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Sample records for ag nanoparticle size

  1. Narrow size distributed Ag nanoparticles grown by spin coating and thermal reduction: effect of processing parameters

    NASA Astrophysics Data System (ADS)

    Ansari, A. A.; Sartale, S. D.

    2016-08-01

    A simple method to grow uniform sized Ag nanoparticles with narrow size distribution on flat support (glass and Si substrates) via spin coating of Ag+ ions (AgNO3) solution followed by thermal reduction in H2 is presented. These grown nanoparticles can be used as model catalytic system to study size dependent oxygen reduction reaction (ORR) activity. Ag nanoparticles formation was confirmed by local surface plasmon resonance and x-ray photoelectron spectroscopy measurements. Influences of process parameters (revolution per minute (rpm), ramp and salt concentration) on grown Ag nanoparticles size, density and size uniformity are studied. With increase in rpm and ramp the size decreases and the particle number density increases, whereas the size dispersion improves. The catalytic activity of the grown Ag particles for ORR is studied and it is found that the catalytic performance is dependent on the size as well as the number density of the grown Ag nanoparticles.

  2. Size-selected ag nanoparticles with five-fold symmetry.

    PubMed

    Gracia-Pinilla, Miguelángel; Ferrer, Domingo; Mejía-Rosales, Sergio; Pérez-Tijerina, Eduardo

    2009-01-01

    Silver nanoparticles were synthesized using the inert gas aggregation technique. We found the optimal experimental conditions to synthesize nanoparticles at different sizes: 1.3 ± 0.2, 1.7 ± 0.3, 2.5 ± 0.4, 3.7 ± 0.4, 4.5 ± 0.9, and 5.5 ± 0.3 nm. We were able to investigate the dependence of the size of the nanoparticles on the synthesis parameters. Our data suggest that the aggregation of clusters (dimers, trimer, etc.) into the active zone of the nanocluster source is the predominant physical mechanism for the formation of the nanoparticles. Our experiments were carried out in conditions that kept the density of nanoparticles low, and the formation of larges nanoparticles by coalescence processes was avoided. In order to preserve the structural and morphological properties, the impact energy of the clusters landing into the substrate was controlled, such that the acceleration energy of the nanoparticles was around 0.1 eV/atom, assuring a soft landing deposition. High-resolution transmission electron microscopy images showed that the nanoparticles were icosahedral in shape, preferentially oriented with a five-fold axis perpendicular to the substrate surface. Our results show that the synthesis by inert gas aggregation technique is a very promising alternative to produce metal nanoparticles when the control of both size and shape are critical for the development of practical applications.

  3. Size-Selected Ag Nanoparticles with Five-Fold Symmetry

    PubMed Central

    2009-01-01

    Silver nanoparticles were synthesized using the inert gas aggregation technique. We found the optimal experimental conditions to synthesize nanoparticles at different sizes: 1.3 ± 0.2, 1.7 ± 0.3, 2.5 ± 0.4, 3.7 ± 0.4, 4.5 ± 0.9, and 5.5 ± 0.3 nm. We were able to investigate the dependence of the size of the nanoparticles on the synthesis parameters. Our data suggest that the aggregation of clusters (dimers, trimer, etc.) into the active zone of the nanocluster source is the predominant physical mechanism for the formation of the nanoparticles. Our experiments were carried out in conditions that kept the density of nanoparticles low, and the formation of larges nanoparticles by coalescence processes was avoided. In order to preserve the structural and morphological properties, the impact energy of the clusters landing into the substrate was controlled, such that the acceleration energy of the nanoparticles was around 0.1 eV/atom, assuring a soft landing deposition. High-resolution transmission electron microscopy images showed that the nanoparticles were icosahedral in shape, preferentially oriented with a five-fold axis perpendicular to the substrate surface. Our results show that the synthesis by inert gas aggregation technique is a very promising alternative to produce metal nanoparticles when the control of both size and shape are critical for the development of practical applications. PMID:20596397

  4. Core-size-dependent catalytic properties of bimetallic Au/Ag core-shell nanoparticles.

    PubMed

    Haldar, Krishna Kanta; Kundu, Simanta; Patra, Amitava

    2014-12-24

    Bimetallic core-shell nanoparticles have recently emerged as a new class of functional materials because of their potential applications in catalysis, surface enhanced Raman scattering (SERS) substrate and photonics etc. Here, we have synthesized Au/Ag bimetallic core-shell nanoparticles with varying the core diameter. The red-shifting of the both plasmonic peaks of Ag and Au confirms the core-shell structure of the nanoparticles. Transmission electron microscopy (TEM) analysis, line scan EDS measurement and UV-vis study confirm the formation of core-shell nanoparticles. We have examined the catalytic activity of these core-shell nanostructures in the reaction between 4-nitrophenol (4-NP) and NaBH4 to form 4-aminophenol (4-AP) and the efficiency of the catalytic reaction is found to be increased with increasing the core size of Au/Ag core-shell nanocrystals. The catalytic efficiency varies from 41.8 to 96.5% with varying core size from 10 to 100 nm of Au/Ag core-shell nanoparticles, and the Au100/Ag bimetallic core-shell nanoparticle is found to be 12-fold more active than that of the pure Au nanoparticles with 100 nm diameter. Thus, the catalytic properties of the metal nanoparticles are significantly enhanced because of the Au/Ag core-shell structure, and the rate is dependent on the size of the core of the nanoparticles.

  5. Oxidation of Ag nanoparticles in aqueous media: Effect of particle size and capping

    NASA Astrophysics Data System (ADS)

    Mikhlin, Yuri L.; Vishnyakova, Elena A.; Romanchenko, Alexander S.; Saikova, Svetlana V.; Likhatski, Maxim N.; Larichev, Yurii V.; Tuzikov, Fedor V.; Zaikovskii, Vladimir I.; Zharkov, Sergey M.

    2014-04-01

    Many applications and environmental impact of silver-bearing nanomaterials critically depend upon their specific reactivity, which is still poorly understood. Here, silver nanoparticles (Ag NPs) of about 3-5 nm and 10-12 nm in diameter, uncapped and capped with L-glucose or citrate, were prepared, characterized using UV-vis absorption spectroscopy, SAXS, TEM, and their (electro)chemical oxidation was examined in comparison with each other and bulk metal applying scanning tunneling microscopy and spectroscopy, cyclic voltammetry, and XPS. A resistive switching effect was found in the tunneling spectra measured in air at the smaller uncapped Ag NPs deposited on HOPG and was interpreted in terms of Ag transfer between the particle and the probe. The anodic oxidation of these Ag NPs in 1 M NaOH yielded 3D Ag2O, while only a layer of "primary" Ag(I) oxide emerged on larger uncapped nanoparticles during the potential sweep. The formation of AgO at higher potentials proceeded readily at the "primary" oxide but was retarded at the smaller NPs. The citrate- and glucose-capping substantially impeded the formation both of Ag2O and AgO. The findings highlighted, particularly, a non-trivial effect of particle size and transient mobilization of Ag species on the reactions of silver nanoparticles.

  6. Prediction of size distribution of Ag nanoparticles synthesized via gamma-ray radiolysis

    NASA Astrophysics Data System (ADS)

    Liang, Jia-liang; Shen, Sheng-wen; Ye, Sheng-ying; Ye, Lü-meng

    2015-09-01

    The spherical shape Ag nanoparticles synthesized via gamma-ray radiolysis were observed with the transmission electron microscope (TEM). Diameters of Ag nanoparticles were measured from the TEM photographs. Statistical analysis showed that the particle diameter complied with a linear-converted Poisson distribution. The distribution parameter, which was the average of diameters, was related to the ultraviolet-visible spectrum peak position of the nanosilver collosol. An empirical equation was established to predicting size distribution of Ag nanoparticles with the peak position. Nanosilver of different sizes could be synthesized by adjusting the intensity of γ-irradiation, the kind and the addition amount of the stabilizing agent. Because particle size affects the physiochemical properties of nanosilver material, results of this paper would be of practical significance for the application of nanosilver.

  7. Size and alloying induced shift in core and valence bands of Pd-Ag and Pd-Cu nanoparticles

    SciTech Connect

    Sengar, Saurabh K.; Mehta, B. R.; Govind

    2014-03-28

    In this report, X-ray photoelectron spectroscopy studies have been carried out on Pd, Ag, Cu, Pd-Ag, and Pd-Cu nanoparticles having identical sizes corresponding to mobility equivalent diameters of 60, 40, and 20 nm. The nanoparticles were prepared by the gas phase synthesis method. The effect of size on valence and core levels in metal and alloy nanoparticles has been studied by comparing the values to those with the 60 nm nanoparticles. The effect of alloying has been investigated by comparing the valence and core level binding energies of Pd-Cu and Pd-Ag alloy nanoparticles with the corresponding values for Pd, Ag, and Cu nanoparticles of identical sizes. These effects have been explained in terms of size induced lattice contractions, alloying induced charge transfer, and hybridization effects. The observation of alloying and size induced binding energy shifts in bimetallic nanoparticles is important from the point of view of hydrogen reactivity.

  8. Raman scattering of 4-aminobenzenethiol sandwiched between Ag nanoparticle and macroscopically smooth Au substrate: effects of size of Ag nanoparticles and the excitation wavelength.

    PubMed

    Kim, Kwan; Choi, Jeong-Yong; Lee, Hyang Bong; Shin, Kuan Soo

    2011-09-28

    A nanogap formed by a metal nanoparticle and a flat metal substrate is one kind of "hot site" for surface-enhanced Raman scattering (SERS). Accordingly, although no Raman signal is observable when 4-aminobenzenethiol (4-ABT), for instance, is self-assembled on a flat Au substrate, a distinct spectrum is obtained when Ag or Au nanoparticles are adsorbed on the pendent amine groups of 4-ABT. This is definitely due to the electromagnetic coupling between the localized surface plasmon of Ag or Au nanoparticle with the surface plasmon polariton of the planar Au substrate, allowing an intense electric field to be induced in the gap even by visible light. To appreciate the Raman scattering enhancement and also to seek the optimal condition for SERS at the nanogap, we have thoroughly examined the size effect of Ag nanoparticles, along with the excitation wavelength dependence, by assembling 4-ABT between planar Au and a variable-size Ag nanoparticle (from 20- to 80-nm in diameter). Regarding the size dependence, a higher Raman signal was observed when larger Ag nanoparticles were attached onto 4-ABT, irrespective of the excitation wavelength. Regarding the excitation wavelength, the highest Raman signal was measured at 568 nm excitation, slightly larger than that at 632.8 nm excitation. The Raman signal measured at 514.5 and 488 nm excitation was an order of magnitude weaker than that at 568 nm excitation, in agreement with the finite-difference time domain simulation. It is noteworthy that placing an Au nanoparticle on 4-ABT, instead of an Ag nanoparticle, the enhancement at the 568 nm excitation was several tens of times weaker than that at the 632.8 nm excitation, suggesting the importance of the localized surface plasmon resonance of the Ag nanoparticles for an effective coupling with the surface plasmon polariton of the planar Au substrate to induce a very intense electric field at the nanogap.

  9. A composition and size controllable approach for Au-Ag alloy nanoparticles

    PubMed Central

    2012-01-01

    A capillary micro-reaction was established for the synthesis of Au-Ag alloy nanoparticles (NPs) with a flexible and controllable composition and grain size by tuning the synthesis temperature, the residence time, or the mole ratio of Au3+:Ag+. By extending the residence time from 5 to 900 s, enhancing the temperature from 120°C to 160°C, or decreasing the mole ratio of Au3+:Ag+ from 1:1 to 1:20, the composition of samples was changed continuously from Au-rich to Ag-rich. The particles became large with the increase of the residence time; however, synthesis temperatures showed less effect on the particle size change. The particle size of the Au-Ag alloy NPs with various composition could be kept by adjusting the mole ratio of Au3+:Ag+. TEM observation displayed that the as-obtained NPs were sphere-like with the smallest average size of 4.0 nm, which is half of those obtained by the traditional flask method. PMID:22513005

  10. Enhanced hydrogenation and reduced lattice distortion in size selected Pd-Ag and Pd-Cu alloy nanoparticles

    SciTech Connect

    Sengar, Saurabh K.; Mehta, B. R.; Kulriya, P. K.; Khan, S. A.

    2013-10-21

    Important correlation between valence band spectra and hydrogenation properties in Pd alloy nanoparticles is established by studying the properties of size selected and monocrystalline Pd, Ag, Cu, Pd-Ag, and Pd-Cu nanoparticles. The X-ray photoelectron spectroscopy and elastic recoil detection analysis show that size induced Pd4d centroid shift is related to enhanced hydrogenation with H/Pd ratio of 0.57 and 0.49 in Pd-Ag and Pd-Cu nanoparticles in comparison to reported bulk values of 0.2 and 0.1, respectively. Pd-alloy nanoparticles show lower hydrogen induced lattice distortion. The reduced distortion and higher hydrogen reactivity of Pd-alloy nanoparticles is important for numerous hydrogen related applications.

  11. Organ-Specific and Size-Dependent Ag Nanoparticle Toxicity in Gills and Intestines of Adult Zebrafish.

    PubMed

    Osborne, Olivia J; Lin, Sijie; Chang, Chong Hyun; Ji, Zhaoxia; Yu, Xuechen; Wang, Xiang; Lin, Shuo; Xia, Tian; Nel, André E

    2015-10-27

    We studied adult zebrafish to determine whether the size of 20 and 110 nm citrate-coated silver nanoparticles (AgC NPs) differentially impact the gills and intestines, known target organs for Ag toxicity in fish. Following exposure for 4 h, 4 days, or 4 days plus a 7 day depuration period, we obtained different toxicokinetic profiles for different particle sizes, as determined by Ag content of the tissues. Ionic AgNO3 served as a positive control. The gills showed a significantly higher Ag content for the 20 nm particles at 4 h and 4 days than the 110 nm particles, while the values were more similar in the intestines. Both particle types were retained in the intestines even after depuration. These toxicokinetics were accompanied by striking size-dependent differences in the ultrastructural features and histopathology in the target organs in response to the particulates. Ag staining of the gills and intestines confirmed prominent Ag deposition in the basolateral membranes for the 20 nm but not for the 110 nm particles. Furthermore, it was possible to link the site of tissue deposition to disruption of the Na(+)/K(+) ion channel, which is also localized to the basolateral membrane. This was confirmed by a reduction in ATPase activity and immunohistochemical detection of the α subunit of this channel in both target organs, with the 20 nm particles causing significantly higher inhibition and disruption than the larger size particles or AgNO3. These results demonstrate the importance of particle size in determining the hazardous impact of AgNPs in the gills and intestines of adult zebrafish.

  12. Organ-Specific and Size-Dependent Ag Nanoparticle Toxicity in Gills and Intestines of Adult Zebrafish.

    PubMed

    Osborne, Olivia J; Lin, Sijie; Chang, Chong Hyun; Ji, Zhaoxia; Yu, Xuechen; Wang, Xiang; Lin, Shuo; Xia, Tian; Nel, André E

    2015-10-27

    We studied adult zebrafish to determine whether the size of 20 and 110 nm citrate-coated silver nanoparticles (AgC NPs) differentially impact the gills and intestines, known target organs for Ag toxicity in fish. Following exposure for 4 h, 4 days, or 4 days plus a 7 day depuration period, we obtained different toxicokinetic profiles for different particle sizes, as determined by Ag content of the tissues. Ionic AgNO3 served as a positive control. The gills showed a significantly higher Ag content for the 20 nm particles at 4 h and 4 days than the 110 nm particles, while the values were more similar in the intestines. Both particle types were retained in the intestines even after depuration. These toxicokinetics were accompanied by striking size-dependent differences in the ultrastructural features and histopathology in the target organs in response to the particulates. Ag staining of the gills and intestines confirmed prominent Ag deposition in the basolateral membranes for the 20 nm but not for the 110 nm particles. Furthermore, it was possible to link the site of tissue deposition to disruption of the Na(+)/K(+) ion channel, which is also localized to the basolateral membrane. This was confirmed by a reduction in ATPase activity and immunohistochemical detection of the α subunit of this channel in both target organs, with the 20 nm particles causing significantly higher inhibition and disruption than the larger size particles or AgNO3. These results demonstrate the importance of particle size in determining the hazardous impact of AgNPs in the gills and intestines of adult zebrafish. PMID:26327297

  13. Size-dependent cytotoxicity of silver nanoparticles in human lung cells: the role of cellular uptake, agglomeration and Ag release

    PubMed Central

    2014-01-01

    Background Silver nanoparticles (AgNPs) are currently one of the most manufactured nanomaterials. A wide range of toxicity studies have been performed on various AgNPs, but these studies report a high variation in toxicity and often lack proper particle characterization. The aim of this study was to investigate size- and coating-dependent toxicity of thoroughly characterized AgNPs following exposure of human lung cells and to explore the mechanisms of toxicity. Methods BEAS-2B cells were exposed to citrate coated AgNPs of different primary particle sizes (10, 40 and 75 nm) as well as to 10 nm PVP coated and 50 nm uncoated AgNPs. The particle agglomeration in cell medium was investigated by photon cross correlation spectroscopy (PCCS); cell viability by LDH and Alamar Blue assay; ROS induction by DCFH-DA assay; genotoxicity by alkaline comet assay and γH2AX foci formation; uptake and intracellular localization by transmission electron microscopy (TEM); and cellular dose as well as Ag release by atomic absorption spectroscopy (AAS). Results The results showed cytotoxicity only of the 10 nm particles independent of surface coating. In contrast, all AgNPs tested caused an increase in overall DNA damage after 24 h assessed by the comet assay, suggesting independent mechanisms for cytotoxicity and DNA damage. However, there was no γH2AX foci formation and no increased production of intracellular reactive oxygen species (ROS). The reasons for the higher toxicity of the 10 nm particles were explored by investigating particle agglomeration in cell medium, cellular uptake, intracellular localization and Ag release. Despite different agglomeration patterns, there was no evident difference in the uptake or intracellular localization of the citrate and PVP coated AgNPs. However, the 10 nm particles released significantly more Ag compared with all other AgNPs (approx. 24 wt% vs. 4–7 wt%) following 24 h in cell medium. The released fraction in cell medium did not induce any

  14. Size-controlled stabilization of the superionic phase to room temperature in polymer-coated AgI nanoparticles.

    PubMed

    Makiura, Rie; Yonemura, Takayuki; Yamada, Teppei; Yamauchi, Miho; Ikeda, Ryuichi; Kitagawa, Hiroshi; Kato, Kenichi; Takata, Masaki

    2009-06-01

    Solid-state ionic conductors are actively studied for their large application potential in batteries and sensors. From the view of future nanodevices, nanoscaled ionic conductors are attracting much interest. Silver iodide (AgI) is a well-known ionic conductor for which the high-temperature alpha-phase shows a superionic conductivity greater than 1 Omega(-1) cm(-1). Below 147 degrees C, alpha-AgI undergoes a phase transition into the poorly conducting beta- and gamma-polymorphs, thereby limiting its applications. Here, we report the facile synthesis of variable-size AgI nanoparticles coated with poly-N-vinyl-2-pyrrolidone (PVP) and the controllable tuning of the alpha- to beta-/gamma-phase transition temperature (Tc). Tc shifts considerably to lower temperatures with decreasing nanoparticle size, leading to a progressively enlarged thermal hysteresis. Specifically, when the size approaches 10-11 nm, the alpha-phase survives down to 30 degrees C--the lowest temperature for any AgI family material. We attribute the suppression of the phase transition not only to the increase of the surface energy, but also to the presence of defects and the accompanying charge imbalance induced by PVP. Moreover, the conductivity of as-prepared 11 nm beta-/gamma-AgI nanoparticles at 24 degrees C is approximately 1.5 x 10(-2) Omega(-1) cm(-1)--the highest ionic conductivity for a binary solid at room temperature. The stabilized superionic phase and the remarkable transport properties at a practical temperature reported here suggest promising applications in silver-ion-based electrochemical devices.

  15. Size-controlled stabilization of the superionic phase to room temperature in polymer-coated AgI nanoparticles

    NASA Astrophysics Data System (ADS)

    Makiura, Rie; Yonemura, Takayuki; Yamada, Teppei; Yamauchi, Miho; Ikeda, Ryuichi; Kitagawa, Hiroshi; Kato, Kenichi; Takata, Masaki

    2009-06-01

    Solid-state ionic conductors are actively studied for their large application potential in batteries and sensors. From the view of future nanodevices, nanoscaled ionic conductors are attracting much interest. Silver iodide (AgI) is a well-known ionic conductor for which the high-temperature α-phase shows a superionic conductivity greater than 1Ω-1cm-1 (ref. 6). Below 147∘C, α-AgI undergoes a phase transition into the poorly conducting β- and γ-polymorphs, thereby limiting its applications. Here, we report the facile synthesis of variable-size AgI nanoparticles coated with poly-N-vinyl-2-pyrrolidone (PVP) and the controllable tuning of the α- to β-/γ-phase transition temperature (Tc↓). Tc↓ shifts considerably to lower temperatures with decreasing nanoparticle size, leading to a progressively enlarged thermal hysteresis. Specifically, when the size approaches 10-11nm, the α-phase survives down to 30∘C-the lowest temperature for any AgI family material. We attribute the suppression of the phase transition not only to the increase of the surface energy, but also to the presence of defects and the accompanying charge imbalance induced by PVP. Moreover, the conductivity of as-prepared 11nm β-/γ-AgI nanoparticles at 24∘C is ~1.5×10-2Ω-1cm-1-the highest ionic conductivity for a binary solid at room temperature. The stabilized superionic phase and the remarkable transport properties at a practical temperature reported here suggest promising applications in silver-ion-based electrochemical devices.

  16. The effect of nanoparticles size on photocatalytic and antimicrobial properties of Ag-Pt/TiO2 photocatalysts

    NASA Astrophysics Data System (ADS)

    Zielińska-Jurek, Anna; Wei, Zhishun; Wysocka, Izabela; Szweda, Piotr; Kowalska, Ewa

    2015-10-01

    Ag-Pt-modified TiO2 nanocomposites were synthesized using the sol-gel method. Bimetallic modified TiO2 nanoparticles exhibited improved photocatalytic activity under visible-light irradiation, better than monometallic Ag/TiO2 and Pt/TiO2 nanoparticles (NPs). All modified powders showed localized surface plasmon resonance (LSPR) in visible region. The photocatalysts' characteristics by X-ray diffractometry (XRD), scanning transmission electron microscopy (STEM), diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption (BET method for specific surface area) showed that sample with the highest photocatalytic activity had anatase structure, about 93 m2/g specific surface area, maximum plasmon absorption at ca. 420 nm and contained small NPs of silver of 6 nm and very fine platinum NPs of 3 nm. The photocatalytic activity was estimated by measuring the decomposition rate of phenol in 0.2 mM aqueous solution under Vis and UV/vis light irradiation. It was found that size of platinum was decisive for the photocatalytic activity under visible light irradiation, i.e., the smaller Pt NPs were, the higher was photocatalytic activity. While, antimicrobial activities, estimated for bacteria Escherichia coli and Staphylococcus aureus, and pathogenic fungi belonging to Candida family, were only observed for photocatalysts containing silver, i.e., Ag/TiO2 and Ag-Pt/TiO2 nanocomposites.

  17. Self-assembled Ag nanoparticle network passivated by a nano-sized ZnO layer for transparent and flexible film heaters

    SciTech Connect

    Seo, Ki-Won; Kim, Han-Ki; Kim, Min-Yi; Chang, Hyo-Sik

    2015-12-15

    We investigated a self-assembled Ag nanoparticle network electrode passivated by a nano-sized ZnO layer for use in high-performance transparent and flexible film heaters (TFFHs). The low temperature atomic layer deposition of a nano-sized ZnO layer effectively filled the uncovered area of Ag network and improved the current spreading in the self-assembled Ag network without a change in the sheet resistance and optical transmittance as well as mechanical flexibility. The time-temperature profiles and heat distribution analysis demonstrate that the performance of the TFTH with the ZnO/Ag network is superior to that of a TFFH with Ag nanowire electrodes. In addition, the TFTHs with ZnO/Ag network exhibited better stability than the TFFH with a bare Ag network due to the effective current spreading through the nano-sized ZnO layer.

  18. State-resolved investigation of the photodesorption dynamics of NO from (NO){sub 2} on Ag nanoparticles of various sizes in comparison with Ag(111)

    SciTech Connect

    Mulugeta, Daniel; Watanabe, Kazuo; Menzel, Dietrich; Freund, Hans-Joachim

    2011-04-28

    The translational and internal state energy distributions of NO desorbed by laser light (2.3, 3.5, and 4.7 eV) from adsorbed (NO){sub 2} on Ag nanoparticles (NPs) (mean diameters, D= 4, 8, and 11 nm) have been investigated by the (1 + 1) resonance enhanced multiphoton ionization technique. For comparison, the same experiments have also been carried out on Ag(111). Detected NO molecules are hyperthermally fast and both rotationally and vibrationally hot, with temperatures well above the sample temperature. The translational and rotational excitations are positively correlated, while the vibrational excitation is decoupled from the other two degrees of freedom. Most of the energy content of the desorbing NO is contained in its translation. The translational and internal energy distributions of NO molecules photodesorbed by 2.3, 3.5, and in part also 4.7 eV light are approximately constant as a function of Ag NPs sizes, and they are the same on Ag(111). This suggests that for these excitations a common mechanism is operative on the bulk single crystal and on NPs, independent of the size regime. Notably, despite the strongly enhanced cross section seen on NP at 3.5 eV excitation energy in p-polarization, i.e., in resonance with the plasmon excitation, the mechanism is also unchanged. At 4.7 eV and for small particles, however, an additional desorption channel is observed which results in desorbates with higher energies in all degrees of freedom. The results are well compatible with our earlier measurements of size-dependent translational energy distributions. We suggest that the broadly constant mechanism over most of the investigated range runs via a transient negative ion state, while at high excitation energy and for small particles the transient state is suggested to be a positive ion.

  19. Study of structural modification of PVA by incorporating Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Saini, Isha; Sharma, Annu; Rozra, Jyoti; Aggarwal, Sanjeev; Dhiman, Rajnish; Sharma, Pawan K.

    2016-05-01

    Nanocomposites of PVA with Ag nanoparticles dispersed in it were synthesized using solution casting method. The morphology and size distribution of Ag nanoparticles embedded in PVA matrix were obtained by transmission electron microscopy (TEM) and Field emission scanning electron microscopy (FE-SEM). Raman spectroscopy was used to examine structural changes taking place inside polyvinyl alcohol (PVA) matrix due to incorporation of Ag nanoparticle. Raman analysis indicates that Ag nanoparticles interact with PVA through H-bonding.

  20. Spin coating of Ag nanoparticles: Effect of reduction

    SciTech Connect

    Ansari, A. A. Sartale, S. D.

    2014-04-24

    A surfactant free method for the growth of Ag nanoparticles on glass substrate by spin coating of Ag ions solution followed by chemical reduction in aqueous hydrazine hydrate (HyH) solution has been presented. Appearance of surface plasmon resonance confirms the formation of Ag nanoparticles. Morphology and absorbance spectra of Ag nanoparticles films are used to examine effect of hydrazine concentration on the growth of Ag nanoparticles. SEM images show uniformly distributed Ag nanoparticles. Rate constant was found to be dependent on HyH concentration as a consequence influence particle size.

  1. Probing the interaction of lysozyme with ciprofloxacin in the presence of different-sized Ag nano-particles by multispectroscopic techniques and isothermal titration calorimetry.

    PubMed

    Pasban Ziyarat, Fatemeh; Asoodeh, Ahmad; Sharif Barfeh, Zahra; Pirouzi, Maliheh; Chamani, Jamshidkhan

    2014-04-01

    The binding of ciprofloxacin to lysozyme in the presence of three Ag nano-particles of varying sizes was for the first time investigated by multispectroscopic and isothermal titration calorimetry techniques at pH 7.4. The results indicated that ciprofloxacin quenched the fluorescence intensity of lysozyme through a static mechanism but in the presence of size-II Ag nano-particles, there were two kinds of interaction behaviors. The interaction between ciprofloxacin and lysozyme occurred via a second type of binding site, whereas in the presence of the Ag nano-particles, some changes occurred. The secondary structure of lysozyme-ciprofloxacin in the presence of Ag nano-particles was determined by circular dichroism. The thermodynamic parameters of the interaction between ciprofloxacin and lysozyme in the presence of Ag nano-particles were measured according to the van't Hoff equation. The enthalpy (ΔH(○)) and entropy (ΔS(○)) changes were calculated to be -49.7 (kJ mol(-1)) and -20.1 (J mol(-1) K(-1)), respectively, which indicated that the interaction of ciprofloxacin with lysozyme was driven mainly by van der Waals forces and hydrogen bonding. In the presence of the three different-sized Ag nano-particles, the enthalpic and the entropic changes were both negative which indicated that hydrogen bonding with van der Waals forces played major roles in the binding between ciprofloxacin and lysozyme. Recent developments in nano-materials offer new pathways for controlling the protein behavior through surface interactions. These data indicate that the recent research on nano-particle/protein interactions will emphasize the importance of such interactions in biological systems with applications including the diagnosis and treatment of human diseases.

  2. Laser-based synthesis of core Ag-shell AgI nanoparticles

    NASA Astrophysics Data System (ADS)

    Tan, Hua; Fan, Wai Yip

    2005-05-01

    A laser-controlled synthesis of silver iodide (AgI) nanoparticles with isolable AgI shell-Ag core stable intermediates is achieved via molecular iodine photodissociation in the presence of pure Ag nanoparticles dispersed in water. Ag nanoparticles were introduced into the solution containing sodium dodecylsulphate surfactants and iodine by ablating a piece of silver foil with a 532 nm pulsed Nd-YAG laser. Transmission electron microscopy images showed that different AgI shell-Ag core sizes could be achieved by controlling the photolysis of I 2 in solution. These nanoparticles were also found to catalyse an atom-economy Grignard-Barbier organic reaction.

  3. Preparation and antibacterial activities of Ag/Ag+/Ag3+ nanoparticle composites made by pomegranate (Punica granatum) rind extract

    NASA Astrophysics Data System (ADS)

    Yang, Hui; Ren, Yan-yu; Wang, Tao; Wang, Chuang

    Nano-silver and its composite materials are widely used in medicine, food and other industries due to their strong conductivity, size effect and other special performances. So far, more microbial researches have been applied, but a plant method is rarely reported. In order to open up a new way to prepare AgNP composites, pomegranate peel extract was used in this work to reduce Ag+ to prepare Ag/Ag+/Ag3+ nanoparticle composites. UV-Vis was employed to detect and track the reduction of Ag+ and the forming process of AgNPs. The composition, structure and size of the crystal were analyzed by XRD and TEM. Results showed that, under mild conditions, pomegranate peel extract reacted with dilute AgNO3 solution to produce Ag/Ag+/Ag3+ nanoparticle composites. At pH = 8 and 10 mmol/L of AgNO3 concentration, the size of the achieved composites ranged between 15 and 35 nm with spherical shapes and good crystallinity. The bactericidal experiment indicated that the prepared Ag/Ag+/Ag3+ nanoparticles had strong antibacterial activity against gram positive bacteria and gram negative bacteria. FTIR analysis revealed that biological macromolecules with groups of sbnd NH2, sbnd OH, and others were distributed on the surface of the newly synthesized Ag/Ag+/Ag3+ nanoparticles. This provided a useful clue to further study the AgNP biosynthesis mechanism.

  4. Influence of size, shape and core–shell interface on surface plasmon resonance in Ag and Ag@MgO nanoparticle films deposited on Si/SiOx

    PubMed Central

    Pinotti, Daniele; Spadaro, Maria Chiara; Paolicelli, Guido; Grillo, Vincenzo; Valeri, Sergio; Pasquali, Luca; Bergamini, Luca; Corni, Stefano

    2015-01-01

    Summary Ag and Ag@MgO core–shell nanoparticles (NPs) with a diameter of d = 3–10 nm were obtained by physical synthesis methods and deposited on Si with its native ultrathin oxide layer SiOx (Si/SiOx). Scanning electron microscopy and transmission electron microscopy (TEM) images of bare Ag NPs revealed the presence of small NP aggregates caused by diffusion on the surface and agglomeration. Atomic resolution TEM gave evidence of the presence of crystalline multidomains in the NPs, which were due to aggregation and multitwinning occurring during NP growth in the nanocluster source. Co-deposition of Ag NPs and Mg atoms in an oxygen atmosphere gave rise to formation of a MgO shell matrix surrounding the Ag NPs. The behaviour of the surface plasmon resonance (SPR) excitation in surface differential reflectivity (SDR) spectra with p-polarised light was investigated for bare Ag and Ag@MgO NPs. It was shown that the presence of MgO around the Ag NPs caused a red shift of the plasmon excitation, and served to preserve its existence after prolonged (five months) exposure to air, realizing the possibility of technological applications in plasmonic devices. The Ag NP and Ag@MgO NP film features in the SDR spectra could be reproduced by classical electrodynamics simulations by treating the NP-containing layer as an effective Maxwell Garnett medium. The simulations gave results in agreement with the experiments when accounting for the experimentally observed aggregation. PMID:25821680

  5. Temperature, pressure, and size dependence of Pd-H interaction in size selected Pd-Ag and Pd-Cu alloy nanoparticles: In-situ X-ray diffraction studies

    SciTech Connect

    Sengar, Saurabh K.; Mehta, B. R.; Kulriya, P. K.

    2014-03-21

    In this study, in-situ X-ray diffraction has been carried out to investigate the effect of temperature and pressure on hydrogen induced lattice parameter variation in size selected Pd-Ag and Pd-Cu alloy nanoparticles. The nanoparticles of three different mobility equivalent diameters (20, 40, and 60 nm) having a narrow size distribution were prepared by gas phase synthesis method. In the present range of temperature (350 K to 250 K) and pressure (10{sup −4} to 100 millibars), no α (H/Pd ≤ 0.03) ↔ β (H/Pd ≥ 0.54) phase transition is observed. At temperature higher than 300 °C or pressure lower than 25 millibars, there is a large difference in the rate at which lattice constant varies as a function of pressure and temperature. Further, the lattice variation with temperature and pressure is also observed to depend upon the nanoparticle size. At lower temperature or higher pressure, size of the nanoparticle seems to be relatively less important. These results are explained on the basis of the relative dominance of physical absorption and diffusion of H in Pd alloy nanoparticles at different temperature and pressure. In the present study, absence of α ↔ β phase transition points towards the advantage of using Pd-alloy nanoparticles in applications requiring long term and repeated hydrogen cycling.

  6. Study of antibacterial activity of Ag and Ag2CO3 nanoparticles stabilized over montmorillonite

    NASA Astrophysics Data System (ADS)

    Sohrabnezhad, Sh.; Pourahmad, A.; Mehdipour Moghaddam, M. J.; Sadeghi, A.

    2015-02-01

    Silver carbonate and silver nanoparticles (NPs) over of stabilizer montmorillonite (MMT) have been synthesized in aqueous and polyol solvent, respectively. Dispersions of silver nanoparticles have been prepared by the reduction of silver nitrate over of MMT in presence and absence of Na2CO3 compound in ethylene glycol. It was observed that montmorillonite was capable of stabilizing formed Ag nanoparticles through the reduction of Ag+ ions in ethylene glycol. Na2CO3 was used as carbonate source in synthesis of Ag2CO3 NPs in water solvent and also for controlling of Ag nanoparticles size in ethylene glycol medium. The samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and ultraviolet-visible diffuse reflectance spectroscopy (DRS). The TEM images showed that Ag NPs size in presence Na2CO3 salts was smaller than without that. The results indicated intercalation of Ag and Ag2CO3 nanoparticles into the montmorillonite clay layers. The diffuse reflectance spectra exhibited a strong surface plasmon resonance (SPR) adsorption peak in the visible region, resulting from Ag nanoparticles. The antibacterial testing results showed that the Ag2CO3-MMT nanocomposite exhibited an antibacterial activity higher than Ag-MMT sample against Escherichia coli.

  7. Comparative Study of Antimicrobial Activity of AgBr and Ag Nanoparticles (NPs)

    PubMed Central

    Suchomel, Petr; Kvitek, Libor; Panacek, Ales; Prucek, Robert; Hrbac, Jan; Vecerova, Renata; Zboril, Radek

    2015-01-01

    The diverse mechanism of antimicrobial activity of Ag and AgBr nanoparticles against gram-positive and gram-negative bacteria and also against several strains of candida was explored in this study. The AgBr nanoparticles (NPs) were prepared by simple precipitation of silver nitrate by potassium bromide in the presence of stabilizing polymers. The used polymers (PEG, PVP, PVA, and HEC) influence significantly the size of the prepared AgBr NPs dependently on the mode of interaction of polymer with Ag+ ions. Small NPs (diameter of about 60–70 nm) were formed in the presence of the polymer with low interaction as are PEG and HEC, the polymers which interact with Ag+ strongly produce nearly two times bigger NPs (120–130 nm). The prepared AgBr NPs were transformed to Ag NPs by the reduction using NaBH4. The sizes of the produced Ag NPs followed the same trends – the smallest NPs were produced in the presence of PEG and HEC polymers. Prepared AgBr and Ag NPs dispersions were tested for their biological activity. The obtained results of antimicrobial activity of AgBr and Ag NPs are discussed in terms of possible mechanism of the action of these NPs against tested microbial strains. The AgBr NPs are more effective against gram-negative bacteria and tested yeast strains while Ag NPs show the best antibacterial action against gram-positive bacteria strains. PMID:25781988

  8. Growth kinetics and size-dependent wetting of Ag/α-Al₂O₃(0001) nanoparticles studied via the plasmonic response.

    PubMed

    Lazzari, Rémi; Jupille, Jacques

    2012-04-01

    The growth of vapour-deposited silver nanoparticles on α-Al₂O₃ was studied in situ from 190 to 675 K by surface differential reflectivity spectroscopy in the UV-visible range. Changes in size, shape and density were derived from the plasmonic response modelled in the framework of interface susceptibilities by assuming that supported clusters were in the form of truncated spheres. The sticking coefficient of silver on alumina is close to one up to T ≃ 575 K before entering a regime of incomplete condensation. The Arrhenius dependence of the saturation density indicates a nucleation on defects at low temperature (T ≤ 300 K) and detrapping above. The particle size D evolution follows temporal power laws, independent of temperature and flux, which characterize the growth (D ∼ t(0.31)) and coalescence (D ∼ t(0.55)) of the film. These are indicative of the growth of isolated particles at constant density and dynamic coalescence, respectively. The wetting angle of the silver clusters is shown to increase during the growth regime, which is assigned to a combination of surface stress and mismatch-induced strain, and to decrease upon coalescence, which is attributed to plastic relaxation. For particles larger than 10 nm in size, the values of contact angle and adhesion energy level off with asymptotic limits (θ(c) = 127.5° ± 1° and 0.48 ± 0.02 J m⁻²) that nicely agree with tabulated data. This work highlights the ability of nanoplasmics to monitor in situ the growth kinetics of thin supported films. PMID:22421238

  9. Influence of size, shape and core-shell interface on surface plasmon resonance in Ag and Ag@MgO nanoparticle films deposited on Si/SiO x.

    PubMed

    D'Addato, Sergio; Pinotti, Daniele; Spadaro, Maria Chiara; Paolicelli, Guido; Grillo, Vincenzo; Valeri, Sergio; Pasquali, Luca; Bergamini, Luca; Corni, Stefano

    2015-01-01

    Ag and Ag@MgO core-shell nanoparticles (NPs) with a diameter of d = 3-10 nm were obtained by physical synthesis methods and deposited on Si with its native ultrathin oxide layer SiO x (Si/SiO x ). Scanning electron microscopy and transmission electron microscopy (TEM) images of bare Ag NPs revealed the presence of small NP aggregates caused by diffusion on the surface and agglomeration. Atomic resolution TEM gave evidence of the presence of crystalline multidomains in the NPs, which were due to aggregation and multitwinning occurring during NP growth in the nanocluster source. Co-deposition of Ag NPs and Mg atoms in an oxygen atmosphere gave rise to formation of a MgO shell matrix surrounding the Ag NPs. The behaviour of the surface plasmon resonance (SPR) excitation in surface differential reflectivity (SDR) spectra with p-polarised light was investigated for bare Ag and Ag@MgO NPs. It was shown that the presence of MgO around the Ag NPs caused a red shift of the plasmon excitation, and served to preserve its existence after prolonged (five months) exposure to air, realizing the possibility of technological applications in plasmonic devices. The Ag NP and Ag@MgO NP film features in the SDR spectra could be reproduced by classical electrodynamics simulations by treating the NP-containing layer as an effective Maxwell Garnett medium. The simulations gave results in agreement with the experiments when accounting for the experimentally observed aggregation.

  10. Accelerated CO2 transport on surface of AgO nanoparticles in ionic liquid BMIMBF4

    PubMed Central

    Ji, Dahye; Kang, Yong Soo; Kang, Sang Wook

    2015-01-01

    The AgO nanoparticles were utilized for a CO2 separation membrane. The AgO nanoparticles were successfully generated in ionic liquid 1-butyl-3-methyl imidazolium tetrafluoroborate (BMIMBF4) by favorable interaction between the surface of particles and the counteranion of BMIMBF4. The generated AgO nanoparticles were confirmed by TEM, and the average size was 20 nm. Coordinative interactions of dissociated AgO particles with BMIM+BF4− were investigated by FT-Raman spectroscopy. When the ionic liquid BMIMBF4 containing AgO nanoparticles was utilized as a CO2 separation membrane, the separation performance was largely enhanced. PMID:26549605

  11. Highly luminescent material based on Alq3:Ag nanoparticles.

    PubMed

    Salah, Numan; Habib, Sami S; Khan, Zishan H

    2013-09-01

    Tris (8-hydroxyquinoline) aluminum (Alq3) is an organic semiconductor molecule, widely used as an electron transport layer, light emitting layer in organic light-emitting diodes and a host for fluorescent and phosphorescent dyes. In this work thin films of pure and silver (Ag), cupper (Cu), terbium (Tb) doped Alq3 nanoparticles were synthesized using the physical vapor condensation method. They were fabricated on glass substrates and characterized by X-ray diffraction, scanning electron microscope (SEM), energy dispersive spectroscopy, atomic force microscope (AFM), UV-visible absorption spectra and studied for their photoluminescence (PL) properties. SEM and AFM results show spherical nanoparticles with size around 70-80 nm. These nanoparticles have almost equal sizes and a homogeneous size distribution. The maximum absorption of Alq3 nanoparticles is observed at 300 nm, while the surface plasmon resonant band of Ag doped sample appears at 450 nm. The PL emission spectra of Tb, Cu and Ag doped Alq3 nanoparticles show a single broad band at around 515 nm, which is similar to that of the pure one, but with enhanced PL intensity. The sample doped with Ag at a concentration ratio of Alq3:Ag = 1:0.8 is found to have the highest PL intensity, which is around 2 times stronger than that of the pure one. This enhancement could be attributed to the surface plasmon resonance of Ag ions that might have increased the absorption and then the quantum yield. These remarkable result suggest that Alq3 nanoparticles incorporated with Ag ions might be quite useful for future nano-optoelectronic devices. PMID:23653126

  12. Noble-metal Ag nanoparticle chains: annealing Ag/Bi superlattice nanowires in vacuum

    NASA Astrophysics Data System (ADS)

    Xu, Shao Hui; Fei, Guang Tao; You, Qiao; Gao, Xu Dong; Huo, Peng Cheng; De Zhang, Li

    2016-09-01

    One-dimensional noble-metal Ag nanoparticle chains have been prepared by electrodepositing Ag/Bi superlattice nanowires in a porous anodic alumina oxide (AAO) template and following an annealing process in vacuum. It is found that Bi, as a sacrificial metal, can be removed completely after annealing at 450 °C with a vacuum degree of 10-5 Torr. The regulation of particle size, shape and interparticle spacing of Ag NP chains has been realized by adjusting the segment length of the Ag/Bi superlattice nanowires and the annealing condition. With an extension of the annealing time, it is observed that Ag particles display the transform trend from ellipsoid to sphere. Our findings could inspire further investigation on the design and fabrication of metal nanoparticle chains.

  13. Noble-metal Ag nanoparticle chains: annealing Ag/Bi superlattice nanowires in vacuum

    NASA Astrophysics Data System (ADS)

    Xu, Shao Hui; Fei, Guang Tao; You, Qiao; Gao, Xu Dong; Huo, Peng Cheng; De Zhang, Li

    2016-09-01

    One-dimensional noble-metal Ag nanoparticle chains have been prepared by electrodepositing Ag/Bi superlattice nanowires in a porous anodic alumina oxide (AAO) template and following an annealing process in vacuum. It is found that Bi, as a sacrificial metal, can be removed completely after annealing at 450 °C with a vacuum degree of 10‑5 Torr. The regulation of particle size, shape and interparticle spacing of Ag NP chains has been realized by adjusting the segment length of the Ag/Bi superlattice nanowires and the annealing condition. With an extension of the annealing time, it is observed that Ag particles display the transform trend from ellipsoid to sphere. Our findings could inspire further investigation on the design and fabrication of metal nanoparticle chains.

  14. Noble-metal Ag nanoparticle chains: annealing Ag/Bi superlattice nanowires in vacuum.

    PubMed

    Xu, Shao Hui; Fei, Guang Tao; You, Qiao; Gao, Xu Dong; Huo, Peng Cheng; De Zhang, Li

    2016-09-16

    One-dimensional noble-metal Ag nanoparticle chains have been prepared by electrodepositing Ag/Bi superlattice nanowires in a porous anodic alumina oxide (AAO) template and following an annealing process in vacuum. It is found that Bi, as a sacrificial metal, can be removed completely after annealing at 450 °C with a vacuum degree of 10(-5) Torr. The regulation of particle size, shape and interparticle spacing of Ag NP chains has been realized by adjusting the segment length of the Ag/Bi superlattice nanowires and the annealing condition. With an extension of the annealing time, it is observed that Ag particles display the transform trend from ellipsoid to sphere. Our findings could inspire further investigation on the design and fabrication of metal nanoparticle chains.

  15. Noble-metal Ag nanoparticle chains: annealing Ag/Bi superlattice nanowires in vacuum.

    PubMed

    Xu, Shao Hui; Fei, Guang Tao; You, Qiao; Gao, Xu Dong; Huo, Peng Cheng; De Zhang, Li

    2016-09-16

    One-dimensional noble-metal Ag nanoparticle chains have been prepared by electrodepositing Ag/Bi superlattice nanowires in a porous anodic alumina oxide (AAO) template and following an annealing process in vacuum. It is found that Bi, as a sacrificial metal, can be removed completely after annealing at 450 °C with a vacuum degree of 10(-5) Torr. The regulation of particle size, shape and interparticle spacing of Ag NP chains has been realized by adjusting the segment length of the Ag/Bi superlattice nanowires and the annealing condition. With an extension of the annealing time, it is observed that Ag particles display the transform trend from ellipsoid to sphere. Our findings could inspire further investigation on the design and fabrication of metal nanoparticle chains. PMID:27487089

  16. Biosynthesis of Au, Ag and Au-Ag nanoparticles using edible mushroom extract

    NASA Astrophysics Data System (ADS)

    Philip, Daizy

    2009-07-01

    Integration of green chemistry principles to nanotechnology is one of the key issues in nanoscience research. There is growing need to develop environmentally benign metal nanoparticle synthesis process that do not use toxic chemicals in the synthesis protocols to avoid adverse effects in medical applications. Here, it is a report on extracellular synthesis method for the preparation of Au, Ag and Au-Ag nanoparticles in water, using the extract of Volvariella volvacea, a naturally occurring edible mushroom, as reducing and protecting agents. Gold nanoparticles of different sizes (20-150 nm) and shapes from triangular nanoprisms to nearly spherical and hexagonal are obtained by this novel method. The size and shape of gold nanoparticles are also found to depend on temperature of the extract. The silver nanoparticles are spherical with size ˜15 nm. There is increased productivity of nanoparticles as shown by sharp and intense surface plasmon resonance bands for the nanoparticles prepared using an excess of the extract. The Au-Ag nanoparticles prepared by co-reduction has only one plasmon band due to alloying of the constituents. All the synthesized nanoparticles are found to be photoluminescent and are highly crystalline as shown by SAED and XRD patterns with fcc phase oriented along the (1 1 1) plane. FTIR measurements were carried out to identify the possible biomolecules responsible for capping and efficient stabilization of the nanoparticles. It is found that Au nanoparticles are bound to proteins through free amino groups and silver nanoparticles through the carboxylate group of the amino acid residues. The position and intensity of the emission band is found to depend on composition of the nanoparticles indicating the possible use in therapeutic applications.

  17. Functionalization of Ag nanoparticles using local hydrophilic pool segment designed on their particle surface

    NASA Astrophysics Data System (ADS)

    Iijima, Motoyuki; Kurumiya, Aki; Esashi, Junki; Miyazaki, Hayato; Kamiya, Hidehiro

    2014-10-01

    The preparation of SiO2-coated Ag nanoparticles dispersible in various organic solvents has been achieved using a solgel reaction of tetraethylorthosilicate (TEOS), in the localized hydrophilic pool segments designed on Ag nanoparticle surfaces. First, oleylamine-capped core Ag nanoparticles were synthesized, followed by ligand exchange with polyethyleneimine (PEI) and further adsorption of an anionic surfactant comprising hydrophilic polyethylene glycol (PEG) chains and hydrophobic alkyl chains, which has previously been reported to improve the stability of nanoparticles in various solvents. Then, a reaction of TEOS with the localized hydrophilic PEI layer on the Ag nanoparticles' surface was conducted by stirring a toluene/TEOS solution of surface-modified Ag nanoparticles at various temperatures. It was found that a SiO2 layer was successfully formed on Ag nanoparticles when the reaction temperature was increased to 60 °C. It was also found, however, that at this elevated temperature, the primary particle size of Ag nanoparticles increased to several tens of nm, attributable to the dissolution and re-reduction of Ag+. Because the surface modifier, PEI and anionic surfactant all remained on the nanoparticle surface during the SiO2 coating process, the prepared SiO2-coated Ag nanoparticles were found to be dispersible in various organic solvents near to their primary particle size.

  18. Phytotoxicity of Ag nanoparticles prepared by biogenic and chemical methods

    NASA Astrophysics Data System (ADS)

    Choudhury, Rupasree; Majumder, Manna; Roy, Dijendra Nath; Basumallick, Srijita; Misra, Tarun Kumar

    2016-06-01

    Silver nanoparticles (Ag NPs) are now widely used as antibacterial and antifungal materials in different consumer products. We report here the preparation of Ag NPs by neem leaves extract ( Azadirachta) reduction and trisodium citrate-sodium borohydride reduction methods, and study of their phytotoxicity. The nanoparticles were characterized by UV-Vis spectroscopy, FTIR, and atomic force microscopy (AFM) techniques. Both neem-coated and citrate-coated Ag NPs exhibit surface plasmon around 400 nm, and their average sizes measured by AFM are about 100 and 20 nm, respectively. Antibacterial and antifungal activities of these nanomaterials have been studied by simple pea seed germination and disk diffusion methods. It has been observed from the growth of root and shoot, citrate-coated Ag NPs significantly affect seedling growth, but neem-coated Ag NPs exhibit somehow mild toxicity toward germination process due to the nutrient supplements from neem. On the other hand, antifungal activity of neem-coated Ag NPs has been found much higher than that of citrate-coated Ag NPs due to the combined effects of antifungal activity of neem and Ag NPs. Present research primarily indicates a possible application of neem-coated Ag NPs as a potential fungicide.

  19. Preparation of conducting silver paste with Ag nanoparticles prepared by e-beam irradiation

    NASA Astrophysics Data System (ADS)

    Sohn, Jong Hwa; Pham, Long Quoc; Kang, Hyun Suk; Park, Ji Hyun; Lee, Byung Cheol; Kang, Young Soo

    2010-11-01

    Conducting silver paste was prepared by using Ag nanoparticles which were synthesized by e-beam irradiation method (from KAERI); its conductivity was comparatively determined with Ag nanoparticles which were prepared by thermolysis method (commercial). The silver nanoparticles with the diameter of approximately 150 nm size prepared by e-beam irradiation were mixed with glass frit and sintered for 1 h at 500 °C. It is presumably concluded that the wt% of silver nanoparticle, size distribution and homogenous dispersibility of Ag nanoparticles in the pastes are the critical factors for the high conductivity of the paste. Among the various wt% of silver nanoparticle in the conducting silver pastes, silver paste with 90 wt% of silver nanoparticle has the highest conductivity as 1.6×10 4 S cm -1. This conductivity value is 1.6 times higher than the Ag pastes which were prepared with silver nanoparticles obtained by thermolysis method.

  20. Synthesis of Cu core Ag shell nanoparticles using chemical reduction method

    NASA Astrophysics Data System (ADS)

    Chinh Trinh, Dung; Dung Dang, Thi My; Khanh Huynh, Kim; Fribourg-Blanc, Eric; Chien Dang, Mau

    2015-01-01

    A simple chemical reduction method is used to prepare colloidal bimetallic Cu-Ag core-shell (Cu@Ag) nanoparticles. Polyvinyl pyrrolidone (PVP) was used as capping agent, and ascorbic acid (C6H8O6) and sodium borohydride (NaBH4) were used as reducing agents. The obtained Cu@Ag nanoparticles were characterized by powder x-ray diffraction (XRD), transmission electron microscopy (TEM) and UV-vis spectrophotometry. The influence of [Ag]/[Cu] molar ratios on the formation of Ag coatings on the Cu particles was investigated. From the TEM results we found that the ratio [Ag+]/[Cu2+] = 0.2 is the best for the stability of Cu@Ag nanoparticles with an average size of 22 nm. It is also found out that adding ammonium hydroxide (NH4OH) makes the obtained Cu@Ag nanoparticles more stable over time when pure deionized water is used as solvent.

  1. Silver nanoparticles: correlating nanoparticle size and cellular uptake with genotoxicity

    PubMed Central

    Butler, Kimberly S.; Peeler, David J.; Casey, Brendan J.; Dair, Benita J.; Elespuru, Rosalie K.

    2015-01-01

    The focus of this research was to develop a better understanding of the pertinent physico-chemical properties of silver nanoparticles (AgNPs) that affect genotoxicity, specifically how cellular uptake influences a genotoxic cell response. The genotoxicity of AgNPs was assessed for three potential mechanisms: mutagenicity, clastogenicity and DNA strand-break-based DNA damage. Mutagenicity (reverse mutation assay) was assessed in five bacterial strains of Salmonella typhimurium and Echerichia coli, including TA102 that is sensitive to oxidative DNA damage. AgNPs of all sizes tested (10, 20, 50 and 100nm), along with silver nitrate (AgNO3), were negative for mutagenicity in bacteria. No AgNPs could be identified within the bacteria cells using transmission electron microscopy (TEM), indicating these bacteria lack the ability to actively uptake AgNPs 10nm or larger. Clastogenicity (flow cytometry-based micronucleus assay) and intermediate DNA damage (DNA strand breaks as measured in the Comet assay) were assessed in two mammalian white blood cell lines: Jurkat Clone E6-1 and THP-1. It was observed that micronucleus and Comet assay end points were inversely correlated with AgNP size, with smaller NPs inducing a more genotoxic response. TEM results indicated that AgNPs were confined within intracellular vesicles of mammalian cells and did not penetrate the nucleus. The genotoxicity test results and the effect of AgNO3 controls suggest that silver ions may be the primary, and perhaps only, cause of genotoxicity. Furthermore, since AgNO3 was not mutagenic in the gram-negative bacterial Ames strains tested, the lack of bacterial uptake of the AgNPs may not be the major reason for the lack of genotoxicity observed. PMID:25964273

  2. Photocurrent enhancements of organic solar cells by altering dewetting of plasmonic Ag nanoparticles

    PubMed Central

    Fleetham, Tyler; Choi, Jea-Young; Choi, Hyung Woo; Alford, Terry; Jeong, Doo Seok; Lee, Taek Sung; Lee, Wook Seong; Lee, Kyeong-Seok; Li, Jian; Kim, Inho

    2015-01-01

    Incorporation of metal nanoparticles into active layers of organic solar cells is one of the promising light trapping approaches. The size of metal nanoparticles is one of key factors to strong light trapping, and the size of thermally evaporated metal nanoparticles can be tuned by either post heat treatment or surface modification of substrates. We deposited Ag nanoparticles on ITO by varying nominal thicknesses, and post annealing was carried out to increase their size in radius. PEDOT:PSS was employed onto the ITO substrates as a buffer layer to alter the dewetting behavior of Ag nanoparticles. The size of Ag nanoparticles on PEDOT:PSS were dramatically increased by more than three times compared to those on the ITO substrates. Organic solar cells were fabricated on the ITO and PEDOT:PSS coated ITO substrates with incorporation of those Ag nanoparticles, and their performances were compared. The photocurrents of the cells with the active layers on PEDOT:PSS with an optimal choice of the Ag nanoparticles were greatly enhanced whereas the Ag nanoparticles on the ITO substrates did not lead to the photocurrent enhancements. The origin of the photocurrent enhancements with introducing the Ag nanoparticles on PEDOT:PSS are discussed. PMID:26388104

  3. Size-controlled dissolution of silver nanoparticles at neutral and acidic pH conditions: kinetics and size changes.

    PubMed

    Peretyazhko, Tanya S; Zhang, Qingbo; Colvin, Vicki L

    2014-10-21

    Silver nanoparticles (Ag(NP)) are widely utilized in increasing number of medical and consumer products due to their antibacterial properties. Once released to aquatic system, Ag(NP) undergoes oxidative dissolution leading to production of toxic Ag(+). Dissolved Ag(+) can have a severe impact on various organisms, including indigenous microbial communities, fungi, alga, plants, vertebrates, invertebrates, and human cells. Therefore, it is important to investigate fate of Ag(NP) and determine physico-chemicals parameters that control Ag(NP) behavior in the natural environment. Nanoparticle size might have a dominant effect on Ag(NP) dissolution in natural waters. In this work, we investigated size-dependent dissolution of AgNP exposed to ultrapure deionized water (pH ≈ 7) and acetic acid (pH 3) and determined changes in nanoparticle size after dissolution. Silver nanoparticles stabilized by thiol functionalized methoxyl polyethylene glycol (PEGSH) of 6 nm (Ag(NP_)6), 9 nm (Ag(NP_)9), 13 nm (Ag(NP_)13), and 70 nm (Ag(NP_)70) were prepared. The results of dissolution experiments showed that the extent of AgNP dissolution in acetic acid was larger than in water. Solubility of Ag(NP) increased with the size decrease and followed the order Ag(NP_)6 > Ag(NP_)9 > Ag(NP_)13 > Ag(NP_)70 in both water and acetic acid. Transmission electron microscopy (TEM) was applied to characterize changes in size and morphology of the AgNP after dissolution in water. Analysis of Ag(NP) by TEM revealed that the particle morphology did not change during dissolution. The particles remained approximately spherical in shape, and no visible aggregation was observed in the samples. TEM analysis also demonstrated that Ag(NP_)6, Ag(NP_)9, and Ag(NP_)13 increased in size after dissolution likely due to Ostwald ripening. PMID:25265014

  4. Application of a new coordination compound for the preparation of AgI nanoparticles

    SciTech Connect

    Mohandes, Fatemeh; Salavati-Niasari, Masoud

    2013-10-15

    Graphical abstract: Silver iodide nanoparticles have been sonochemically synthesized by using silver salicylate complex, [Ag(HSal)], as silver precursor. A series of control experiments were carried out to investigate the effects of solvent, surfactant concentration, sonication time and temperature on the morphology of AgI nanostructures. - Highlights: • Silver salicylate as a new precursor was applied to fabricate γ-AgI nanoparticles. • To further decrease the particle size of AgI, SDS was used as surfactant. • The effect of preparation parameters on the particle size of AgI was investigated. - Abstract: AgI nanoparticles have been sonochemically synthesized by using silver salicylate, [Ag(HSal)], as silver precursor. To investigate the effects of solvent, surfactant concentration, sonication time and temperature on the morphology of AgI nanostructures, several experiments were carried out. The products were characterized by SEM, TEM, XRD, TGA/DTA, UV–vis, and FT-IR. Based on the experimental findings in this research, it was found that the size of AgI nanoparticles was dramatically dependent on the silver precursor, sonochemical irradiation, and surfactant concentration. Sodium dodecyl sulfate (SDS) was applied as surfactant. When the concentration of SDS was 0.055 mM, very uniform sphere-like AgI nanoparticles with grain size of about 25–30 nm were obtained. These results indicated that the high concentration of SDS could prevent the aggregation between colloidal nanoparticles due to its steric hindrance effect.

  5. Transport of silver nanoparticles (AgNPs) in soil.

    PubMed

    Sagee, Omer; Dror, Ishai; Berkowitz, Brian

    2012-07-01

    The effect of soil properties on the transport of silver nanoparticles (AgNPs) was studied in a set of laboratory column experiments, using different combinations of size fractions of a Mediterranean sandy clay soil. The AgNPs with average size of ~30nm yielded a stable suspension in water with zeta potential of -39mV. Early breakthrough of AgNPs in soil was observed in column transport experiments. AgNPs were found to have high mobility in soil with outlet relative concentrations ranging from 30% to 70%, depending on experimental conditions. AgNP mobility through the column decreased when the fraction of smaller soil aggregates was larger. The early breakthrough pattern was not observed for AgNPs in pure quartz columns nor for bromide tracer in soil columns, suggesting that early breakthrough is related to the nature of AgNP transport in natural soils. Micro-CT and image analysis used to investigate structural features of the soil, suggest that soil aggregate size strongly affects AgNP transport in natural soil. The retention of AgNPs in the soil column was reduced when humic acid was added to the leaching solution, while a lower flow rate (Darcy velocity of 0.17cm/min versus 0.66cm/min) resulted in higher retention of AgNPs in the soil. When soil residual chloride was exchanged by nitrate prior to column experiments, significantly improved mobility of AgNPs was observed in the soil column. These findings point to the importance of AgNP-soil chemical interactions as a retention mechanism, and demonstrate the need to employ natural soils rather than glass beads or quartz in representative experimental investigations.

  6. Photocurrent enhancement of chemically synthesized Ag nanoparticle-embedded BiFeO3 thin films

    NASA Astrophysics Data System (ADS)

    Maruyama, Rika; Sakamoto, Wataru; Yuitoo, Isamu; Takeuchi, Teruaki; Hayashi, Koichiro; Yogo, Toshinobu

    2016-10-01

    BiFeO3 and Ag nanoparticle-embedded BiFeO3 thin films were prepared on Pt/TiO x /SiO2/Si and MgO(100) substrates using colloidal silver and BiFeO3 metal-organic precursor solutions. Colloidal silver solution was prepared by a chemical reductive method using NaBH4 as a reductant. The prepared Ag nanoparticles exhibited characteristic optical absorption properties based on their surface plasmon resonance related to particle size. The synthesized BiFeO3 and Ag nanoparticle/BiFeO3 thin films demonstrated rapid on/off responses of photocurrent to visible light. The Ag nanoparticle-incorporated BiFeO3 film exhibited a 2-4-fold higher photocurrent than the BiFeO3 film. Optical and ferroelectric properties did not change markedly even when Ag nanoparticles were embedded in the BiFeO3 thin film within the quantities of this study. Furthermore, in the Ag nanoparticle/BiFeO3 composite structure, Ag nanoparticles were introduced in the near-metallic state with maintained their nanometer size. In the Ag nanoparticle-embedded BiFeO3 film, photoinduced charge separation and transport of photoexcited carriers were enhanced by the surface plasmon effect of nanosized Ag particles as well as the internal bias electric field existed in the narrow-bandgap BiFeO3 thin film.

  7. Highly quasi-monodisperse ag nanoparticles on titania nanotubes by impregnative aqueous ion exchange.

    PubMed

    Toledo-Antonio, J A; Cortes-Jácome, M A; Angeles-Chavez, C; López-Salinas, E; Quintana, P

    2009-09-01

    Silver nanoparticles were homogenously dispersed on titania nanotubes (NT), which were prepared by alkali hydrothermal methodology and dried at 373 K. Ag(+) incorporation was done by impregnative ion exchange of aqueous silver nitrate onto NT. First, Ag(+) ions incorporate into the layers of nanotube walls, and then, upon heat treatment under N(2) at 573 and 673 K, they migrate and change into Ag(2)O and Ag(0) nanoparticles, respectively. In both cases, Ag nanoparticles are highly dispersed, decorating the nanotubes in a polka-dot pattern. The Ag particle size distribution is very narrow, being ca. 4 +/- 2 nm without any observable agglomeration. The reduction of Ag(2)O into Ag(0) octahedral nanoparticles occurs spontaneously and topotactically when annealing, without the aid of any reducing agent. The population of Ag(0) nanoparticles can be controlled by adjusting the annealing temperature. An electron charge transfer from NT support to Ag(0) nanoparticles, because of a strong interaction, is responsible for considerable visible light absorption in Ag(0) nanoparticles supported on NT.

  8. Transport of engineered silver (Ag) nanoparticles through partially fractured sandstones.

    PubMed

    Neukum, Christoph; Braun, Anika; Azzam, Rafig

    2014-08-01

    Transport behavior and fate of engineered silver nanoparticles (AgNP) in the subsurface is of major interest concerning soil and groundwater protection in order to avoid groundwater contamination of vital resources. Sandstone aquifers are important groundwater resources which are frequently used for public water supply in many regions of the world. The objective of this study is to get a better understanding of AgNP transport behavior in partially fractured sandstones. We executed AgNP transport studies on partially fissured sandstone drilling cores in laboratory experiments. The AgNP concentration and AgNP size in the effluent were analyzed using flow field-flow fractionation mainly. We employed inverse mathematical models on the measured AgNP breakthrough curves to identify and quantify relevant transport processes. Physicochemical filtration, time-dependent blocking due to filling of favorable attachment sites and colloid-facilitated transport were identified as the major processes for AgNP mobility. Physicochemical filtration was found to depend on solute chemistry, mineralogy, pore size distribution and probably on physical and chemical heterogeneity. Compared to AgNP transport in undisturbed sandstone matrix reported in the literature, their mobility in partially fissured sandstone is enhanced probably due to larger void spaces and higher hydraulic conductivity.

  9. Size distributions of chemically synthesized Ag nanocrystals

    NASA Astrophysics Data System (ADS)

    Thøgersen, Annett; Bonsak, Jack; Fosli, Carl Huseby; Muntingh, Georg

    2011-08-01

    Silver nanocrystals made by a chemical reduction of silver salts (AgNO3) by sodium borohydride (NaBH4) were studied using transmission electron microscopy and light scattering simulations. For various AgNO3/NaBH4 molar ratios, the size distributions of the nanocrystals were found to be approximately log-normal. In addition, a linear relation was found between the mean nanocrystal size and the molar ratio. In order to relate the size distribution of Ag nanocrystals of the various molar ratios to the scattering properties of Ag nanocrystals in solar cell devices, light scattering simulations of Ag nanocrystals in Si, SiO2, SiN, and Al2O3 matrices were carried out using MiePlot. These light scattering spectra for the individual nanocrystal sizes were combined into light scattering spectra for the fitted size distributions. The evolution of these scattering spectra with respect to an increasing mean nanocrystal size was then studied. From these findings, it is possible to find the molar ratio for which the corresponding nanocrystal size distribution has maximum scattering at a particular wavelength in the desired matrix.

  10. Morphological and electrochemical characterization of electrodeposited Zn–Ag nanoparticle composite coatings

    SciTech Connect

    Punith Kumar, M.K.; Srivastava, Chandan

    2013-11-15

    Silver nanoparticles with an average size of 23 nm were chemically synthesized and used to fabricate Zn–Ag composite coatings. The Zn–Ag composite coatings were generated by electrodeposition method using a simple sulfate plating bath dispersed with 0.5, 1 and 1.5 g/l of Ag nanoparticles. Scanning electron microscopy, X-ray diffraction and texture co-efficient calculations revealed that Ag nanoparticles appreciably influenced the morphology, micro-structure and texture of the deposit. It was also noticed that agglomerates of Ag nanoparticles, in the case of high bath load conditions, produced defects and dislocations on the deposit surface. Ag nanoparticles altered the corrosion resistance property of Zn–Ag composite coatings as observed from Tafel polarization, electrochemical impedance analysis and an immersion test. Reduction in corrosion rate with increased charge transfer resistance was observed for Zn–Ag composite coatings when compared to a pure Zn coating. However, the particle concentration in the plating bath and their agglomeration state directly influenced the surface morphology and the subsequent corrosion behavior of the deposits. - Highlights: • Synthesis of Ag nanoparticles with an average size of 23 nm • Fabrication of Zn/nano Ag composite coating on mild steel • Composite coatings showed better corrosion resistance. • Optimization of particle concentration is necessary.

  11. Annealing behaviour of c-SiO 2 implanted layer distributed with high density Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Liu, Zhengxin; Wang, Honghong

    1997-01-01

    High volume density Ag nanoparticles embedded in c-SiO 2 matrix have been prepared by Ag ion implantation at an energy of 200 keV and a current density of about 20 μA/cm 2 to a nominal dose of 6.7 × 10 16ions/cm 2 at RT. Bright-field transmission electron microscopy (TEM) image indicates that Ag nanoparticles show two groups of sizes: the larger diameter is about 25 nm and the smaller is less than 10 nm. RBS spectra show that the distribution of implanted Ag atoms is bimodal which is associated with the two groups of nanoparticles above. Thermal stability of the implanted layer which consists of Ag nanoparticles, dissolved Ag atoms and c-SiO 2 matrix has been investigated by RBS, TEM and Raman spectroscopy. RBS spectra prove that little migration of Ag atoms is found and Ag nanoparticles are considerably stable at 300°C annealing. Though the obvious change in the distribution of Ag is observed at 400°C annealing in RBS spectra, TEM image identifies that both the larger and the smaller Ag nanoparticles still exist at relatively stable state. Following 750°C annealing, Ag atoms drastically move, and furthermore, the bimodal character of the distribution disappears. On the other hand, the amorphized SiO 2 implanted layer recrystal after 300°C, 400°C annealing.

  12. Synthesis and Characterization of BSA Conjugated Silver Nanoparticles (Ag/BSA Nanoparticles) and Evaluation of Biological Properties of Ag/BSA Nanoparticles and Ag/BSA Nanoparticles Loaded Poly(hydroxy butyrate valerate) PHBV Films

    NASA Astrophysics Data System (ADS)

    Ambaye, Almaz

    Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa are the etiological agents of several infectious diseases. Antibiotic resistance by these three microbes has emerged as a prevalent problem due in part to the misuse of existing antibiotics and the lack of novel antibiotics. Nanoparticles have emerged as an alternative antibacterial agents to conventional antibiotics owing to their high surface area to volume ratio and their unique chemical and physical properties. Among the nanoparticles, silver nanoparticles have gained increasing attention because silver nanoparticles exhibit antibacterial activity against a range of gram positive and gram negative bacteria. Nanoparticles of well-defined chemistry and morphology can be used in broad biomedical applications, especially in bone tissue engineering applications, where bone infection by bacteria can be acute and lethal. It is commonly noted in the literature that the activity of nanoparticles against microorganisms is dependent upon the size and concentration of the nanoparticles as well as the chemistry of stabilizing agent. To the best of our knowledge, a comprehensive study that evaluates the antibacterial activity of well characterized silver nanoparticles in particular Bovine Serum Albumin (BSA) stabilized against S. aureus and E. coli and cytotoxicity level of BSA stabilized silver nanoparticles towards osteoblast cells (MC3T3-E1) is currently lacking. Therefore, the primary objective of this study was to characterize protein conjugated silver nanoparticles prepared by chemical reduction of AgNO3 and BSA mixture. The formation of Ag/BSA nanoparticles was studied by UV-Vis spectroscopy. The molar ratio of silver to BSA in the Ag/BSA nanoparticles was established to be 27+/- 3: 1, based on Thermogravimetric Analysis and Atomic Absorption Spectroscopy. Based on atomic force microscopy, dynamic light scattering,and transmission electron microscopy(TEM) measurements, the particle size (diameter) of

  13. High Resolution PDF Measurements on Ag Nanoparticles

    SciTech Connect

    Rocha, Tulio C. R.; Martin, Chris; Kycia, Stefan; Zanchet, Daniela

    2009-01-29

    The quantitative analysis of structural defects in Ag nanoparticles was addressed in this work. We performed atomic scale structural characterization by a combination of x-ray diffraction (XRD) using the Pair Distribution Function analysis (PDF) and High Resolution Transmission Electron Microscopy (HRTEM). The XRD measurements were performed using an innovative instrumentation setup to provide high resolution PDF patterns.

  14. Preparation of highly dispersed core/shell-type titania nanocapsules containing a single Ag nanoparticle.

    PubMed

    Sakai, Hideki; Kanda, Takashi; Shibata, Hirobumi; Ohkubo, Takahiro; Abe, Masahiko

    2006-04-19

    Core/shell-type titania nanocapsules containing a single Ag nanoparticle were prepared. Ag nanoparticles were prepared using the reduction of silver nitrate with hydrazine in the presence of cetyltrimethylammonium bromide (CTAB) as protective agent. The sol-gel reaction of titanium tetraisopropoxide (TTIP) was used to prepare core/shell-type titania nanocapsules with CTAB-coated Ag nanoparticles as the core. TEM observations revealed that the size of the core (Ag particle) and the thickness of the shell (titania) of the core/shell particles obtained are about 10 nm and 5-10 nm, respectively. In addition, the nanocapsules were found to be dispersed in the medium as individual particles without aggregation. Moreover, titania coating caused the surface plasmon absorption of Ag nanoparticles to shift toward the longer wavelength side. PMID:16608315

  15. A simple way to prepare Cupric oleate capped AgI nanoparticles

    SciTech Connect

    Song Meirong; Zhang Zhijun . E-mail: s234soow@henu.edu.cn

    2004-12-02

    Cupric oleate capped AgI (Cu(OA){sub 2}-AgI) nanoparticles were prepared by a simple method and they have good dispersibility in organic solvents. X-ray diffraction (XRD), transmission electron microscope (TEM), FTIR, X-ray photoelectron spectrometer (XPS) and ultraviolet-visible (UV-vis) spectrometer were used to characterize the Cu(OA){sub 2}-AgI nanoparticles. The results show that the mean size is about 80 nm; the modified reagent has been chemically bonded on the surface of AgI. In addition, new absorption peaks in the UV region appear.

  16. Thermal Behavior of Ag Micro/Nano Wires Formed by Low-Temperature Sintering of Ag Nanoparticles

    NASA Astrophysics Data System (ADS)

    Wang, Wen; Zhong, Yinghui; Li, Dongxue; Wang, Pan; Cai, Yuwei; Duan, Zhiyong

    2015-12-01

    Ag nanoparticles of 30 nm size were deposited onto a Si substrate to form Ag microwires. The nanoparticles were transformed into continuous Ag wires with low-temperature heat treatment at temperatures not higher than 200°C. The morphology, electrical properties, and interface of the sintered Ag nanoparticle wires are described. It is shown that the neck between the nanoparticles begins to form at 150°C, and obvious metallization was found at 170°C. The changes of the crystal structure of the Ag wires at different sintering temperatures were analyzed by x-ray diffractometry. The grain boundary resistance decreased as the crystal grain size increased above 130 nm. The corresponding resistivity of the microstructure is close to that of the bulk. Through the comparison between the Mayadas-Shatzkes's model and experimental data, the range of the grain boundary reflection coefficient C at different temperatures is obtained. This research lays the foundation for the study of nanoimprint lithography with a pseudoplastic metal nanoparticle fluid.

  17. M4Ag44(p-MBA)30 Molecular Nanoparticles

    NASA Astrophysics Data System (ADS)

    Conn, Brian E.

    In recent years, molecular nanoparticles have attracted much attention due to their unique physical, optical, and electronic properties. The properties of molecular nanoparticles are shown to deviate from their larger bulk counterparts, due to quantum confinement effects and large surface-to-volume ratios. As the size of the nanoparticle shrinks to a cluster of metal atoms (<3 nm in diameter), there is an emergence of a HOMO-LUMO band gap, which is not present in transitional d-block metals. The HOMO-LUMO band gap gives rise to discrete electronic states, leading to new chemical and physical properties. Molecular nanoparticles have had a substantial impact across a diverse range of fields, including catalysis, sensing, photochemistry, optoelectronic, energy conversion, and medicine. Currently many of the synthetic procedures for molecular nanoparticles require low temperatures, long incubation times, multistep purification and hazardous reagents that produce low yields and polydisperse molecular nanoparticles with poor stability. Although silver has very desirable physical properties, good relative abundance and low cost, gold molecular nanoparticles have been widely favored owing to their proved stability and ease of use. Unlike gold, silver is notorious for its susceptibility to oxidation, i.e., tarnishing, which has limited the development of silver-based nanotechnologies. Despite two decades of synthetic efforts, silver molecular nanoparticles that are inert or have long-term stability have remained unrealized. Herein we report a simple synthetic protocol for producing ultrastable M4Ag44(p-MBA)30 nanoparticles as a single-sized molecular product and in exceptionally large quantities. The stability, purity, and yield are substantially better than other metal nanoparticles, including gold, due to several stabilization mechanisms. Also, reported are the structural and mechanical properties of extended crystalline solids of Na4Ag44(p-MBA)30 from large-scale quantum

  18. Aging Induced Ag Nanoparticle Rearrangement under Ambient Atmosphere and Consequences for Nanoparticle-Enhanced DNA Biosensing

    PubMed Central

    Peng, Hsin-I; Krauss, Todd D.; Miller, Benjamin L.

    2010-01-01

    Localized surface plasmons of metallic nanoparticles can strongly amplify the magnitude of the surrounding electric field. This in turn enhances fluorescence from nearby fluorophores. However, little is known regarding how time-dependent changes in nanoparticle structure due to exposure to the ambient environment affect their behavior in plasmonic devices. Here, we report the interesting finding that the aging of a nanostructured Ag substrate in ambient atmosphere markedly improves the fluorescence signal of a plasmonic-based DNA detection system. The effect can be observed with an exposure time as short as two days, and a nearly 17-fold signal enhancement can be achieved with 30 days of aging. Analysis of substrate surface topography by atomic force microscopy (AFM) reveals a substantial change in nanoparticle morphology as the substrates age despite being covalently attached to a solid dry substrate. Nanoparticle morphological changes also manifest in extinction spectra. This process can be further accelerated by light. Together, our findings address the important question of Ag nanoparticle stability over time and its potential ramifications for plasmon-enabled sensors. They also imply that nanoparticle aging may be used strategically to tune nanoparticle size and geometry and plasmon spectrum, which may be beneficial for studies on plasmonics as well as sensor optimization. PMID:20857925

  19. Subsurface synthesis and characterization of Ag nanoparticles embedded in MgO.

    PubMed

    Vilayurganapathy, S; Devaraj, A; Colby, R; Pandey, A; Varga, T; Shutthanandan, V; Manandhar, S; El-Khoury, P Z; Kayani, Asghar; Hess, W P; Thevuthasan, S

    2013-03-01

    Metal nanoparticles exhibit a localized surface plasmon resonance (LSPR) which is very sensitive to the size and shape of the nanoparticle and the surrounding dielectric medium. The coupling between the electromagnetic radiation and the localized surface plasmon in metallic nanoparticles results in a sizable enhancement of the incident fields, making them possible candidates for plasmonic applications. In particular, partially exposed metallic nanoparticles distributed in a dielectric matrix can provide prime locations for LSPR spectroscopy and sensing. We report the synthesis and characterization of a plasmonic substrate consisting of Ag nanoparticles partially buried in MgO. Ag nanoparticles of different shapes and size distributions were synthesized below the surface of MgO by implanting 200 keV Ag(+) ions followed by annealing at 1000 °C for 10 and 30 h. A detailed optical and structural characterization was carried out to understand the evolution of the Ag nanoparticle and size distribution inside the MgO matrix. Micro x-ray diffraction (Micro-XRD) was employed to investigate the structural properties and estimate the crystallite size. The nanoparticles evolved from a spherical to a faceted morphology with annealing time, assuming an octahedral shape truncated at the (001) planes, as visualized from aberration-corrected transmission electron microscopy (TEM) images. The nanoparticles embedded in MgO were shown to be pure metallic Ag using atom probe tomography (APT). The nanoparticles were partially exposed to the surface by employing plasma etch techniques to remove the overlaying MgO. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were employed to study the surface morphology and obtain a height distribution for the partially exposed nanoparticles. PMID:23403363

  20. Subsurface synthesis and characterization of Ag nanoparticles embedded in MgO

    NASA Astrophysics Data System (ADS)

    Vilayurganapathy, S.; Devaraj, A.; Colby, R.; Pandey, A.; Varga, T.; Shutthanandan, V.; Manandhar, S.; El-Khoury, P. Z.; Kayani, Asghar; Hess, W. P.; Thevuthasan, S.

    2013-03-01

    Metal nanoparticles exhibit a localized surface plasmon resonance (LSPR) which is very sensitive to the size and shape of the nanoparticle and the surrounding dielectric medium. The coupling between the electromagnetic radiation and the localized surface plasmon in metallic nanoparticles results in a sizable enhancement of the incident fields, making them possible candidates for plasmonic applications. In particular, partially exposed metallic nanoparticles distributed in a dielectric matrix can provide prime locations for LSPR spectroscopy and sensing. We report the synthesis and characterization of a plasmonic substrate consisting of Ag nanoparticles partially buried in MgO. Ag nanoparticles of different shapes and size distributions were synthesized below the surface of MgO by implanting 200 keV Ag+ ions followed by annealing at 1000 °C for 10 and 30 h. A detailed optical and structural characterization was carried out to understand the evolution of the Ag nanoparticle and size distribution inside the MgO matrix. Micro x-ray diffraction (Micro-XRD) was employed to investigate the structural properties and estimate the crystallite size. The nanoparticles evolved from a spherical to a faceted morphology with annealing time, assuming an octahedral shape truncated at the (001) planes, as visualized from aberration-corrected transmission electron microscopy (TEM) images. The nanoparticles embedded in MgO were shown to be pure metallic Ag using atom probe tomography (APT). The nanoparticles were partially exposed to the surface by employing plasma etch techniques to remove the overlaying MgO. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were employed to study the surface morphology and obtain a height distribution for the partially exposed nanoparticles.

  1. Size-Controlled Dissolution of Organic-Coated Silver Nanoparticles

    SciTech Connect

    Ma, Rui; Levard, Clément; Marinakos, Stella M.; Cheng, Yingwen; Liu, Jie; Michel, F. Marc; Brown, Jr., Gordon E.; Lowry, Gregory V.

    2012-04-02

    The solubility of Ag NPs can affect their toxicity and persistence in the environment. We measured the solubility of organic-coated silver nanoparticles (Ag NPs) having particle diameters ranging from 5 to 80 nm that were synthesized using various methods, and with different organic polymer coatings including poly(vinylpyrrolidone) and gum arabic. The size and morphology of Ag NPs were characterized by transmission electron microscopy (TEM). X-ray absorption fine structure (XAFS) spectroscopy and synchrotron-based total X-ray scattering and pair distribution function (PDF) analysis were used to determine the local structure around Ag and evaluate changes in crystal lattice parameters and structure as a function of NP size. Ag NP solubility dispersed in 1 mM NaHCO{sub 3} at pH 8 was found to be well correlated with particle size based on the distribution of measured TEM sizes as predicted by the modified Kelvin equation. Solubility of Ag NPs was not affected by the synthesis method and coating as much as by their size. Based on the modified Kelvin equation, the surface tension of Ag NPs was found to be {approx}1 J/m{sup 2}, which is expected for bulk fcc (face centered cubic) silver. Analysis of XAFS, X-ray scattering, and PDFs confirm that the lattice parameter, {alpha}, of the fcc crystal structure of Ag NPs did not change with particle size for Ag NPs as small as 6 nm, indicating the absence of lattice strain. These results are consistent with the finding that Ag NP solubility can be estimated based on TEM-derived particle size using the modified Kelvin equation for particles in the size range of 5-40 nm in diameter.

  2. Monodispersed bimetallic PdAg nanoparticles with twinned structures: Formation and enhancement for the methanol oxidation

    PubMed Central

    Yin, Zhen; Zhang, Yining; Chen, Kai; Li, Jing; Li, Wenjing; Tang, Pei; Zhao, Huabo; Zhu, Qingjun; Bao, Xinhe; Ma, Ding

    2014-01-01

    Monodispersed bimetallic PdAg nanoparticles can be fabricated through the emulsion-assisted ethylene glycol (EG) ternary system. Different compositions of bimetallic PdAg nanoparticles, Pd80Ag20, Pd65Ag35 and Pd46Ag54 can be obtained via adjusting the reaction parameters. For the formation process of the bimetallic PdAg nanoparticles, there have two-stage growth processes: firstly, nucleation and growth of the primary nanoclusters; secondly, formation of the secondary nanoparticles with the size-selection and relax process via the coalescence or aggregation of the primary nanoclusters. The as-prepared PdAg can be supported on the carbon black without any post-treatment, which exhibited high electro-oxidation activity towards methanol oxidation under alkaline media. More importantly, carbon-supported Pd80Ag20 nanoparticles reveal distinctly superior activities for the methanol oxidation, even if compared with commercial Pt/C electro-catalyst. It is concluded that the enhanced activity is dependant on the unique twinning structure with heterogeneous phase due to the dominating coalescence growth in EG ternary system. PMID:24608736

  3. Green and Tunable Decoration of Graphene with Spherical Nanoparticles Based on Laser Ablation in Water: A Case of Ag Nanoparticle/Graphene Oxide Sheet Composites.

    PubMed

    He, Hui; Wang, Haibo; Li, Kai; Zhu, Jun; Liu, Jianshuang; Meng, Xiangdong; Shen, Xiaoshuang; Zeng, Xianghua; Cai, Weiping

    2016-02-23

    A simple and green strategy is presented to decorate graphene with nanoparticles, based on laser ablation of targets in graphene auqeous solution. Ag and graphene oxide (GO) are chosen as model materials. The surface of GO sheets is strongly anchored with spherical Ag nanoparticles. The density and size of the Ag nanoparticles can be easily tuned by laser ablation conditions. Further, the GO sheets can be decorated with other nanoparticles from simple metals or semiconductors to multicomponent hybrids. Additionally, the Ag nanoparticle/GO sheet colloids can be utilized as blocks to build three-dimensional structures, such as sandwich membranes by evaporation-induced self-assembly. These graphene-based composite materials could be very useful in catalysis, sensors, and nanodevices. Particularly, the Ag nanoparticle/GO sheet sandwich composite membranes exhibit excellent surface-enhanced Raman scattering performance and possess the huge potential in trace-detecting persistent organic pollutants in the environment.

  4. Spectral investigation of nonlinear local field effects in Ag nanoparticles

    SciTech Connect

    Sato, Rodrigo Takeda, Yoshihiko; Ohnuma, Masato; Oyoshi, Keiji

    2015-03-21

    The capability of Ag nanoparticles to modulate their optical resonance condition, by optical nonlinearity, without an external feedback system was experimentally demonstrated. These optical nonlinearities were studied in the vicinity of the localized surface plasmon resonance (LSPR), using femtosecond pump-and-probe spectroscopy with a white-light continuum probe. Transient transmission changes ΔT/T exhibited strong photon energy and particle size dependence and showed a complex and non-monotonic change with increasing pump light intensity. Peak position and change of sign redshift with increasing pump light intensity demonstrate the modulation of the LSPR. These features are discussed in terms of the intrinsic feedback via local field enhancement.

  5. The characteristics of novel bimodal Ag-TiO2 nanoparticles generated by hybrid laser-ultrasonic technique

    NASA Astrophysics Data System (ADS)

    Hamad, Abubaker; Li, Lin; Liu, Zhu; Zhong, Xiang Li; Burke, Grace; Wang, Tao

    2016-04-01

    Silver-titania (Ag-TiO2) nanoparticles with smaller Ag nanoparticles attached to larger TiO2 nanoparticles were generated by hybrid ultrasonic vibration and picosecond laser ablation of Ag and Ti bulk targets in deionised water, for the first time. The laser has a wavelength of 1064 nm and a pulse duration of 10 ps. It was observed that without the ultrasonic vibration, Ag and TiO2 nanoparticles did not combine, thus the role of ultrasonic vibration is essential. In addition, colloidal TiO2 and Ag nanoparticles were generated separately for comparison under the same laser beam characteristics and process conditions. The absorption spectra of colloidal Ag-TiO2 cluster nanoparticles were examined by UV-Vis spectroscopy, and size distribution was characterised using transmission electron microscopy. The morphology and composition of Ag-TiO2 nanoparticles were examined using scanning transmission electron microscopy in high-angle annular dark field, and energy-dispersive X-ray spectroscopy. The crystalline structures were investigated by X-ray diffraction. The size of larger TiO2 particles was in the range 30-150 nm, and the smaller-sized Ag nanoparticles attached to the TiO2 was mainly in the range of 10-15 nm. The yield is more than 50 % with the remaining nanoparticles in the form of uncombined Ag and TiO2. The nanoparticles generated had strong antibacterial effects as tested against E. coli. A discussion is given on the role of ultrasonic vibration in the formation of Ag-TiO2 hybrid nanoparticles by picosecond laser ablation.

  6. Bio-inspired sustainable and green synthesis of plasmonic Ag/AgCl nanoparticles for enhanced degradation of organic compound from aqueous phase.

    PubMed

    Devi, Th Babita; Ahmaruzzaman, M

    2016-09-01

    In the current study, we report the utilization of the biogenic potential of Benincasa hispida (ash gourd) peel extract for the synthesis of Ag embedded AgCl nanoparticles nanoparticles (Ag/AgCl NPs) without the use of any external organic solvents. The appearance of dark brown color from the pale yellow color confirmed the formation of Ag/AgCl nanoparticles which was further validated by absorbance peak using UV-visible spectroscopy. The phytochemicals (flavones) present in the B. hispida peel extract acts as a reducing/stabilizing agents. The morphology and size of the synthesized NPs were characterized by transmission electron microscope (TEM), selected area electron microscope (SAED) and high resolution transmission electron microscope (HR-TEM). FT-IR spectra of the B. hispida peel extract and after the development of nanoparticles are determined to identify the functional groups responsible for the conversion of metal ions to metal nanoparticles. The synthesized nanoparticles showed an excellent photocatalytic property in the degradation of toxic dye like malachite green oxalate under sunlight irradiation. For the first time, malachite green oxalate dye was degraded by Ag/AgCl nanoparticles under sunlight irradiation. PMID:27246560

  7. Bio-inspired sustainable and green synthesis of plasmonic Ag/AgCl nanoparticles for enhanced degradation of organic compound from aqueous phase.

    PubMed

    Devi, Th Babita; Ahmaruzzaman, M

    2016-09-01

    In the current study, we report the utilization of the biogenic potential of Benincasa hispida (ash gourd) peel extract for the synthesis of Ag embedded AgCl nanoparticles nanoparticles (Ag/AgCl NPs) without the use of any external organic solvents. The appearance of dark brown color from the pale yellow color confirmed the formation of Ag/AgCl nanoparticles which was further validated by absorbance peak using UV-visible spectroscopy. The phytochemicals (flavones) present in the B. hispida peel extract acts as a reducing/stabilizing agents. The morphology and size of the synthesized NPs were characterized by transmission electron microscope (TEM), selected area electron microscope (SAED) and high resolution transmission electron microscope (HR-TEM). FT-IR spectra of the B. hispida peel extract and after the development of nanoparticles are determined to identify the functional groups responsible for the conversion of metal ions to metal nanoparticles. The synthesized nanoparticles showed an excellent photocatalytic property in the degradation of toxic dye like malachite green oxalate under sunlight irradiation. For the first time, malachite green oxalate dye was degraded by Ag/AgCl nanoparticles under sunlight irradiation.

  8. Nanotoxicity of silver nanoparticles to red blood cells: size dependent adsorption, uptake, and hemolytic activity.

    PubMed

    Chen, Li Qiang; Fang, Li; Ling, Jian; Ding, Cheng Zhi; Kang, Bin; Huang, Cheng Zhi

    2015-03-16

    Silver nanoparticles (AgNPs) are increasingly being used as antimicrobial agents and drug carriers in biomedical fields. However, toxicological information on their effects on red blood cells (RBCs) and the mechanisms involved remain sparse. In this article, we examined the size dependent nanotoxicity of AgNPs using three different characteristic sizes of 15 nm (AgNPs15), 50 nm (AgNPs50), and 100 nm (AgNPs100) against fish RBCs. Optical microscopy and transmission electron microscopy observations showed that AgNPs exhibited a size effect on their adsorption and uptake by RBCs. The middle sized AgNPs50, compared with the smaller or bigger ones, showed the highest level of adsorption and uptake by the RBCs, suggesting an optimal size of ∼50 nm for passive uptake by RBCs. The toxic effects determined based on the hemolysis, membrane injury, lipid peroxidation, and antioxidant enzyme production were fairly size and dose dependent. In particular, the smallest sized AgNPs15 displayed a greater ability to induce hemolysis and membrane damage than AgNPs50 and AgNPs100. Such cytotoxicity induced by AgNPs should be attributed to the direct interaction of the nanoparticle with the RBCs, resulting in the production of oxidative stress, membrane injury, and subsequently hemolysis. Overall, the results suggest that particle size is a critical factor influencing the interaction between AgNPs and the RBCs.

  9. Room-temperature solution synthesis of Ag nanoparticle functionalized molybdenum oxide nanowires and their catalytic applications

    NASA Astrophysics Data System (ADS)

    Dong, Wenjun; Huang, Huandi; Zhu, Yanjun; Li, Xiaoyun; Wang, Xuebin; Li, Chaorong; Chen, Benyong; Wang, Ge; Shi, Zhan

    2012-10-01

    A simple chemical solution route for the synthesis of large-scale high-quality Ag nanoparticle functionalized molybdenum oxide nanowire at room temperature has been developed. In the synthesis, the protonated amine was intercalated into the molybdenum bronze layers to reduce the electrostatic force of the lamellar structures, and then the Ag nanoparticle functionalized long nanowires could be easily induced by a redox reaction between a molybdenum oxide-amine intermediate and Ag+ at room temperature. The intercalation lamellar structures improved the nucleation and growth of the Ag nanoparticles, with the result that uniform Ag nanoparticles occurred on the surface of the MoO3 nanowire. In this way Ag nanoparticles with average sizes of around 6 nm, and high-purity nanowires with mean diameter of around 50 nm and with typical lengths of several tens to hundreds of micrometers were produced. The heteronanostructured nanowires were intricately and inseparably connected to each other with hydrogen bonds and/or bridge oxygen atoms and packed together, forming a paper-like porous network film. The Ag-MoO3 nanowire film performs a promoted catalytic property for the epoxidation of cis-cyclooctene, and the heteronanostructured nanowire film sensor shows excellent sensing performance to hydrogen and oxygen at room temperature.

  10. Mechanisms of Toxicity of Ag Nanoparticles in Comparison to Bulk and Ionic Ag on Mussel Hemocytes and Gill Cells

    PubMed Central

    Katsumiti, Alberto; Gilliland, Douglas; Arostegui, Inmaculada; Cajaraville, Miren P.

    2015-01-01

    Silver nanoparticles (Ag NPs) are increasingly used in many products and are expected to end up in the aquatic environment. Mussels have been proposed as marine model species to evaluate NP toxicity in vitro. The objective of this work was to assess the mechanisms of toxicity of Ag NPs on mussel hemocytes and gill cells, in comparison to ionic and bulk Ag. Firstly, cytotoxicity of commercial and maltose stabilized Ag NPs was screened in parallel with the ionic and bulk forms at a wide range of concentrations in isolated mussel cells using cell viability assays. Toxicity of maltose alone was also tested. LC50 values were calculated and the most toxic Ag NPs tested were selected for a second step where sublethal concentrations of each Ag form were tested using a wide array of mechanistic tests in both cell types. Maltose-stabilized Ag NPs showed size-dependent cytotoxicity, smaller (20 nm) NPs being more toxic than larger (40 and 100 nm) NPs. Maltose alone provoked minor effects on cell viability. Ionic Ag was the most cytotoxic Ag form tested whereas bulk Ag showed similar cytotoxicity to the commercial Ag NPs. Main mechanisms of action of Ag NPs involved oxidative stress and genotoxicity in the two cell types, activation of lysosomal AcP activity, disruption of actin cytoskeleton and stimulation of phagocytosis in hemocytes and increase of MXR transport activity and inhibition of Na-K-ATPase in gill cells. Similar effects were observed after exposure to ionic and bulk Ag in the two cell types, although generally effects were more marked for the ionic form. In conclusion, results suggest that most observed responses were due at least in part to dissolved Ag. PMID:26061169

  11. Synthesis and characterization of Au-core Ag-shell nanoparticles from unmodified apoferritin

    SciTech Connect

    Li, T.; Chattopadhyay, S.; Shibata, T.; Cook, R. E.; Miller, J. T.; Suthiwangcharoen, N.; Lee, S.; Winans, R. E.; Lee, B.

    2012-01-01

    Narrow-size distributed, water-soluble Au-core Ag-shell nanoparticles with a size range from 1 to 5 nm are synthesized using unmodified apoferritin as a template. Fast protein liquid chromatography reveals that the nanoparticles are formed inside the apoferritin cavity and are stable in aqueous solution. Electron microscopy shows that the particles are uniform in size and composed of both Au and Ag. In addition, extended X-ray absorption fine structure confirms that the particles have a core-shell structure with a Au core covered with a Ag shell. By varying the loading amounts of the silver precursor, the Ag shell thickness is controlled from one layer to several layers.

  12. Preparation and antibacterial activity of Fe3O4@Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Gong, Ping; Li, Huimin; He, Xiaoxiao; Wang, Kemin; Hu, Jianbing; Tan, Weihong; Zhang, Shouchun; Yang, Xiaohai

    2007-07-01

    Bifunctional Fe3O4@Ag nanoparticles with both superparamagnetic and antibacterial properties were prepared by reducing silver nitrate on the surface of Fe3O4 nanoparticles using the water-in-oil microemulsion method. Formation of well-dispersed nanoparticles with sizes of 60 ± 20 nm was confirmed by transmission electron microscopy and dynamic light scattering. X-ray diffraction patterns and UV-visible spectroscopy indicated that both Fe3O4 and silver are present in the same particle. The superparamagnetism of Fe3O4@Ag nanoparticles was confirmed with a vibrating sample magnetometer. Their antibacterial activity was evaluated by means of minimum inhibitory concentration value, flow cytometry, and antibacterial rate assays. The results showed that Fe3O4@Ag nanoparticles presented good antibacterial performance against Escherichia coli (gram-negative bacteria), Staphylococcus epidermidis (gram-positive bacteria) and Bacillus subtilis (spore bacteria). Furthermore, Fe3O4@Ag nanoparticles can be easily removed from water by using a magnetic field to avoid contamination of surroundings. Reclaimed Fe3O4@Ag nanoparticles can still have antibacterial capability and can be reused.

  13. Surface spin polarization induced ferromagnetic Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Shih, Po-Hsun; Li, Wen-Hsien; Wu, Sheng Yun

    2016-05-01

    We report on the observation of ferromagnetic spin polarized moments in 4.5 nm Ag nanoparticles. Both ferromagnetic and diamagnetic responses to an applied magnetic field were detected. The spin polarized moments shown under non-linear thermoinduced magnetization appeared on the surface atoms, rather than on all the atoms in particles. The saturation magnetization departed substantially from the Bloch T3/2-law, showing the existence of magnetic anisotropy. The Heisenberg ferromagnetic spin wave model for Ha-aligned moments was then employed to identify the magnetic anisotropic energy gap of ~0.12 meV. Our results may be understood by assuming the surface magnetism model, in which the surface atoms give rise to polarized moments while the core atoms produce diamagnetic responses.

  14. Evaluation of the Cytotoxic Behavior of Fungal Extracellular Synthesized Ag Nanoparticles Using Confocal Laser Scanning Microscope

    PubMed Central

    Salaheldin, Taher A.; Husseiny, Sherif M.; Al-Enizi, Abdullah M.; Elzatahry, Ahmed; Cowley, Alan H.

    2016-01-01

    Silver nanoparticles have been synthesized by subjecting a reaction medium to a Fusarium oxysporum biomass at 28 °C for 96 h. The biosynthesized Ag nanoparticles were characterized on the basis of their anticipated peak at 405 nm using UV-Vis-NIR spectroscopy. Structural confirmation was evident from the characteristic X-ray diffraction (XRD) pattern, high-resolution transmission electron Microscopy (HRTEM) and the particle size analyzer. The Ag nanoparticles were of dimension 40 ± 5 nm and spherical in shape. The study mainly focused on using the confocal laser scanning microscope (CLSM) to examine the cytotoxic activities of fungal synthesized Ag nanoparticles on a human breast carcinoma cell line MCF7 cell, which featured remarkable vacuolation, thus indicating a potent cytotoxic activity. PMID:26950118

  15. Evaluation of the Cytotoxic Behavior of Fungal Extracellular Synthesized Ag Nanoparticles Using Confocal Laser Scanning Microscope.

    PubMed

    Salaheldin, Taher A; Husseiny, Sherif M; Al-Enizi, Abdullah M; Elzatahry, Ahmed; Cowley, Alan H

    2016-03-03

    Silver nanoparticles have been synthesized by subjecting a reaction medium to a Fusarium oxysporum biomass at 28 °C for 96 h. The biosynthesized Ag nanoparticles were characterized on the basis of their anticipated peak at 405 nm using UV-Vis-NIR spectroscopy. Structural confirmation was evident from the characteristic X-ray diffraction (XRD) pattern, high-resolution transmission electron Microscopy (HRTEM) and the particle size analyzer. The Ag nanoparticles were of dimension 40 ± 5 nm and spherical in shape. The study mainly focused on using the confocal laser scanning microscope (CLSM) to examine the cytotoxic activities of fungal synthesized Ag nanoparticles on a human breast carcinoma cell line MCF7 cell, which featured remarkable vacuolation, thus indicating a potent cytotoxic activity.

  16. Magnetic hyperthermia in brick-like Ag@Fe3O4 core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Brollo, M. E. F.; Orozco-Henao, J. M.; López-Ruiz, R.; Muraca, D.; Dias, C. S. B.; Pirota, K. R.; Knobel, M.

    2016-01-01

    Heating efficiency of multifunctional Ag@Fe3O4 brick-like nanoparticles under alternating magnetic field was investigated by means of specific absorption rate (SAR) measurements, and compared with equivalent measurements for plain magnetite and dimer heteroparticles. The samples were synthesized by thermal decomposition reactions and present narrow size polydispersity and high degree of crystallinity. The SAR values are analyzed using the superparamagnetic theory, in which the basic morphology, size and dispersion of sizes play key roles. The results suggest that these novel brick-like nanoparticles are good candidates for hyperthermia applications, displaying heating efficiencies comparable with the most efficient plain nanoparticles.

  17. In situ biosynthesis of Ag, Au and bimetallic nanoparticles using Piper pedicellatum C.DC: green chemistry approach.

    PubMed

    Tamuly, Chandan; Hazarika, Moushumi; Borah, Sarat Ch; Das, Manash R; Boruah, Manas P

    2013-02-01

    The synthesis of Ag, Au and Ag-Au bimetallic nanoparticles using Piper pedicellatum C.DC leaf extract is demonstrated here. The rapid formation of stable Ag and Au nanoparticles has been found using P. pedicellatum C.DC leaf extract in aqueous medium at normal atmospheric condition. Competitive reduction of Ag(+) and Au(3+) ions present simultaneously in solution during exposure to P. pedicellatum C.DC leaf extract leads to the synthesis of bimetallic Ag-Au nanoparticles in solution. Transmission electron microscopy (TEM) analysis revealed that the Ag nanoparticles predominantly form spherical in shape with the size range of 2.0±0.5-30.0±1.2 nm. In case of Au nanoparticles, the particles are spherical in shape along with few triangular, hexagonal and pentagonal shaped nanoparticles also observed. X-ray diffraction (XRD) studies revealed that the nanoparticles were face centered cubic (fcc) in shape. Fourier transform infrared spectroscopy (FTIR) showed nanoparticles were capped with plant compounds. The chemical constituents, viz. catechin, gallic acid, courmaric acid and protocatechuic acid of the leaf extract were identified which may act as a reducing, stabilizing and capping agent. The expected reaction mechanism in the formation of Ag and Au nanoparticles is also reported. PMID:23107941

  18. In situ biosynthesis of Ag, Au and bimetallic nanoparticles using Piper pedicellatum C.DC: green chemistry approach.

    PubMed

    Tamuly, Chandan; Hazarika, Moushumi; Borah, Sarat Ch; Das, Manash R; Boruah, Manas P

    2013-02-01

    The synthesis of Ag, Au and Ag-Au bimetallic nanoparticles using Piper pedicellatum C.DC leaf extract is demonstrated here. The rapid formation of stable Ag and Au nanoparticles has been found using P. pedicellatum C.DC leaf extract in aqueous medium at normal atmospheric condition. Competitive reduction of Ag(+) and Au(3+) ions present simultaneously in solution during exposure to P. pedicellatum C.DC leaf extract leads to the synthesis of bimetallic Ag-Au nanoparticles in solution. Transmission electron microscopy (TEM) analysis revealed that the Ag nanoparticles predominantly form spherical in shape with the size range of 2.0±0.5-30.0±1.2 nm. In case of Au nanoparticles, the particles are spherical in shape along with few triangular, hexagonal and pentagonal shaped nanoparticles also observed. X-ray diffraction (XRD) studies revealed that the nanoparticles were face centered cubic (fcc) in shape. Fourier transform infrared spectroscopy (FTIR) showed nanoparticles were capped with plant compounds. The chemical constituents, viz. catechin, gallic acid, courmaric acid and protocatechuic acid of the leaf extract were identified which may act as a reducing, stabilizing and capping agent. The expected reaction mechanism in the formation of Ag and Au nanoparticles is also reported.

  19. Bimetallic PdAg nanoparticle arrays from monolayer films of diblock copolymer micelles

    NASA Astrophysics Data System (ADS)

    Ehret, E.; Beyou, E.; Mamontov, G. V.; Bugrova, T. A.; Prakash, S.; Aouine, M.; Domenichini, B.; Cadete Santos Aires, F. J.

    2015-07-01

    The self-assembly technique provides a highly efficient route to generate well-ordered structures on a nanometer scale. In this paper, well-ordered arrays of PdAg alloy nanoparticles on flat substrates with narrow distributions of particle size (6-7 nm) and interparticle spacing (about 60 nm) were synthesized by the block copolymer micelle approach. A home-made PS-b-P4VP diblock copolymer was prepared to obtain a micellar structure in toluene. Pd and Ag salts were then successfully loaded in the micellar core of the PS-b-P4VP copolymer. A self-assembled monolayer of the loaded micelles was obtained by dipping the flat substrate in the solution. At this stage, the core of the micelles was still loaded with the metal precursor rather than with a metal. Physical and chemical reducing methods were used to reduce the metal salts embedded in the P4VP core into PdAg nanoparticles. HRTEM and EDX indicated that Pd-rich PdAg alloy nanoparticles were synthesized by chemical or physical reduction; UV-visible spectroscopy observations confirmed that metallic PdAg nanoparticles were quickly formed after chemical reduction; XPS measurements revealed that the PdAg alloy nanoparticles were in a metallic state after a short time of exposure to O2 plasma and after hydrazine reduction.

  20. Controlled formation of ag nanoparticles by means of long-chain sodium polyacrylates in dilute solution.

    PubMed

    Huber, Klaus; Witte, Thomas; Hollmann, Jutta; Keuker-Baumann, Susanne

    2007-02-01

    A new tool is presented to control formation of Ag nanoparticles. Small amounts of silver ions were added to dilute solutions of long-chain sodium polyacrylates (NaPA). Four NaPA samples covering a molar mass regime of 97 kD < or = Mw < or = 650 kD have been used. With amounts of added Ag(+) as low as 1-2% of the COO(-) groups of the polyanionic chains, significant changes could already be induced in the NaPA coils with 650 kD. If the NaPA concentration was kept below 0.1 g/L, the coils with 650 kD exhibited a significant coil shrinking in stable solutions. At larger NaPA concentrations, addition of Ag+ initiates an aggregation of the polyacrylate coils toward compact structures. Coil shrinking and aggregation was revealed by means of time-resolved static light scattering. If exposed to UV-radiation, small Ag particles formed within the shrunken anionic polyacrylate coils. The Ag nanoparticles were identified by means of an enhanced light scattering and a characteristic plasmon absorption band around 410 nm. No such Ag particle formation could be observed even at 5 times larger concentrations of Ag(+) and NaPA if the two smallest polyacrylate samples have been used under otherwise equal conditions. This molar mass sensitive response of NaPA to Ag(+)-addition suggests an interesting phenomenon: if the coil size of the NaPa chains, which act as Ag(+) collectors, is large enough, local Ag(+) concentration in these coil-shaped Ag(+) containers exceeds a critical value, and irradiation with UV generates Ag nanoparticles. PMID:17263389

  1. Evidence for avoidance of Ag nanoparticles by earthworms (Eisenia fetida).

    PubMed

    Shoults-Wilson, W A; Zhurbich, Oksana I; McNear, David H; Tsyusko, Olga V; Bertsch, Paul M; Unrine, Jason M

    2011-03-01

    Silver nanoparticles have been incorporated into a wide variety of consumer products, ideally acting as antimicrobial agents. Silver exposure has long been known to cause toxic effects to a wide variety of organisms, making large scale production of silver nanoparticles a potential hazard to environmental systems. Here we describe the first evidence that an organism may be able to sense manufactured nanoparticles in a complex, environmentally relevant exposure and that the presence of nanoparticles alters the organism's behavior. We found that earthworms (Eisenia fetida) consistently avoid soils containing silver nanoparticles and AgNO(3) at similar concentrations of Ag. However, avoidance of silver nanoparticles occurred over 48 h, while avoidance of AgNO(3) was immediate. It was determined that avoidance of silver nanoparticles could not be explained by release of silver ions or any changes in microbial communities caused by the introduction of Ag. This leads us to conclude that the earthworms were in some way sensing the presence of nanoparticles over the course of a 48 h exposure and choosing to avoid exposure to them. Our results demonstrate that nanoparticle interactions with organisms may be unpredictable and that these interactions may result in ecologically significant effects on behavior at environmentally relevant concentrations. PMID:21229389

  2. Characterization of Silver/Bovine Serum Albumin (Ag/BSA) nanoparticles structure: morphological, compositional, and interaction studies.

    PubMed

    Gebregeorgis, A; Bhan, C; Wilson, O; Raghavan, D

    2013-01-01

    The primary objective of this study was to elucidate the structure of protein conjugated silver nanoparticles prepared by chemical reduction of AgNO(3) and bovine serum albumin (BSA) mixture. The role of BSA in the formation of Ag/BSA nanoparticles was established by UV-Vis Spectroscopy. The association of silver with BSA in Ag/BSA nanoparticles was studied by the decrease in the intensity of absorbance peak at 278 nm in UV-Vis spectra and shift in cathodic peak potential in cyclic voltammogram. The molar ratio of silver to BSA in the Ag/BSA nanoparticles is 27:1, as ascertained by thermogravimetric analysis and atomic absorption spectrometry. Based on atomic force microscopy, dynamic light scattering and transmission electron microscopy (TEM) measurements, the average particle size of nanoparticles was found to be range of 11-15 nm. TEM image showed that the nanoparticle has two distinct phases and selected area electron diffraction pattern of nanoparticles indicated that the silver phase in Ag/BSA is fcc. X-ray photo electron spectroscopy measurements of freshly prepared and argon sputtered nanoparticles provided evidence that the outer and inner region of nanoparticles are mainly composed of BSA and silver respectively. The structural and compositional findings of nanoparticles could have a strong bearing on the bioavailability and antimicrobial activity of nanoparticles.

  3. Artificial silver sulfide Ag2S: Crystal structure and particle size in deposited powders

    NASA Astrophysics Data System (ADS)

    Sadovnikov, S. I.; Gusev, A. I.; Rempel, A. A.

    2015-07-01

    Chemical deposition from aqueous solutions of silver nitrate and sodium sulfide was used for synthesis of coarse-crystalline and nanocrystalline silver sulfide Ag2S powders. Sodium citrate was used as a complexing and stabilizing agent during synthesis. X-ray diffraction study shows that synthesized Ag2S powders have monoclinic (space group P21/c) α-Ag2S acanthite type crystal structure. The unit cell of artificial monoclinic silver sulfide Ag2S contains four Ag2S formula units and has the following parameters: a = 0.42264 nm, b = 0.69282 nm, c = 0.95317 nm and β = 125.554°. The size of silver sulfide particles in deposited powders was estimated by the X-ray diffraction and BET methods. By varying the ratio between the concentrations of reagents in the initial reaction mixture it is possible to deposit Ag2S nanoparticles with average size ranging in the interval from ∼1000 to ∼30 nm. Ag2S nanopowders have no deformation distortions of the crystal lattice practically because the microstrains ε in the synthesized powders do not exceed 0.15%. All the Ag2S powders with different particle size have an identical morphology.

  4. Beet Juice-Induced Green Fabrication of Plasmonic AgCl/Ag Nanoparticles

    EPA Science Inventory

    A simple, green, and fast approach (complete within 5 min) was explored for the fabrication of hybrid AgCl/Ag plasmonic nanoparticles under microwave (MW) irradiation. In this method, beet juice served as a reducing reagent, which is an abundant sugar-rich agricultural produce. I...

  5. Exposure medium: key in identifying free Ag+ as the exclusive species of silver nanoparticles with acute toxicity to Daphnia magna.

    PubMed

    Shen, Mo-Hai; Zhou, Xiao-Xia; Yang, Xiao-Ya; Chao, Jing-Bo; Liu, Rui; Liu, Jing-Fu

    2015-04-10

    It is still not very clear what roles the various Ag species play in the toxicity of silver nanoparticles (AgNPs). In this study, we found that traditional exposure media result in uncontrollable but consistent physicochemical transformation of AgNPs, causing artifacts in determination of median lethal concentration (LC50) and hindering the identification of Ag species responsible for the acute toxicity of AgNPs to Daphnia magna. This obstacle was overcome by using 8 h exposure in 0.1 mmol L(-1) NaNO3 medium, in which we measured the 8-h LC50 of seven AgNPs with different sizes and coatings, and determined the concentrations of various Ag species. The LC50 as free Ag(+) of the seven AgNPs (0.37-0.44 μg L(-1)) agreed very well with that of AgNO3 (0.40 μg L(-1)), and showed the lowest value compared to that as total Ag, total Ag(+), and dissolved Ag, demonstrating free Ag(+) is exclusively responsible for the acute toxicity of AgNPs to D. magna, while other Ag species in AgNPs have no contribution to the acute toxicity. Our results demonstrated the great importance of developing appropriate exposure media for evaluating risk of nanomaterials.

  6. Exposure Medium: Key in Identifying Free Ag+ as the Exclusive Species of Silver Nanoparticles with Acute Toxicity to Daphnia magna

    NASA Astrophysics Data System (ADS)

    Shen, Mo-Hai; Zhou, Xiao-Xia; Yang, Xiao-Ya; Chao, Jing-Bo; Liu, Rui; Liu, Jing-Fu

    2015-04-01

    It is still not very clear what roles the various Ag species play in the toxicity of silver nanoparticles (AgNPs). In this study, we found that traditional exposure media result in uncontrollable but consistent physicochemical transformation of AgNPs, causing artifacts in determination of median lethal concentration (LC50) and hindering the identification of Ag species responsible for the acute toxicity of AgNPs to Daphnia magna. This obstacle was overcome by using 8 h exposure in 0.1 mmol L-1 NaNO3 medium, in which we measured the 8-h LC50 of seven AgNPs with different sizes and coatings, and determined the concentrations of various Ag species. The LC50 as free Ag+ of the seven AgNPs (0.37-0.44 μg L-1) agreed very well with that of AgNO3 (0.40 μg L-1), and showed the lowest value compared to that as total Ag, total Ag+, and dissolved Ag, demonstrating free Ag+ is exclusively responsible for the acute toxicity of AgNPs to D. magna, while other Ag species in AgNPs have no contribution to the acute toxicity. Our results demonstrated the great importance of developing appropriate exposure media for evaluating risk of nanomaterials.

  7. Exposure Medium: Key in Identifying Free Ag+ as the Exclusive Species of Silver Nanoparticles with Acute Toxicity to Daphnia magna

    PubMed Central

    Shen, Mo-Hai; Zhou, Xiao-Xia; Yang, Xiao-Ya; Chao, Jing-Bo; Liu, Rui; Liu, Jing-Fu

    2015-01-01

    It is still not very clear what roles the various Ag species play in the toxicity of silver nanoparticles (AgNPs). In this study, we found that traditional exposure media result in uncontrollable but consistent physicochemical transformation of AgNPs, causing artifacts in determination of median lethal concentration (LC50) and hindering the identification of Ag species responsible for the acute toxicity of AgNPs to Daphnia magna. This obstacle was overcome by using 8 h exposure in 0.1 mmol L−1 NaNO3 medium, in which we measured the 8-h LC50 of seven AgNPs with different sizes and coatings, and determined the concentrations of various Ag species. The LC50 as free Ag+ of the seven AgNPs (0.37–0.44 μg L−1) agreed very well with that of AgNO3 (0.40 μg L−1), and showed the lowest value compared to that as total Ag, total Ag+, and dissolved Ag, demonstrating free Ag+ is exclusively responsible for the acute toxicity of AgNPs to D. magna, while other Ag species in AgNPs have no contribution to the acute toxicity. Our results demonstrated the great importance of developing appropriate exposure media for evaluating risk of nanomaterials. PMID:25858866

  8. Gamma ray irradiated AgFeO{sub 2} nanoparticles with enhanced gas sensor properties

    SciTech Connect

    Wang, Xiuhua; Shi, Zhijie; Yao, Shangwu; Liao, Fan; Ding, Juanjuan; Shao, Mingwang

    2014-11-15

    AgFeO{sub 2} nanoparticles were synthesized via a facile hydrothermal method and irradiated by various doses of gamma ray. The products were characterized with X-ray powder diffraction, UV–vis absorption spectrum and transmission electron microscope. The results revealed that the crystal structure, morphology and size of the samples remained unchanged after irradiation, while the intensity of UV–Vis spectra increased with irradiation dose increasing. In addition, gamma ray irradiation improved the performance of gas sensor based on the AgFeO{sub 2} nanoparticles including the optimum operating temperature and sensitivity, which might be ascribed to the generation of defects. - Graphical abstract: Gamma ray irradiation improved the performance of gas sensor based on the AgFeO{sub 2} nanoparticles including sensitivity and optimum operating temperature, which might be ascribed to the generation of defects. - Highlights: • AgFeO{sub 2} nanoparticles were synthesized and irradiated with gamma ray. • AgFeO{sub 2} nanoparticles were employed to fabricate gas sensors to detect ethanol. • Gamma ray irradiation improved the sensitivity and optimum operating temperature.

  9. Underlying mechanisms in size control of uniform nanoparticles.

    PubMed

    Sugimoto, Tadao

    2007-05-01

    Insights are given into underlying mechanisms for size control of uniform nanoparticles in liquid phases. At the outset, instead of the classical nucleation theories, which are hardly applicable to the size control of uniform particles, a fundamental equation for the nucleation of monodisperse particles, derived for their size control on the basis of the LaMer model, is introduced. This equation was derived on three assumptions: (1) There is a mass balance between the supply rate of solute and its consumption rate for nucleation and growth of the generated nuclei; (2) The supply rate of solute is independent of the subsequent precipitation events; (3) The nucleation rate is controlled only by the growth of the preformed nuclei at a fixed supply rate of solute. Thus, this nucleation theory is applicable to a system in which the precursor solute is supplied by slow irreversible generation in a closed system or by continuous feed from outside in an open system. However, it is inapplicable even if only one of these three assumptions is not fulfilled. Examples of applicable and inapplicable systems are listed, and finally discussion is focused on the underlying mechanisms of size control in some unique processes chosen from them, such as hydrolysis-induced precipitation of AgCl nanoparticles, double-jet precipitation of AgCl nanoparticles in a reverse micelle system to resolve the mechanism of particle formation in general reverse micelle systems, and a gel-sol process for the formation of nanoparticles of anatase TiO2.

  10. Influence of temperature and precursor concentration on the synthesis of HDA-capped Ag{sub 2}Se nanoparticles

    SciTech Connect

    Mlambo, M.; Moloto, M.J.; Moloto, N.; Mdluli, P.S.

    2013-06-01

    Graphical abstract: The temperature effect on the growth and size of silver selenide nanoparticles with the size distribution and XRD patterns. Highlights: ► The HDA-capped Ag{sub 2}Se nanoparticles were synthesized via the colloidal route. ► Temperature and monomer concentration of the reaction were varied. ► The concentration as a factor influenced particles with a decrease observed as the amount of Ag{sup +} ion source is increased. ► Temperature has expected influence on the growth of particles resulting in increase as the temperature is increased. ► TEM images shows spherical particles and their orthorhombic phase from structural analysis by XRD. - Abstract: The size dependent of temperature and precursor concentration on the synthesis of hexadecylamine capped Ag{sub 2}Se nanoparticles via the colloidal route were studied using the combination of optical and structural analysis. The as-prepared Ag{sub 2}Se nanoparticles showed the quantum confinement with all the obtained absorption band edges blue-shifted from the bulk and their corresponding emission maxima displaying a red-shift from band edges characterised by UV–vis absorption and photoluminescence spectroscopy. The particle sizes were obtained from transmission electron microscopy analysis. The increase in precursor concentration resulted in a decrease in nanoparticle sizes. The increase in reaction temperature showed an increase in the nanoparticle sizes, when the critical temperature at 160 °C was reached, the nanoparticle sizes decreased.

  11. Biofabrication of Ag nanoparticles using Moringa oleifera leaf extract and their antimicrobial activity

    PubMed Central

    Prasad, TNVKV; Elumalai, EK

    2011-01-01

    Objective To formulate a simple rapid procedure for bioreduction of silver nanoparticles using aqueous leaves extract of Moringa oleifera (M. oleifera). Methods 10 mL of leaf extract was mixed to 90 mL of 1 mM aqueous of AgNO3 and was heated at 60 - 80 °C for 20 min. A change from brown to reddish color was observed. Characterization using UV-Vis spectrophotometry, Transmission Electron Microscopy (TEM) was performed. Results TEM showed the formation of silver nanoparticles with an average size of 57 nm. Conclusions M. oleifera demonstrates strong potential for synthesis of silver nanoparticles by rapid reduction of silver ions (Ag+ to Ag0). Biological methods are good competents for the chemical procedures, which are eco-friendly and convenient. PMID:23569809

  12. Facile synthesis of Ag2S nanoparticles functionalized by carbon-containing citrate shell

    NASA Astrophysics Data System (ADS)

    Sadovnikov, S. I.; Gusev, A. I.; Gerasimov, E. Yu.; Rempel, A. A.

    2015-12-01

    Silver sulfide nanoparticles with non-toxic citrate shell are synthesized by chemical bath deposition from aqueous mixtures of silver nitrate and sodium sulfide in the presence of sodium citrate used as a complexing and stabilizing agent. The prepared nanoparticles have Ag2S core with monoclinic crystal structure functionalized by a carbon-containing citrate shell. By varying the concentrations of reagents it was possible to prepare core-shell nanoparticles with pre-assigned size of Ag2S core from 10 and 50 nm and pre-assigned thickness from 1.5 to 10 nm of citrate shell. A probable mechanism of formation of carbon-containing citrate shell on Ag2S core has been proposed.

  13. Synthesis of silver nanoparticles deposited on silica by γ-irradiation and preparation of PE/Ag nano compound masterbatches

    NASA Astrophysics Data System (ADS)

    Nguyen, Thi Kim Lan; Trinh Nguyen, Thuy Ai; Phu Dang, Van; Duy Nguyen, Ngoc; Le, Anh Quoc; Hien Nguyen, Quoc

    2013-12-01

    Silver nanoparticles (AgNPs) deposited on silica were synthesized by gamma Co-60 irradiation of Ag+ dispersion in silica/ethanol/water mixture (9/80/20:w/v/v). The reduction of Ag+ is occurred by hydrated electron (e-aq) and hydrogen atom (H•) generated during radiolysis of ethanol/water. The conversion doses (Ag+ → Ag0) were determined by UV-Vis spectroscopy. The synthesized AgNPs/silica were characterized by transmission electron microscopy (TEM) and x-ray diffraction (XRD), which showed the size of AgNPs to be in the range of 5-40 nm for Ag+ concentrations from 5 to 20 mM. Masterbatches of PE/AgNPs/silica compound with silver content from 250 to 1000 mg kg-1 were also prepared. These masterbatches can be suitably used for various applications such as antimicrobial food containers and packing films, etc.

  14. Immobilization of Highly Dispersed Ag Nanoparticles on Carbon Nanotubes Using Electron-Assisted Reduction for Antibacterial Performance.

    PubMed

    Yan, Xiaoliang; Li, Sha; Bao, Jiehua; Zhang, Nan; Fan, Binbin; Li, Ruifeng; Liu, Xuguang; Pan, Yun-Xiang

    2016-07-13

    Silver nanoparticles (Ag NPs) supported on certain materials have been widely used as disinfectants. Yet, to date, the antibacterial activity of the supported Ag NPs is still far below optimum. This is mainly associated with the easy aggregation of Ag NPs on the supporting materials. Herein, an electron-assisted reduction (EAR) method, which is operated at temperatures as low as room temperature and without using any reduction reagent, was employed for immobilizing highly dispersed Ag NPs on aminated-CNTs (Ag/A-CNTs). The average Ag NPs size on the EAR-prepared Ag/A-CNTs is only 3.8 nm, which is much smaller than that on the Ag/A-CNTs fabricated from the traditional thermal calcination (25.5 nm). Compared with Ag/A-CNTs fabricated from traditional thermal calcination, EAR-prepared Ag/A-CNTs shows a much better antibacterial activity to E. coli/S. aureus and antifouling performance to P. subcordiformis/T. lepidoptera. This is mainly originated from the significantly enhanced Ag(+) ion releasing rate and highly dispersed Ag NPs with small size on the EAR-prepared Ag/A-CNTs. The findings from the present work are helpful for fabricating supported Ag NPs with small size and high dispersion for efficient antibacterial process. PMID:27327238

  15. Synthesis and formation mechanism of Ag-Ni alloy nanoparticles at room temperature

    NASA Astrophysics Data System (ADS)

    Yan, Shi; Sun, Dongbai; Tan, Yuanyuan; Xing, Xueqing; Yu, Hongying; Wu, Zhonghua

    2016-11-01

    Ag-Ni nanoparticles were prepared with a chemical reduction method in the presence of polyvinylpyrrolidone (PVP) used as a stabilizing agent. During the synthesis of Ag-Ni nanoparticles, silver nitrate was used as the Ag+ source while nickel sulfate hexahydrate was used as Ni2+ source. Mixed solutions of Ag+ source and Ni2+ source were used as the precursors and sodium borohydride was used as the reducing agent. Five ratios of Ag+/Ni2+ (9:1, 3:1, 1:1, 1:3, and 1:9) suspensions were prepared in the corresponding precursors. Ag-Ni alloy nanoparticles were obtained with this method at room temperature. Scanning electronic microscope (SEM), energy dispersive spectrum (EDS), high resolution transmission electron microscope (HRTEM) were used to characterize the morphology, composition and crystal structure of the nanoparticles. The crystal structure was also investigated with X-ray diffraction (XRD). In all five Ag/Ni ratios, two kinds of particle structures were observed that are single crystal structure and five-fold twinned structure respectively. Free energy of nanoparticles with different crystal structures were calculated at each Ag/Ni ratio. Calculated results revealed that, with identical volume, free energy of single crystal particle is lower than multi-twinned particle and the difference becomes smaller with the increase of particle size; increase of Ni content will lead the increase of free energy for both structures. Formation of different crystal structures are decided by the structure of the original nuclei at the very early stage of the reduction process.

  16. The preparation and characterization of nanoparticle Ag-SiO2 composite films with super low refractive index

    NASA Astrophysics Data System (ADS)

    Sun, Yu-Long; Wang, Jian; Li, Shou-Yi; He, Xin; Wang, Cheng-Wei

    2014-09-01

    The spin coating technique is used to prepare the porous Ag-SiO2 composite films, and the subsequent annealing process makes the nanoparticle Ag-SiO2 composite films formed. As the increase of the annealing temperature from 300 °C to 500 °C, the size of Ag-SiO2 composite nanoparticles gradually decreases. The SEM, TEM and XRD measurements of Ag-SiO2 composite films indicate that the single crystal metal nanoparticles are uniformly embedded into the SiO2 particles, forming Ag-SiO2 composite nanoparticles. The SPR absorption spectra of the Ag-SiO2 composite films show the content of metal Ag increases with the increase of annealing temperature, but when the annealing temperature increases to 500 °C, the SPR absorption is not observed on the absorption spectra although the total absorption of Ag-SiO2 composite films is enhanced. Furthermore, the optical constants of Ag-SiO2 composite films have been determined based on the measurement of ellipsometric parameters. It is more important the refractive index lower than 1 is obtained after annealing process of Ag-SiO2 composite films under 300 and 400 °C, but the extinction coefficient is low, which makes the film have low absorption.

  17. Synthesis and characterization of AgCl nanoparticles produced by laser ablation of Ag in NaCl solution

    NASA Astrophysics Data System (ADS)

    Mahmoodi, Afsaneh; Shoorshinie, Seyedeh Zahra; Dorranian, Davoud

    2016-04-01

    In this work, the structural and optical properties of silver chloride nanoparticles produced by laser ablation of Ag plate in NaCl solution were investigated. Five different concentrations of NaCl solution were used as the ablation environment. The beam of a Q-switched Nd:YAG laser of 1064 nm wavelength and 7 ns pulse width was employed to irradiate the Ag target in NaCl solutions. Fluence of laser pulse was 1.5 J/cm2, and repetition rate was 5 Hz. Samples were prepared using 1500 pulses. Produced nanoparticles were characterized using UV-visible-NIR absorption, and transmission spectrum, transmission electron microscopy, scanning electron microscopy, X-ray diffraction pattern, photoluminescence spectrum, and dynamic light scattering method. Results show that laser ablation is a promising method to produce AgCl nanoparticles. Size of nanoparticles, their lattice structure, and bandgap energy as well as the production rate may be controlled by the concentration of NaCl in the ablation environment.

  18. The IP6 micelle-stabilized small Ag cluster for synthesizing Ag-Au alloy nanoparticles and the tunable surface plasmon resonance effect

    NASA Astrophysics Data System (ADS)

    Wang, Na; Wen, Ying; Wang, Yao; Zhang, Rui; Chen, Xiyao; Ling, Bo; Huan, Shuangyan; Yang, Haifeng

    2012-04-01

    The stable small Ag seeds (size in diameter < 10 nm) were obtained in the presence of inositol hexakisphosphoric (IP6) micelles. Then Ag-Au bimetallic nanoparticles were synthesized through a replacement reaction with the rapid interdiffusion process between such small Ag seeds in nanoclusters and HAuCl4. Adjusting the dosage of HAuCl4 resulted in different products, which possessed unique surface plasmon resonances (SPR). The morphologies of the as-made nanoparticles were observed using transmission electron microscopy and field emission scanning electron microscopy and their compositions were determined by energy-dispersive x-ray spectroscopy. Among them, the Ag-Au alloy nanoparticles with the cauliflower-like structure had a suitable SPR for highly sensitive Raman detection application as a surface-enhanced Raman scattering (SERS) substrate with a long-term stability of six months.

  19. Label-Free Detection of Ag+ Based on Gold Nanoparticles and Ag+-Specific DNA.

    PubMed

    Pu, Wendan; Zhao, Zhao; Wu, Liping; Liu, Yue; Zhao, Huawen

    2015-08-01

    A sensitive label-free method was presented for the determination of silver ion (Ag+) in this paper. Cytosine-rich DNA (C-DNA) was used as Ag+ specific DNA. Without Ag+ in the solution, fluorescence of fluorescein (FAM) is quenched by C-DNA stabilized gold nanoparticles (AuNPs) in high salt environment. When Ag+ is present in the solution, however, Ag+-mediated cytosine-Ag+-cytosine (C-Ag+-C) base pairs induced the C-DNA folding into a hairpin structure, which can not stabilize AuNPs in high salt environment, thus causing AuNPs aggregation. After centrifugation to remove the aggregated AuNPs, the quenching ability of the supernatant for FAM is decreased and the fluorescence intensity of solution increases with increasing the Ag+ concentration. Due to the highly specific interaction of the C-DNA towards Ag+ and the strong fluorescent quenching ability of AuNPs for FAM, the method has high selectivity and sensitivity for Ag+. Under the optimal conditions, the fluorescence intensity at 515 nm increased linearly with the concentration of Ag+ ranging from 15 nM to 700 nM, and the detection limit was determined as 6 nM based on 3 σ/slope. This method is simple, sensitive, and may be applied to other detection systems by selecting the appropriate DNA sequences. PMID:26369112

  20. Extranuclear dynamics of 111Ag(→111Cd) doped in AgI nanoparticles

    NASA Astrophysics Data System (ADS)

    Sato, W.; Mizuuchi, R.; Irioka, N.; Komatsuda, S.; Kawata, S.; Taoka, A.; Ohkubo, Y.

    2014-08-01

    Dynamic behavior of the extranuclear field relative to the 111Ag(→111Cd) probe nucleus introduced in a superionic conductor silver iodide (AgI) was investigated by means of the time-differential perturbed angular correlation technique. For poly-N-vinyl-2-pyrrolidone (PVP)-coated AgI nanoparticles, we observed nuclear spin relaxation of the probe at room temperature. This result signifies that Ag+ ions in the polymer-coated sample make hopping motion from site to site at this low temperature. The activation energy for the dynamic motion was successfully estimated to be 46(10) meV. The first atomic-level observation of the temperature-dependent dynamic behavior of Ag+ ions in the polymer-coated AgI is reported.

  1. Ag(I)-triggered one-pot synthesis of Ag nanoparticles onto natural nanorods as a multifunctional nanocomposite for efficient catalysis and adsorption.

    PubMed

    Tian, Guangyan; Wang, Wenbo; Mu, Bin; Kang, Yuru; Wang, Aiqin

    2016-07-01

    A multifunctional palygorskite/polyaniline/Ag nanoparticles (PAL/PANI/AgNPs) nanocomposite was prepared at room temperature using a simple one-pot in-situ polymerization reaction of aniline monomers triggered by Ag(I) on the surface of natural PAL nanorods. Ag(I) served as both the oxidant and the precursor of the AgNPs, which initiated the polymerization of aniline monomers on PAL nanorods while simultaneously being reduced to form Ag(0) nanoparticles (AgNPs). The in-situ formed AgNPs were evenly distributed on the surface of the PAL nanorods because the interfacial effect of PAL prevents their aggregation. The density and size of the AgNPs and the catalytic activity of the nanocomposites could be controlled by altering the molar ratio of aniline to Ag(I). The performance evaluation revealed that the nanocomposites could be used as highly active catalysts, which rapidly catalyzed the reduction of 4-nitrophenol (4-NP) within 2min and Congo red (CR) within 10min. The nanocomposites are also an effective adsorbent for H2PO4(-) able to remove 99.40% of H2PO4(-) (only 61.77% for raw PAL) from a solution with an initial concentration of 50mg/L. This multifunctional nanocomposite synthesized by a simple one-pot approach is a promising material for environmental applications.

  2. [Three-dimensional vertically aligned CNTs coated by Ag nanoparticles for surface-enhanced Raman scattering].

    PubMed

    Zhang, Xiao-Lei; Zhang, Jie; Fan, Tuo; Ren, Wen-Jie; Lai, Chun-Hong

    2014-09-01

    In order to make surface-enhanced Raman scattering (SERS) substrates contained more "hot spots" in a three-dimensional (3D) focal volume, and can be adsorbed more probe molecules and metal nanoparticles, to obtain stronger Raman spectral signal, a new structure based on vertically aligned carbon nanotubes (CNTs) coated by Ag nanoparticles for surface Raman enhancement is presented. The vertically aligned CNTs are synthesized by chemical vapor deposition (CVD). A silver film is first deposited on the vertically aligned CNTs by magnetron sputtering. The samples are then annealed at different temperature to cause the different size silver nanoparticles to coat on the surface and sidewalls of vertically aligned CNTs. The result of scanning electron microscopy(SEM) shows that Ag nanoparticles are attached onto the sidewalls and tips of the vertically aligned CNTs, as the annealing temperature is different , pitch size, morphology and space between the silver nanoparticles is vary. Rhodamine 6G is served as the probe analyte. Raman spectrum measurement indicates that: the higher the concentration of R6G, the stronger the Raman intensity, but R6G concentration increase with the enhanced Raman intensity varies nonlinearly; when annealing temperature is 450 °C, the average size of silver nanoparticles is about 100 to 120 nm, while annealing temperature is 400 °C, the average size is about 70 nm, and the Raman intensity of 450 °C is superior to the annealing temperature that of 400 °C and 350 °C. PMID:25532342

  3. Monodispersed bimetallic PdAg nanoparticles with twinned structures: formation and enhancement for the methanol oxidation.

    PubMed

    Yin, Zhen; Zhang, Yining; Chen, Kai; Li, Jing; Li, Wenjing; Tang, Pei; Zhao, Huabo; Zhu, Qingjun; Bao, Xinhe; Ma, Ding

    2014-01-01

    Monodispersed bimetallic PdAg nanoparticles can be fabricated through the emulsion-assisted ethylene glycol (EG) ternary system. Different compositions of bimetallic PdAg nanoparticles, Pd₈₀Ag₂₀, Pd₆₅Ag₃₅ and Pd₄₆Ag₅₄ can be obtained via adjusting the reaction parameters. For the formation process of the bimetallic PdAg nanoparticles, there have two-stage growth processes: firstly, nucleation and growth of the primary nanoclusters; secondly, formation of the secondary nanoparticles with the size-selection and relax process via the coalescence or aggregation of the primary nanoclusters. The as-prepared PdAg can be supported on the carbon black without any post-treatment, which exhibited high electro-oxidation activity towards methanol oxidation under alkaline media. More importantly, carbon-supported Pd₈₀Ag₂₀ nanoparticles reveal distinctly superior activities for the methanol oxidation, even if compared with commercial Pt/C electro-catalyst. It is concluded that the enhanced activity is dependant on the unique twinning structure with heterogeneous phase due to the dominating coalescence growth in EG ternary system. PMID:24608736

  4. Phase transitions in CuS-Ag2S nanoparticle system

    NASA Astrophysics Data System (ADS)

    Sheela Christy, R.; Thanka Kumaran, J. T.; Bansal, C.; Brightson, M.

    2016-02-01

    (Ag2)xCu1-xS, x = .2, .4, .6 and .8 nanoparticles were synthesized by the solvothermal method. The as-synthesized nanoparticles were characterized by X-ray diffraction to study the crystal structure and size. The surface morphologies of the above samples were studied using scanning electron microscope. As there is continuous shift in the lower wavelength absorption edge of the UV-VIS spectrum of these samples with concentration, (Ag2)xCu1-xS nanoparticles can be tuned to different band gap energies by varying the composition. The D.C. electrical resistance was measured in the temperature range 310-485 K. As Ag2S transforms from monoclinic to bcc at around 450 K, copper sulfide nanoparticles also shows a phase transition at around 470 K, the effects of these two transitions are seen in the resistance measurements and in the UV-VIS spectra of the entire system. The electrical resistance of (Ag2)xCu1-xS nanoparticles rapidly reduces as more and more copper sulfide is added.

  5. Vibrational Dynamics and Thermodynamics of AgCu nanoparticles

    NASA Astrophysics Data System (ADS)

    Kara, Abdelkader; Yildirim, Handan; Rahman, Talat S.; Ferrando, Ricardo

    2006-03-01

    We present results of a systematic study of the structure, vibrational dynamics and thermodynamics of AgnCu34-n nanoparticles including. The starting structure were generated using a structural optimization using a genetic algorithm [1]. Using the embedded atom method potentials, we have calculated the vibrational densities of states for all stoichiometries and the corresponding vibrational free energies, in the harmonic approximations. At 300K, the vibrational free energy is found to behave linearly with the increasing number of Ag atoms in the nanoparticles. The vibrational contributions to the free energy increase from 5.5% for Ag0Cu34 to 8.3% Ag34Cu0. Selected force constants for several nanoparticles were calculated using density functional theory (DFT) and were found to be very close to those determined using EAM potentials. [1] G. Rossi, A. Rapallo, C. Mottet, A. Fortunelli, F. Baletto and R. Ferrando Phys. Rev. Lett, 93, 105503 (2004)

  6. Collagen-chitosan scaffold modified with Au and Ag nanoparticles: Synthesis and structure

    NASA Astrophysics Data System (ADS)

    Rubina, M. S.; Kamitov, E. E.; Zubavichus, Ya. V.; Peters, G. S.; Naumkin, A. V.; Suzer, S.; Vasil'kov, A. Yu.

    2016-03-01

    Nowadays, the dermal biomimetic scaffolds are widely used in regenerative medicine. Collagen-chitosan scaffold one of these materials possesses antibacterial activity, good compatibility with living tissues and has been already used as a wound-healing material. In this article, collagen-chitosan scaffolds modified with Ag and Au nanoparticles have been synthesized using novel method - the metal-vapor synthesis. The nanocomposite materials are characterized by XPS, TEM, SEM and synchrotron radiation-based X-ray techniques. According to XRD data, the mean size of the nanoparticles (NPs) is 10.5 nm and 20.2 nm in Au-Collagen-Chitosan (Au-CollCh) and Ag-Collagen-Chitosan (Ag-CollCh) scaffolds, respectively in fair agreement with the TEM data. SAXS analysis of the composites reveals an asymmetric size distribution peaked at 10 nm for Au-CollCh and 25 nm for Ag-CollCh indicative of particle's aggregation. According to SEM data, the metal-carrying scaffolds have layered structure and the nanoparticles are rather uniformly distributed on the surface material. XPS data indicate that the metallic nanoparticles are in their unoxidized/neutral states and dominantly stabilized within the chitosan-rich domains.

  7. Magnetic properties of Co/Ag core/shell nanoparticles prepared by successive reactions in microemulsions

    NASA Astrophysics Data System (ADS)

    Rivas, J.; Garcia-Bastida, A. J.; Lopez-Quintela, M. A.; Ramos, C.

    2006-05-01

    Co nanoparticles with an Ag covering layer have been prepared by successive reactions in microemulsions. Their magnetic behavior was studied as a function of heat treatment. It was confirmed that, under the experimental conditions of this study, the size of the Co nuclei is limited by the reactant concentration, whereas the Ag covering is fixed by microemulsion droplet size. The as-prepared particles contain mainly Co 3O 4 nuclei, and present high effective moments that agree with the spin state of Co 3+. The observed magnetic behaviors were explained taking into account the intra- and inter-particle structural evolution of the particle assemblies annealed under different experimental conditions.

  8. Spectroscopic Study on Eu3+ Doped Borate Glasses Containing Ag Nanoparticles and Ag Aggregates.

    PubMed

    Fu, Shaobo; Zheng, Hui; Zhang, Jinsu; Li, Xiangping; Sun, Jiashi; Hua, Ruinian; Dong, Bin; Xia, Haiping; Chen, Baojiu

    2015-01-01

    Transparent Eu(3+)-doped borate glasses containing Ag nanoparticles and Ag aggregates with composition (40 - x) CaO-59.5B2O3-0.5Eu2O3-xAgNO3 were prepared by a simple one-step melt-quenching technique. The X-ray diffraction (XRD) patterns of the glasses reveal amorphous structural properties and no diffraction peaks belonging to metal Ag particles. Ag particles and Ag aggregates were observed from the absorption spectra. Effective energy transfers from the Ag aggregates to the Eu3+ ions were observed in the excitation spectra from monitoring the intrinsic emission of Eu3+x .5D0 --> 7F2. The glasses with higher Ag content can be effectively excited by light in a wide wavelength region, indicating that these glasses have potential application in the solid state lighting driven by semiconductor light emitting diodes (LEDs). The emission spectra of the samples with higher Ag contents exhibit plenteous spectral components covering the full visible region from violet to red, thus indicating that these glass materials possess an excellent and tunable color rendering index. The color coordinates for all the glass samples were calculated by using the intensity-corrected emission spectra and the standard data issued by the CIE (Commission International de l' Eclairage) in 1931. It was found that the color coordinates for most samples with higher Ag contents fall into the white region in the color space. PMID:26328363

  9. Enhanced formation of silver nanoparticles in Ag+-NOM-iron(II, III) systems and antibacterial activity studies.

    PubMed

    Adegboyega, Nathaniel F; Sharma, Virender K; Siskova, Karolina M; Vecerova, Renata; Kolar, Milan; Zbořil, Radek; Gardea-Torresdey, Jorge L

    2014-03-18

    This work reports the role of iron redox pair (Fe(3+)/Fe(2+)) in the formation of naturally occurring silver nanoparticles (AgNPs) in the aquatic environment. The results showed that Fe(3+) or Fe(2+) ions in the mixtures of Ag(+) and natural organic matter enhanced the formation of AgNPs. The formation of AgNPs depended on pH and types of organic matter. Increase in pH enhanced the formation of AgNPs, and humic acids as ligands showed higher formation of AgNPs compared to fulvic acids. The observed results were described by considering the potentials of redox pairs of silver and iron species and the possible species involved in reducing silver ions to AgNPs. Dynamic light scattering and transmission electron microscopy measurements of AgNPs revealed mostly bimodal size distribution with decrease in size of AgNPs due to iron species in the reaction mixture. Minimum inhibitory concentration of AgNPs needed to inhibit the growth of various bacterial species suggested the role of surfaces of tested Gram-positive and Gram-negative bacteria. Stability study of AgNPs, formed in Ag(+)-humic acid/fulvic acids-Fe(3+) mixtures over a period of several months showed high stability of the particles with significant increase in surface plasmon resonance peak. The environmental implications of the results in terms of fate, transport, and ecotoxicity of organic-coated AgNPs are briefly presented. PMID:24524189

  10. Effects of silver and gold nanoparticles of different sizes in human pulmonary fibroblasts.

    PubMed

    Ávalos, Alicia; Haza, Ana Isabel; Mateo, Diego; Morales, Paloma

    2015-01-01

    Silver and gold nanoparticles (Ag-AuNPs) are currently some of the most manufactured nanomaterials. Accordingly, the hazards associated with human exposure to Ag-AuNPs should be investigated to facilitate the risk assessment process. In particular, because pulmonary exposure to Ag-AuNPs occurs during handling of these nanoparticles, it is necessary to evaluate the toxic response in pulmonary cells. The aim of this study was to evaluate the in vitro mechanisms of toxicity of different sizes of silver (4.7 and 42 nm) and gold nanoparticles (30, 50 and 90 nm) in human pulmonary fibroblasts (HPF). The toxicity was evaluated by observing cell viability and oxidative stress parameters. Data showed that AgNPs-induced cytotoxicity was size-dependent, whereas the AuNPs of the three sizes showed similar cytotoxicity. Silver nanoparticles of 4.7 nm were much more toxic than the large silver nanoparticles and the AuNPs. However, the pre-treatment with the antioxidant, N-acetyl-L-cysteine, protected HPF cells against treatment with Ag-AuNPs. The oxidative stress parameters revealed significant increase in reactive oxygen species levels, depletion of glutathione level and slight, but not statistically significant inactivation of superoxide dismutase, suggesting generation of oxidative stress. Hence, care has to be taken while processing and formulating the Ag-AuNPs till their final finished product.

  11. Chemical and phase distributions in a multilayered organic matter-Ag nanoparticle thin film system

    NASA Astrophysics Data System (ADS)

    Michel, F. M.; Levard, C.; Wang, Y.; Choi, Y.; Eng, P.; Brown, G. E.

    2010-12-01

    Rapid development of nanotechnologies raises concern regarding the environmental impact of nanoparticles on ecosystems. Among the types of nanoparticles currently in production, metallic silver is the most widely used in nanotechnology (1). Synthetic Ag nanoparticles (Ag-NPs) are most often used for their antimicrobial and antifungal properties that are, in part, explained by the release of highly toxic Ag+ species (2). While such properties are desirable in certain applied cases, the release of Ag-NPs and soluble Ag+ species to the environment is expected to impact biota as well as soil and water quality (3). With the production of Ag-NPs projected to increase (1), the amount of Ag-NPs that will be released to the environment through waste streams is also likely to increase. As such, a deeper understanding of the fundamental processes associated with Ag-NPs toxicity and reactivity is needed to evaluate their impact on the environment. We have studied the interaction during aging of poly-acrylic acid (PAA) and Ag-NPs with average particle sizes of 20 ±5 nm. The sample studied was composed of thin films of PAA and Ag-NPs deposited on a Si-wafer support. PAA served as a model compound and a simplified surrogate for exopolysaccharide, an organic substance produced through metabolic activity by most microorganisms. We applied a novel combination of long-period x-ray standing wave fluorescence yield (XSW-FY) spectroscopy, grazing-incidence x-ray diffraction (GI-XRD), and XRD-based standing wave profiles (XSW-XRD) to obtain chemical- and phase-specific information on this sample. After 24 hours, we observed the formation of AgCl(s) in the PAA film of the sample, which suggests oxidation and dissolution of a portion of the Ag-NPs during aging, resulting in the release of Ag+. In addition, we see partitioning of Cl and Br, both present initially in the PAA, to the intact Ag-NPs thin film. To our knowledge, this is the first application of this suite of techniques to this

  12. Synthesis and anti-bacterial activity of Cu, Ag and Cu-Ag alloy nanoparticles: A green approach

    SciTech Connect

    Valodkar, Mayur; Modi, Shefaly; Pal, Angshuman; Thakore, Sonal

    2011-03-15

    Research highlights: {yields} Synthesis of novel nanosized copper-silver alloys of different compositions. {yields} Completely green approach for synthesis of water soluble bimetallic nanoparticle. {yields} Interesting anti-bacterial activity of as synthesized metal and alloy nanoparticle. -- Abstract: Metallic and bimetallic nanoparticles of copper and silver in various proportions were prepared by microwave assisted chemical reduction in aqueous medium using the biopolymer, starch as a stabilizing agent. Ascorbic acid was used as the reducing agent. The silver and copper nanoparticles exhibited surface plasmon absorption resonance maxima (SPR) at 416 and 584 nm, respectively; while SPR for the Cu-Ag alloys appeared in between depending on the alloy composition. The SPR maxima for bimetallic nanoparticles changes linearly with increasing copper content in the alloy. Transmission electron micrograph (TEM) showed monodispersed particles in the range of 20 {+-} 5 nm size. Both silver and copper nanoparticles exhibited emission band at 485 and 645 nm, respectively. The starch-stabilized nanoparticles exhibited interesting antibacterial activity with both gram positive and gram negative bacteria at micromolar concentrations.

  13. Stability of Ag nanoparticles dispersed in amphiphilic organic matrix

    NASA Astrophysics Data System (ADS)

    Suvorova, Elena I.; Klechkovskaya, Vera V.; Kopeikin, Victor V.; Buffat, Philippe A.

    2005-02-01

    Nano- and thin-film technologies based on novel systems associating metals particles to polymer matrix open a broad range of different applications. Such composites were found to be more efficient and safe, for instance, in biomedical needs. The Ag/poly(N-vinyl-2-pyrrolidone) (Ag/PVP) composite investigated in the present work is a new bactericide mean applied in complicated cases of infected burns and purulent wounds. High-resolution transmission electron microscopy (HRTEM) and X-ray energy-dispersive (EDS) microanalysis were used to bring chemical and structural information in a study of the properties and stability of thin-film nanocomposite whih consisted of Ag nanoparticles dispersed in water-soluble organic matrix poly(N-vinyl-2-pyrrolidone). The nanostructural investigation of Ag/PVP composite by HRTEM and EDS exposed to SO 2 and H 2S from the atmosphere and some traces of S-containing substances explains the limited stability of this system by a structural modification associated with a phase change and formation of Ag 2S and Ag 2SO 3. However, formation of the hardly water-soluble Ag 2S and Ag 2SO 3 salts may play an important role in the suppression of bacterial growth. On the one hand, silver could block S-H groups in vital proteins and conduced to their destruction, in that way revealing the antibacterial power. On the other hand, antiseptic properties of Ag consist in binding the products of the protein decay.

  14. In situ nanoparticle sizing with zeptomole sensitivity.

    PubMed

    Batchelor-McAuley, Christopher; Ellison, Joanna; Tschulik, Kristina; Hurst, Philip L; Boldt, Regine; Compton, Richard G

    2015-08-01

    We present the basis for an entirely new approach to in situ nanoparticle sizing. Nanoparticles containing just 12 zeptomoles (1 zeptomole = 10(-21) moles) of silver, are detected via in situ particle coulometry. These stochastic charge measurements correspond to the transfer of only 7000-8000 electrons, yielding direct information relating to the individual nanoparticle volumes. The resulting particle size distribution (average equivalent radius 5 nm) obtained via nanoparticle coulometry is in excellent correspondence with that attained from TEM analysis. Moreover, the measurable particle size limit by this electrochemical method is shown to be significantly below that of more common optical nanoparticle tracking techniques, and as such can be viewed as a potential disruptive nano-technology.

  15. Ag nanoparticle dispersed PbTiO3 percolative composite thin film with high permittivity

    NASA Astrophysics Data System (ADS)

    Wang, Zongrong; Hu, Tao; Tang, Liwen; Ma, Ning; Song, Chenlu; Han, Gaorong; Weng, Wenjian; Du, Piyi

    2008-12-01

    Ag nanoparticle dispersed PbTiO3 percolative composite thin films were prepared in situ by sol-gel method using Pb(NO3)2, Ti(C4H9O)4, and AgNO3 as raw materials and lactic acid along with citric acid as complexing agent. The size of the Ag nanoparticles measured by ultraviolet-visible spectra is about 3nm. The percolation effect occurs in composite thin films. The composite exhibits relatively high dielectric constant which is about five times higher than that of PbTiO3 thin film and comparatively low dielectric loss comparable to pure PbTiO3 system. It is highly attractive in application of high quality dielectric devices and miniaturization.

  16. An extracellular enzyme synthesizes narrow-sized silver nanoparticles in both water and methanol

    NASA Astrophysics Data System (ADS)

    Rai, Tripti; Panda, Debashis

    2015-03-01

    Cellulase reduces silver ions in both aqueous and methanolic media yielding stable narrow-sized silver nanoparticles (Ag-NP) at room temperature. The synthesized nanoparticles have been characterized by various spectroscopic, microscopic methods. The redox potentials of tyrosine residues and protein backbone play an instrumental role to reduce the metal ions. The average size of nanoparticles formed in aqueous medium is of 5.04 ± 3.50 nm. Post-synthesis of Ag-NP secondary structure of enzyme is completely lost whereas upon incubation with chemically synthesized Ag-NP a significant gain in secondary structure is observed. Cellulase as a capping ligand stabilizes the silver nanoparticles even in methanol.

  17. Trimetallic nanostructures: the case of AgPd/Pt multiply twinned nanoparticles

    PubMed Central

    Khanal, Subarna; Bhattarai, Nabraj; Velázquez-Salazar, J. Jesús; Bahena, Daniel; Soldano, German; Ponce, Arturo; Mariscal, Marcelo M.; Mejía-Rosales, Sergio; José-Yacamán, Miguel

    2013-01-01

    We report the synthesis, structural characterization, and atomistic simulations of AgPd/Pt trimetallic (TM) nanoparticles. Two types of structure were synthesized using a relatively facile chemical method: multiply twinned core-shell, and hollow particles. The nanoparticles were small in size, with an average diameter of 11 nm and a narrow distribution, and their characterization by aberration corrected scanning transmission electron microscopy allowed us to probe the structure of the particles at atomistic level. In some nanoparticles, the formation of a hollow structure was also observed, that facilitates the alloying of Ag and Pt in the shell region and the segregation of Ag atoms in the surface, affecting the catalytic activity and stability. We also investigated the growth mechanism of the nanoparticles using grand canonical Monte Carlo simulations, and we have found that Pt regions grow at overpotentials on the AgPd nanoalloys, forming 3D islands at the early stages of the deposition process. We found very good agreement between the simulated structures and those observed experimentally. PMID:24165796

  18. Polyvinyl alcohol electrospun nanofibers containing Ag nanoparticles used as sensors for the detection of biogenic amines.

    PubMed

    Marega, Carla; Maculan, Jenny; Andrea Rizzi, Gian; Saini, Roberta; Cavaliere, Emanuele; Gavioli, Luca; Cattelan, Mattia; Giallongo, Giuseppe; Marigo, Antonio; Granozzi, Gaetano

    2015-02-20

    Polyvinyl alcohol (PVA) electrospun nanofibers containing Ag nanoparticles (NPs) have been deposited on glass substrates. The aim of the work was to test the feasibility of this approach for the detection of biogenic amines by using either the Ag localized surface plasmon resonance quenching caused by the adsorption of amines on Ag NPs or by detecting the amines by surface enhanced Raman spectroscopy (SERS) after adsorption, from the gas phase, on the metal NPs. Two different approaches have been adopted. In the first one an ethanol/water solution containing AgNO3 was used directly in the electrospinning apparatus. In this way, a simple heat treatment of the nanofibers mat was sufficient to obtain the formation of Ag NPs inside the nanofibers and a partial cross-link of PVA. In the second procedure, the Ag NPs were deposited on PVA nanofibers by using the supersonic cluster beam deposition method, so that a beam of pure Ag NPs of controlled size was obtained. Exposure of the PVA mat to the beam produced a uniform distribution of the NPs on the nanofibers surface. Ethylendiamine vapors and volatile amines released from fresh shrimp meat were chemisorbed on the nanofibers mats. A SERS spectrum characterized by a diagnostic Ag-N stretching vibration at 230 cm(-1) was obtained. The results allow to compare the two different approaches in the detection of ammines.

  19. Ag nanoparticles generated using bio-reduction and -coating cause microbial killing without cell lysis.

    PubMed

    Gade, Aniket; Adams, Joshua; Britt, David W; Shen, Fen-Ann; McLean, Joan E; Jacobson, Astrid; Kim, Young-Cheol; Anderson, Anne J

    2016-04-01

    Cost-effective "green" methods of producing Ag nanoparticles (NPs) are being examined because of the potential of these NPs as antimicrobials. Ag NPs were generated from Ag ions using extracellular metabolites from a soil-borne Pythium species. The NPs were variable in size, but had one dimension less than 50 nm and were biocoated; aggregation and coating changed with acetone precipitation. They had dose-dependent lethal effects on a soil pseudomonad, Pseudomonas chlororaphis O6, and were about 30-fold more effective than Ag(+) ions. A role of reactive oxygen species in cell death was demonstrated by use of fluorescent dyes responsive to superoxide anion and peroxide accumulation. Also mutants of the pseudomonad, defective in enzymes that protect against oxidative stress, were more sensitive than the wild type strain; mutant sensitivity differed between exposure to Ag NPs and Ag(+) ions demonstrating a nano-effect. Imaging of bacterial cells treated with the biocoated Ag NPs revealed no cell lysis, but there were changes in surface properties and cell height. These findings support that biocoating the NPs results in limited Ag release and yet they retained potent antimicrobial activity. PMID:26805711

  20. Polyvinyl alcohol electrospun nanofibers containing Ag nanoparticles used as sensors for the detection of biogenic amines

    NASA Astrophysics Data System (ADS)

    Marega, Carla; Maculan, Jenny; Rizzi, Gian Andrea; Saini, Roberta; Cavaliere, Emanuele; Gavioli, Luca; Cattelan, Mattia; Giallongo, Giuseppe; Marigo, Antonio; Granozzi, Gaetano

    2015-02-01

    Polyvinyl alcohol (PVA) electrospun nanofibers containing Ag nanoparticles (NPs) have been deposited on glass substrates. The aim of the work was to test the feasibility of this approach for the detection of biogenic amines by using either the Ag localized surface plasmon resonance quenching caused by the adsorption of amines on Ag NPs or by detecting the amines by surface enhanced Raman spectroscopy (SERS) after adsorption, from the gas phase, on the metal NPs. Two different approaches have been adopted. In the first one an ethanol/water solution containing AgNO3 was used directly in the electrospinning apparatus. In this way, a simple heat treatment of the nanofibers mat was sufficient to obtain the formation of Ag NPs inside the nanofibers and a partial cross-link of PVA. In the second procedure, the Ag NPs were deposited on PVA nanofibers by using the supersonic cluster beam deposition method, so that a beam of pure Ag NPs of controlled size was obtained. Exposure of the PVA mat to the beam produced a uniform distribution of the NPs on the nanofibers surface. Ethylendiamine vapors and volatile amines released from fresh shrimp meat were chemisorbed on the nanofibers mats. A SERS spectrum characterized by a diagnostic Ag-N stretching vibration at 230 cm-1 was obtained. The results allow to compare the two different approaches in the detection of ammines.

  1. Green synthesis, characterization, photocatalytic, fluorescence and antimicrobial activities of Cochlospermum gossypium capped Ag2S nanoparticles.

    PubMed

    Ayodhya, Dasari; Veerabhadram, Guttena

    2016-04-01

    The study describes a simple and green method for the synthesis of silver sulfide nanoparticles (Ag2S NPs) using gum kondagogu (Cochlospermum gossypium) (GK). The synthesized NPs were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), fluorescence, UV-vis absorption, zeta potential and thermogravimetric analysis (TGA) techniques. The optical properties and quantum confinement effect of the products were confirmed by means of spectroscopic measurements. The morphologies and sizes were characterized by SEM and TEM. The Ag2S NPs were spherical in shape with an effective diameter size of 25 nm. The photocatalytic property of Ag2S NPs was evaluated by the degradation of fluorescein (FL) dye under solar light. The effect of Ag2SNPs on the photocatalytic degradation of FL dye and influence of other parameters such as Ag2S loading, H2O2, temperature and under solar light irradiation was also evaluated. The degradation reaction follows the pseudo-first order kinetics. The apparent reaction rate was used to calculate the apparent activation energy (Ea=13.95 kJ/mol) of the degradation process. The activation thermodynamic parameters (ΔG*, ΔH* and ΔS*) were obtained from variable temperature kinetic studies. The interaction between Ag2S NPs and bovine serum albumin (BSA) was studied by using fluorescence spectroscopic measurements. The synthesized Ag2S NPs were showing good antimicrobial activity.

  2. Resonant surface enhancement of Raman scattering of Ag nanoparticles on silicon substrates fabricated by dc sputtering

    SciTech Connect

    Fang Yingcui; Li Xiaxi; Blinn, Kevin; Mahmoud, Mahmoud A.; Liu Meilin

    2012-09-15

    Ag nanoparticles (AgNPs) were deposited onto silicon substrates by direct current (dc) magnetron sputtering. The influences of sputtering power and sputtering time on the AgNP film morphology were studied using atomic force microscopy. The particle size was successfully tuned from 19 nm to 53 nm by varying the sputtering time at a dc power of 10 W. When Rhodamine 6 G (R6G) was used as the probe molecule, the AgNP films showed significant surface enhanced Raman scattering effect. In particular, it is found that larger particles show stronger enhancement for lower concentrations of R6G while smaller particles display stronger enhancement for higher concentrations of R6G.

  3. Purification of Nanoparticles by Size and Shape

    PubMed Central

    Robertson, James D.; Rizzello, Loris; Avila-Olias, Milagros; Gaitzsch, Jens; Contini, Claudia; Magoń, Monika S.; Renshaw, Stephen A.; Battaglia, Giuseppe

    2016-01-01

    Producing monodisperse nanoparticles is essential to ensure consistency in biological experiments and to enable a smooth translation into the clinic. Purification of samples into discrete sizes and shapes may not only improve sample quality, but also provide us with the tools to understand which physical properties of nanoparticles are beneficial for a drug delivery vector. In this study, using polymersomes as a model system, we explore four techniques for purifying pre-formed nanoparticles into discrete fractions based on their size, shape or density. We show that these techniques can successfully separate polymersomes into monodisperse fractions. PMID:27271538

  4. Purification of Nanoparticles by Size and Shape

    NASA Astrophysics Data System (ADS)

    Robertson, James D.; Rizzello, Loris; Avila-Olias, Milagros; Gaitzsch, Jens; Contini, Claudia; Magoń, Monika S.; Renshaw, Stephen A.; Battaglia, Giuseppe

    2016-06-01

    Producing monodisperse nanoparticles is essential to ensure consistency in biological experiments and to enable a smooth translation into the clinic. Purification of samples into discrete sizes and shapes may not only improve sample quality, but also provide us with the tools to understand which physical properties of nanoparticles are beneficial for a drug delivery vector. In this study, using polymersomes as a model system, we explore four techniques for purifying pre-formed nanoparticles into discrete fractions based on their size, shape or density. We show that these techniques can successfully separate polymersomes into monodisperse fractions.

  5. Large 2D-arrays of size-controllable silver nanoparticles prepared by hybrid deposition

    NASA Astrophysics Data System (ADS)

    Dieu Thuy Ung, Thi; Hoa Nguyen, Thi; Liem Nguyen, Quang

    2016-09-01

    Two main results are presented in this paper. (i) Silver nanoparticles (AgNPs) with uniform size-distribution and controllability in the range of 20-50 nm were synthesized by seeding and growing at ambient conditions. The single-crystal Ag nano-seeds were created by reduction of AgNO3 in presence of citrate surfactant at 70 °C. Then, importantly, the fresh AgCl precursor was used in the presence of polyvinylpyrrolidone to adjust the reaction rate with ascorbic acid to generate Ag for growing on the surface of single-crystal Ag nano-seeds. The AgNPs size could be well-controlled by varying the amount of Ag nano-seeds while keeping the AgCl precursor concentration to be constant. (ii) The large 2D-arrays with homogeneous and dense monolayers of AgNPs were prepared on ITO substrates by hybrid method, in which the key technological point is the surface functionalization of AgNPs using mixed alkanethiols (dodecanethiol:octadecanethiol = 6:1). We have used the fabricated 2D-arrays from the 50 nm AgNPs as a surface enhanced Raman scattering substrate to take the Raman scattering spectra of rhodamine B (RhB), glucose and viral pathogen (H5N1) at very low concentrations of 10-10 M, 10-12 M and 4 ng μl-1, respectively.

  6. Large 2D-arrays of size-controllable silver nanoparticles prepared by hybrid deposition

    NASA Astrophysics Data System (ADS)

    Dieu Thuy Ung, Thi; Hoa Nguyen, Thi; Liem Nguyen, Quang

    2016-09-01

    Two main results are presented in this paper. (i) Silver nanoparticles (AgNPs) with uniform size-distribution and controllability in the range of 20–50 nm were synthesized by seeding and growing at ambient conditions. The single-crystal Ag nano-seeds were created by reduction of AgNO3 in presence of citrate surfactant at 70 °C. Then, importantly, the fresh AgCl precursor was used in the presence of polyvinylpyrrolidone to adjust the reaction rate with ascorbic acid to generate Ag for growing on the surface of single-crystal Ag nano-seeds. The AgNPs size could be well-controlled by varying the amount of Ag nano-seeds while keeping the AgCl precursor concentration to be constant. (ii) The large 2D-arrays with homogeneous and dense monolayers of AgNPs were prepared on ITO substrates by hybrid method, in which the key technological point is the surface functionalization of AgNPs using mixed alkanethiols (dodecanethiol:octadecanethiol = 6:1). We have used the fabricated 2D-arrays from the 50 nm AgNPs as a surface enhanced Raman scattering substrate to take the Raman scattering spectra of rhodamine B (RhB), glucose and viral pathogen (H5N1) at very low concentrations of 10‑10 M, 10‑12 M and 4 ng μl‑1, respectively.

  7. Energetics of the formation of Cu-Ag core–shell nanoparticles

    DOE PAGES

    Chandross, Michael

    2014-10-06

    Our work presents molecular dynamics and Monte Carlo simulations aimed at developing an understanding of the formation of core–shell Cu-Ag nanoparticles. The effects of surface and interfacial energies were considered and used to form a phenomenological model that calculates the energy gained upon the formation of a core–shell structure from two previously distinct, non-interacting nanoparticles. In most cases, the core–shell structure was found to be energetically favored. Specifically, the difference in energy as a function of the radii of the individual Cu and Ag particles was examined, with the assumption that a core–shell structure forms. In general, it was foundmore » that the energetic gain from forming such a structure increased with increasing size of the initial Ag particle. This result was interpreted as a result of the reduction in surface energy. Moreover, for two separate particles, both Cu and Ag contribute to the surface energy; however, for a core–shell structure, the only contribution to the surface energy is from the Ag shell and the Cu contribution is changed to a Cu–Ag interfacial energy, which is always smaller.« less

  8. Energetics of the formation of Cu-Ag core–shell nanoparticles

    SciTech Connect

    Chandross, Michael

    2014-10-06

    Our work presents molecular dynamics and Monte Carlo simulations aimed at developing an understanding of the formation of core–shell Cu-Ag nanoparticles. The effects of surface and interfacial energies were considered and used to form a phenomenological model that calculates the energy gained upon the formation of a core–shell structure from two previously distinct, non-interacting nanoparticles. In most cases, the core–shell structure was found to be energetically favored. Specifically, the difference in energy as a function of the radii of the individual Cu and Ag particles was examined, with the assumption that a core–shell structure forms. In general, it was found that the energetic gain from forming such a structure increased with increasing size of the initial Ag particle. This result was interpreted as a result of the reduction in surface energy. Moreover, for two separate particles, both Cu and Ag contribute to the surface energy; however, for a core–shell structure, the only contribution to the surface energy is from the Ag shell and the Cu contribution is changed to a Cu–Ag interfacial energy, which is always smaller.

  9. Facile synthesis of near-monodisperse Ag@Ni core-shell nanoparticles and their application for catalytic generation of hydrogen.

    PubMed

    Guo, Huizhang; Chen, Yuanzhi; Chen, Xiaozhen; Wen, Ruitao; Yue, Guang-Hui; Peng, Dong-Liang

    2011-05-13

    Magnetically recyclable Ag-Ni core-shell nanoparticles have been fabricated via a simple one-pot synthetic route using oleylamine both as solvent and reducing agent and triphenylphosphine as a surfactant. As characterized by transmission electron microscopy (TEM), the as-synthesized Ag-Ni core-shell nanoparticles exhibit a very narrow size distribution with a typical size of 14.9 ± 1.2 nm and a tunable shell thickness. UV-vis absorption spectroscopy study shows that the formation of a Ni shell on Ag core can damp the surface plasmon resonance (SPR) of the Ag core and lead to a red-shifted SPR absorption peak. Magnetic measurement indicates that all the as-synthesized Ag-Ni core-shell nanoparticles are superparamagnetic at room temperature, and their blocking temperatures can be controlled by modulating the shell thickness. The as-synthesized Ag-Ni core-shell nanoparticles exhibit excellent catalytic properties for the generation of H(2) from dehydrogenation of sodium borohydride in aqueous solutions. The hydrogen generation rate of Ag-Ni core-shell nanoparticles is found to be much higher than that of Ag and Ni nanoparticles of a similar size, and the calculated activation energy for hydrogen generation is lower than that of many bimetallic catalysts. The strategy employed here can also be extended to other noble-magnetic metal systems.

  10. Growth and characterization of ZnO multipods on functional surfaces with different sizes and shapes of Ag particles

    NASA Astrophysics Data System (ADS)

    A, Kamalianfar; S, A. Halim; Mahmoud Godarz, Naseri; M, Navasery; Fasih, Ud Din; J, A. M. Zahedi; Kasra, Behzad; K, P. Lim; A Lavari, Monghadam; S, K. Chen

    2013-08-01

    Three-dimensional ZnO multipods are successfully synthesized on functional substrates using the vapor transport method in a quartz tube. The functional surfaces, which include two different distributions of Ag nanoparticles and a layer of commercial Ag nanowires, are coated onto silicon substrates before the growth of ZnO nanostructures. The structures and morphologies of the ZnO/Ag heterostructures are investigated using X-ray diffraction and field emission scanning electron microscopy. The sizes and shapes of the Ag particles affect the growth rates and initial nucleations of the ZnO structures, resulting in different numbers and shapes of multipods. They also influence the orientation and growth quality of the rods. The optical properties are studied by photoluminescence, UV-vis, and Raman spectroscopy. The results indicate that the surface plasmon resonance strongly depends on the sizes and shapes of the Ag particles.

  11. Synthesis and thermal behavior of tin-based alloy (Sn-Ag-Cu) nanoparticles.

    PubMed

    Roshanghias, Ali; Yakymovych, Andriy; Bernardi, Johannes; Ipser, Herbert

    2015-03-19

    The prominent melting point depression of nanoparticles has been the subject of a considerable amount of research. For their promising applications in electronics, tin-based nano-alloys such as near-eutectic Sn-Ag-Cu (SAC) alloys have been synthesized via various techniques. However, due to issues such as particle aggregation and oxidation or introduced impurities, the application of these nano-size particles has been confined or aborted. For instance, thermal investigations by DTA/DSC in a large number of studies revealed exothermic peaks in the range of 240-500 °C, i.e. above the melting point of SAC nanoparticles, with different and quite controversial explanations for this unclear phenomenon. This represents a considerable drawback for the application of nanoparticles. Correspondingly, in the current study, the thermal stability of SAC nanoparticles has been investigated via electron microscopy, XRD, FTIR, and DSC/TG analysis. It was found that the nanoparticles consist mainly of a metallic β-Sn core and an amorphous tin hydroxide shell structure. The SnO crystalline phase formation from this amorphous shell has been associated with the exothermic peaks on the first heating cycle of the nanoparticles, followed by a disproportionation reaction into metallic Sn and SnO₂.The results also revealed that the surfactant and reducing agent cannot only affect the size and size distribution of the nanoparticles, they might also alter the ratio between the amorphous shell and the crystalline core in the structure of particles. PMID:25757694

  12. Size controlled biogenic silver nanoparticles as antibacterial agent against isolates from HIV infected patients.

    PubMed

    Suganya, K S Uma; Govindaraju, K; Kumar, V Ganesh; Dhas, T Stalin; Karthick, V; Singaravelu, G; Elanchezhiyan, M

    2015-06-01

    Silver nanoparticles (AgNPs) are synthesized using biological sources due to its high specificity in biomedical applications. Herein, we report the size and shape controlled synthesis of AgNPs using the aqueous extract of blue green alga, Spirulina platensis. Size, shape and elemental composition of AgNPs were characterized using UV-vis spectroscopy, Fluorescence spectroscopy, FT-IR (Fourier Transform-Infrared Spectroscopy), FT-RS (Fourier Transform-Raman Spectroscopy), SEM-EDAX (Scanning Electron Microscopy-Energy Dispersive X-ray analysis) and HR-TEM (High Resolution Transmission Electron Microscopy). AgNPs were stable, well defined and monodispersed (spherical) with an average size of 6 nm. The synthesized AgNPs were tested for its antibacterial potency against isolates obtained from HIV patients. PMID:25769122

  13. Catalytic Properties of AgPt Nanoshells as a Function of Size: Larger Outer Diameters Lead to Improved Performances.

    PubMed

    Rodrigues, Thenner S; da Silva, Anderson G M; Gonçalves, Mariana C; Fajardo, Humberto V; Balzer, Rosana; Probst, Luiz F D; da Silva, Alisson H M; Assaf, Jose M; Camargo, Pedro H C

    2016-09-13

    We report herein a systematic investigation on the effect of the size of silver (Ag) nanoparticles employed as starting materials over the morphological features and catalytic performances of AgPt nanoshells produced by a combination of galvanic replacement between Ag and PtCl6(2-) and PtCl6(2-) reduction by hydroquinone. More specifically, we focused on Ag nanoparticles of four different sizes as starting materials, and found that the outer diameter, shell thickness, and the number of Pt surface atoms of the produced nanoshells increased with the size of the starting Ag nanoparticles. The produced AgPt nanoshells were supported into SiO2, and the catalytic performances of the AgPt/SiO2 nanocatalysts toward the gas-phase oxidation of benzene, toluene, and o-xylene (BTX oxidation) followed the order: AgPt 163 nm/SiO2 > AgPt 133 nm/SiO2 > AgPt 105 nm/SiO2 > AgPt 95 nm/SiO2. Interestingly, bigger AgPt nanoshell sizes lead to better catalytic performances in contrast to the intuitive prediction that particles having larger outer diameters tend to present poorer catalytic activities due to their lower surface to volume ratios as compared to smaller particles. This is in agreement with the H2 chemisorption results, and can be assigned to the increase in the Pt surface area with size due to the presence of smaller NPs islands at the surface of the nanoshells having larger outer diameters. This result indicates that, in addition to the overall diameters, the optimization of the surface morphology may play an important role over the optimization of catalytic activities in metal-based nanocatalysts, which can be even more pronounced that the size effect. Our data demonstrate that the control over surface morphology play a very important role relative to the effect of size to the optimization of catalytic performances in catalysts based on noble-metal nanostructures. PMID:27556904

  14. Effective medium analysis of thermally evaporated Ag nanoparticle films for plasmonic enhancement in organic solar cell

    NASA Astrophysics Data System (ADS)

    Haidari, Gholamhosain; Hajimahmoodzadeh, Morteza; Fallah, Hamid Reza; Varnamkhasti, Mohsen Ghasemi

    2015-09-01

    Films of silver nanoparticles have optical properties that are useful for applications such as plasmonic light trapping in solar cells. We report on the simple fabrication of Ag nanoparticle films via thermal evaporation, with and without subsequent annealing. These films result in a random array of particles of various shapes and sizes. The modeling of such a vast collection of particles is still beyond reach of the modern computers. We show that it is possible to represent the silver island films by the Bergman effective mediums with the same optical properties. The effective medium method provides us with deep insight about the shape, the size and the distribution of nanoparticles. The far field simulations of solar cells, in which the silver island film is replaced with an effective medium layer, show a reduction in the absorption of active layer. Besides, the near field simulations based on finite-difference time-domain technique demonstrate that the near field effects on active layer absorption are negligible and this method highlights the importance of nanoparticles shapes. The PCPDTBT:PCBM solar cells with embedded silver island films are fabricated, and it is found that their performances show the similar trend. This insight can be used for the optical analysis of thermally evaporated Ag nanoparticle films for the improvement of organic solar cells.

  15. Effect of cysteine and humic acids on bioavailability of Ag from Ag nanoparticles to a freshwater snail

    USGS Publications Warehouse

    Luoma, Samuel N.; Tasha Stoiber,; Croteau, Marie-Noele; Isabelle Romer,; Ruth Merrifeild,; Jamie Lead,

    2016-01-01

    Metal-based engineered nanoparticles (NPs) will undergo transformations that will affect their bioavailability, toxicity and ecological risk when released to the environment, including interactions with dissolved organic material. The purpose of this paper is to determine how interactions with two different types of organic material affect the bioavailability of silver nanoparticles (AgNPs). Silver uptake rates by the pond snail Lymnaea stagnalis were determined after exposure to 25 nmol l-1 of Ag as PVP AgNPs, PEG AgNPs or AgNO3, in the presence of either Suwannee River humic acid or cysteine, a high-affinity thiol-rich organic ligand. Total uptake rate of Ag from the two NPs was either increased or not strongly affected in the presence of 1 – 10 mg 1-1 humic acid. Humic substances contain relatively few strong ligands for Ag explaining their limited effects on Ag uptake rate. In contrast, Ag uptake rate was substantially reduced by cysteine. Three components of uptake from the AgNPs were quantified in the presence of cysteine using a biodynamic modeling approach: uptake of dissolved Ag released by the AgNPs, uptake of a polymer or large (>3kD) Ag-cysteine complex and uptake of the nanoparticle itself. Addition of 1:1 Ag:cysteine reduced concentrations of dissolved Ag, which contributed to, but did not fully explain the reductions in uptake. A bioavailable Ag-cysteine complex (> 3kD) appeared to be the dominant avenue of uptake from both PVP AgNPs and PEG AgNPs in the presence of cysteine. Quantifying the different avenues of uptake sets the stage for studies to assess toxicity unique to NPs.

  16. Carbon supported Ag nanoparticles as high performance cathode catalyst for H2/O2 anion exchange membrane fuel cell

    PubMed Central

    Xin, Le; Zhang, Zhiyong; Wang, Zhichao; Qi, Ji; Li, Wenzhen

    2013-01-01

    A solution phase-based nanocapsule method was successfully developed to synthesize non-platinum metal catalyst—carbon supported Ag nanoparticles (Ag/C). XRD patterns and TEM image show Ag nanoparticles with a small average size (5.4 nm) and narrow size distribution (2–9 nm) are uniformly dispersed on the carbon black Vulcan XC-72 support. The intrinsic activity and pathway of oxygen reduction reaction (ORR) on the Ag/C and commercial Pt/C were investigated using rotating ring disk electrode (RRDE) tests at room temperature. The results confirmed that the 4-electron pathway of ORR proceeds on small Ag nanoparticles, and showed comparable ORR activities on the self-prepared Ag/C and a commercial Pt/C. A single H2-O2 anion exchange membrane fuel cell (AEMFC) with the Ag/C cathode catalyst exhibited an open circuit potential of 0.98 V and a peak power density of 190 mW/cm2 at 80°C. PMID:24790944

  17. Shape manipulation of ion irradiated Ag nanoparticles embedded in lithium niobate

    NASA Astrophysics Data System (ADS)

    Wolf, Steffen; Rensberg, Jura; Johannes, Andreas; Thomae, Rainer; Smit, Frederick; Neveling, Retief; Moodley, Mathew; Bierschenk, Thomas; Rodriguez, Matias; Afra, Boshra; Hasan, Shakeeb Bin; Rockstuhl, Carsten; Ridgway, Mark; Bharuth-Ram, Krish; Ronning, Carsten

    2016-04-01

    Spherical silver nanoparticles were prepared by means of ion beam synthesis in lithium niobate. The embedded nanoparticles were then irradiated with energetic 84Kr and 197Au ions, resulting in different electronic energy losses between 8.1 and 27.5 keV nm-1 in the top layer of the samples. Due to the high electronic energy losses of the irradiating ions, molten ion tracks are formed inside the lithium niobate in which the elongated Ag nanoparticles are formed. This process is strongly dependent on the initial particle size and leads to a broad aspect ratio distribution. Extinction spectra of the samples feature the extinction maximum with shoulders on either side. While the maximum is caused by numerous remaining spherical nanoparticles, the shoulders can be attributed to elongated particles. The latter could be verified by COMSOL simulations. The extinction spectra are thus a superposition of the spectra of all individual particles.

  18. Shape manipulation of ion irradiated Ag nanoparticles embedded in lithium niobate.

    PubMed

    Wolf, Steffen; Rensberg, Jura; Johannes, Andreas; Thomae, Rainer; Smit, Frederick; Neveling, Retief; Moodley, Mathew; Bierschenk, Thomas; Rodriguez, Matias; Afra, Boshra; Bin Hasan, Shakeeb; Rockstuhl, Carsten; Ridgway, Mark; Bharuth-Ram, Krish; Ronning, Carsten

    2016-04-01

    Spherical silver nanoparticles were prepared by means of ion beam synthesis in lithium niobate. The embedded nanoparticles were then irradiated with energetic (84)Kr and (197)Au ions, resulting in different electronic energy losses between 8.1 and 27.5 keV nm(-1) in the top layer of the samples. Due to the high electronic energy losses of the irradiating ions, molten ion tracks are formed inside the lithium niobate in which the elongated Ag nanoparticles are formed. This process is strongly dependent on the initial particle size and leads to a broad aspect ratio distribution. Extinction spectra of the samples feature the extinction maximum with shoulders on either side. While the maximum is caused by numerous remaining spherical nanoparticles, the shoulders can be attributed to elongated particles. The latter could be verified by COMSOL simulations. The extinction spectra are thus a superposition of the spectra of all individual particles. PMID:26902734

  19. Pulsed laser deposition of Mg-Al layered double hydroxide with Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Matei, A.; Birjega, R.; Vlad, A.; Luculescu, C.; Epurescu, G.; Stokker-Cheregi, F.; Dinescu, M.; Zavoianu, R.; Pavel, O. D.

    2013-03-01

    Powdered layered double hydroxides (LDHs)—also known as hydrotalcite-like (HT)—compounds have been widely studied due to their applications as catalysts, anionic exchangers or host materials for inorganic or organic molecules. Assembling thin films of nano-sized LDHs onto flat solid substrates is an expanding area of research, with promising applications as sensors, corrosion-resistant coatings, components in optical and magnetic devices. The exploitation of LDHs as vehicles to carry dispersed metal nanoparticles onto a substrate is a new approach to obtain composite thin films with prospects for biomedical and optical applications. We report the deposition of thin films of Ag nanoparticles embedded in a Mg-Al layered double hydroxide matrix by pulsed laser deposition (PLD). The Ag-LDH powder was prepared by co-precipitation at supersaturation and pH = 10 using aqueous solutions of Mg and Al nitrates, Na hydroxide and carbonate, and AgNO3, having atomic ratios of Mg/Al = 3 and Ag/Al = 0.55. The target to be used in laser ablation experiments was a dry pressed pellet obtained from the prepared Ag-LDH powder. Three different wavelengths of a Nd:YAG laser (266, 532 and 1064 nm) working at a repetition rate of 10 Hz were used. X-Ray diffraction (XRD), atomic force microscopy (AFM), scanning electron microscopy (SEM), and secondary ions mass spectrometry (SIMS) were used to investigate the structure, surface morphology and composition of the deposited films.

  20. Breathing Raman modes in Ag2S nanoparticles obtained from F9 zeolite matrix

    NASA Astrophysics Data System (ADS)

    Delgado-Beleño, Y.; Cortez-Valadez, M.; Martinez-Nuñez, C. E.; Britto Hurtado, R.; Alvarez, Ramón A. B.; Rocha-Rocha, O.; Arizpe-Chávez, H.; Perez-Rodríguez, A.; Flores-Acosta, M.

    2015-12-01

    Ag2S nanoparticles were synthesized with a combination of synthetic F9, silver nitrate (AgNO3) and monohydrated sodium sulfide (Na2S9H2O). An ionic exchange was achieved via hydrothermal reaction. Nanoparticles with a predominant size ranging from 2 to 3 nm were obtained through Transmission Electron Microscopy (TEM). The nanoparticles feature a phase P21/n (14) monoclinic structure. A Raman band can be observed at around 250 cm-1 in the nanoparticles. Furthermore, the vibrational properties and stability parameters of the clusters (AgS)n, (with n = 2-9) were studied by the Density Functional Theory (DFT). The approximation levels used with DFT were: Local Spin Density Approximation (LSDA) and Becke's three-parameter and the gradient corrected functional of Lee, Yang and Puar (B3LYP) in combination with the basis set LANL2DZ (the effective core potentials and associated double-zeta valence). The Radial Breathing Mode (RBM) for B3LYP was found between 227 and 295 cm-1 as well as in longer wavelengths for LSDA.

  1. Enhanced and tunable optical quantum efficiencies from plasmon bandwidth engineering in bimetallic CoAg nanoparticles

    NASA Astrophysics Data System (ADS)

    Malasi, A.; Taz, H.; Ehrsam, M.; Goodwin, J.; Garcia, H.; Kalyanaraman, R.

    2016-10-01

    Plasmonic nanoparticles are amongst the most effective ways to resonantly couple optical energy into and out of nanometer sized volumes. However, controlling and/or tuning the transfer of this incident energy to the surrounding near and far field is one of the most interesting challenges in this area. Due to the dielectric properties of metallic silver (Ag), its nanoparticles have amongst the highest radiative quantum efficiencies (η), i.e., the ability to radiatively transfer the incident energy to the surrounding. Here we report the discovery that bimetallic nanoparticles of Ag made with immiscible and plasmonically weak Co metal can show comparable and/or even higher η values. The enhancement is a result of the narrowing of the plasmon bandwidth from these bimetal systems. The phenomenological explanation of this effect based on the dipolar approximation points to the reduction in radiative losses within the Ag nanoparticles when in contact with cobalt. This is also supported by a model of coupling between poor and good conductors based on the surface to volume ratio. This study presents a new type of bandwidth engineering, one based on using bimetal nanostructures, to tune and/or enhance the quality factor and quantum efficiency for near and far-field plasmonic applications.

  2. Nanoparticle Ag-enhanced textured-powder Bi-2212/Ag wire technology

    NASA Astrophysics Data System (ADS)

    Kellams, J. N.; McIntyre, P.; Pogue, N.; Vandergrifft, J.

    2015-12-01

    A new approach to the preparation of cores for Bi-2212/Ag wire is being developed. Nanoparticle Ag is homogeneously dispersed in Bi-2212 fine powder, and the mixture is uniaxially compressed to form highly textured, cold-sintered core rods. The rods can be assembled in a silver matrix, drawn to form multifilament wire, and restacked and drawn to form multifilament wire. Preliminary studies using tablet geometry demonstrate that a nonmelt heat treatment produces densification, grain growth, intergrowth among grains, and macroscopic current transport. The status of the development is reported.

  3. Antibacterial properties of silver nanoparticles in three different sizes and their nanocomposites with a new waterborne polyurethane

    PubMed Central

    Liu, Hung-Li; Dai, Shenghong A; Fu, Keng-Yen; Hsu, Shan-hui

    2010-01-01

    Silver nanoparticles (AgNPs) are strong bactericidal agents but they are also cytotoxic. Embedding them in a polymer matrix may reduce their cytotoxic effect. In the present study, AgNPs in three average sizes were tested for their antibacterial activities and cytotoxicity. Nanocomposites from a new waterborne polyetherurethane (PEU) ionomer and AgNPs were prepared without the use of any crosslinker. It was observed that the antibacterial activity of AgNPs against Escherichia coli started at the effective concentration of 0.1–1 ppm, while that against Staphylococcus aureus started at higher concentrations of 1–10 ppm. Cytotoxicity of AgNPs was observed at the concentration of 10 ppm. AgNPs with smaller average size showed greater antibacterial activity as well as cytotoxicity. The PEU synthesized in this study showed high tensile strength, and the addition of AgNPs at all sizes further increased its thermal stability. The delicate surface features of nanophases, however, were only observed in nanocomposites with either small-or medium-sized AgNPs. PEU-Ag nanocomposites had a strong bacteriostatic effect on the growth of E. coli and S. aureus. The proliferation of endothelial cells on PEU-Ag nanocomposites was enhanced, whereas the platelet adhesion was reduced. The expression of endothelial nitric oxide synthase gene was upregulated on PEU-Ag containing small-sized AgNPs (30 ppm) or medium-sized AgNPs (60 ppm). This effect was not as remarkable in nanocomposites from large-sized AgNPs. Overall, nanocomposites from the PEU and 60 ppm of the medium-sized (5 nm) AgNPs showed the best biocompatibility and antibacterial activity. Addition of smaller or larger AgNPs did not produce as substantial an effect in PEU, especially for the larger AgNPs. PMID:21187943

  4. Synthesis of polydopamine at the femtoliter scale and confined fabrication of Ag nanoparticles on surfaces.

    PubMed

    Guardingo, M; Esplandiu, M J; Ruiz-Molina, D

    2014-10-25

    Nanoscale polydopamine motifs are fabricated on surfaces by deposition of precursor femtolitre droplets using an AFM tip and employed as confined reactors to fabricate Ag nanoparticle patterns by in situ reduction of a Ag(+) salt. PMID:25195667

  5. Photodeposition of Ag or Pt onto TiO2 nanoparticles decorated on step edges of HOPG.

    PubMed

    Taing, James; Cheng, Ming H; Hemminger, John C

    2011-08-23

    Ordered linear arrays of titanium dioxide nanoparticles were fabricated on highly oriented pyrolytic graphite utilizing a step edge decoration method. Ag- or Pt-based nanoparticles were then photodeposited onto the titanium dioxide nanoparticles (∼18 nm) to simultaneously verify photocatalytic activity and to demonstrate a viable route to load the titanium dioxide nanoparticles with metals. Scanning electron microscopy and atomic force microscopy determined the morphology, size, and distribution of the particles. X-ray photoelectron spectroscopy confirmed the identity of the titanium dioxide nanoparticles, and transmission electron microscopy showed that some of the particles were rutile single crystals. Energy-dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy determined the chemical composition of the metal-based nanoparticles selectively loaded on the linear arrays of titanium dioxide nanoparticles.

  6. Nanomedicine: Sizing up targets with nanoparticles

    NASA Astrophysics Data System (ADS)

    Minchin, Rod

    2008-01-01

    Nanoparticles have many potential medical applications but their behaviour in the body is poorly understood. New studies in mice show that particles that don't have targeting molecules attached can selectively enter certain organs solely on the basis of their charge and size.

  7. Self-organization and photo-induced formation of cyanine dye aggregates on the plasmonic Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Starovoytov, Anton A.; Nabiullina, Rezida D.; Toropov, Nikita A.

    2016-04-01

    The optical properties of hybrid film based on plasmon Ag nanoparticles of different size and cyanine dyes with different length of conjugation chain depending on the relative position of the plasmon resonance and the absorption of organic molecules were studied. The absorption spectra of the films revealed several molecular forms, such as all-trans- and cisisomers, dimers and J-aggregate, which also exist in pure organic films without Ag nanoparticles. It's shown that the absorption of aggregate bands increased after exposure by nanosecond laser on the hybrid films due to photo-induced additional self-organization of aggregates. In the presence of Ag nanoparticles, laser radiation leads to the change of molecular forms at a comparatively low threshold.

  8. Fabrication of Ag-Decorated CaTiO₃ Nanoparticles and Their Enhanced Photocatalytic Activity for Dye Degradation.

    PubMed

    Xian, T; Yang, H; Huo, Y S; Ma, J Y; Zhang, H M; Su, J Y; Feng, W J

    2016-01-01

    CaTiO₃nanoparticles of 30-40 nm in size were synthesized via a polyacrylamide gel route. Ag nanoparticles with size of 8-16 nm were deposited onto CaTiO₃particles by a photochemical reduction method to yield CaTiO₃@Ag composites. The photocatalytic activity of prepared samples was evaluated by degrading methyl orange under ultraviolet irradiation. It is demonstrated that Ag-decorated CaTiO₃ particles exhibit an enhanced photocatalytic activity compared to bare CaTiO₃ particles. After 60 min of photocatalysis, the degradation percentage of MO increases from 54% for bare CaTiO₃particles to 72% for CaTiO₃@Ag composites. This can be explained by the fact that photogenerated electrons are captured by Ag nanoparticles and photogenerated holes are therefore increasingly available to react with OH⁻/H₂O to generate hydroxyl (·OH) radicals. ·OH radicals were detected by fluorimetry using terephthalic acid as a probe molecule, revealing an enhanced yield on the irradiated CaTiO₃@Ag composites. In addition, it is found that the addition of ethanol, which acts as an ·OH scavenger, leads to a quenching of ·OH radicals and simultaneous decrease in the photocatalytic efficiency. This suggests that ·OH radicals are the dominant active species responsible for the dye degradation. PMID:27398489

  9. In situ growth of Ag nanoparticles on α-Ag2WO4 under electron irradiation: probing the physical principles

    NASA Astrophysics Data System (ADS)

    San-Miguel, Miguel A.; da Silva, Edison Z.; Zannetti, Sonia M.; Cilense, Mario; Fabbro, Maria T.; Gracia, Lourdes; Andrés, Juan; Longo, Elson

    2016-06-01

    Exploiting the plasmonic behavior of Ag nanoparticles grown on α-Ag2WO4 is a widely employed strategy to produce efficient photocatalysts, ozone sensors, and bactericides. However, a description of the atomic and electronic structure of the semiconductor sites irradiated by electrons is still not available. Such a description is of great importance to understand the mechanisms underlying these physical processes and to improve the design of silver nanoparticles to enhance their activities. Motivated by this, we studied the growth of silver nanoparticles to investigate this novel class of phenomena using both transmission electron microscopy and field emission scanning electron microscopy. A theoretical framework based on density functional theory calculations (DFT), together with experimental analysis and measurements, were developed to examine the changes in the local geometrical and electronic structure of the materials. The physical principles for the formation of Ag nanoparticles on α-Ag2WO4 by electron beam irradiation are described. Quantum mechanical calculations based on DFT show that the (001) of α-Ag2WO4 displays Ag atoms with different coordination numbers. Some of them are able to diffuse out of the surface with a very low energy barrier (less than 0.1 eV), thus, initiating the growth of metallic Ag nanostructures and leaving Ag vacancies in the bulk material. These processes increase the structural disorder of α-Ag2WO4 as well as its electrical resistance as observed in the experimental measurements.

  10. In situ growth of Ag nanoparticles on α-Ag2WO4 under electron irradiation: probing the physical principles.

    PubMed

    San-Miguel, Miguel A; da Silva, Edison Z; Zannetti, Sonia M; Cilense, Mario; Fabbro, Maria T; Gracia, Lourdes; Andrés, Juan; Longo, Elson

    2016-06-01

    Exploiting the plasmonic behavior of Ag nanoparticles grown on α-Ag2WO4 is a widely employed strategy to produce efficient photocatalysts, ozone sensors, and bactericides. However, a description of the atomic and electronic structure of the semiconductor sites irradiated by electrons is still not available. Such a description is of great importance to understand the mechanisms underlying these physical processes and to improve the design of silver nanoparticles to enhance their activities. Motivated by this, we studied the growth of silver nanoparticles to investigate this novel class of phenomena using both transmission electron microscopy and field emission scanning electron microscopy. A theoretical framework based on density functional theory calculations (DFT), together with experimental analysis and measurements, were developed to examine the changes in the local geometrical and electronic structure of the materials. The physical principles for the formation of Ag nanoparticles on α-Ag2WO4 by electron beam irradiation are described. Quantum mechanical calculations based on DFT show that the (001) of α-Ag2WO4 displays Ag atoms with different coordination numbers. Some of them are able to diffuse out of the surface with a very low energy barrier (less than 0.1 eV), thus, initiating the growth of metallic Ag nanostructures and leaving Ag vacancies in the bulk material. These processes increase the structural disorder of α-Ag2WO4 as well as its electrical resistance as observed in the experimental measurements. PMID:27114472

  11. Conversion of Ag nanowires to AgCI nanowires decorated with Au nanoparticles and their photocatalytic activity.

    SciTech Connect

    Sun, Y.; Center for Nanoscale Materials

    2010-02-11

    A two-step approach has been developed to synthesize AgCl nanowires decorated with Au nanoparticles by using Ag nanowires as chemical templates. In the first step, the Ag nanowires are oxidized with FeCl{sub 3} followed by a simultaneous precipitation reaction between Ag{sup +} and Cl{sup -} ions at room temperature, resulting in conversion of the Ag nanowires to AgCl nanowires as well as reduction of Fe{sup 3+} to Fe{sup 2+} ions. In the second step, the Fe{sup 2+} ions generated in the first step reduce Au precursors (e.g., NaAuCl{sub 4}) to deposit Au nanoparticles on the surfaces of the AgCl nanowires, resulting in the formation of AgCl:Au composite nanowires. Because of strong surface plasmon resonance and chemical inertness of Au nanoparticles, the as-synthesized AgCl:Au nanowires exhibit enhanced absorption coefficient in the visible region and enhanced chemical stability to prevent them from degradation and aggregation. These unique properties enable the AgCl:Au nanowires to be used as a class of promising plasmonic photocatalysts driven by visible light. Preliminary results demonstrate these composite nanowires can efficiently decompose organics, such as methylene blue molecules, under illumination of white light.

  12. Electrochemiluminescent metallopolymer-nanoparticle composites: nanoparticle size effects.

    PubMed

    Devadoss, Anitha; Dickinson, Calum; Keyes, Tia E; Forster, Robert J

    2011-03-15

    Metallopolymer-gold nanocomposites have been synthesized in which the metal complex-Au nanoparticle (NP) mole ratio is systematically varied by mixing solutions of 4-(dimethylamino) pyridine protected gold nanoparticles and a [Ru(bpy)(2)PVP(10)](2+) metallopolymer; bpy is 2,2'-bipyridyl and PVP is poly-(4-vinylpyridine). The impact of changing the gold nanoparticle diameter ranging from 4.0 ± 0.5 to 12.5 ± 1 nm has been investigated. The photo induced emission of the metallopolymer undergoes static quenching by the metal nanoparticles irrespective of their size. When the volume ratio of Au NP-Ru is 1, the quenching efficiency increases from 38% to 93% on going from 4.0 ± 0.5 to 12.5 ± 1 nm diameter nanoparticles while the radius of the quenching sphere remains unaffected at 75 ± 5 Å. The conductivity of thin films is initially unaffected by nanoparticle incorporation until a percolation threshold is reached at a mole ratio of 4.95 × 10(-2) after which the conductivity increases before reaching a maximum. For thin films of the nanocomposites on electrodes, the electrochemiluminescence intensity of the nanocomposite initially increases as nanoparticles are added before decreasing for the highest loadings. The electrochemiluminescence intensity increases with increasing nanoparticle diameter. The electrochemiluminescence (ECL) emission intensity of the nanocomposite formed using 12.5 nm particles at mole ratios between 5 × 10(-3) and 10 × 10(-3) is approximately 7-fold higher than that found for the parent metallopolymer. The application of these materials for low cost ECL-based point of care devices is discussed.

  13. LSP spectral changes correlating with SERS activation and quenching for R6G on immobilized Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Futamata, M.; Maruyama, Y.

    2008-10-01

    In terms of chemical enhancement in Surface Enhanced Raman Scattering (SERS), we investigated the effect of halide and other anions to rhodamine 6G (R6G) adsorbed Ag particles that were immobilized on the substrates. The residual species on chemically prepared Ag particles such as citrate or a-carbon were thoroughly substituted by various anions, e.g., Cl-, Br-, I-, SCN-, CN-, or S2O3 2- anions, whose adsorption features are elucidated by the formation constants for AgX2 ( m-1)-, here X denotes the above anions. In particular, Cl-, Br-, or SCN- ions activated SERS of R6G via intrinsic electronic interaction with Ag, whereas CN-, S2O3 2-, or I- anions quenched it due to their exclusive adsorption onto the Ag surfaces. We found that the activation process with the anions commonly yields a marked blue-shift of the coupled plasmon peak from ca. 650-700 to 500-550 nm in elastic scattering. It is rationalized by slight increase of the gap size between adjacent Ag nanoparticles by only ca. 1 nm based on theoretical simulations. This is probably caused by slight dissolution, oxidative etching, of the particles according to large formation constants of the complexes. Consequently, partly remaining negative charges on the Ag surface, and a slight increase in the gap size, providing huge electric field, facilitated R6G cations to adsorb on the nanoparticles, especially at the junction.

  14. Characterization and Evaluation of Reverse Osmosis Membranes Modified with Ag2O Nanoparticles to Improve Performance.

    PubMed

    Al-Hobaib, Abdullah S; Al-Sheetan, Khalid M; Shaik, Mohammed Rafi; Al-Andis, Naser M; Al-Suhybani, M S

    2015-12-01

    The objective of this work was to prepare and characterize a new and highly efficient modified membrane by in situ interfacial polymerization on porous polysulfone supports. The process used m-phenylenediamine and trimesoyl chloride in hexane, incorporating silver oxide Ag2O nanoparticles of varied concentrations from 0.001 to 0.1 wt%. Ag2O nanoparticles were prepared at different sizes varying between 20 and 50 nm. The modified membranes were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), atomic force microscopy (AFM), transmission electron microscopy (TEM), and contact angle measurement. The results showed a smooth membrane surface and average surface roughness from 31 to 74 nm. Moreover, hydrophilicity improved and the contact angle decreased to 41° at 0.009 wt% silver oxide. The performances of the developed membranes were investigated by measuring permeate fluxes and salt rejection capability by passing NaCl solutions (2000 ppm) through the membranes at 225 psi. The results showed that the flux increased from 26 to 40.5 L/m(2) h, while the salt rejection was high, at 99 %, with 0.003 wt% Ag2O nanoparticles.

  15. Characterization and Evaluation of Reverse Osmosis Membranes Modified with Ag2O Nanoparticles to Improve Performance

    NASA Astrophysics Data System (ADS)

    Al-Hobaib, Abdullah S.; AL-Sheetan, Khalid M.; Shaik, Mohammed Rafi; Al-Andis, Naser M.; Al-Suhybani, M. S.

    2015-09-01

    The objective of this work was to prepare and characterize a new and highly efficient modified membrane by in situ interfacial polymerization on porous polysulfone supports. The process used m-phenylenediamine and trimesoyl chloride in hexane, incorporating silver oxide Ag2O nanoparticles of varied concentrations from 0.001 to 0.1 wt%. Ag2O nanoparticles were prepared at different sizes varying between 20 and 50 nm. The modified membranes were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), atomic force microscopy (AFM), transmission electron microscopy (TEM), and contact angle measurement. The results showed a smooth membrane surface and average surface roughness from 31 to 74 nm. Moreover, hydrophilicity improved and the contact angle decreased to 41° at 0.009 wt% silver oxide. The performances of the developed membranes were investigated by measuring permeate fluxes and salt rejection capability by passing NaCl solutions (2000 ppm) through the membranes at 225 psi. The results showed that the flux increased from 26 to 40.5 L/m2 h, while the salt rejection was high, at 99 %, with 0.003 wt% Ag2O nanoparticles.

  16. The synthesis of Pt/Ag bimetallic nanoparticles using a successive solution plasma process.

    PubMed

    Kim, Sung Min; Lee, Sang Yul; Lee, Min Hyung; Kim, Jung Wan

    2014-12-01

    A successive solution plasma process was developed for the synthesis of Pt/Ag bimetallic nanoparticles. Ag nanoparticles were made first by applying a high voltage of bipolar pulsed DC to anode and cathode electrodes composed of Ag rods. The solution containing Ag nanoparticles was discharged successively using Pt electrodes. The joule heating and electrolysis between electrodes generated vapors, and solution plasma was sustained due to progressive ionization and excitation in the vapor phase. The maximum current and voltage breakdown was observed at approximately 8.9 A and 900 V with an interval of 25 μs, which indicated that an intense solution plasma was sustained continuously. The Pt-on-Ag heterogeneous nanostructures formed, and finally, the Ag nanoparticles were completely covered by Pt nanoparticles after a discharge duration of 1,200 s. PMID:25970983

  17. Chromatographic analysis of phytochemicals components present in mangifera indica leaves for the synthesis of silver nanoparticles by AgNO3 reduction

    NASA Astrophysics Data System (ADS)

    Martínez-Bernett, D.; Silva-Granados, A.; Correa-Torres, S. N.; Herrera, A.

    2016-02-01

    It was studied the green synthesis of silver nanoparticles (AgNPs) from the reduction of a silver nitrate solution (1 and 10mM) in the presence of an extract of mangifera indica leaves. Phytochemicals components present in extracts of mango leaves were determined using a GC-MS chromatograph. The results showed the presence of the phenolic compound pyrogallol (26.9% wt/5mL of extract) and oleic acid (29.1% wt/5mL of extract), which are useful for the reduction of the metallic salt AgNO3 and the stabilization of silver nanoparticles. The synthesized nanoparticles were characterized by UV visible spectroscopy (UV-vis), evidencing absorbances at wavelengths of 417nm (AgNPs-1) and 414nm (AgNPs- 10), which are characteristic peaks of this metallic nanoparticles. Scanning Electron Microscopy (SEM) was used to determine the size of the synthesized nanoparticles. A particle size of about 28±7nm was observed for the AgNPs-1 sample and 26±5nm for the AgNPs-10. This suggests the advantages of green chemistry to obtain silver nanoparticles with a narrow size distribution.

  18. The size distribution of 'gold standard' nanoparticles.

    PubMed

    Bienert, Ralf; Emmerling, Franziska; Thünemann, Andreas F

    2009-11-01

    The spherical gold nanoparticle reference materials RM 8011, RM 8012, and RM 8013, with a nominal radius of 5, 15, and 30 nm, respectively, have been available since 2008 from NIST. These materials are recommended as standards for nanoparticle size measurements and for the study of the biological effects of nanoparticles, e.g., in pre-clinical biomedical research. We report on determination of the size distributions of these gold nanoparticles using different small-angle X-ray scattering (SAXS) instruments. Measurements with a classical Kratky type SAXS instrument are compared with a synchrotron SAXS technique. Samples were investigated in situ, positioned in capillaries and in levitated droplets. The number-weighted size distributions were determined applying model scattering functions based on (a) Gaussian, (b) log-normal, and (c) Schulz distributions. The mean radii are 4.36 +/- 0.04 nm (RM 8011), 12.20 +/- 0.03 nm (RM 8012), and 25.74 +/- 0.27 nm (RM 8013). Low polydispersities, defined as relative width of the distributions, were detected with values of 0.067 +/- 0.006 (RM 8011), 0.103 +/- 0.003, (RM 8012), and 0.10 +/- 0.01 (RM 8013). The results are in agreement with integral values determined from classical evaluation procedures, such as the radius of gyration (Guinier) and particle volume (Kratky). No indications of particle aggregation and particle interactions--repulsive or attractive--were found. We recommend SAXS as a standard method for a fast and precise determination of size distributions of nanoparticles.

  19. Raman bands in Ag nanoparticles obtained in extract of Opuntia ficus-indica plant

    NASA Astrophysics Data System (ADS)

    Bocarando-Chacon, J.-G.; Cortez-Valadez, M.; Vargas-Vazquez, D.; Rodríguez Melgarejo, F.; Flores-Acosta, M.; Mani-Gonzalez, P. G.; Leon-Sarabia, E.; Navarro-Badilla, A.; Ramírez-Bon, R.

    2014-05-01

    Silver nanoparticles have been obtained in an extract of Opuntia ficus-indica plant. The size and distribution of nanoparticles were quantified by atomic force microscopy (AFM). The diameter was estimated to be about 15 nm. In addition, energy dispersive X-ray spectroscopy (EDX) peaks of silver were observed in these samples. Three Raman bands have been experimentally detected at 83, 110 and 160 cm-1. The bands at 83 and 110 cm-1 are assigned to the silver-silver Raman modes (skeletal modes) and the Raman mode located at 160 cm-1 has been assigned to breathing modes. Vibrational assignments of Raman modes have been carried out based on the Density Functional Theory (DFT) quantum mechanical calculation. Structural and vibrational properties for small Agn clusters with 2≤n≤9 were determined. Calculated Raman modes for small metal clusters have an approximation trend of Raman bands. These Raman bands were obtained experimentally for silver nanoparticles (AgNP).

  20. Thermal co-reduction approach to vary size of silver nanoparticle: its microbial and cellular toxicology.

    PubMed

    Dasgupta, Nandita; Ranjan, Shivendu; Rajendran, Bhavapriya; Manickam, Venkatraman; Ramalingam, Chidambaram; Avadhani, Ganesh S; Kumar, Ashutosh

    2016-03-01

    In recent years, silver nanoparticles (AgNPs) have attracted considerable interest in the field of food, agriculture and pharmaceuticals mainly due to its antibacterial activity. AgNPs have also been reported to possess toxic behavior. The toxicological behavior of nanomaterials largely depends on its size and shape which ultimately depend on synthetic protocol. A systematic and detailed analysis for size variation of AgNP by thermal co-reduction approach and its efficacy toward microbial and cellular toxicological behavior is presented here. With the focus to explore the size-dependent toxicological variation, two different-sized NPs have been synthesized, i.e., 60 nm (Ag60) and 85 nm (Ag85). A detailed microbial toxicological evaluation has been performed by analyzing minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC), diameter of inhibition zone (DIZ), growth kinetics (GrK), and death kinetics (DeK). Comparative cytotoxicological behavior was analyzed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. It has been concluded by this study that the size of AgNPs can be varied, by varying the concentration of reactants and temperature called as "thermal co-reduction" approach, which is one of the suitable approaches to meet the same. Also, the smaller AgNP has shown more microbial and cellular toxicity. PMID:25943508

  1. Exposure-dependent Ag+ release from silver nanoparticles and its complexation in AgS2 sites in primary murine macrophages

    NASA Astrophysics Data System (ADS)

    Veronesi, G.; Aude-Garcia, C.; Kieffer, I.; Gallon, T.; Delangle, P.; Herlin-Boime, N.; Rabilloud, T.; Carrière, M.

    2015-04-01

    Silver nanoparticle (AgNP) toxicity is related to their dissolution in biological environments and to the binding of the released Ag+ ions in cellulo; the chemical environment of recombined Ag+ ions is responsible for their toxicological outcome, moreover it is indicative of the cellular response to AgNP exposure, and can therefore shed light on the mechanisms governing AgNP toxicity. This study probes the chemistry of Ag species in primary murine macrophages exposed to AgNPs by making use of X-ray Absorption Fine Structure spectroscopy under cryogenic conditions: the linear combination analysis of the near-edge region of the spectra provides the fraction of Ag+ ions released from the AgNPs under a given exposure condition and highlights their complexation with thiolate groups; the ab initio modelling of the extended spectra allows measuring the Ag-S bond length in cellulo. Dissolution rates depend on the exposure scenario, chronicity leading to higher Ag+ release than acute exposure; Ag-S bond lengths are 2.41 +/- 0.03 Å and 2.38 +/- 0.01 Å in acute and chronic exposure respectively, compatible with digonal AgS2 coordination. Glutathione is identified as the most likely putative ligand for Ag+. The proposed method offers a scope for the investigation of metallic nanoparticle dissolution and recombination in cellular models.Silver nanoparticle (AgNP) toxicity is related to their dissolution in biological environments and to the binding of the released Ag+ ions in cellulo; the chemical environment of recombined Ag+ ions is responsible for their toxicological outcome, moreover it is indicative of the cellular response to AgNP exposure, and can therefore shed light on the mechanisms governing AgNP toxicity. This study probes the chemistry of Ag species in primary murine macrophages exposed to AgNPs by making use of X-ray Absorption Fine Structure spectroscopy under cryogenic conditions: the linear combination analysis of the near-edge region of the spectra provides

  2. Effects of silver nanoparticles with different sizes on photochemical responses of polythiophene-fullerene thin films.

    PubMed

    You, Jing; Leonard, Kwati; Takahashi, Yukina; Yonemura, Hiroaki; Yamada, Sunao

    2014-01-21

    Effects of size and coverage density of silver nanoparticles (AgPs) on the fluorescence emission and fluorescence lifetime of poly(3-hexylthiophene-2,5-diyl) (P3HT) thin films were investigated. AgPs of 64 nm diameter showed greater effects on the fluorescence decay process of P3HT films as compared with 7 nm AgPs. The fluorescence lifetime (FL) of P3HT decreased from 0.61 to 0.22 ns in the presence of 64 nm AgPs, while no appreciable change (0.60 ns) was seen in the case of 7 nm AgPs. The results suggest that the 64 nm AgPs showed a greater effect on the enhancement of the decay rate of excited P3HT. The photoelectric conversion of thin films consisting of P3HT and phenyl-C61-butyric acid methyl ester (PCBM) was also investigated. AgPs of 7 or 64 nm diameters were first deposited on indium-tin-oxide substrates with controlled surface coverage densities from ~1 to 40%. When the coverage densities of deposited AgPs were ~20% for both 7 and 64 nm, the enhancement of photoelectric conversion efficiency reached maximum. The degree of enhancement in the case of 64 nm AgPs was larger than in the case of 7 nm AgPs. PMID:24292622

  3. Raman gas sensing of modified Ag nanoparticle SERS

    NASA Astrophysics Data System (ADS)

    Myoung, NoSoung; Yoo, Hyung Keun; Hwang, In-Wook

    2014-03-01

    Recent progress in modified Surface Enhanced Raman Scattering (SERS) using Ag nanoparticles makes them promising optical technique for direct gas sensing of interest. However, SERS has been shown to provide sub ppb level detection of the compounds in the vapor phase. The major problem with the sensitivity scaling-up was in the development of fabrication technology for stability and reproducibility of SERS substrates. We report an optimization of 1-propanethiol coated multiple Ag nanoparticle layers on SiO2 substrate as well as new records of real-time, simultaneous vapor phase detection of toluene and 1-2 dichlorobenzene by the radiation of fiber optic coupled 785 nm diode laser and spectrograph. Multiple depositions of Ag NPs were loaded on SiO2 and soaked in 1-propanethiol solution for 24 hours to modify the surface into hydrophobic due to the characteristics of vapor phase of our interests. Raman bands at 1003 cm-1 and 1130 cm-1 for toluene and 12DCB, respectively were compared to 1089 cm-1 and each gas concentration in 1000 mL flask were calculated as a function of each vapor phase ratio. The saturation of toluene and 12DCB were limited only by 800 ppm and the detectable range was 0.6-800 ppm.

  4. Surface-enhanced Raman scattering from Ag nanoparticles formed by visible laser irradiation of thermally annealed AgO{sub x} thin films

    SciTech Connect

    Fujimaki, Makoto; Awazu, Koichi; Tominaga, Junji; Iwanabe, Yasuhiko

    2006-10-01

    Visible laser irradiation of AgO{sub x} thin films forms Ag nanoparticles, which then results in surface-enhanced Raman scattering (SERS). The efficiency of this Ag nanoparticle formation strongly depends on the properties of the AgO{sub x} thin films. Thermal annealing causes changes in physical properties such as deoxidization of the films and aggregation of Ag atoms in the films. In the present research, the effects of the changes induced by thermal annealing on SERS efficiency were examined. It was found that AgO{sub x} thin films annealed at 300 deg. C for 5 min in a N{sub 2} atmosphere were suitable for the formation of Ag nanoparticles effective for SERS, while films that were not annealed were not. From these results, it was deduced that the Ag aggregation resulting from thermal annealing in AgO{sub x} thin films promotes the Ag nanoparticle formation.

  5. Green synthesis, characterization, photocatalytic, fluorescence and antimicrobial activities of Cochlospermum gossypium capped Ag2S nanoparticles.

    PubMed

    Ayodhya, Dasari; Veerabhadram, Guttena

    2016-04-01

    The study describes a simple and green method for the synthesis of silver sulfide nanoparticles (Ag2S NPs) using gum kondagogu (Cochlospermum gossypium) (GK). The synthesized NPs were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), fluorescence, UV-vis absorption, zeta potential and thermogravimetric analysis (TGA) techniques. The optical properties and quantum confinement effect of the products were confirmed by means of spectroscopic measurements. The morphologies and sizes were characterized by SEM and TEM. The Ag2S NPs were spherical in shape with an effective diameter size of 25 nm. The photocatalytic property of Ag2S NPs was evaluated by the degradation of fluorescein (FL) dye under solar light. The effect of Ag2SNPs on the photocatalytic degradation of FL dye and influence of other parameters such as Ag2S loading, H2O2, temperature and under solar light irradiation was also evaluated. The degradation reaction follows the pseudo-first order kinetics. The apparent reaction rate was used to calculate the apparent activation energy (Ea=13.95 kJ/mol) of the degradation process. The activation thermodynamic parameters (ΔG*, ΔH* and ΔS*) were obtained from variable temperature kinetic studies. The interaction between Ag2S NPs and bovine serum albumin (BSA) was studied by using fluorescence spectroscopic measurements. The synthesized Ag2S NPs were showing good antimicrobial activity. PMID:26894846

  6. SiO(2) /TiO(2) hollow nanoparticles decorated with Ag nanoparticles: enhanced visible light absorption and improved light scattering in dye-sensitized solar cells.

    PubMed

    Hwang, Sun Hye; Shin, Dong Hoon; Yun, Juyoung; Kim, Chanhoi; Choi, Moonjung; Jang, Jyongsik

    2014-04-01

    Hollow SiO2 /TiO2 nanoparticles decorated with Ag nanoparticles (NPs) of controlled size (Ag@HNPs) were fabricated in order to enhance visible-light absorption and improve light scattering in dye-sensitized solar cells (DSSCs). They exhibited localized surface plasmon resonance (LSPR) and the LSPR effects were significantly influenced by the size of the Ag NPs. The absorption peak of the LSPR band dramatically increased with increasing Ag NP size. The LSPR of the large Ag NPs mainly increased the light absorption at short wavelengths, whereas the scattering from the SiO2 /TiO2 HNPs improved the light absorption at long wavelengths. This enabled the working electrode to use the full solar spectrum. Furthermore, the SiO2 layer thickness was adjusted to maximize the LSPR from the Ag NPs and avoid corrosion of the Ag NPs by the electrolyte. Importantly, the power conversion efficiency (PCE) increased from 7.1 % with purely TiO2 -based DSSCs to 8.1 % with HNP-based DSSCs, which is an approximately 12 % enhancement and can be attributed to greater light scattering. Furthermore, the PCEs of Ag@HNP-based DSSCs were 11 % higher (8.1 vs. 9.0 %) than the bare-HNP-based DSSCs, which can be attributed to LSPR. Together, the PCE of Ag@HNP-based DSSCs improved by a total of 27 %, from 7.1 to 9.0 %, due to these two effects. This comparative research will offer guidance in the design of multifunctional nanomaterials and the optimization of solar-cell performance.

  7. Synthesis of triangular Au core-Ag shell nanoparticles

    SciTech Connect

    Rai, Akhilesh; Chaudhary, Minakshi; Ahmad, Absar; Bhargava, Suresh; Sastry, Murali . E-mail: msastry@tatachemicals.com

    2007-07-03

    In this paper, we demonstrate a simple and reproducible method for the synthesis of triangular Au core-Ag shell nanoparticles. The triangular gold core is obtained by the reduction of gold ions by lemongrass extract. Utilizing the negative charge on the gold nanotriangles, silver ions are bound to their surface and thereafter reduced by ascorbic acid under alkaline conditions. The thickness of the silver shell may be modulated by varying the pH of the reaction medium. The formation of the Au core-Ag shell triangular nanostructures has been followed by UV-vis-NIR Spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy (TEM) and atomic force microscopy (AFM) measurements. The sharp vertices of the triangles coupled with the core-shell structure is expected to have potential for application in surface enhanced Raman spectroscopy and in the sensitive detection of biomolecules.

  8. Continuous syntheses of Pd@Pt and Cu@Ag core-shell nanoparticles using microwave-assisted core particle formation coupled with galvanic metal displacement.

    PubMed

    Miyakawa, Masato; Hiyoshi, Norihito; Nishioka, Masateru; Koda, Hidekazu; Sato, Koichi; Miyazawa, Akira; Suzuki, Toshishige M

    2014-08-01

    Continuous synthesis of Pd@Pt and Cu@Ag core-shell nanoparticles was performed using flow processes including microwave-assisted Pd (or Cu) core-nanoparticle formation followed by galvanic displacement with a Pt (or Ag) shell. The core-shell structure and the nanoparticle size were confirmed using high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) observation and EDS elemental mapping. The Pd@Pt nanoparticles with a particle size of 6.5 ± 0.6 nm and a Pt shell thickness of ca. 0.25 nm were synthesized with appreciably high Pd concentration (Pd 100 mM). This shell thickness corresponds to one atomic layer thickness of Pt encapsulating the Pd core metal. The particle size of core Pd was controlled by tuning the initial concentrations of Na2[PdCl4] and PVP. Core-shell Cu@Ag nanoparticles with a particle size of 90 ± 35 nm and an Ag shell thickness of ca. 3.5 nm were obtained using similar sequential reactions. Oxidation of the Cu core was suppressed by the coating of Cu nanoparticles with the Ag shell. PMID:24948122

  9. New one-pot synthesis of Au and Ag nanoparticles using green rust reactive particle as a micro-reactor.

    PubMed

    Ayadi, Sondra; Perca, Cristian; Legrand, Ludovic

    2013-01-01

    A new, simple, and fast one-pot synthesis of supported Au or Ag nanoparticles is implemented, for which a reactive Fe(II)-bearing green rust inorganic particle is used as an individual micro-reactor acting as both the reducing agent and support for the resulting metal nanoparticles. The mechanism involves both the solid-state oxidation of the green rust support (sulfate or carbonate) and the reduction-precipitation of soluble metal precursor. The resulting nanohybrids have a platy inorganic part supporting about one to ten nanoparticles with sizes in the 20 to 120 nm range. PMID:23433071

  10. New one-pot synthesis of Au and Ag nanoparticles using green rust reactive particle as a micro-reactor

    NASA Astrophysics Data System (ADS)

    Ayadi, Sondra; Perca, Cristian; Legrand, Ludovic

    2013-02-01

    A new, simple, and fast one-pot synthesis of supported Au or Ag nanoparticles is implemented, for which a reactive Fe(II)-bearing green rust inorganic particle is used as an individual micro-reactor acting as both the reducing agent and support for the resulting metal nanoparticles. The mechanism involves both the solid-state oxidation of the green rust support (sulfate or carbonate) and the reduction-precipitation of soluble metal precursor. The resulting nanohybrids have a platy inorganic part supporting about one to ten nanoparticles with sizes in the 20 to 120 nm range.

  11. New one-pot synthesis of Au and Ag nanoparticles using green rust reactive particle as a micro-reactor.

    PubMed

    Ayadi, Sondra; Perca, Cristian; Legrand, Ludovic

    2013-02-22

    A new, simple, and fast one-pot synthesis of supported Au or Ag nanoparticles is implemented, for which a reactive Fe(II)-bearing green rust inorganic particle is used as an individual micro-reactor acting as both the reducing agent and support for the resulting metal nanoparticles. The mechanism involves both the solid-state oxidation of the green rust support (sulfate or carbonate) and the reduction-precipitation of soluble metal precursor. The resulting nanohybrids have a platy inorganic part supporting about one to ten nanoparticles with sizes in the 20 to 120 nm range.

  12. New one-pot synthesis of Au and Ag nanoparticles using green rust reactive particle as a micro-reactor

    PubMed Central

    2013-01-01

    A new, simple, and fast one-pot synthesis of supported Au or Ag nanoparticles is implemented, for which a reactive Fe(II)-bearing green rust inorganic particle is used as an individual micro-reactor acting as both the reducing agent and support for the resulting metal nanoparticles. The mechanism involves both the solid-state oxidation of the green rust support (sulfate or carbonate) and the reduction-precipitation of soluble metal precursor. The resulting nanohybrids have a platy inorganic part supporting about one to ten nanoparticles with sizes in the 20 to 120 nm range. PMID:23433071

  13. Effect of Synthesis Techniques on Crystallization and Optical Properties of Ag-Cu Bimetallic Nanoparticles

    NASA Astrophysics Data System (ADS)

    Xiong, Ziye; Qin, Fen; Huang, Po-Shun; Nettleship, Ian; Lee, Jung-Kun

    2016-04-01

    Silver (Ag)-copper (Cu) bimetallic nanoparticles (NPs) were synthesized by the reduction of silver nitrate and copper (II) acetate monohydrate using ethylene glycol in a microwave (MW) heating system with controlled reaction times ranging from 5 min to 30 min. The molar ratio Ag/Cu was varied from 1:1 to 1:3. The effect of reaction conditions on the bimetallic NPs structures and compositions were characterized by x-ray photoelectron spectroscopy, x-ray diffraction and transmission electron microscopy. The average particle size was approximately 150 nm. The surface plasmon resonance (SPR) of Ag-Cu bimetallic NPs was investigated by monitoring the SPR band peak behavior via UV/Vis spectrophotometry. The resonance peak positions and peak widths varied due to the different structures of the bimetallic NPs created under the synthesis conditions. In the MW heating method, the reduction of Cu was increased and Cu was inhomogeneously deposited over the Ag cores. As the composition of Cu becoming higher in the Ag-Cu bimetallic NPs, the absorption between 400 nm to 600 nm was greatly enhanced.

  14. Synthesis and thermal behavior of tin-based alloy (Sn-Ag-Cu) nanoparticles

    NASA Astrophysics Data System (ADS)

    Roshanghias, Ali; Yakymovych, Andriy; Bernardi, Johannes; Ipser, Herbert

    2015-03-01

    The prominent melting point depression of nanoparticles has been the subject of a considerable amount of research. For their promising applications in electronics, tin-based nano-alloys such as near-eutectic Sn-Ag-Cu (SAC) alloys have been synthesized via various techniques. However, due to issues such as particle aggregation and oxidation or introduced impurities, the application of these nano-size particles has been confined or aborted. For instance, thermal investigations by DTA/DSC in a large number of studies revealed exothermic peaks in the range of 240-500 °C, i.e. above the melting point of SAC nanoparticles, with different and quite controversial explanations for this unclear phenomenon. This represents a considerable drawback for the application of nanoparticles. Correspondingly, in the current study, the thermal stability of SAC nanoparticles has been investigated via electron microscopy, XRD, FTIR, and DSC/TG analysis. It was found that the nanoparticles consist mainly of a metallic β-Sn core and an amorphous tin hydroxide shell structure. The SnO crystalline phase formation from this amorphous shell has been associated with the exothermic peaks on the first heating cycle of the nanoparticles, followed by a disproportionation reaction into metallic Sn and SnO2.The results also revealed that the surfactant and reducing agent cannot only affect the size and size distribution of the nanoparticles, they might also alter the ratio between the amorphous shell and the crystalline core in the structure of particles.The prominent melting point depression of nanoparticles has been the subject of a considerable amount of research. For their promising applications in electronics, tin-based nano-alloys such as near-eutectic Sn-Ag-Cu (SAC) alloys have been synthesized via various techniques. However, due to issues such as particle aggregation and oxidation or introduced impurities, the application of these nano-size particles has been confined or aborted. For

  15. Synthesis of ZnS:Ag,Co water-soluble blue afterglow nanoparticles and application in photodynamic activation

    NASA Astrophysics Data System (ADS)

    Ma, Lun; Zou, Xiaoju; Hossu, Marius; Chen, Wei

    2016-08-01

    Silver and cobalt co-doped ZnS (ZnS:Ag,Co) water-soluble afterglow nanoparticles were synthesized using a wet chemistry method followed by aging at room temperature. The nanoparticles had a cubic zinc blende structure with average sizes of approximately 4 nm and emitted a blue fluorescence emission centered at 441 nm due to radiative transitions from surface defects to Ag+ luminescent centers. Intense afterglow emission peaking at 475 nm from the obtained nanoparticles was observed and was red-shifted compared to the fluorescence emission peak. X-ray photoelectron spectroscopy revealed a large increase of O/S ratio, indicating a surface oxidation process during aging. The S vacancies produced accordingly may contribute to form more electron traps and enhance afterglow. The ZnS:Ag,Co afterglow nanoparticles have a very low dark-toxicity and are applied as a light source for photodynamic therapy activation by conjugating with protoporphyrin together. Our preliminary study has shown that the ZnS:Ag,Co afterglow nanoparticles can significantly reduce the x-ray dosage used in activation and thus may be a very promising candidate for future x-ray excited photodynamic therapy in deep cancer treatment.

  16. Size and Aging Effects on Antimicrobial Efficiency of Silver Nanoparticles Coated on Polyamide Fabrics Activated by Atmospheric DBD Plasma.

    PubMed

    Zille, Andrea; Fernandes, Margarida M; Francesko, Antonio; Tzanov, Tzanko; Fernandes, Marta; Oliveira, Fernando R; Almeida, Luís; Amorim, Teresa; Carneiro, Noémia; Esteves, Maria F; Souto, António P

    2015-07-01

    This work studies the surface characteristics, antimicrobial activity, and aging effect of plasma-pretreated polyamide 6,6 (PA66) fabrics coated with silver nanoparticles (AgNPs), aiming to identify the optimum size of nanosilver exhibiting antibacterial properties suitable for the manufacture of hospital textiles. The release of bactericidal Ag(+) ions from a 10, 20, 40, 60, and 100 nm AgNPs-coated PA66 surface was a function of the particles' size, number, and aging. Plasma pretreatment promoted both ionic and covalent interactions between AgNPs and the formed oxygen species on the fibers, favoring the deposition of smaller-diameter AgNPs that consequently showed better immediate and durable antimicrobial effects against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus bacteria. Surprisingly, after 30 days of aging, a comparable bacterial growth inhibition was achieved for all of the fibers treated with AgNPs <100 nm in size. The Ag(+) in the coatings also favored the electrostatic stabilization of the plasma-induced functional groups on the PA66 surface, thereby retarding the aging process. At the same time, the size-related ratio (Ag(+)/Ag(0)) of the AgNPs between 40 and 60 nm allowed for the controlled release of Ag(+) rather than bulk silver. Overall, the results suggest that instead of reducing the size of the AgNPs, which is associated with higher toxicity, similar long-term effects can be achieved with larger NPs (40-60 nm), even in lower concentrations. Because the antimicrobial efficiency of AgNPs larger than 30 nm is mainly ruled by the release of Ag(+) over time and not by the size and number of the AgNPs, this parameter is crucial for the development of efficient antimicrobial coatings on plasma-treated surfaces and contributes to the safety and durability of clothing used in clinical settings.

  17. Ultrafine Au and Ag Nanoparticles Synthesized from Self-Assembled Peptide Fibers and Their Excellent Catalytic Activity.

    PubMed

    Xu, Wenlong; Hong, Yue; Hu, Yuanyuan; Hao, Jingcheng; Song, Aixin

    2016-07-18

    The self-assembly of an amphiphilic peptide molecule to form nanofibers facilitated by Ag(+) ions was investigated. Ultrafine AgNPs (NPs=nanoparticles) with an average size of 1.67 nm were synthesized in situ along the fibers due to the weak reducibility of the -SH group on the peptide molecule. By adding NaBH4 to the peptide solution, ultrafine AgNPs and AuNPs were synthesized with an average size of 1.35 and 1.18 nm, respectively. The AuNPs, AgNPs, and AgNPs/nanofibers all exhibited excellent catalytic activity toward the reduction of 4-nitrophenol, with turnover frequency (TOF) values of 720, 188, and 96 h(-1) , respectively. Three dyes were selected for catalytic degradation by the prepared nanoparticles and the nanoparticles showed selective catalysis activity toward the different dyes. It was a surprising discovery that the ultrafine AuNPs in this work had an extremely high catalytic activity toward methylene blue, with a reaction rate constant of 0.21 s(-1) and a TOF value of 1899 h(-1) .

  18. Y{sub 2}O{sub 3}:Eu{sup 3+} (5 mol%) with Ag nanoparticles prepared by citrate precursor

    SciTech Connect

    Ferrari, J.L.; Cebim, M.A.; Pires, A.M.; Couto dos Santos, M.A.

    2010-09-15

    Y{sub 2}O{sub 3}:Eu{sup 3+} (5 mol% Eu{sup 3+}) and Y{sub 2}O{sub 3}:Eu{sup 3+} (5 mol% Eu{sup 3+}) containing 1 mol% of Ag nanoparticles were prepared by heat treatment of a viscous resin obtained via citrate precursor. TEM and EDS analyses showed that Y{sub 2}O{sub 3}:Eu{sup 3+} (5 mol% Eu{sup 3+}) is formed by nanoparticles with an average size of 12 nm, which increases to 30 nm when Ag is present because the effect of metal induced crystallization occurs. Ag nanoparticles with a size of 9 nm dispersed in Y{sub 2}O{sub 3}:Eu{sup 3+} (5 mol% Eu{sup 3+}) were obtained and the surface plasmon effect on Ag nanoparticles was observed. The emission around 612 nm assigned to the Eu{sup 3+} ({sup 5}D{sub 0{yields}}{sup 7}F{sub 2}) transition enhanced when the Ag nanoparticles were present in the Y{sub 2}O{sub 3}:Eu{sup 3+} luminescent material. - Graphical abstract: The presence of Ag nanoparticles together Y{sub 2}O{sub 3}:Eu{sup 3+} 5 mol% phosphor showed to affect directly the optical and crystallinity of the material. Luminescence spectra show directly the effect observed.

  19. Polymer Assisted Core-shell Ag-C nanoparticles Synthesis via Green hydrothermal Technique

    NASA Astrophysics Data System (ADS)

    Williams, James; Mishra, Sanjay

    2009-03-01

    Core-Shell Ag-C nanoparticles were synthesized in the presence of glucose through a one-pot green hydrothermal wet chemical process. An aqueous solution of glucose and Ag nitrate was hydrothermally treated to produce porous carbonaceous shell over silver core nanoparticles. The growth of carbon shells was regulated by either of the polymers (poly) vinyl pyrrolidone (PVP) or poly vinyl alcohol (PVA). The two polymers were compared to take a measure of different tunable sizes of cores, and shells. The effects of hydrothermal temperature, time, and concentration of reagents on the final formation of nanostructures were studied using UV-vis extinction spectra, transmission electron microscope, and Raman spectroscopy. The polymer molecules were found to be incorporated into carbonaceous shell. The resulting opacity of the shell was found to be hydrothermal time and temperature dependent. The shell structure was found to be more uniform with PVP than PVA. Furthermore, the polymer concentration was found to influence size and shape of the core-silver particles as well. The core-shelled nanoparticles have surfaces with organic groups capable of assembling with different reagents that could be useful in drug-delivery, optical nanodevices or biochemistry.

  20. Dendritic macromolecules supported Ag nanoparticles as efficient catalyst for the reduction of 4-nitrophenol

    NASA Astrophysics Data System (ADS)

    Safari, Javad; Zarnegar, Zohre; Sadeghi, Masoud; Enayati-Najafabadi, Azadeh

    2016-12-01

    Polymer supported Ag nanoparticles, generated in situ by silver nitrate (AgNO3) reduction under reaction conditions, catalyzed the hydrogenation of 4-nitrophenol with high efficiency in water at room temperature in the presence of an excess amount of NaBH4. Amphiphilic linear-dendritic copolymers containing a poly(ethylene glycol) (PEG) core and poly(2-ethyl-2-oxazoline)-poly(ε-caprolactone) arms were able to load the Ag nanoparticles. The Ag nanoparticles with a diameter of 8-10 nm were found to show a comparable catalytic activity towards formation of the aromatic amine as single product with short reaction time.

  1. Reversibly phototunable TiO{sub 2} photonic crystal modulated by Ag nanoparticles' oxidation/reduction

    SciTech Connect

    Liu Jian; Zhou Jinming; Ye Changqing; Li Mingzhu; Wang Jingxia; Jiang Lei; Song Yanlin

    2011-01-10

    We report a reversibly phototunable photonic crystal system whose reflectance at the stop band position can be modulated by alternating UV/visible (UV/Vis) irradiation. The phototunable system consists of Ag nanoparticles and TiO{sub 2} photonic crystal. The stop bands intensity of Ag loaded TiO{sub 2} photonic crystals were found to be dependent on the redox states of Ag nanoparticles. The quasi 'on' and 'off' states of the stop band were reversibly modulated by the Ag nanoparticles' oxidation/reduction through alternating UV/Vis light irradiation.

  2. Redox-Robust Pentamethylferrocene Polymers and Supramolecular Polymers, and Controlled Self-Assembly of Pentamethylferricenium Polymer-Embedded Ag, AgI, and Au Nanoparticles.

    PubMed

    Gu, Haibin; Ciganda, Roberto; Castel, Patricia; Vax, Amélie; Gregurec, Danijela; Irigoyen, Joseba; Moya, Sergio; Salmon, Lionel; Zhao, Pengxiang; Ruiz, Jaime; Hernández, Ricardo; Astruc, Didier

    2015-12-01

    We report the first pentamethylferrocene (PMF) polymers and the redox chemistry of their robust polycationic pentamethylferricenium (PMFium) analogues. The PMF polymers were synthesized by ring-opening metathesis polymerization (ROMP) of a PMF-containing norbornene derivative by using the third-generation Grubbs ruthenium metathesis catalyst. Cyclic voltammetry studies allowed us to determine confidently the number of monomer units in the polymers through the Bard-Anson method. Stoichiometric oxidation by using ferricenium hexafluorophosphate quantitatively and instantaneously provided fully stable (even in aerobic solutions) blue d(5) Fe(III) metallopolymers. Alternatively, oxidation of the PMF-containing polymers was conducted by reactions with Ag(I) or Au(III) , to give PMFium polymer-embedded Ag and Au nanoparticles (NPs). In the presence of I2 , oxidation by using Ag(I) gave polymer-embedded Ag/AgI NPs and AgNPs at the surface of AgI NPs. Oxidation by using Au(III) also produced an Au(I) intermediate that was trapped and characterized. Engineered single-electron transfer reactions of these redox-robust nanomaterial precursors appear to be a new way to control their formation, size, and environment in a supramolecular way.

  3. Redox-Robust Pentamethylferrocene Polymers and Supramolecular Polymers, and Controlled Self-Assembly of Pentamethylferricenium Polymer-Embedded Ag, AgI, and Au Nanoparticles.

    PubMed

    Gu, Haibin; Ciganda, Roberto; Castel, Patricia; Vax, Amélie; Gregurec, Danijela; Irigoyen, Joseba; Moya, Sergio; Salmon, Lionel; Zhao, Pengxiang; Ruiz, Jaime; Hernández, Ricardo; Astruc, Didier

    2015-12-01

    We report the first pentamethylferrocene (PMF) polymers and the redox chemistry of their robust polycationic pentamethylferricenium (PMFium) analogues. The PMF polymers were synthesized by ring-opening metathesis polymerization (ROMP) of a PMF-containing norbornene derivative by using the third-generation Grubbs ruthenium metathesis catalyst. Cyclic voltammetry studies allowed us to determine confidently the number of monomer units in the polymers through the Bard-Anson method. Stoichiometric oxidation by using ferricenium hexafluorophosphate quantitatively and instantaneously provided fully stable (even in aerobic solutions) blue d(5) Fe(III) metallopolymers. Alternatively, oxidation of the PMF-containing polymers was conducted by reactions with Ag(I) or Au(III) , to give PMFium polymer-embedded Ag and Au nanoparticles (NPs). In the presence of I2 , oxidation by using Ag(I) gave polymer-embedded Ag/AgI NPs and AgNPs at the surface of AgI NPs. Oxidation by using Au(III) also produced an Au(I) intermediate that was trapped and characterized. Engineered single-electron transfer reactions of these redox-robust nanomaterial precursors appear to be a new way to control their formation, size, and environment in a supramolecular way. PMID:26494439

  4. Size-dependent thermopower of nickel nanoparticles

    SciTech Connect

    Singh, Jaiveer; Kaurav, N.; Okram, Gunadhor S.

    2014-04-24

    Nickel nanoparticles (Ni-NPs) were prepared by thermal decomposition method using Trioctylphosphine (TOP) and Oleylamine (OA). The average particle size (D) estimated from X-ray diffraction (XRD) using Scherrer equation, to be 1-10nm, systematically decreases with increasing concentration of TOP at constant OA concentration. The observed thermopower strongly depends on particle size particularly at low temperatures reaching a very high value of ∼ 10{sup 5} μV/K (at 20 K), and is attributed to the enhanced grain-boundary scattering combined with quantum confinement.

  5. Tunable Au-Ag nanobowl arrays for size-selective plasmonic biosensing.

    PubMed

    Jana, Debrina; Lehnhoff, Emily; Bruzas, Ian; Robinson, Jendai; Lum, William; Sagle, Laura

    2016-08-01

    Selectivity is often a major obstacle for localized surface plasmon resonance-based biosensing in complex biological solutions. An additional degree of selectivity can be achieved through the incorporation of shape complementarity on the nanoparticle surface. Here, we report the versatile fabrication of substrate-bound Au-Ag nanobowl arrays through the galvanic ion replacement of silver nanodisk arrays. Both localized surface plasmon resonance (LSPR) and surface enhanced Raman spectroscopy (SERS) were carried out to detect the binding of analytes of varying size to the nanobowl arrays. Large increases in the LSPR and SERS response were measured for analytes that were small enough to enter the nanobowls, compared to those too large to come into contact with the interior of the nanobowls. This size-selective sensing should prove useful in both size determination and differentiation of large analytes in biological solutions, such as viruses, fungi, and bacterial cells.

  6. Impact of Ag nanoparticle exposure on p,p'-DDE bioaccumulation by Cucurbita pepo (zucchini) and Glycine max (soybean).

    PubMed

    De La Torre-Roche, Roberto; Hawthorne, Joseph; Musante, Craig; Xing, Baoshan; Newman, Lee A; Ma, Xingmao; White, Jason C

    2013-01-15

    The effect of nanoparticle (NP), bulk, or ionic Ag exposure on dichlorodiphenyldichloroethylene (p,p'-DDE; DDT metabolite) accumulation by Glycine max L. (soybean) and Cucurbita pepo L. (zucchini) was investigated. The plants were grown in 125-mL jars of vermiculite amended with 500 or 2000 mg/L of bulk or NP Ag; ion controls at 5 and 20 mg/L were established. During 19 d of growth, plants were amended with solution containing 100 ng/mL of p,p'-DDE. Total shoot p,p'-DDE levels in non-Ag exposed G. max and C. pepo were 500 and 970 ng, respectively; total root DDE content was 13,700 and 20,300 ng, respectively. Ag decreased the p,p'-DDE content of G. max tissues by up to 40%, with NP exposure resulting in less contaminant uptake than bulk Ag. Total Ag content of exposed G. max ranged from 50.5 to 373 μg; NP-exposed plants had 1.9-2.2 times greater overall Ag than corresponding bulk particle treatments and also significantly greater relative Ag transport to shoot tissues. Bulk and NP Ag at 500 mg/L suppressed DDE uptake by C. pepo by 21-29%, although Ag exposure at 2000 mg/L had no impact on contaminant uptake. Similar to G. max , C. pepo whole plant Ag content ranged from 50.5 to 182 μg, with tissue element content generally being greater for NP exposed plants. These findings show that the Ag may significantly alter the accumulation and translocation of cocontaminants in agricultural systems. Notably, the cocontaminant interactions vary both with Ag particle size (NP vs bulk) and plant species. Future investigations will be needed to clarify the mechanisms responsible for the cocontaminant interactions and assess the impact on overall exposure and risk.

  7. Laser induced mechanisms controlling the size distribution of metallic nanoparticles.

    PubMed

    Liu, Zeming; Vitrant, Guy; Lefkir, Yaya; Bakhti, Said; Destouches, Nathalie

    2016-09-21

    This paper describes a model to simulate changes in the size distribution of metallic nanoparticles (NPs) in TiO2 films upon continuous wave light excitation. Interrelated laser induced physical and chemical processes initiated directly by photon absorption or by plasmon induced thermal heating are considered. Namely the model takes into account the NP coalescence, Ostwald ripening, the reduction of silver ions and the oxidation of metallic NPs, competitive mechanisms that can lead to counter-intuitive behaviors depending on the exposure conditions. Theoretical predictions are compared successfully to the experimental results deduced from a thorough analysis of scanning transmission electron microscopy (STEM) pictures of Ag:TiO2 films processed with a scanning visible laser beam at different speeds. Ag:TiO2 systems are considered for many applications in solar energy conversion, photocatalysis or secured data printing. Numerical investigations of such a system provide a better understanding of light induced growth and shrinking processes and open up prospects for designing more efficient photocatalytic devices based on metal NP doped TiO2 or for improving the size homogeneity in self-organized metallic NP patterns, for instance. PMID:27539293

  8. Ag nanoparticle decorated nanoporous ZnO microrods and their enhanced photocatalytic activities.

    PubMed

    Deng, Quan; Duan, Xiaowei; Ng, Dickon H L; Tang, Haibin; Yang, Yong; Kong, Mingguang; Wu, Zhikun; Cai, Weiping; Wang, Guozhong

    2012-11-01

    Nanostructured Ag nanoparticles (Ag-NPs)/nanoporous ZnO micrometer-rods (n-ZnO MRs) have been synthesized by a two-step method. The n-ZnO MRs was initially prepared by solvothermal-assisted heat treatment. The rods had the diameter ranged from 90 to 150 nm and length between 0.5 and 3 μm. They were found to be porous and were composited of ZnO nanopartiles with size of about 20 nm. In the second stage, Ag-NPs with a diameter of 20-50 nm were anchored onto the surface of the as-prepared n-ZnO MRs by a photoreduction method. The Ag-NPs/n-ZnO MRs were evaluated for their ability to degrade methylene blue (MB) solution under visible to ultraviolet (UV) light irradiation. The rate of degradation of the as-prepared Ag-NPs/n-ZnO MRs was more than twice and nearly 5.6 times faster than that of using bare n-ZnO MRs under the UV and solar light irradiation, respectively. The formation of Schottky barriers in the regions between the Ag-NPs and n-ZnO MRs had improved the charge separation and consequently enhanced the efficiency of the degradation process. Moreover, the as-prepared hybrid structure exhibited high photostability, and 98% of degradation efficiency could be maintained even after being used five times. This endurance was attributed to the retardation of photocorrosion of ZnO as a result of the low concentration of surface defects in the as-prepared n-ZnO MRs. It also minimized the surface defects of the as-prepared n-ZnO MRs and consequently further inhibited the photocorrosion of ZnO when the deposited Ag-NPs were much more inclined to combine with the chemisorbed oxygen.

  9. A simple and large-scale strategy for the preparation of Ag nanoparticles supported on resin-derived carbon and their antibacterial properties

    NASA Astrophysics Data System (ADS)

    Wang, Baoli; Tian, Chungui; Zheng, Chunying; Wang, Lei; Fu, Honggang

    2009-01-01

    A simple strategy was developed for preparing stable Ag nanoparticles supported on carbon by carbonizing Ag+/acrylic acid type ion-exchange resin complexes under N2 atmosphere. The products were characterized by x-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV-visible absorption spectroscopy. The results indicated that the Ag nanoparticles were well dispersed on the surface of carbon, and their size could be regulated by tuning the carbonization temperature. The antibacterial assay showed that the Ag/C composites possess good antibacterial properties that are determined largely by the Ag particle size. Furthermore, the composites are very stable and they do not show obviously change even after storing at ambient conditions for more than one year.

  10. High Yield Seedless Synthesis of Uniform Silver Nanoparticles with Different Sizes.

    PubMed

    Xi, Chunxiao; Song, Yahui; Zhang, Jihui; Zhang, Dongmei; Xia, Haibing

    2016-06-01

    Currently, seed-mediated growth method is the dominant strategy for synthesis of silver nanoparticles (Ag NPs) with different sizes. However, it is complicated for the researchers with limited chemistry-training. In this work, monodisperse, quasi-spherical Ag NPs with different sizes were successfully produced in high yield by adding a trace amount of NaBH4 solution into the mixtures of AgNO3, ascorbic acid and cetyltrimethylammonium chloride (CTAC) as surfactants. It was found that the sizes of as-prepared Ag NPs can be tuned from 20 nm to 50 nm by adjusting the NaBH4 concentration at optimal pH (about 6.33) and CTAC concentration (0.02-0.06 M). The surface-enhanced Raman scattering (SERS) activity of 50 nm Ag NPs shows an enhanced enhancement factor for 4-aminothiophenol (4-ATP) molecules (2.5 x 10(7) for a(1) mode). Moreover, Raman signals (a(g) mode) of 4,4'-dimercaptoazobenzene (DMAB) molecules were also observed due to the laser-induced transformation of 4-ATP molecules on the surfaces of 50 nm Ag NPs during SERS measurement. Furthermore, the transformation of probe molecules on the surfaces of metal NPs during SERS measurement have to be considered. PMID:27427638

  11. Ablation and optical third-order nonlinearities in Ag nanoparticles

    PubMed Central

    Torres-Torres, Carlos; Peréa-López, Néstor; Reyes-Esqueda, Jorge Alejandro; Rodríguez-Fernández, Luis; Crespo-Sosa, Alejandro; Cheang-Wong, Juan Carlos; Oliver, Alicia

    2010-01-01

    The optical damage associated with high intensity laser excitation of silver nanoparticles (NPs) was studied. In order to investigate the mechanisms of optical nonlinearity of a nanocomposite and their relation with its ablation threshold, a high-purity silica sample implanted with Ag ions was exposed to different nanosecond and picosecond laser irradiations. The magnitude and sign of picosecond refractive and absorptive nonlinearities were measured near and far from the surface plasmon resonance (SPR) of the Ag NPs with a self-diffraction technique. Saturable optical absorption and electronic polarization related to self-focusing were identified. Linear absorption is the main process involved in nanosecond laser ablation, but non-linearities are important for ultrashort picosecond pulses when the absorptive process become significantly dependent on the irradiance. We estimated that near the resonance, picosecond intraband transitions allow an expanded distribution of energy among the NPs, in comparison to the energy distribution resulting in a case of far from resonance, when the most important absorption takes place in silica. We measured important differences in the ablation threshold and we estimated that the high selectiveness of the SPR of Ag NPs as well as their corresponding optical nonlinearities can be strongly significant for laser-induced controlled explosions, with potential applications for biomedical photothermal processes. PMID:21187944

  12. Single molecule detection using SERS study in PVP functionalized Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Garg, Parul; Dhara, S.

    2013-02-01

    Non-spherical functionalized Ag nanoparticles (NPs) with homogenous size ˜ 40 nm have been grown using soft chemical route. Solution of silver nitrate and polyvinylpyrrolidone is reduced in excess of ethylene glycol for the preparation of the NPs. Substrates has been prepared by dip coating of the NPs on c-Si for Raman studies. Rhodamine (R6G) is used as a test molecule to study the surface enhanced Raman spectroscopy (SERS) effect. A single molecule detection of R6G along with an enhancement factor of ˜ 4×103 orders of magnitude in the intensity, for the concentration as low as 10-12 M using polymer coated Ag NPs as SERS substrates, has been achieved.

  13. Role of silver nanoparticles (AgNPs) on the cardiovascular system.

    PubMed

    Gonzalez, Carmen; Rosas-Hernandez, Hector; Ramirez-Lee, Manuel Alejandro; Salazar-García, Samuel; Ali, Syed F

    2016-03-01

    With the advent of nanotechnology, the use and applications of silver nanoparticles (AgNPs) have increased, both in consumer products as well as in medical devices. However, little is known about the effects of these nanoparticles on human health, more specific in the cardiovascular system, since this system represents an important route of action in terms of distribution, bioaccumulation and bioavailability of the different circulating substances in the bloodstream. A collection of studies have addressed the effects and applications of different kinds of AgNPs (shaped, sized, coated and functionalized) in several components of the cardiovascular system, such as endothelial cells, isolated vessels and organs as well as integrative animal models, trying to identify the underlying mechanisms involved in their actions, to understand their implication in the field of biomedicine. The purpose of the present review is to summarize the most relevant studies to date of AgNPs effects in the cardiovascular system and provide a broader picture of the potential toxic effects and exposure risks, which in turn will allow pointing out the directions of further research as well as new applications of these versatile nanomaterials.

  14. Role of silver nanoparticles (AgNPs) on the cardiovascular system.

    PubMed

    Gonzalez, Carmen; Rosas-Hernandez, Hector; Ramirez-Lee, Manuel Alejandro; Salazar-García, Samuel; Ali, Syed F

    2016-03-01

    With the advent of nanotechnology, the use and applications of silver nanoparticles (AgNPs) have increased, both in consumer products as well as in medical devices. However, little is known about the effects of these nanoparticles on human health, more specific in the cardiovascular system, since this system represents an important route of action in terms of distribution, bioaccumulation and bioavailability of the different circulating substances in the bloodstream. A collection of studies have addressed the effects and applications of different kinds of AgNPs (shaped, sized, coated and functionalized) in several components of the cardiovascular system, such as endothelial cells, isolated vessels and organs as well as integrative animal models, trying to identify the underlying mechanisms involved in their actions, to understand their implication in the field of biomedicine. The purpose of the present review is to summarize the most relevant studies to date of AgNPs effects in the cardiovascular system and provide a broader picture of the potential toxic effects and exposure risks, which in turn will allow pointing out the directions of further research as well as new applications of these versatile nanomaterials. PMID:25543135

  15. Fluoride-induced reduction of Ag(I) cation leading to formation of silver mirrors and luminescent Ag-nanoparticles.

    PubMed

    Maity, Krishnendu; Panda, Dillip K; Lochner, Eric; Saha, Sourav

    2015-03-01

    In aprotic solvents, Lewis basic F(-) anion reduces Lewis acidic Ag(I) cation to Ag(0), forming metallic silver mirrors on the inner surfaces of reaction vessels and luminescent Ag-nanoparticles (AgNPs) in supernatant solutions, which emit blue light upon UV irradiation. The F(-)-induced formation of silver mirrors and AgNPs was confirmed through X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), fluorescence spectroscopy, and mass spectrometry, whereas the Ag(I)-induced oxidation of F(-) to Ḟ radical, followed by its conversion to HF2(-) via H-abstraction and H-bonding, was evident from (19)F NMR spectroscopy. This redox reaction is deactivated in water, as the reducing power of hydrated F(-) diminishes drastically. Less Lewis basic Cl(-), Br(-), and I(-) ions do not reduce Ag(I) to Ag(0), instead they can only form Ag(I) halide precipitates irrespective of protic or aprotic solvents. The Ag-coated surfaces, luminescent AgNPs, and Ḟ radicals produced by this unprecedented redox reaction could be exploited as electrodes, light-emitting materials, and radical initiators, respectively.

  16. Size-dependent melting of Bi nanoparticles

    NASA Astrophysics Data System (ADS)

    Olson, E. A.; Efremov, M. Yu.; Zhang, M.; Zhang, Z.; Allen, L. H.

    2005-02-01

    Nanocalorimetry was used to investigate the melting of Bi nanoparticles. The particles were formed by evaporating Bi onto a silicon nitride substrate, which was then heated. The particles self-assemble into truncated spherical particles. Below 5-nm average film thickness, mean particle sizes increased linearly with deposition thickness but increased rapidly for 10-nm-thick films. As expected, small particles were found to exhibit size-dependent melting temperatures less than the bulk melting temperature (e.g., ΔT =67K for a 3-nm radius particle). The measured melting temperatures for particles below ˜7nm in radius, however, were ˜50K above the value predicted by the homogeneous melting model. We discuss this discrepancy in terms of a possible size-dependent crystal structure change and the superheating of the solid phase.

  17. Plasmonic properties of Ag nanoparticles embedded in GeO2-SiO2 matrix by atom beam sputtering.

    PubMed

    Mohapatra, Satyabrata

    2016-02-01

    Nanocomposite thin films containing Ag nanoparticles embedded in the GeO2-SiO2 matrix were synthesized by the atom beam co-sputtering technique. The structural, optical and plasmonic properties and the chemical composition of the nanocomposite thin films were studied by transmission electron microscopy (TEM) with energy dispersive X-ray spectroscopy (EDX), UV-visible absorption spectroscopy and X-ray photoelectron spectroscopy (XPS). UV-visible absorption studies on Ag-SiO2 nanocomposites revealed the presence of a strong localized surface plasmon resonance (LSPR) peak characteristic of Ag nanoparticles at 413 nm, which showed a blue shift of 26 nm (413 to 387 nm) along with a significant broadening and drastic decrease in intensity with the incorporation of 16 at% of Ge into the SiO2 matrix. TEM studies on Ag-GeO2-SiO2 nanocomposite thin films confirmed the presence of Ag nanoparticles with an average size of 3.8 nm in addition to their aggregates with an average size of 16.2 nm. Thermal annealing in air resulted in strong enhancement in the intensity of the LSPR peak, which showed a regular red shift of 51 nm (from 387 to 438 nm) with the increase in annealing temperature up to 500 °C. XPS studies showed that annealing in air resulted in oxidation of excess Ge atoms in the nanocomposite into GeO2. Our work demonstrates the possibility of controllably tuning the LSPR of Ag nanoparticles embedded in the GeO2-SiO2 matrix by single-step thermal annealing, which is interesting for optical applications.

  18. High-value utilization of lignin to synthesize Ag nanoparticles with detection capacity for Hg²⁺.

    PubMed

    Shen, Zuguang; Luo, Yuqiong; Wang, Qun; Wang, Xiaoying; Sun, Runcang

    2014-09-24

    This study reports the rapid preparation of silver nanoparticles (AgNPs) from Tollens' reagent under microwave irradiation. In the synthesis, lignin with reducing groups and spatial three-dimensional structure was used as reducing and stabilizing agents without other chemical reagents, and the effects of the ratio of lignin to Ag(+), reaction temperature, and heating time on the synthesis of AgNPs were investigated. The obtained AgNPs were further characterized by UV-vis, Malvern particle size, TEM, XRD, and XPS analyses. The structural changes of lignin before and after reaction were also studied by FT-IR, (1)H NMR, (13)C NMR, and GC-MS. The results revealed that the obtained AgNPs were mostly spherical with diameters of around 24 nm. The optimum reaction conditions were a ratio 50 mg of lignin to 0.3 mM of Ag(+), a microwave irradiation temperature of 60 °C, and a heating time of 10 min. Moreover, AgNPs redispersed well in water and ethanol after centrifugation for the removal of lignin. During the formation of AgNPs, lignin was oxidized, and the side chains of lignin were partly disrupted into small molecules, such as hydrocarbon and alcohol. The resultant lignin-AgNPs showed highly selective sensing detection for Hg(2+), and the color of the lignin-AgNP solution containing Hg(2+) decreased gradually with increasing amounts of Hg(2+) within seconds, but the other 19 metal ions had little effect on the color and surface plasmon absorption band of the lignin-AgNPs. Also, there was a linear relationship between the absorbance and Hg(2+) concentration, with a limit of detection concentration of 23 nM. This study provides not only a new way to take advantage of agricultural and forestry residues, but also a green and rapid method for the synthesis of AgNPs to detect the toxic ion Hg(2+) selectively and sensitively.

  19. The Antimicrobial Properties of Silver Nanoparticles in Bacillus subtilis Are Mediated by Released Ag+ Ions

    PubMed Central

    Hsueh, Yi-Huang; Lin, Kuen-Song; Ke, Wan-Ju; Hsieh, Chien-Te; Chiang, Chao-Lung; Tzou, Dong-Ying; Liu, Shih-Tung

    2015-01-01

    The superior antimicrobial properties of silver nanoparticles (Ag NPs) are well-documented, but the exact mechanisms underlying Ag-NP microbial toxicity remain the subject of intense debate. Here, we show that Ag-NP concentrations as low as 10 ppm exert significant toxicity against Bacillus subtilis, a beneficial bacterium ubiquitous in the soil. Growth arrest and chromosomal DNA degradation were observed, and flow cytometric quantification of propidium iodide (PI) staining also revealed that Ag-NP concentrations of 25 ppm and above increased membrane permeability. RedoxSensor content analysis and Phag-GFP expression analysis further indicated that reductase activity and cytosolic protein expression decreased in B. subtilis cells treated with 10–50 ppm of Ag NPs. We conducted X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) analyses to directly clarify the valence and fine structure of Ag atoms in B. subtilis cells placed in contact with Ag NPs. The results confirmed the Ag species in Ag NP-treated B. subtilis cells as Ag2O, indicating that Ag-NP toxicity is likely mediated by released Ag+ ions from Ag NPs, which penetrate bacterial cells and are subsequently oxidized intracellularly to Ag2O. These findings provide conclusive evidence for the role of Ag+ ions in Ag-NP microbial toxicity, and suggest that the impact of inappropriately disposed Ag NPs to soil and water ecosystems may warrant further investigation. PMID:26669836

  20. The Antimicrobial Properties of Silver Nanoparticles in Bacillus subtilis Are Mediated by Released Ag+ Ions.

    PubMed

    Hsueh, Yi-Huang; Lin, Kuen-Song; Ke, Wan-Ju; Hsieh, Chien-Te; Chiang, Chao-Lung; Tzou, Dong-Ying; Liu, Shih-Tung

    2015-01-01

    The superior antimicrobial properties of silver nanoparticles (Ag NPs) are well-documented, but the exact mechanisms underlying Ag-NP microbial toxicity remain the subject of intense debate. Here, we show that Ag-NP concentrations as low as 10 ppm exert significant toxicity against Bacillus subtilis, a beneficial bacterium ubiquitous in the soil. Growth arrest and chromosomal DNA degradation were observed, and flow cytometric quantification of propidium iodide (PI) staining also revealed that Ag-NP concentrations of 25 ppm and above increased membrane permeability. RedoxSensor content analysis and Phag-GFP expression analysis further indicated that reductase activity and cytosolic protein expression decreased in B. subtilis cells treated with 10-50 ppm of Ag NPs. We conducted X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) analyses to directly clarify the valence and fine structure of Ag atoms in B. subtilis cells placed in contact with Ag NPs. The results confirmed the Ag species in Ag NP-treated B. subtilis cells as Ag2O, indicating that Ag-NP toxicity is likely mediated by released Ag+ ions from Ag NPs, which penetrate bacterial cells and are subsequently oxidized intracellularly to Ag2O. These findings provide conclusive evidence for the role of Ag+ ions in Ag-NP microbial toxicity, and suggest that the impact of inappropriately disposed Ag NPs to soil and water ecosystems may warrant further investigation. PMID:26669836

  1. Oleate-Assisted Room Temperature Synthesis and High Photocatalytic Activity of Ag3PO4 Nanoparticles for no Decomposition

    NASA Astrophysics Data System (ADS)

    Huang, Lijun; Yin, Shu; Guo, Chongshen; Huang, Yunfang; Wang, Ming; Dong, Qiang; Li, Huihui; Kimura, Takeshi; Tanaka, Miyuki; Sato, Tsugio

    2012-06-01

    An oleate-assisted approach was used to synthesize nanosized spherical silver phosphate (Ag3PO4) in different solvents. The silver phosphate nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), ultraviolet-visible-infrared diffuse reflectance spectroscopy (DRS), thermogravimetric analysis (TDA), and surface area measurement by nitrogen adsorption and decomposition evolution of NOx gas. The as-prepared nanoparticles showed narrow size distribution. The black colored nanoparticles could absorb most of visible light with a wavelength up to 530 nm. The DeNOx experiments revealed that the nanosized Ag3PO4 possessed a photocatalytic ability being superior to commercial P25 sample both in ultraviolet light and visible light regions.

  2. Synthesis of positively charged silver nanoparticles via photoreduction of AgNO3 in branched polyethyleneimine/HEPES solutions.

    PubMed

    Tan, Siliu; Erol, Melek; Attygalle, Athula; Du, Henry; Sukhishvili, Svetlana

    2007-09-11

    Branched polyethyleneimine (BPEI) and 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES) were used collaboratively to reduce silver nitrate under UV irradiation for the synthesis of positively charged silver nanoparticles. The effects of molar ratio of the ingredients and the molecular weight of BPEI on the particle size and distribution were investigated. The mechanism for the reduction of Ag+ ions in the BPEI/HEPES mixtures entails oxidative cleavage of BPEI chains that results in the formation of positively charged BPEI fragments enriched with amide groups as well as in the production of formaldehyde, which serves as a reducing agent for Ag+ ions. The resultant silver nanoparticles are positively charged due to protonation of surface amino groups. Importantly, these positively charged Ag nanoparticles demonstrate superior SERS activity over negatively charged citrate reduced Ag nanoparticles for the detection of thiocyanate and perchlorate ions; therefore, they are promising candidates for sensing and detection of a variety of negatively charged analytes in aqueous solutions using surface-enhanced Raman spectroscopy (SERS). PMID:17705409

  3. Hydroquinone-assisted synthesis of branched au-ag nanoparticles with polydopamine coating as highly efficient photothermal agents.

    PubMed

    Li, Jing; Wang, Wenjing; Zhao, Liang; Rong, Li; Lan, Shijie; Sun, Hongchen; Zhang, Hao; Yang, Bai

    2015-06-01

    Despite the success of galvanic replacement in preparing hollow nanostructures with diversified morphologies via the replacement reaction between sacrificial metal nanoparticles (NPs) seeds and less active metal ions, limited advances are made for producing branched alloy nanostructures. In this paper, we report an extended galvanic replacement for preparing branched Au-Ag NPs with Au-rich core and Ag branches using hydroquinone (HQ) as the reductant. In the presence of HQ, the preformed Ag seeds are replaceable by Au and, in turn, supply the growth of Ag branches. By altering the feed ratio of Ag seeds, HAuCl4, and HQ, the size and morphology of the NPs are tunable. Accordingly, the surface plasmon resonance absorption is tuned to near-infrared (NIR) region, making the branched NPs as potential materials in photothermal therapy. The branched NPs are further coated with polydopamine (PDA) shell via dopamine polymerization at room temperature. In comparison with bare NPs, PDA-coated branched Au-Ag (Au-Ag@PDA) NPs exhibit improved stability, biocompatibility, and photothermal performance. In vitro experiments indicate that the branched Au-Ag@PDA NPs are competitive agents for photothermal ablation of cancer cells. PMID:25969998

  4. Hydroquinone-assisted synthesis of branched au-ag nanoparticles with polydopamine coating as highly efficient photothermal agents.

    PubMed

    Li, Jing; Wang, Wenjing; Zhao, Liang; Rong, Li; Lan, Shijie; Sun, Hongchen; Zhang, Hao; Yang, Bai

    2015-06-01

    Despite the success of galvanic replacement in preparing hollow nanostructures with diversified morphologies via the replacement reaction between sacrificial metal nanoparticles (NPs) seeds and less active metal ions, limited advances are made for producing branched alloy nanostructures. In this paper, we report an extended galvanic replacement for preparing branched Au-Ag NPs with Au-rich core and Ag branches using hydroquinone (HQ) as the reductant. In the presence of HQ, the preformed Ag seeds are replaceable by Au and, in turn, supply the growth of Ag branches. By altering the feed ratio of Ag seeds, HAuCl4, and HQ, the size and morphology of the NPs are tunable. Accordingly, the surface plasmon resonance absorption is tuned to near-infrared (NIR) region, making the branched NPs as potential materials in photothermal therapy. The branched NPs are further coated with polydopamine (PDA) shell via dopamine polymerization at room temperature. In comparison with bare NPs, PDA-coated branched Au-Ag (Au-Ag@PDA) NPs exhibit improved stability, biocompatibility, and photothermal performance. In vitro experiments indicate that the branched Au-Ag@PDA NPs are competitive agents for photothermal ablation of cancer cells.

  5. Maximizing the photo catalytic and photo response properties of multimodal plasmonic Ag/WO(3-x) heterostructure nanorods by variation of the Ag size.

    PubMed

    Ghosh, Sirshendu; Saha, Manas; Paul, Sumana; De, S K

    2015-11-21

    High quality nearly monodisperse colloidal WO3-x nanorods with an aspect ratio ∼18 were synthesized using the thermal decomposition technique. The effects of a capping agent and an activating agent on the nanorod aspect ratio have been studied. Excess carrier concentration due to large oxygen vacancy and smaller width of the nanorods compared to the Bohr exciton radius gives rise to an increase of the band gap. Shape anisotropy in nanorods results in two plasmonic absorbance bands at about 890 nm and 5900 nm corresponding to short axis and long axis plasmon modes. The short axis mode reveals an excellent plasmonic sensitivity of ∼345 nm per refractive index. A plasmonic photocatalysis process based on WO3-x nanorods has been developed to synthesize Ag/WO3-x heterostructures consisting of multiple Ag dots with ∼2 nm size, randomly decorated on the surface of the WO3-x nanorods. Long time irradiation leads to an increase in the size (5 nm) of Ag nanocrystals concomitant with decrease in the number of Ag nanocrystals attached per WO3-x nanorod. Plasmonic photocatalysis followed by thermal annealing produces only one Ag nanocrystal of size ∼10 nm on each WO3-x nanorod. Red shifting and broadening of plasmon bands of Ag nanocrystals and WO3-x nanorods confirm the formation of heterostructures between the metal and semiconductor. Detailed transmission electron micrograph analysis indicates the epitaxial growth of Ag nanocrystals onto WO3-x nanorods. A high photocurrent gain of about 4000 is observed for Ag (10 nm)/WO3-x heterostructures. The photodegradation rate for Rhodamine-B and methylene blue is maximum for Ag (10 nm)/WO3-x heterostructures due to efficient electron transfer from WO3-x nanorods to Ag nanocrystals. Metal plasmon-semiconductor exciton coupling, prominent plasmon absorbance of metal nanoparticles, and formation of an epitaxial interface are found to be the important factors to achieve the maximum photocatalytic activity and fabrication of a

  6. Ag nanoparticle-ZnO nanowire hybrid nanostructures as enhanced and robust antimicrobial textiles via a green chemical approach.

    PubMed

    Li, Zhou; Tang, Haoying; Yuan, Weiwei; Song, Wei; Niu, Yongshan; Yan, Ling; Yu, Min; Dai, Ming; Feng, Siyu; Wang, Menghang; Liu, Tengjiao; Jiang, Peng; Fan, Yubo; Wang, Zhong Lin

    2014-04-11

    A new approach for fabrication of a long-term and recoverable antimicrobial nanostructure/textile hybrid without increasing the antimicrobial resistance is demonstrated. Using in situ synthesized Ag nanoparticles (NPs) anchored on ZnO nanowires (NWs) grown on textiles by a 'dip-in and light-irradiation' green chemical method, we obtained ZnONW@AgNP nanocomposites with small-size and uniform Ag NPs, which have shown superior performance for antibacterial applications. These new Ag/ZnO/textile antimicrobial composites can be used for wound dressings and medical textiles for topical and prophylactic antibacterial treatments, point-of-use water treatment to improve the cleanliness of water and antimicrobial air filters to prevent bioaerosols accumulating in ventilation, heating, and air-conditioning systems.

  7. Ag nanoparticle-ZnO nanowire hybrid nanostructures as enhanced and robust antimicrobial textiles via a green chemical approach

    NASA Astrophysics Data System (ADS)

    Li, Zhou; Tang, Haoying; Yuan, Weiwei; Song, Wei; Niu, Yongshan; Yan, Ling; Yu, Min; Dai, Ming; Feng, Siyu; Wang, Menghang; Liu, Tengjiao; Jiang, Peng; Fan, Yubo; Wang, Zhong Lin

    2014-04-01

    A new approach for fabrication of a long-term and recoverable antimicrobial nanostructure/textile hybrid without increasing the antimicrobial resistance is demonstrated. Using in situ synthesized Ag nanoparticles (NPs) anchored on ZnO nanowires (NWs) grown on textiles by a ‘dip-in and light-irradiation’ green chemical method, we obtained ZnONW@AgNP nanocomposites with small-size and uniform Ag NPs, which have shown superior performance for antibacterial applications. These new Ag/ZnO/textile antimicrobial composites can be used for wound dressings and medical textiles for topical and prophylactic antibacterial treatments, point-of-use water treatment to improve the cleanliness of water and antimicrobial air filters to prevent bioaerosols accumulating in ventilation, heating, and air-conditioning systems.

  8. Unaffected features of BSA stabilized Ag nanoparticles after storage and reconstitution in biological relevant media.

    PubMed

    Valenti, Laura E; Giacomelli, Carla E

    2015-08-01

    Silver-coated orthopedic implants and silver composite materials have been proposed to produce local biocidal activity at low dose to reduce post-surgery infection that remains one of the major contributions to the patient morbidity. This work presents the synthesis combined with the characterization, colloidal stability in biological relevant media, antimicrobial activity and handling properties of silver nanoparticles (Ag-NP) before and after freeze dry and storage. The nanomaterial was synthesized in aqueous solution with simple, reproducible and low-cost strategies using bovine serum albumin (BSA) as the stabilizing agent. Ag-NP were characterized by means of the size distribution and morphology (UV-vis spectra, dynamic light scattering measurements and TEM images), charge as a function of the pH (zeta potential measurements) and colloidal stability in biological relevant media (UV-vis spectra and dynamic light scattering measurements). Further, the interactions between the protein and Ag-NP were evaluated by surface enhanced Raman spectroscopy (SERS) and the antimicrobial activity was tested with two bacteria strains (namely Staphylococcus aureus and Staphylococcus epidermidis) mainly present in the infections caused by implants and prosthesis in orthopedic surgery. Finally, the Ag-NP dispersed in aqueous solution were dried and stored as long-lasting powders that were easily reconstituted without losing their stability and antimicrobial properties. The proposed methods to stabilize Ag-NP not only produce stable dispersions in media of biological relevance but also long-lasting powders with optimal antimicrobial activity in the nanomolar range. This level is much lower than the cytotoxicity determined in vitro on osteoblasts, osteoclasts and osteoarthritic chondrocytes. The synthesized Ag-NP can be incorporated as additive of biomaterials or pharmaceutical products to confer antimicrobial activity in a powdered form in different formulations, dispersed in

  9. Pulmonary Toxicity of Instilled Silver Nanoparticles: Influence of Size, Coating and Rat Strain

    PubMed Central

    Seiffert, Joanna; Hussain, Farhana; Wiegman, Coen; Li, Feng; Bey, Leo; Baker, Warren; Porter, Alexandra; Ryan, Mary P.; Chang, Yan; Gow, Andrew; Zhang, Junfeng; Zhu, Jie; Tetley, Terry D.; Chung, Kian Fan

    2015-01-01

    Particle size and surface chemistry are potential determinants of silver nanoparticle (AgNP) respiratory toxicity that may also depend on the lung inflammatory state. We compared the effects of intratracheally-administered AgNPs (20nm and 110nm; polyvinylpyrrolidone (PVP) and citrate-capped; 0.1 mg/Kg) in Brown-Norway (BN) and Sprague-Dawley (SD) rats. In BN rats, there was both a neutrophilic and eosinophilic response, while in SD rats, there was a neutrophilic response at day 1, greatest for the 20nm citrate-capped AgNPs. Eosinophilic cationic protein was increased in bronchoalveolar lavage (BAL) in BN and SD rats on day 1. BAL protein and malondialdehyde levels were increased in BN rats at 1 and 7 days, and BAL KC, CCL11 and IL-13 levels at day 1, with increased expression of CCL11 in lung tissue. Pulmonary resistance increased and compliance decreased at day 1, with persistence at day 7. The 20nm, but not the 110 nm, AgNPs increased bronchial hyperresponsiveness on day 1, which continued at day 7 for the citrate-capped AgNPs only. The 20nm versus the 110 nm size were more proinflammatory in terms of neutrophil influx, but there was little difference between the citrate-capped versus the PVP-capped AgNPs. AgNPs can induce pulmonary eosinophilic and neutrophilic inflammation with bronchial hyperresponsiveness, features characteristic of asthma. PMID:25747867

  10. Ion beam shaping of Au nanoparticles in silica: Particle size and concentration dependence

    SciTech Connect

    Dawi, E. A.; Mink, M. P.; Vredenberg, A. M.; Habraken, F. H. P. M.; Rizza, G.

    2009-04-01

    Irradiation with swift heavy ions of spherical Au nanoparticles confined within a silica matrix shapes them into prolate nanorods and nanowires whose principal axes are aligned along the beam direction. In the present paper, we investigate the role that is played by the initial nanoparticle size and concentration in this so-called ion-shaping mechanism. We have produced silica films wherein Au nanoparticles with average diameters of 15, 30, and 45 nm were embedded within a single plane and have irradiated these films at 300 K at normal incidence with 18, 25, and 54 MeV Ag ions. We demonstrate the existence of both threshold and saturation fluences for the elongation effects mentioned. The values of these critical fluences depend both on the ion energy and the initial nanoparticle size. Moreover, we show that 45 nm Au particles are not deformed when irradiated with 18 MeV Ag ions, such that this value corresponds to an energy threshold for the deformation process. As far as the influence of the nanoparticle concentration on the shaping characteristics is concerned, we have found that above the critical irradiation fluence, the deformation effect becomes very sensitive to the initial concentration of the nanoparticles.

  11. Controlled protein embedment onto Au/Ag core-shell nanoparticles for immuno-labeling of nanosilver surface.

    PubMed

    Lee, In Hwan; Lee, Jeong Min; Jung, Yongwon

    2014-05-28

    Difficulties in stable conjugation of biomolecules to nanosilver surfaces have severely limited the use of silver nanostructures in biological applications. Here, we report a facile antibody conjugation onto gold/silver (Au/Ag) core-shell nanoparticles by stable and uniform embedment of an antibody binding protein, protein G, in silver nanoshells. A rigid helical peptide linker with a terminal cysteine residue was fused to protein G. A mixture of the peptide-fused protein G and space-filling free peptide was reacted with gold nanoparticles (AuNPs) to form a protein G-linked peptide layer on the particle surface. Uniform silver nanoshells were successfully formed on these protein G-AuNPs, while stably embedding protein G-linked peptide layers. Protein G specifically targets the Fc region of an antibody and thus affords properly orientated antibodies on the particle surface. Compared to Au nanoparticles of similar size with randomly adsorbed antibodies, the present immuno-labeled Au/Ag core-shell nanoparticles offered nearly 10-fold higher sensitivities for naked-eye detection of surface bound antigens. In addition, small dye molecules that were bonded to the peptide layer on Au nanoparticles exhibited highly enhanced surface-enhanced Raman scattering (SERS) signals upon Ag shell formation. The present strategy provides a simple but efficient way to conjugate antibodies to nanosilver surfaces, which will greatly facilitate wider use of the superior optical properties of silver nanostructures in biological applications. PMID:24801432

  12. SERS detection and antibacterial activity from uniform incorporation of Ag nanoparticles with aligned Si nanowires

    NASA Astrophysics Data System (ADS)

    Chen, Chia-Yun; Hsu, Li-Jen; Hsiao, Po-Hsuan; Yu, Chang-Tze Ricky

    2015-11-01

    We present a facile, reliable and controllable two-steps electroless deposition for uniformly decorating the silver (Ag) nanoparticles (NPs) on the highly aspect ratio of silicon (Si) nanowire arrays. Different from the direct Ag-loading process, which is normally challenged by the non-uniform coating of Ag, the formation of Ag NPs using such innovative electroless process is no longer to be limited at top nanowire surfaces solely; instead, each Ag+/Si interface can initiate the galvanic reduction of Ag+ ions, thus resulting in the uniform formation of Ag NPs on the entire Si nanowire arrays. In addition, systematic explorations of surface-enhanced Raman scattering (SERS) capability as well as antibacterial activity of the Ag/Si-incorporated nanostructures were performed, and the optimized Ag loadings on Si nanowire-based substrates along with the kinetic investigations were further revealed, which may benefit their practical applications in sensing, medical and biological needs.

  13. Facile Decoration of Polyaniline Fiber with Ag Nanoparticles for Recyclable SERS Substrate.

    PubMed

    Mondal, Sanjoy; Rana, Utpal; Malik, Sudip

    2015-05-20

    Facile synthesis of polyaniline@Ag composite has been successfully demonstrated by a simple solution-dipping method using high-aspect-ratio benzene tetracarboxylic acid-doped polyaniline (BDP) fiber as a nontoxic reducing agent as well as template cum stabilizer. In BDP@Ag composite, BDP fibers are decorated with spherical Ag nanoparticles (Ag NPs), and the population of Ag NPs on BDP fibers is controlled by changing the molar concentration of AgNO3. Importantly, Ag-NP-decorated BDP fibers (BDP@Ag composites) have been evolved as a sensitive materials for the detection of trace amounts of 4-mercaptobenzoic acid and rhodamine 6G as an analyte of surface-enhanced Raman scattering (SERS), and the detection limit is down to nanomolar concentrations with excellent recyclability. Furthermore, synthesized BDP@Ag composites are applied simultaneously as an active SERS substrate and a superior catalyst for reduction of 4-nitrothiophenol.

  14. Influence of electron beam irradiation on structural and optical properties of α-Ag2WO4 nanoparticles.

    PubMed

    A, Sreedevi; K P, Priyanka; K K, Babitha; S, Ganesh; Varghese, T

    2016-09-01

    The influence of 8MeV electron beam irradiation on the structural and optical properties of silver tungstate (α-Ag2WO4) nanoparticles synthesized by chemical precipitation method was investigated. The dose dependent effect of electron irradiation was investigated by various characterization techniques such as, X-ray diffraction, scanning electron microscopy, UV-vis absorption spectroscopy, photoluminescence and Raman spectroscopy. Systematic studies confirm that electron beam irradiation induces non-stoichiometry, defects and particle size variation on α-Ag2WO4, which in turn results changes in optical band gap, photoluminescence spectra and Raman bands.

  15. Optical properties of Ag nanoparticle-polymer composite film based on two-dimensional Au nanoparticle array film

    PubMed Central

    2014-01-01

    The nanocomposite polyvinyl pyrrolidone (PVP) films containing Ag nanoparticles and Rhodamine 6G are prepared on the two-dimensional distinctive continuous ultrathin gold nanofilms. We investigate the optical properties and the fluorescence properties of silver nanoparticles-PVP polymer composite films influenced by Ag nanoparticles and Au nanoparticles. Absorption spectral analysis suggests that the prominently light absorption in Ag nanowire/PVP and Ag nanowire/PVP/Au film arises from the localized surface plasmon resonance of Ag nanowire and Au nanofilm. The enhanced fluorescence is observed in the presence of Ag nanowire and Au nanofilm, which is attributed to the excitation of surface plasmon polariton resonance of Ag nanowire and Au nanofilm. The gold nanofilm is proven to be very effective fluorescence resonance energy transfer donors. The fabricated novel structure, gold ultrathin continuous nanofilm, possesses high surface plasmon resonance properties and prominent fluorescence enhancement effect. Therefore, the ultrathin continuous gold nanofilm is an active substrate on nanoparticle-enhanced fluorescence. PMID:24685186

  16. The impact of Ag nanoparticles on the parameters of DSS- cells sensitized by Z907

    NASA Astrophysics Data System (ADS)

    Ibrayev, N. Kh; Aimukhanov, A. K.; Zeinidenov, A. K.

    2016-02-01

    Research of influence of Ag nanoparticles are in-process undertaken on absorption and on parameters CVC DSS-cells sensitized Z907. It is set that with the height of concentration Ag nanoparticles in tape to the concentration of 0.3% wt%. the absorbance of Z907 in a short-wave stripe grew to the value 1,6. It is set that under reaching the concentration of Ag nanoparticles in the cell of value the 0.3% wt%. efficiency of cell increased to 2.2%.

  17. Preparing of Highly Conductive Patterns on Flexible Substrates by Screen Printing of Silver Nanoparticles with Different Size Distribution

    NASA Astrophysics Data System (ADS)

    Ding, Jin; Liu, Jun; Tian, Qingyong; Wu, Zhaohui; Yao, Weijing; Dai, Zhigao; Liu, Li; Wu, Wei

    2016-09-01

    A facile one-step polyol method is employed to synthesize the Ag nanoparticles (NPs) in large scale. The Ag NPs with different average diameter (from 52 to 120 nm) and particle size distribution are prepared by changing the mass ratio of AgNO3 and PVP. Furthermore, the as-obtained Ag NPs are prepared as conductive inks, which could be screen printed on various flexible substrates and formed as conductive patterns after sintering treatment. During the reaction process, PVP is used as the capping reagent for preventing the agglomeration of Ag NPs, and the influence of the mass ratio of AgNO3 and PVP to the size distribution of Ag NPs is investigated. The results of electronic properties reveal that the conductivity of printed patterns is highly dependent on the size distribution of as-obtained Ag NPs. Among all the samples, the optimal conductivity is obtained when the mass ratio of AgNO3 and PVP is 1:0.4. Subsequently, the sintering time and temperature are further investigated for obtaining the best conductivity; the optimal electrical resistivity value of 3.83 μΩ · cm is achieved at 160 °C for 75 min, which is close to the resistivity value of the bulk silver (1.58 μΩ · cm). Significantly, there are many potential advantages in printed electronics applications because of the as-synthesized Ag NPs with a low sintering temperature and low electrical resistivity.

  18. Innovative method to avoid the reduction of silver ions to silver nanoparticles \\left( A{{g}^{+}}\\to Ag{}^\\circ \\right) in silver ion conducting based polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Aziz, Shujahadeen B.; Abidin, Zul Hazrin Z.; Kadir, M. F. Z.

    2015-03-01

    In this research work an innovative method is used to prevent the silver ion reduction in solid polymer electrolytes. The x-ray diffraction (XRD) results reveal the disruption of the crystalline nature of chitosan (CS) and formation of silver nanoparticles upon addition of silver triflate (AgTf) salt. The UV-vis measurement confirms the existence of silver nanoparticles via the broad surface plasmon resonance (SPR) peak. Upon the addition of Al2O3 nanoparticles the SPR peak intensity is greatly reduced. The amorphous domain of the CS:silver triflate (CS:AgTf) system increases with the addition of Al2O3 nanoparticles up to 4 wt.%. Deconvolution of the XRD results reveals that a larger crystallite size is obtained for higher Al2O3 concentrations and the peaks due to silver nanoparticles almost disappear. Scanning electron microscope (SEM) analyses show that Al2O3 nanoparticles are well dispersed at low concentrations and the leakage of chains of silver nanoparticles to the membrane surface almost disappear. The XRD, UV-vis, SEM and energy-dispersive x-ray (EDX) results strongly support that the reduction of silver ions to silver nanoparticles (Ag+ → Ag°) in the CS:silver triflate system is significantly avoided upon the addition of an Al2O3 filler.

  19. Size-separation of silver nanoparticles using sucrose gradient centrifugation

    SciTech Connect

    Suresh, Anil K.; Pelletier, Dale A.; Moon, Ji Won; Phelps, Tommy; Doktycz, Mitchel John

    2015-08-28

    Size and shape distributions of nanoparticles can drastically contribute to the overall properties of nanoparticles, thereby influencing their interaction with different chemotherapeutic molecules, biological organisms and or materials and cell types. Therefore, to exploit the proper use of nanoparticles for various biomedical and biosensor applications, it is important to obtain well-separated monodispersed nanoparticles. However, gaining precise control over the morphological characteristics of nanoparticles during their synthesis is often a challenging task. Consequently, post-synthesis separation of nanoparticles is necessary. In the present study, we demonstrate the successful one-pot post-synthesis separation of anisotropic silver nanoparticles to near modispersities using sucrose density gradient sedimentation. The separation of the nanoparticles was evidenced based on optical confirmation, and spectrophotometric and transmission electron microscopy measurements. Our results clearly demonstrate the facile separation of anisotropic silver nanoparticles using sucrose density gradient sedimentation and can enable the use of nanoparticles for various biomedical applications.

  20. Size-separation of silver nanoparticles using sucrose gradient centrifugation

    DOE PAGES

    Suresh, Anil K.; Pelletier, Dale A.; Moon, Ji Won; Phelps, Tommy; Doktycz, Mitchel John

    2015-08-28

    Size and shape distributions of nanoparticles can drastically contribute to the overall properties of nanoparticles, thereby influencing their interaction with different chemotherapeutic molecules, biological organisms and or materials and cell types. Therefore, to exploit the proper use of nanoparticles for various biomedical and biosensor applications, it is important to obtain well-separated monodispersed nanoparticles. However, gaining precise control over the morphological characteristics of nanoparticles during their synthesis is often a challenging task. Consequently, post-synthesis separation of nanoparticles is necessary. In the present study, we demonstrate the successful one-pot post-synthesis separation of anisotropic silver nanoparticles to near modispersities using sucrose density gradientmore » sedimentation. The separation of the nanoparticles was evidenced based on optical confirmation, and spectrophotometric and transmission electron microscopy measurements. Our results clearly demonstrate the facile separation of anisotropic silver nanoparticles using sucrose density gradient sedimentation and can enable the use of nanoparticles for various biomedical applications.« less

  1. Mixed-valence metal oxide nanoparticles as electrochemical half-cells: substituting the Ag/AgCl of reference electrodes by CeO(2-x) nanoparticles.

    PubMed

    Nagarale, Rajaram K; Hoss, Udo; Heller, Adam

    2012-12-26

    Cations of mixed valence at surfaces of metal oxide nanoparticles constitute electrochemical half-cells, with potentials intermediate between those of the dissolved cations and those in the solid. When only cations at surfaces of the particles are electrochemically active, the ratio of electrochemically active/all cations is ~0.1 for 15 nm diameter CeO(2-x) particles. CeO(2-x) nanoparticle-loaded hydrogel films on printed carbon and on sputtered gold constitute reference electrodes having a redox potential similar to that of Ag/AgCl in physiological (0.14 M) saline solutions. In vitro the characteristics of potentially subcutaneously implantable glucose monitoring sensors made with CeO(2-x) nanoparticle reference electrodes are undistinguishable from those of sensors made with Ag/AgCl reference electrodes. Cerium is 900 times more abundant than silver, and commercially produced CeO(2-x) nanoparticle solutions are available at prices well below those of the Ag/AgCl pastes used in the annual manufacture of ~10(9) reference electrodes of glucose monitoring strips for diabetes management. PMID:23171288

  2. Bioimpacts of nanoparticle size: why it matters?

    PubMed

    Barar, Jaleh

    2015-01-01

    During the last two decades, applications of nanotechnology are delivered to benefit the human society. The fact is that various nanomaterials are able to be tailor made to achieve desired properties. In biomedical field, nanotechnology has created great excitements to advance both diagnosis and therapy areas - the field so-called nanomedicines in different forms of nanoparticles (NPs) and nanosystems (NSs). It is noteworthy to mention NPs/NSs do not act similarly in the biological milieu, in which their biological behaviors/ impacts varies with size, morphology, and physicochemical characteristics. On the other hand, nanomedicines impacts on biological systems seem to be influenced by its possible interaction(s) with different bioelements of cell membrane, in particular the endocytic pathway(s) by which NPs/NSs can be internalized and localized. This latter phenomenon is influenced by membrane viscoelastic property, polymerization/depolymerization of cytoskeletal system, and the particle specification itself. Among all other properties of NPs/NSs, as shown by various researchers, the size is an important parameter in the fate of the particle. Accordingly, in-depth efforts to unravel the size dependent effects of nanomedicins can provide insights to design and develop more efficacious NSs with greater benefits and lower side effects. This editorial aims to highlight some important aspects of size dependent impacts NPs/NSs. PMID:26457247

  3. Surface modification of oleylamine-capped Ag-Cu nanoparticles to fabricate low-temperature-sinterable Ag-Cu nanoink

    NASA Astrophysics Data System (ADS)

    Kim, Na Rae; Jong Lee, Yung; Lee, Changsoo; Koo, Jahyun; Lee, Hyuck Mo

    2016-08-01

    By treating oleylamine (OA)-capped Ag-Cu nanoparticles with tetramethylammonium hydroxide (TMAH), we obtained metal nanoparticles that are suspended in polar solvents and sinterable at low temperatures. The simple process with ultra sonication enables synthesis of monodispersed and high purity nanoparticles in an organic base, where the resulting nanoparticles are dispersible in polar solvents such as ethanol and isopropyl alcohol. To investigate the surface characteristics, we conducted Fourier-transform infrared and zeta-potential analyses. After thermal sintering at 200 °C, which is approximately 150 °C lower than the thermal decomposition temperature of OA, an electrically conductive thin film was obtained. Electrical resistivity measurements of the TMAH-treated ink demonstrate that surface modified nanoparticles have a low resistivity of 13.7 × 10-6 Ω cm. These results confirm the prospects of using low-temperature sinterable nanoparticles as the electrode layer for flexible printed electronics without damaging other stacked polymer layers.

  4. Oxidative Stress Mechanisms Caused by Ag Nanoparticles (NM300K) are Different from Those of AgNO3: Effects in the Soil Invertebrate Enchytraeus crypticus

    PubMed Central

    Ribeiro, Maria J.; Maria, Vera L.; Scott-Fordsmand, Janeck J.; Amorim, Mónica J. B.

    2015-01-01

    The mechanisms of toxicity of Ag nanoparticles (NPs) are unclear, in particular in the terrestrial environment. In this study the effects of AgNP (AgNM300K) were assessed in terms of oxidative stress in the soil worm Enchytraeus crypticus, using a range of biochemical markers [catalase (CAT), glutathione peroxidase (GPx), glutathione S-transferase (GST), glutathione reductase (GR), total glutathione (TG), metallothionein (MT), lipid peroxidation (LPO)]. E. crypticus were exposed during 3 and 7 days (d) to the reproduction EC20, EC50 and EC80 levels of both AgNP and AgNO3. AgNO3 induced oxidative stress earlier (3 d) than AgNP (7 d), both leading to LPO despite the activation of the anti-redox system. MT increased only for AgNP. The Correspondence Analysis showed a clear separation between AgNO3 and AgNP, with e.g., CAT being the main descriptor for AgNP for 7 d. LPO, GST and GPx were for both 3 and 7 d associated with AgNO3, whereas MT and TG were associated with AgNP. These results may reflect a delay in the effects of AgNP compared to AgNO3 due to the slower release of Ag+ ions from the AgNP, although this does not fully explain the observed differences, i.e., we can conclude that there is a nanoparticle effect. PMID:26287225

  5. Solution structure of peptide AG4 used to form silver nanoparticles

    SciTech Connect

    Lee, Eunjung; Kim, Dae-Hee; Woo, Yoonkyung; Hur, Ho-Gil; Lim, Yoongho

    2008-11-21

    The preparation of silver nanoparticles (AgNPs) is of great interest due to their various biological activities, such as observed in their antimicrobial and wound healing actions. Moreover, the formation of AgNPs using silver-binding peptide has certain advantages because they can be made in aqueous solution at ambient temperature. The solution structure of the silver-binding peptide AG4 was determined using nuclear magnetic resonance spectroscopy, and the site of the AG4 interaction with AgNPs was elucidated.

  6. Loading Ag nanoparticles on Cd(II) boron imidazolate framework for photocatalysis

    NASA Astrophysics Data System (ADS)

    Liu, Min; Zhang, De-Xiang; Chen, Shumei; Wen, Tian

    2016-05-01

    An amine-functionalized Cd(II) boron imidazolate framework (BIF-77) with three-dimensional open structure has been successfully synthesized, which can load Ag nanoparticles (NPs) for photocatalytic degradation of methylene blue (MB).

  7. Maximizing the photo catalytic and photo response properties of multimodal plasmonic Ag/WO3-x heterostructure nanorods by variation of the Ag size

    NASA Astrophysics Data System (ADS)

    Ghosh, Sirshendu; Saha, Manas; Paul, Sumana; de, S. K.

    2015-10-01

    High quality nearly monodisperse colloidal WO3-x nanorods with an aspect ratio ~18 were synthesized using the thermal decomposition technique. The effects of a capping agent and an activating agent on the nanorod aspect ratio have been studied. Excess carrier concentration due to large oxygen vacancy and smaller width of the nanorods compared to the Bohr exciton radius gives rise to an increase of the band gap. Shape anisotropy in nanorods results in two plasmonic absorbance bands at about 890 nm and 5900 nm corresponding to short axis and long axis plasmon modes. The short axis mode reveals an excellent plasmonic sensitivity of ~345 nm per refractive index. A plasmonic photocatalysis process based on WO3-x nanorods has been developed to synthesize Ag/WO3-x heterostructures consisting of multiple Ag dots with ~2 nm size, randomly decorated on the surface of the WO3-x nanorods. Long time irradiation leads to an increase in the size (5 nm) of Ag nanocrystals concomitant with decrease in the number of Ag nanocrystals attached per WO3-x nanorod. Plasmonic photocatalysis followed by thermal annealing produces only one Ag nanocrystal of size ~10 nm on each WO3-x nanorod. Red shifting and broadening of plasmon bands of Ag nanocrystals and WO3-x nanorods confirm the formation of heterostructures between the metal and semiconductor. Detailed transmission electron micrograph analysis indicates the epitaxial growth of Ag nanocrystals onto WO3-x nanorods. A high photocurrent gain of about 4000 is observed for Ag (10 nm)/WO3-x heterostructures. The photodegradation rate for Rhodamine-B and methylene blue is maximum for Ag (10 nm)/WO3-x heterostructures due to efficient electron transfer from WO3-x nanorods to Ag nanocrystals. Metal plasmon-semiconductor exciton coupling, prominent plasmon absorbance of metal nanoparticles, and formation of an epitaxial interface are found to be the important factors to achieve the maximum photocatalytic activity and fabrication of a high speed

  8. Green synthesis of size controllable gold nanoparticles

    NASA Astrophysics Data System (ADS)

    Mohan Kumar, Kesarla; Mandal, Badal Kumar; Kiran Kumar, Hoskote A.; Maddinedi, Sireesh Babu

    2013-12-01

    A facile rapid green eco-friendly method to synthesize gold nanoparticles (Au NPs) of tunable size using aqueous Terminalia arjuna fruit extracts has been demonstrated herein. Formation of Au NPs was confirmed by Surface Plasmon Resonance (SPR) study at 528 nm using UV-visible spectrophotometer. The time of reduction, size and morphological variations of Au NPs were studied with varying quantities of T. arjuna fruit aqueous extracts. Synthesized Au NPs were characterized using UV-visible spectroscopy, Fourier transformed infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), transmission electron microscopy (TEM) and Energy dispersive X-ray spectroscopy (EDAX). Polyphenols responsible for reduction of Au3+ to Au0 were identified using High Performance Liquid Chromatography (HPLC) as ascorbic acid, gallic acid and pyrogallol. The oxidized forms of polyphenols formed coordination with surface of Au NPs which protected their further growth and aggregation. We also propose a plausible mechanism how to tune size and shape of Au NPs by varying the quantity of extracts. Thus obtained Au NPs were stable for more than four months.

  9. Effect of electrode material on characteristics of non-volatile resistive memory consisting of Ag2S nanoparticles

    NASA Astrophysics Data System (ADS)

    Jang, Jaewon

    2016-07-01

    In this study, Ag2S nanoparticles are synthesized and used as the active material for two-terminal resistance switching memory devices. Sintered Ag2S films are successfully crystallized on plastic substrates with synthesized Ag2S nanoparticles, after a relatively low-temperature sintering process (200 °C). After the sintering process, the crystallite size is increased from 6.8 nm to 80.3 nm. The high ratio of surface atoms to inner atoms of nanoparticles reduces the melting point temperature, deciding the sintering process temperature. In order to investigate the resistance switching characteristics, metal/Ag2S/metal structures are fabricated and tested. The effect of the electrode material on the non-volatile resistive memory characteristics is studied. The bottom electrochemically inert materials, such as Au and Pt, were critical for maintaining stable memory characteristics. By using Au and Pt inert bottom electrodes, we are able to significantly improve the memory endurance and retention to more than 103 cycles and 104 sec, respectively.

  10. Localized surface plasmon behavior of Ag-Cu alloy nanoparticles stabilized by rice-starch and gelatin

    SciTech Connect

    Singh, Manish Kumar; Mandal, R. K.; Manda, Premkumar; Singh, A. K.

    2015-10-15

    The purpose of this communication was to understand localized surface plasmon behavior of a series of Ag-Cu alloy nanoparticles capped by rice-starch and gelatin. The structures of dried powders were investigated with the help of X-ray diffraction. The analysis revealed Ag-rich and Cu-rich phases with maximum solid solubility of Cu ∼9 atom per cent; 8 atom per cent and Ag ∼ 16 atom per cent; 14 atom per cent in rice-starch and gelatin capped samples respectively. Transmission electron microscope was used for knowing the particle size as well as to supplement FCC phase formations of Ag-rich and Cu-rich solid phases arrived at based on X-ray diffraction studies. The UV-Vis spectra of sols were examined for the formation and stability of alloy nanoparticles. The temporal evolution of LSPR curves gave us to assert that the sol is stable for more than two months. Small angle X-ray scattering in the sol state was extensively utilized to understand nature of suspensions in terms of fractals. Such a study is important for having a correlation between LSPR behaviors with those of nanoparticle dispersion in aqueous media. It is believed that this work will be a contribution to the emerging field of plasmonics that include applications in the area of photophysical processes and photochemical reactions.

  11. Localized surface plasmon behavior of Ag-Cu alloy nanoparticles stabilized by rice-starch and gelatin

    NASA Astrophysics Data System (ADS)

    Singh, Manish Kumar; Manda, Premkumar; Singh, A. K.; Mandal, R. K.

    2015-10-01

    The purpose of this communication was to understand localized surface plasmon behavior of a series of Ag-Cu alloy nanoparticles capped by rice-starch and gelatin. The structures of dried powders were investigated with the help of X-ray diffraction. The analysis revealed Ag-rich and Cu-rich phases with maximum solid solubility of Cu ˜9 atom per cent; 8 atom per cent and Ag ˜ 16 atom per cent; 14 atom per cent in rice-starch and gelatin capped samples respectively. Transmission electron microscope was used for knowing the particle size as well as to supplement FCC phase formations of Ag-rich and Cu-rich solid phases arrived at based on X-ray diffraction studies. The UV-Vis spectra of sols were examined for the formation and stability of alloy nanoparticles. The temporal evolution of LSPR curves gave us to assert that the sol is stable for more than two months. Small angle X-ray scattering in the sol state was extensively utilized to understand nature of suspensions in terms of fractals. Such a study is important for having a correlation between LSPR behaviors with those of nanoparticle dispersion in aqueous media. It is believed that this work will be a contribution to the emerging field of plasmonics that include applications in the area of photophysical processes and photochemical reactions.

  12. The role of exopolymeric substances in the bioaccumulation and toxicity of Ag nanoparticles to algae.

    PubMed

    Zhou, Kaijun; Hu, Yi; Zhang, Luqing; Yang, Kun; Lin, Daohui

    2016-01-01

    Exopolymeric substances (EPS) have an important role in bioaccumulation and toxicity of nanoparticles (NPs) to algae, which warrants specific studies. The interaction of EPS with citrate and polyvinyl pyrrolidone (PVP) coated AgNPs (C-AgNPs and P-AgNPs, respectively) and its roles in bioaccumulation and toxicity of the AgNPs to Chlorella pyrenoidosa were investigated. The amino and aromatic carboxylic groups in the EPS were involved in the EPS-AgNP interactions. Compared with Ag(+), C-AgNPs had comparable total bioaccumulation but greater absorption by intact algae with EPS; P-AgNPs had the smallest total bioaccumulation and were mainly adsorbed on algal surfaces. With EPS removed, the total bioaccumulations and surface adsorptions for the three Ag species decreased but the cell internalizations increased; the 96 h half growth inhibition concentrations decreased, indicating EPS alleviated the algal toxicity of Ag. The cell-internalized but not the adsorbed AgNPs could contribute to the nanotoxicity. The EPS could bind both AgNPs and Ag(+), and thus inhibited the cell internalization and the nanotoxicity. However, the EPS-bound Ag on the cell surfaces would migrate along with the algae and be biologically amplified in the aquatic food chains, presenting ecological risks. These results are helpful for understanding the fate and ecological effects of NPs. PMID:27615743

  13. The role of exopolymeric substances in the bioaccumulation and toxicity of Ag nanoparticles to algae

    PubMed Central

    Zhou, Kaijun; Hu, Yi; Zhang, Luqing; Yang, Kun; Lin, Daohui

    2016-01-01

    Exopolymeric substances (EPS) have an important role in bioaccumulation and toxicity of nanoparticles (NPs) to algae, which warrants specific studies. The interaction of EPS with citrate and polyvinyl pyrrolidone (PVP) coated AgNPs (C-AgNPs and P-AgNPs, respectively) and its roles in bioaccumulation and toxicity of the AgNPs to Chlorella pyrenoidosa were investigated. The amino and aromatic carboxylic groups in the EPS were involved in the EPS-AgNP interactions. Compared with Ag+, C-AgNPs had comparable total bioaccumulation but greater absorption by intact algae with EPS; P-AgNPs had the smallest total bioaccumulation and were mainly adsorbed on algal surfaces. With EPS removed, the total bioaccumulations and surface adsorptions for the three Ag species decreased but the cell internalizations increased; the 96 h half growth inhibition concentrations decreased, indicating EPS alleviated the algal toxicity of Ag. The cell-internalized but not the adsorbed AgNPs could contribute to the nanotoxicity. The EPS could bind both AgNPs and Ag+, and thus inhibited the cell internalization and the nanotoxicity. However, the EPS-bound Ag on the cell surfaces would migrate along with the algae and be biologically amplified in the aquatic food chains, presenting ecological risks. These results are helpful for understanding the fate and ecological effects of NPs. PMID:27615743

  14. The role of exopolymeric substances in the bioaccumulation and toxicity of Ag nanoparticles to algae

    NASA Astrophysics Data System (ADS)

    Zhou, Kaijun; Hu, Yi; Zhang, Luqing; Yang, Kun; Lin, Daohui

    2016-09-01

    Exopolymeric substances (EPS) have an important role in bioaccumulation and toxicity of nanoparticles (NPs) to algae, which warrants specific studies. The interaction of EPS with citrate and polyvinyl pyrrolidone (PVP) coated AgNPs (C-AgNPs and P-AgNPs, respectively) and its roles in bioaccumulation and toxicity of the AgNPs to Chlorella pyrenoidosa were investigated. The amino and aromatic carboxylic groups in the EPS were involved in the EPS-AgNP interactions. Compared with Ag+, C-AgNPs had comparable total bioaccumulation but greater absorption by intact algae with EPS; P-AgNPs had the smallest total bioaccumulation and were mainly adsorbed on algal surfaces. With EPS removed, the total bioaccumulations and surface adsorptions for the three Ag species decreased but the cell internalizations increased; the 96 h half growth inhibition concentrations decreased, indicating EPS alleviated the algal toxicity of Ag. The cell-internalized but not the adsorbed AgNPs could contribute to the nanotoxicity. The EPS could bind both AgNPs and Ag+, and thus inhibited the cell internalization and the nanotoxicity. However, the EPS-bound Ag on the cell surfaces would migrate along with the algae and be biologically amplified in the aquatic food chains, presenting ecological risks. These results are helpful for understanding the fate and ecological effects of NPs.

  15. Reducing Strength Prevailing at Root Surface of Plants Promotes Reduction of Ag+ and Generation of Ag0/Ag2O Nanoparticles Exogenously in Aqueous Phase

    PubMed Central

    Pardha-Saradhi, Peddisetty; Yamal, Gupta; Peddisetty, Tanuj; Sharmila, Peddisetty; Nagar, Shilpi; Singh, Jyoti; Nagarajan, Rajamani; Rao, Kottapalli S.

    2014-01-01

    Potential of root system of plants from wide range of families to effectively reduce membrane impermeable ferricyanide to ferrocyanide and blue coloured 2,6-dichlorophenol indophenol (DCPIP) to colourless DCPIPH2 both under non-sterile and sterile conditions, revealed prevalence of immense reducing strength at root surface. As generation of silver nanoparticles (NPs) from Ag+ involves reduction, present investigations were carried to evaluate if reducing strength prevailing at surface of root system can be exploited for reduction of Ag+ and exogenous generation of silver-NPs. Root system of intact plants of 16 species from 11 diverse families of angiosperms turned clear colorless AgNO3 solutions, turbid brown. Absorption spectra of these turbid brown solutions showed silver-NPs specific surface plasmon resonance peak. Transmission electron microscope coupled with energy dispersive X-ray confirmed the presence of distinct NPs in the range of 5–50 nm containing Ag. Selected area electron diffraction and powder X-ray diffraction patterns of the silver NPs showed Bragg reflections, characteristic of crystalline face-centered cubic structure of Ag0 and cubic structure of Ag2O. Root system of intact plants raised under sterile conditions also generated Ag0/Ag2O-NPs under strict sterile conditions in a manner similar to that recorded under non-sterile conditions. This revealed the inbuilt potential of root system to generate Ag0/Ag2O-NPs independent of any microorganism. Roots of intact plants reduced triphenyltetrazolium to triphenylformazon and impermeable ferricyanide to ferrocyanide, suggesting involvement of plasma membrane bound dehydrogenases in reduction of Ag+ and formation of Ag0/Ag2O-NPs. Root enzyme extract reduced triphenyltetrazolium to triphenylformazon and Ag+ to Ag0 in presence of NADH, clearly establishing potential of dehydrogenases to reduce Ag+ to Ag0, which generate Ag0/Ag2O-NPs. Findings presented in this manuscript put forth a novel, simple

  16. DNA origami based Au-Ag-core-shell nanoparticle dimers with single-molecule SERS sensitivity

    NASA Astrophysics Data System (ADS)

    Prinz, J.; Heck, C.; Ellerik, L.; Merk, V.; Bald, I.

    2016-03-01

    DNA origami nanostructures are a versatile tool to arrange metal nanostructures and other chemical entities with nanometer precision. In this way gold nanoparticle dimers with defined distance can be constructed, which can be exploited as novel substrates for surface enhanced Raman scattering (SERS). We have optimized the size, composition and arrangement of Au/Ag nanoparticles to create intense SERS hot spots, with Raman enhancement up to 1010, which is sufficient to detect single molecules by Raman scattering. This is demonstrated using single dye molecules (TAMRA and Cy3) placed into the center of the nanoparticle dimers. In conjunction with the DNA origami nanostructures novel SERS substrates are created, which can in the future be applied to the SERS analysis of more complex biomolecular targets, whose position and conformation within the SERS hot spot can be precisely controlled.DNA origami nanostructures are a versatile tool to arrange metal nanostructures and other chemical entities with nanometer precision. In this way gold nanoparticle dimers with defined distance can be constructed, which can be exploited as novel substrates for surface enhanced Raman scattering (SERS). We have optimized the size, composition and arrangement of Au/Ag nanoparticles to create intense SERS hot spots, with Raman enhancement up to 1010, which is sufficient to detect single molecules by Raman scattering. This is demonstrated using single dye molecules (TAMRA and Cy3) placed into the center of the nanoparticle dimers. In conjunction with the DNA origami nanostructures novel SERS substrates are created, which can in the future be applied to the SERS analysis of more complex biomolecular targets, whose position and conformation within the SERS hot spot can be precisely controlled. Electronic supplementary information (ESI) available: Additional information about materials and methods, designs of DNA origami templates, height profiles, additional SERS spectra, assignment of DNA

  17. In-situ preparation of binary-phase silver nanoparticles at a high Ag+ concentration.

    PubMed

    Ullah, Md Habib; Kim, Il; Ha, Chang-Sik

    2006-03-01

    Stable and monodisperse silver nanoparticles (NPs) have been synthesized using high metal salt concentration (up to 0.735 M) through a simple but novel technique. It is based on one-step procedure that uses glycerol for reducing Ag+ in the presence of o-phenylenediamine (o-PDA) resulting the nanoparticles are in two forms (one water-soluble, the other a precipitated). The water-soluble phase contains NPs that have a bimodal size distribution (2-3 and 5-6 nm); the other comprises precipitated NPs, having a unimodal size distribution (2-3 nm). The water-soluble NPs are covalently bonded to the aromatic amine molecules to form isolated units, while the precipitated nanoparticles are embedded in the networks formed by cross-linking between COOH groups of hydroxypyruvic acid (oxidized form of glycerol) and NH2 groups of o-PDA molecules. We used transmission electron microscopy (TEM), UV-Vis spectroscopy, X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) to characterize the silver products obtained.

  18. Deposition of Ag nanoparticles on fluoroalkylsilane self-assembled monolayers with varying chain length

    NASA Astrophysics Data System (ADS)

    Zuo, Juan; Keil, Patrick; Valtiner, Markus; Thissen, Peter; Grundmeier, Guido

    2008-12-01

    Silver nanoparticles were prepared by means of electron beam evaporation of silver on top of self-assembled fluoroalkylsilane monolayers with different fluoroalkyl chain length. The surface properties of the different self-assembled monolayers (SAMs) were evaluated by surface energy measurements and X-ray photoelectron spectroscopy. The morphology of the silver nanostructures, characterized by their size, size distribution, shape and interparticle separation, was observed to be dependent on the chemical composition, fluoroalkyl chain length and surface energy of the sub-layer as well as the degradation of the monolayer during the deposition process. The resulting morphology of the evaporated Ag nanostructures on the different surfaces could be explained based on the basis of surface energy and the role of ordering, disordering and defects of the monolayers caused by the impinging silver atoms during evaporation. Depending on the fluoroalkyl chain length significant changes in the chemical and physical structure of the SAMs after the evaporation process could be detected.

  19. Anti-inflammatory effects of silver-polyvinyl pyrrolidone (Ag-PVP) nanoparticles in mouse macrophages infected with live Chlamydia trachomatis

    PubMed Central

    Yilma, Abebayehu N; Singh, Shree R; Dixit, Saurabh; Dennis, Vida A

    2013-01-01

    Chlamydia trachomatis is a very common sexually transmissible infection in both developing and developed countries. A hallmark of C. trachomatis infection is the induction of severe inflammatory responses which play critical roles in its pathogenesis. Antibiotics are the only treatment option currently available for controlling C. trachomatis infection; however, they are efficacious only when administered early after an infection. The objectives of this study are to explore alternative strategies in the control and regulation of inflammatory responses triggered by a C. trachomatis infection. We employed silver-polyvinyl pyrrolidone (Ag-PVP) nanoparticles, which have been shown to possess anti-inflammatory properties, as our target and the in vitro mouse J774 macrophage model of C. trachomatis infection. Our hypothesis is that small sizes of Ag-PVP nanoparticles will control inflammatory mediators triggered by a C. trachomatis infection. Cytotoxicity studies using Ag-PVP nanoparticles of 10, 20, and 80 nm sizes revealed >80% macrophage viability up to a concentration of 6.25 μg/mL, with the 10 nm size being the least toxic. All sizes of Ag-PVP nanoparticles, especially the 10 nm size, reduced the levels of the prototypic cytokines, tumor necrosis factor (TNF) and interleukin (IL)-6, as elicited from C. trachomatis infected macrophages. Additionally, Ag-PVP nanoparticles (10 nm) selectively inhibited a broad spectrum of other cytokines and chemokines produced by infected macrophages. Of significance, Ag-PVP nanoparticles (10 nm) caused perturbations in a variety of upstream (toll like receptor 2 [TLR2], nucleotide-binding oligomerization-protein 2 [NOD2], cluster of differentiation [CD]40, CD80, and CD86) and downstream (IL-1 receptor-associated kinase 3 [IRAK3] and matrix metallopeptidase 9 [MMP9]) inflammatory signaling pathways by downregulating their messenger ribonucleic acid (mRNA) gene transcript expressions as induced by C. trachomatis in macrophages

  20. Fabrication of plasmonic AgBr/Ag nanoparticles-sensitized TiO2 nanotube arrays and their enhanced photo-conversion and photoelectrocatalytic properties

    NASA Astrophysics Data System (ADS)

    Wang, Qingyao; Qiao, Jianlei; Jin, Rencheng; Xu, Xiaohui; Gao, Shanmin

    2015-03-01

    Plasmonic photosensitizer AgBr/Ag nanospheres supported on TiO2 nanotube arrays (TiO2 NTs) are prepared by successive ionic layer adsorption and reaction (SILAR) technique followed by photoreduction methods. The structural and surface morphological properties of AgBr/Ag nanoparticles sensitized TiO2 NTs and their photoelectrochemical performance are investigated and discussed. A detailed formation mechanism of the TiO2 NTs/AgBr/Ag is proposed. The TiO2 NTs/AgBr/Ag exhibit excellent photocurrent and photoelectrocatalytic activities under visible light irradiation. Efficient utilization of solar energy to create electron-hole pairs is attributed to the significant visible light response and surface plasmon resonance of Ag nanoparticles. This finding indicates that the high photosensitivity of the TiO2 NTs-based surface plasmon resonance materials could be applied toward the development of new plasmonic visible-light-sensitive photovoltaic fuel cells and photocatalysts.

  1. Ultrasensitive and Rapid Determination of Folic Acid Using Ag Nanoparticles Enhanced 1, 10-Phenantroline-Terbium (III) Sensitized Fluorescence.

    PubMed

    Hassanzadeh, Robab; Lotfi, Ali; Bagheri, Nafiseh; Hassanzadeh, Javad

    2016-09-01

    A novel spectrofluorimetric probe based on Ag nanoparticle (AgNPs)-enhanced terbium (III) (Tb) fluorescence was introduced for the sensitive determination of folic acid (FA). The effect of gold and silver nanoparticles in different size was investigated on the well-known Tb sensitized fluorescence emission of 1, 10-phenantroline (Phen). The greatest fluorescence intensity was observed in the presence of AgNPs with a diameter of ~6 nm maybe due to their highest surface area. Furthermore, it's discovered that FA can form Tb-Phen -FA ternary complexes and cause a notable diminution in this enhanced fluorescence system. Based on this finding, a high sensitive and selective method was developed for the determination of FA. Effects of various parameters like Ag NPs, Phen and Tb(3+) concentration and pH of media were investigated. In the optimum circumstances, the fluorescence emission of AgNPs-Phen-Tb collection was declined linearly by increasing the concentration of FA in the range of 0.5 to 110 nmol L(-1). Limits of detection and quantification were achieved to be 0.21 and 0.62 nmol  L(-1), respectively. The method has good linearity, recovery, reproducibility and sensitivity, and was adequately exploited to follow FA content in pharmaceutical, fortified flour and human urine samples.

  2. Mesoporous TiO2 nanoparticles containing Ag ion with excellent antimicrobial activity at remarkable low silver concentrations.

    PubMed

    Naik, Kshipra; Chatterjee, Amrita; Prakash, Halan; Kowshik, Meenal

    2013-04-01

    Mesoporous Ag-TiO2 nanoparticles with TiO2 homogenous anatase crystalline phase was synthesized using a one-pot sol-gel method. The sample was calcined at 100 degrees C and characterized by XRD, HR TEM, EDAX, IR spectroscopy, DRS, N2 adsorption-desorption isotherm and Brunauer-Emmett-Teller (BET) analysis. The BET surface area of the sample was 266 m2/g and the crystallite size as calculated using Scherrer formula was 3.76 nm. The Ag-TiO2 nanoparticles exhibited excellent antimicrobial activity against representative Gram-positive and Gram-negative bacterial cultures and Candida albicans. Complete inhibition of microorganisms was achieved at a very low Ag-TiO2 concentration, in the range of 1.0 to 20 microg/mL (effective Ag concentrations were 11.7 to 234 ppb) in less than 2 h under ambient conditions, without the requirement of photoactivation. Silver ion release studies showed that about 18% of silver ions were present in solution. Thus, it may be inferred that the antimicrobial activity is due to Ag ions released from the TiO2 matrix. The mesoporous nature and antimicrobial activity at low concentrations without photoactivation are important aspects which make this material an excellent candidate for potential application as disinfectant and/or antimicrobial agent.

  3. Impact of Ag and Al₂O₃ nanoparticles on soil organisms: in vitro and soil experiments.

    PubMed

    Fajardo, C; Saccà, M L; Costa, G; Nande, M; Martin, M

    2014-03-01

    In vitro analyses were conducted to assess the impact of Al2O3 and Ag nanoparticles on two common soil bacteria, Bacillus cereus and Pseudomonas stutzeri. Al2O3 nanoparticles did not show significant toxicity at any dose or time assayed, whereas exposure to 5 mg L(-1) Ag nanoparticles for 48 h caused bactericidal effects. Moreover, alterations at the morphological level were observed by transmission electron microscopy (TEM); Ag but not Al2O3 nanoparticles evoked the entrance of B. cereus cells in an early sporulation stage and both nanoparticles penetrated P. stutzeri cells. At the molecular level, a dramatic increase (8.2-fold) in katB gene expression was found in P. stutzeri following Al2O3 nanoparticles exposure, indicative of an oxidative stress-defence system enhancement in this bacterium. In the microcosm experiment, using two different natural soils, Al2O3 or Ag nanoparticles did not affect the Caenorhabditis elegans toxicity endpoints growth, survival, or reproduction. However, differences in microbial phylogenetic compositions were detected by fluorescence in situ hybridization (FISH). The use of katB- and pykA-based sequences showed that the microbial transcriptional response to nanoparticle exposure decreased, suggesting a decrease in cellular activity. These changes were attributable to both the nanoparticles treatment and soil characteristics, highlighting the importance of considering the soil matrix on a case by case basis.

  4. Persistence of Silver Nanoparticles in the Rat Lung: Influence of Dose, Size and Chemical Composition

    PubMed Central

    Anderson, Donald S; Silva, Rona M; Lee, Danielle; Edwards, Patricia C.; Sharmah, Arjun; Guo, Ting; Pinkerton, Kent E; Van Winkle, Laura S

    2014-01-01

    Increasing silver nanoparticle (AgNP) use in sprays, consumer products and medical devices has raised concerns about potential health effects. While previous studies have investigated AgNPs, most were limited to a single particle size or surface coating. In this study, we investigated the effect of size, surface coating and dose on the persistence of silver in the lung following exposure to AgNP. Adult male rats were intratracheally instilled with four different AgNPs: 20 or 110nm in size and coated with either citrate or polyvinylpyrrolidone (PVP) at 0.5 or 1.0mg/kg doses. Silver retention was assessed in the lung at 1, 7 and 21 days post exposure. ICP-MS quantification demonstrated that citrate coated AgNPs persisted in the lung to 21 days with greater than 90% retention, while PVP coated AgNP had less than 30% retention. Localization of silver in lung tissue at one day post exposure demonstrated decreased silver in proximal airways exposed to 110nm particles compared with 20nm AgNPs. In terminal bronchioles one day post exposure, silver was localized to surface epithelium but was more prominent in the basement membrane at 7 days. Silver positive macrophages in bronchoalveolar lavage fluid decreased more quickly after exposure to particles coated with PVP. We conclude that PVP coated AgNPs had less retention in the lung tissue over time and larger particles were more rapidly cleared from large airways than smaller particles. The 20nm citrate particles the greatest effect; increasing lung macrophages even 21days after exposure and resulted in the greatest silver retention in lung tissue. PMID:25231189

  5. Core–shell Ag@SiO{sub 2} nanoparticles of different silica shell thicknesses: Preparation and their effects on photoluminescence of lanthanide complexes

    SciTech Connect

    Kang, Jie; Li, Yuan; Chen, Yingnan; Wang, Ailing; Yue, Bin; Qu, Yanrong; Zhao, Yongliang; Chu, Haibin

    2015-11-15

    Highlights: • Ag@SiO{sub 2} nanoparticles of different silica shell thicknesses were prepared via the Stöber process. • Sm and Dy complexes with benzoate, 1,10-phenanthroline and 2,2′-bipyridine were synthesized. • The complex-doped Ag@SiO{sub 2} composites show stronger luminescent intensities than pure complexes. • The luminescent intensities of the composites strongly depend on the SiO{sub 2} shell thickness. - Abstract: Three kinds of almost spherical core–shell Ag@SiO{sub 2} nanoparticles of different silica shell thicknesses (10, 25 and 80 nm) were prepared via the Stöber process. The Ag core nanoparticles were prepared by reducing silver nitrate with sodium citrate. The size, morphology and structure of core–shell Ag@SiO{sub 2} nanoparticles were characterized by transmission electron microscopy. Subsequently, eight kinds of lanthanide complexes with benzoate, 1,10-phenanthroline and 2,2′-bipyridine were synthesized. The composition of the lanthanide complexes was characterized by elemental analysis, IR and UV spectra. Finally, lanthanide complexes were attached to the surface of Ag@SiO{sub 2} nanoparticles to form lanthanide-complex-doped Ag@SiO{sub 2} nanocomposites. The results show that the complex-doped Ag@SiO{sub 2} nanocomposites display much stronger luminescence intensities than the lanthanide complexes. Furthermore, the luminescence intensities of the lanthanide-complex-doped Ag@SiO{sub 2} nanocomposites with SiO{sub 2} shell thickness of 25 nm are stronger than those of the nanocomposites with SiO{sub 2} shell thickness of 10 and 80 nm.

  6. Surface plasmon enhanced photoluminescence in amorphous silicon carbide films by adjusting Ag island film sizes

    NASA Astrophysics Data System (ADS)

    Yu, Wei; Wang, Xin-Zhan; Dai, Wan-Lei; Lu, Wan-Bing; Liu, Yu-Mei; Fu, Guang-Sheng

    2013-05-01

    Ag island films with different sizes are deposited on hydrogenated amorphous silicon carbide (α-SiC:H) films, and the influences of Ag island films on the optical properties of the α-SiC:H films are investigated. Atomic force microscope images show that Ag nanoislands are formed after Ag coating, and the size of the Ag islands increases with increasing Ag deposition time. The extinction spectra indicate that two resonance absorption peaks which correspond to out-of-plane and in-plane surface plasmon modes of the Ag island films are obtained, and the resonance peak shifts toward longer wavelength with increasing Ag island size. The photoluminescence (PL) enhancement or quenching depends on the size of Ag islands, and PL enhancement by 1.6 times on the main PL band is obtained when the sputtering time is 10 min. Analyses show that the influence of surface plasmons on the PL of α-SiC:H is determined by the competition between the scattering and absorption of Ag islands, and PL enhancement is obtained when scattering is the main interaction between the Ag islands and incident light.

  7. Effect of Ag nanoparticle concentration on the electrical and ferroelectric properties of Ag/P(VDF-TrFE) composite films

    PubMed Central

    Paik, Haemin; Choi, Yoon-Young; Hong, Seungbum; No, Kwangsoo

    2015-01-01

    We investigated the effect of the Ag nanoparticles on the ferroelectric and piezoelectric properties of Ag/poly(vinylidenefluoride-trifluoroethylene) (P(VDF-TrFE)) composite films. We found that the remanent polarization and direct piezoelectric coefficient increased up to 12.14 μC/cm2 and 20.23 pC/N when the Ag concentration increased up to 0.005 volume percent (v%) and decreased down to 9.38 μC/cm2 and 13.45 pC/N when it increased up to 0.01 v%. Further increase in Ag concentration resulted in precipitation of Ag phase and significant leakage current that hindered any meaningful measurement of the ferroelectric and piezoelectric properties. 46% increase of the remanent polarization value and 27% increase of the direct piezoelectric coefficient were observed in the film with the 0.005 v% of the Ag nanoparticles added without significant changes to the crystalline structure confirmed by both X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) experiments. These enhancements of both the ferroelectric and piezoelectric properties are attributed to the increase in the effective electric field induced by the reduction in the effective volume of P(VDF-TrFE) that results in more aligned dipoles. PMID:26336795

  8. Effect of Ag nanoparticle concentration on the electrical and ferroelectric properties of Ag/P(VDF-TrFE) composite films

    DOE PAGES

    Paik, Haemin; Choi, Yoon -Young; Hong, Seungbum; No, Kwangsoo

    2015-09-04

    We investigated the effect of the Ag nanoparticles on the ferroelectric and piezoelectric properties of Ag/poly(vinylidenefluoride-trifluoroethylene) (P(VDF-TrFE)) composite films. We found that the remanent polarization and direct piezoelectric coefficient increased up to 12.14 μC/cm2 and 20.23 pC/N when the Ag concentration increased up to 0.005 volume percent (v%) and decreased down to 9.38 μC/cm2 and 13.45 pC/N when it increased up to 0.01 v%. Further increase in Ag concentration resulted in precipitation of Ag phase and significant leakage current that hindered any meaningful measurement of the ferroelectric and piezoelectric properties. 46% increase of the remanent polarization value and 27% increasemore » of the direct piezoelectric coefficient were observed in the film with the 0.005 v% of the Ag nanoparticles added without significant changes to the crystalline structure confirmed by both X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) experiments. The enhancements of both the ferroelectric and piezoelectric properties are attributed to the increase in the effective electric field induced by the reduction in the effective volume of P(VDF-TrFE) that results in more aligned dipoles.« less

  9. Effect of Ag nanoparticle concentration on the electrical and ferroelectric properties of Ag/P(VDF-TrFE) composite films

    SciTech Connect

    Paik, Haemin; Choi, Yoon -Young; Hong, Seungbum; No, Kwangsoo

    2015-09-04

    We investigated the effect of the Ag nanoparticles on the ferroelectric and piezoelectric properties of Ag/poly(vinylidenefluoride-trifluoroethylene) (P(VDF-TrFE)) composite films. We found that the remanent polarization and direct piezoelectric coefficient increased up to 12.14 μC/cm2 and 20.23 pC/N when the Ag concentration increased up to 0.005 volume percent (v%) and decreased down to 9.38 μC/cm2 and 13.45 pC/N when it increased up to 0.01 v%. Further increase in Ag concentration resulted in precipitation of Ag phase and significant leakage current that hindered any meaningful measurement of the ferroelectric and piezoelectric properties. 46% increase of the remanent polarization value and 27% increase of the direct piezoelectric coefficient were observed in the film with the 0.005 v% of the Ag nanoparticles added without significant changes to the crystalline structure confirmed by both X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) experiments. The enhancements of both the ferroelectric and piezoelectric properties are attributed to the increase in the effective electric field induced by the reduction in the effective volume of P(VDF-TrFE) that results in more aligned dipoles.

  10. Silica Cladding of Ag Nanoparticles for High Stability and Surface-Enhanced Raman Spectroscopy Performance

    NASA Astrophysics Data System (ADS)

    Zhao, Miaomiao; Guo, Hao; Liu, Wenyao; Tang, Jun; Wang, Lei; Zhang, Binzhen; Xue, Chenyang; Liu, Jun; Zhang, Wendong

    2016-09-01

    For high-precision biochemical sensing, surface-enhanced Raman spectroscopy (SERS) has been demonstrated to be a highly sensitive spectroscopic analytical method and Ag is considered to be the best material for SERS performance. Due to the high surface activity of Ag nanoparticles, the high stability of Ag nanostructures, especially in moist environments, is one of the key issues that need to be solved. A method for silica (SiO2) cladding of Ag nanoparticles (NPs) is demonstrated here for high sensitivity and long-term stability when putted in aqueous solution. The chemically inert, transparent, hydrophilic, and bio-compatible SiO2 surface acts as the protection layer for the Ag nanoparticles, which can also enhance the Raman intensity to a certain extent. In our study, the Ag@SiO2 core-shell substrate can detect crystal violet solutions with molar concentrations down to 10-12 M. After 24 h of immersion, the reduction in Raman scattering intensity is about 85 % for sole Ag NP films, compared to 12 % for the Ag coated with a 10-nm SiO2 layer. This thickness was found to be optimum for Ag@SiO2 core-shell substrates with long-term stability and high SERS activity.

  11. Silica Cladding of Ag Nanoparticles for High Stability and Surface-Enhanced Raman Spectroscopy Performance.

    PubMed

    Zhao, Miaomiao; Guo, Hao; Liu, Wenyao; Tang, Jun; Wang, Lei; Zhang, Binzhen; Xue, Chenyang; Liu, Jun; Zhang, Wendong

    2016-12-01

    For high-precision biochemical sensing, surface-enhanced Raman spectroscopy (SERS) has been demonstrated to be a highly sensitive spectroscopic analytical method and Ag is considered to be the best material for SERS performance. Due to the high surface activity of Ag nanoparticles, the high stability of Ag nanostructures, especially in moist environments, is one of the key issues that need to be solved. A method for silica (SiO2) cladding of Ag nanoparticles (NPs) is demonstrated here for high sensitivity and long-term stability when putted in aqueous solution. The chemically inert, transparent, hydrophilic, and bio-compatible SiO2 surface acts as the protection layer for the Ag nanoparticles, which can also enhance the Raman intensity to a certain extent. In our study, the Ag@SiO2 core-shell substrate can detect crystal violet solutions with molar concentrations down to 10(-12) M. After 24 h of immersion, the reduction in Raman scattering intensity is about 85 % for sole Ag NP films, compared to 12 % for the Ag coated with a 10-nm SiO2 layer. This thickness was found to be optimum for Ag@SiO2 core-shell substrates with long-term stability and high SERS activity. PMID:27637895

  12. A Micro-Raman Study of Live, Single Red Blood Cells (RBCs) Treated with AgNO3 Nanoparticles

    PubMed Central

    Bankapur, Aseefhali; Barkur, Surekha; Chidangil, Santhosh; Mathur, Deepak

    2014-01-01

    Silver nanoparticles (Ag NPs) are known to exhibit broad antimicrobial activity. However, such activity continues to raise concerns in the context of the interaction of such NPs with biomolecules. In a physiological environment NPs interact with individual biological cells either by penetrating through the cell membrane or by adhering to the membrane. We have explored the interaction of Ag NPs with single optically-trapped, live erythrocytes (red blood cells, RBCs) using Raman Tweezers spectroscopy. Our experiments reveal that Ag NPs induce modifications within an RBC that appear to be irreversible. In particular we are able to identify that the heme conformation in an RBC transforms from the usual R-state (oxy-state) to the T-state (deoxy-state). We rationalize our observations by proposing a model for the nanoparticle cytotoxicity pathway when the NP size is larger than the membrane pore size. We propose that the interaction of Ag NPs with the cell surface induces damage brought about by alteration of intracellular pH caused by the blockage of the cell membrane transport. PMID:25057913

  13. Dependence of SERS enhancement on the chemical composition and structure of Ag/Au hybrid nanoparticles.

    PubMed

    Chaffin, Elise; O'Connor, Ryan T; Barr, James; Huang, Xiaohua; Wang, Yongmei

    2016-08-01

    Noble metal nanoparticles (NPs) such as silver (Ag) and gold (Au) have unique plasmonic properties that give rise to surface enhanced Raman scattering (SERS). Generally, Ag NPs have much stronger plasmonic properties and, hence, provide stronger SERS signals than Au NPs. However, Ag NPs lack the chemical stability and biocompatibility of comparable Au NPs and typically exhibit the most intense plasmonic resonance at wavelengths much shorter than the optimal spectral region for many biomedical applications. To overcome these issues, various experimental efforts have been devoted to the synthesis of Ag/Au hybrid NPs for the purpose of SERS detections. However, a complete understanding on how the SERS enhancement depends on the chemical composition and structure of these nanoparticles has not been achieved. In this study, Mie theory and the discrete dipole approximation have been used to calculate the plasmonic spectra and near-field electromagnetic enhancements of Ag/Au hybrid NPs. In particular, we discuss how the electromagnetic enhancement depends on the mole fraction of Au in Ag/Au alloy NPs and how one may use extinction spectra to distinguish between Ag/Au alloyed NPs and Ag-Au core-shell NPs. We also show that for incident laser wavelengths between ∼410 nm and 520 nm, Ag/Au alloyed NPs provide better electromagnetic enhancement than pure Ag, pure Au, or Ag-Au core-shell structured NPs. Finally, we show that silica-core Ag/Au alloy shelled NPs provide even better performance than pure Ag/Au alloy or pure solid Ag and pure solid Au NPs. The theoretical results presented will be beneficial to the experimental efforts in optimizing the design of Ag/Au hybrid NPs for SERS-based detection methods. PMID:27497571

  14. Dependence of SERS enhancement on the chemical composition and structure of Ag/Au hybrid nanoparticles

    NASA Astrophysics Data System (ADS)

    Chaffin, Elise; O'Connor, Ryan T.; Barr, James; Huang, Xiaohua; Wang, Yongmei

    2016-08-01

    Noble metal nanoparticles (NPs) such as silver (Ag) and gold (Au) have unique plasmonic properties that give rise to surface enhanced Raman scattering (SERS). Generally, Ag NPs have much stronger plasmonic properties and, hence, provide stronger SERS signals than Au NPs. However, Ag NPs lack the chemical stability and biocompatibility of comparable Au NPs and typically exhibit the most intense plasmonic resonance at wavelengths much shorter than the optimal spectral region for many biomedical applications. To overcome these issues, various experimental efforts have been devoted to the synthesis of Ag/Au hybrid NPs for the purpose of SERS detections. However, a complete understanding on how the SERS enhancement depends on the chemical composition and structure of these nanoparticles has not been achieved. In this study, Mie theory and the discrete dipole approximation have been used to calculate the plasmonic spectra and near-field electromagnetic enhancements of Ag/Au hybrid NPs. In particular, we discuss how the electromagnetic enhancement depends on the mole fraction of Au in Ag/Au alloy NPs and how one may use extinction spectra to distinguish between Ag/Au alloyed NPs and Ag-Au core-shell NPs. We also show that for incident laser wavelengths between ˜410 nm and 520 nm, Ag/Au alloyed NPs provide better electromagnetic enhancement than pure Ag, pure Au, or Ag-Au core-shell structured NPs. Finally, we show that silica-core Ag/Au alloy shelled NPs provide even better performance than pure Ag/Au alloy or pure solid Ag and pure solid Au NPs. The theoretical results presented will be beneficial to the experimental efforts in optimizing the design of Ag/Au hybrid NPs for SERS-based detection methods.

  15. Dependence of SERS enhancement on the chemical composition and structure of Ag/Au hybrid nanoparticles.

    PubMed

    Chaffin, Elise; O'Connor, Ryan T; Barr, James; Huang, Xiaohua; Wang, Yongmei

    2016-08-01

    Noble metal nanoparticles (NPs) such as silver (Ag) and gold (Au) have unique plasmonic properties that give rise to surface enhanced Raman scattering (SERS). Generally, Ag NPs have much stronger plasmonic properties and, hence, provide stronger SERS signals than Au NPs. However, Ag NPs lack the chemical stability and biocompatibility of comparable Au NPs and typically exhibit the most intense plasmonic resonance at wavelengths much shorter than the optimal spectral region for many biomedical applications. To overcome these issues, various experimental efforts have been devoted to the synthesis of Ag/Au hybrid NPs for the purpose of SERS detections. However, a complete understanding on how the SERS enhancement depends on the chemical composition and structure of these nanoparticles has not been achieved. In this study, Mie theory and the discrete dipole approximation have been used to calculate the plasmonic spectra and near-field electromagnetic enhancements of Ag/Au hybrid NPs. In particular, we discuss how the electromagnetic enhancement depends on the mole fraction of Au in Ag/Au alloy NPs and how one may use extinction spectra to distinguish between Ag/Au alloyed NPs and Ag-Au core-shell NPs. We also show that for incident laser wavelengths between ∼410 nm and 520 nm, Ag/Au alloyed NPs provide better electromagnetic enhancement than pure Ag, pure Au, or Ag-Au core-shell structured NPs. Finally, we show that silica-core Ag/Au alloy shelled NPs provide even better performance than pure Ag/Au alloy or pure solid Ag and pure solid Au NPs. The theoretical results presented will be beneficial to the experimental efforts in optimizing the design of Ag/Au hybrid NPs for SERS-based detection methods.

  16. Temperature and size-dependent Hamaker constants for metal nanoparticles

    NASA Astrophysics Data System (ADS)

    Jiang, K.; Pinchuk, P.

    2016-08-01

    Theoretical values of the Hamaker constant have been calculated for metal nanoparticles using Lifshitz theory. The theory describes the Hamaker constant in terms of the permittivity of the interacting bodies. Metal nanoparticles exhibit an internal size effect that alters the dielectric permittivity of the particle when its size falls below the mean free path of the conducting electrons. This size dependence of the permittivity leads to size-dependence of the Hamaker constant for metal nanoparticles. Additionally, the electron damping and the plasma frequency used to model the permittivity of the particle exhibit temperature-dependence, which lead to temperature dependence of the Hamaker constant. In this work, both the size and temperature dependence for gold, silver, copper, and aluminum nanoparticles is demonstrated. The results of this study might be of interest for studying the colloidal stability of nanoparticles in solution.

  17. Fabrication of flexible superhydrophobic films by lift-up soft-lithography and decoration with Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Yao, Tongjie; Wang, Chuanxi; Lin, Quan; Li, Xiao; Chen, Xiaolu; Wu, Jie; Zhang, Junhu; Yu, Kui; Yang, Bai

    2009-02-01

    Superhydrophobic films with excellent flexibility have been fabricated by combining the lift-up soft-lithography technique and chemical reduction of [Ag(NH3)2]+ ions to Ag nanoparticles (NPs) on the surface of silica spheres which are patterned on the polydimethylsiloxane (PDMS) films. Scanning electron microscopy (SEM) images reveal the presence of raspberry-like hierarchical structures on the PDMS films. The influence of the amount of Ag NPs and the size of the silica spheres on the wettability of the soft films is investigated carefully. Because PDMS films are elastomeric materials, our superhydrophobic films offer great flexibility. The resulting films can be easily transferred from one substrate surface to another without destroying their superhydrophobicity. These flexible and superhydrophobic films can be used repeatedly to satisfy a wide range of applications.

  18. A novel green synthesis of Fe3O4-Ag core shell recyclable nanoparticles using Vitis vinifera stem extract and its enhanced antibacterial performance

    NASA Astrophysics Data System (ADS)

    Venkateswarlu, Sada; Natesh Kumar, B.; Prathima, B.; Anitha, K.; Jyothi, N. V. V.

    2015-01-01

    We described a novel and eco-friendly method for preparing Fe3O4-Ag core shell nanoparticles (CSNPs) with high magnetism and potent antibacterial activity. The Fe3O4-Ag CSNPs were obtained using waste material of Vitis vinifera (grape) stem extract as the green solvent, reducing and capping agent. The result recorded from X-ray powder diffraction (XRD), UV-vis spectrum, energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FT-IR) supports the biosynthesis and characterization of Fe3O4-Ag CSNPs. From transmission electron microscopy (TEM) the size of the Fe3O4-Ag nanoparticles was measured below 50 nm; high-resolution TEM (HRTEM) indicates the core shell structure; and selected area electron diffraction (SAED) has revealed polycrystalline nature. Vibrating sample magnetometer (VSM) shows the ferromagnetic nature of Fe3O4-Ag CSNPs at room temperature with saturation magnetization of 15.74 emu/g. Further, these biogenic nanoparticles were highly hazardous to microorganisms. The antibacterial activity of biogenic Fe3O4-Ag CSNPs showed potent inhibitory activity against both Gram-positive and Gram-negative pathogens. These nanoparticles may also be reusable because of its excellent ferromagnetic property.

  19. Hydrogen treatment-improved uniform deposition of Ag nanoparticles on ZnO nanorod arrays and their visible-light photocatalytic and surface-enhanced Raman scattering properties

    PubMed Central

    2013-01-01

    ZnO nanorod arrays were synthesized by chemical bath deposition. After heat treatment in hydrogen or air, Ag nanoparticles were deposited on ZnO nanorod arrays by photo-reduction method. The size of Ag nanoparticles as well as the surface morphology, structure, composition, and optical property of ZnO nanorod arrays before and after the deposition of Ag nanoparticles were characterized by SEM, XRD, EDS, and UV/VIS/NIR spectrophotometer. As compared to the samples with heat treatment in air or without heat treatment, the ZnO nanorod arrays after heat treatment in hydrogen allowed Ag nanoparticles to be deposited more uniformly, densely, and numerously. Also, they exhibited higher efficiency for the visible light-driven photocatalytic degradation of Rhodamine 6G (R6G) dye. The effects of the amount of Ag nanoparticles, initial dye concentration, and temperature on the photocatalytic degradation efficiency were investigated. Furthermore, they also exhibited better surface-enhanced Raman scattering property for the detection of R6G dyes. PMID:23866904

  20. Silver sulfide nanoparticles (Ag2S-NPs) are taken up by plants and are phytotoxic.

    PubMed

    Wang, Peng; Menzies, Neal W; Lombi, Enzo; Sekine, Ryo; Blamey, F Pax C; Hernandez-Soriano, Maria C; Cheng, Miaomiao; Kappen, Peter; Peijnenburg, Willie J G M; Tang, Caixian; Kopittke, Peter M

    2015-01-01

    Silver nanoparticles (NPs) are used in more consumer products than any other nanomaterial and their release into the environment is unavoidable. Of primary concern is the wastewater stream in which most silver NPs are transformed to silver sulfide NPs (Ag2S-NPs) before being applied to agricultural soils within biosolids. While Ag2S-NPs are assumed to be biologically inert, nothing is known of their effects on terrestrial plants. The phytotoxicity of Ag and its accumulation was examined in short-term (24 h) and longer-term (2-week) solution culture experiments with cowpea (Vigna unguiculata L. Walp.) and wheat (Triticum aestivum L.) exposed to Ag2S-NPs (0-20 mg Ag L(-1)), metallic Ag-NPs (0-1.6 mg Ag L(-1)), or ionic Ag (AgNO3; 0-0.086 mg Ag L(-1)). Although not inducing any effects during 24-h exposure, Ag2S-NPs reduced growth by up to 52% over a 2-week period. This toxicity did not result from their dissolution and release of toxic Ag(+) in the rooting medium, with soluble Ag concentrations remaining below 0.001 mg Ag L(-1). Rather, Ag accumulated as Ag2S in the root and shoot tissues when plants were exposed to Ag2S-NPs, consistent with their direct uptake. Importantly, this differed from the form of Ag present in tissues of plants exposed to AgNO3. For the first time, our findings have shown that Ag2S-NPs exert toxic effects through their direct accumulation in terrestrial plant tissues. These findings need to be considered to ensure high yield of food crops, and to avoid increasing Ag in the food chain. PMID:25686712

  1. Ag Nanoparticles (Ag NM300K) in the Terrestrial Environment: Effects at Population and Cellular Level in Folsomia candida (Collembola)

    PubMed Central

    Mendes, Luís André; Maria, Vera L.; Scott-Fordsmand, Janeck J.; Amorim, Mónica J. B.

    2015-01-01

    The effects of nanomaterials have been primarily assessed based on standard ecotoxicity guidelines. However, by adapting alternative measures the information gained could be enhanced considerably, e.g., studies should focus on more mechanistic approaches. Here, the environmental risk posed by the presence of silver nanoparticles (Ag NM300K) in soil was investigated, anchoring population and cellular level effects, i.e., survival, reproduction (28 days) and oxidative stress markers (0, 2, 4, 6, 10 days). The standard species Folsomia candida was used. Measured markers included catalase (CAT), glutathione reductase (GR), glutathione S-transferase (GST), total glutathione (TG), metallothionein (MT) and lipid peroxidation (LPO). Results showed that AgNO3 was more toxic than AgNPs at the population level: reproduction EC20 and EC50 was ca. 2 and 4 times lower, respectively. At the cellular level Correspondence Analysis showed a clear separation between AgNO3 and AgNP throughout time. Results showed differences in the mechanisms, indicating a combined effect of released Ag+ (MT and GST) and of AgNPs (CAT, GR, TG, LPO). Hence, clear advantages from mechanistic approaches are shown, but also that time is of importance when measuring such responses. PMID:26473892

  2. TiN nanoparticles: small size-selected fabrication and their quantum size effect

    PubMed Central

    2012-01-01

    Size-selected TiN nanoclusters in the range of 4 to 20 nm have been produced by an ionized cluster beam, which combines a glow-discharge sputtering with an inert gas condensation technique. With this method, by controlling the experimental conditions, it was possible to produce nanoparticles with a high control in size. The size distribution of TiN nanoparticles was determined before deposition by mass spectroscopy and confirmed by atomic force microscopy. The size distribution was also analyzed using a high-resolution transmission electron micrograph. The photoluminescence [PL] spectra of TiN nanoparticles at different sizes were also experimentally investigated. We reported, for the first time, the strong visible luminescence of TiN nanoparticles on Si (111) wafer due to the reduced size. We also discussed the PL intensity as a function of the nanoparticle size distribution. PMID:22252375

  3. TiN nanoparticles: small size-selected fabrication and their quantum size effect.

    PubMed

    Hernández Mainet, Luis Carlos; Cabrera, Luis Ponce; Rodriguez, Eugenio; Cruz, Abel Fundora; Santana, Guillermo; Menchaca, Jorge Luis; Pérez-Tijerina, Eduardo

    2012-01-01

    Size-selected TiN nanoclusters in the range of 4 to 20 nm have been produced by an ionized cluster beam, which combines a glow-discharge sputtering with an inert gas condensation technique. With this method, by controlling the experimental conditions, it was possible to produce nanoparticles with a high control in size. The size distribution of TiN nanoparticles was determined before deposition by mass spectroscopy and confirmed by atomic force microscopy. The size distribution was also analyzed using a high-resolution transmission electron micrograph. The photoluminescence [PL] spectra of TiN nanoparticles at different sizes were also experimentally investigated. We reported, for the first time, the strong visible luminescence of TiN nanoparticles on Si (111) wafer due to the reduced size. We also discussed the PL intensity as a function of the nanoparticle size distribution. PMID:22252375

  4. 1,10-Phenanthroline as an accelerator for Ag nanoparticle-catalysed electroless copper deposition

    NASA Astrophysics Data System (ADS)

    Liu, Chia-Ru; Chou, Nan-Kuang; Li, Cheng-Hsing; Chen, Ho-Rei; Lee, Chien-Liang

    2014-10-01

    1,10-Phenanthroline (phen) can be successfully used as an accelerator for Ag-catalysed electroless copper deposition (ECD) processes. Electrochemical quartz crystal microbalance analyses indicate that the mass activity in terms of thickness of deposited Cu layer and average ECD rate within a deposition time of 110 s for Ag nanoparticles activated by phen are 7.86 × 10-3 μm μg-1 and 1.43 × 10-4 μm μg-1 s-1, respectively, whereas Ag nanoparticles without phen cannot catalyse the reaction. Furthermore, Tafel and cyclic voltammetric results show that the addition of phen to the ECD bath significantly enhances the ability of the Ag nanoparticles to catalyse the oxidation of HCHO and suppresses the formation of CuO.

  5. Impact of water composition on association of Ag and CeO₂ nanoparticles with aquatic macrophyte Elodea canadensis.

    PubMed

    Van Koetsem, Frederik; Xiao, Yi; Luo, Zhuanxi; Du Laing, Gijs

    2016-03-01

    In this study, the potential association of (citrate-stabilized) Ag (14.1 ± 1.0 nm) and CeO2 (6.7 ± 1.2 nm) engineered nanoparticles (ENPs), or their ionic counterparts, with the submerged aquatic plant Elodea canadensis, was examined and, in particular, parameters affecting the distribution of the nanoparticles (or metal ions) between plant biomass and the water phase were assessed using five distinct aqueous matrices (i.e. tap water, 10 % Hoagland's solution and three natural surface water samples). Individual plants were exposed to varying concentrations of Ag and CeO2 ENPs or Ag(+) and Ce(3+) ions during 72-h-lasting batch experiments. A dose-dependent increase of silver or cerium in plant biomass was observed for both the nanoparticles and the ions, whereby exposure to the latter systematically resulted in significantly higher biomass concentrations. Furthermore, the apparent plant uptake of CeO2 ENPs appeared to be higher than that for Ag ENPs when comparing similar exposure concentrations. These findings suggest that association with E. canadensis might be affected by particle characteristics such as size, composition, surface charge or surface coating. Moreover, the stability of the ENPs or ions in suspension/solution may be another important aspect affecting plant exposure and uptake. The association of the nanoparticles or ions with E. canadensis was affected by the physicochemical characteristics of the water sample. The silver biomass concentration was found to correlate significantly with the electrical conductivity (EC), dry residue (DR) and Cl(-), K, Na and Mg content in the case of Ag ENPs or with the EC, inorganic carbon (IC) and Cl(-), NO3 (-), Na and Mg content in the case of Ag(+) ions, whereas significant relationships between the cerium biomass concentration and the EC, DR, IC and Ca content or the pH, EC, DR, IC and Cl(-), Ca and Mg content were obtained for CeO2 ENPs or Ce(3+) ions, respectively. Results also indicated that the Ag

  6. [Contribution of Particle Size and Surface Coating of Silver Nanoparticles to Its Toxicity in Marine Diatom Skeletonema costatum].

    PubMed

    Huang, Jun; Yi, Jun; Qiang, Li-yuan; Cheng, Jin-ping

    2016-05-15

    Due to the unique antibacterial properties, silver nanoparticles (AgNPs) have been widely used in commercial applications. In this study, the toxicity of three kinds of AgNPs with different sizes and surface coatings to marine diatom Skeletonema costatum (S. costatum) was studied, which was one of the dominant species in estuarine and coastal areas. All three kinds of tested AgNPs inhibited the growth of exposed S. costatum under acute exposure condition, and the order of toxicity was 10 nm-OA > 10 nm-PVP > 20 nm-PVP. Given the condition of similar particle size, oil amine surface coated AgNPs were more toxic than polyvinyl pyrrolidone (PVP) surface coated AgNPs in S. costatum in term of cytotoxicity. With the same surface coating, the toxicity of AgNPs in S. costatum was affected by its hydrodynamic diameter and exposure concentrations. When the concentration of AgNPs was less than 500 µg · L⁻¹, larger sized AgNPs showed greater toxicity; When the concentration was greater than or equal to 500 µg · L⁻¹, smaller AgNPs exhibited greater toxicity. At molecular level, 50 µg · L⁻¹ 10nm-PVP significantly upregulated expression level of 3HfcpA (P < 0.05) and significantly downregulated expression level of Dl (P < 0.05), and 500 µg · L⁻¹ 10nm-OA significantly upregulated 3HfcpA expression (P < 0.05), while 20 nm-PVP treatment group didn't show any significant change. Exposed diatom demonstrated sensitive photosynthesis response to small size and PVP coated silver nanoparticles at molecular level. This study suggested that the toxicity of AgNPs to marine microalgae was largely controlled by the particle size, surface coating, exposure medium, exposure concentration and other factors. The smaller the particle size, the greater the toxicity of AgNPs, and the particle size of AgNPs played an important role in the toxicity of AgNPs in marine diatom S. costatum.

  7. [Contribution of Particle Size and Surface Coating of Silver Nanoparticles to Its Toxicity in Marine Diatom Skeletonema costatum].

    PubMed

    Huang, Jun; Yi, Jun; Qiang, Li-yuan; Cheng, Jin-ping

    2016-05-15

    Due to the unique antibacterial properties, silver nanoparticles (AgNPs) have been widely used in commercial applications. In this study, the toxicity of three kinds of AgNPs with different sizes and surface coatings to marine diatom Skeletonema costatum (S. costatum) was studied, which was one of the dominant species in estuarine and coastal areas. All three kinds of tested AgNPs inhibited the growth of exposed S. costatum under acute exposure condition, and the order of toxicity was 10 nm-OA > 10 nm-PVP > 20 nm-PVP. Given the condition of similar particle size, oil amine surface coated AgNPs were more toxic than polyvinyl pyrrolidone (PVP) surface coated AgNPs in S. costatum in term of cytotoxicity. With the same surface coating, the toxicity of AgNPs in S. costatum was affected by its hydrodynamic diameter and exposure concentrations. When the concentration of AgNPs was less than 500 µg · L⁻¹, larger sized AgNPs showed greater toxicity; When the concentration was greater than or equal to 500 µg · L⁻¹, smaller AgNPs exhibited greater toxicity. At molecular level, 50 µg · L⁻¹ 10nm-PVP significantly upregulated expression level of 3HfcpA (P < 0.05) and significantly downregulated expression level of Dl (P < 0.05), and 500 µg · L⁻¹ 10nm-OA significantly upregulated 3HfcpA expression (P < 0.05), while 20 nm-PVP treatment group didn't show any significant change. Exposed diatom demonstrated sensitive photosynthesis response to small size and PVP coated silver nanoparticles at molecular level. This study suggested that the toxicity of AgNPs to marine microalgae was largely controlled by the particle size, surface coating, exposure medium, exposure concentration and other factors. The smaller the particle size, the greater the toxicity of AgNPs, and the particle size of AgNPs played an important role in the toxicity of AgNPs in marine diatom S. costatum. PMID:27506055

  8. Hydroxyapatite supported Ag3PO4 nanoparticles with higher visible light photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Hong, Xiaoting; Wu, Xiaohui; Zhang, Qiuyun; Xiao, Mingfeng; Yang, Gelin; Qiu, Meirong; Han, Guocheng

    2012-03-01

    Hydroxyapatite supported Ag3PO4 nanocomposites have been synthesized by a wet impregnation process. UV-vis absorption spectra show a red shift of the absorption edges for the composite systems compared to pure hydroxyapatite support. The surface structure and morphology of the nanocomposites were characterized by Brunauer-Emmett-Teller (BET) apparatus, X-ray diffraction (XRD), transmission electron microscopy (TEM). The results suggest that Ag3PO4 nanoparticles (6-17 nm in diameter) are well dispersed on the hydroxyapatite support and Ag3PO4 nanoparticles density is larger for the higher Ag+ loading sample. The as-prepared nanocomposite photocatalysts showed a pronounced photocatalytic activity upon decomposition of methylene blue dye in aqueous solution under both visible light (wavelength > 400 nm) and UV-vis light irradiation. A synergic mechanism of inherent photocatalytic capability of Ag3PO4 and the accelerated electron/hole separation resulting from the photoinduced electrons captured by the slow-released Ag+ at the interface of Ag3PO4 and hydroxyapatite is proposed for the nanocomposites on the enhancement of photocatalytic performance in comparison to that of pure Ag3PO4 nanoparticles. The support of hydroxyapatite may also act as an absorbent which favors the mass transfer in heterogeneous photocatalysis reaction.

  9. In situ plasmonic Ag nanoparticle anchored TiO2 nanotube arrays as visible-light-driven photocatalysts for enhanced water splitting

    NASA Astrophysics Data System (ADS)

    Ge, Ming-Zheng; Cao, Chun-Yan; Li, Shu-Hui; Tang, Yu-Xin; Wang, Lu-Ning; Qi, Ning; Huang, Jian-Ying; Zhang, Ke-Qin; Al-Deyab, S. S.; Lai, Yue-Kun

    2016-02-01

    ). It was found that the hydrogen production rate of the Ag@TiO2 NTAs prepared with ultrasonication-assisted deposition for 5 min was approximately 15 times higher than that of its pristine TiO2 NTAs counterpart. The highly efficient photocatalytic hydrogen evolution is attributed to the SPR effect of Ag for enhanced visible light absorption and boosting the photogenerated electron-hole separation/transfer. This strategy is promising for the design and construction of high efficiency TiO2 based photocatalysts for solar energy conversion. Electronic supplementary information (ESI) available: EDS and mapping spectra of Ag@TiO2 NTAs with an ultrasonication-assisted deposition time of 5 min, the size distribution of Ag nanoparticles of Ag@TiO2 NTAs with different deposition times, SEM images and EDS spectra of TiO2 NTAs with an ultrasonication-assisted deposition time of 5 min with 5, 20, and 40 mM AgNO3, photocurrent responses and hydrogen production rate of as-prepared pure TiO2 NTAs and Ag@TiO2 NTAs with an ultrasonication-assisted deposition time of 5 min with different concentrations of AgNO3. See DOI: 10.1039/c5nr08341a

  10. Size- and coating-dependent cytotoxicity and genotoxicity of silver nanoparticles evaluated using in vitro standard assays.

    PubMed

    Guo, Xiaoqing; Li, Yan; Yan, Jian; Ingle, Taylor; Jones, Margie Yvonne; Mei, Nan; Boudreau, Mary D; Cunningham, Candice K; Abbas, Mazhar; Paredes, Angel M; Zhou, Tong; Moore, Martha M; Howard, Paul C; Chen, Tao

    2016-11-01

    The physicochemical characteristics of silver nanoparticles (AgNPs) may greatly alter their toxicological potential. To explore the effects of size and coating on the cytotoxicity and genotoxicity of AgNPs, six different types of AgNPs, having three different sizes and two different coatings, were investigated using the Ames test, mouse lymphoma assay (MLA) and in vitro micronucleus assay. The genotoxicities of silver acetate and silver nitrate were evaluated to compare the genotoxicity of nanosilver to that of ionic silver. The Ames test produced inconclusive results for all types of the silver materials due to the high toxicity of silver to the test bacteria and the lack of entry of the nanoparticles into the cells. Treatment of L5718Y cells with AgNPs and ionic silver resulted in concentration-dependent cytotoxicity, mutagenicity in the Tk gene and the induction of micronuclei from exposure to nearly every type of the silver materials. Treatment of TK6 cells with these silver materials also resulted in concentration-dependent cytotoxicity and significantly increased micronucleus frequency. With both the MLA and micronucleus assays, the smaller the AgNPs, the greater the cytotoxicity and genotoxicity. The coatings had less effect on the relative genotoxicity of AgNPs than the particle size. Loss of heterozygosity analysis of the induced Tk mutants indicated that the types of mutations induced by AgNPs were different from those of ionic silver. These results suggest that AgNPs induce cytotoxicity and genotoxicity in a size- and coating-dependent manner. Furthermore, while the MLA and in vitro micronucleus assay (in both types of cells) are useful to quantitatively measure the genotoxic potencies of AgNPs, the Ames test cannot. PMID:27441588

  11. Size Selective Green Synthesis of Silver and Gold Nanoparticles: Enhanced Antibacterial Efficacy of Resveratrol Capped Silver Sol.

    PubMed

    Shukla, Shashi P; Roy, Mainak; Mukherjee, Poulomi; Das, Laboni; Neogy, Suman; Srivastava, Dinesh; Adhikari, Soumyakanti

    2016-03-01

    In view of potential biomedical application of the noble metal nanoparticles, we report a size controlled yet simple and green synthesis of resveratrol stabilized silver and gold nanoparticles having low polydispersity of size. Here, resveratrol plays two simultaneous roles, reducing the metal ions and providing efficient capping of the small nanoparticles. This gives rise to specific size of silver and gold nanoparticles at specific ratios of metal to resveratrol. The particles have been characterized by XRD and transmission electron microscopy. The nanoparticle sols are stable for months. The UV Visible absorption spectra of the silver sol show the plasmon peak of spherical nanoparticles, presence of which is further reflected in the TEM images. Size of the silver particles obtained is in between 11 to 21 nm depending on the ratio of resveratrol to metal ion used. Resveratrol capped silver nanoparticles exhibit high antibacterial activity against Gram negative wild type E coli BW (25113). The minimum inhibitory concentration (MIC) of nano-silver against the bacterium has been estimated to be 6.48 μg/ml, which is significantly lower than that reported in some earlier as well as recent publications. Reaction of gold ions with resveratrol, on the other hand, produces gold nanoparticles of sizes varying from 7 to 29 nm at different ratios of resveratrol to the metal ions. Particles with higher size and aspect ratio are formed at lower concentration of the capping agent whereas particles with very small size and pseudo-spherical morphology are formed at higher capping concentration. Difference in the formation kinetics of silver and gold nanoparticles has been attributed to the different growth mechanisms in the two cases. Possible modes of anchorage of resveratrol to silver nanoparticles have been investigated using surface enhanced resonance Raman spectroscopy (SERS) which shows that the silver nanoparticles are capped by resveratrol molecule primarily through O-Ag

  12. Nanoparticles of Ag with a Pt and Pd rich surface supported on carbon as a new catalyst for the oxygen electroreduction reaction (ORR) in acid electrolytes: Part 1

    NASA Astrophysics Data System (ADS)

    Pech-Pech, I. E.; Gervasio, Dominic F.; Godínez-Garcia, A.; Solorza-Feria, O.; Pérez-Robles, J. F.

    2015-02-01

    Silver (Ag) nanoparticles enriched with platinum (Pt) and palladium (Pd) on their surfaces (Ag@Pt0.1Pd0.1) are supported on Vulcan XC-72 carbon (C) to form a new catalyst (Ag@Pt0.1Pd0.1/C) for the oxygen reduction reaction (ORR) in acid electrolytes. This catalyst is prepared in one pot by reducing Ag and then Pt and Pd metal salts with sodium borohydride in the presence of trisodium citrate then adding XC-72 while applying intense ultrasound. The metallic Ag@Pt0.1Pd0.1 nanoparticles contain 2 weight percent of Pt, are spherical and have an average size less than 10 nm as determined by X-ray diffraction (XRD) and transmission electron microscopy (TEM). At the ORR potentials, Ag nanoparticles on carbon (Ag/C) rapidly lose Ag by dissolution and show no more catalytic activity for the ORR than the carbon support, whereas Ag@Pt0.1Pd0.1/C is a stable catalyst and exhibits 1.4 and 1.6 fold greater specific activity, also 3.6 and 2.8 fold greater mass activity for ORR in 0.5 M H2SO4 solution than comparable Pt/C and Pt0.5Pd0.5/C catalysts with the same Pt loading as determined for thin-films of these catalysts on a rotating-disk electrode (TF-RDE). Using silver nanoparticles increases Pt utilization and therefore decreases Pt-loading and cost of a catalyst for a proton exchange membrane fuel cell (PEMFC) electrode.

  13. New SERS-active alumina-based sorbents containing Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Yurova, Nadezhda S.; Markina, Natalia E.; Galushka, Victor V.; Burashnikova, Marina M.; Zakharevich, Andrey M.; Markin, Alexey V.; Rusanova, Tatiana Y.

    2016-04-01

    New SERS-active materials were obtained by preparation of alumina with embedded silver nanoparticles and their application both as sorbents for pre-concentration and SERS platforms was studied. The influence of ionic strength on Ag NPs size, absorption spectra and SERS signal was investigated. Synthesized materials were examined by Raman spectroscopy, scanning electron microscopy, and UV-visible spectroscopy. The optimal conditions for SERSmeasurements were chosen. Synthesized materials were applied for pre-concentration of model analytes (Rhodamine 6G, folic acid and pyrene) and their SERS detection directly within the sorbent. It was shown that the recovery of analytes could be improved by alumina modification. The combination of surface-enhanced Raman spectroscopy with preconcentration is a promising instrument for analytical applications.

  14. Oligogermanes as molecular precursors for germanium(0) nanoparticles: Size control and size-dependent fluorescence

    SciTech Connect

    Schrick, Aaron C.; Weinert, Charles S.

    2013-10-15

    Graphical abstract: Catenated germanium compounds are employed as molecular precursors for germanium(0) nanoparticles. The size of the nanoparticles, and their fluorescence spectra, depend on the number of catenated germanium atoms present in the precursor. - Highlights: • We have used oligogermanes for the size-specific synthesis of germanium(0) nanoparticles. • The size of the nanomaterials obtained depends directly on the degree of catenation present in the oligogermane precursor. • The nanoparticles are shown to exhibit size-dependent fluorescence. • Oligogermanes will function as useful precursors for the synthesis of a variety of nanomaterials. - Abstract: Germanium nanoparticles were synthesized in solution from novel oligogermane molecular precursors. The size of the nanoparticles obtained is directly related to the number of catenated germanium atoms present in the oligogermane precursor and the nanoparticles exhibit size-dependent fluorescence. The germanium nanoparticles were also characterized by TEM, powder XRD, FTIR, EDS and XPS methods. This method appears to be a promising new route for the synthesis of germanium nanoparticles since the size of the materials obtained can be controlled by the choice of the oligogermane used as the precursor.

  15. Core-shell AgSiO2-protoporphyrin IX nanoparticle: Effect of the Ag core on reactive oxygen species generation

    NASA Astrophysics Data System (ADS)

    Lismont, M.; Pá; ez-Martinez, C.; Dreesen, L.

    2015-03-01

    Photodynamic therapy (PDT) for cancer is based on the use of a light sensitive molecule to produce, under specific irradiation, toxic reactive oxygen species (ROS). A way to improve the therapy efficiency is to increase the amount of produced ROS near cancer cells. This aim can be achieved by using a metal enhanced process arising when an optically active molecule is located near a metallic nanoparticle (NP). Here, the coupling effect between silver (Ag) NPs and protoporphyrin IX (PpIX) molecules, a clinically approved photosensitizer, is studied compared first, to PpIX fluorescence yield and second, to ROS production efficiency. By applying a modified Stöber process, PpIX was encapsulated into a silica (SiO2) shell, surrounding a 60 nm sized Ag core. We showed that, compared to SiO2-PpIX NPs, Ag coated SiO2-PpIX NPs dramatically decreased PpIX fluorescence together with singlet oxygen production efficiency. However, after incubation time in the dark, the amount of superoxide anions generated by the Ag doped sample was higher than the control sample one.

  16. Nanoparticle size detection limits by single particle ICP-MS for 40 elements.

    PubMed

    Lee, Sungyun; Bi, Xiangyu; Reed, Robert B; Ranville, James F; Herckes, Pierre; Westerhoff, Paul

    2014-09-01

    The quantification and characterization of natural, engineered, and incidental nano- to micro-size particles are beneficial to assessing a nanomaterial's performance in manufacturing, their fate and transport in the environment, and their potential risk to human health. Single particle inductively coupled plasma mass spectrometry (spICP-MS) can sensitively quantify the amount and size distribution of metallic nanoparticles suspended in aqueous matrices. To accurately obtain the nanoparticle size distribution, it is critical to have knowledge of the size detection limit (denoted as Dmin) using spICP-MS for a wide range of elements (other than a few available assessed ones) that have been or will be synthesized into engineered nanoparticles. Herein is described a method to estimate the size detection limit using spICP-MS and then apply it to nanoparticles composed of 40 different elements. The calculated Dmin values correspond well for a few of the elements with their detectable sizes that are available in the literature. Assuming each nanoparticle sample is composed of one element, Dmin values vary substantially among the 40 elements: Ta, U, Ir, Rh, Th, Ce, and Hf showed the lowest Dmin values, ≤10 nm; Bi, W, In, Pb, Pt, Ag, Au, Tl, Pd, Y, Ru, Cd, and Sb had Dmin in the range of 11-20 nm; Dmin values of Co, Sr, Sn, Zr, Ba, Te, Mo, Ni, V, Cu, Cr, Mg, Zn, Fe, Al, Li, and Ti were located at 21-80 nm; and Se, Ca, and Si showed high Dmin values, greater than 200 nm. A range of parameters that influence the Dmin, such as instrument sensitivity, nanoparticle density, and background noise, is demonstrated. It is observed that, when the background noise is low, the instrument sensitivity and nanoparticle density dominate the Dmin significantly. Approaches for reducing the Dmin, e.g., collision cell technology (CCT) and analyte isotope selection, are also discussed. To validate the Dmin estimation approach, size distributions for three engineered nanoparticle samples were

  17. Effect of toxicity of Ag nanoparticles on SERS spectral variance of bacteria

    NASA Astrophysics Data System (ADS)

    Cui, Li; Chen, Shaode; Zhang, Kaisong

    2015-02-01

    Ag nanoparticles (NPs) have been extensively utilized in surface-enhanced Raman scattering (SERS) spectroscopy for bacterial identification. However, Ag NPs are toxic to bacteria. Whether such toxicity can affect SERS features of bacteria and interfere with bacterial identification is still unknown and needed to explore. Here, by carrying out a comparative study on non-toxic Au NPs with that on toxic Ag NPs, we investigated the influence of nanoparticle concentration and incubation time on bacterial SERS spectral variance, both of which were demonstrated to be closely related to the toxicity of Ag NPs. Sensitive spectral alterations were observed on Ag NPs with increase of NPs concentration or incubation time, accompanied with an obvious decrease in number of viable bacteria. In contrast, SERS spectra and viable bacterial number on Au NPs were rather constant under the same conditions. A further analysis on spectral changes demonstrated that it was cell response (i.e. metabolic activity or death) to the toxicity of Ag NPs causing spectral variance. However, biochemical responses to the toxicity of Ag were very different in different bacteria, indicating the complex toxic mechanism of Ag NPs. Ag NPs are toxic to a great variety of organisms, including bacteria, fungi, algae, protozoa etc., therefore, this work will be helpful in guiding the future application of SERS technique in various complex biological systems.

  18. Effect of toxicity of Ag nanoparticles on SERS spectral variance of bacteria.

    PubMed

    Cui, Li; Chen, Shaode; Zhang, Kaisong

    2015-02-25

    Ag nanoparticles (NPs) have been extensively utilized in surface-enhanced Raman scattering (SERS) spectroscopy for bacterial identification. However, Ag NPs are toxic to bacteria. Whether such toxicity can affect SERS features of bacteria and interfere with bacterial identification is still unknown and needed to explore. Here, by carrying out a comparative study on non-toxic Au NPs with that on toxic Ag NPs, we investigated the influence of nanoparticle concentration and incubation time on bacterial SERS spectral variance, both of which were demonstrated to be closely related to the toxicity of Ag NPs. Sensitive spectral alterations were observed on Ag NPs with increase of NPs concentration or incubation time, accompanied with an obvious decrease in number of viable bacteria. In contrast, SERS spectra and viable bacterial number on Au NPs were rather constant under the same conditions. A further analysis on spectral changes demonstrated that it was cell response (i.e. metabolic activity or death) to the toxicity of Ag NPs causing spectral variance. However, biochemical responses to the toxicity of Ag were very different in different bacteria, indicating the complex toxic mechanism of Ag NPs. Ag NPs are toxic to a great variety of organisms, including bacteria, fungi, algae, protozoa etc., therefore, this work will be helpful in guiding the future application of SERS technique in various complex biological systems. PMID:25291503

  19. DNA-modulated photo-transformation of AgCl to silver nanoparticles: visiting the formation mechanism.

    PubMed

    Wang, Guoqing; Mitomo, Hideyuki; Matsuo, Yasutaka; Niikura, Kenichi; Maeda, Mizuo; Ijiro, Kuniharu

    2015-08-15

    Solution-phase synthesis and post-synthetic bio-modification have continued to play a dominant role in preparation of nanostructured biomaterials. Heterogeneous nucleation and growth that occur much more often in nature, however, remain rarely explored in nano-biomaterials research. We have newly developed a DNA-modulated photoconversion approach to uniform silver nanoparticles that afford DNA-directed recognition and multi-mode imaging. The present study was aimed at understanding the rapid heterogeneous nucleation and growth of AgNPs at the solid-liquid interface with the aid of DNA. Dynamic changes in absorbance, size and morphology of silver nanostructures were monitored and analyzed to clarify the growth kinetics, which indicated a synthetic route involving synchronous growth of silver nanostructures and the fragmentation and consumption of AgCl. Various stabilizers, including polymer and amino acids, were assessed and compared with respect to the efficacy in photoconversion of AgCl. DNA was found to offer the best monodispersity and the smallest diameter for the resultant AgNPs, due to its strong interactions to silver species as well as excellent charge dispersion ability. By controlling the physicochemical property of DNA through choice of pH and ionic strength, we have demonstrated tunable structure and composition of the nanoparticles.

  20. Using femtosecond lasers to modify sizes of gold nanoparticles

    NASA Astrophysics Data System (ADS)

    da Silva Cordeiro, Thiago; Almeida de Matos, Ricardo; Silva, Flávia Rodrigues de Oliveira; Vieira, Nilson D.; Courrol, Lilia C.; Samad, Ricardo E.

    2016-04-01

    Metallic nanoparticles are important on several scientific, medical and industrial areas. The control of nanoparticles characteristics has fundamental importance to increase the efficiency on the processes and applications in which they are employed. The metallic nanoparticles present specific surface plasmon resonances (SPR). These resonances are related with the collective oscillations of the electrons presents on the metallic nanoparticle. The SPR is determined by the potential defined by the nanoparticle size and geometry. There are several methods of producing gold nanoparticles, including the use of toxic chemical polymers. We already reported the use of natural polymers, as for example, the agar-agar, to produce metallic nanoparticles under xenon lamp irradiation. This technique is characterized as a "green" synthesis because the natural polymers are inoffensive to the environment. We report a technique to produce metallic nanoparticles and change its geometrical and dimensional characteristics using a femtosecond laser. The 1 ml initial solution was irradiate using a laser beam with 380 mW, 1 kHz and 40 nm of bandwidth centered at 800 nm. The setup uses an Acousto-optic modulator, Dazzler, to change the pulses spectral profiles by introduction of several orders of phase, resulting in different temporal energy distributions. The use of Dazzler has the objective of change the gold nanoparticles average size by the changing of temporal energy distributions of the laser pulses incident in the sample. After the laser irradiation, the gold nanoparticles average diameter were less than 15 nm.

  1. Ag Nanoparticles (Ag NM300K) in the Terrestrial Environment: Effects at Population and Cellular Level in Folsomia candida (Collembola).

    PubMed

    Mendes, Luís André; Maria, Vera L; Scott-Fordsmand, Janeck J; Amorim, Mónica J B

    2015-10-01

    The effects of nanomaterials have been primarily assessed based on standard ecotoxicity guidelines. However, by adapting alternative measures the information gained could be enhanced considerably, e.g., studies should focus on more mechanistic approaches. Here, the environmental risk posed by the presence of silver nanoparticles (Ag NM300K) in soil was investigated, anchoring population and cellular level effects, i.e., survival, reproduction (28 days) and oxidative stress markers (0, 2, 4, 6, 10 days). The standard species Folsomia candida was used. Measured markers included catalase (CAT), glutathione reductase (GR), glutathione S-transferase (GST), total glutathione (TG), metallothionein (MT) and lipid peroxidation (LPO). Results showed that AgNO₃ was more toxic than AgNPs at the population level: reproduction EC₂₀ and EC₅₀ was ca. 2 and 4 times lower, respectively. At the cellular level Correspondence Analysis showed a clear separation between AgNO₃ and AgNP throughout time. Results showed differences in the mechanisms, indicating a combined effect of released Ag⁺ (MT and GST) and of AgNPs (CAT, GR, TG, LPO). Hence, clear advantages from mechanistic approaches are shown, but also that time is of importance when measuring such responses. PMID:26473892

  2. The influence of Ag nanoparticles on random laser from dye-doped nematic liquid crystals

    NASA Astrophysics Data System (ADS)

    Ye, Lihua; Liu, Bo; Li, Fangjie; Feng, Yangyang; Cui, Yiping; Lu, Yanqing

    2016-10-01

    The threshold energy and electric field response characteristic of random laser have been investigated in dye-doped nematic liquid crystal (DDNLC) with the addition of different concentrations of Ag nanoparticles (NPs). Due to the localized surface plasmon resonance (LSPR) induced by Ag NPs, random laser from DDNLC with Ag NP doping had a lower threshold energy. From another point of view, nematic liquid crystals (LCs) in a DDNLC cell with the addition of Ag NPs could be more easily influenced by the electric field, which allowed the random laser to be controlled at a lower applied voltage. The turn-off time and turn-on time of random laser also decreased in the DDNLC cells with increasing the concentration of Ag NPs. This is due to the enhancement of the electro-optical characteristic of LC and the restoring force imparted by the locally ordered LCs induced by the Ag NPs, respectively.

  3. Ag2Mo3O10 Nanorods Decorated with Ag2S Nanoparticles: Visible-Light Photocatalytic Activity, Photostability, and Charge Transfer.

    PubMed

    Chen, Xianjie; Liu, Fenglin; Yan, Xiaodong; Yang, Yang; Chen, Qian; Wan, Juan; Tian, Lihong; Xia, Qinghua; Chen, Xiaobo

    2015-12-14

    Ag2Mo3O10 nanorods decorated with Ag2 S nanoparticles have been synthesized by an anion-exchange route. With thiourea as the sulfur source, sulfur ions replace [Mo3O10](2-) units of active sites on the surface of Ag2Mo3O10 nanorods, forming Ag2Mo3O10 nanorods decorated with Ag2S nanoparticles. This induces enhanced absorption in the visible-light region. Ag2 S nanoparticles decorate the surface of Ag2Mo3O10 nanorods uniformly with a suitable amount of thiourea. The Ag2S/Ag2Mo3O10 nanoheterostructure enhances the photocatalytic activity on the degradations of Rhodamine B and glyphosate under visible light. This enhancement is attributed to the improved absorption of visible light and effective separation of charge carriers in the nanoheterostructure. Meanwhile, the Ag2S/Ag2Mo3O10 nanoheterostructure displays good photocatalytic stability based on cyclic photocatalytic experiments.

  4. Formation of Ag Nanoparticles on β-Ag2WO4 through Electron Beam Irradiation: A Synergetic Computational and Experimental Study.

    PubMed

    Roca, Roman A; Gouveia, Amanda F; Lemos, Pablo S; Gracia, Lourdes; Andrés, Juan; Longo, Elson

    2016-09-01

    In the present work, a combined theoretical and experimental study was performed on the structure, optical properties, and growth of Ag nanoparticles in metastable β-Ag2WO4 microcrystals. This material was synthesized using the precipitation method without the presence of surfactants. The structural behavior was analyzed using X-ray diffraction and Raman and infrared spectroscopy. Field-emission scanning electron microscopy revealed the presence of irregular spherical-like Ag nanoparticles on the β-Ag2WO4 microcrystals, which were induced by electron beam irradiation under high vacuum conditions. A detailed analysis of the optimized β-Ag2WO4 geometry and theoretical results enabled interpretation of both the Raman and infrared spectra and provided deeper insight into rationalizing the observed morphology. In addition, first-principles calculations, within the quantum theory of atoms in molecules framework, provided an in-depth understanding of the nucleation and early evolution of Ag nanoparticles. The Ag nucleation and formation is the result of structural and electronic changes of the [AgO6] and [AgO5] clusters as a constituent building block of β-Ag2WO4, which is consistent with Ag metallic formation. PMID:27533109

  5. Synthesis of Ag/CNT hybrid nanoparticles and fabrication of their nylon-6 polymer nanocomposite fibers for antimicrobial applications.

    PubMed

    Rangari, Vijaya K; Mohammad, Ghouse M; Jeelani, Shaik; Hundley, Angel; Vig, Komal; Singh, Shree Ram; Pillai, Shreekumar

    2010-03-01

    Ag-coated CNTs hybrid nanoparticles (Ag/CNTs) were prepared by ultrasonic irradiation of dimethylformamide (DMF) and silver (I) acetate precursors in the presence of CNTs. The morphology of Ag/CNTs was characterized using x-ray diffraction and transmission electron microscopy (TEM) techniques. The Nylon-6 powder and 1 wt% Ag/CNTs mixture was dispersed uniformly using a noncontact spinning technique. The dried mixture was melted in a single screw extrusion machine and then extruded through an orifice. Extruded filaments were later stretched and stabilized by sequentially passing them through a set of tension adjusters and a secondary heater. The Nylon-6/Ag/CNT hybrid polymer nanocomposite (HPNC) fibers, which were of approximately 80 microm size, were tested for their tensile properties. The failure stress and modulus of the extruded HPNC fibers (doped with 1% Ag/CNTs) was about 72.19 % and 342.62% higher than the neat extruded Nylon-6 fiber, respectively. DSC results indicated an increase in the thermal stability and crystallization for HPNC fibers. The antibacterial activity of the Ag-coated CNTs, commercial Ag, neat Nylon-6 and plain CNTs were evaluated. Ag-coated CNTs at 25 microg demonstrated good antimicrobial activity against four common bacterial pathogens as tested by the Kirby-Bauer assay. The mean diameters of the zones of inhibition were 27.9 +/- 6.72 mm, 19.4 +/- 3.64 mm, 21.9 +/- 4.33 mm, and 24.1 +/- 4.14 mm, respectively, for Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli and Salmonella enterica serovar Typhimurium. By comparison, those obtained using the broad spectrum antibiotic amoxicillin-clavulanic acid were 37.7 +/- 2.13 mm, 28.6 +/- 4.27 mm, 22.6 +/- 1.27 mm, and 27.0 +/- 1.41 mm, respectively, for the same strains. The zones of inhibition obtained for Nylon-6 Ag-coated CNT powder at 25 microg were also high, ranging from 15.2 to 25.3 mm in contrast to commercial silver or neat Nylon-6, which did not inhibit the bacterial

  6. Synthesis of Ag/CNT hybrid nanoparticles and fabrication of their Nylon-6 polymer nanocomposite fibers for antimicrobial applications

    NASA Astrophysics Data System (ADS)

    Rangari, Vijaya K.; Mohammad, Ghouse M.; Jeelani, Shaik; Hundley, Angel; Vig, Komal; Ram Singh, Shree; Pillai, Shreekumar

    2010-03-01

    Ag-coated CNTs hybrid nanoparticles (Ag/CNTs) were prepared by ultrasonic irradiation of dimethylformamide (DMF) and silver (I) acetate precursors in the presence of CNTs. The morphology of Ag/CNTs was characterized using x-ray diffraction and transmission electron microscopy (TEM) techniques. The Nylon-6 powder and 1 wt% Ag/CNTs mixture was dispersed uniformly using a noncontact spinning technique. The dried mixture was melted in a single screw extrusion machine and then extruded through an orifice. Extruded filaments were later stretched and stabilized by sequentially passing them through a set of tension adjusters and a secondary heater. The Nylon-6/Ag/CNT hybrid polymer nanocomposite (HPNC) fibers, which were of ~ 80 µm size, were tested for their tensile properties. The failure stress and modulus of the extruded HPNC fibers (doped with 1% Ag/CNTs) was about 72.19 % and 342.62% higher than the neat extruded Nylon-6 fiber, respectively. DSC results indicated an increase in the thermal stability and crystallization for HPNC fibers. The antibacterial activity of the Ag-coated CNTs, commercial Ag, neat Nylon-6 and plain CNTs were evaluated. Ag-coated CNTs at 25 µg demonstrated good antimicrobial activity against four common bacterial pathogens as tested by the Kirby-Bauer assay. The mean diameters of the zones of inhibition were 27.9 ± 6.72 mm, 19.4 ± 3.64 mm, 21.9 ± 4.33 mm, and 24.1 ± 4.14 mm, respectively, for Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli and Salmonella enterica serovar Typhimurium. By comparison, those obtained using the broad spectrum antibiotic amoxicillin-clavulanic acid were 37.7 ± 2.13 mm, 28.6 ± 4.27 mm, 22.6 ± 1.27 mm, and 27.0 ± 1.41 mm, respectively, for the same strains. The zones of inhibition obtained for Nylon-6 Ag-coated CNT powder at 25 µg were also high, ranging from 15.2 to 25.3 mm in contrast to commercial silver or neat Nylon-6, which did not inhibit the bacterial strains tested. Further, the

  7. Speciation and Lability of Ag-, AgCl- and Ag2S-Nanoparticles in Soil Determined by X-ray Absorption Spectroscopy and Diffusive Gradients in Thin Films

    EPA Science Inventory

    Long-term speciation and lability of silver (Ag-), silver chloride (AgCl-) and silver sulfide nanoparticles (Ag2S-NPs) in soil were studied by X-ray absorption spectroscopy (XAS), and newly developed "nano" Diffusive Gradients in Thin Films (DGT) devices. These nano-D...

  8. Deposition of Nanostructured Thin Film from Size-Classified Nanoparticles

    NASA Technical Reports Server (NTRS)

    Camata, Renato P.; Cunningham, Nicholas C.; Seol, Kwang Soo; Okada, Yoshiki; Takeuchi, Kazuo

    2003-01-01

    Materials comprising nanometer-sized grains (approximately 1_50 nm) exhibit properties dramatically different from those of their homogeneous and uniform counterparts. These properties vary with size, shape, and composition of nanoscale grains. Thus, nanoparticles may be used as building blocks to engineer tailor-made artificial materials with desired properties, such as non-linear optical absorption, tunable light emission, charge-storage behavior, selective catalytic activity, and countless other characteristics. This bottom-up engineering approach requires exquisite control over nanoparticle size, shape, and composition. We describe the design and characterization of an aerosol system conceived for the deposition of size classified nanoparticles whose performance is consistent with these strict demands. A nanoparticle aerosol is generated by laser ablation and sorted according to size using a differential mobility analyzer. Nanoparticles within a chosen window of sizes (e.g., (8.0 plus or minus 0.6) nm) are deposited electrostatically on a surface forming a film of the desired material. The system allows the assembly and engineering of thin films using size-classified nanoparticles as building blocks.

  9. Sequential laser and ultrasonic wave generation of TiO2@Ag core-shell nanoparticles and their anti-bacterial properties.

    PubMed

    Hamad, Abubaker Hassan; Li, Lin; Liu, Zhu; Zhong, Xiang Li; Wang, Tao

    2016-02-01

    Core-shell nanoparticles have unusual physical, chemical and biological properties. Until now, for the Ag and TiO2 combination, only Ag core and TiO2 shell nanoparticles have been practically demonstrated. In this investigation, novel TiO2@Ag core-shell (TiO2 core and Ag shell) nanoparticles were produced via ultrasonic vibration of Ag-TiO2 compound nanoparticles. A bulk Ti/Ag alloy plate was used to generate colloidal Ag-TiO2 compound nanoparticles via picosecond laser ablation in deionised water. The colloidal nanoparticles were then sonicated in an ultrasonic bath to generate TiO2@Ag core-shell nanoparticles. They were characterised using a UV-VIS spectrometer, transmission electron microscopy (TEM), high-angle annular dark-field-Scanning transmission electron microscopy (HAADF-STEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). The Ag-TiO2 compound and the TiO2@Ag core-shell nanoparticles were examined for their antibacterial activity against Escherichia coli (E. coli) JM109 strain bacteria and compared with those of Ag and TiO2 nanoparticles. The antibacterial activity of the core-shell nanoparticles was slightly better than that of the compound nanoparticles at the same concentration under standard laboratory light conditions and both were better than the TiO2 nanoparticles but not as good as the Ag nanoparticles.

  10. Extracellular Polymeric Substances (EPS) of Freshwater Biofilms Stabilize and Modify CeO2 and Ag Nanoparticles

    PubMed Central

    Kroll, Alexandra; Behra, Renata; Kaegi, Ralf; Sigg, Laura

    2014-01-01

    Streams are potential receiving compartments for engineered nanoparticles (NP). In streams, NP may remain dispersed or settle to the benthic compartment. Both dispersed and settling NP can accumulate in benthic biofilms called periphyton that are essential to stream ecosystems. Periphytic organisms excrete extracellular polymeric substances (EPS) that interact with any material reaching the biofilms. To understand the interaction of NP with periphyton it is therefore crucial to study the interaction of NP with EPS. We investigated the influence of EPS on the physicochemical properties of selected NP (CeO2, Ag) under controlled conditions at pH 6, 7.6, 8.6 and light or dark exposure. We extracted EPS from five different periphyton communities, characterized the extracts, and exposed CeO2 and carbonate-stabilized Ag NP (0.5 and 5 mg/L, both 25 nm primary particle size) and AgNO3 to EPS (10 mg/L) over two weeks. We measured NP size distribution, shape, primary particle size, surface plasmon resonance, and dissolution. All EPS extracts were composed of biopolymers, building blocks of humic substances, low molecular weight (Mr) acids, and small amphiphilic or neutral compounds in varying concentrations. CeO2 NP were stabilized by EPS independent of pH and light/dark while dissolution increased over time in the dark at pH 6. EPS induced a size increase in Ag NP in the light with decreasing pH and the formation of metallic Ag NP from AgNO3 at the same conditions via EPS-enhanced photoreduction. NP transformation and formation were slower in the extract with the lowest biopolymer and low Mr acid concentrations. Periphytic EPS in combination with naturally varying pH and light/dark conditions influence the properties of the Ag and CeO2 NP tested and thus the exposure conditions within biofilms. Our results indicate that periphytic organisms may be exposed to a constantly changing mixture of engineered and naturally formed Ag NP and Ag+. PMID:25333364

  11. Hyperspectral reflected light microscopy of plasmonic Au/Ag alloy nanoparticles incubated as multiplex chromatic biomarkers with cancer cells.

    PubMed

    Patskovsky, Sergiy; Bergeron, Eric; Rioux, David; Simard, Mikaël; Meunier, Michel

    2014-10-21

    A hyperspectral microscopy system based on a reflected light method for plasmonic nanoparticle (NP) imaging was designed and compared with a conventional darkfield method for spatial localization and spectroscopic identification of single Au, Ag and Au/Ag alloy NPs incubated with fixed human cancer cell preparations. A new synthesis protocol based on co-reduction of Au and Ag salts combined with the seeded growth technique was used for the fabrication of monodispersed alloy NPs with sizes ranging from 30 to 100 nm in diameter. We validated theoretically and experimentally the performance of 60 nm Au, Ag and Au/Ag (50 : 50) NPs as multiplexed biological chromatic markers for biomedical diagnostics and optical biosensing. The advantages of the proposed reflected light microscopy method are presented for NP imaging in a complex and highly diffusing medium such as a cellular environment. The obtained information is essential for the development of a high throughput, selective and efficient strategy for cancer detection and treatment. PMID:25133743

  12. Photocatalytic performance of Ag doped SnO2 nanoparticles modified with curcumin

    NASA Astrophysics Data System (ADS)

    Vignesh, K.; Hariharan, R.; Rajarajan, M.; Suganthi, A.

    2013-07-01

    Visible light active Ag doped SnO2 nanoparticles modified with curcumin (Cur-Ag-SnO2) have been prepared by a combined precipitation and chemical impregnation route. The optical properties, phase structures and morphologies of the as-prepared nanoparticles were characterized using UV-visible diffuse reflectance spectra (UV-vis-DRS), X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). The surface area was measured by Brunauer. Emmett. Teller (B.E.T) analysis. Compared to bare SnO2, the surface modified photocatalysts (Ag-SnO2 and Cur-Ag-SnO2) showed a red shift in the visible region. The photocatalytic activity was monitored via the degradation of rose bengal (RB) dye and the results revealed that Cur-Ag-SnO2 shows better photocatalytic activity than that of Ag-SnO2 and SnO2. The superior photocatalytic activity of Cur-Ag-SnO2 could be attributed to the effective electron-hole separation by surface modification. The effect of photocatalyst concentration, initial dye concentration and electron scavenger on the photocatalytic activity was examined in detail. Furthermore, the antifungal activity of the photocatalysts and the reusability of Cur-Ag-SnO2 were tested.

  13. The disinfection performance and mechanisms of Ag/lysozyme nanoparticles supported with montmorillonite clay.

    PubMed

    Jiang, Jing; Zhang, Chang; Zeng, Guang-Ming; Gong, Ji-Lai; Chang, Ying-Na; Song, Biao; Deng, Can-Hui; Liu, Hong-Yu

    2016-11-01

    The fabrication of montmorillonite (Mt) decorated with lysozyme-modified silver nanoparticles (Ag/lyz-Mt) was reported. The lysozyme (lyz) was served as both reducing and capping reagent. Coupling the bactericidal activity of the lyz with AgNPs, along with the high porous structure and large specific surface area of the Mt, prevented aggregation of AgNPs and promoted nanomaterial-bacteria interactions, resulting in a greatly enhanced bactericidal capability against both Gram positive and Gram negative bacteria. This paper systematically elucidated the bactericidal mechanisms of Ag/lyz-Mt. Direct contact between the Ag/lyz-Mt surface and the bacterial cell was essential to the disinfection. Physical disruption of bacterial membrane was considered to be one of the bactericidal mechanisms of Ag/lyz-Mt. Results revealed that Ag(+) was involved in the bactericidal activity of Ag/lyz-Mt via tests conducted using Ag(+) scavengers. A positive ROS (reactive oxygen species) scavenging test indirectly confirmed the involvement of ROS (O2(-), H2O2, and OH) in the bactericidal mechanism. Furthermore, the concentrations of individual ROS were quantified. Results showed that Ag/lyz-Mt nanomaterial could be a promising bactericide for water disinfection.

  14. The disinfection performance and mechanisms of Ag/lysozyme nanoparticles supported with montmorillonite clay.

    PubMed

    Jiang, Jing; Zhang, Chang; Zeng, Guang-Ming; Gong, Ji-Lai; Chang, Ying-Na; Song, Biao; Deng, Can-Hui; Liu, Hong-Yu

    2016-11-01

    The fabrication of montmorillonite (Mt) decorated with lysozyme-modified silver nanoparticles (Ag/lyz-Mt) was reported. The lysozyme (lyz) was served as both reducing and capping reagent. Coupling the bactericidal activity of the lyz with AgNPs, along with the high porous structure and large specific surface area of the Mt, prevented aggregation of AgNPs and promoted nanomaterial-bacteria interactions, resulting in a greatly enhanced bactericidal capability against both Gram positive and Gram negative bacteria. This paper systematically elucidated the bactericidal mechanisms of Ag/lyz-Mt. Direct contact between the Ag/lyz-Mt surface and the bacterial cell was essential to the disinfection. Physical disruption of bacterial membrane was considered to be one of the bactericidal mechanisms of Ag/lyz-Mt. Results revealed that Ag(+) was involved in the bactericidal activity of Ag/lyz-Mt via tests conducted using Ag(+) scavengers. A positive ROS (reactive oxygen species) scavenging test indirectly confirmed the involvement of ROS (O2(-), H2O2, and OH) in the bactericidal mechanism. Furthermore, the concentrations of individual ROS were quantified. Results showed that Ag/lyz-Mt nanomaterial could be a promising bactericide for water disinfection. PMID:27318738

  15. Synthesis of Starch-Stabilized Ag Nanoparticles and Hg2+ Recognition in Aqueous Media

    NASA Astrophysics Data System (ADS)

    Fan, Yingju; Liu, Zhen; Wang, Le; Zhan, Jinhua

    2009-10-01

    The starch-stabilized Ag nanoparticles were successfully synthesized via a reduction approach and characterized with SPR UV/Vis spectroscopy, TEM, and HRTEM. By utilizing the redox reaction between Ag nanoparticles and Hg2+, and the resulted decrease in UV/Vis signal, we develop a colorimetric method for detection of Hg2+ ion. A linear relationship stands between the absorbance intensity of the Ag nanoparticles and the concentration of Hg2+ ion over the range from 10 ppb to 1 ppm at the absorption of 390 nm. The detection limit for Hg2+ ions in homogeneous aqueous solutions is estimated to be ~5 ppb. This system shows excellent selectivity for Hg2+ over other metal ions including Na+, K+, Ba2+, Mg2+, Ca2+, Fe3+, and Cd2+. The results shown herein have potential implications in the development of new colorimetric sensors for easy and selective detection and monitoring of mercuric ions in aqueous solutions.

  16. Particle size dependence of the surface-enhanced Raman scattering properties of densely arranged two-dimensional assemblies of Au(core)-Ag(shell) nanospheres.

    PubMed

    Sugawa, Kosuke; Akiyama, Tsuyoshi; Tanoue, Yoshimasa; Harumoto, Takashi; Yanagida, Sayaka; Yasumori, Atsuo; Tomita, Shohei; Otsuki, Joe

    2015-09-01

    We investigated the dependence of the surface-enhanced Raman scattering (SERS) activity of densely arranged two-dimensional assemblies of spherical Au(core)-Ag(shell) nanoparticles (Au/AgNSs) on the nanoparticle diameter. The size-controlled Au/AgNSs were synthesized using the Au nanosphere seed-mediated growth method without any bulky stabilizers. The diameters of the Au/AgNSs were 38, 53, and 90 nm and the ratio of the total diameter to the Au core diameter was adjusted to ca. 2.0. Extinction spectra of the colloidal solutions of these nanoparticles exhibited the prominent peak of the localized surface plasmon resonance (LSPR) of Ag and therefore the Au/AgNSs exhibited LSPR properties almost the same as Ag nanospheres. It was confirmed from SEM observation that the organic solvent-mediated liquid-liquid interface assembly technique easily generated densely arranged two-dimensional assemblies of the nanospheres. The extinction spectra of all the assemblies exhibited a prominent broad peak ranging from 500 nm to the near-infrared region, which is assigned to the longitudinal LSPR mode of the coupling nanospheres. The extinction intensity increased with increasing nanosphere diameter. The SERS activities of these assemblies were investigated using p-aminothiophenol as a probe molecule. The result revealed that the enhancement factor (EF) of the Raman signal dramatically increased upon increasing the particle diameter. The maximum EF obtained with a laser excitation wavelength of 785 nm was 1.90 × 10(6) for a nanosphere diameter of 90 nm. This renders the two-dimensional assemblies of the plasmonic Au/AgNSs promising for the development of highly sensitive SERS sensor platforms due to their strong electromagnetic effect.

  17. Beet juice utilization: Expeditious green synthesis of nobel metal nanoparticles (Ag, Au, Pt, and Pd) using microwaves

    EPA Science Inventory

    Metal nanoparticles of Ag, Au, Pt, and Pd were prepared in aqueous solutions via a rapid microwave-assisted green method using beet juice, an abundant sugar-rich agricultural produce, served as both a reducing and a capping reagent. The Ag nanoparticles with capping prepared by b...

  18. Measuring the Hydrodynamic Size of Nanoparticles Using Fluctuation Correlation Spectroscopy

    NASA Astrophysics Data System (ADS)

    Dominguez-Medina, Sergio; Chen, Sishan; Blankenburg, Jan; Swanglap, Pattanawit; Landes, Christy F.; Link, Stephan

    2016-05-01

    Fluctuation correlation spectroscopy (FCS) is a well-established analytical technique traditionally used to monitor molecular diffusion in dilute solutions, the dynamics of chemical reactions, and molecular processes inside living cells. In this review, we present the recent use of FCS for measuring the size of colloidal nanoparticles in solution. We review the theoretical basis and experimental implementation of this technique and its advantages and limitations. In particular, we show examples of the use of FCS to measure the size of gold nanoparticles, monitor the rotational dynamics of gold nanorods, and investigate the formation of protein coronas on nanoparticles.

  19. Monodispersed biocompatible Ag2S nanoparticles: Facile extracellular bio-fabrication using the gamma-proteobacterium, S. oneidensis

    SciTech Connect

    Suresh, Anil K; Doktycz, Mitchel John; Wang, Wei; Moon, Ji Won; Gu, Baohua; Meyer III, Harry M; Hensley, Dale K; Retterer, Scott T; Allison, David P; Phelps, Tommy Joe; Pelletier, Dale A

    2011-01-01

    Interest in engineered metal and semiconductor nanocrystallites continues to grow due to their unique size and or shape dependent optoelectronic, physicochemical and biological properties. Therefore identifying novel non-hazardous nanoparticle synthesis routes that address hydrophilicity, size and shape control and production costs have become a priority. In the present illustration we report for the first time the efficient generation of extracellular Ag2S nanoparticles by the metal reducing bacterium, Shewanella oneidensis. The particles are nearly monodispersed with homogeneous shape distributions and are produced under ambient temperatures and pressures at high yield, 85 % theoretical maximum. UV-vis and Fourier transform infrared spectroscopy, dynamic light scattering, X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy measurements confirmed the formation, optical properties, purity, and crystallinity of the as-synthesized particles. Further characterization revealed that the particles consist of spheres in the size range of 1-22 nm, with an average size of 9 3 nm and are capped by a detachable protein/peptide surface coat. Toxicity assessments of these silver sulfide nanoparticles on Gram-negative Escherichia coli and Shewanella oneidensis and Gram-positive Bacillus subtilis bacterial systems as well as eukaryotic; mouse lung epithelial (C 10) and macrophage (RAW-264.7) cells showed that the particles were non-inhibitory or non-cytotoxic to both these systems. Our results provide a facile, eco-friendly and economical route for the fabrication of technologically important semiconducting Ag2S nanoparticles which are dispersible and biocompatible; thus providing excellent potential for their uses in optical imaging and electronic devices, and solar cell applications.

  20. Dual layer hollow fiber PVDF ultra-filtration membranes containing Ag nano-particle loaded zeolite with longer term anti-bacterial capacity in salt water.

    PubMed

    Shi, Huyan; Xue, Lixin; Gao, Ailin; Zhou, Qingbo

    2016-01-01

    Dual layer polyvinylidene fluoride (PVDF), antibacterial, hollow fiber, ultra-filtration composite membranes with antibacterial particles (silver (Ag) nano-particles loaded zeolite (Z-Ag)) in the outer layer were prepared with high water flux and desired pore sizes. The amounts of Ag(+) released from the composite membranes, freshly made and stored in water and salt solution, were measured. The result indicated that dual layer PVDF antibacterial hollow fiber containing Z-Ag (M-1-Ag) still possessed the ability of continuous release of Ag(+) even after exposure to water with high ionic content, showing a longer term resistance to bacterial adhesion and antibacterial activity than membrane doped with Z-Ag(+) (M-1). Results from an anti-adhesion and bacteria killing test with Escherichia coli supported that the antibacterial efficiency of dual hollow fiber PVDF membranes with Z-Ag was much higher than those with Z-Ag(+) after long time storage in water or exposure to phosphate buffered saline (PBS) solution. This novel hollow fiber membrane may find applications in constructing sea water pretreatment devices with long term antifouling capability for the desalination processes.

  1. Dual layer hollow fiber PVDF ultra-filtration membranes containing Ag nano-particle loaded zeolite with longer term anti-bacterial capacity in salt water.

    PubMed

    Shi, Huyan; Xue, Lixin; Gao, Ailin; Zhou, Qingbo

    2016-01-01

    Dual layer polyvinylidene fluoride (PVDF), antibacterial, hollow fiber, ultra-filtration composite membranes with antibacterial particles (silver (Ag) nano-particles loaded zeolite (Z-Ag)) in the outer layer were prepared with high water flux and desired pore sizes. The amounts of Ag(+) released from the composite membranes, freshly made and stored in water and salt solution, were measured. The result indicated that dual layer PVDF antibacterial hollow fiber containing Z-Ag (M-1-Ag) still possessed the ability of continuous release of Ag(+) even after exposure to water with high ionic content, showing a longer term resistance to bacterial adhesion and antibacterial activity than membrane doped with Z-Ag(+) (M-1). Results from an anti-adhesion and bacteria killing test with Escherichia coli supported that the antibacterial efficiency of dual hollow fiber PVDF membranes with Z-Ag was much higher than those with Z-Ag(+) after long time storage in water or exposure to phosphate buffered saline (PBS) solution. This novel hollow fiber membrane may find applications in constructing sea water pretreatment devices with long term antifouling capability for the desalination processes. PMID:27148717

  2. Decorated TiO2 Nanoparticles with La and Ag Elements to Improve Photocatalytic Activity Under Visible Light for the Degradation of MO.

    PubMed

    Wang, Qinghua; Gao, Xuechuan; Zhang, Renfei; Shen, Beibei; Tan, Zhibing; Li, Zhao; Yu, Shiyong

    2016-04-01

    Visible-light photocatalyst of TiO2/La/Ag nanocomposites were successfully synthesized via the conventional sol-gel method and reducing agent of Ag+. The photocatalytic activities were evaluated by methyl orange (MO) degradation. They have remarkable photocatalytic activities compared to TiO2-Anatase, which is thanks to the separation of electron-hole pairs by Ag nanoparticles and lanthanum. The products were characterized by a series of techniques such as X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and Uv-vis. The results show that spherical nanocomposites have been prepared with the size 300 nm and Ag nanoparticles (~10 nm) are dispersed uniformly onto the surface of TiO2/La, which forms TiO2/La/Ag nanocomposites. TiO2/La/Ag nanocomposites have good absorption in the visible region (700 nm > λ > 400 nm). The reasons are as follows: (1) the efficient separation of photogenerated electrons and holes of the photocatalysts on the surface of TiO2/La/Ag nanocomposites and (2) a wide visible-light photoabsorption range (700 nm > λ > 400 nm). Therefore, this study may provide some new idea for the rational design and the facile synthesis of composite catalysts with a green, efficient pathway. PMID:27451670

  3. Effect of Ag nanowire addition into nanoparticle paste on the conductivity of Ag patterns printed by gravure offset method.

    PubMed

    Ok, Ki-Hun; Lee, Chan-Jae; Kwak, Min-Gi; Choi, Duck-Kyun; Kim, Kwang-Seok; Jung, Seung-Boo; Kim, Jong-Woong

    2014-11-01

    This paper focuses on the effect of Ag nanowire addition into a commercial Ag nanopaste and the printability evaluation of the mixed paste by the gravure offset printing methodology. Ag nanowires were synthesized by a modified polyol method, and a small amount of them was added into a commercial metallic paste based on Ag nanoparticles of 50 nm in diameter. Two annealing temperatures were selected for comparison, and electrical conductivity was measured by four point probe method. As a result, the hybrid mixture could be printed by the gravure offset method for patterning fine lines up to 15 μm width with sharp edges and scarce spreading. The addition of the Ag nanowires was significantly efficient for enhancement of electrical conductivity of the printed lines annealed at a low temperature (150 degrees C), while the effect was somewhat diluted in case of high temperature annealing (200 degrees C). The experimental results were discussed with the conduction mechanism in the printed conductive circuits with a schematic description of the electron flows in the printed lines.

  4. In vitro assessment of Ag2O nanoparticles toxicity against Gram-positive and Gram-negative bacteria.

    PubMed

    Negi, Harshita; Rathinavelu Saravanan, Palaniyandi; Agarwal, Tithi; Ghulam Haider Zaidi, Mohd; Goel, Reeta

    2013-01-01

    In view of antibiotic resistance among pathogens, the present study is to address the toxicity of Ag2O nanoparticles against the Gram-positive and Gram-negative bacteria through in vitro assays. The preliminary screening by agar diffusion assay confirms the antibacterial activity of Ag2O nanoparticles against all the test bacteria. Comparative antibacterial activity of Ag2O nanoparticles and respective antibiotics reveals their broad range of activity and lower inhibitory dose against the used bacterial strains. Further, they can inhibit E. coli with an effective dose of 0.036 mg/ml within 1 h of exposure time as determined by luciferin based ATP assay. Moreover, the Ag2O nanoparticles exhibit higher antibacterial efficacy against Gram-negative bacteria than Gram-positive bacteria, as revealed by their MIC & MBC values. Therefore, Ag2O nanoparticles pave the way for a new generation of antibacterial agents against the emerging multidrug resistant pathogens.

  5. Novel method for the preparation of core-shell nanoparticles with movable Ag core and polystyrene loop shell

    SciTech Connect

    Liu Weijun; Zhang Zhicheng . E-mail: lwj3600@ustc.edu; He Weidong; Zheng Cheng; Ge Xuewu; Li, Jian; Liu Huarong; Jiang Hao

    2006-04-15

    Core/shell nanoparticles with movable silver (Ag) core and polystyrene (PSt) shell (Ag at PSt nanoparticle) were successfully synthesized at room temperature and under ambient pressure via two steps: {gamma}-irradiation and interfacial-initiated polymerization. Firstly, mono-dispersed Ag nanoparticles with diameters 20 nm were synthesized in inversed microemulsion by reducing silver nitrate under {gamma}-irradiation. Then, Ag nanoparticles were coated with PSt via interfacial-initiated polymerization with cumene hydroperoxide/ferrous sulfate/disodium ethylenediaminetetraacetate/sodium formaldehyde sulfoxylate (CHPO-Fe {sup 2+}-EDTA-SFS) as the redox initiation pair. The resulted Ag at PSt nanoparticles were identified by transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray powder diffraction (XRD) and X-ray photoelectron spectroscopy (XPS)

  6. Visible-light photocatalytic degradation of methylene blue with laser-induced Ag/ZnO nanoparticles

    NASA Astrophysics Data System (ADS)

    Whang, Thou-Jen; Hsieh, Mu-Tao; Chen, Huang-Han

    2012-01-01

    The preparation of Ag doped ZnO nanoparticles conducted through the method of laser-induction is presented in this work. The Ag/ZnO nanoparticles attained from various weight percentages of added AgNO3 relative to ZnO were applied under visible-light irradiation for evaluating the heterogeneous photocatalytic degradations of methylene blue (MB) solutions. It was shown that the catalytic behavior of Ag/ZnO nanoparticles in the visible-light range is notably improved through the Ag deposition onto ZnO nanoparticles by the method of laser-induction with a maximum effectiveness of 92% degradation. The properties of the nanoparticles were characterized by the employments of UV-vis spectroscopy (UV-vis), X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), and selected-area electron diffraction (SAED).

  7. Speciation and lability of Ag-, AgCl-, and Ag2S-nanoparticles in soil determined by X-ray absorption spectroscopy and diffusive gradients in thin films.

    PubMed

    Sekine, R; Brunetti, G; Donner, E; Khaksar, M; Vasilev, K; Jämting, Å K; Scheckel, K G; Kappen, P; Zhang, H; Lombi, E

    2015-01-20

    Long-term speciation and lability of silver (Ag-), silver chloride (AgCl-), and silver sulfide nanoparticles (Ag2S-NPs) in soil were studied by X-ray absorption spectroscopy (XAS), and newly developed “nano” Diffusive Gradients in Thin Films (DGT) devices. These nano-DGT devices were designed specifically to avoid confounding effects when measuring element lability in the presence of nanoparticles. The aging profile and stabilities of the three nanoparticles and AgNO3 (ionic Ag) in soil were examined at three different soil pH values over a period of up to 7 months. Transformation of ionic Ag, Ag-NP and AgCl-NPs were dependent on pH. AgCl formation and persistence was observed under acidic conditions, whereas sulfur-bound forms of Ag dominated in neutral to alkaline soils. Ag2S-NPs were found to be very stable under all conditions tested and remained sulfur bound after 7 months of incubation. Ag lability was characteristically low in soils containing Ag2S-NPs. Other forms of Ag were linked to higher DGT-determined lability, and this varied as a function of aging and related speciation changes as determined by XAS. These results clearly indicate that Ag2S-NPs, which are the most environmentally relevant form of Ag that enter soils, are chemically stable and have profoundly low Ag lability over extended periods. This may minimize the long-term risks of Ag toxicity in the soil environment. PMID:25436975

  8. Size and shape of rhenium nanoparticles.

    SciTech Connect

    Yang, N.; Mickelson, G. E.; Greenlay, N.; Kelly, S. D.; Vila, F. D.; Kas, J.; Rehr, J. J.; Bare, S. R.; X-Ray Science Division; UOP LLC; EXAFS; Univ. of Washington

    2007-01-01

    In this paper the results from a detailed XAFS characterization of supported rhenium nanoparticles are presented. The Re nanoparticles are formed by the reduction of dispersed supported rhenium oxide in the presence of moist hydrogen. The shape of the wet-reduced Re clusters is determined by comparing the EXAFS spectra of Re-metal to the Re-wet-reduced clusters to 6 {angstrom}. A decrease in the signal from the 4th and 7th Re shells is an indication of sheet-like rather than spherical-like particles.

  9. Size and Shape of Rhenium Nanoparticles

    SciTech Connect

    Yang, N.; Mickelson, G. E.; Greenlay, N.; Bare, Simon R.; Kelly, S. D.; Vila, F. D.; Kas, J.; Rehr, J. J.

    2007-02-02

    In this paper the results from a detailed XAFS characterization of supported rhenium nanoparticles are presented. The Re nanoparticles are formed by the reduction of dispersed supported rhenium oxide in the presence of moist hydrogen. The shape of the wet--reduced Re clusters is determined by comparing the EXAFS spectra of Re-metal to the Re-wet-reduced clusters to 6 A. A decrease in the signal from the 4th and 7th Re shells is an indication of sheet-like rather than spherical-like particles.

  10. Impact of ZnO and Ag Nanoparticles on Bacterial Growth and Viability

    NASA Astrophysics Data System (ADS)

    Olson, M. S.; Digiovanni, K. A.

    2007-12-01

    Hundreds of consumer products containing nanomaterials are currently available in the U.S., including computers, clothing, cosmetics, sports equipment, medical devices and product packaging. Metallic nanoparticles can be embedded in or coated on product surfaces to provide antimicrobial, deodorizing, and stain- resistant properties. Although these products have the potential to provide significant benefit to the user, the impact of these products on the environment remains largely unknown. The purpose of this project is to study the effect of metallic nanoparticles released to the environment on bacterial growth and viability. Inhibition of bacterial growth was tested by adding doses of suspended ZnO and Ag nanoparticles into luria broth prior to inoculation of Escherichia coli cells. ZnO particles (approximately 40 nm) were obtained commercially and Ag particles (12-14 nm) were fabricated by reduction of silver nitrate with sodium borohydride. Toxicity assays were performed to test the viability of E. coli cells exposed to both ZnO and Ag nanoparticles using the LIVE/DEAD BacLight bacterial viability kit (Invitrogen). Live cells stain green whereas cells with compromised membranes that are considered dead or dying stain red. Cells were first grown, stained, and exposed to varying doses of metallic nanoparticles, and then bacterial viability was measured hourly using fluorescence microscopy. Results indicate that both ZnO and Ag nanoparticles inhibit the growth of E. coli in liquid media. Preliminary results from toxicity assays confirm the toxic effect of ZnO and Ag nanoparticles on active cell cultures. Calculated death rates resulting from analyses of toxicity studies will be presented.

  11. Surface modification of oleylamine-capped Ag-Cu nanoparticles to fabricate low-temperature-sinterable Ag-Cu nanoink.

    PubMed

    Kim, Na Rae; Lee, Yung Jong; Lee, Changsoo; Koo, Jahyun; Lee, Hyuck Mo

    2016-08-26

    By treating oleylamine (OA)-capped Ag-Cu nanoparticles with tetramethylammonium hydroxide (TMAH), we obtained metal nanoparticles that are suspended in polar solvents and sinterable at low temperatures. The simple process with ultra sonication enables synthesis of monodispersed and high purity nanoparticles in an organic base, where the resulting nanoparticles are dispersible in polar solvents such as ethanol and isopropyl alcohol. To investigate the surface characteristics, we conducted Fourier-transform infrared and zeta-potential analyses. After thermal sintering at 200 °C, which is approximately 150 °C lower than the thermal decomposition temperature of OA, an electrically conductive thin film was obtained. Electrical resistivity measurements of the TMAH-treated ink demonstrate that surface modified nanoparticles have a low resistivity of 13.7 × 10(-6) Ω cm. These results confirm the prospects of using low-temperature sinterable nanoparticles as the electrode layer for flexible printed electronics without damaging other stacked polymer layers. PMID:27454465

  12. Silver Nanoparticles Incite Size and Dose-Dependent Developmental Phenotypes and Nanotoxicity in Zebrafish Embryos

    PubMed Central

    Browning, Lauren M.; Lee, Kerry J.; Nallathamby, Prakash D.; Xu, Xiao-Hong Nancy

    2013-01-01

    Nanomaterials possess distinctive physicochemical properties and promise a wide range of applications, from advanced technology to leading-edge medicine. However, their effects on living organisms remain largely unknown. Here we report that the purified silver nanoparticles (Ag NPs, 97 ± 13 nm) incite specific developmental stage embryonic phenotypes and nanotoxicity in a dose-dependent manner, upon acute exposure of given-stage embryos to the NPs (0–24 pM) for only 2 h. The critical concentrations of the NPs that cause 50% of embryos develop normally for cleavage, early-gastrula, early-segmentation, late-segmentation, and hatching stage zebrafish embryos are 3.5, 4, 6, 6, and 8 pM, respectively, showing that the earlier developmental stage embryos are much more sensitive to the effects of the NPs than the later stage. Interestingly, distinctive phenotypes (head abnormality and no eyes) are observed only in cleavage and early-gastrula stage embryos treated with the NPs, showing the stage-specific effects of the NPs. By comparing with our study of the smaller Ag NPs (13.1 ± 2.5 nm), we found that the embryonic phenotypes strikingly depend upon the sizes of Ag NPs and embryonic developmental stages. These notable findings suggest that the Ag NPs are unlike any conventional chemicals or ions. They can potentially enable target specific study and therapy for early embryonic development in size, stage, dose, and exposure-duration dependent manners. PMID:24024906

  13. Localized surface plasmon resonance-based hybrid Au-Ag nanoparticles for detection of Staphylococcus aureus enterotoxin B

    NASA Astrophysics Data System (ADS)

    Zhu, Shaoli; Du, ChunLei; Fu, Yongqi

    2009-09-01

    A triangular hybrid Au-Ag nanoparticles array was proposed for the purpose of biosensing in this paper. Constructing the hybrid nanoparticles, an Au thin film is capped on the Ag nanoparticles which are attached on glass substrate. The hybrid nanoparticles array was designed by means of finite-difference and time-domain (FDTD) algorithm-based computational numerical calculation and optimization. Sensitivity of refractive index of the hybrid nanoparticles array was obtained by the computational calculation and experimental detection. Moreover, the hybrid nanoparticles array can prevent oxidation of the pure Ag nanoparticles from atmosphere environment because the Au protective layer was deposited on top of the Ag nanoparticles so as to isolate the Ag particles from the atmosphere. We presented a novel surface covalent link method between the localized surface plasmon resonance (LSPR) effect-based biosensors with hybrid nanoparticles array and the detected target molecules. The generated surface plasmon wave from the array carries the biological interaction message into the corresponding spectra. Staphylococcus aureus enterotoxin B (SEB), a small protein toxin was directly detected at nanogramme per milliliter level using the triangular hybrid Au-Ag nanoparticles. Hence one more option for the SEB detection is provided by this way.

  14. Preparing of Highly Conductive Patterns on Flexible Substrates by Screen Printing of Silver Nanoparticles with Different Size Distribution.

    PubMed

    Ding, Jin; Liu, Jun; Tian, Qingyong; Wu, Zhaohui; Yao, Weijing; Dai, Zhigao; Liu, Li; Wu, Wei

    2016-12-01

    A facile one-step polyol method is employed to synthesize the Ag nanoparticles (NPs) in large scale. The Ag NPs with different average diameter (from 52 to 120 nm) and particle size distribution are prepared by changing the mass ratio of AgNO3 and PVP. Furthermore, the as-obtained Ag NPs are prepared as conductive inks, which could be screen printed on various flexible substrates and formed as conductive patterns after sintering treatment. During the reaction process, PVP is used as the capping reagent for preventing the agglomeration of Ag NPs, and the influence of the mass ratio of AgNO3 and PVP to the size distribution of Ag NPs is investigated. The results of electronic properties reveal that the conductivity of printed patterns is highly dependent on the size distribution of as-obtained Ag NPs. Among all the samples, the optimal conductivity is obtained when the mass ratio of AgNO3 and PVP is 1:0.4. Subsequently, the sintering time and temperature are further investigated for obtaining the best conductivity; the optimal electrical resistivity value of 3.83 μΩ · cm is achieved at 160 °C for 75 min, which is close to the resistivity value of the bulk silver (1.58 μΩ · cm). Significantly, there are many potential advantages in printed electronics applications because of the as-synthesized Ag NPs with a low sintering temperature and low electrical resistivity. PMID:27644238

  15. Biogenic synthesis of Au and Ag nanoparticles by Indian propolis and its constituents.

    PubMed

    Roy, Nayan; Mondal, Samiran; Laskar, Rajibul A; Basu, Saswati; Mandal, Debabrata; Begum, Naznin Ara

    2010-03-01

    In an attempt to find natural, environmentally benign, green-chemical agents for the synthesis of metal nanoparticles, we have demonstrated for the first time the excellent efficiency of ethanol and water extracts of a natural, non-toxic material, Indian propolis and two of its chemical constituents, pinocembrin and galangin in the rapid synthesis of stable Ag and Au nanoparticles having wide spectrum of fascinating morphologies. Both of these two extracts were found to be extremely efficient in the synthesis of Ag and Au nanoparticles under alkaline condition. For a given metal ion precursor, the kinetics of particle synthesis were remarkably similar in all the cases, as it is evident from the absorption spectra monitored over time. Moreover they exhibited similar redox behavior under alkaline condition (pH approximately 10.62). The efficiency of the ethanol and water extracts of Indian propolis towards Ag and Au nanoparticles synthesis was compared with that of naturally occurring hydroxyflavonoids, pinocembrin and galangin isolated from Indian propolis; which are equally efficient in the rapid synthesis of Ag and Au nanoparticles and stabilization of the resultant particles.

  16. Preparation of graphene-Ag nanoparticles hybrids and their SERS activities

    NASA Astrophysics Data System (ADS)

    Wang, Xinyu; Wang, Ning; Gong, Tiancheng; Zhu, Yong; Zhang, Jie

    2016-11-01

    Surface-enhanced Raman scattering (SERS) substrates based on graphene and Ag nanoparticles hybrid structures with low cost, high uniformity were prepared by a standard process of immobilization of silver nanoparticles with 3-aminopropyltrimethoxysilane (APTMS). Thermal annealing was used for removing residual APTMS and adjusting the morphology of silver nanoparticles, and the effectiveness of this method was verified experimentally. The influence of annealing temperature, dipping duration, and APTMS volume on the distribution of Ag nanoparticles and Raman enhancement was investigated experimentally and analyzed in detail. Our samples were prepared under the preparation conditions of 10% ν/ν APTMS, dipping time of 48 h, annealing temperature of 450 °C, duration of 30 min, and Ar flow rate of 40 sccm. SERS activities with enhancement of 107 and relative standard deviation of <20% were observed using rhodamine 6G (R6G) as probe molecule with a concentration of 10-6 M and 10-7 M.

  17. Green synthesis, characterization of Au-Ag core-shell nanoparticles using gripe water and their applications in nonlinear optics and surface enhanced Raman studies

    NASA Astrophysics Data System (ADS)

    Kirubha, E.; Palanisamy, P. K.

    2014-12-01

    In recent years there has been excessive progress in the ‘green’ chemistry approach for the synthesis of gold and silver nanoparticles. Bimetallic nanoparticles have gained special significance due to their unique tunable optical properties. Herein we report a facile one-pot, eco-friendly synthesis of Au-Ag bimetallic core-shell nanoparticles using gripe water as reducing as well as stabilizing agent. The as-synthesized Au-Ag nanoparticles are characterized using UV-Vis spectroscopy to determine the surface plasmon resonance, and using transmission electron microscopy to study the morphology and the particle size. The optical nonlinearity of the bimetallic nanoparticles investigated by z-scan technique using femtosecond Ti:sapphire is in the order of 109. The nonlinear optical parameters such as the nonlinear refractive index n2, nonlinear absorption coefficient β and the third order nonlinear susceptibility χ3 are measured for various wavelengths from 700 nm to 950 nm. The Au-Ag nanoparticles are also used in surface enhanced Raman spectroscopic studies to enhance the Raman signals of rhodamine 6G.

  18. Effects of size restriction on donor-acceptor recombination in AgBr

    NASA Astrophysics Data System (ADS)

    Rodney, Paul J.; Marchetti, Alfred P.; Fauchet, Philippe M.

    2000-08-01

    The behavior of donor-acceptor (DA) recombination luminescence in quantum confined AgBr has been investigated. The DA luminescence decay, after pulsed excitation, became longer lived as the nanocluster size decreased. This result differs from theoretical expectations and from observations with AgI nanoclusters. The DA lifetime increase with decreasing size is due to an increase in yield and lifetime of ``free'' excitons that slowly dissociate into ``close'' donor-acceptor pairs, giving rise to an ``exciton dribbling'' effect.

  19. The enhanced SERS effect of Ag/ZnO nanoparticles through surface hydrophobic modification

    NASA Astrophysics Data System (ADS)

    Li, Zhenjiang; Zhu, Kaixing; Zhao, Qian; Meng, Alan

    2016-07-01

    Ag/ZnO nanocomposites modified by a mixture of stearic acid (SA) and polyvinylpyrrolidone (PVP) were obtained using a heating reflux method. Fourier transform infrared spectroscopy (FT-IR) suggests that organic SA/PVP was bonded onto the surface of Ag/ZnO nanocrystals, converting the wettability property of the nanostructures from hydrophilic to hydrophobic. The modified Ag/ZnO nanostructures were confirmed as effective Raman substrates, with a 3-fold signal enhancement compared to the ordinary hydrophilic Ag/ZnO substrate for detecting Rh B molecules due to the hydrophobic condensation effect. It is expected that the modified Ag/ZnO nanoparticles have potential for SERS-based rapid detection of molecules.

  20. Ag nanowire percolating network embedded in indium tin oxide nanoparticles for printable transparent conducting electrodes

    SciTech Connect

    Jeong, Jin-A; Kim, Han-Ki

    2014-02-17

    Solution-based printable transparent conducting electrodes consisting of Ag nanowire (NW) and indium tin oxide (ITO) nanoparticles (NPs) were fabricated by simple brush painting at room temperature under atmospheric ambient conditions. Effectively embedding the Ag NW percolating network into the ITO NPs provided a conduction path, led to a metallic conduction behavior of the ITO NPs/Ag NW/ITO NPs multilayer and supplied electrons into the ITO NPs. The optimized ITO NPs/Ag NW/ITO NPs multilayer showed a sheet resistance of 16.57 Ω/sq and an optical transparency of 79.50% without post annealing. Based on high resolution transmission electron microscope analysis, we investigated the microstructure and interface structure of the ITO NPs/Ag NW/ITO NPs multilayer electrodes and suggested a possible mechanism to explain the low resistivity of the multilayers.

  1. Low-temperature ferromagnetic properties in Co-doped Ag{sub 2}Se nanoparticles

    SciTech Connect

    Yang, Fengxia E-mail: xia9020@hust.edu.cn; Yu, Gen; Han, Chong; Liu, Tingting; Zhang, Duanming; Xia, Zhengcai E-mail: xia9020@hust.edu.cn

    2014-01-06

    β-Ag{sub 2}Se is a topologically nontrivial insulator. The magnetic properties of Co-doped Ag{sub 2}Se nanoparticles with Co concentrations up to 40% were investigated. The cusp of zero-field-cooling magnetization curves and the low-temperature hysteresis loops were observed. With increasing concentration of Co{sup 2+} ions mainly substituting Ag{sub I} sites in the Ag{sub 2}Se structure, the resistivity, Curie temperature T{sub c}, and magnetization increased. At 10 T, a sharp drop of resistance near T{sub c} was detected due to Co dopants. The ferromagnetic behavior in Co-doped Ag{sub 2}Se might result from the intra-layer ferromagnetic coupling and surface spin. This magnetic semiconductor is a promising candidate in electronics and spintronics.

  2. Influence of particle size on persistence and clearance of aerosolized silver nanoparticles in the rat lung.

    PubMed

    Anderson, Donald S; Patchin, Esther S; Silva, Rona M; Uyeminami, Dale L; Sharmah, Arjun; Guo, Ting; Das, Gautom K; Brown, Jared M; Shannahan, Jonathan; Gordon, Terry; Chen, Lung Chi; Pinkerton, Kent E; Van Winkle, Laura S

    2015-04-01

    The growing use of silver nanoparticles (AgNPs) in consumer products raises concerns about potential health effects. This study investigated the persistence and clearance of 2 different size AgNPs (20 and 110 nm) delivered to rats by single nose-only aerosol exposures (6 h) of 7.2 and 5.4 mg/m(3), respectively. Rat lung tissue was assessed for silver accumulations using inductively-coupled plasma mass spectrometry (ICP-MS), autometallography, and enhanced dark field microscopy. Involvement of tissue macrophages was assessed by scoring of silver staining in bronchoalveolar lavage fluid (BALF). Silver was abundant in most macrophages at 1 day post-exposure. The group exposed to 20 nm AgNP had the greatest number of silver positive BALF macrophages at 56 days post-exposure. While there was a significant decrease in the amount of silver in lung tissue at 56 days post-exposure compared with 1 day following exposure, at least 33% of the initial delivered dose was still present for both AgNPs. Regardless of particle size, silver was predominantly localized within the terminal bronchial/alveolar duct junction region of the lung associated with extracellular matrix and within epithelial cells. Inhalation of both 20 and 110 nm AgNPs resulted in a persistence of silver in the lung at 56 days post-exposure and local deposition as well as accumulation of silver at the terminal bronchiole alveolar duct junction. Further the smaller particles, 20 nm AgNP, produced a greater silver burden in BALF macrophages as well as greater persistence of silver positive macrophages at later timepoints (21 and 56 days). PMID:25577195

  3. Influence of Particle Size on Persistence and Clearance of Aerosolized Silver Nanoparticles in the Rat Lung

    PubMed Central

    Anderson, Donald S.; Patchin, Esther S.; Silva, Rona M.; Uyeminami, Dale L.; Sharmah, Arjun; Guo, Ting; Das, Gautom K.; Brown, Jared M.; Shannahan, Jonathan; Gordon, Terry; Chen, Lung Chi; Pinkerton, Kent E.; Van Winkle, Laura S.

    2015-01-01

    The growing use of silver nanoparticles (AgNPs) in consumer products raises concerns about potential health effects. This study investigated the persistence and clearance of 2 different size AgNPs (20 and 110 nm) delivered to rats by single nose-only aerosol exposures (6 h) of 7.2 and 5.4 mg/m3, respectively. Rat lung tissue was assessed for silver accumulations using inductively-coupled plasma mass spectrometry (ICP-MS), autometallography, and enhanced dark field microscopy. Involvement of tissue macrophages was assessed by scoring of silver staining in bronchoalveolar lavage fluid (BALF). Silver was abundant in most macrophages at 1 day post-exposure. The group exposed to 20 nm AgNP had the greatest number of silver positive BALF macrophages at 56 days post-exposure. While there was a significant decrease in the amount of silver in lung tissue at 56 days post-exposure compared with 1 day following exposure, at least 33% of the initial delivered dose was still present for both AgNPs. Regardless of particle size, silver was predominantly localized within the terminal bronchial/alveolar duct junction region of the lung associated with extracellular matrix and within epithelial cells. Inhalation of both 20 and 110 nm AgNPs resulted in a persistence of silver in the lung at 56 days post-exposure and local deposition as well as accumulation of silver at the terminal bronchiole alveolar duct junction. Further the smaller particles, 20 nm AgNP, produced a greater silver burden in BALF macrophages as well as greater persistence of silver positive macrophages at later timepoints (21 and 56 days). PMID:25577195

  4. Zeta-potential and particle size studies of silver sulphide nanoparticles

    NASA Astrophysics Data System (ADS)

    Sharma, Vikash; Tarachand, Ganesan, V.; Okram, Gunadhor S.

    2016-05-01

    Silver sulfide (Ag2S) nanoparticles (NPs) were prepared successfully for the first time using diethylene glycol (DEG) as a surfactant. X-ray diffraction (XRD) data revealed single phase nature of the compound and energy-dispersive X-ray (EDX) confirmed its nominal composition. Their sizes were 43 nm from XRD, 50 nm from atomic force microscopy (AFM) and 19 nm & 213 nm from dynamic light scattering (DLS); their differences have been discussed. Autotitration study of zeta potential of these NPs in deionized water by DLS at different pH values confirmed an isoelectric point at pH = 5.14 and their very unstable nature in deionized water.

  5. Plasmonic effect of Ag nanoparticles in a SiON antireflective coating: engineering rules and physical barrier

    NASA Astrophysics Data System (ADS)

    Lecler, S.; Bastide, S.; Tan, J.; Qu, M.; Slaoui, A.; Fix, T.

    2016-10-01

    Surface plasmon polaritons have been proposed in the architectures of several solar cells as a way to enhance light collection and thus to increase their efficiency. Here, Ag nanoparticles (NPs) are embedded in a SiON antireflective layer using an electroless technique. The plasmonic effects are modeled and observed experimentally for NPs 5 to 200 nm in size. The systematic comparison of scattering and extinction efficiencies computed as a function of the NPs and surrounding medium properties allows establishing engineering rules, validated by the experimental measurements. The fact that Ag NPs larger than 30 nm mainly contribute to light scattering and therefore to optical path enlargement (green-red light), whereas those smaller than 15 nm absorb light by light trapping (blue-green), is demonstrated and physically explained. A physical barrier making it impossible to shift the dominant resonance beyond 650 nm is pointed out.

  6. Tuning the SERS Response with Ag-Au Nanoparticle-Embedded Polymer Thin Film Substrates.

    PubMed

    Rao, V Kesava; Radhakrishnan, T P

    2015-06-17

    Development of facile routes to the fabrication of thin film substrates with tunable surface enhanced Raman scattering (SERS) efficiency and identification of the optimal conditions for maximizing the enhancement factor (EF) are significant in terms of both fundamental and application aspects of SERS. In the present work, polymer thin films with embedded bimetallic nanoparticles of Ag-Au are fabricated by a simple two-stage protocol. Ag nanoparticles are formed in the first stage, by the in situ reduction of silver nitrate by the poly(vinyl alcohol) (PVA) film through mild thermal annealing, without any additional reducing agent. In the second stage, aqueous solutions of chloroauric acid spread on the Ag-PVA thin film under ambient conditions, lead to the galvanic displacement of Ag by Au in situ inside the film, and the formation of Ag-Au particles. Evolution of the morphology of the bimetallic nanoparticles into hollow cage structures and the distribution of Au on the nanoparticles are revealed through electron microscopy and energy dispersive X-ray spectroscopy. The localized surface plasmon resonance (LSPR) extinction of the nanocomposite thin film evolves with the Ag-Au composition; theoretical simulation of the extinction spectra provides insight into the observed trends. The Ag-Au-PVA thin films are found to be efficient substrates for SERS. The EF follows the variation of the LSPR extinction vis-à-vis the excitation laser wavelength, but with an offset, and the maximum SERS effect is obtained at very low Au content; experiments with Rhodamine 6G showed EFs on the order of 10(8) and a limit of detection of 0.6 pmol. The present study describes a facile and simple fabrication of a nanocomposite thin film that can be conveniently deployed in SERS investigations, and the utility of the bimetallic system to tune and maximize the EF.

  7. All-thiol-stabilized Ag44 and Au12Ag32 nanoparticles with single-crystal structures.

    PubMed

    Yang, Huayan; Wang, Yu; Huang, Huaqi; Gell, Lars; Lehtovaara, Lauri; Malola, Sami; Häkkinen, Hannu; Zheng, Nanfeng

    2013-01-01

    Noble metal nanoparticles stabilized by organic ligands are important for applications in assembly, site-specific bioconjugate labelling and sensing, drug delivery and medical therapy, molecular recognition and molecular electronics, and catalysis. Here we report crystal structures and theoretical analysis of three Ag44(SR)30 and three Au12Ag32(SR)30 intermetallic nanoclusters stabilized with fluorinated arylthiols (SR=SPhF, SPhF2 or SPhCF3). The nanocluster forms a Keplerate solid of concentric icosahedral and dodecahedral atom shells, protected by six Ag2(SR)5 units. Positive counterions in the crystal indicate a high negative charge of 4(-) per nanoparticle, and density functional theory calculations explain the stability as an 18-electron superatom shell closure in the metal core. Highly featured optical absorption spectra in the ultraviolet-visible region are analysed using time-dependent density functional perturbation theory. This work forms a basis for further understanding, engineering and controlling of stability as well as electronic and optical properties of these novel nanomaterials. PMID:24005600

  8. All-thiol-stabilized Ag44 and Au12Ag32 nanoparticles with single-crystal structures.

    PubMed

    Yang, Huayan; Wang, Yu; Huang, Huaqi; Gell, Lars; Lehtovaara, Lauri; Malola, Sami; Häkkinen, Hannu; Zheng, Nanfeng

    2013-01-01

    Noble metal nanoparticles stabilized by organic ligands are important for applications in assembly, site-specific bioconjugate labelling and sensing, drug delivery and medical therapy, molecular recognition and molecular electronics, and catalysis. Here we report crystal structures and theoretical analysis of three Ag44(SR)30 and three Au12Ag32(SR)30 intermetallic nanoclusters stabilized with fluorinated arylthiols (SR=SPhF, SPhF2 or SPhCF3). The nanocluster forms a Keplerate solid of concentric icosahedral and dodecahedral atom shells, protected by six Ag2(SR)5 units. Positive counterions in the crystal indicate a high negative charge of 4(-) per nanoparticle, and density functional theory calculations explain the stability as an 18-electron superatom shell closure in the metal core. Highly featured optical absorption spectra in the ultraviolet-visible region are analysed using time-dependent density functional perturbation theory. This work forms a basis for further understanding, engineering and controlling of stability as well as electronic and optical properties of these novel nanomaterials.

  9. Enhanced Raman Scattering of Silicon Nanowires by Ag Nanoparticles in-situ Decoration

    NASA Astrophysics Data System (ADS)

    Peng, Zeping; Hu, Hailong; Wang, Shijie; Shen, Zexiang; Xiong, Qihua

    2010-08-01

    Recently, metallic nanoparticles decorated semiconductor nanowires, especially silicon, attract considerable attention, due to their potential applications in photocatalysis, photovoltaics, surface enhanced Raman scattering and biosensing. A common method that has been used to decorate silicon nanowires with metallic nanoparticles, e.g. Au or Pt, is galvanic displacement, in which metallic ions are reduced with electrons supplied by virtue of silicon half-cell reaction. Here we report a method to decorate silicon nanowires with Ag nanoparticles by surface reduction, in which a freshly etched silicon surface reduces Ag ions in-situ in aqueous silver nitrate solution. The as-grown Ag nanoparticles exhibit either highly single crystallinity or twinning boundaries, with most probably diameter ˜25 nm (Figure 1). Raman mapping experiments suggest that 1st order Raman band of silicon nanowires exhibit uniform contrast along wire axis for pristine silicon nanowires, while for Ag nanoparticle decorated silicon nanowires a series of "hot-spot," i.e., substantially enhanced Raman scattering were discovered along the wire axis. This was explained by local electric field enhancement due to Ag nanoparticle "nano-antenna," which was supported by the correlation between atomic force microscopy (AFM) analysis and Raman mapping (Figure 2). The enhancement is more or less delocalized in Raman mapping due to diffraction limit in our far-field mapping experiments. In addition, we also noticed a new side band feature ˜495 cm-1 for nanowires appeared after HF etching, this new feature sustained after sequential Oxygen plasma and UV/ozone treatment which excluded the possibility due to any possible surface dangling bonds. We now suspect this feature is due to porosity resulted from HF etching and it is now being subjected to further investigations.

  10. Enzyme Induced Formation of Monodisperse Hydrogel Nanoparticles Tunable in Size

    SciTech Connect

    Bocharova, Vera; Sharp, Danna; Jones, Aaron; Cheng, Shiwang; Griffin, Philip J.; Agapov, Alexander L.; Voylov, Dmitry; Wang, Yangyang; Kisliuk, Alexander; Melman, Artem; Sokolov, Alexei P.

    2015-03-09

    Here, we report a novel approach to synthesize monodisperse hydrogel nanoparticles that are tunable in size. The distinctive feature of our approach is the use of a multicopper oxidase enzyme, laccase, as both a biocatalyst and template for nanoparticle growth. We utilize the ferroxidase activity of laccase to initiate localized production of iron(III) cations from the oxidation of iron(II) cations. We demonstrate that nanoparticles are formed in a dilute polymer solution of alginate as a result of cross-linking between alginate and enzymatically produced iron(III) cations. Exerting control over the enzymatic reaction allows for nanometer-scale tuning of the hydrogel nanoparticle radii in the range of 30–100 nm. Moreover, the nanoparticles and their growth kinetics were characterized via dynamic light scattering, atomic force microscopy, and UV–vis spectroscopy. Our finding opens up a new avenue for the synthesis of tunable nanoscale hydrogel particles for biomedical applications.

  11. Plasmon-enhanced UV and blue upconverted emissions of Tm3+-doped 12CaO·7Al2O3 nanocrystals by attaching Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Zhu, Hancheng; Liu, Yuxue; Zhao, Dongxing; Zhang, Meng; Yang, Jian; Yan, Duanting; Liu, Chunguang; Xu, Changshan; Layfield, Carter; Ma, Li; Wang, Xiaojun

    2016-09-01

    Tm3+-doped 12CaO·7Al2O3 (C12A7) nanocrystals with the grain size of 360 nm have been fabricated by chemical co-precipitation method. Up-converted emissions at 367, 457, 476, 648, and 682 nm, corresponding to the 1D2 → 3H6, 1D2 → 3F4, 1G4 → 3H6, 1G4 → 3F4, and 3F3 → 3H6 transitions, respectively, are observed under 808 nm excitation. Plasmon-enhanced ultraviolet (UV) and blue upconverted emissions of Tm3+-doped C12A7 nanocrystals have been achieved by attaching Ag nanoparticles onto the surface of nanocrystals. The enhancement of the upconverted emissions is highly wavelength-dependent. The emission intensities of the sample with Ag+ concentration of 5.0 × 10-3 mol/L at 367 and 476 nm are enhanced about 10 and 3 times, respectively, relative to the sample without Ag attachment. The enhancement mechanism can be ascribed to surface plasmon resonance due to the highly localized electric field and the increased radiative decay rate around Ag nanoparticles. Our results suggest that Tm3+-doped C12A7 nanocrystals by attaching Ag nanoparticles might be a potential material for upconversion, compact and tunable short-wavelength lasers.

  12. Enhanced photo-catalytic activity of Sr and Ag co-doped TiO2 nanoparticles for the degradation of Direct Green-6 and Reactive Blue-160 under UV & visible light.

    PubMed

    Naraginti, Saraschandra; Thejaswini, T V L; Prabhakaran, D; Sivakumar, A; Satyanarayana, V S V; Arun Prasad, A S

    2015-10-01

    This work is focused on sol-gel synthesis of silver and strontium co-doped TiO2 nanoparticles and their utilization as photo-catalysts in degradation of two textile dyes. Effect of pH, intensity of light, amount of photo-catalyst, concentration of dye, sensitizers, etc., were studied to optimize conditions for obtaining enhanced photo-catalytic activity of synthesized nanoparticles. XRD, BET, HR-TEM, EDAX and UV-Vis (diffused reflectance mode) techniques were used to characterize the nanoparticles. Interestingly, band gap of Sr and Ag co-doped TiO2 nanoparticles showed considerable narrowing (2.6 eV) when compared to Ag doped TiO2 (2.7 eV) and undoped TiO2 (3.17 eV) nanoparticles. Incorporation of Ag and Sr in the lattice of TiO2 could bring isolated energy levels near conduction and valence bands thus narrowing band gap. The XRD analysis shows that both Ag and Sr nanoparticles are finely dispersed on the surface of titania framework, without disturbing its crystalline structure. TEM images indicate that representative grain sizes of Ag-doped TiO2 & Sr and Ag co-doped TiO2 nanoparticles are in the range of 8-20 nm and 11-25 nm, respectively. Effective degradation of Direct Green-6 (DG-6) and Reactive Blue-160 (RB-160) under UV and visible light has been achieved using the photo-catalysts. Sr and Ag co-doped TiO2 photo-catalysts showed higher catalytic activity during degradation process in visible region when compared to Ag-doped and undoped TiO2 nanoparticles which could be attributed to the interactive effect caused by band gap narrowing and enhancement in charge separation. For confirming degradation of the dyes, total organic carbon (TOC) content was monitored periodically.

  13. Bioaccumulation of Zn and Ag Nanoparticles in the Earthworms (Eisenia fetida)

    NASA Astrophysics Data System (ADS)

    Ha, Lee Seung; Sung-Dae, Kim; Yi, Yang Song; Byeong-Gweon, Lee

    2014-05-01

    Many studies are carried out to evaluate environmental effects of engineered nanoparticles (ENPs). Most of the previous studies primarily focused on the effects of nanoparticles into the aquatic environment and human. Model studies predict that ENPs released into environment would transferred primarily to the soil of the terrestrial environment. Despite this prediction, biogeochemical behavior of ENPs in soil environment as well as bioavailability of ENPs to soil-dwelling organisms such as earthworm, springtail, isopod and nematodes are poorly understood. The main goal of this study was to compare the bioaccumulation factor (BAFs) and subcellular partitioning of nanoparticles in the soil-dwelling earthworm (Eisenia fetida) from ENP (ZnO and Ag nanoparticles) or ionic metal (Zn2+, Ag+) contaminated soil. And the sequential extraction was also used to determine the mobility of metals in soil which could be used as to predict bioavailability and compare that with bioaccumulation factor. The radiotracer method was employed to trace the transfer of ENPs and ionic metal among different environmental media and animals. Radiolabeled 65ZnO, 110mAgNPs coated with PVP or citrate were synthesized in the laboratory and their chemical and biological behavior was compared to ionic 65Zn and 110mAg. The BAFs of Zn and Ag in the earthworms were determined after animals exposed to the contaminated soils. After the 7 days of elimination phase, subcellular partitioning of metals were also obtained. BAF for ZnO(0.06) was 31 times lower than that for Zn ion (1.86), suggesting that ZnO was less bioavailable than its ionic form from contaminated soil. On the other hands, BAFs for AgNPs coated with PVP (0.12) or with citrate (0.11) were comparable to those for Ag ion (0.17), indicating that Ag from contaminated soil was bioavailable in a similar rate regardless of chemical forms. The subcellular partitioning results showed that bioaccumulated Zn from Zn ion and ZnO contaminated soil were

  14. Contribution of Eu ions on the precipitation of silver nanoparticles in Ag-Eu co-doped borate glasses

    SciTech Connect

    Jiao, Qing; Qiu, Jianbei; Zhou, Dacheng; Xu, Xuhui

    2014-03-01

    Graphical abstract: - Highlights: • Silver nanoparticles are precipitated from the borate glasses during the melting process without any further heat treatment. • The reduction of Eu{sup 3+} ions to Eu{sup 2+} ions is presented in this material. • The intensity of Ag{sup +} luminescence. • The introduction of Eu ions accelerated the reaction between Eu{sup 2+} ions and silver ions inducing the silver clusters formation. - Abstract: Ag{sup +} doped sodium borate glasses with different Eu ions concentration were prepared by the melt-quenching method. The absorption at about 410 nm which was caused by the surface plasmon resonance (SPR) of Ag nanoparticles (NPs) is promoted with increasing of Eu ions concentration. Meanwhile, the luminescent spectra showed that the emission intensity of Ag{sup +} decreased while that of the Ag aggregates increased simultaneously. The results indicated that the Ag ions intend to form the high-polymeric state such as Ag aggregates and nanoparticles with increasing of europium ions. Owing to the self-reduction of Eu{sup 3+} to Eu{sup 2+} in our glass system, it revealed that Ag{sup +} has been reduced by the neighboring Eu{sup 2+} which leads to the formation of Ag aggregates and the precipitation of Ag NPs in the matrix. In addition, energy transfer (ET) process from Ag{sup +}/Ag aggregates to the Eu{sup 3+} was investigated for the enhancement of Eu{sup 3+} luminescence.

  15. Scalable preparation of ultrathin silica-coated Ag nanoparticles for SERS application.

    PubMed

    Hu, Yanjie; Shi, Yunli; Jiang, Hao; Huang, Guangjian; Li, Chunzhong

    2013-11-13

    Silica-coated Ag nanoparticles (Ag@SiO2 NPs) have been successfully prepared by a scalable flame spray pyrolysis (FSP) technique with production rate up to 4 g/h in laboratory-scale. The ultrathin SiO2 shell, with a thickness 1 nm, not only effectively avoids the intersintering of Ag nanoparticles core at the high temperature, but also serves as a protective layer of the SERS-active nanostructure. The silica-coated Ag nanoparticles form agglomerates in the large temperature gradient zone, which with several nanometers gaps from each other but not contact. Such an intriguing feature can result in more Raman hot-spots generated at the gaps among Ag core active sites, which will beneficial for the whole SERS substrate enhancement. The results demonstrate that a maximum enhancement factor can reach ~10(5) with a detectable concentration as low as 10(-10) M for rhodamine 6G (R6G) molecules, indicating that the as-obtained unique nanostructure will be a promising candidate for SERS applications. PMID:24117322

  16. 77 FR 75169 - Silver Nanoparticles (AgNPs); Information and Comment Request

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-19

    ... HUMAN SERVICES Centers for Disease Control and Prevention Silver Nanoparticles (AgNPs); Information and Comment Request AGENCY: National Institute for Occupational Safety and Health (NIOSH) of the Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Request...

  17. Ag Nanoparticle/Polydopamine-Coated Inverse Opals as Highly Efficient Catalytic Membranes.

    PubMed

    Choi, Gwan H; Rhee, Do Kyung; Park, A Reum; Oh, Min Jun; Hong, Sunghwan; Richardson, Joseph J; Guo, Junling; Caruso, Frank; Yoo, Pil J

    2016-02-10

    Polymeric three-dimensional inverse-opal (IO) structures provide unique structural properties useful for various applications ranging from optics to separation technologies. Despite vast needs for IO functionalization to impart additional chemical properties, this task has been seriously challenged by the intrinsic limitation of polymeric porous materials that do not allow for the easy penetration of waterborne moieties or precursors. To overcome this restriction, we present a robust and straightforward method of employing a dipping-based surface modification with polydopamine (PDA) inside the IO structures, and demonstrate their application to catalytic membranes via synthetic incorporation of Ag nanoparticles. The PDA coating offers simultaneous advantages of achieving the improved hydrophilicity required for the facilitated infiltration of aqueous precursors and successful creation of nucleation sites for a reduction of growth of the Ag nanoparticles. The resulting Ag nanoparticle-incorporated IO structures are utilized as catalytic membranes for the reduction of 4-nitrophenol to its amino derivatives in the presence of NaBH4. Synergistically combined characteristics of high reactivity of Ag nanoparticles along with a greatly enhanced internal surface area of IO structures enable the implementation of remarkably improved catalytic performance, exhibiting a good conversion efficiency greater than 99% while minimizing loss in the membrane permeability. PMID:26780371

  18. Ag Nanoparticle/Polydopamine-Coated Inverse Opals as Highly Efficient Catalytic Membranes.

    PubMed

    Choi, Gwan H; Rhee, Do Kyung; Park, A Reum; Oh, Min Jun; Hong, Sunghwan; Richardson, Joseph J; Guo, Junling; Caruso, Frank; Yoo, Pil J

    2016-02-10

    Polymeric three-dimensional inverse-opal (IO) structures provide unique structural properties useful for various applications ranging from optics to separation technologies. Despite vast needs for IO functionalization to impart additional chemical properties, this task has been seriously challenged by the intrinsic limitation of polymeric porous materials that do not allow for the easy penetration of waterborne moieties or precursors. To overcome this restriction, we present a robust and straightforward method of employing a dipping-based surface modification with polydopamine (PDA) inside the IO structures, and demonstrate their application to catalytic membranes via synthetic incorporation of Ag nanoparticles. The PDA coating offers simultaneous advantages of achieving the improved hydrophilicity required for the facilitated infiltration of aqueous precursors and successful creation of nucleation sites for a reduction of growth of the Ag nanoparticles. The resulting Ag nanoparticle-incorporated IO structures are utilized as catalytic membranes for the reduction of 4-nitrophenol to its amino derivatives in the presence of NaBH4. Synergistically combined characteristics of high reactivity of Ag nanoparticles along with a greatly enhanced internal surface area of IO structures enable the implementation of remarkably improved catalytic performance, exhibiting a good conversion efficiency greater than 99% while minimizing loss in the membrane permeability.

  19. Facile synthesis of S-Ag nanocomposites and Ag2S short nanorods by the interaction of sulfur with AgNO3 in PEG400

    NASA Astrophysics Data System (ADS)

    Zhang, Yan-Li; Xie, Xin-Yuan; Liang, Ming; Xie, Shu-Ming; Chen, Jie-Mei; Zheng, Wen-Jie

    2016-06-01

    A facile, eco-friendly and inexpensive method to prepare Ag2S short nanorods and S-Ag nanocomposites using sublimed sulfur, AgNO3, PVP and PEG400 was studied. According to x-ray diffraction and scanning electron microscopy of the Ag2S, the products are highly crystalline and pure Ag2S nanorods with diameters of 70-160 nm and lengths of 200-360 nm. X-ray diffraction of the S-Ag nanocomposites shows that we obtained cubic Ag and S nanoparticles. Transmission electron microscopy shows that the molar ratio of PVP to Ag+ plays an important role in controlling the size and morphology of the S-Ag nanocomposites. When the molar ratio of PVP to Ag+ was 10:1, smaller sizes, better dispersibility and narrower distribution of S-Ag nanocomposites with diameters of 10-40 nm were obtained. The formation mechanism of the S-Ag nanocomposites was studied by designing a series of experiments using ultraviolet-visible measurement, and it was found that S nanoparticles are produced first and act as seed crystals; then Ag+ becomes Ag nanocrystals on the surfaces of the S nanoparticles by the reduction of PVP. PEG400 acts as a catalyzer, accelerating the reaction rate, and protects the S-Ag nanocomposites from reacting to produce Ag2S. The antimicrobial experiments show that the S-Ag nanocomposites have greater antimicrobial activity on Staphylococcus aureus, Aspergillus niger and blue mold than Ag nanoparticles.

  20. Facile synthesis of S–Ag nanocomposites and Ag2S short nanorods by the interaction of sulfur with AgNO3 in PEG400

    NASA Astrophysics Data System (ADS)

    Zhang, Yan-Li; Xie, Xin-Yuan; Liang, Ming; Xie, Shu-Ming; Chen, Jie-Mei; Zheng, Wen-Jie

    2016-06-01

    A facile, eco-friendly and inexpensive method to prepare Ag2S short nanorods and S–Ag nanocomposites using sublimed sulfur, AgNO3, PVP and PEG400 was studied. According to x-ray diffraction and scanning electron microscopy of the Ag2S, the products are highly crystalline and pure Ag2S nanorods with diameters of 70–160 nm and lengths of 200–360 nm. X-ray diffraction of the S–Ag nanocomposites shows that we obtained cubic Ag and S nanoparticles. Transmission electron microscopy shows that the molar ratio of PVP to Ag+ plays an important role in controlling the size and morphology of the S–Ag nanocomposites. When the molar ratio of PVP to Ag+ was 10:1, smaller sizes, better dispersibility and narrower distribution of S–Ag nanocomposites with diameters of 10–40 nm were obtained. The formation mechanism of the S–Ag nanocomposites was studied by designing a series of experiments using ultraviolet–visible measurement, and it was found that S nanoparticles are produced first and act as seed crystals; then Ag+ becomes Ag nanocrystals on the surfaces of the S nanoparticles by the reduction of PVP. PEG400 acts as a catalyzer, accelerating the reaction rate, and protects the S–Ag nanocomposites from reacting to produce Ag2S. The antimicrobial experiments show that the S–Ag nanocomposites have greater antimicrobial activity on Staphylococcus aureus, Aspergillus niger and blue mold than Ag nanoparticles.

  1. β-Cyclodextrin coated SiO₂@Au@Ag core-shell nanoparticles for SERS detection of PCBs.

    PubMed

    Lu, Yilin; Yao, Guohua; Sun, Kexi; Huang, Qing

    2015-09-01

    A new type of surface-enhanced Raman scattering (SERS) substrate consisting of β-cyclodextrin (β-CD) coated SiO2@Au@Ag nanoparticles (SiO2@Au@Ag@CD NPs) has been achieved. Our protocol was a simplified approach as the fabrication and modification of the silver shell were realized in a single-step reaction by taking advantage of β-CD as both the reducing and stabilizing agents. The as-synthesized SiO2@Au@Ag@CD NPs were uniform in size and demonstrated high SERS activity and reproducibility. The substrates consisting of the SiO2@Au@Ag@CD NPs were employed for SERS detection of polychlorinated biphenyls (PCBs) including PCB-3, PCB-29 and PCB-77. The SERS detection sensitivity was significantly improved due to enrichment of more PCB molecules captured by β-CD on the substrate surface, as confirmed by the appearance of the new Raman bands which are attributed to the complexes between β-CD and PCBs according to the theoretical simulation. Therefore, this work presents a novel approach to the fabrication of effective SERS substrates that can be employed for rapid determination of trace amounts of PCBs in the environment with high detection sensitivity and recognition selectivity. PMID:25478906

  2. Does Nanoparticle Activity Depend upon Size and Crystal Phase?

    PubMed Central

    Jiang, Jingkun; Oberdörster, Günter; Elder, Alison; Gelein, Robert; Mercer, Pamela; Biswas, Pratim

    2010-01-01

    A method to investigate the dependence of the physicochemical properties of nanoparticles (e.g. size, surface area and crystal phase) on their oxidant generating capacity is proposed and demonstrated for TiO2 nanoparticles. Gas phase synthesis methods that allow for strict control of size and crystal phase were used to prepare TiO2 nanoparticles. The reactive oxygen species (ROS) generating capacity of these particles was then measured. The size dependent ROS activity was established using TiO2 nanoparticles of 9 different sizes (4 – 195 nm) but the same crystal phase. For a fixed total surface area, an S-shaped curve for ROS generation per unit surface area was observed as a function of particle size. The highest ROS activity per unit area was observed for 30 nm particles, and observed to be constant above 30 nm. There was a decrease in activity per unit area as size decreased from 30 nm to 10 nm; and again constant for particles smaller than 10 nm. The correlation between crystal phase and oxidant capacity was established using TiO2 nanoparticles of 11 different crystal phase combinations but similar size. The ability of different crystal phases of TiO2 nanoparticles to generate ROS was highest for amorphous, followed by anatase, and then anatase/rutile mixtures, and lowest for rutile samples. Based on evaluation of the entire dataset, important dose metrics for ROS generation are established. Their implications of these ROS studies on biological and toxicological studies using nanomaterials are discussed. PMID:20827377

  3. Enhanced photocatalysis by coupling of anatase TiO2 film to triangular Ag nanoparticle island.

    PubMed

    Xu, Jinxia; Xiao, Xiangheng; Ren, Feng; Wu, Wei; Dai, Zhigao; Cai, Guangxu; Zhang, Shaofeng; Zhou, Juan; Mei, Fei; Jiang, Changzhong

    2012-01-01

    In order to overcome the low utilization ratio of solar light and high electron-hole pair recombination rate of TiO2, the triangular Ag nanoparticle island is covered on the surface of the TiO2 thin film. Enhancement of the photocatalytic activity of the Ag/TiO2 nanocomposite system is observed. The increase of electron-hole pair generation is caused by the enhanced near-field amplitudes of localized surface plasmon of the Ag nanoparticles. The efficiently suppressed recombination of electron-hole pair caused by the metal-semiconductor contact can also enhance the photocatalytic activity of the TiO2 film. PMID:22548875

  4. Enhanced resistive switching effect in Ag nanoparticle embedded BaTiO{sub 3} thin films

    SciTech Connect

    Au, K.; Wang, Juan; Bao, Z. Y.; Dai, J. Y.; Gao, X. S.; Liu, J. M.

    2013-07-14

    Ag nanoparticle (NP) embedded BaTiO{sub 3} (BTO) thin films on SrRuO{sub 3}-coated SrTiO{sub 3} (STO) substrates are prepared by the integrated nanocluster beam deposition and laser-molecular beam epitaxy. Enhanced resistive switching, up to an ON/OFF ration of 10{sup 4}, has been achieved at low switching voltage (less than 1 V) without a forming voltage. These characteristics make such nanocomposite film very promising for application of low voltage non-volatile random access memory. The enhanced resistive switching effect may be attributed to the charge storage effect of the Ag nanoparticles and easy formation of Ag filament inside the BTO film.

  5. Enhanced photocatalysis by coupling of anatase TiO2 film to triangular Ag nanoparticle island

    PubMed Central

    2012-01-01

    In order to overcome the low utilization ratio of solar light and high electron-hole pair recombination rate of TiO2, the triangular Ag nanoparticle island is covered on the surface of the TiO2 thin film. Enhancement of the photocatalytic activity of the Ag/TiO2 nanocomposite system is observed. The increase of electron-hole pair generation is caused by the enhanced near-field amplitudes of localized surface plasmon of the Ag nanoparticles. The efficiently suppressed recombination of electron-hole pair caused by the metal-semiconductor contact can also enhance the photocatalytic activity of the TiO2 film. PMID:22548875

  6. Adsorption of DNA on colloidal Ag nanoparticles: effects of nanoparticle surface charge, base content and length of DNA.

    PubMed

    Abbasian, Sara; Moshaii, Ahmad; Nikkhah, Maryam; Farkhari, Nahid

    2014-04-01

    The adsorption of single and double stranded DNA on colloidal silver nanoparticles has been studied to investigate the effects of surface charge of the nanoparticles, the composition of the oligonucleotide and its length on the adsorption characteristics. The results explain that the nanoparticle surface charge is a key parameter determining the propensity of oligonucleotides to adsorb on nanoparticles. The adsorption also depends on the length and composition of oligonucleotide. The protective effects of both single and double stranded DNA against salt-induced aggregation dramatically increase as the DNA length increases. In contrast to other available reports, we observed that long oligonucleotides (single-stranded and double stranded) can well be adsorbed on the nanoparticles as the short ones leading to almost complete protection of nanoparticles against salt induced aggregation and hence are not suitable for the sensing applications. Finally, the light scattering from the Ag nanoparticles has been simulated and the results compared with the experiments. Our understanding should improve development of colorimetric assays for DNA detection based on aggregation of unmodified metallic nanoparticles.

  7. Synthesis, characterization, and evaluation of antibacterial effect of Ag nanoparticles against Escherichia coli O157:H7 and methicillin-resistant Staphylococcus aureus (MRSA).

    PubMed

    Paredes, Daissy; Ortiz, Claudia; Torres, Rodrigo

    2014-01-01

    Silver nanoparticles (AgNPs) have been shown great interest because of their potential antibacterial effect. Recently, this has been increased due to resistance in some pathogenic bacteria strains to conventional antibiotics, which has initiated new studies to search for more effective treatments against resistant microorganisms. For these reasons, AgNPs have become an important approach for applications in nanobiotechnology in the development of antibiotic treatment of different bacterial infections. This study was aimed at synthesizing AgNPs using cysteine as a reducer agent and cetyl-tri-methyl-ammonium bromide as a stabilizer in order to obtain more efficient treatment against the pathogen bacteria Escherichia coli O157:H7. These AgNPs were characterized through UV-Vis spectroscopy, transmission electron microscopy, and dynamic light scattering. From these analyses, formation of spherical nanoparticles with an average size of 55 nm was confirmed. Finally, minimal inhibitory concentration (MIC) and minimal bactericide concentration (MBC) of these AgNPs against pathogenic strains E. coli O157:H7 and methicillin-resistant Staphylococcus aureus (MRSA) were determined in both solid and liquid media. MIC and MBC values were around 0.25 μg/mL and 1 μg/mL, respectively. These parameters were comparable to those reported in the literature and were even more effective than other synthesized AgNPs.

  8. Synthesis, characterization, and evaluation of antibacterial effect of Ag nanoparticles against Escherichia coli O157:H7 and methicillin-resistant Staphylococcus aureus (MRSA)

    PubMed Central

    Paredes, Daissy; Ortiz, Claudia; Torres, Rodrigo

    2014-01-01

    Silver nanoparticles (AgNPs) have been shown great interest because of their potential antibacterial effect. Recently, this has been increased due to resistance in some pathogenic bacteria strains to conventional antibiotics, which has initiated new studies to search for more effective treatments against resistant microorganisms. For these reasons, AgNPs have become an important approach for applications in nanobiotechnology in the development of antibiotic treatment of different bacterial infections. This study was aimed at synthesizing AgNPs using cysteine as a reducer agent and cetyl-tri-methyl-ammonium bromide as a stabilizer in order to obtain more efficient treatment against the pathogen bacteria Escherichia coli O157:H7. These AgNPs were characterized through UV-Vis spectroscopy, transmission electron microscopy, and dynamic light scattering. From these analyses, formation of spherical nanoparticles with an average size of 55 nm was confirmed. Finally, minimal inhibitory concentration (MIC) and minimal bactericide concentration (MBC) of these AgNPs against pathogenic strains E. coli O157:H7 and methicillin-resistant Staphylococcus aureus (MRSA) were determined in both solid and liquid media. MIC and MBC values were around 0.25 μg/mL and 1 μg/mL, respectively. These parameters were comparable to those reported in the literature and were even more effective than other synthesized AgNPs. PMID:24729707

  9. Preparation of mesoporous cadmium sulfide nanoparticles with moderate pore size

    SciTech Connect

    Han Zhaohui Zhu, Huaiyong; Shi, Jeffrey; Parkinson, Gordon; Lu, G.Q.

    2007-03-15

    The preparation of cadmium sulfide nanoparticles that have a moderate pore size is reported. This preparation method involves a hydrothermal process that produces a precursor mixture and a following acid treatment of the precursor to get the porous material. The majority of the particles have a pore size close to 20nm, which complements and fills in the gap between the existing cadmium sulfide materials, which usually have a pore size either less than 10nm or are well above 100nm.

  10. Size and Crystallinity in Protein-Templated Inorganic Nanoparticles

    SciTech Connect

    Jolley, Craig C.; Uchida, Masaki; Reichhardt, Courtney; Harrington, Richard; Kang, Sebyung; Klem, Michael T.; Parise, John B.; Douglas, Trevor

    2010-12-01

    Protein cages such as ferritins and virus capsids have been used as containers to synthesize a wide variety of protein-templated inorganic nanoparticles. While identification of the inorganic crystal phase has been successful in some cases, very little is known about the detailed nanoscale structure of the inorganic component. We have used pair distribution function analysis of total X-ray scattering to measure the crystalline domain size in nanoparticles of ferrihydrite, {gamma}-Fe{sub 2}O{sub 3}, Mn{sub 3}O{sub 4}, CoPt, and FePt grown inside 24-meric ferritin cages from H. sapiens and P. furiosus. The material properties of these protein-templated nanoparticles are influenced by processes at a variety of length scales: the chemistry of the material determines the precise arrangement of atoms at very short distances, while the interior volume of the protein cage constrains the maximum nanoparticle size attainable. At intermediate length scales, the size of coherent crystalline domains appears to be constrained by the arrangement of crystal nucleation sites on the interior of the cage. On the basis of these observations, some potential synthetic strategies for the control of crystalline domain size in protein-templated nanoparticles are suggested.

  11. Effect of Metallic Glass Particle Size on the Contact Resistance of Ag/Metallic Glass Electrode

    NASA Astrophysics Data System (ADS)

    Park, Jin Man; Park, Keum Hwan; Park, Eun Soo; Hong, Seok-Moo; Kim, Se Yun; Jee, Sang Soo; Lee, Eun Sung; Kim, Suck Jun; Kim, Ki Buem; Kim, Do Hyang; Eckert, Jürgen

    2015-06-01

    In this study, electrically conductive Al-based metallic glass (MG) has been applied as an alternative of oxide glass in silver paste. Al85Ni5Y8Co2 MG powder was produced by gas atomization process and simultaneously classified depending on the size of powder. The wetting behavior of MG was dramatically altered by the degree of crystallinity and the size of MG powder, resulting in the different sinterability of silver (Ag) and contact area between Si emitter and Ag. The Ag electrode with smaller MG powder shows much denser structure of Ag and larger contact area, leading to low contact resistance, 0.69 ± 0.38 at p-type and 0.56 ± 0.13 mΩcm2 at n-type emitter.

  12. Synthesis and the enhanced visible-light-driven photocatalytic activity of BiVO4 nanocrystals coupled with Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Wang, W. Z.; Meng, Shan; Tan, Miao; Jia, L. J.; Zhou, Y. X.; Wu, Shuang; Huang, X. W.; Liang, Y. J.; Shi, H. L.

    2015-03-01

    BiVO4 nanocrystals coupled with Ag nanoparticles (Ag-BiVO4 heterogeneous nanostructures) have been prepared by a new strategy via combining a hydrothermal route with a polyol process, in which BiVO4 nanocrystals were first synthesized by a hydrothermal route, and then, Ag nanoparticles were grown on the surfaces of the presynthesized BiVO4 nanocrystals through a polyol process. The photocatalytic evaluations demonstrate that BiVO4 nanocrystals coupled with Ag nanoparticles exhibit the enhanced visible-light-driven photocatalytic activity for the degradation of methylene blue (MB) and rhodamine B (RhB). The energy alignment and diffuse reflectance property of Ag-BiVO4 heterogeneous nanostructures demonstrate that Ag nanoparticles attached on the surfaces of BiVO4 nanocrystals play double roles for the enhanced visible-light-driven photocatalytic activity. First, the Ag nanoparticles grown on the surfaces of BiVO4 nanocrystals may act as electron sinks to retard the recombination of the photogenerated electrons and holes in BiVO4 so as to improve the charge separation on its surfaces. Second, the Ag nanoparticles increase the visible light absorption of the Ag-BiVO4 photocatalyst due to surface plasmon resonance (SPR) of Ag nanoparticles. These double roles of Ag nanoparticles make Ag-BiVO4 heterogeneous nanostructures to exhibit the enhanced photocatalytic activity to decompose MB and RhB under visible light irradiation, compared to the pure BiVO4 nanocrystals. The enhanced photocatalytic activity is attributed to the charge transfer from BiVO4 to the attached Ag nanoparticles as well as SPR absorption of Ag nanoparticles. The present work not only provides an efficient route to enhance visible-light-driven photocatalytic activity of BiVO4, but also offers a new strategy for fabricating metal-semiconductor heterogeneous nanostructure photocatalysts, which are expected to show considerable potential applications in solar-driven wastewater treatment and water

  13. Engineered nanoparticles interacting with cells: size matters

    PubMed Central

    2014-01-01

    With the rapid advancement of nanoscience and nanotechnology, detailed knowledge of interactions between engineered nanomaterials and cells, tissues and organisms has become increasingly important, especially in regard to possible hazards to human health. This review intends to give an overview of current research on nano-bio interactions, with a focus on the effects of NP size on their interactions with live cells. We summarize common techniques to characterize NP size, highlight recent work on the impact of NP size on active and passive cellular internalization and intracellular localization. Cytotoxic effects are also discussed. PMID:24491160

  14. Size- and shape-dependent clinical and mycological efficacy of silver nanoparticles on dandruff

    PubMed Central

    Anwar, Mohammad F; Yadav, Deepak; Jain, Swati; Kapoor, Sumeet; Rastogi, Shweta; Arora, Indu; Samim, Mohammed

    2016-01-01

    Dandruff is a prominent scalp problem caused by the growth of fungus Malassezia furfur, potentially cascading into dermal inflammation, itching, and tissue damage. The present work outlines a detailed analysis of the treatment of scalp infection using silver nanomaterials (Ag NMs), and focuses on biocidal activity owing to manipulation of size, shape, and structure. Monodisperse silver spherical nanoparticles (NPs) and nanorods (NRs) were synthesized by chemical routes that were characterized using analytical and spectroscopic techniques. Ag NMs demonstrated enhanced biocidal tendencies compared to market available drugs, itracanozole and ketoconazole, showing greater zones of inhibition. The obtained 20 nm and 50 nm spherical-shaped NPs and 50 nm NRs showed concentration-, size-, and shape-dependent antifungal activity, with 20 nm spherical-shaped NPs exhibiting excellent potency. Minimum inhibitory concentration for 20 nm was lowest at 0.2 mg/mL in comparison to 0.3 mg/mL for NRs. Primary irritation index was 0.33 and 0.16 for 20 nm and 50 nm spherical-shaped NPs, respectively, while 50 nm rod-shaped NMs exhibited negligible redness. An in vivo model for M. furfur infection was generated by passing fungi subcutaneously in rats’ skin. Again, 20 nm particles showed best normalization of skin after 10 days on regular dosing, in comparison with bigger and rod-shaped particles. The statistical clinical score was highest for Ag nanorods, followed by 50 nm Ag NPs-treated animals. It was observed that 20 nm spherical particles exhibited the lowest score (0) compared with others as well as with antifungal drugs. Biochemical analysis performed by checking antioxidant enzymatic activities indicated tissue repair and normalization of enzymes and protein concentration by Ag NPs. PMID:26792991

  15. Size- and shape-dependent clinical and mycological efficacy of silver nanoparticles on dandruff.

    PubMed

    Anwar, Mohammad F; Yadav, Deepak; Jain, Swati; Kapoor, Sumeet; Rastogi, Shweta; Arora, Indu; Samim, Mohammed

    2016-01-01

    Dandruff is a prominent scalp problem caused by the growth of fungus Malassezia furfur, potentially cascading into dermal inflammation, itching, and tissue damage. The present work outlines a detailed analysis of the treatment of scalp infection using silver nanomaterials (Ag NMs), and focuses on biocidal activity owing to manipulation of size, shape, and structure. Monodisperse silver spherical nanoparticles (NPs) and nanorods (NRs) were synthesized by chemical routes that were characterized using analytical and spectroscopic techniques. Ag NMs demonstrated enhanced biocidal tendencies compared to market available drugs, itracanozole and ketoconazole, showing greater zones of inhibition. The obtained 20 nm and 50 nm spherical-shaped NPs and 50 nm NRs showed concentration-, size-, and shape-dependent antifungal activity, with 20 nm spherical-shaped NPs exhibiting excellent potency. Minimum inhibitory concentration for 20 nm was lowest at 0.2 mg/mL in comparison to 0.3 mg/mL for NRs. Primary irritation index was 0.33 and 0.16 for 20 nm and 50 nm spherical-shaped NPs, respectively, while 50 nm rod-shaped NMs exhibited negligible redness. An in vivo model for M. furfur infection was generated by passing fungi subcutaneously in rats' skin. Again, 20 nm particles showed best normalization of skin after 10 days on regular dosing, in comparison with bigger and rod-shaped particles. The statistical clinical score was highest for Ag nanorods, followed by 50 nm Ag NPs-treated animals. It was observed that 20 nm spherical particles exhibited the lowest score (0) compared with others as well as with antifungal drugs. Biochemical analysis performed by checking antioxidant enzymatic activities indicated tissue repair and normalization of enzymes and protein concentration by Ag NPs. PMID:26792991

  16. Size Dependent Phase Diagrams of Nickel-Carbon Nanoparticles

    NASA Astrophysics Data System (ADS)

    Magnin, Y.; Zappelli, A.; Amara, H.; Ducastelle, F.; Bichara, C.

    2015-11-01

    The carbon rich phase diagrams of nickel-carbon nanoparticles, relevant to catalysis and catalytic chemical vapor deposition synthesis of carbon nanotubes, are calculated for system sizes up to about 3 nm (807 Ni atoms). A tight binding model for interatomic interactions drives the grand canonical Monte Carlo simulations used to locate solid, core shell and liquid stability domains, as a function of size, temperature, and carbon chemical potential or concentration. Melting is favored by carbon incorporation from the nanoparticle surface, resulting in a strong relative lowering of the eutectic temperature and a phase diagram topology different from the bulk one. This should lead to a better understanding of the nanotube growth mechanisms.

  17. Fungal biomolecules assisted biosynthesis of Au-Ag alloy nanoparticles and evaluation of their catalytic property.

    PubMed

    Tripathi, Ravi Mani; Gupta, Rohit Kumar; Bhadwal, Akhshay Singh; Singh, Priti; Shrivastav, Archana; Shrivastav, B R

    2015-08-01

    The catalytic reduction of methylene blue was studied using biosynthesised gold-silver (Au-Ag) alloy nanoparticles (NPs). The fungal biomass of Trichoderma harzianum was used as a reducing and stabilising agent in the synthesis of Au-Ag alloy NPs. The synthesised NPs were well characterised by UV-vis spectroscopy, dynamic light scattering, X-ray diffraction, transmission electron microscopy, energy dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. The plausible synthesis mechanism involved in the formation of Au-Ag alloy NPs was also discussed with diagrammatic representation. A series of experiments was performed to investigate the catalytic activity of the as-prepared Au-Ag alloy NPs and found that the alloy NPs show excellent catalytic activity. PMID:26224346

  18. Photostability of gold nanoparticles with different shapes: the role of Ag clusters.

    PubMed

    Attia, Yasser A; Buceta, David; Requejo, Félix G; Giovanetti, Lisandro J; López-Quintela, M Arturo

    2015-07-14

    Anisotropic gold nanostructures prepared by the seed method in the presence of Ag ions have been used to study their photostability to low-power UV irradiation (254 nm) at room temperature. It has been observed that, whereas spheres are very stable to photoirradiation, rods and prisms suffer from photocorrosion and finally dissolve completely with the production of Au(III) ions. Interpretation of these differences is based on the presence of semiconductor-like Ag clusters, adsorbed onto rods and prisms, able to photocorrode the Au nanoparticles, which are absent in the case of Au spheres. We further show direct evidence of the presence of Ag clusters in Au nanorods by XANES. These results confirm a previous hypothesis (J. Am. Chem. Soc., 2014, 136, 1182-1185) about the major influence of very stable small Ag clusters, not only on the anisotropic formation of nanostructures but also on their photostability.

  19. Stellated Ag-Pt bimetallic nanoparticles: An effective platform for catalytic activity tuning

    PubMed Central

    Liu, Hui; Ye, Feng; Yao, Qiaofeng; Cao, Hongbin; Xie, Jianping; Lee, Jim Yang; Yang, Jun

    2014-01-01

    The usefulness of Pt-based nanomaterials for catalysis can be greatly enhanced by coupling morphology engineering to the strategic presence of a second or even third metal. Here we demonstrate the design and preparation of stellated Ag-Pt bimetallic nanoparticles where significant activity difference between the methanol oxidation reaction (MOR) and the oxygen reduction reaction (ORR) may be realized by relegating Ag to the core or by hollowing out the core. In particular the stellated Pt surface, with an abundance of steps, edges, corner atoms, and {111} facets, is highly effective for the ORR but is ineffective for MOR. MOR activity is only observed in the presence of a Ag core through electronic coupling to the stellated Pt shell. The bimetallic Ag-Pt stellates therefore demonstrate the feasibility of tuning a Pt surface for two very different structure sensitive catalytic reactions. Stellated bimetallics may therefore be an effective platform for highly tunable catalyst designs. PMID:24495979

  20. Fabrication of high aspect ratio nanogrid transparent electrodes via capillary assembly of Ag nanoparticles.

    PubMed

    Kang, Juhoon; Park, Chang-Goo; Lee, Su-Han; Cho, Changsoon; Choi, Dae-Geun; Lee, Jung-Yong

    2016-06-01

    In this report, we describe the fabrication of periodic Ag nanogrid electrodes by capillary assembly of silver nanoparticles (AgNPs) along patterned nanogrid templates. By assembling the AgNPs into these high-aspect-ratio nanogrid patterns, we can obtain high-aspect-ratio nanogratings, which can overcome the inherent trade-off between the optical transmittance and the sheet resistance of transparent electrodes. The junction resistance between the AgNPs is effectively reduced by photochemical welding and post-annealing. The fabricated high-aspect-ratio nanogrid structure with a line width of 150 nm and a height of 450 nm has a sheet resistance of 15.2 Ω sq(-1) and an optical transmittance of 85.4%. PMID:27187802

  1. Fractal structure formation from Ag nanoparticle films on insulating substrates.

    PubMed

    Tang, Jing; Li, Zhiyong; Xia, Qiangfei; Williams, R Stanley

    2009-07-01

    Two dimensional (2D) fractal structures were observed to form from fairly uniform Ag island films (equivalent mass thicknesses of 1.5 and 5 nm) on insulating silicon dioxide surfaces (thermally grown silicon oxide on Si or quartz) upon immersion in deionized water. This result is distinctly different from the previously observed three-dimensional (3D) growth of faceted Ag nanocrystals on conductive surfaces (ITO and graphite) as the result of an electrochemical Ostwald ripening process, which also occurs on native oxide covered silicon surfaces as reported here. The fractal structures formed by diffusion-limited aggregation (DLA) of Ag species on the insulating surfaces. We present the experimental observation of this phenomenon and discuss some possible mechanisms for the DLA formation. PMID:19496573

  2. Tuning size and thermal hysteresis in bistable spin crossover nanoparticles.

    PubMed

    Galán-Mascarós, José Ramón; Coronado, Eugenio; Forment-Aliaga, Alicia; Monrabal-Capilla, María; Pinilla-Cienfuegos, Elena; Ceolin, Marcelo

    2010-06-21

    Nanoparticles of iron(II) triazole salts have been prepared from water-organic microemulsions. The mean size of the nanoparticles can be tuned down to 6 nm in diameter, with a narrow size distribution. A sharp spin transition from the low spin (LS) to the high spin (HS) state is observed above room temperature, with a 30-40-K-wide thermal hysteresis. The same preparation can yield second generation nanoparticles containing molecular alloys by mixing triazole with triazole derivatives, or from metallic mixtures of iron(II) and zinc(II). In these nanoparticles of 10-15 nm, the spin transition "moves" towards lower temperatures, reaching a 316 K limit for the cooling down transition and maintaining a thermal hysteresis over 15-20-K-wide. The nanoparticles were characterized by dynamic light scattering, TEM, and AFM, after deposition on gold or silicon surfaces. The spin transition was characterized by magnetic susceptibility measurements and EXAFS (in solid samples after solvent removal) and also by the color change between the LS (violet) and HS (colorless) states in an organic solvent suspension. The discovery of bistable magnetic nanoparticles of 6 nm with a wide thermal hysteresis above room temperature showcases the actual possibilities of spin crossover materials for nanotechnological applications. PMID:20503990

  3. Size-dependent structure of silver nanoparticles under high pressure

    SciTech Connect

    Koski, Kristie Jo

    2008-12-31

    Silver noble metal nanoparticles that are<10 nm often possess multiply twinned grains allowing them to adopt shapes and atomic structures not observed in bulk materials. The properties exhibited by particles with multiply twinned polycrystalline structures are often far different from those of single-crystalline particles and from the bulk. I will present experimental evidence that silver nanoparticles<10 nm undergo a reversible structural transformation under hydrostatic pressures up to 10 GPa. Results for nanoparticles in the intermediate size range of 5 to 10 nm suggest a reversible linear pressure-dependent rhombohedral distortion which has not been previously observed in bulk silver. I propose a mechanism for this transitiion that considers the bond-length distribution in idealized multiply twinned icosahedral particles. Results for nanoparticles of 3.9 nm suggest a reversible linear pressure-dependent orthorhombic distortion. This distortion is interpreted in the context of idealized decahedral particles. In addition, given these size-dependent measurements of silver nanoparticle compression with pressure, we have constructed a pressure calibration curve. Encapsulating these silver nanoparticles in hollow metal oxide nanospheres then allows us to measure the pressure inside a nanoshell using x-ray diffraction. We demonstrate the measurement of pressure gradients across nanoshells and show that these nanoshells have maximum resolved shear strengths on the order of 500 MPa to IGPa.

  4. Evaluation of Postharvest Washing on Removal of Silver Nanoparticles (AgNPs) from Spinach Leaves.

    PubMed

    Zhang, Zhiyun; Guo, Huiyuan; Carlisle, Thomas; Mukherjee, Arnab; Kinchla, Amanda; White, Jason C; Xing, Baoshan; He, Lili

    2016-09-21

    There is increasing use of silver nanoparticles (AgNPs) as pesticides for fruits and vegetables due to the particles' unique antimicrobial and insecticidal properties. However, residual AgNPs in harvested produce may transfer through the food chain and pose a potential risk to public health. The objective of this study is to determine whether postharvest washing can effectively remove AgNPs that had accumulated on fresh produce. Ten microliters of commercially available 40 nm citrate coated AgNPs (0.4 mg/L) was dropped to a (1 × 1 cm(2)) spot on spinach leaves, followed by washing with deionized water (DI water), Tsunami 100 (80 mg/L), or Clorox bleach (200 mg/L). Then, the AgNP removal efficiency of the three treatments was evaluated by surface-enhanced Raman spectroscopy (SERS), scanning electron microscopy (SEM)-energy dispersive spectrometry (EDS), and inductively coupled plasma mass spectrometry (ICP-MS). ICP-MS results showed that deionized water removed statistically insignificant amounts of total Ag (5%), whereas Tsunami 100 and Clorox bleach yielded 21 and 10% decreases in total Ag, respectively (P < 0.05). The increased removal efficiency resulted from AgNP dissolution and Ag(+) release upon contact with the oxidizing agents in Tsunami 100 (peroxyacetic acid, hydrogen peroxide) and Clorox bleach (sodium hypochlorite). According to the SERS results, the deionized water and Tsunami 100 treatments removed nonsignificant amounts of AgNPs. Clorox bleach decreased Ag NPs by >90% (P < 0.05); however, SEM-EDS images revealed the formation of large silver chloride (AgCl) crystals (162 ± 51 nm) on the leaf, which explained the low total Ag removal from ICP-MS. This study indicates current factory washing methods for fresh produce may not be effective in reducing AgNPs (by water and Tsunami 100) and total Ag (by all three means). This highlights the necessity to develop an efficient washing method for NP removal from food surfaces in the future. PMID:27548506

  5. Evaluation of Postharvest Washing on Removal of Silver Nanoparticles (AgNPs) from Spinach Leaves.

    PubMed

    Zhang, Zhiyun; Guo, Huiyuan; Carlisle, Thomas; Mukherjee, Arnab; Kinchla, Amanda; White, Jason C; Xing, Baoshan; He, Lili

    2016-09-21

    There is increasing use of silver nanoparticles (AgNPs) as pesticides for fruits and vegetables due to the particles' unique antimicrobial and insecticidal properties. However, residual AgNPs in harvested produce may transfer through the food chain and pose a potential risk to public health. The objective of this study is to determine whether postharvest washing can effectively remove AgNPs that had accumulated on fresh produce. Ten microliters of commercially available 40 nm citrate coated AgNPs (0.4 mg/L) was dropped to a (1 × 1 cm(2)) spot on spinach leaves, followed by washing with deionized water (DI water), Tsunami 100 (80 mg/L), or Clorox bleach (200 mg/L). Then, the AgNP removal efficiency of the three treatments was evaluated by surface-enhanced Raman spectroscopy (SERS), scanning electron microscopy (SEM)-energy dispersive spectrometry (EDS), and inductively coupled plasma mass spectrometry (ICP-MS). ICP-MS results showed that deionized water removed statistically insignificant amounts of total Ag (5%), whereas Tsunami 100 and Clorox bleach yielded 21 and 10% decreases in total Ag, respectively (P < 0.05). The increased removal efficiency resulted from AgNP dissolution and Ag(+) release upon contact with the oxidizing agents in Tsunami 100 (peroxyacetic acid, hydrogen peroxide) and Clorox bleach (sodium hypochlorite). According to the SERS results, the deionized water and Tsunami 100 treatments removed nonsignificant amounts of AgNPs. Clorox bleach decreased Ag NPs by >90% (P < 0.05); however, SEM-EDS images revealed the formation of large silver chloride (AgCl) crystals (162 ± 51 nm) on the leaf, which explained the low total Ag removal from ICP-MS. This study indicates current factory washing methods for fresh produce may not be effective in reducing AgNPs (by water and Tsunami 100) and total Ag (by all three means). This highlights the necessity to develop an efficient washing method for NP removal from food surfaces in the future.

  6. Size analysis of nanoparticles extracted from W/O emulsions.

    PubMed

    Nagelreiter, C; Kotisch, H; Heuser, T; Valenta, C

    2015-07-01

    Nanosized particles are frequently used in many different applications, especially TiO2 nanoparticles as physical filters in sunscreens to protect the skin from UV radiation. However, concerns have arisen about possible health issues caused by nanoparticles and therefore, the assessment of the occurrence of nanoparticles is important in pharmaceutical and cosmetic formulations. In a previous work of our group, a method was presented to extract nanoparticles from O/W emulsions. But to respond to the needs of dry and sensitive skin, sunscreens of the water-in-oil emulsion type are available. In these, assessment of present nanoparticles is also an important issue, so the present study offers a method for extracting nanoparticles from W/O emulsions. Both methods emanate from the same starting point, which minimizes both effort and cost before the beginning of the assessment. By addition of NaOH pellets and centrifugation, particles were extracted from W/O emulsions and measured for their size and surface area by laser diffraction. With the simple equation Q=A/S a distinction between nanoparticles and microparticles was achieved in W/O emulsions, even in commercially available samples. The present method is quick and easy to implement, which makes it cost-effective. PMID:25907509

  7. Size analysis of nanoparticles extracted from W/O emulsions.

    PubMed

    Nagelreiter, C; Kotisch, H; Heuser, T; Valenta, C

    2015-07-01

    Nanosized particles are frequently used in many different applications, especially TiO2 nanoparticles as physical filters in sunscreens to protect the skin from UV radiation. However, concerns have arisen about possible health issues caused by nanoparticles and therefore, the assessment of the occurrence of nanoparticles is important in pharmaceutical and cosmetic formulations. In a previous work of our group, a method was presented to extract nanoparticles from O/W emulsions. But to respond to the needs of dry and sensitive skin, sunscreens of the water-in-oil emulsion type are available. In these, assessment of present nanoparticles is also an important issue, so the present study offers a method for extracting nanoparticles from W/O emulsions. Both methods emanate from the same starting point, which minimizes both effort and cost before the beginning of the assessment. By addition of NaOH pellets and centrifugation, particles were extracted from W/O emulsions and measured for their size and surface area by laser diffraction. With the simple equation Q=A/S a distinction between nanoparticles and microparticles was achieved in W/O emulsions, even in commercially available samples. The present method is quick and easy to implement, which makes it cost-effective.

  8. Fabrication of high aspect ratio nanogrid transparent electrodes via capillary assembly of Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Kang, Juhoon; Park, Chang-Goo; Lee, Su-Han; Cho, Changsoon; Choi, Dae-Geun; Lee, Jung-Yong

    2016-05-01

    In this report, we describe the fabrication of periodic Ag nanogrid electrodes by capillary assembly of silver nanoparticles (AgNPs) along patterned nanogrid templates. By assembling the AgNPs into these high-aspect-ratio nanogrid patterns, we can obtain high-aspect-ratio nanogratings, which can overcome the inherent trade-off between the optical transmittance and the sheet resistance of transparent electrodes. The junction resistance between the AgNPs is effectively reduced by photochemical welding and post-annealing. The fabricated high-aspect-ratio nanogrid structure with a line width of 150 nm and a height of 450 nm has a sheet resistance of 15.2 Ω sq-1 and an optical transmittance of 85.4%.In this report, we describe the fabrication of periodic Ag nanogrid electrodes by capillary assembly of silver nanoparticles (AgNPs) along patterned nanogrid templates. By assembling the AgNPs into these high-aspect-ratio nanogrid patterns, we can obtain high-aspect-ratio nanogratings, which can overcome the inherent trade-off between the optical transmittance and the sheet resistance of transparent electrodes. The junction resistance between the AgNPs is effectively reduced by photochemical welding and post-annealing. The fabricated high-aspect-ratio nanogrid structure with a line width of 150 nm and a height of 450 nm has a sheet resistance of 15.2 Ω sq-1 and an optical transmittance of 85.4%. Electronic supplementary information (ESI) available. See DOI: 10.1039/c6nr01896c

  9. In situ synthesis of size-controlled, stable silver nanoparticles within ultrashort peptide hydrogels and their anti-bacterial properties.

    PubMed

    Reithofer, Michael R; Lakshmanan, Anupama; Ping, Andy T K; Chin, Jia M; Hauser, Charlotte A E

    2014-08-01

    We have developed a silver-releasing biomaterial with promising potential for wound healing applications. The material is made of ultrashort peptides which can self-assemble in water to form hydrogels. Silver nanoparticles (Ag NPs) were synthesized in situ within the biomaterial, using only UV irradiation and no additional chemical reducing agents. The synthetic strategy allows precise control of the nanoparticle size, with the network of peptide fibers preventing aggregation of Ag NPs. The biomaterial shows increased mechanical strength compared to the hydrogel control. We observed a sustained release of Ag NPs over a period of 14 days. This is a crucial prerequisite for effective anti-bacterial therapy. The ability to inhibit bacterial growth was tested using different bacterial strains, namely gram-negative Escherichia coli and Pseudomonas aeruginosa and gram-positive Staphylococcus aureus. Inhibition of bacterial growth was observed for all strains. The best results were obtained for Pseudomonas aeruginosa which is known for exhibiting multidrug resistance. Biocompatibility studies on HDFa cells, using Ag NP-containing hydrogels, did not show any significant influence on cell viability. We propose this silver-releasing hydrogel as an excellent biomaterial with great potential for applications in wound healing due to its low silver content, sustained silver nanoparticle release and biocompatibility.

  10. Raman enhancement of rhodamine adsorbed on Ag nanoparticles self-assembled into nanowire-like arrays

    PubMed Central

    2011-01-01

    This work reports on Raman scattering of rhodamine (R6G) molecules absorbed on either randomly distributed or grating-like arrays of approximately 8-nm Ag nanoparticles developed by inert gas aggregation. Optimal growth and surface-enhanced Raman scattering (SERS) parameters have been obtained for the randomly distributed nanoparticles, while effects related to the aging of the silver nanoparticles were studied. Grating-like arrays of nanoparticles have been fabricated using line arrays templates formed either by fracture-induced structuring or by standard lithographic techniques. Grating structures fabricated by both methods exhibit an enhancement of the SERS signal, in comparison to the corresponding signal from randomly distributed Ag nanoparticles, as well as a preferential enhancement in the areas of the sharp features, and a dependence on the polarization direction of the incident exciting laser beam, with respect to the orientation of the gratings structuring. The observed spectroscopic features are consistent with a line-arrangement of hot-spots due to the self- alignment of metallic nanoparticles, induced by the grating-like templates. PMID:22168792

  11. M3Ag17(SPh)12 Nanoparticles and Their Structure Prediction.

    PubMed

    Wickramasinghe, Sameera; Atnagulov, Aydar; Yoon, Bokwon; Barnett, Robert N; Griffith, Wendell P; Landman, Uzi; Bigioni, Terry P

    2015-09-16

    Although silver nanoparticles are of great fundamental and practical interest, only one structure has been determined thus far: M4Ag44(SPh)30, where M is a monocation, and SPh is an aromatic thiolate ligand. This is in part due to the fact that no other molecular silver nanoparticles have been synthesized with aromatic thiolate ligands. Here we report the synthesis of M3Ag17(4-tert-butylbenzene-thiol)12, which has good stability and an unusual optical spectrum. We also present a rational strategy for predicting the structure of this molecule. First-principles calculations support the structural model, predict a HOMO-LUMO energy gap of 1.77 eV, and predict a new "monomer mount" capping motif, Ag(SR)3, for Ag nanoparticles. The calculated optical absorption spectrum is in good correspondence with the measured spectrum. Heteroatom substitution was also used as a structural probe. First-principles calculations based on the structural model predicted a strong preference for a single Au atom substitution in agreement with experiment.

  12. Repeated dose (28-day) administration of silver nanoparticles of varied size and coating does not significantly alter the indigenous murine gut microbiome.

    PubMed

    Wilding, Laura A; Bassis, Christine M; Walacavage, Kim; Hashway, Sara; Leroueil, Pascale R; Morishita, Masako; Maynard, Andrew D; Philbert, Martin A; Bergin, Ingrid L

    2016-01-01

    Silver nanoparticles (AgNPs) have been used as antimicrobials in a number of applications, including topical wound dressings and coatings for consumer products and biomedical devices. Ingestion is a relevant route of exposure for AgNPs, whether occurring unintentionally via Ag dissolution from consumer products, or intentionally from dietary supplements. AgNP have also been proposed as substitutes for antibiotics in animal feeds. While oral antibiotics are known to have significant effects on gut bacteria, the antimicrobial effects of ingested AgNPs on the indigenous microbiome or on gut pathogens are unknown. In addition, AgNP size and coating have been postulated as significantly influential towards their biochemical properties and the influence of these properties on antimicrobial efficacy is unknown. We evaluated murine gut microbial communities using culture-independent sequencing of 16S rRNA gene fragments following 28 days of repeated oral dosing of well-characterized AgNPs of two different sizes (20 and 110 nm) and coatings (PVP and Citrate). Irrespective of size or coating, oral administration of AgNPs at 10 mg/kg body weight/day did not alter the membership, structure or diversity of the murine gut microbiome. Thus, in contrast to effects of broad-spectrum antibiotics, repeat dosing of AgNP, at doses equivalent to 2000 times the oral reference dose and 100-400 times the effective in vitro anti-microbial concentration, does not affect the indigenous murine gut microbiome.

  13. [Preparation Polyacrylonitrile/Ag Nanoparticle Composite Nanofibers Via an Elelctrospinning Technique and Their Surface Enhanced Raman Scattering Study].

    PubMed

    Song, Wei; Li, Ting-ting; Wang, Xu; Zhao, Bing

    2015-07-01

    In this paper, we have prepared polyacrylonitrile (PAN) /Ag nanoparticle composite nanofibers as a surface enhanced Raman scattering (SERS) substrate via an electrospinning technique. First, the PAN and AgNO3 were dissolved in N, N'-dimethylformamide solvent to get PAN/Ag seed solution; then the PAN/Ag seed solution was electrospun for the preparation of PAN/Ag seed composite nanofibers; Finally, the PAN/Ag seed composite nanofibers were treated by hydrazine hydrate to syn- thesize PAN/Ag nanoparticle composite nanofibers. The as-prepared PAN/Ag nanoparticle composite nanofibers were mixed with the probes for the SERS detection to get the SERS spectrum of the probes. The PAN/Ag nanoparticle composite nanofibers substate showed a good SERS signal when the concentration of PATP is as low as 10(-6) mol x L(-1). Furthermore, this kind of SERS substrate could be large-scale prepared, which showed a high commercial value. PMID:26717748

  14. Kinetic stability of hematite nanoparticles: the effect ofparticle sizes

    SciTech Connect

    He, Y. thomas; Wan, Jiamin; Tokunaga, Tetsu

    2006-11-16

    Nanoparticles are ubiquitous in environment and arepotentially important in many environmental processes such as sorption,coprecipitation, redox reactions, and dissolution. To investigateparticle size effects on nanoparticle aggregation and stability, thisstudy tested aggregation behavior of 12(+-2), 32(+-3), and 65(+-3) nm(hydrated radius) hematite particles under environmental relevant pH andionic strength conditions. The results showed that at the same ionicstrength and pH conditions, different particle sizes show differenttendency to aggregate. At the same ionic strength, aggregation rates arehigher for smaller particles. The critical coagulation concentration alsodepends on particle size, and decreases as particle size decreases. Asthe particle size decreases, fast aggregation shifted to lower pH. Thismay be related to a dependence of PZC on particle size originating fromchange of structure and surface energy characteristics as particle sizedecreases. Under the same conditions, aggregation occurs faster asparticle concentration increases. Even though the nanoparticles ofdifferent sizes show different response to the same pH and ionicstrength, DLVO theory can be used to qualitatively understand hematitenanoparticle aggregation behavior.

  15. Synthesis, Characterizations of Superparamagnetic Fe3O4-Ag Hybrid Nanoparticles and Their Application for Highly Effective Bacteria Inactivation.

    PubMed

    Tung, Le Minh; Cong, Nguyen Xuan; Huy, Le Thanh; Lan, Nguyen Thi; Phan, Vu Ngoc; Hoa, Nguyen Quang; Vinh, Le Khanh; Thinh, Nguyen Viet; Tai, Le Thanh; Ngo, Duc-The; Mølhave, Kristian; Huy, Tran Quang; Le, Anh-Tuan

    2016-06-01

    In recent years, outbreaks of infectious diseases caused by pathogenic micro-organisms pose a serious threat to public health. In this work, Fe3O4-Ag hybrid nanoparticles were synthesized by simple chemistry method and these prepared nanoparticles were used to investigate their antibacterial properties and mechanism against methicilline-resistant Staphylococcus aureus (MRSA) pathogen. The formation of dimer-like nanostructure of Fe3O4-Ag hybrid NPs was confirmed by X-ray diffraction and High-resolution Transmission Electron Microscopy. Our biological analysis revealed that the Fe3O4-Ag hybrid NPs showed more noticeable bactericidal activity than that of plain Fe3O4 NPs and Ag-NPs. We suggest that the enhancement in bactericidal activity of Fe3O4-Ag hybrid NPs might be likely from main factors such as: (i) enhanced surface area property of hybrid nanoparticles; (ii) the high catalytic activity of Ag-NPs with good dispersion and aggregation stability due to the iron oxide magnetic carrier, and (iii) large direct physical contacts between the bacterial cell membrane and the hybrid nanoparticles. The superparamagnetic hybrid nanoparticles of iron oxide magnetic nanoparticles decorated with silver nanoparticles can be a potential candidate to effectively treat infectious MRSA pathogen with recyclable capability, targeted bactericidal delivery and minimum release into environment. PMID:27427651

  16. Microstructure of interface between Si chip and tape-type Ag nanoparticle sheet

    NASA Astrophysics Data System (ADS)

    Mutoh, Hayato; Moriyama, Naoki; Kaneko, Keiya; Miyazawa, Yasuyuki; Kida, Hitoshi

    2014-08-01

    A Ag nanoparticles-based technology for joining semiconductor materials through sintering has been developed. Currently, a paste consisting of Ag nanoparticles is used for die bonding in the electronics industry. A binder-free Ag nanojoining material has been developed for fabricating electronic devices. In this study, we investigated the joining ability of this binder-free tape-type Ag nanojoining material with respect to Si chips. A paste-type Ag nanojoining material that contained an organic binder was also investigated for comparison. The microstructures of the Si-joining material interfaces were observed using a focused ion beam system. The cleaved surfaces of the joints were observed using scanning electron microscopy. High-quality joints that contained only a few pores could be formed between a Au thin film electroplated on the Si chip and the tape-type material after sintering, owing to the simplicity of the joining process and the binder-free nature of the joining material.

  17. Color-Controlled Ag Nanoparticles and Nanorods within Confined Mesopores: Microwave-Assisted Rapid Synthesis and Application in Plasmonic Catalysis under Visible-Light Irradiation.

    PubMed

    Mori, Kohsuke; Verma, Priyanka; Hayashi, Ryunosuke; Fuku, Kojirou; Yamashita, Hiromi

    2015-08-10

    Color-controlled spherical Ag nanoparticles (NPs) and nanorods, with features that originate from their particle sizes and morphologies, can be synthesized within the mesoporous structure of SBA-15 by the rapid and uniform microwave (MW)-assisted alcohol reduction method in the absence or presence of surface-modifying organic ligands. The obtained several Ag catalysts exhibit different catalytic activities in the H2 production from ammonia borane (NH3 BH3 , AB) under dark conditions, and higher catalytic activity is observed by smaller yellow Ag NPs in spherical form. The catalytic activities are specifically enhanced under the light irradiation for all Ag catalysts. In particular, under light irradiation, the blue Ag nanorod shows a maximum enhancement of more than twice that observed in the dark. It should be noted that the order of increasing catalytic performance is in close agreement with the order of absorption intensity owing to the Ag localized surface plasmon resonance (LSPR) at irradiation light wavelength. Upon consideration of infrared thermal effect, wavelength dependence on catalytic activity, and effect of radical scavengers, it can be concluded that the dehydrogenation of AB is promoted by change of charge density of the Ag NP surface derived from LSPR. The LSPR-enhanced catalytic activity can be further realized in the tandem reaction consisting of dehydrogenation of AB and hydrogenation of 4-nitrophenol, in which a similar tendency in the enhancement of catalytic activity is observed.

  18. Size tuning of Ag-decorated TiO₂ nanotube arrays for improved bactericidal capacity of orthopedic implants.

    PubMed

    Esfandiari, N; Simchi, A; Bagheri, R

    2014-08-01

    Surface modification of orthopedic implants using titanium dioxide nanotubes and silver nanoparticles (SNs) is a promising approach to prevent bacteria adhesion, biofilm formation, and implant infection. Herein, we utilized a straightforward and all-solution process to prepare silver-decorated TiO2 nanotube arrays with surface density of 10(3) to 10(4) per µm(2). With controlling the synthesis conditions, hexagonal closed-packed nanotubes with opening diameter of 30-100 nm that are decorated with SNs with varying sizes (12-40 nm) were prepared. Various analytical techniques were utilized to characterize the size, morphology, distribution, valance state, surface roughness, and composition of the prepared antibacterial films. The bactericidal capacity of the films were studied on Escherichia coli (E. coli) by drop-test method and correlated with the size and percentage of Ag as well as the surface density of TiO2 nanotube arrays. Synergetic effect of TiO2 nanotubes and SNs on the antibacterial activity of the composite films is shown. The bactericidal capacity is found to depend on the size characteristics of the Ag-TiO2 coating. The highest antibacterial activity is obtained for TiO2 nanotubes with opening diameter of about 100 nm and SNs with an average size of 20 nm. MTT assay using osteoblast MG63 cells was performed to examine the cell viability. We suggest that release rate of the silver ions is an important factor controlling the antibacterial activity. Additionally, the size dependency of the bactericidal capacity implies that electrical coupling between silver and TiO2 nanotubes and improved hydrophobicity of the coating might influence the bacterial behavior of the hybrid nanostructures.

  19. Natural water as the test medium for Ag and CuO nanoparticle hazard evaluation: An interlaboratory case study.

    PubMed

    Heinlaan, Margit; Muna, Marge; Knöbel, Melanie; Kistler, David; Odzak, Niksa; Kühnel, Dana; Müller, Josefine; Gupta, Govind Sharan; Kumar, Ashutosh; Shanker, Rishi; Sigg, Laura

    2016-09-01

    Engineered nanoparticles (NPs) have realistic potential of reaching natural waterbodies and of exerting toxicity to freshwater organisms. The toxicity may be influenced by the composition of natural waters as crucial NP properties are influenced by water constituents. To tackle this issue, a case study was set up in the framework of EU FP7 NanoValid project, performing an interlaboratory hazard evaluation of NPs in natural freshwater. Ag and CuO NPs were selected as model NPs because of their potentially high toxicity in the freshwater. Daphnia magna (OECD202) and Danio rerio embryo (OECD236) assays were used to evaluate NP toxicity in natural water, sampled from Lake Greifen and Lake Lucerne (Switzerland). Dissolution of the NPs was evaluated by ultrafiltration, ultracentrifugation and metal specific sensor bacteria. Ag NP size was stable in natural water while CuO NPs agglomerated and settled rapidly. Ag NP suspensions contained a large fraction of Ag(+) ions and CuO NP suspensions had low concentration of Cu(2+) ions. Ag NPs were very toxic (48 h EC50 1-5.5 μg Ag/L) to D. magna as well as to D. rerio embryos (96 h EC50 8.8-61 μg Ag/L) in both standard media and natural waters with results in good agreement between laboratories. CuO NP toxicity to D. magna differed significantly between the laboratories with 48 h EC50 0.9-11 mg Cu/L in standard media, 5.7-75 mg Cu/L in Lake Greifen and 5.5-26 mg Cu/L in Lake Lucerne. No toxicity of CuO NP to zebrafish embryos was detected up to 100 mg/L independent of the medium used. The results show that Ag and CuO NP toxicity may be higher in natural water than in the standard media due to differences in composition. NP environmental hazard evaluation can and should be carried out in natural water to obtain more realistic estimates on the toxicity.

  20. Natural water as the test medium for Ag and CuO nanoparticle hazard evaluation: An interlaboratory case study.

    PubMed

    Heinlaan, Margit; Muna, Marge; Knöbel, Melanie; Kistler, David; Odzak, Niksa; Kühnel, Dana; Müller, Josefine; Gupta, Govind Sharan; Kumar, Ashutosh; Shanker, Rishi; Sigg, Laura

    2016-09-01

    Engineered nanoparticles (NPs) have realistic potential of reaching natural waterbodies and of exerting toxicity to freshwater organisms. The toxicity may be influenced by the composition of natural waters as crucial NP properties are influenced by water constituents. To tackle this issue, a case study was set up in the framework of EU FP7 NanoValid project, performing an interlaboratory hazard evaluation of NPs in natural freshwater. Ag and CuO NPs were selected as model NPs because of their potentially high toxicity in the freshwater. Daphnia magna (OECD202) and Danio rerio embryo (OECD236) assays were used to evaluate NP toxicity in natural water, sampled from Lake Greifen and Lake Lucerne (Switzerland). Dissolution of the NPs was evaluated by ultrafiltration, ultracentrifugation and metal specific sensor bacteria. Ag NP size was stable in natural water while CuO NPs agglomerated and settled rapidly. Ag NP suspensions contained a large fraction of Ag(+) ions and CuO NP suspensions had low concentration of Cu(2+) ions. Ag NPs were very toxic (48 h EC50 1-5.5 μg Ag/L) to D. magna as well as to D. rerio embryos (96 h EC50 8.8-61 μg Ag/L) in both standard media and natural waters with results in good agreement between laboratories. CuO NP toxicity to D. magna differed significantly between the laboratories with 48 h EC50 0.9-11 mg Cu/L in standard media, 5.7-75 mg Cu/L in Lake Greifen and 5.5-26 mg Cu/L in Lake Lucerne. No toxicity of CuO NP to zebrafish embryos was detected up to 100 mg/L independent of the medium used. The results show that Ag and CuO NP toxicity may be higher in natural water than in the standard media due to differences in composition. NP environmental hazard evaluation can and should be carried out in natural water to obtain more realistic estimates on the toxicity. PMID:27357482

  1. Ag2CrO4 nanoparticles loaded on two-dimensional large surface area graphite-like carbon nitride sheets: simple synthesis and excellent photocatalytic performance.

    PubMed

    Shi, Lei; Liang, Lin; Wang, Fangxiao; Liu, Mengshuai; Sun, Jianmin

    2016-04-01

    Graphite-like carbon nitride (g-C3N4) with a large surface area was prepared through thermal condensation of guanidine hydrochloride at 650 °C. Various amounts of silver chromate (Ag2CrO4) nanoparticles with small size were highly loaded on the g-C3N4 by a simple co-precipitation method at room temperature. The chemical constituents, surface structure and optical properties of the resultant Ag2CrO4/g-C3N4 composites were thoroughly characterized. And the photocatalytic performances were evaluated by degradation of Rhodamine B (RhB) and phenol, the experimental results indicated that the as-prepared Ag2CrO4/g-C3N4 composites presented excellent photocatalytic activity under visible-light irradiation. With the mass ratio of Ag2CrO4 to g-C3N4 at 1 : 2, the Ag2CrO4/g-C3N4 composites exhibited optimal photocatalytic activity for degrading RhB, approximately 6.1 and 10.4 times higher than those on pure g-C3N4 and bare Ag2CrO4 particles. The improved photocatalytic activity was mainly attributed to the combined effect including the larger surface area, highly dispersed smaller Ag2CrO4 nanoparticles, stronger visible absorption and higher charge separation efficiency of the Ag2CrO4/g-C3N4 composites. Moreover, the possible mechanism for the photocatalytic activity was tentatively proposed.

  2. Ag2CrO4 nanoparticles loaded on two-dimensional large surface area graphite-like carbon nitride sheets: simple synthesis and excellent photocatalytic performance.

    PubMed

    Shi, Lei; Liang, Lin; Wang, Fangxiao; Liu, Mengshuai; Sun, Jianmin

    2016-04-01

    Graphite-like carbon nitride (g-C3N4) with a large surface area was prepared through thermal condensation of guanidine hydrochloride at 650 °C. Various amounts of silver chromate (Ag2CrO4) nanoparticles with small size were highly loaded on the g-C3N4 by a simple co-precipitation method at room temperature. The chemical constituents, surface structure and optical properties of the resultant Ag2CrO4/g-C3N4 composites were thoroughly characterized. And the photocatalytic performances were evaluated by degradation of Rhodamine B (RhB) and phenol, the experimental results indicated that the as-prepared Ag2CrO4/g-C3N4 composites presented excellent photocatalytic activity under visible-light irradiation. With the mass ratio of Ag2CrO4 to g-C3N4 at 1 : 2, the Ag2CrO4/g-C3N4 composites exhibited optimal photocatalytic activity for degrading RhB, approximately 6.1 and 10.4 times higher than those on pure g-C3N4 and bare Ag2CrO4 particles. The improved photocatalytic activity was mainly attributed to the combined effect including the larger surface area, highly dispersed smaller Ag2CrO4 nanoparticles, stronger visible absorption and higher charge separation efficiency of the Ag2CrO4/g-C3N4 composites. Moreover, the possible mechanism for the photocatalytic activity was tentatively proposed. PMID:26937621

  3. Size-dependent magnetic properties of iron oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Patsula, Vitalii; Moskvin, Maksym; Dutz, Silvio; Horák, Daniel

    2016-01-01

    Uniform iron oxide nanoparticles in the size range from 10 to 24 nm and polydisperse 14 nm iron oxide particles were prepared by thermal decomposition of Fe(III) carboxylates in the presence of oleic acid and co-precipitation of Fe(II) and Fe(III) chlorides by ammonium hydroxide followed by oxidation, respectively. While the first method produced hydrophobic oleic acid coated particles, the second one formed hydrophilic, but uncoated, nanoparticles. To make the iron oxide particles water dispersible and colloidally stable, their surface was modified with poly(ethylene glycol) and sucrose, respectively. Size and size distribution of the nanoparticles was determined by transmission electron microscopy, dynamic light scattering and X-ray diffraction. Surface of the PEG-functionalized and sucrose-modified iron oxide particles was characterized by Fourier transform infrared (FT-IR) and Raman spectroscopy and thermogravimetric analysis (TGA). Magnetic properties were measured by means of vibration sample magnetometry and specific absorption rate in alternating magnetic fields was determined calorimetrically. It was found, that larger ferrimagnetic particles showed higher heating performance than smaller superparamagnetic ones. In the transition range between superparamagnetism and ferrimagnetism, samples with a broader size distribution provided higher heating power than narrow size distributed particles of comparable mean size. Here presented particles showed promising properties for a possible application in magnetic hyperthermia.

  4. Coupling of Ag Nanoparticle with Inverse Opal Photonic Crystals as a Novel Strategy for Upconversion Emission Enhancement of NaYF4: Yb(3+), Er(3+) Nanoparticles.

    PubMed

    Shao, Bo; Yang, Zhengwen; Wang, Yida; Li, Jun; Yang, Jianzhi; Qiu, Jianbei; Song, Zhiguo

    2015-11-18

    Rare-earth-ion-doped upconversion (UC) nanoparticles have generated considerable interest because of their potential application in solar cells, biological labeling, therapeutics, and imaging. However, the applications of UC nanoparticles were still limited because of their low emission efficiency. Photonic crystals and noble metal nanoparticles are applied extensively to enhance the UC emission of rare earth ions. In the present work, a novel substrate consisting of inverse opal photonic crystals and Ag nanoparticles was prepared by the template-assisted method, which was used to enhance the UC emission of NaYF4: Yb(3+), Er(3+) nanoparticles. The red or green UC emissions of NaYF4: Yb(3+), Er(3+) nanoparticles were selectively enhanced on the inverse opal substrates because of the Bragg reflection of the photonic band gap. Additionally, the UC emission enhancement of NaYF4: Yb(3+), Er(3+) nanoparticles induced by the coupling of metal nanoparticle plasmons and photonic crystal effects was realized on the Ag nanoparticles included in the inverse opal substrate. The present results demonstrated that coupling of Ag nanoparticle with inverse opal photonic crystals provides a useful strategy to enhance UC emission of rare-earth-ion-doped nanoparticles. PMID:26496243

  5. Coupling of Ag Nanoparticle with Inverse Opal Photonic Crystals as a Novel Strategy for Upconversion Emission Enhancement of NaYF4: Yb(3+), Er(3+) Nanoparticles.

    PubMed

    Shao, Bo; Yang, Zhengwen; Wang, Yida; Li, Jun; Yang, Jianzhi; Qiu, Jianbei; Song, Zhiguo

    2015-11-18

    Rare-earth-ion-doped upconversion (UC) nanoparticles have generated considerable interest because of their potential application in solar cells, biological labeling, therapeutics, and imaging. However, the applications of UC nanoparticles were still limited because of their low emission efficiency. Photonic crystals and noble metal nanoparticles are applied extensively to enhance the UC emission of rare earth ions. In the present work, a novel substrate consisting of inverse opal photonic crystals and Ag nanoparticles was prepared by the template-assisted method, which was used to enhance the UC emission of NaYF4: Yb(3+), Er(3+) nanoparticles. The red or green UC emissions of NaYF4: Yb(3+), Er(3+) nanoparticles were selectively enhanced on the inverse opal substrates because of the Bragg reflection of the photonic band gap. Additionally, the UC emission enhancement of NaYF4: Yb(3+), Er(3+) nanoparticles induced by the coupling of metal nanoparticle plasmons and photonic crystal effects was realized on the Ag nanoparticles included in the inverse opal substrate. The present results demonstrated that coupling of Ag nanoparticle with inverse opal photonic crystals provides a useful strategy to enhance UC emission of rare-earth-ion-doped nanoparticles.

  6. An evaluation of the influence of size and radiation in silver nanoparticle toxicity

    EPA Science Inventory

    The antimicrobial properties of silver nanoparticles (AgNP) have made them popular in textile manufacturing, medical technology, and biomedical applications. Studies suggest that after ingestion, nanomaterials are distributed throughout the body to different organs, possibly incl...

  7. Photocatalytic Properties of TiO2 Thin Films Modified with Ag and Pt Nanoparticles Deposited by Gas Flow Sputtering.

    PubMed

    Maicu, M; Glöss, D; Frach, Peter; Hecker, D; Gerlach, G; Córdoba, José M

    2015-09-01

    In this work, a gas flow sputtering (GFS) process which allows the production and deposition of metal nanoparticles (NPs) in a vacuum environment is described. Aim of the study is to prove the potential of this technology for the fabrication of new TiO2 films with enhanced photocatalytic properties. For this purpose, Ag and Pt NPs have been produced and deposited on photocatalytic float glass coated with TiO2 thin films by magnetron sputtering. The influence of the process parameters and of the metal amount on the final properties of the particles (quantity, size, size distribution, oxidation state etc.,) was widely investigated. Moreover, the effect of the NPs on the photocatalytic activity of the resulting materials was evaluated for the case of the decomposition of stearic acid (SA) during UV-A irradiation. The reduction of the water contact angle (WCA) during the irradiation period was measured in order to test the photo-induced super-hydrophilicity (PSH).

  8. Size Selective Green Synthesis of Silver and Gold Nanoparticles: Enhanced Antibacterial Efficacy of Resveratrol Capped Silver Sol.

    PubMed

    Shukla, Shashi P; Roy, Mainak; Mukherjee, Poulomi; Das, Laboni; Neogy, Suman; Srivastava, Dinesh; Adhikari, Soumyakanti

    2016-03-01

    In view of potential biomedical application of the noble metal nanoparticles, we report a size controlled yet simple and green synthesis of resveratrol stabilized silver and gold nanoparticles having low polydispersity of size. Here, resveratrol plays two simultaneous roles, reducing the metal ions and providing efficient capping of the small nanoparticles. This gives rise to specific size of silver and gold nanoparticles at specific ratios of metal to resveratrol. The particles have been characterized by XRD and transmission electron microscopy. The nanoparticle sols are stable for months. The UV Visible absorption spectra of the silver sol show the plasmon peak of spherical nanoparticles, presence of which is further reflected in the TEM images. Size of the silver particles obtained is in between 11 to 21 nm depending on the ratio of resveratrol to metal ion used. Resveratrol capped silver nanoparticles exhibit high antibacterial activity against Gram negative wild type E coli BW (25113). The minimum inhibitory concentration (MIC) of nano-silver against the bacterium has been estimated to be 6.48 μg/ml, which is significantly lower than that reported in some earlier as well as recent publications. Reaction of gold ions with resveratrol, on the other hand, produces gold nanoparticles of sizes varying from 7 to 29 nm at different ratios of resveratrol to the metal ions. Particles with higher size and aspect ratio are formed at lower concentration of the capping agent whereas particles with very small size and pseudo-spherical morphology are formed at higher capping concentration. Difference in the formation kinetics of silver and gold nanoparticles has been attributed to the different growth mechanisms in the two cases. Possible modes of anchorage of resveratrol to silver nanoparticles have been investigated using surface enhanced resonance Raman spectroscopy (SERS) which shows that the silver nanoparticles are capped by resveratrol molecule primarily through O-Ag

  9. In situ assembly of well-dispersed Ag nanoparticles (AgNPs) on electrospun carbon nanofibers (CNFs) for catalytic reduction of 4-nitrophenol.

    PubMed

    Zhang, Peng; Shao, Changlu; Zhang, Zhenyi; Zhang, Mingyi; Mu, Jingbo; Guo, Zengcai; Liu, Yichun

    2011-08-01

    Carbon nanofibers/silver nanoparticles (CNFs/AgNPs) composite nanofibers were fabricated by two steps consisting of the preparation of the CNFs by electrospinning and the hydrothermal growth of the AgNPs on the CNFs. The as-prepared nanofibers were characterized by scanning electron microscopy, energy dispersive spectroscopy, transmission electron microscopy, X-ray diffraction, resonant Raman spectra, thermal gravimetric and differential thermal analysis, and X-ray photoelectron spectroscopy, respectively. The results indicated that not only were AgNPs (25-50 nm) successfully grown on the CNFs but also the AgNPs were distributed without aggregation on the CNFs. Further more, by adjusting the parameters in hydrothermal processing, the content of silver supported on the CNFs could be easily controlled. The catalytic activities of the CNFs/AgNPs composite nanofibers to the reduction of 4-nitrophenol (4-NP) with NaBH(4) were tracked by UV-visible spectroscopy. It was suggested that the CNFs/AgNPs composite nanofibers exhibited high catalytic activity in the reduction of 4-NP, which might be attributed to the high surface areas of AgNPs and synergistic effect on delivery of electrons between CNFs and AgNPs. And, the catalytic efficiency was enhanced with the increasing of the content of silver on the CNFs/AgNPs composite nanofibers. Notably, the CNFs/AgNPs composite nanofibers could be easily recycled due to their one-dimensional nanostructural property.

  10. Plasmonic core-shell nanoparticles for SERS detection of the pesticide thiram: size- and shape-dependent Raman enhancement.

    PubMed

    Guo, Pengzhen; Sikdar, Debabrata; Huang, Xiqiang; Si, Kae Jye; Xiong, Wei; Gong, Shu; Yap, Lim Wei; Premaratne, Malin; Cheng, Wenlong

    2015-02-21

    We systematically investigated the size- and shape-dependent SERS activities of plasmonic core-shell nanoparticles towards detection of the pesticide thiram. Monodisperse Au@Ag nanocubes (NCs) and Au@Ag nanocuboids (NBs) were synthesized and their Ag shell thickness was precisely adjusted from ∼1 nm to ∼16 nm. All these nanoparticles were used as SERS substrates for thiram detection, and the Raman intensities with three different lasers (514 nm, 633 nm and 782 nm) were recorded and compared. Our results clearly show that: (1) the excitation wavelength discriminated particle shapes regardless of particle sizes, and the maximized Raman enhancement was observed when the excitation wavelength approaches the SERS peak (provided there is significant local electric field confinement on the plasmonic nanostructures at that wavelength); (2) at the optimized laser wavelength, the maximum Raman enhancement was achieved at a certain threshold of particle size (or silver coating thickness). By exciting particles at their optimized sizes with the corresponding optimized laser wavelengths, we achieved a detection limit of roughly around 100 pM and 80 pM for NCs and NBs, respectively.

  11. Liquid-liquid interface assisted synthesis of size- and thickness-controlled Ag nanoplates

    SciTech Connect

    Jin Mingshang; Kuang Qin; Han Xiguang; Xie Shuifen; Xie Zhaoxiong; Zheng Lansun

    2010-06-15

    Here we proposed a synthetic method of high-purity Ag nanoplates by the reduction of aqueous Ag{sup +} ions at the aqueous-organic interface with the reductant ferrocene. We demonstrated that the as-prepared Ag nanoplates can be widely tunable from 600 nm to 7 {mu}m in size and from 10 to 35 nm in thickness, simply by adjusting the component of organic phase. To our knowledge, there are few methods to tailor the size and the thickness of metal nanoplates in such a large range although many efforts have been made aiming to realize it. Our proposed synthetic strategy is rapid, template-free, seed-less, and high-yield, and could be applied to synthesize analogous two-dimensional nanostructures of other noble metals, such as Pt, Au, and Pd. - Graphical abstract: High-purity Ag nanoplates were synthesized by the reduction of aqueous Ag{sup +} ions at the aqueous-organic interface with the reductant ferrocene, the size and thickness of which were widely tunable.

  12. Selective photochemical synthesis of Ag nanoparticles on position-controlled ZnO nanorods for the enhancement of yellow-green light emission

    NASA Astrophysics Data System (ADS)

    Park, Hyeong-Ho; Zhang, Xin; Lee, Keun Woo; Sohn, Ahrum; Kim, Dong-Wook; Kim, Joondong; Song, Jin-Won; Choi, Young Su; Lee, Hee Kwan; Jung, Sang Hyun; Lee, In-Geun; Cho, Young-Dae; Shin, Hyun-Beom; Sung, Ho Kun; Park, Kyung Ho; Kang, Ho Kwan; Park, Won-Kyu; Park, Hyung-Ho

    2015-12-01

    A novel technique for the selective photochemical synthesis of silver (Ag) nanoparticles (NPs) on ZnO nanorod arrays is established by combining ultraviolet-assisted nanoimprint lithography (UV-NIL) for the definition of growth sites, hydrothermal reaction for the position-controlled growth of ZnO nanorods, and photochemical reduction for the decoration of Ag NPs on the ZnO nanorods. During photochemical reduction, the size distribution and loading of Ag NPs on ZnO nanorods can be tuned by varying the UV-irradiation time. The photochemical reduction is hypothesized to facilitate the adsorbed citrate ions on the surface of ZnO, allowing Ag ions to preferentially form Ag NPs on ZnO nanorods. The ratio of visible emission to ultraviolet (UV) emission for the Ag NP-decorated ZnO nanorod arrays, synthesized for 30 min, is 20.5 times that for the ZnO nanorod arrays without Ag NPs. The enhancement of the visible emission is believed to associate with the surface plasmon (SP) effect of Ag NPs. The Ag NP-decorated ZnO nanorod arrays show significant SP-induced enhancement of yellow-green light emission, which could be useful in optoelectronic applications. The technique developed here requires low processing temperatures (120 °C and lower) and no high-vacuum deposition tools, suitable for applications such as flexible electronics.A novel technique for the selective photochemical synthesis of silver (Ag) nanoparticles (NPs) on ZnO nanorod arrays is established by combining ultraviolet-assisted nanoimprint lithography (UV-NIL) for the definition of growth sites, hydrothermal reaction for the position-controlled growth of ZnO nanorods, and photochemical reduction for the decoration of Ag NPs on the ZnO nanorods. During photochemical reduction, the size distribution and loading of Ag NPs on ZnO nanorods can be tuned by varying the UV-irradiation time. The photochemical reduction is hypothesized to facilitate the adsorbed citrate ions on the surface of ZnO, allowing Ag ions to

  13. Modulation of Human Macrophage Responses to Mycobacterium tuberculosis by Silver Nanoparticles of Different Size and Surface Modification

    PubMed Central

    Sarkar, Srijata; Leo, Bey Fen; Carranza, Claudia; Chen, Shu; Rivas-Santiago, Cesar; Porter, Alexandra E.; Ryan, Mary P.; Gow, Andrew; Chung, Kian Fan; Tetley, Teresa D.; Zhang, Junfeng (Jim); Georgopoulos, Panos G.; Ohman-Strickland, Pamela A.; Schwander, Stephan

    2015-01-01

    Exposure to silver nanoparticles (AgNP) used in consumer products carries potential health risks including increased susceptibility to infectious pathogens. Systematic assessments of antimicrobial macrophage immune responses in the context of AgNP exposure are important because uptake of AgNP by macrophages may lead to alterations of innate immune cell functions. In this study we examined the effects of exposure to AgNP with different particle sizes (20 and 110 nm diameters) and surface chemistry (citrate or polyvinlypyrrolidone capping) on cellular toxicity and innate immune responses against Mycobacterium tuberculosis (M.tb) by human monocyte-derived macrophages (MDM). Exposures of MDM to AgNP significantly reduced cellular viability, increased IL8 and decreased IL10 mRNA expression. Exposure of M.tb-infected MDM to AgNP suppressed M.tb-induced expression of IL1B, IL10, and TNFA mRNA. Furthermore, M.tb-induced IL-1β, a cytokine critical for host resistance to M.tb, was inhibited by AgNP but not by carbon black particles indicating that the observed immunosuppressive effects of AgNP are particle specific. Suppressive effects of AgNP on the M.tb-induced host immune responses were in part due to AgNP-mediated interferences with the TLR signaling pathways that culminate in the activation of the transcription factor NF-κB. AgNP exposure suppressed M.tb-induced expression of a subset of NF-κB mediated genes (CSF2, CSF3, IFNG, IL1A, IL1B, IL6, IL10, TNFA, NFKB1A). In addition, AgNP exposure increased the expression of HSPA1A mRNA and the corresponding stress-induced Hsp72 protein. Up-regulation of Hsp72 by AgNP can suppress M.tb-induced NF-κB activation and host immune responses. The observed ability of AgNP to modulate infectious pathogen-induced immune responses has important public health implications. PMID:26580078

  14. Modulation of Human Macrophage Responses to Mycobacterium tuberculosis by Silver Nanoparticles of Different Size and Surface Modification.

    PubMed

    Sarkar, Srijata; Leo, Bey Fen; Carranza, Claudia; Chen, Shu; Rivas-Santiago, Cesar; Porter, Alexandra E; Ryan, Mary P; Gow, Andrew; Chung, Kian Fan; Tetley, Teresa D; Zhang, Junfeng Jim; Georgopoulos, Panos G; Ohman-Strickland, Pamela A; Schwander, Stephan

    2015-01-01

    Exposure to silver nanoparticles (AgNP) used in consumer products carries potential health risks including increased susceptibility to infectious pathogens. Systematic assessments of antimicrobial macrophage immune responses in the context of AgNP exposure are important because uptake of AgNP by macrophages may lead to alterations of innate immune cell functions. In this study we examined the effects of exposure to AgNP with different particle sizes (20 and 110 nm diameters) and surface chemistry (citrate or polyvinlypyrrolidone capping) on cellular toxicity and innate immune responses against Mycobacterium tuberculosis (M.tb) by human monocyte-derived macrophages (MDM). Exposures of MDM to AgNP significantly reduced cellular viability, increased IL8 and decreased IL10 mRNA expression. Exposure of M.tb-infected MDM to AgNP suppressed M.tb-induced expression of IL1B, IL10, and TNFA mRNA. Furthermore, M.tb-induced IL-1β, a cytokine critical for host resistance to M.tb, was inhibited by AgNP but not by carbon black particles indicating that the observed immunosuppressive effects of AgNP are particle specific. Suppressive effects of AgNP on the M.tb-induced host immune responses were in part due to AgNP-mediated interferences with the TLR signaling pathways that culminate in the activation of the transcription factor NF-κB. AgNP exposure suppressed M.tb-induced expression of a subset of NF-κB mediated genes (CSF2, CSF3, IFNG, IL1A, IL1B, IL6, IL10, TNFA, NFKB1A). In addition, AgNP exposure increased the expression of HSPA1A mRNA and the corresponding stress-induced Hsp72 protein. Up-regulation of Hsp72 by AgNP can suppress M.tb-induced NF-κB activation and host immune responses. The observed ability of AgNP to modulate infectious pathogen-induced immune responses has important public health implications. PMID:26580078

  15. Green synthesis and applications of Au-Ag bimetallic nanoparticles

    NASA Astrophysics Data System (ADS)

    Meena Kumari, M.; Jacob, John; Philip, Daizy

    2015-02-01

    This paper reports for the first time the synthesis of bimetallic nanoparticles at room temperature using the fruit juice of pomegranate. Simultaneous reduction of gold and silver ions in different molar ratios leads to the formation of alloy as well as core-shell nanostructures. The nanoparticles have been characterized using UV-vis spectroscopy, transmission electron microscopy, Fourier Transform Infrared Spectroscopy and X-ray diffraction. The synthesized alloy particles are used as catalysts in the reduction of 2-, 3-, 4-nitrophenols to the corresponding amines and in the degradation of methyl orange. The reduction kinetics for all the reactions follows pseudo-first order. The rate constants follow the order k4-nitrophenol < k2-nitrophenol < k3-nitrophenol. Thermal conductivity is measured as a function of volume fraction and it is observed that the incorporation of the alloy nanoparticles enhances the thermal conductivity of the base fluid (water) showing nanofluid application. The nitric oxide and hydroxyl radical scavenging activity shown by the nanoparticles promise the potential application in biomedical field.

  16. Green synthesis and applications of Au-Ag bimetallic nanoparticles.

    PubMed

    Meena Kumari, M; Jacob, John; Philip, Daizy

    2015-02-25

    This paper reports for the first time the synthesis of bimetallic nanoparticles at room temperature using the fruit juice of pomegranate. Simultaneous reduction of gold and silver ions in different molar ratios leads to the formation of alloy as well as core-shell nanostructures. The nanoparticles have been characterized using UV-vis spectroscopy, transmission electron microscopy, Fourier Transform Infrared Spectroscopy and X-ray diffraction. The synthesized alloy particles are used as catalysts in the reduction of 2-, 3-, 4-nitrophenols to the corresponding amines and in the degradation of methyl orange. The reduction kinetics for all the reactions follows pseudo-first order. The rate constants follow the order k4-nitrophenolnanoparticles enhances the thermal conductivity of the base fluid (water) showing nanofluid application. The nitric oxide and hydroxyl radical scavenging activity shown by the nanoparticles promise the potential application in biomedical field. PMID:25218228

  17. Size distribution effects on the fate and transport of nanoparticles in porous media

    NASA Astrophysics Data System (ADS)

    Taghavy, A.; Abriola, L. M.

    2013-12-01

    Application of conventional continuum-based particle transport models generally requires implementing a single representative particle diameter as a model input parameter. In reality however, particles typically exhibit a particle size distribution (PSD). The implications of this simplification on the prediction of nanoparticle (NP) transport, attachment, and reaction, however, have not been systematically explored. In this presentation, we present a one-dimensional random-walk particle-tracking (RWPT) transport model capable of accounting for NPs that exhibit a size distribution. The model is implemented in a previously developed and verified hybrid Eulerian-Lagrangian particle (HELP) simulator and applied to quantify the potential approximation that is associated with an 'average particle' approach to representing poly-dispersed populations of NPs. Porous medium, flow, and NP properties are chosen consistent with those reported in a previous transport column study for silver NPs (nAg). Particles from a poly-dispersed (PD) family and a representative mono-dispersed (MD) family, with a diameter equal to the mass-based average of particle diameters from the former family, are numerically introduced into a sand column. PD particles are either normally distributed or from an experimental PSD. Simulation results explore the influence of the PSD on (1) the transport of stable suspensions of nanoparticles, and (2) the fate of reactive nanoparticles (e.g., nAg dissolution). Our findings suggest that use of an 'average particle' approach yields a different pattern for the spatial retention of NPs and underestimates the overall dissolution reaction kinetics, in comparison to predictions derived using a more realistic PSD.

  18. Porous silicon nanowire arrays decorated by Ag nanoparticles for surface enhanced Raman scattering study

    NASA Astrophysics Data System (ADS)

    Su, L.; Xu, H. J.; Chan, Y. F.; Sun, X. M.

    2012-02-01

    A large scale and highly ordered Ag nanoparticle-decorated porous silicon nanowire array was fabricated for a uniform and reproducible surface-enhanced Raman scattering (SERS) substrate. The overall process for the proposed structure is simple and reliable with the use of only chemical etching and metal reduction processes. The SERS sensitivity of the novel substrate as low as 10-16 M for rhodamine 6G (R6G) and the Raman enhancement factor as high as 10^14 were obtained. The excellent SERS performances were mainly attributed to the strong local electromagnetic effect which is associated with the formation of large-quantity Ag nanoparticles on porous silicon nanowire array and the existence of semiconductor silicon nanowires. Significantly, the quadratic relation between the logarithmic concentrations and the logarithmic integrated Raman peak intensities provided quantitative detection of R6G. Our results open new possibilities for applying SERS to trace detection of low-concentration biomolecules.

  19. Changes in silver nanoparticles exposed to human synthetic stomach fluid: Effectsof particle size and surface chemistry

    EPA Science Inventory

    The significant rise in consumer products and applications utilizing the antibacterial properties of silver nanoparticles (AgNPs) has increased the possibility of human exposure. The mobility and bioavailability of AgNPs through the ingestion pathway will depend, in part, on prop...

  20. Tuning the properties of ZnO, hematite, and Ag nanoparticles by adjusting the surface charge.

    PubMed

    Zhang, Jianhui; Dong, Guanjun; Thurber, Aaron; Hou, Yayi; Gu, Min; Tenne, Dmitri A; Hanna, C B; Punnoose, Alex

    2012-03-01

    A poly (acryl acid) (PAA) post-treatment method is performed to modify the surface charge of ZnO nanospheres, hematite nanocubes, and Ag nanoprisms from highly positive to very negative by adjusting the PAA concentration, to and greatly modify their photoluminescence, cytotoxicity, magnetism, and surface plasmon resonance. This method provides a general way to tune the nanoparticle properties for broad physicochemical and biological applications. PMID:22298490

  1. Investigation of magnetic field enriched surface enhanced resonance Raman scattering performance using Fe3O4@Ag nanoparticles for malaria diagnosis

    NASA Astrophysics Data System (ADS)

    Yuen, Clement; Liu, Quan

    2014-03-01

    Recently, we have demonstrated the magnetic field-enriched surface-enhanced resonance Raman spectroscopy (SERRS) of β-hematin by using nanoparticles with iron oxide core and silver shell (Fe3O4@Ag) for the potential application in the early malaria diagnosis. In this study, we investigate the dependence of the magnetic field-enriched SERRS performance of β-hematin on the different core and shell sizes of the Fe3O4@Ag nanoparticles. We note that the core and shell parameters are critical in the realization of the optimal magnetic field-enrich SERRS β-hematin signal. These results are consistent with our simulations that will guide the optimization of the magnetic SERRS performance for the potential early diagnosis in the malaria disease.

  2. Fabrication of Au@Ag core-shell nanoparticles using polyelectrolyte multilayers as nanoreactors.

    PubMed

    Zhang, Xin; Wang, Hui; Su, Zhaohui

    2012-11-01

    A new synthetic strategy has been developed for the fabrication of Au-Ag bimetallic core-shell nanoparticles (NPs) using polyelectrolyte multilayers (PEMs) as unique nanoreactors. Bimetallic NPs composed of Au core and Ag shell were successively incorporated into PEMs by repeating anion/cation exchange/reduction cycle multiple times in a stepwise manner. The strategy described here allows for the facile preparation of Au@Ag core-shell NPs with well-controlled core and shell dimensions and geometrically tunable optical properties by simply varying the number of ion-exchange/reduction cycles in the PEM matrix. The strategy can be extended to synthesize in situ other core-shell NPs in polymer matrix.

  3. Raman scattering of linear chains of strongly coupled Ag nanoparticles on SWCNTs

    PubMed Central

    Valmalette, Jean-Christophe; Tan, Zhenquan; Abe, Hiroya; Ohara, Satoshi

    2014-01-01

    We compare the Raman scattering properties of hybrid nanostructures consisting of Ag nanoparticles (NPs) in disordered and aligned arrangements on single-walled carbon nanotubes (SWCNTs) as a result of chemical and photoreduction methods. In the latter case, the unique structure of the very small Ag NP (from 4 to 7 nm) chains generated an extremely large mode at 969 cm−1 that was assigned to the sulphate-silver interaction at the NP surface. Another strong mode was present at 1201 cm−1 and was assigned to an IR-active mode of sodium dodecyl sulphate (SDS); this mode was observed because the symmetry changes altered the selection rules. We demonstrate that both the UV photoreduction of silver and the presence of SWCNTs are necessary to produce this very strong Raman scattering. The Raman modes of the SWCNTs are also significantly modified by the presence of Ag NP chains along the nanotubes. PMID:24912409

  4. Production of antibacterial colored viscose fibers using in situ prepared spherical Ag nanoparticles.

    PubMed

    Emam, Hossam E; Mowafi, Salwa; Mashaly, Hamada M; Rehan, Mohamed

    2014-09-22

    In situ incorporation technique was used for coloration and acquiring excellent antibacterial properties for viscose fibers by silver nanoparticles (AgNPs). AgNPs were prepared in situ and incorporated in viscose matrix directly without using any other reducing and stabilizing agents. The main objective of this research was to successfully employ the reducing and stabilizing features of cellulose to produce nanosilver-viscose composites. Coloration of fibers after in situ AgNPs incorporation is related to surface plasmon resonance of silver. Colorimetric data were recorded as a function of washings to characterize the final colored fibers. Fastness properties and silver release were all measured to study the washable and wear off properties. Depending on the silver concentration, yellowish colored fibers with different shades were produced. Good fastness properties were obtained after 20 washings without using any crosslinker or binder. The colored fibers had excellent antibacterial activities against Escherichia coli, even after 20 washings. PMID:24906741

  5. Synthesis of spindle-shaped AgI/TiO2 nanoparticles with enhanced photocatalytic performance

    NASA Astrophysics Data System (ADS)

    Yang, Liu; Gao, Minggang; Dai, Bin; Guo, Xuhong; Liu, Zhiyong; Peng, Banghua

    2016-11-01

    A novel synthetic route has been developed to prepare silver iodide (AgI) loaded spindle-shaped TiO2 nanoparticles (NPs). The morphology and crystallinity characterization revealed that small AgI NPs, with an average diameter of 15 nm were dispersed on the surface and interior of nanoporous anatase TiO2 support. High-resolution transmission electron microscopy (HRTEM), Brunauer-Emmett-Teller (BET) surface area, Raman and X-ray photoelectron spectroscopy (XPS) were used to identify the nanoporous structure of TiO2 and the existence of AgI NPs. Diffuse reflectance spectra (DRS) showed that AgI/TiO2 composite exhibited a remarkable enhancement of visible light absorption, which is ascribed to the addition of AgI. For illustrating the superior property of this hybrid as photocatalyst, the degradation experiments were carried out for processing rhodamine B (RhB) solution under visible light irradiation and it was found that the photocatalytic activity was dramatically improved for AgI/TiO2 compared with nanoporous TiO2 and commercial P25 TiO2. The enhanced photocatalytic properties could be attributed to the large surface area of porous TiO2, good stability of AgI particles, and the effective charge separation due to the synergetic effect between AgI and TiO2 that can facilitate the separation of electron-hole pairs. Our novel composite based on nanoporous spindle-shaped TiO2 represents a promising new pathway for the design of high-performance photocatalysts for environmental applications.

  6. Rapid synthesis of ordered hexagonal mesoporous silica and their incorporation with Ag nanoparticles by solution plasma

    SciTech Connect

    Pootawang, Panuphong; Saito, Nagahiro; Takai, Osamu; Lee, Sang Yul

    2012-10-15

    Graphical abstract: Overall reactions of mesoporous silica and AgNPs-incorporated mesoporous silica syntheses by solution plasma process (SPP). Highlights: ► SPP for rapid synthesis of mesoporous silica. ► SPP for rapid synthesis of mesoporous silica and AgNPs incorporation. ► Higher surface area and larger pore diameter of mesoporous silica synthesized by SPP. -- Abstract: Rapid synthesis of silica with ordered hexagonal mesopore arrangement was obtained using solution plasma process (SPP) by discharging the mixture of P123 triblock copolymer/TEOS in acid solution. SPP, moreover, was utilized for Ag nanoparticles (AgNPs) incorporation in silica framework as one-batch process using silver nitrate (AgNO{sub 3}) solution as precursor. The turbid silicate gel was clearly observed after discharge for 1 min and the white precipitate formed at 3 min. The mesopore with hexagonal arrangement and AgNPs were observed in mesoporous silica. Two regions of X-ray diffraction patterns (2θ < 2° and 2θ = 35–90°) corresponded to the mesoporous silica and Ag nanocrystal characteristics. Comparing with mesoporous silica prepared by a conventional sol–gel route, surface area and pore diameter of mesoporous silica prepared by solution plasma were observed to be larger. In addition, the increase in Ag loading resulted in the decrease in surface area with insignificant variation in the pore diameter of mesoporous silica. SPP could be successfully utilized not only to enhance gelation time but also to increase surface area and pore diameter of mesoporous silica.

  7. Exploiting Size-Dependent Drag and Magnetic Forces for Size-Specific Separation of Magnetic Nanoparticles

    PubMed Central

    Rogers, Hunter B.; Anani, Tareq; Choi, Young Suk; Beyers, Ronald J.; David, Allan E.

    2015-01-01

    Realizing the full potential of magnetic nanoparticles (MNPs) in nanomedicine requires the optimization of their physical and chemical properties. Elucidation of the effects of these properties on clinical diagnostic or therapeutic properties, however, requires the synthesis or purification of homogenous samples, which has proved to be difficult. While initial simulations indicated that size-selective separation could be achieved by flowing magnetic nanoparticles through a magnetic field, subsequent in vitro experiments were unable to reproduce the predicted results. Magnetic field-flow fractionation, however, was found to be an effective method for the separation of polydisperse suspensions of iron oxide nanoparticles with diameters greater than 20 nm. While similar methods have been used to separate magnetic nanoparticles before, no previous work has been done with magnetic nanoparticles between 20 and 200 nm. Both transmission electron microscopy (TEM) and dynamic light scattering (DLS) analysis were used to confirm the size of the MNPs. Further development of this work could lead to MNPs with the narrow size distributions necessary for their in vitro and in vivo optimization. PMID:26307980

  8. Anisotropic effective medium properties from interacting Ag nanoparticles in silicon dioxide.

    PubMed

    Menegotto, Thiago; Horowitz, Flavio

    2014-05-01

    Films containing a layer of Ag nanoparticles embedded in silicon dioxide were produced by RF magnetron sputtering. Optical transmittance measurements at several angles of incidence (from normal to 75°) revealed two surface plasmon resonance (SPR) peaks, which depend on electric field direction: one in the ultraviolet and another red-shifted from the dilute Ag/SiO₂ system resonance at 410 nm. In order to investigate the origin of this anisotropic behavior, the structural properties were determined by transmission electron microscopy, revealing the bidimensional plane distribution of Ag nanoparticles with nearly spherical shape as well as the filling factor of metal in the composite. A simple model linked to these experimental parameters allowed description of the most relevant features of the SPR positions, which, depending on the field direction, were distinctly affected by the coupling of oscillations between close nanoparticles, as described by a modified Drude-Lorentz dielectric function introduced into the Maxwell-Garnett relation. This approach allowed prediction of the resonance for light at 75° incidence from the SPR position for light at normal incidence, in good agreement with experimental observation. PMID:24921871

  9. Enzyme Induced Formation of Monodisperse Hydrogel Nanoparticles Tunable in Size

    DOE PAGES

    Bocharova, Vera; Sharp, Danna; Jones, Aaron; Cheng, Shiwang; Griffin, Philip J.; Agapov, Alexander L.; Voylov, Dmitry; Wang, Yangyang; Kisliuk, Alexander; Melman, Artem; et al

    2015-03-09

    Here, we report a novel approach to synthesize monodisperse hydrogel nanoparticles that are tunable in size. The distinctive feature of our approach is the use of a multicopper oxidase enzyme, laccase, as both a biocatalyst and template for nanoparticle growth. We utilize the ferroxidase activity of laccase to initiate localized production of iron(III) cations from the oxidation of iron(II) cations. We demonstrate that nanoparticles are formed in a dilute polymer solution of alginate as a result of cross-linking between alginate and enzymatically produced iron(III) cations. Exerting control over the enzymatic reaction allows for nanometer-scale tuning of the hydrogel nanoparticle radiimore » in the range of 30–100 nm. Moreover, the nanoparticles and their growth kinetics were characterized via dynamic light scattering, atomic force microscopy, and UV–vis spectroscopy. Our finding opens up a new avenue for the synthesis of tunable nanoscale hydrogel particles for biomedical applications.« less

  10. Electrochemical Nanoparticle Sizing Via Nano-Impacts: How Large a Nanoparticle Can be Measured?

    PubMed Central

    Bartlett, Thomas R; Sokolov, Stanislav V; Compton, Richard G

    2015-01-01

    The field of nanoparticle (NP) sizing encompasses a wide array of techniques, with electron microscopy and dynamic light scattering (DLS) having become the established methods for NP quantification; however, these techniques are not always applicable. A new and rapidly developing method that addresses the limitations of these techniques is the electrochemical detection of NPs in solution. The ‘nano-impacts’ technique is an excellent and qualitative in situ method for nanoparticle characterization. Two complementary studies on silver and silver bromide nanoparticles (NPs) were used to assess the large radius limit of the nano-impact method for NP sizing. Noting that by definition a NP cannot be larger than 100 nm in diameter, we have shown that the method quantitatively sizes at the largest limit, the lower limit having been previously reported as ∼6 nm.1 PMID:26491639

  11. Cyto/hemocompatible magnetic hybrid nanoparticles (Ag2S-Fe3O4) with luminescence in the near-infrared region as promising theranostic materials.

    PubMed

    Hocaoglu, Ibrahim; Asik, Didar; Ulusoy, Gulen; Grandfils, Christian; Ojea-Jimenez, Isaac; Rossi, François; Kiraz, Alper; Doğan, Nurcan; Acar, Havva Yagci

    2015-09-01

    Small hybrid nanoparticles composed of highly biocompatible Ag2S quantum dots (QD) emitting in the near-infrared region and superparamagnetic iron oxide (SPION) are produced in a simple extraction method utilizing ligand exchange mechanism. Hybrid nanoparticles luminesce at the same wavelength as the parent QD, therefore an array of hybrid nanoparticles with emission between 840 and 912nm were easily produced. Such hybrid structures have (1) strong luminescence in the medical imaging window eliminating the autofluoresence of cells as effective optical probes, (2) strong magnetic response for magnetic targeting and (3) good cyto/hemocompatibility. An interesting size dependent cytotoxicity behavior was observed in HeLa and NIH/3T3 cell lines: smallest particles are internalized significantly more by both of the cell lines, yet showed almost no significant cytotoxicity in HeLa between 10 and 25μg/mL Ag concentration but were most toxic in NIH/3T3 cells. Cell internalization and hence the cytotoxicity enhanced when cells were incubated with the hybrid nanoparticles under magnetic field, especially with the hybrid nanoparticles containing larger amounts of SPION in the hybrid composition. These results prove them as effective optical imaging agents and magnetic delivery vehicles. Combined with the known advantages of SPIONs as a contrast agent in MRI, these particles are a step forward for new theranostics for multimode imaging and magnetic targeting. PMID:26101820

  12. Cyto/hemocompatible magnetic hybrid nanoparticles (Ag2S-Fe3O4) with luminescence in the near-infrared region as promising theranostic materials.

    PubMed

    Hocaoglu, Ibrahim; Asik, Didar; Ulusoy, Gulen; Grandfils, Christian; Ojea-Jimenez, Isaac; Rossi, François; Kiraz, Alper; Doğan, Nurcan; Acar, Havva Yagci

    2015-09-01

    Small hybrid nanoparticles composed of highly biocompatible Ag2S quantum dots (QD) emitting in the near-infrared region and superparamagnetic iron oxide (SPION) are produced in a simple extraction method utilizing ligand exchange mechanism. Hybrid nanoparticles luminesce at the same wavelength as the parent QD, therefore an array of hybrid nanoparticles with emission between 840 and 912nm were easily produced. Such hybrid structures have (1) strong luminescence in the medical imaging window eliminating the autofluoresence of cells as effective optical probes, (2) strong magnetic response for magnetic targeting and (3) good cyto/hemocompatibility. An interesting size dependent cytotoxicity behavior was observed in HeLa and NIH/3T3 cell lines: smallest particles are internalized significantly more by both of the cell lines, yet showed almost no significant cytotoxicity in HeLa between 10 and 25μg/mL Ag concentration but were most toxic in NIH/3T3 cells. Cell internalization and hence the cytotoxicity enhanced when cells were incubated with the hybrid nanoparticles under magnetic field, especially with the hybrid nanoparticles containing larger amounts of SPION in the hybrid composition. These results prove them as effective optical imaging agents and magnetic delivery vehicles. Combined with the known advantages of SPIONs as a contrast agent in MRI, these particles are a step forward for new theranostics for multimode imaging and magnetic targeting.

  13. Toxicological Effects of Caco-2 Cells Following Short-Term and Long-Term Exposure to Ag Nanoparticles

    PubMed Central

    Chen, Ni; Song, Zheng-Mei; Tang, Huan; Xi, Wen-Song; Cao, Aoneng; Liu, Yuanfang; Wang, Haifang

    2016-01-01

    Extensive utilization increases the exposure of humans to Ag nanoparticles (NPs) via the oral pathway. To comprehensively address the action of Ag NPs to the gastrointestinal systems in real situations, i.e., the long-term low-dose exposure, we evaluated and compared the toxicity of three Ag NPs (20–30 nm with different surface coatings) to the human intestine cell Caco-2 after 1-day and 21-day exposures, using various biological assays. In both the short- and long-term exposures, the variety of surface coating predominated the toxicity of Ag NPs in a descending order of citrate-coated Ag NP (Ag-CIT), bare Ag NP (Ag-B), and poly (N-vinyl-2-pyrrolidone)-coated Ag NP (Ag-PVP). The short-term exposure induced cell growth inhibition and death. The cell viability loss appeared after cells were exposed to 0.7 μg/mL Ag-CIT, 0.9 μg/mL Ag-B or >1.0 μg/mL Ag-PVP for 24 h. The short-term and higher-dose exposure also induced reactive oxygen species (ROS) generation, mitochondrial damage, cell membrane leakage, apoptosis, and inflammation (IL-8 level). The long-term exposure only inhibited the cell proliferation. After 21-day exposure to 0.4 μg/mL Ag-CIT, the cell viability dropped to less than 50%, while cells exposed to 0.5 μg/mL Ag-PVP remained normal as the control. Generally, 0.3 μg/mL is the non-toxic dose for the long-term exposure of Caco-2 cells to Ag NPs in this study. However, cells presented inflammation after exposure to Ag NPs with the non-toxic dose in the long-term exposure. PMID:27338357

  14. Synthesis and visible-light-induced catalytic activity of Ag2S-coupled TiO2 nanoparticles and nanowires

    NASA Astrophysics Data System (ADS)

    Xie, Yi; Heo, Sung Hwan; Kim, Yong Nam; Yoo, Seung Hwa; Cho, Sung Oh

    2010-01-01

    We present the synthesis and visible-light-induced catalytic activity of Ag2S-coupled TiO2 nanoparticles (NPs) and TiO2 nanowires (NWs). Through a simple wet chemical process from a mixture of peroxo titanic acid (PTA) solution, thiourea and AgAc, a composite of Ag2S NPs and TiO2 NPs with sizes of less than 7 nm was formed. When the NP composite was further treated with NaOH solution followed by annealing at ambient conditions, a new nanocomposite material comprising Ag2S NPs on TiO2 NWs was created. Due to the coupling with such a low bandgap material as Ag2S, the TiO2 nanocomposites could have a visible-light absorption capability much higher than that of pure TiO2. As a result, the synthesized Ag2S/TiO2 nanocomposites exhibited much higher catalytic efficiency for the decomposition of methyl orange than commercial TiO2 (Degussa P25, Germany) under visible light.

  15. Electronic Coupling and Optimal Gap Size Between Two Metal Nanoparticles

    SciTech Connect

    Zhao, Ke; Troparevsky, Claudia; Xiao, Di; Eguiluz, Adolfo G; Zhang, Zhenyu

    2009-01-01

    We study the electronic coupling between two silver nanoparticles using ab initio density functional theory for real atoms. We show that the electronic coupling depends on both the gap size of the dimer system and the relative orientation of the particles. As the two particles are separated from touching contact, the dimer undergoes a bond-breaking step, which also establishes the striking existence of an optimal gap size dened by a maximal static polarizability of the dimer. For some dimers, the electronic coupling before the bond breaking can be strong enough to give rise to a net magnetic moment of the dimer, even though the isolated particles are nonmagnetic. These ndings may prove to be instrumental in understanding and controlling the optical, magnetic, electrical, and chemical properties of closely-packed nanoparticle aggregates.

  16. Size Dependent Phase Diagrams of Nickel-Carbon Nanoparticles.

    PubMed

    Magnin, Y; Zappelli, A; Amara, H; Ducastelle, F; Bichara, C

    2015-11-13

    The carbon rich phase diagrams of nickel-carbon nanoparticles, relevant to catalysis and catalytic chemical vapor deposition synthesis of carbon nanotubes, are calculated for system sizes up to about 3 nm (807 Ni atoms). A tight binding model for interatomic interactions drives the grand canonical Monte Carlo simulations used to locate solid, core shell and liquid stability domains, as a function of size, temperature, and carbon chemical potential or concentration. Melting is favored by carbon incorporation from the nanoparticle surface, resulting in a strong relative lowering of the eutectic temperature and a phase diagram topology different from the bulk one. This should lead to a better understanding of the nanotube growth mechanisms. PMID:26613451

  17. Size dependence of non-magnetic thickness in YIG nanoparticles

    NASA Astrophysics Data System (ADS)

    Niyaifar, M.; Mohammadpour, H.; Dorafshani, M.; Hasanpour, A.

    2016-07-01

    This study is focused on particle size dependence of structural and magnetic properties in yttrium iron garnet (Y3Fe5O12) nanoparticles. A series of YIG samples with different particle size were produced by varying the annealing temperatures. The X-ray analysis revealed an inverse correlation between lattice parameter and the crystallite size. The normal distribution is used for fitting the particles size distribution which is extracted from scanning electron micrographs. Also, by using the results of vibrating sample magnetometer, the magnetic diameter was calculated based on Langevin model in order to investigate the variation of dead layer thickness. Furthermore, the observed line broadening in Mössbauer spectra confirmed the increase of non-magnetic thickness due to the reduction of particle size.

  18. Antibacterial activity and reusability of CNT-Ag and GO-Ag nanocomposites

    NASA Astrophysics Data System (ADS)

    Kim, Ji Dang; Yun, Hyosuk; Kim, Gwui Cheol; Lee, Chul Won; Choi, Hyun Chul

    2013-10-01

    A facile approach to the synthesis of novel CNT-Ag and GO-Ag antibacterial materials, in which thiol groups are utilized as linkers to secure silver (Ag) nanoparticles to the CNT and GO surfaces without agglomeration, is reported. The resulting CNT-Ag and GO-Ag samples were characterized by performing TEM, XRD, Auger, XPS, and Raman measurements, which revealed that in these antibacterial materials size-similar and quasi-spherical Ag nanoparticles are anchored to the CNT and GO surfaces. The Ag nanoparticles in CNT-Ag and GO-Ag have narrow size distributions with average diameters of 2.6 and 3.5 nm respectively. The antibacterial activities of CNT-Ag and GO-Ag against Escherichia coli were assessed with the paper-disk diffusion method and by determining the minimal inhibitory concentrations (MICs). CNT-Ag was found to have higher antibacterial activity than the reference Ag colloid. Moreover, both CNT-Ag and GO-Ag retain more than 50% of their original antibacterial activities after 20 washes with detergent, which indicates their potential as antibacterial materials for laboratory and medical purposes.

  19. Preparation of the egg membrane bandage contained the antibacterial Ag nanoparticles

    SciTech Connect

    Zhang, Jin; Duan, Guangwen; Fu, Yunzhi; Zhao, Jinsheng

    2015-02-15

    Silver nanoparticles were synthesized using a rapid, single step, and completely green biosynthetic method employing aqueous aloe leaf extracts as both the reducing and capping agent. Transmission electron microscopy analysis revealed the average size of silver nanoparticles approximately 18.05 nm. Fourier transform infrared spectroscopy observation showed the estimation of two kinds of binding sites between aqueous aloe leaf and aqueous aloe leaf with silver nanoparticles. In addition, the critical roles of the concentration of silver nitrate, temperature, and reaction time in the formation of silver nanoparticles had been illustrated. Furthermore, silver nanoparticles were deposited on egg membrane bandage, forming a new egg membrane bandage that contained silver nanoparticles that exhibiting excellent antibacterial effects against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus, which was 2.5 times stronger than the commercially available bandage. - Graphical Abstract: Display Omitted.

  20. Role of proteins in controlling selenium nanoparticle size

    NASA Astrophysics Data System (ADS)

    Dobias, J.; Suvorova, E. I.; Bernier-Latmani, R.

    2011-05-01

    This work investigates the potential for harnessing the association of bacterial proteins to biogenic selenium nanoparticles (SeNPs) to control the size distribution and the morphology of the resultant SeNPs. We conducted a proteomic study and compared proteins associated with biogenic SeNPs produced by E. coli to chemically synthesized SeNPs as well as magnetite nanoparticles. We identified four proteins (AdhP, Idh, OmpC, AceA) that bound specifically to SeNPs and observed a narrower size distribution as well as more spherical morphology when the particles were synthesized chemically in the presence of proteins. A more detailed study of AdhP (alcohol dehydrogenase propanol-preferring) confirmed the strong affinity of this protein for the SeNP surface and revealed that this protein controlled the size distribution of the SeNPs and yielded a narrow size distribution with a three-fold decrease in the median size. These results support the assertion that protein may become an important tool in the industrial-scale synthesis of SeNPs of uniform size and properties.

  1. Drastic nickel ion removal from aqueous solution by curcumin-capped Ag nanoparticles

    NASA Astrophysics Data System (ADS)

    Bettini, S.; Pagano, R.; Valli, L.; Giancane, G.

    2014-08-01

    A completely green synthesis protocol has been adopted to obtain silver nanoaggregates capped by the natural compound (1E, 6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-diene), also known as curcumin. The synthesis has been monitored by infrared, Raman, visible and fluorescence spectroscopies. Characterization confirms that curcumin reduces and caps the nanoparticles, and such a procedure allows its solubility in water and drastically increases curcumin stability. Silver nanoparticles (AgNPs)/curcumin complex has been dispersed in a water solution containing a known nickel ion concentration. After three days, a grey precipitate is observed and nickel concentration in the solution is reduced by about 70%.A completely green synthesis protocol has been adopted to obtain silver nanoaggregates capped by the natural compound (1E, 6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-diene), also known as curcumin. The synthesis has been monitored by infrared, Raman, visible and fluorescence spectroscopies. Characterization confirms that curcumin reduces and caps the nanoparticles, and such a procedure allows its solubility in water and drastically increases curcumin stability. Silver nanoparticles (AgNPs)/curcumin complex has been dispersed in a water solution containing a known nickel ion concentration. After three days, a grey precipitate is observed and nickel concentration in the solution is reduced by about 70%. Electronic supplementary information (ESI) available. See DOI: 10.1039/c4nr02583k

  2. Preparation of an agar-silver nanoparticles (A-AgNp) film for increasing the shelf-life of fruits.

    PubMed

    Gudadhe, Janhavi A; Yadav, Alka; Gade, Aniket; Marcato, Priscyla D; Durán, Nelson; Rai, Mahendra

    2014-12-01

    Preparation of protective coating possessing antimicrobial properties is present day need as they increase the shelf life of fruits and vegetables. In the present study, preparation of agar-silver nanoparticle film for increasing the shelf life of fruits is reported. Silver nanoparticles (Ag-NPs) biosynthesised using an extract of Ocimum sanctum leaves, were mixed with agar-agar to prepare an agar-silver nanoparticles (A-AgNp) film. This film was surface-coated over the fruits, Citrus aurantifolium (Thornless lime) and Pyrus malus (Apple), and evaluated for the determination of antimicrobial activity of A-AgNp films using disc diffusion method, weight loss and shelf life of fruits. This study demonstrates that these A-AgNp films possess antimicrobial activity and also increase the shelf life of fruits. PMID:25429496

  3. Dielectric performance of polymer-based composites containing core-shell Ag@TiO2 nanoparticle fillers

    NASA Astrophysics Data System (ADS)

    Liang, Fei; Zhang, Lu; Lu, Wen-Zhong; Wan, Qian-Xing; Fan, Gui-Fen

    2016-02-01

    This paper reports composites prepared by embedding core-shell Ag@TiO2 fillers into polytetrafluoroethylene. Ag nanoparticles were homogeneously coated with TiO2, to give a shell thickness of approximately ˜8-10 nm. The composite containing Ag@TiO2 nanoparticles with rutile shells exhibited better dielectric properties than the composite containing Ag@TiO2 nanoparticles with anatase shells. The relative permittivity (ɛr) of the composite containing 70 vol. % filler was approximately 240 at 100 Hz, which was more than 100 times higher than that of pure polytetrafluoroethylene (ɛr = 2.1). An effective medium percolation theory model is used to account for the dielectric constant of the composite.

  4. Ultrafast image-based dynamic light scattering for nanoparticle sizing

    NASA Astrophysics Data System (ADS)

    Zhou, Wu; Zhang, Jie; Liu, Lili; Cai, Xiaoshu

    2015-11-01

    An ultrafast sizing method for nanoparticles is proposed, called as UIDLS (Ultrafast Image-based Dynamic Light Scattering). This method makes use of the intensity fluctuation of scattered light from nanoparticles in Brownian motion, which is similar to the conventional DLS method. The difference in the experimental system is that the scattered light by nanoparticles is received by an image sensor instead of a photomultiplier tube. A novel data processing algorithm is proposed to directly get correlation coefficient between two images at a certain time interval (from microseconds to milliseconds) by employing a two-dimensional image correlation algorithm. This coefficient has been proved to be a monotonic function of the particle diameter. Samples of standard latex particles (79/100/352/482/948 nm) were measured for validation of the proposed method. The measurement accuracy of higher than 90% was found with standard deviations less than 3%. A sample of nanosilver particle with nominal size of 20 ± 2 nm and a sample of polymethyl methacrylate emulsion with unknown size were also tested using UIDLS method. The measured results were 23.2 ± 3.0 nm and 246.1 ± 6.3 nm, respectively, which is substantially consistent with the transmission electron microscope results. Since the time for acquisition of two successive images has been reduced to less than 1 ms and the data processing time in about 10 ms, the total measuring time can be dramatically reduced from hundreds seconds to tens of milliseconds, which provides the potential for real-time and in situ nanoparticle sizing.

  5. Ultrafast image-based dynamic light scattering for nanoparticle sizing

    SciTech Connect

    Zhou, Wu; Zhang, Jie; Liu, Lili; Cai, Xiaoshu

    2015-11-15

    An ultrafast sizing method for nanoparticles is proposed, called as UIDLS (Ultrafast Image-based Dynamic Light Scattering). This method makes use of the intensity fluctuation of scattered light from nanoparticles in Brownian motion, which is similar to the conventional DLS method. The difference in the experimental system is that the scattered light by nanoparticles is received by an image sensor instead of a photomultiplier tube. A novel data processing algorithm is proposed to directly get correlation coefficient between two images at a certain time interval (from microseconds to milliseconds) by employing a two-dimensional image correlation algorithm. This coefficient has been proved to be a monotonic function of the particle diameter. Samples of standard latex particles (79/100/352/482/948 nm) were measured for validation of the proposed method. The measurement accuracy of higher than 90% was found with standard deviations less than 3%. A sample of nanosilver particle with nominal size of 20 ± 2 nm and a sample of polymethyl methacrylate emulsion with unknown size were also tested using UIDLS method. The measured results were 23.2 ± 3.0 nm and 246.1 ± 6.3 nm, respectively, which is substantially consistent with the transmission electron microscope results. Since the time for acquisition of two successive images has been reduced to less than 1 ms and the data processing time in about 10 ms, the total measuring time can be dramatically reduced from hundreds seconds to tens of milliseconds, which provides the potential for real-time and in situ nanoparticle sizing.

  6. Ultrafast image-based dynamic light scattering for nanoparticle sizing.

    PubMed

    Zhou, Wu; Zhang, Jie; Liu, Lili; Cai, Xiaoshu

    2015-11-01

    An ultrafast sizing method for nanoparticles is proposed, called as UIDLS (Ultrafast Image-based Dynamic Light Scattering). This method makes use of the intensity fluctuation of scattered light from nanoparticles in Brownian motion, which is similar to the conventional DLS method. The difference in the experimental system is that the scattered light by nanoparticles is received by an image sensor instead of a photomultiplier tube. A novel data processing algorithm is proposed to directly get correlation coefficient between two images at a certain time interval (from microseconds to milliseconds) by employing a two-dimensional image correlation algorithm. This coefficient has been proved to be a monotonic function of the particle diameter. Samples of standard latex particles (79/100/352/482/948 nm) were measured for validation of the proposed method. The measurement accuracy of higher than 90% was found with standard deviations less than 3%. A sample of nanosilver particle with nominal size of 20 ± 2 nm and a sample of polymethyl methacrylate emulsion with unknown size were also tested using UIDLS method. The measured results were 23.2 ± 3.0 nm and 246.1 ± 6.3 nm, respectively, which is substantially consistent with the transmission electron microscope results. Since the time for acquisition of two successive images has been reduced to less than 1 ms and the data processing time in about 10 ms, the total measuring time can be dramatically reduced from hundreds seconds to tens of milliseconds, which provides the potential for real-time and in situ nanoparticle sizing. PMID:26628172

  7. Kinetics of protein adsorption on gold nanoparticle with variable protein structure and nanoparticle size.

    PubMed

    Khan, S; Gupta, A; Verma, N C; Nandi, C K

    2015-10-28

    The spontaneous protein adsorption on nanomaterial surfaces and the formation of a protein corona around nanoparticles are poorly understood physical phenomena, with high biological relevance. The complexity arises mainly due to the poor knowledge of the structural orientation of the adsorbed proteins onto the nanoparticle surface and difficulties in correlating the protein nanoparticle interaction to the protein corona in real time scale. Here, we provide quantitative insights into the kinetics, number, and binding orientation of a few common blood proteins when they interact with citrate and cetyltriethylammoniumbromide stabilized spherical gold nanoparticles with variable sizes. The kinetics of the protein adsorption was studied experimentally by monitoring the change in hydrodynamic diameter and zeta potential of the nanoparticle-protein complex. To understand the competitive binding of human serum albumin and hemoglobin, time dependent fluorescence quenching was studied using dual fluorophore tags. We have performed molecular docking of three different proteins--human serum albumin, bovine serum albumin, and hemoglobin--on different nanoparticle surfaces to elucidate the possible structural orientation of the adsorbed protein. Our data show that the growth kinetics of a protein corona is exclusively dependent on both protein structure and surface chemistry of the nanoparticles. The study quantitatively suggests that a general physical law of protein adsorption is unlikely to exist as the interaction is unique and specific for a given pair. PMID:26520545

  8. Kinetic trapping through coalescence and the formation of patterned Ag-Cu nanoparticles

    NASA Astrophysics Data System (ADS)

    Grammatikopoulos, Panagiotis; Kioseoglou, Joseph; Galea, Antony; Vernieres, Jerome; Benelmekki, Maria; Diaz, Rosa E.; Sowwan, Mukhles

    2016-05-01

    In recent years, due to its inherent flexibility, magnetron-sputtering has been widely used to synthesise bi-metallic nanoparticles (NPs) via subsequent inert-gas cooling and gas-phase condensation of the sputtered atomic vapour. Utilising two separate sputter targets allows for good control over composition. Simultaneously, it involves fast kinetics and non-equilibrium processes, which can trap the nascent NPs into metastable configurations. In this study, we observed such configurations in immiscible, bi-metallic Ag-Cu NPs by scanning transmission electron microscopy (S/TEM) and electron energy-loss spectroscopy (EELS), and noticed a marked difference in the shape of NPs belonging to Ag- and Cu-rich samples. We explained the formation of Janus or Ag@Cu core/shell metastable structures on the grounds of in-flight mixed NP coalescence. We utilised molecular dynamics (MD) and Monte Carlo (MC) computer simulations to demonstrate that such configurations cannot occur as a result of nanoalloy segregation. Instead, sintering at relatively low temperatures can give rise to metastable structures, which eventually can be stabilised by subsequent quenching. Furthermore, we compared the heteroepitaxial diffusivities along various surfaces of both Ag and Cu NPs, and emphasised the differences between the sintering mechanisms of Ag- and Cu-rich NP compositions: small Cu NPs deform as coherent objects on large Ag NPs, whereas small Ag NPs dissolve into large Cu NPs, with their atoms diffusing along specific directions. Taking advantage of this observation, we propose controlled NP coalescence as a method to engineer mixed NPs of a unique, patterned core@partial-shell structure, which we refer to as a ``glass-float'' (ukidama) structure.In recent years, due to its inherent flexibility, magnetron-sputtering has been widely used to synthesise bi-metallic nanoparticles (NPs) via subsequent inert-gas cooling and gas-phase condensation of the sputtered atomic vapour. Utilising two

  9. Surface modification of nanoporous alumina layers by deposition of Ag nanoparticles. Effect of alumina pore diameter on the morphology of silver deposit and its influence on SERS activity

    NASA Astrophysics Data System (ADS)

    Pisarek, Marcin; Nowakowski, Robert; Kudelski, Andrzej; Holdynski, Marcin; Roguska, Agata; Janik-Czachor, Maria; Kurowska-Tabor, Elżbieta; Sulka, Grzegorz D.

    2015-12-01

    Self-organized Al2O3 nanoporous/nanotubular (Al2O3-NP) oxide layers decorated with silver nanoparticles (Ag-NPs) exhibiting specific properties may serve as attractive SERS substrates for investigating the interactions between an adsorbate and adsorbent, or as stable platforms for detecting various organic compounds. This article presents the influence of the size of the alumina nanopores with a deposit of silver nanoparticles obtained by the magnetron sputtering technique on the morphology of silver film. Moreover, the effect of pore diameter on the intensity of SERS spectra in Ag-NPs/Al2O3-NP/Al composites has also been estimated. For such investigations we used pyridine as a probe molecule, since it has a large cross-section for Raman scattering. To characterize the morphology of the composite oxide layer Ag-NPs/Al2O3-NP/Al, before and after deposition of Ag-NPs by PVD methods (Physical Vapor Deposition), we used scanning electron microscopy (SEM) and atomic force microscopy (AFM). The surface analytical technique of surface-enhanced Raman spectroscopy (SERS) was used to investigate the surface activity of the composite. The results obtained show that, for a carefully controlled amount of Ag (0.020 mg/cm2 - deposited on the top of alumina nanopores whose average size varies from ∼86 nm up to ∼320 nm) in the composites investigated, pore size significantly affects SERS enhancement. We obtained distinctly higher intensities of SERS spectra for substrates with an Ag-NPs deposit having a larger diameter of the alumina nanopores. AFM results suggest that both the lateral and perpendicular distribution of Ag-NPs within and on the top of the largest pores is responsible for the highest SERS activity of the resulting Ag-NPs/Al2O3-NP/Al composite layer, since it produces a variety of cavities and slits which function as resonators for the adsorbed molecules. The Ag-NPs/MeOx-NP/Me composite layers obtained ensure a good reproducibility of the SERS measurements. a

  10. Synthesis of silver nanoparticles by solar irradiation of cell-free Bacillus amyloliquefaciens extracts and AgNO3.

    PubMed

    Wei, Xuetuan; Luo, Mingfang; Li, Wei; Yang, Liangrong; Liang, Xiangfeng; Xu, Lin; Kong, Peng; Liu, Huizhou

    2012-01-01

    Silver nanoparticles (AgNPs) were obtained by solar irradiation of cell-free extracts of Bacillusamyloliquefaciens and AgNO3. Light intensity, extract concentration, and NaCl addition influenced the synthesis of AgNPs. Under optimized conditions (solar intensity 70,000 lx, extract concentration 3 mg/mL, and NaCl content 2 mM), 98.23±0.06% of the Ag+ (1 mM) was reduced to AgNPs within 80 min, and the ζ-potential of AgNPs reached -70.84±0.66 mV. TEM (Transmission electron microscopy) and XRD (X-ray diffraction) analysis confirmed that circular and triangular crystalline AgNPs with mean diameter of 14.6 nm were synthesized. Since heat-inactivated extracts also mediated the formation of AgNPs, enzymatic reactions are likely not involved in AgNPs formation. A high absolute ζ-potential value of the AgNPs, possibly caused by interaction with proteins likely explains the high stability of AgNPs suspensions. AgNPs showed antimicrobial activity against Bacillussubtilis and Escherichiacoli in liquid and solid medium.

  11. Comparison of Ag and SiO2 Nanoparticles for Light Trapping Applications in Silicon Thin Film Solar Cells.

    PubMed

    Theuring, Martin; Wang, Peng Hui; Vehse, Martin; Steenhoff, Volker; von Maydell, Karsten; Agert, Carsten; Brolo, Alexandre G

    2014-10-01

    Plasmonic and photonic light trapping structures can significantly improve the efficiency of solar cells. This work presents an experimental and computational comparison of identically shaped metallic (Ag) and nonmetallic (SiO2) nanoparticles integrated to the back contact of amorphous silicon solar cells. Our results show comparable performance for both samples, suggesting that minor influence arises from the nanoparticle material. Particularly, no additional beneficial effect of the plasmonic features due to metallic nanoparticles could be observed. PMID:26278435

  12. Partitioning of silver and chemical speciation of free Ag in soils amended with nanoparticles

    PubMed Central

    2013-01-01

    Background Knowledge about silver nanoparticles in soils is limited even if soils are a critical pathway for their environmental fate. In this paper, speciation results have been acquired using a silver ion selective electrode in three different soils. Results Soil organic matter and pH were the most important soil properties controlling the occurrence of silver ions in soils. In acidic soils, more free silver ions are available while in the presence of organic matter, ions were tightly bound in complexes. The evolution of the chemical speciation of the silver nanoparticles in soils was followed over six months. Conclusion During the first few hours, there appeared to be a strong sorption of the silver with soil ligands, whereas over time, silver ions were released, the final concentration being approximately 10 times higher than at the beginning. Ag release was associated with either the oxidation of the nanoparticles or a dissociation of adsorbed silver from the soil surfaces. PMID:23617903

  13. Development of Novel Cadmium-Free AgInS2 Semiconductor Nanoparticles.

    PubMed

    Yang, Wentao; Gong, Xiaoqun; Chang, Jin

    2016-03-01

    AgInS2 (AIS) semiconductor nanoparticles as the novel alternatives to cadmium- or lead-containing semiconductors have attracted much attention both on the theory and application research, based on their tunable fluorescence emission wavelengths, high photostability and low toxicity of chemical composition. The bandgap of AIS nanoparticles can be adjusted from 1.54 to 2.03 eV, which makes AIS nanocrystalline suitable for applications in solar energy conversion. Moreover, the fluorescence emission wavelengths can be tuned in the near-infrared regions, and thus make it the next-generation low-toxicity materials for the applications in bioimaging. In this review, the research progress of the AIS nanoparticles is summarized, including synthetic methods, properties and the possibilities to influence their shape and crystallographic structure. Furthermore, we discuss the potential applications of this novel material in photocatalysis, solar energy conversion and biological area. PMID:27455616

  14. Development of Novel Cadmium-Free AgInS2 Semiconductor Nanoparticles.

    PubMed

    Yang, Wentao; Gong, Xiaoqun; Chang, Jin

    2016-03-01

    AgInS2 (AIS) semiconductor nanoparticles as the novel alternatives to cadmium- or lead-containing semiconductors have attracted much attention both on the theory and application research, based on their tunable fluorescence emission wavelengths, high photostability and low toxicity of chemical composition. The bandgap of AIS nanoparticles can be adjusted from 1.54 to 2.03 eV, which makes AIS nanocrystalline suitable for applications in solar energy conversion. Moreover, the fluorescence emission wavelengths can be tuned in the near-infrared regions, and thus make it the next-generation low-toxicity materials for the applications in bioimaging. In this review, the research progress of the AIS nanoparticles is summarized, including synthetic methods, properties and the possibilities to influence their shape and crystallographic structure. Furthermore, we discuss the potential applications of this novel material in photocatalysis, solar energy conversion and biological area.

  15. Kinetic trapping through coalescence and the formation of patterned Ag-Cu nanoparticles.

    PubMed

    Grammatikopoulos, Panagiotis; Kioseoglou, Joseph; Galea, Antony; Vernieres, Jerome; Benelmekki, Maria; Diaz, Rosa E; Sowwan, Mukhles

    2016-05-14

    In recent years, due to its inherent flexibility, magnetron-sputtering has been widely used to synthesise bi-metallic nanoparticles (NPs) via subsequent inert-gas cooling and gas-phase condensation of the sputtered atomic vapour. Utilising two separate sputter targets allows for good control over composition. Simultaneously, it involves fast kinetics and non-equilibrium processes, which can trap the nascent NPs into metastable configurations. In this study, we observed such configurations in immiscible, bi-metallic Ag-Cu NPs by scanning transmission electron microscopy (S/TEM) and electron energy-loss spectroscopy (EELS), and noticed a marked difference in the shape of NPs belonging to Ag- and Cu-rich samples. We explained the formation of Janus or Ag@Cu core/shell metastable structures on the grounds of in-flight mixed NP coalescence. We utilised molecular dynamics (MD) and Monte Carlo (MC) computer simulations to demonstrate that such configurations cannot occur as a result of nanoalloy segregation. Instead, sintering at relatively low temperatures can give rise to metastable structures, which eventually can be stabilised by subsequent quenching. Furthermore, we compared the heteroepitaxial diffusivities along various surfaces of both Ag and Cu NPs, and emphasised the differences between the sintering mechanisms of Ag- and Cu-rich NP compositions: small Cu NPs deform as coherent objects on large Ag NPs, whereas small Ag NPs dissolve into large Cu NPs, with their atoms diffusing along specific directions. Taking advantage of this observation, we propose controlled NP coalescence as a method to engineer mixed NPs of a unique, patterned core@partial-shell structure, which we refer to as a "glass-float" (ukidama) structure. PMID:27119383

  16. Ag(0) nanoparticles containing cotton fabric: Synthesis, characterization, color data and antibacterial action.

    PubMed

    Emam, Hossam E; Zahran, M K

    2015-04-01

    The main objective of the current research was to successfully employ the reducing and stabilizing features of xanthan gum to synthesize nanosilver, then coating cotton fabrics with the net produced nanosilver in order to obtain finished fabrics valuable in medical applications. Pre-hydrolyzed xanthan gum was used to reduce Ag(+) to Ag(0) in nano size using a simple one-step rapid synthetic route. The reduction step was followed up by measuring the concentration of reducing sugars eliminated in the reaction medium. The optimum concentration of xanthan gum was 3g/L to reduce 1 mmol/L Ag(+), as 2.66 ± 0.4 g/L was the maximum concentration of reducing sugars obtained in the reaction. Transmission microscope images show that the AgNPs are spherical in shape with mean size 9.1 ± 4.8 nm. Cotton fabrics were then coated with the produced AgNPs using pad-dry-cure method. Well dispersed layer from Ag(0) on cotton surface was showed under electron microscope. The biocidal activities of the coated fabrics were tested against Staphylococcus aureus and showed excellent results for antibacterial even after 20 washing cycles. This method has the advantage of not necessitating aggressive conditions such as the presence of organic solvents to produce durable antibacterial cotton fabrics.

  17. Size evolution of ion beam synthesized Pb nanoparticles in Al

    NASA Astrophysics Data System (ADS)

    Wang, Huan; Zhu, Hongzhi

    2014-07-01

    The size evolution of Pb nanoparticles (NPs) synthesized by ion implantation in an epitaxial Al film has been experimentally investigated. The average radius R of Pb NPs was determined as a function of implantation fluence f. The R( f) data were analyzed using various growth models. Our observations suggest that the size evolution of Pb NPs is controlled by the diffusion-limited growth kinetics ( R 2∝ f). With increasing implantation current density, the diffusion coefficient of Pb atoms in Al is evident to be enhanced. By a comparative analysis of the R( f) data, values of the diffusion coefficient of Pb in Al were obtained.

  18. Size distributions of metal nanoparticles in polyelectrolyte gels

    NASA Astrophysics Data System (ADS)

    Svergun, D. I.; Shtykova, E. V.; Dembo, A. T.; Bronstein, L. M.; Platonova, O. A.; Yakunin, A. N.; Valetsky, P. M.; Khokhlov, A. R.

    1998-12-01

    Small-angle x-ray scattering is used to study size distributions of noble metal nanoparticles embedded in polyelectrolyte hydrogels with oppositely charged surfactants. A procedure is proposed to subtract matrix scattering and to extract pure scattering due to the nanoparticles allowing to evaluate their size distribution functions by means of a regularization technique. Two kinds of collapsed gel-surfactant complexes were studied: a complex of a cationic gel of poly(diallyldimethylammonium chloride) with an anionic surfactant sodium dodecyl sulfate (PDADMACl/SDS), and that of an anionic gel of poly(methacrylic acid) with a cationic surfactant cetylpyridinium chloride (PMA/CPC). Addition of a gold compound (HAuCl4ṡ3H2O) to the PDADMACl/SDS system forms the metal compound clusters and leads to a partial distortion of the gel structure. After subsequent reduction of the gold compound with sodium borohydride (NaBH4) ordering in the gel disappears and gold nanoparticles are formed. Their size distribution includes a fraction of small particles with approximately the same size as the compound clusters before reduction and a fraction of larger particles with the radii up to 40 nm. For the collapsed PDADMACl/SDS gels, aging does not change the size distribution profile; for the noncollapsed PDADMACl gels without surfactant, metal particles are found to grow with time. This suggests that the aggregation of metal colloids is prevented by the ordering in the collapsed gel-surfactant complex. The addition of HAuCl4ṡ3H2O and the subsequent reduction of the metal ions in the PMA/CPC system does not distort the gel structure as the degree of incorporation of AuCl4- ions is very low. Particle sizes in the PMA/CPC system are found to be somewhat larger than those in the PDADMACl/SDS system. The PDADMACl/SDS gels loaded with the PtCl4 compound were also studied to analyze the influence of the reducing agent type on the particle size distribution distributions. Fast reduction

  19. Effects of soil and dietary exposures to Ag nanoparticles and AgNO₃ in the terrestrial isopod Porcellionides pruinosus.

    PubMed

    Tourinho, Paula S; van Gestel, Cornelis A M; Jurkschat, Kerstin; Soares, Amadeu M V M; Loureiro, Susana

    2015-10-01

    The effects of Ag-NPs and AgNO3 on the isopod Porcellionides pruinosus were determined upon soil and dietary exposures. Isopods avoided Ag in soil, with EC50 values of ∼16.0 and 14.0 mg Ag/kg for Ag-NPs and AgNO3, respectively. Feeding inhibition tests in soil showed EC50s for effects on consumption ratio of 127 and 56.7 mg Ag/kg, respectively. Although similar EC50s for effects on biomass were observed for nanoparticulate and ionic Ag (114 and 120 mg Ag/kg dry soil, respectively), at higher concentrations greater biomass loss was found for AgNO3. Upon dietary exposure, AgNO3 was more toxic, with EC50 for effects on biomass change being >1500 and 233 mg Ag/kg for Ag-NPs and AgNO3, respectively. The difference in toxicity between Ag-NPs and AgNO3 could not be explained from Ag body concentrations. This suggests that the relation between toxicity and bioavailability of Ag-NPs differs from that of ionic Ag in soils.

  20. Self-reduction and size controlled synthesis of silver nanoparticles on carbon nanospheres by grafting triazine-based molecular layer for conductivity improvement

    NASA Astrophysics Data System (ADS)

    Sang, Jing; Aisawa, Sumio; Hirahara, Hidetoshi; Kudo, Takahiro; Mori, Kunio

    2016-02-01

    A facile, self-reduction and size controlled synthesis method has been explored to fabricate silver nanoparticles (Ag NPs) on carbon nanosphere (CNs) under mild conditions. Without using predeposition of seed metals and reducing agent, a uniform and complete layer of Ag NPs was formed through grafting a molecular layer on CNs surfaces under UV irradiation. The size and thickness of Ag NPs were effectively tuned by adjusting the UV irradiation time. This direct formation of Ag NPs was attributed to self seed in aqueous Ag(NH3)2+ complex solution through a triazine-based silane coupling agent molecular layer, even at 25 °C. Scanning electron microscopy (SEM), Transmission electron microscope (TEM), and X-ray photoelectron spectroscopy (XPS) were employed to characterize the Ag NPs' properties. A substantial conductivity improvement of prepared Ag NPs on carbon nanosphere was demonstrated. The presented method is simple and environmentally friendly and thus should be of significant value for the industrial fabrication of Ag NPs on carbon nanosphere in conduct electricity paint and coating applications.

  1. In vivo genotoxicity assesment of silver nanoparticles of different sizes by the Somatic Mutation and Recombination Test (SMART) on Drosophila.

    PubMed

    Ávalos, Alicia; Haza, Ana Isabel; Drosopoulou, Elena; Mavragani-Tsipidou, Penelope; Morales, Paloma

    2015-11-01

    Silver nanoparticles (AgNPs) with antimicrobial activity are by far the most commercialized nano-compound. They are commonly used in medical products and devices, food storage materials, cosmetics and industrial products. Despite the increasing human exposure to AgNPs, they remain a controversial research area with regard to their toxic and genotoxic effects to biological systems. Although previous data have suggested that AgNPs induce toxicity in vitro, the in vivo studies on this topic are very limited. In the present study, the potential genotoxic activity of AgNPs of different sizes (4.7 and 42 nm) was evaluated using the in vivo Somatic Mutation and Recombination Test (SMART) in Drosophila melanogaster. Larvae were treated with 25, 30 and 50 μg/ml of AgNPs 4.7 nm, and 250, 500 and 1000 μg/ml of AgNPs 42 nm. Data showed that AgNPs at the applied concentrations did not modify the spontaneous frequencies of spots indicating lack of mutagenic and recombinogenic activity. However, both AgNPs induced pigmentation defects and reduction in locomotor ability in adult flies. Therefore, further experiments must be carried out to gain a better understanding of the mechanism of action of AgNPs to ensure their safe use. PMID:26169716

  2. Global optimization of bimetallic cluster structures. II. Size-matched Ag-Pd, Ag-Au, and Pd-Pt systems.

    PubMed

    Rossi, Giulia; Ferrando, Riccardo; Rapallo, Arnaldo; Fortunelli, Alessandro; Curley, Benjamin C; Lloyd, Lesley D; Johnston, Roy L

    2005-05-15

    Genetic algorithm global optimization of Ag-Pd, Ag-Au, and Pd-Pt clusters is performed. The 34- and 38-atom clusters are optimized for all compositions. The atom-atom interactions are modeled by a semiempirical potential. All three systems are characterized by a small size mismatch and a weak tendency of the larger atoms to segregate at the surface of the smaller ones. As a result, the global minimum structures exhibit a larger mixing than in Ag-Cu and Ag-Ni clusters. Polyicosahedral structures present generally favorable energetic configurations, even though they are less favorable than in the case of the size-mismatched systems. A comparison between all the systems studied here and in the previous paper (on size-mismatched systems) is presented.

  3. Size Effect of Ruthenium Nanoparticles in Catalytic Carbon Monoxide Oxidation

    SciTech Connect

    Joo, Sang Hoon; Park, Jeong Y.; Renzas, J. Russell; Butcher, Derek R.; Huang, Wenyu; Somorjai, Gabor A.

    2010-04-04

    Carbon monoxide oxidation over ruthenium catalysts has shown an unusual catalytic behavior. Here we report a particle size effect on CO oxidation over Ru nanoparticle (NP) catalysts. Uniform Ru NPs with a tunable particle size from 2 to 6 nm were synthesized by a polyol reduction of Ru(acac){sub 3} precursor in the presence of poly(vinylpyrrolidone) stabilizer. The measurement of catalytic activity of CO oxidation over two-dimensional Ru NPs arrays under oxidizing reaction conditions (40 Torr CO and 100 Torr O{sub 2}) showed an activity dependence on the Ru NP size. The CO oxidation activity increases with NP size, and the 6 nm Ru NP catalyst shows 8-fold higher activity than the 2 nm catalysts. The results gained from this study will provide the scientific basis for future design of Ru-based oxidation catalysts.

  4. Symmetry and Size of Membrane Protein Polyhedral Nanoparticles

    NASA Astrophysics Data System (ADS)

    Li, Di; Kahraman, Osman; Haselwandter, Christoph A.

    2016-09-01

    In recent experiments [T. Basta et al., Proc. Natl. Acad. Sci. U.S.A. 111, 670 (2014)] lipids and membrane proteins were observed to self-assemble into membrane protein polyhedral nanoparticles (MPPNs) with a well-defined polyhedral protein arrangement and characteristic size. We develop a model of MPPN self-assembly in which the preferred symmetry and size of MPPNs emerge from the interplay of protein-induced lipid bilayer deformations, topological defects in protein packing, and thermal effects. With all model parameters determined directly from experiments, our model correctly predicts the observed symmetry and size of MPPNs. Our model suggests how key lipid and protein properties can be modified to produce a range of MPPN symmetries and sizes in experiments.

  5. Size-dependent color tuning of efficiently luminescent germanium nanoparticles.

    PubMed

    Shirahata, Naoto; Hirakawa, Daigo; Masuda, Yoshitake; Sakka, Yoshio

    2013-06-18

    It is revealed that rigorous control of the size and surface of germanium nanoparticles allows fine color tuning of efficient fluorescence emission in the visible region. The spectral line widths of each emission were very narrow (<500 meV). Furthermore, the absolute fluorescence quantum yields of each emission were estimated to be 4-15%, which are high enough to be used as fluorescent labeling tags. In this study, a violet-light-emitting nanoparticle is demonstrated to be a new family of luminescent Ge. Such superior properties of fluorescence were observed from the fractions separated from one mother Ge nanoparticle sample by the fluorescent color using our developed combinatorial column technique. It is commonly believed that a broad spectral line width frequently observed from Ge nanoparticle appears because of an indirect band gap nature inherited even in nanostructures, but the present study argues that such a broad luminescence spectrum is expressed as an ensemble of different spectral lines and can be separated into the fractions emitting light in each wavelength region by the appropriate postsynthesis process.

  6. Water-soluble multidentate polymers compactly coating Ag2S quantum dots with minimized hydrodynamic size and bright emission tunable from red to second near-infrared region

    NASA Astrophysics Data System (ADS)

    Gui, Rijun; Wan, Ajun; Liu, Xifeng; Yuan, Wen; Jin, Hui

    2014-04-01

    Hydrodynamic size-minimized quantum dots (QDs) have outstanding physicochemical properties for applications in multicolor molecular and cellular imaging at the level of single molecules and nanoparticles. In this study, we have reported the aqueous synthesis of Ag2S QDs by using thiol-based multidentate polymers as capping reagents. By regulating the composition of the precursors (AgNO3 and sulfur-N2H4.H2O complex) and multidentate polymers (poly(acrylic acid)-graft-cysteamine-graft-ethylenediamine), as well as the reaction time, Ag2S QDs (2.6-3.7 nm) are prepared, displaying tunable photoluminescence (PL) emission from red to the second near-infrared region (687-1096 nm). The small hydrodynamic thickness (1.6-1.9 nm) of the multidentate polymers yields a highly compact coating for the QDs, which results in the bright fluorescent QDs with high PL quantum yields (QYs: 14.2-16.4%). Experimental results confirm that the QDs have high PL stability and ultralow cytotoxicity, as well as high PLQYs and small hydrodynamic sizes (4.5-5.6 nm) similar to fluorescent proteins (27-30 kDa), indicating the feasibility of highly effective PL imaging in cells and living animals.Hydrodynamic size-minimized quantum dots (QDs) have outstanding physicochemical properties for applications in multicolor molecular and cellular imaging at the level of single molecules and nanoparticles. In this study, we have reported the aqueous synthesis of Ag2S QDs by using thiol-based multidentate polymers as capping reagents. By regulating the composition of the precursors (AgNO3 and sulfur-N2H4.H2O complex) and multidentate polymers (poly(acrylic acid)-graft-cysteamine-graft-ethylenediamine), as well as the reaction time, Ag2S QDs (2.6-3.7 nm) are prepared, displaying tunable photoluminescence (PL) emission from red to the second near-infrared region (687-1096 nm). The small hydrodynamic thickness (1.6-1.9 nm) of the multidentate polymers yields a highly compact coating for the QDs, which results in

  7. Preparation of AgInS2 nanoparticles by a facile microwave heating technique; study of effective parameters, optical and photovoltaic characteristics

    NASA Astrophysics Data System (ADS)

    Tadjarodi, Azadeh; Cheshmekhavar, Amir Hossein; Imani, Mina

    2012-12-01

    In this work, AgInS2 (AIS) semiconductor nanoparticles were synthesized by an efficient and facile microwave heating technique using several sulfur sources and solvents in the different reaction times. The SEM images presented the particle morphology for all of the obtained products in the arranged reaction conditions. The particle size of 70 nm was obtained using thioacetamide (TAA), ethylene glycol (EG) as the sulfur source and solvent, respectively at the reaction time of 5 min. It was found that the change of the mentioned parameters lead to alter on the particle size of the resulting products. The average particle size was estimated using a microstructure measurement program and Minitab statistical software. The optical band gap energy of 1.96 eV for the synthesized AIS nanoparticles was determined by the diffuse reflectance spectroscopy (DRS). AgInS2/CdS/CuInSe2 heterojunction solar cell was constructed and photovoltaic parameters, i.e., open-circuit voltage (Voc), short-circuit current (Jsc) and fill factor (FF) were estimated by photocurrent-voltage (I-V) curve. The calculated fill factor of 30% and energy conversion efficiency of 1.58% revealed the capability of AIS nanoparticles to use in the solar cell devices.

  8. Synthesis, characterization, and 3D-FDTD simulation of Ag@SiO2 nanoparticles for shell-isolated nanoparticle-enhanced Raman spectroscopy.

    PubMed

    Uzayisenga, Viviane; Lin, Xiao-Dong; Li, Li-Mei; Anema, Jason R; Yang, Zhi-Lin; Huang, Yi-Fan; Lin, Hai-Xin; Li, Song-Bo; Li, Jian-Feng; Tian, Zhong-Qun

    2012-06-19

    Au-seed Ag-growth nanoparticles of controllable diameter (50-100 nm), and having an ultrathin SiO(2) shell of controllable thickness (2-3 nm), were prepared for shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS). Their morphological, optical, and material properties were characterized; and their potential for use as a versatile Raman signal amplifier was investigated experimentally using pyridine as a probe molecule and theoretically by the three-dimensional finite-difference time-domain (3D-FDTD) method. We show that a SiO(2) shell as thin as 2 nm can be synthesized pinhole-free on the Ag surface of a nanoparticle, which then becomes the core. The dielectric SiO(2) shell serves to isolate the Raman-signal enhancing core and prevent it from interfering with the system under study. The SiO(2) shell also hinders oxidation of the Ag surface and nanoparticle aggregation. It significantly improves the stability and reproducibility of surface-enhanced Raman scattering (SERS) signal intensity, which is essential for SERS applications. Our 3D-FDTD simulations show that Ag-core SHINERS nanoparticles yield at least 2 orders of magnitude greater enhancement than Au-core ones when excited with green light on a smooth Ag surface, and thus add to the versatility of our SHINERS method.

  9. E-beam deposited Ag-nanoparticles plasmonic organic solar cell and its absorption enhancement analysis using FDTD-based cylindrical nano-particle optical model.

    PubMed

    Kim, Richard S; Zhu, Jinfeng; Park, Jeung Hun; Li, Lu; Yu, Zhibin; Shen, Huajun; Xue, Mei; Wang, Kang L; Park, Gyechoon; Anderson, Timothy J; Pei, Qibing

    2012-06-01

    We report the plasmon-assisted photocurrent enhancement in Ag-nanoparticles (Ag-NPs) embedded PEDOT:PSS/P3HT:PCBM organic solar cells, and systematically investigate the causes of the improved optical absorption based on a cylindrical Ag-NPs optical model which is simulated with a 3-Dimensional finite difference time domain (FDTD) method. The proposed cylindrical Ag-NPs optical model is able to explain the optical absorption enhancement by the localized surface plasmon resonance (LSPR) modes, and to provide a further understanding of Ag-NPs shape parameters which play an important role to determine the broadband absorption phenomena in plasmonic organic solar cells. A significant increase in the power conversion efficiency (PCE) of the plasmonic solar cell was experimentally observed and compared with that of the solar cells without Ag-NPs. Finally, our conclusion was made after briefly discussing the electrical effects of the fabricated plasmonic organic solar cells.

  10. One pot synthesis of Ag nanoparticle modified ZnO microspheres in ethylene glycol medium and their enhanced photocatalytic performance

    SciTech Connect

    Tian Chungui; Li Wei; Pan Kai; Zhang Qi; Tian Guohui; Zhou Wei; Fu Honggang

    2010-11-15

    Ag nanoparticles (NPs) modified ZnO microspheres (Ag/ZnO microspheres) were prepared by a facile one pot strategy in ethylene glycol (EG) medium. The EG played two important roles in the synthesis: it could act as a reaction media for the formation of ZnO and reduce Ag{sup +} to Ag{sup 0}. A series of the characterizations indicated the successful combination of Ag NPs with ZnO microspheres. It was shown that Ag modification could greatly enhance the photocatalytic efficiency of ZnO microspheres by taking the photodegradation of Rhodamine B as a model reaction. With appropriate ratio of Ag and ZnO, Ag/ZnO microspheres showed the better photocatalytic performance than commercial Degussa P-25 TiO{sub 2}. Photoluminescence and surface photovoltage spectra demonstrated that Ag modification could effectively inhibit the recombination of the photoinduced electron and holes of ZnO. This is responsible for the higher photocatalytic activity of Ag/ZnO composites. -- Graphical abstract: A 'one-pot' strategy was developed for preparing the Ag/ZnO microspheres in ethylene glycol. The composites exhibited superior photocatalytic performance for photodegradation of Rhodamine B dye in water. Display Omitted

  11. Antibacterial property of Ag nanoparticle-impregnated N-doped titania films under visible light

    NASA Astrophysics Data System (ADS)

    Wong, Ming-Show; Chen, Chun-Wei; Hsieh, Chia-Chun; Hung, Shih-Che; Sun, Der-Shan; Chang, Hsin-Hou

    2015-07-01

    Photocatalysts produce free radicals upon receiving light energy; thus, they possess antibacterial properties. Silver (Ag) is an antibacterial material that disrupts bacterial physiology. Our previous study reported that the high antibacterial property of silver nanoparticles on the surfaces of visible light-responsive nitrogen-doped TiO2 photocatalysts [TiO2(N)] could be further enhanced by visible light illumination. However, the major limitation of this Ag-TiO2 composite material is its durability; the antibacterial property decreased markedly after repeated use. To overcome this limitation, we developed TiO2(N)/Ag/TiO2(N) sandwich films in which the silver is embedded between two TiO2(N) layers. Various characteristics, including silver and nitrogen amounts, were examined in the composite materials. Various analyses, including electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and ultraviolet-visible absorption spectrum and methylene blue degradation rate analyses, were performed. The antibacterial properties of the composite materials were investigated. Here we revealed that the antibacterial durability of these thin films is substantially improved in both the dark and visible light, by which bacteria, such as Escherichia coli, Streptococcus pyogenes, Staphylococcus aureus, and Acinetobacter baumannii, could be efficiently eliminated. This study demonstrated a feasible approach to improve the visible-light responsiveness and durability of antibacterial materials that contain silver nanoparticles impregnated in TiO2(N) films.

  12. Antibacterial property of Ag nanoparticle-impregnated N-doped titania films under visible light

    PubMed Central

    Wong, Ming-Show; Chen, Chun-Wei; Hsieh, Chia-Chun; Hung, Shih-Che; Sun, Der-Shan; Chang, Hsin-Hou

    2015-01-01

    Photocatalysts produce free radicals upon receiving light energy; thus, they possess antibacterial properties. Silver (Ag) is an antibacterial material that disrupts bacterial physiology. Our previous study reported that the high antibacterial property of silver nanoparticles on the surfaces of visible light-responsive nitrogen-doped TiO2 photocatalysts [TiO2(N)] could be further enhanced by visible light illumination. However, the major limitation of this Ag-TiO2 composite material is its durability; the antibacterial property decreased markedly after repeated use. To overcome this limitation, we developed TiO2(N)/Ag/TiO2(N) sandwich films in which the silver is embedded between two TiO2(N) layers. Various characteristics, including silver and nitrogen amounts, were examined in the composite materials. Various analyses, including electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and ultraviolet–visible absorption spectrum and methylene blue degradation rate analyses, were performed. The antibacterial properties of the composite materials were investigated. Here we revealed that the antibacterial durability of these thin films is substantially improved in both the dark and visible light, by which bacteria, such as Escherichia coli, Streptococcus pyogenes, Staphylococcus aureus, and Acinetobacter baumannii, could be efficiently eliminated. This study demonstrated a feasible approach to improve the visible-light responsiveness and durability of antibacterial materials that contain silver nanoparticles impregnated in TiO2(N) films. PMID:26156001

  13. Antibacterial property of Ag nanoparticle-impregnated N-doped titania films under visible light.

    PubMed

    Wong, Ming-Show; Chen, Chun-Wei; Hsieh, Chia-Chun; Hung, Shih-Che; Sun, Der-Shan; Chang, Hsin-Hou

    2015-07-09

    Photocatalysts produce free radicals upon receiving light energy; thus, they possess antibacterial properties. Silver (Ag) is an antibacterial material that disrupts bacterial physiology. Our previous study reported that the high antibacterial property of silver nanoparticles on the surfaces of visible light-responsive nitrogen-doped TiO2 photocatalysts [TiO2(N)] could be further enhanced by visible light illumination. However, the major limitation of this Ag-TiO2 composite material is its durability; the antibacterial property decreased markedly after repeated use. To overcome this limitation, we developed TiO2(N)/Ag/TiO2(N) sandwich films in which the silver is embedded between two TiO2(N) layers. Various characteristics, including silver and nitrogen amounts, were examined in the composite materials. Various analyses, including electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and ultraviolet-visible absorption spectrum and methylene blue degradation rate analyses, were performed. The antibacterial properties of the composite materials were investigated. Here we revealed that the antibacterial durability of these thin films is substantially improved in both the dark and visible light, by which bacteria, such as Escherichia coli, Streptococcus pyogenes, Staphylococcus aureus, and Acinetobacter baumannii, could be efficiently eliminated. This study demonstrated a feasible approach to improve the visible-light responsiveness and durability of antibacterial materials that contain silver nanoparticles impregnated in TiO2(N) films.

  14. Size-dependent interaction of silica nanoparticles with different surfactants in aqueous solution.

    PubMed

    Kumar, Sugam; Aswal, Vinod K; Kohlbrecher, Joachim

    2012-06-26

    The size-dependent interaction of anionic silica nanoparticles with ionic (anionic and cationic) and nonionic surfactants has been studied using small-angle neutron scattering (SANS). The surfactants used are anionic sodium dodecyl sulfate (SDS), cationic dodecyltrimethyl ammonium bromide (DTAB), and nonionic decaoxyethylene n-dodecylether (C(12)E(10)). The measurements have been carried out for three different sizes of silica nanoparticles (8, 16, and 26 nm) at fixed concentrations (1 wt % each) of nanoparticles and surfactants. It is found that irrespective of the size of the nanoparticles there is no significant interaction evolved between like-charged nanoparticles and the SDS micelles leading to any structural changes. However, the strong attraction of oppositely charged DTAB micelles with silica nanoparticles results in the aggregation of nanoparticles. The number of micelles mediating the nanoparticle aggregation increases with the size of the nanoparticle. The aggregates are characterized by fractal structure where the fractal dimension is found to be constant (D ≈ 2.3) independent of the size of the nanoparticles and consistent with diffusion-limited-aggregation-type fractal morphology in these systems. In the case of nonionic surfactant C(12)E(10), micelles interact with the individual silica nanoparticles. The number of adsorbed micelles per nanoparticle increases drastically whereas the percentage of adsorbed micelles on nanoparticles decreases with the increase in the size of the nanoparticles. PMID:22655980

  15. Tailoring Size and Coverage Density of Silver Nanoparticles on Monodispersed Polymer Spheres as Highly Sensitive SERS Substrates.

    PubMed

    Hu, Yougen; Zhao, Tao; Zhu, Pengli; Zhu, Yu; Liang, Xianwen; Sun, Rong; Wong, Ching-Ping

    2016-09-01

    Silver nanoparticles (AgNPs) were deposited onto the monodispersed carboxylic polystyrene (CPS) spheres by an improved in situ reduction method. The size and coverage density of the AgNPs on the surface of CPS spheres could be easily tailored by tuning the concentrations of carboxylic functional groups and silver precursor. The morphologies and structures of the resulting CPS/Ag hybrid particles were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), UV-Vis-NIR spectrometer and X-ray photoelectron spectroscopy (XPS), etc. The surface enhanced Raman scattering (SERS) performances of the resulting uniform CPS/Ag hybrid particles were investigated using 4-aminobenzenethiol (4-ABT) as the probe molecule. The optimized CPS/Ag hybrid particles show high enhancement factor (EF) of 2.71×10(7) , low limit of detection (LOD) of 10(-10)  m and good reproducibility with relative standard deviation (RSD) of 9.64 %. The good SERS improvement properties demonstrate these hybrid particles could be employed as simple and effective substrates in the SERS spectroscopy. PMID:27511618

  16. Determination of Anthracene on Ag-Au Alloy Nanoparticles/Overoxidized-Polypyrrole Composite Modified Glassy Carbon Electrodes

    PubMed Central

    Mailu, Stephen N.; Waryo, Tesfaye T.; Ndangili, Peter M.; Ngece, Fanelwa R.; Baleg, Abd A.; Baker, Priscilla G.; Iwuoha, Emmanuel I.

    2010-01-01

    A novel electrochemical sensor for the detection of anthracene was prepared by modifying a glassy carbon electrode (GCE) with over-oxidized polypyrrole (PPyox) and Ag-Au (1:3) bimetallic nanoparticles (Ag-AuNPs). The composite electrode (PPyox/Ag-AuNPs/GCE) was prepared by potentiodynamic polymerization of pyrrole on GCE followed by its overoxidation in 0.1 M NaOH. Ag-Au bimetallic nanoparticles were chemically prepared by the reduction of AgNO3 and HAuCl4 using C6H5O7Na3 as the reducing agent as well as the capping agent and then immobilized on the surface of the PPyox/GCE. The nanoparticles were characterized by UV-visible spectroscopy technique which confirmed the homogeneous formation of the bimetallic alloy nanoparticles. Transmission electron microscopy showed that the synthesized bimetallic nanoparticles were in the range of 20–50 nm. The electrochemical behaviour of anthracene at the PPyox/Ag-AuNPs/GCE with Ag: Au atomic ratio 25:75 (1:3) exhibited a higher electrocatalytic effect compared to that observed when GCE was modified with each constituent of the composite (i.e., PPyox, Ag-AuNPs) and bare GCE. A linear relationship between anodic current and anthracene concentration was attained over the range of 3.0 × 10−6 to 3.56 × 10−4 M with a detection limit of 1.69 × 10−7 M. The proposed method was simple, less time consuming and showed a high sensitivity. PMID:22163419

  17. Separation of monodisperse alginate nanoparticles and effect of particle size on transport of vitamin E.

    PubMed

    Li, Qian; Liu, Chen-Guang; Yu, Yu

    2015-06-25

    Four batches of oleoyl alginate ester (OAE) nanoparticles with narrow size distribution were rapidly separated from the initial batch of nanoparticles by means of centrifugation at the relative centrifugal force (RCF) between 270×g and 6750×g after adjusting the zeta potential. The size of nanoparticles decreased with increasing speed of centrifugation, and the polydispersity of nanoparticles significantly decreased. As particle size increased the loading capacity also increased, while transport across Caco-2 cells and the cellular uptake of nanoparticles in jejunum decreased. Endocytosis of nanoparticles around 50nm/120nm, 420nm and 730nm occur mainly via clathrin-mediated endocytosis, caveolae-mediated endocytosis and macropinocytosis respectively. These results show that centrifugation could separate nanoparticles with appropriate zeta potential into different sizes and the transport and cellular uptake of OAE polysaccharide nanoparticles were size dependent.

  18. Study of Ag-Pd bimetallic nanoparticles modified glassy carbon electrode for detection of L-cysteine

    NASA Astrophysics Data System (ADS)

    Murugavelu, M.; Karthikeyan, B.

    2014-11-01

    Ag-Pd bimetallic nanoparticles (Ag-Pd BNPs) as an enhanced sensing material with improved electronic transmission rates in the electrochemical sensing of L-cysteine (L-cys) has been reported. The morphology of Ag-Pd BNPs was characterized with X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and cyclic voltammetry (CV). Oxidation of L-cys on Ag-Pd BNPs is investigated in detail by discussing the effect of the structure and from the electrocatalytic oxidation of L-cys. We found that the Ag-Pd BNPs exhibited high electrocatalytic activity towards L-cys oxidation in neutral condition and could be used for the development of nonenzymatic L-cys sensor. Based on the efficient catalytic ability of Ag-Pd BNPs, the fabricated biosensor exhibited a wide linear range of responses to the L-cys with the concentration detection limit of nearly down to 2 mM with fast response time.

  19. Preparation of Novel Europium Complex Doped Ag@SiO2 Nanoparticles with Intense Fluorescence.

    PubMed

    Liu, Bing; Yin, Dongguang; Song, Kailin; Yang, Juan Ou; Wang, Chengcheng; Wu, Minghong

    2015-01-01

    In this study, a new europium complex of 4,4'-bis (1",1",1",2",2",3",3"-heptafluoro-4",6"- hexanedion-6"-yl)-o-terpheny-Eu(3+)-4,7-diphenyl-1,10-phenanthroline-2,9-dicarboxylic acid-(3-aminopropyl) trimethoxysilane (BHHT-Eu(3+)-DPPDA-APTMS) was prepared first. Then novel core-shell Ag@SiO2 nanoparticles with BHHT-Eu(3+)-DPPDA-APTMS doped in shell were synthesized by a facile water-in-oil microemulsion method. The properties of the prepared complex and nanoparticles, and the effect of metal enhanced fluorescence for the nanoparticles were investigated. The prepared nanopartilces exhibited intense fluorescence, uniform morphology and good water-solubility. The fluorescent intensities of silver core-present nanopartciles were significant higher than that of silver core-absent nanoparticles owing to the metal enhanced fluorescence of silver core. It is expectable that the as-prepared nanoparticles can serve as a potential fluorescent nanoprobe, applying in high sensitive biological and medical detections.

  20. Spectral anion sensing and γ-radiation induced magnetic modifications of polyphenol generated Ag-nanoparticles

    NASA Astrophysics Data System (ADS)

    Ansari, Zarina; Dhara, Susmita; Bandyopadhyay, Bilwadal; Saha, Abhijit; Sen, Kamalika

    2016-03-01

    A fast one step bio-synthesis for in situ preparation of silver nanoparticles is proposed. The method involves reduction of AgNO3 with an aqueous extract of peanut skin, which is a good source of polyphenols. The silver nanoparticles thus synthesized were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), UV-Vis absorption spectroscopy, Fourier Transform infrared (FTIR) spectroscopy and magnetic measurements. Effect of low dose γ irradiation during the synthesis was studied and their physico-chemical properties were compared with those produced without irradiation. On the contrary to the diamagnetic behavior of bulk silver, the silver nanoparticles thus prepared show a significant ferromagnetic moment component. Variable time exposure to γ-irradiation results in an exponential decay of ferromagnetic component. A freshly prepared solution of silver nanoparticles shows selective spectral changes towards iodide ions at trace concentration (below 50 μM) among a series of 16 other competing anions. The prepared nanoparticles are therefore suitable for anion sensing application.

  1. Assessing Pistia stratiotes for phytoremediation of silver nanoparticles and Ag(I) contaminated waters.

    PubMed

    Hanks, Nicole A; Caruso, Joseph A; Zhang, Peng

    2015-12-01

    To study the phytoremediation capabilities of Pistia stratiotes in silver nanoparticle (AgNP) and silver ion contaminated wastewaters, individual plants were grown in media spiked with different concentrations of silver nanoparticle and silver ions (0.02, 0.2, and 2 mg L(-1)). Control experiments were carried out at the same time for comparison purposes. Visual changes in the plants were also recorded periodically during each experiment. Total silver concentrations were monitored in the media before, during, and at the termination of the experiments. In addition, analysis of total silver in plant root and leaf samples after termination were carried out to determine the effect of the different media concentrations. The results showed that P. stratiotes can survive in AgNP and ions under 0.02 mg L(-1) and contaminants are retained within the plant. The use of P. stratiotes as a phytoremediator shows potential in removing heavy metal nanoparticles and is competitive in its removal of the ion counterpart. Even higher concentrations of silver, regardless of form, can be reduced to lower levels than the World Health Organization's maximum contamination limit.

  2. The antibacterial properties of a novel chitosan-Ag-nanoparticle composite.

    PubMed

    Sanpui, Pallab; Murugadoss, A; Prasad, P V Durga; Ghosh, Siddhartha Sankar; Chattopadhyay, Arun

    2008-05-31

    Escherichia coli expressing recombinant green fluorescent protein was used to test the bactericidal efficacy of a newly synthesized chitosan-Ag-nanoparticle composite. The composite was found to have significantly higher antimicrobial activity than its components at their respective concentrations. The one-pot synthesis method led to the formation of small Ag nanoparticles attached to the polymer which can be dispersed in media of pH< or =6.3. The presence of a small percentage (2.15%, w/w) of metal nanoparticles in the composite was enough to significantly enhance inactivation of E. coli as compared with unaltered chitosan. Fluorescence spectroscopy indicated that bacterial growth stopped immediately after exposure of E. coli to the composite, with release of cellular green fluorescent protein into the medium at a faster rate than with chitosan. Fluorescence confocal laser scanning and scanning electron microscopy showed attachment of the bacteria to the composite and their subsequent fragmentation. Native protein gel electrophoresis experiments indicated no effect of the composite on bacterial proteins.

  3. Sonochemically synthesized Ag nanoparticles as a SERS active substrate and effect of surfactant

    NASA Astrophysics Data System (ADS)

    Dar, Nitzan; Chen, Kuang-Yu; Nien, Yung-Tang; Perkas, Nina; Gedanken, Aharon; Chen, In-Gann

    2015-03-01

    Surface enhanced Raman scattering (SERS) enables the detection of substances at low concentrations using silver or gold nanostructure. The SERS technique has many applications, such as environmental detection and biosensing. Sonochemistry is an excellent and cheap deposition technique for coating substrates in a form of nanostructure at ambient temperature. It can also be utilized to prepare large SERS substrates. Here, we used the advantages of sonochemistry to deposit solid SERS substrates immobilized on GaN nanostructure. Morphology was studied by scanning electron microscopy. The elemental composition and the spatial distribution were examined by energy dispersive X-ray spectroscopy. The crystal structure and atomic presence was confirmed by X-ray diffraction. SERS substrates were examined with the analytes crystal violet (10-5 M) and rhodamine 6G (10-6 M), they showed prominent characteristic peaks. We discovered that the SERS intensity of poly-vinyl-pyrrolidinone aided sonochemical deposition of Ag nanoparticles was increased. The reason for the effect is morphological changes of the Ag nanoparticles. Smaller nanoparticles were fabricated, which increase their SERS intensity.

  4. Strain Hardening and Size Effect in Five-fold Twinned Ag Nanowires.

    PubMed

    Narayanan, Sankar; Cheng, Guangming; Zeng, Zhi; Zhu, Yong; Zhu, Ting

    2015-06-10

    Metallic nanowires usually exhibit ultrahigh strength but low tensile ductility owing to their limited strain hardening capability. Here we study the unique strain hardening behavior of the five-fold twinned Ag nanowires by nanomechanical testing and atomistic modeling. In situ tensile tests within a scanning electron microscope revealed strong strain hardening behavior of the five-fold twinned Ag nanowires. Molecular dynamics simulations showed that such strain hardening was critically controlled by twin boundaries and pre-existing defects. Strain hardening was size dependent; thinner nanowires achieved more hardening and higher ductility. The size-dependent strain hardening was found to be caused by the obstruction of surface-nucleated dislocations by twin boundaries. Our work provides mechanistic insights into enhancing the tensile ductility of metallic nanostructures by engineering the internal interfaces and defects.

  5. Nanosized Fe3O4 an efficient PCR yield enhancer-Comparative study with Au, Ag nanoparticles.

    PubMed

    Kambli, Priyanka; Kelkar-Mane, Varsha

    2016-05-01

    Nanomaterials-assisted PCR is a promising field of nanobiotechnology that amalgamates nanomaterials into the conventional PCR system to achieve better amplification of desired product. With literature documenting the variable effects of these nanomaterials on the PCR yield and amplification; it was thought worthwhile to compare the PCR enhancing efficiency of three transition metal nanoparticles in form of stable colloidal suspensions at varying concentrations.The nanoparticles(NPs) of silver, gold and magnetite were chemically synthesized by reducing their respective salts and characterized using UV-vis spectroscopy. Their morphology was assessed using nanoparticle tracking system and AFM. The effect of these nanofluids on amplification of 800 bp prokaryotic DNA template with 30% GC content was studied using conventional thermal cycler. The reaction kinetics for all the three nanofluids yielded a Gaussian curve of amplification with varying concentrations. The ammonium salt of oleic acid coated magnetite (Fe3O4) nanoparticles at a concentration of 0.72 × 10(-2)nM and average size of 33 nm demonstrated highest amplification efficiency of 190% as compared to the citrate stabilized AgNP-25 nm (45%) and AuNP-15.19 nm (134%) using a conventional PCR system. The major reasons that allow Fe3O4 NPs outperform the other 2 transition metal NP's seem to be attributed to its heat conduction property as well as effective adsorption of PCR components onto the ammonium salt of oleic acid coated magnetite nanofluids. The data from our study offers valuable information for the application of ferrofluids as economically, efficient and effective alternative for nanomaterial-assisted PCR yield enhancers.

  6. Nanosized Fe3O4 an efficient PCR yield enhancer-Comparative study with Au, Ag nanoparticles.

    PubMed

    Kambli, Priyanka; Kelkar-Mane, Varsha

    2016-05-01

    Nanomaterials-assisted PCR is a promising field of nanobiotechnology that amalgamates nanomaterials into the conventional PCR system to achieve better amplification of desired product. With literature documenting the variable effects of these nanomaterials on the PCR yield and amplification; it was thought worthwhile to compare the PCR enhancing efficiency of three transition metal nanoparticles in form of stable colloidal suspensions at varying concentrations.The nanoparticles(NPs) of silver,