peaks of the CW and pulsed SERRS spectra converged, suggesting that lower peak power, high repetition rate systems may be more effective excitation sources for SERRS. Transmission electron microscopy of pulsed laser-irradiated silver particles showed significant sample damage and morphological changes. This problem was overcome with the use of a recirculating large-volume flow cell system, providing a fresh sample for each measurement. A picosecond-resolved time delay experiment found that SERRS intensity decreased by ,60% when exposed to a 400 nm pump pulse and probed with a 529 nm pulse. As the time delay between pump and probe increased the system recovered gradually to ,60% of the original SERRS intensity after 50 ps, where it remained constant. This suggests that the surface bonding between the silver and the dye is significantly perturbed, with some nanoscale diffusion occurring of the dye away from the metal surface. Hence chemical enhancement is temporarily prevented and electromagnetic enhancement is reduced as a function of 1/r3 as the dye moves away from the surface. Additionally, transient heating of the colloidal particles caused by the pulsed laser may also lead to plasmon shifts and changes in absorption intensity. Other factors such as surface annealing or decomposition of the silver particle or dye due the extreme temperature conditions may account for the permanent loss in SERRS intensity. Copyright © 2005 John Wiley & Sons, Ltd. [source] Silver Nanoparticles with Controlled Dispersity and Their Assembly into SuperstructuresADVANCED ENGINEERING MATERIALS, Issue 5 2010Karsten Moh In this paper we report on the influence of particle size distribution, particle substrate interaction, and drying behavior on the self-assembly process using ligand stabilized silver particles. Two-dimensional particle arrays were characterized using transmission electron microscopy and extensive image analysis. The formation of such structures was observed in situ using an environmental scanning electron microscope in WET-STEM mode. The results confirm that a small particle size distribution is crucial for the formation of regular particle patterns with long range order, but also the particle substrate interaction and the particle density have an influence on the degree of ordering. Additionally, we find that separated binary particle assemblies keep the orientation of their two-dimensional hexagonal lattices over alternating domains of small and big particles. This is probably enabled due to the formation of dislocations and a small change of the course of the lattice lines within the respective boundary. [source] Plasmonic Enhancement or Energy Transfer?ADVANCED FUNCTIONAL MATERIALS, Issue 13 2009Its Potential for Light-Emitting Devices, Lanthanide-Doped Silicate Glasses, On the Luminescence of Gold-, Silver- Abstract With the technique of synchrotron X-ray activation, molecule-like, non-plasmonic gold and silver particles in soda-lime silicate glasses can be generated. The luminescence energy transfer between these species and lanthanide(III) ions is studied. As a result, a significant lanthanide luminescence enhancement by a factor of up to 250 under non-resonant UV excitation is observed. The absence of a distinct gold and silver plasmon resonance absorption, respectively, the missing nanoparticle signals in previous SAXS and TEM experiments, the unaltered luminescence lifetime of the lanthanide ions compared to the non-enhanced case, and an excitation maximum at 300,350,nm (equivalent to the absorption range of small noble metal particles) indicate unambiguously that the observed enhancement is due to a classical energy transfer between small noble metal particles and lanthanide ions, and not to a plasmonic field enhancement effect. It is proposed that very small, molecule-like noble metal particles (such as dimers, trimers, and tetramers) first absorb the excitation light, undergo a singlet-triplet intersystem crossing, and finally transfer the energy to an excited multiplet state of adjacent lanthanide(III) ions. X-ray lithographic microstructuring and excitation with a commercial UV LED show the potential of the activated glass samples as bright light-emitting devices with tunable emission colors. [source] Mechanisms Controlling Crystal Habits of Gold and Silver ColloidsADVANCED FUNCTIONAL MATERIALS, Issue 7 2005C. Lofton Abstract Examples of gold and silver anisotropic colloids, such as prisms and rods, have appeared in the literature for many years. In most cases, the morphologies of these thermodynamically unfavorable particles have been explained by the particular reaction environment in which they were synthesized. The mechanisms used to explain the growth generally fall into two categories, one in which chemically adsorbed molecules regulate the growth of specific crystal faces kinetically, and the other where micelle-forming surfactants physically direct the shape of the particle. This paper raises questions about the growth of anisotropic metal colloids that the current mechanisms cannot adequately address, specifically, the formation of multiple shapes in a single homogeneous reaction and the appearance of similar structures in very different synthesis schemes. These observations suggest that any growth mechanism should primarily take into consideration nucleation and kinetics, and not only thermodynamics or physical constrictions. The authors suggest an alternative mechanism where the presence and orientation of twin planes in these face-centered cubic (fcc) metals direct the shape of the growing particles. This explanation follows that used for silver halide crystals, and has the advantage of explaining particle growth in many synthesis methods. In this mechanism, twin planes generate reentrant grooves, favorable sites for the attachment of adatoms. Shape and structural data are presented for gold and silver particles synthesized using several different techniques to support this new model. Triangular prisms are suggested to contain a single twin plane which directs that growth of the initial seed in two dimensions, but limits the final size of the prism. Hexagonal platelets are suggested to contain two parallel twin planes that allow the fast growing edges to regenerate one another, allowing large sizes and aspect ratios to form. Rods and wires were found to have a fivefold symmetry, which may only allow growth in one dimension. It is expected that a superior mechanistic understanding will permit shape-selective synthesis schemes to be developed. [source] Highly Surface-roughened "Flower-like" Silver Nanoparticles for Extremely Sensitive Substrates of Surface-enhanced Raman ScatteringADVANCED MATERIALS, Issue 45 2009Hongyan Liang Abstract Surface-enhanced Raman scattering (SERS) is a new optical spectroscopic analysis technique with potential for highly sensitive detection of molecules. Recently, many efforts have been made to find SERS substrates with high sensitivity and reproducibility. In this Research News article, we provide a focused review on the synthesis of monodispersed silver particles with a novel, highly roughened, "flower-like" morphology by reducing silver nitrate with ascorbic acid in aqueous solutions. The nanometer-scale surface roughness of the particles can provide several hot spots on a single particle, which significantly increases SERS enhancement. The incident polarization-dependent SERS of individual particles is also studied. Although the different "hot spots" on a single particle can have a strong polarization dependency, the total Raman signals from an individual particle usually have no obvious polarization dependency. Moreover, these flower-like silver particles can be measured by SERS with high enhancement several times, which indicates the high stability of the hot spots. Hence, the flower-like silver particles here can serve as highly sensitive and reproducible SERS substrates. [source] A green process for preparing silver nanoparticles using spinning disk reactorAICHE JOURNAL, Issue 2 2008Clifford Y. Tai Abstract The main theme of this research was to synthesize nanoparticles using green materials in a spinning disk reactor (SDR), which is a type of Higee equipment. The reducing agent and protecting agent were glucose and starch, respectively, either of which is an inexpensive and nontoxic material. Silver particles were prepared by continuously pumping two solutions, which were a mixture of AgNO3 aqueous solution containing protecting agent and another mixture of NaOH aqueous solution containing the reducing agent, into the chamber of the SDR, where a liquid,liquid reaction took place. The reaction time was less than 10 min, which was much shorter than the traditional methods. After washing and redispersing, silver particles of 10 nm or smaller were obtained, and the redispersed aqueous suspensions were stable for more than 40 days with or without the addition of a dispersing agent. A high-gravity process that combines economic benefit with environmental benignancy was successfully developed to produce silver nanoparticles. © 2007 American Institute of Chemical Engineers AIChE J, 2008 [source] Surface-enhanced resonance Raman scattering using pulsed and continuous-wave laser excitationJOURNAL OF RAMAN SPECTROSCOPY, Issue 6-7 2005Rachael E. Littleford Abstract Pulsed and continuous-wave (CW) lasers were compared as excitation sources for surface-enhanced resonance Raman scattering (SERRS). CW excitation provided SERRS spectra with a greater signal-to-noise ratio and more sensitive detection by a factor of ,50 compared with the high peak power, low repetition rate pulsed configuration used. The SERRS intensity using a pulsed laser produced a non-linear response with respect to changes in power of the laser. At powers of less than ,0.012 mW, the absolute intensity under the peaks of the CW and pulsed SERRS spectra converged, suggesting that lower peak power, high repetition rate systems may be more effective excitation sources for SERRS. Transmission electron microscopy of pulsed laser-irradiated silver particles showed significant sample damage and morphological changes. This problem was overcome with the use of a recirculating large-volume flow cell system, providing a fresh sample for each measurement. A picosecond-resolved time delay experiment found that SERRS intensity decreased by ,60% when exposed to a 400 nm pump pulse and probed with a 529 nm pulse. As the time delay between pump and probe increased the system recovered gradually to ,60% of the original SERRS intensity after 50 ps, where it remained constant. This suggests that the surface bonding between the silver and the dye is significantly perturbed, with some nanoscale diffusion occurring of the dye away from the metal surface. Hence chemical enhancement is temporarily prevented and electromagnetic enhancement is reduced as a function of 1/r3 as the dye moves away from the surface. Additionally, transient heating of the colloidal particles caused by the pulsed laser may also lead to plasmon shifts and changes in absorption intensity. Other factors such as surface annealing or decomposition of the silver particle or dye due the extreme temperature conditions may account for the permanent loss in SERRS intensity. Copyright © 2005 John Wiley & Sons, Ltd. [source] Adsorption of 3- and 4-benzoylpyridine on colloidal silver particles: a surface-enhanced Raman scattering studyJOURNAL OF RAMAN SPECTROSCOPY, Issue 12 2004Joydeep Chowdhury Abstract Surface-enhanced Raman scattering (SERS) spectra of 3- and 4-benzoylpyridine (BP) adsorbed on silver hydrosols were compared with the FTIR and normal Raman spectra in bulk and in solution. With a small fractional change in adsorbate concentration, the SER spectra of isomeric BPs show significant changes in their features, indicating different orientational changes of the different parts of the flexible molecule on the colloidal silver surface with adsorbate concentration. The appearance of a broad, long-wavelength band in the absorption spectra of the silver sol due to solute-induced coagulation of colloidal silver particles is found to be red shifted with increase in adsorbate concentration. The SER excitation profiles indicate that the resonance of the Raman excitation radiation with the new aggregation band contributes more to the SERS intensity than that with the original sol band. Copyright © 2004 John Wiley & Sons, Ltd. [source] Production of monodisperse silver colloids by reduction with hydrazine: the effect of chloride and aggregation on SER(R)S signal intensity,JOURNAL OF RAMAN SPECTROSCOPY, Issue 2 2004U. Nickel Abstract SER(R)S spectra with high signal intensity of Nile Blue A sulfate and 1,1,-diethyl-2,2,-cyanine iodide present in low concentration (,0.05 µM) can be recorded by employing certain silver sols in the absence of any chloride and without highly aggregated particles. The sols have been prepared by reduction of silver nitrate with hydrazine hydrate in a special procedure at a carefully established pH. In the presence of chloride, the maximum SER(R)S signal observed for a ca. 0.5 µM solution of Nile Blue A is of similar magnitude employing either a silver sol according to Lee and Meisel or our sol C, which contains nearly exclusively single silver particles with diameters of about 50 nm. Without added chloride, however, only our sol produces SER(R)S spectra with similar intensity as with chloride. Because the influence of chloride and coagulation on the intensity of the SER(R)S-signal can be controlled by varying the additives to our silver sol, further experiments of this kind can help to elucidate how these two parameters influence the magnitude of the SERS enhancement. Copyright © 2004 John Wiley & Sons, Ltd. [source] Effect of Silver on the Sintering and Grain-Growth Behavior of Barium TitanateJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 12 2000Chin-Yi Chen Silver and its alloys frequently are used as electrode material for BaTiO3 -based dielectrics. In the present study, a small amount of fine silver particles have been intimately mixed with BaTiO3 powder. The sintering and grain-growth behavior of the silver-doped BaTiO3 in air are investigated. The solubility of silver in BaTiO3, as revealed by lattice-parameter measurement, electrical measurement, and electron probe microanalysis, is <300 ppm. The densification of BaTiO3 is slowed slightly by the addition of silver inclusions. However, the presence of a small amount (<0.3 wt%) of silver increases the amount and size of abnormal grains. When the silver content is >0.3 wt%, the grain growth of BaTiO3 then is prohibited by the silver inclusions. [source] Behavior of Silver and Palladium Mixtures during HeatingJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2000Terry Garino The behavior of mixtures of silver and palladium during heating in both air and an inert atmosphere was studied using X-ray diffractometry (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), dilatometry, and scanning electron microscopy (SEM). In situ high-temperature XRD studies on a commercial 20% palladium material with submicrometer-sized particles indicated that an intermetallic phase, most likely Ag3Pd, formed in air between 300° and 400°C, the same temperature range where a 13% linear expansion was measured by dilatometry. The DSC data indicated an exothermic peak at 340°C, a temperature where the TGA results indicated that the material had picked up only 0.2% oxygen, compared with the maximum of 1.4% at 525°C. No PdO was detected by XRD at 400°C, which suggests that oxygen was being incorporated in the intermetallic. Microstructural examination using SEM indicated that larger particles, with internal pores, had formed after heating in air to 375°C. When the material was heated in argon for 1 h at 400°C, no intermetallic phase or alloy formed, and minimal expansion occurred. When mixtures of larger silver particles (5,30 ,m) with palladium particles (1,3 ,m) were heated in air, the maximum amount of expansion that occurred increased from 0% for pure palladium up to a maximum of 18% at 75% silver. This result supports the conclusion that expansion is a result of formation of this new phase, in the presence of oxygen, not of the oxidation of the palladium. [source] Nanoanalysis by a high-resolution energy filtering transmission electron microscopeMICROSCOPY RESEARCH AND TECHNIQUE, Issue 3 2004Masanori Mitome Abstract An energy-filtering transmission electron microscope with 300 kV acceleration voltage was developed and the spatial resolution of elemental distribution images was improved. Observing oxygen monolayers in Al11O3N9, it was shown that the actual resolution attained is up to 0.5 nm. Surface plasmon loss images of silver particles were taken with a resolution of better than 0.4 nm. Furthermore, the sensitivity is sufficiently high to distinguish indium content differences of 2.5 atomic percent in InxAl1-xAs. This performance is good enough to analyze elemental distribution with atomic-level resolution. Furthermore, since analysis with the energy-filtering microscope is easy and practical, nanoanalysis may come into wide use not only in academic fields but also in industry. Microsc. Res. Tech. 63:140,148, 2004. © 2004 Wiley-Liss, Inc. [source] The role of a third component on the conductivity behavior of ternary epoxy/Ag conductive compositesPOLYMER COMPOSITES, Issue 4 2002W. Jia Conductive adhesives, based on highly filled silver particles dispersed in a liquid epoxy resin, with an aliphatic amine [diethyltriamine (DETA)] as a curing agent, were investigated. A third component was added to the epoxy/Ag system to obtain composites of better conductivity, or similar conductivity but at lower silver contents, to modify the conductive adhesive properties, and also to reduce cost. Epoxy/Ag/carbon black (CB), epoxy/Ag/carbon fibrils (CF), epoxy/Ag/SiO2 and epoxy/Ag/dispersant composites were thus studied. The effect of high curing temperature on the uniformity and resulting conductivity level was also studied. The studied systems, excluding the epoxy/Ag/CB composite, exhibited enhanced conductivities. The microstructure of most of the systems was studied by scanning electron microscopy (SEM). The micrographs produced have served to establish structure-property relations for better understanding of the observed phenomena. [source] Multilayer Substrate-Mediated Tuning Resonance of Plasmon and SERS EF of Nanostructured Silver,CHEMPHYSCHEM, Issue 12 2010Lian C. T. Shoute Dr. Abstract A thin-film of dielectric on a reflecting surface constituting a multilayer substrate modulates light intensity due to the interference effect. A nanostructure consisting of randomly oriented silver particles of different shapes, sizes, and interparticle spacings supports multiple plasmon resonances and is observed to have a broad extinction spectrum that spans the entire visible region. Combining the two systems by fabricating the nanostructure on the thin-dielectric film of the multilayer substrate yields a new composite structure which is observed to modulate both the extinction spectrum and the SERS EF (surface enhanced Raman scattering enhancement factor) of the nanostructure as the thickness of the thin-film dielectric is varied. The frequency and intensity of the visible extinction spectrum vary dramatically with the dielectric thickness and in the intermediate thickness range the spectrum has no visible band. The SERS EF determined for the composite structure as a function of the thin-film dielectric thickness varies by several orders of magnitude. Strong correlation between the magnitude of the SERS EF and the extinction intensity is observed over the entire dielectric thickness range indicating that the extinction spectrum corresponds to the excitation of the plasmon resonances of the nanostructure. A significant finding which has potential applications is that the composite structure has synergic effect to boost SERS EF of the nanostructure by an order of magnitude or more compared to the same nanostructure on an unlayered substrate. [source] Rational Design of Ag/TiO2 Nanosystems by a Combined RF-Sputtering/Sol-Gel ApproachCHEMPHYSCHEM, Issue 18 2009Lidia Armelao Dr. Abstract The present work is devoted to the preparation of Ag/TiO2 nanosystems by an original synthetic strategy, based on the radio-frequency (RF) sputtering of silver particles on titania-based xerogels prepared by the sol,gel (SG) route. This approach takes advantage of the synergy between the microporous xerogel structure and the infiltration power characterizing RF-sputtering, whose combination enables the obtainment of a tailored dispersion of Ag-containing particles into the titania matrix. In addition, the system,s chemico-physical features can be tuned further through proper ex situ thermal treatments in air at 400 and 600,°C. The synthesized composites are extensively characterized by the joint use of complementary techniques, that is, X-ray photoelectron and X-ray excited Auger electron spectroscopies (XPS, XE-AES), secondary ion mass spectrometry (SIMS), glancing incidence X-ray diffraction (GIXRD), field emission scanning electron microscopy (FE,SEM), transmission electron microscopy (TEM), electron diffraction (ED), high-angle annular dark field scanning TEM (HAADF,STEM), energy-filtered TEM (EF,TEM) and optical absorption spectroscopy. Finally, the photocatalytic performances of selected samples in the decomposition of the azo-dye Plasmocorinth B are preliminarily investigated. The obtained results highlight the possibility of tailoring the system characteristics over a broad range, directly influencing their eventual functional properties. [source] Photoinduced Reduction of Silver inside Microscale Polyelectrolyte CapsulesCHEMPHYSCHEM, Issue 10 2003Dmitry G. Shchukin Dr. Every cloud has a silver lining. The use of poly(styrene sulfonate)/poly(allylamine hydrochloride) (PSS/PAH) polyelectrolyte capsules as microreactors is described for the photochemical synthesis of nanosized silver particles, exclusively, inside a restricted volume of capsule (see graphic). The formed Ag nanoparticles are not aggregated and have an average diameter of 8 nm. The resulting Ag-filled polyelectrolyte capsules can find applications as catalytic microreactors and medical agents. [source] | |||||||||||||