scholarly journals Au@Ag Core@Shell Nanoparticles Synthesized with Rumex hymenosepalus as Antimicrobial Agent

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Jesús Mauro Adolfo Villalobos-Noriega ◽  
Ericka Rodríguez-León ◽  
César Rodríguez-Beas ◽  
Eduardo Larios-Rodríguez ◽  
Maribel Plascencia-Jatomea ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Bimetallic Nanoparticles ◽  
Lag Phase ◽  
Core Shell ◽  
Root Extract ◽  
Dependent Manner ◽  
X Ray ◽  
Transmission Electron ◽  
Gold Silver ◽  
Vis Spectroscopy

AbstractIn this work, we used a sequential method of synthesis for gold–silver bimetallic nanoparticles with core@shell structure (Au@AgNPs). Rumex hymenosepalus root extract (Rh), which presents high content in catechins and stilbenes, was used as reductor agent in nanoparticles synthesis. Size distribution obtained by Transmission Electron Microscopy (TEM) gives a mean diameter of 36 ± 11 nm for Au@AgNPs, 24 ± 4 nm for gold nanoparticles (AuNPs), and 13 ± 3 nm for silver nanoparticles (AgNPs). The geometrical shapes of NPs were principally quasi-spherical. The thickness of the silver shell over AuNPs is around 6 nm and covered by active biomolecules onto the surface. Nanoparticles characterization included high angle annular dark field images (HAADF) recorded with a scanning transmission electron microscope (STEM), Energy-Dispersive X-ray Spectroscopy (EDS), X-Ray Diffraction (XRD), UV–Vis Spectroscopy, Zeta Potential, and Dynamic Light Scattering (DLS). Fourier Transform Infrared Spectrometer (FTIR), and X-ray Photoelectron Spectroscopy (XPS) show that nanoparticles are stabilized by extract molecules. A growth kinetics study was performed using the Gompertz model for microorganisms exposed to nanomaterials. The results indicate that AgNPs and Au@AgNPs affect the lag phase and growth rate of Escherichia coli and Candida albicans in a dose-dependent manner, with a better response for Au@AgNPs

scholarly journals Core-Shell Au@Ag Nanoparticles Synthesized with Polyphenols as Antimicrobial Agents

2021 ◽  
Author(s):  
Jesús Mauro Adolfo Villalobos-Noriega ◽  
Ericka Rodríguez Leon ◽  
César Rodríguez-Beas ◽  
Eduardo Larios-Rodríguez ◽  
Maribel Plascencia-Jatomea ◽  
...  
Keyword(s):  
Growth Kinetic ◽  
Antimicrobial Agents ◽  
Bimetallic Nanoparticles ◽  
Kinetic Curve ◽  
Core Shell ◽  
Root Extract ◽  
X Ray ◽  
Transmission Electron ◽  
Gold Silver ◽  
Vis Spectroscopy

Abstract In this work, we used a sequential method of synthesis for gold-silver bimetallic nanoparticles with core@shell structure (Au@AgNPs). Rumex hymenosepalus root extract (Rh), which presents high content in catechins and stilbenes, was used as reductor agent in nanoparticles synthesis. Size distribution obtained by Transmission Electron Microscopy (TEM) give a diameter mean of 36 nm for Au@AgNPs, and 24 nm for gold nanoparticles (AuNPs). The geometrical shapes of NPs were principally quasi-spherical. The thickness of silver shell over AuNPs are around 6 nm and covered by active biomolecules onto surface. Microstructural characterization included high angle annular dark field images (HAADF) recorded with a scanning transmission electron microscope (STEM), Energy-Dispersive X-ray Spectroscopy (EDS), X-Ray Diffraction (XRD), UV-Vis Spectroscopy, and Zeta Potential. Also, a growth kinetic curve analysis using the Gompertz model for Staphylococcus aureus (Gram-positive), Escherichia coli (Gram-negative), and Candida albicans (yeast) were carried out for Au@AgNPs and monometallic AuNPs and AgNPs. Interestingly, Gompertz analysis indicates that Au@AgNPs present a higher effect on the growth kinetic of microorganisms than shown by monometallic nanoparticles.

scholarly journals Microwave-assisted preparation of ZnS and ZnSe nanocrystals with different morphologies for photodegradation process of organic dyes

2019 ◽  
Author(s):  
Katarzyna Matras-Postolek ◽  
A. Zaba ◽  
S. Sovinska ◽  
D. Bogdal
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Organic Dyes ◽  
Zinc Sulphide ◽  
Conventional Heating ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy

Zinc sulphide (ZnS) and zinc selenide (ZnSe) and manganese-doped and un-doped with different morphologies from 1D do 3D microflowers were successfully fabricated in only a few minutes by solvothermal reactions under microwave irradiation. In order to compare the effect of microwave heating on the properties of obtained  nanocrystals, additionally the synthesis under conventional heating was conducted additionally in similar conditions. The obtained nanocrystals were systematically characterized in terms of structural and optical properties using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV-Vis spectroscopy (DR UV-Vis), Fourier-transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area analysis. The photocatalytic activity of ZnSe, ZnS, ZnS:Mn and ZnSe:Mn nanocrystals with different morphologies was evaluated by the degradation of methyl orange (MO) and Rhodamine 6G (R6G), respectively. The results show that Mn doped NCs samples had higher coefficient of degradation of organic dyes under ultraviolet irradiation (UV).

One-Pot Hydrothermal Synthesis of Sulfur-Doped SnO2 Nanoparticles and their Enhanced Photocatalytic Properties

NANO ◽  
2016 ◽  
Vol 11 (03) ◽  
pp. 1650035 ◽  
Author(s):  
Lin Ma ◽  
Limei Xu ◽  
Xuyao Xu ◽  
Xiaoping Zhou ◽  
Lingling Zhang
Keyword(s):  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Sno2 Nanoparticles ◽  
Light Response ◽  
One Pot ◽  
X Ray ◽  
Transmission Electron ◽  
Light Region ◽  
Vis Spectroscopy

Sulfur-doped SnO2 nanoparticles with ultrafine sizes have been successfully prepared by a one-pot hydrothermal method. The obtained samples are characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), high resolution transmission electron microscopy (HRTEM), thermogravimetric (TG), analyzer UV-Vis spectroscopy, photoluminescence (PL) and electrochemical impedance spectroscopy (EIS). The experimental results indicate that the doping level of sulfur element as well as the bandgaps of SnO2 can be controlled to a certain extent by varying the amount of L-cysteine (L-cys). When evaluated as photocatalysts in the degradation of rhodamine B (RhB) and reduction of Cr(VI) under visible light region, the resultant sulfur-doped SnO2 nanoparticles demonstrate obviously enhanced photocatalytic activities due to the markedly improved visible light response and effective separation of the photo-generated electron–hole pairs.

scholarly journals Efficient Method for the Concentration Determination of Fmoc Groups Incorporated in the Core-Shell Materials by Fmoc–Glycine

Molecules ◽  
2020 ◽  
Vol 25 (17) ◽  
pp. 3983
Author(s):  
Elżbieta Szczepańska ◽  
Beata Grobelna ◽  
Jacek Ryl ◽  
Amanda Kulpa ◽  
Tadeusz Ossowski ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Core Shell ◽  
Amino Groups ◽  
The Core ◽  
Transmission Electron ◽  
Model Sample ◽  
Vis Spectroscopy ◽  
Fmoc Group ◽  
Synthesis Procedure

In this paper, we described the synthesis procedure of TiO2@SiO2 core-shell modified with 3-(aminopropyl)trimethoxysilane (APTMS). The chemical attachment of Fmoc–glycine (Fmoc–Gly–OH) at the surface of the core-shell structure was performed to determine the amount of active amino groups on the basis of the amount of Fmoc group calculation. We characterized nanostructures using various methods: transmission electron microscope (TEM), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS) to confirm the modification effectiveness. The ultraviolet-visible spectroscopy (UV-vis) measurement was adopted for the quantitative determination of amino groups present on the TiO2@SiO2 core-shell surface by determination of Fmoc substitution. The nanomaterials were functionalized by Fmoc–Gly–OH and then the fluorenylmethyloxycarbonyl (Fmoc) group was cleaved using 20% (v/v) solution of piperidine in DMF. This reaction led to the formation of a dibenzofulvene–piperidine adduct enabling the estimation of free Fmoc groups by measurement the maximum absorption at 289 and 301 nm using UV-vis spectroscopy. The calculations of Fmoc loading on core-shell materials was performed using different molar absorption coefficient: 5800 and 6089 dm3 × mol−1 × cm−1 for λ = 289 nm and both 7800 and 8021 dm3 × mol−1 × cm−1 for λ = 301 nm. The obtained results indicate that amount of Fmoc groups present on TiO2@SiO2–(CH2)3–NH2 was calculated at 6 to 9 µmol/g. Furthermore, all measurements were compared with Fmoc–Gly–OH used as the model sample.

scholarly journals Fe based core–shell model catalysts for the reaction of CO2 with H2

2020 ◽  
Vol 131 (1) ◽  
pp. 119-128 ◽  
Author(s):  
Johann Kirchner ◽  
Christian Zambrzycki ◽  
Zeynep Baysal ◽  
Robert Güttel ◽  
Sven Kureti
Keyword(s):  
Shell Model ◽  
Photoelectron Spectroscopy ◽  
Major Product ◽  
Model Catalysts ◽  
Core Shell ◽  
Core Size ◽  
X Ray ◽  
Transmission Electron ◽  
Spent Catalysts ◽  
Temperature Programmed

Abstract Fe@SiO2 core–shell model catalysts were investigated for the conversion of CO2 and H2 into CH4, CO and H2O. For evaluation of the effect of core size on the catalytic activity, samples with Fe particle sizes of 4, 6 and 8 nm were prepared. Fresh and spent catalysts were thoroughly characterized by X-ray diffraction, 57Fe Mössbauer spectroscopy, transmission electron microscopy, temperature programmed hydrogenation and X-ray photoelectron spectroscopy. As a result, the yield of the major product CO as well as CH4 was increased with Fe core size. Additionally, growing Fe cores led to stronger carburization and higher amount of reactive carbide entities, which drive the CH4 formation. Finally, formation of inactive bulk carbon deposition is strongly suppressed for the core–shell catalysts in comparison to bulk iron oxide catalysts used for CO2 hydrogenation.

Characterization of Highly Luminescent LaPO4:Eu3+/LaPO4 One-Dimensional Core/Shell Heterostructures

2008 ◽  
Vol 8 (3) ◽  
pp. 1266-1271 ◽  
Author(s):  
Wenbo Bu ◽  
Jianlin Shi
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Core Shell ◽  
Trap States ◽  
Hydrothermal Conditions ◽  
One Dimensional ◽  
X Ray ◽  
Luminescence Efficiency ◽  
Transmission Electron

Highly luminescent LaPO4:Eu3+/LaPO4 one-dimensional (1D) core/shell heterostructures were successfully synthesized by a mild and simple self-aggregation process under refluxing or hydrothermal conditions. The resulting 1D core/shell heterostructures were characterized using a variety of techniques including X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), and X-ray photoelectron spectroscopy (XPS) to demonstrate successful coating by the crystalline LaPO4. In addition, a possible formation mechanism for this core/shell heterostructure was proposed. Finally, the photoluminescence property of the LaPO4:Eu3+/LaPO4 1D core/shell heterostructures was investigated in detail, which illustrates that the core/shell heterostructures remarkably increase the luminescence efficiency because the LaPO4 shells effectively eliminate surface trap-states and suppress the energy quenching in the energy-transfer processes.

Synthesis and characterization of thermosensitive and polarity-sensitive fluorescent PNIPAM-coated gold nanoparticles

e-Polymers ◽  
2017 ◽  
Vol 17 (1) ◽  
pp. 65-70 ◽  
Author(s):  
Chunhua Luo ◽  
Meijuan Qian ◽  
Qiujing Dong
Keyword(s):  
Photoelectron Spectroscopy ◽  
Au Nanoparticles ◽  
Synthesis And Characterization ◽  
Strong Fluorescence ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Grafting Through ◽  
Polarity Sensitive

AbstractThermosensitive PNIPAM-coated Au nanoparticles (AuNPs@P(NIPAM-co-MADMAC)) were synthesized by the radical “grafting through” copolymerization of 4-methacryloyloxy-4′-dimethylaminochalcone (MADMAC), MAEL-capped AuNPs and N-isopropylacrylamide (NIPAM) using azobisisobutyronitrile (AIBN) as the initiator. AuNPs@P(NIPAM-co-MADMAC) were characterized by transmission electron microscopy (TEM), ultraviolet-visible (UV-Vis) spectroscopy, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), 1H nuclear magnetic resonance (NMR), and Fourier transform infrared (FTIR) spectroscopy. AuNPs@P(NIPAM-co-MADMAC) exhibited thermo-sensitivity from poly(NIPAM-co-MADMAC) chains and sensitive fluorescence from the MADMAC group. AuNPs@P(NIPAM-co-MADMAC) showed weak fluorescence after the temperature increased from 25°C to 45°C, or after β-cyclodextrin (β-CD) was added. Furthermore, it exhibited strong fluorescence when the solvent was changed to ethanol or chloroform.

Synthesis of Self-Stratifying Polyacrylate Latex Containing Silicon

2012 ◽  
Vol 151 ◽  
pp. 337-340 ◽  
Author(s):  
Yu Feng Li ◽  
Hong Chao Wang ◽  
Zhong Yuan Xiang ◽  
Xiao Hui Gao
Keyword(s):  
Photoelectron Spectroscopy ◽  
Raw Materials ◽  
Core Shell ◽  
Size Distributions ◽  
X Ray ◽  
Organic Silicon ◽  
Air Interface ◽  
Transmission Electron ◽  
Core Shell Structure ◽  
Thermal Stability Of

Self-stratifying polyacrylate latex containing silicon was synthesized via semi-continuous emulsion polymerization, using organic silicon and acrylate as raw materials. Transmission electron microscope(TEM) characterization indicated that the particles were form uniform analogous core-shell structure and dynamic light scattering(DLS) analysis possessed narrow size distributions. The results of X-ray photoelectron spectroscopy(XPS) proved the propensity of silicon enrichment at film-air interface, which revealed self-stratifying phenomenon. The thermal stability of the latex films determined by thermogravimetric analysis(TGA) was increased 24 °C as the join of organic silicon.

scholarly journals Laser-Assisted Synthesis and Oxygen Generation of Nickel Nanoparticles

Materials ◽  
2020 ◽  
Vol 13 (18) ◽  
pp. 4068
Author(s):  
Jakub Wawrzyniak ◽  
Jakub Karczewski ◽  
Jacek Ryl ◽  
Katarzyna Grochowska ◽  
Katarzyna Siuzdak
Keyword(s):  
Photoelectron Spectroscopy ◽  
Nickel Nanoparticles ◽  
Size Control ◽  
Metallic Nickel ◽  
X Ray ◽  
Oxygen Generation ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Order Of Magnitude ◽  
Current Densities

Nowadays, more than ever, environmental awareness is being taken into account when it comes to the design of novel materials. Herein, the pathway to the creation of a colloid of spherical, almost purely metallic nickel nanoparticles (NPs) through pulsed laser ablation in ethanol is presented. A complex description of the colloid is provided through UV-vis spectroscopy and dynamic light scattering analysis, ensuring insight into laser-induced nanoparticle homogenization and size-control of the NPs. The transmission electron spectroscopy revealed spherical nanoparticles with a narrow size distribution, whereas the energy-dispersive X-ray spectroscopy accompanied by the X-ray photoelectron spectroscopy revealed their metallic nature. Furthermore, an example of the application of the colloidal nanoparticles is presented, where a quick, five-min ultrasound modification results in over an order of magnitude higher current densities in the titania-based electrode for the oxygen evolution reaction.

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