Synthesis and Characterization of Silica-Lead Sulfide Core Shell Nanospheres For Applications in Optoelectronic Devices

2021 ◽  
Author(s):  
Anderson Klay Romero-Jaime ◽  
Milka del Carmen Acosta-Enríquez ◽  
Diana Vargas-Hernández ◽  
Judith Celina Tánori-Córdova ◽  
Horacio Antolín Pineda-León ◽  
...  
Keyword(s):  
Chemical Composition ◽  
Lead Sulfide ◽  
Photoelectron Spectroscopy ◽  
Core Shell ◽  
Shell System ◽  
Quantum Confinement Effects ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Spectrum Shift

Abstract Nanoscale miniaturization of chalcogenides semiconductors, such as lead sulfide (galena), can generate interesting quantum confinement effects in the field of optoelectronic applications. At this work, a process in order to obtain SiO2 nanospheres coated with Galena, as the denominated core-shell system, is developed, this process it is based in Stöber’s method, where only the magnetic stirring was replaced by an ultrasonic bath, to achieve well rounded, and highly stable silica nanoparticles with diameters average of 70 nm. The PbS shell cover presents a thickness of 10 nm around. Nanostructures chemical composition, morphology and optical properties were determined by Transmission Electron Microscopy and UV-Vis spectroscopy, respectively. As a result, the nano shells correspond to cubic PbS, presenting some interplanar distances of 2.95 Å and 3.41 Å; this nano shell also shown a toward blue optical spectrum shift and a remarkable increase in its band gap, 3.75 eV, was obtained, compared with the PbS bulk value. The chemical composition it is studied by energy scattering spectroscopy, and X-ray photoelectron spectroscopy analyzes.

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.

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.

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 Synthesis and characterization of silica–lead sulfide core–shell nanospheres for applications in optoelectronic devices

2021 ◽  
Author(s):  
A. K. Romero-Jaime ◽  
M. C. Acosta-Enríquez ◽  
D. Vargas-Hernández ◽  
J. C. Tánori-Córdova ◽  
H. A. Pineda León ◽  
...  
Keyword(s):  
Lead Sulfide ◽  
Optoelectronic Devices ◽  
Synthesis And Characterization ◽  
Core Shell

scholarly journals Structural Factors Inducing Cracking of Brass Fittings

Materials ◽  
2021 ◽  
Vol 14 (12) ◽  
pp. 3255
Author(s):  
Lenka Kunčická ◽  
Michal Jambor ◽  
Adam Weiser ◽  
Jiří Dvořák
Keyword(s):  
Chemical Composition ◽  
Plastic Flow ◽  
Beta Phase ◽  
Alpha Phase ◽  
Structural Factors ◽  
Transmission Electron ◽  
Medical Gas ◽  
Hot Die Forging ◽  
Multiple Step

Cu–Zn–Pb brasses are popular materials, from which numerous industrially and commercially used components are fabricated. These alloys are typically subjected to multiple-step processing—involving casting, extrusion, hot forming, and machining—which can introduce various defects to the final product. The present study focuses on the detailed characterization of the structure of a brass fitting—i.e., a pre-shaped medical gas valve, produced by hot die forging—and attempts to assess the factors beyond local cracking occurring during processing. The analyses involved characterization of plastic flow via optical microscopy, and investigations of the phenomena in the vicinity of the crack, for which we used scanning and transmission electron microscopy. Numerical simulation was implemented not only to characterize the plastic flow more in detail, but primarily to investigate the probability of the occurrence of cracking based on the presence of stress. Last, but not least, microhardness in specific locations of the fitting were examined. The results reveal that the cracking occurring in the location with the highest probability of the occurrence of defects was most likely induced by differences in the chemical composition; the location the crack in which developed exhibited local changes not only in chemical composition—which manifested as the presence of brittle precipitates—but also in beta phase depletion. Moreover, as a result of the presence of oxidic precipitates and the hard and brittle alpha phase, the vicinity of the crack exhibited an increase in microhardness, which contributed to local brittleness.

scholarly journals Synthesis and characterization of Fe, Co, and Ni colloids in 2-mercaptoethanol

2020 ◽  
Vol 10 ◽  
pp. 184798042096688
Author(s):  
Galo Cárdenas-Triviño ◽  
Sergio Triviño-Matus
Keyword(s):  
Electron Microscopy ◽  
Electron Diffraction ◽  
Colloidal Dispersions ◽  
Synthesis And Characterization ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Chemical Liquid Deposition ◽  
Liquid Deposition

Metal colloids in 2-mercaptoethanol using nanoparticles (NPs) of iron (Fe), cobalt (Co), and nickel (Ni) were prepared by chemical liquid deposition method. Transmission electron microscopy, electron diffraction, UV-VIS spectroscopy, and scanning electron microscopy with electron dispersive X-ray spectroscopy characterized the resulting colloidal dispersions. The NPs exhibited sizes with ranges from 9.8 nm for Fe, 3.7 nm for Co, and 7.2 nm for Ni. The electron diffraction shows the presence of the metals in its elemental state Fe (0), Co (0), and Ni (0) and also some compounds FeO (OH), CoCo2S4, and NiNi2S4.

Characterization of columns grown during KrF laser micromachining of Al2O3–TiC ceramics

2003 ◽  
Vol 18 (5) ◽  
pp. 1123-1130 ◽  
Author(s):  
V. Oliveira ◽  
R. Vilar
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Laser Pulses ◽  
Formation Mechanisms ◽  
X Ray ◽  
Reducing Conditions ◽  
Transmission Electron ◽  
Column Formation ◽  
Krf Laser

This paper aims to contribute to the understanding of column formation mechanisms in Al2O3–TiC ceramics micromachined using excimer lasers. Chemical and structural characterization of columns grown in Al2O3–TiC composite processed with 200 KrF laser pulses at 10 J/cm2 was carried out by scanning electron microscopy, transmission electron microscopy, x-ray photoelectron spectroscopy, and x-ray diffraction analysis. Fully developed columns consist of a core of unprocessed material surrounded by an outer layer of Al2TiO5, formed in oxidizing conditions, and an inner layer, formed in reducing conditions, composed of TiC and Al3Ti or an AlTi solid solution. Possible mechanisms of column formation are discussed.

Fullerene-Gold Core-Shell Structures and Their Self-Assemblies

2017 ◽  
Vol 16 (02) ◽  
pp. 1650029
Author(s):  
R. Sepahvand ◽  
S. Alihosseini ◽  
M. Adeli ◽  
P. Sasanpour
Keyword(s):  
Citric Acid ◽  
Self Assembly ◽  
Size Structure ◽  
Shell Structures ◽  
Core Shell ◽  
Hybrid Nanomaterial ◽  
Gold Core ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Gold Nps

Hybrid nanomaterials consisting of functionalized fullerene and gold nanoparticle (NP) have been synthesized. Fullerene was functionalized by citric acid and used as reducing and capping agent for preparation of gold NPs. Functionalization of fullerene by use of citric acid was performed by enzymatic and thermal approaches. The core-shell structures containing gold NPs as core and fullerene as shell (gold/fullerene) were prepared. It was found that method and density of functionalization of fullerene effect final structure and therefore their physicochemical property of hybrid nanomaterial dramatically. Ultraviolet-visible (UV-Vis) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, dynamic light scattering (DLS), atomic force microscopy (AFM), transmission electron microscopy (TEM) were used to analyze the structure of the synthesized hybrid nanomaterial and also study their self-assembly and physicochemical properties. Effect of the size, structure and morphology (e.g., agglomeration) of the synthesized hybrid nanomaterial on their UV-Vis absorption behavior has been also verified by theoretical modeling.

Study on Dispersion and Characterization of Functionalized MWCNTs Prepared by Wet Oxidation

2014 ◽  
Vol 661 ◽  
pp. 8-13 ◽  
Author(s):  
Intan Syaffinazzilla Zaine ◽  
N.A.M. Napiah ◽  
Azmi Mohamad Yusof ◽  
A.N. Alias ◽  
A.M.M. Ali ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Relative Intensity ◽  
Colloidal Stability ◽  
Structural Defects ◽  
Wet Oxidation ◽  
Defect Level ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Functionalized Mwcnts

The MWCNTs was functionalized by refluxing commercial MWCNTs (a-MWCNTs) in concentrated HNO3/H2SO4 (3:1 v/v) at 100°C for 6 hours. The dispersion of a-MWCNTs and functionalized MWCNTs (f-MWCNTs) were observed after 1 hour sonication in ethanol. Both samples were characterized by UV-vis spectroscopy for dispersion behavior. The dried f-MWCNTs and a-MWCNTs were characterized by Raman spectroscopy to estimate the defect level. The morphology of the samples were analyzed by Transmission Electron Microscopy (TEM). The f-MWCNTs was well dispersed in ethanol within 2 weeks of observations period. The colloidal stability of a-MWCNTs was low as it was easily sediment after 24 hours. The UV-vis spectra of f-MWCNTs show maximum absorbance at 250 nm meanwhile no absorbance was observed for a-MWCNTs. Analysis from Raman spectrum shows that the f-MWCNTs have relative intensity of 1.101 which is higher than a-MWCNTs that have relative intensity of 0.935. The image from TEM revealed that the f-MWCNTs have structural defects and the absence of amorphous carbon on sidewall meanwhile the a-MWCNTs indicate otherwise.

Preparation and Characterization of γ-Fe2O3-ZnFe2O4 Composite Nanoparticles

2013 ◽  
Vol 873 ◽  
pp. 152-157
Author(s):  
Long Long Chen ◽  
Jun Ming Li ◽  
Xiao Min Gong ◽  
Jian Li
Keyword(s):  
Photoelectron Spectroscopy ◽  
Chemical Species ◽  
Composite Nanoparticles ◽  
X Ray Diffraction ◽  
Ferrite Core ◽  
Phase Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Chemically Induced

Using a chemically induced transition in an FeCl2 solution, γ-Fe2O3 nanoparticles can be prepared from an amorphous precursor composed of FeOOH and Mg (OH)2. Surface modification by adding ZnCl2 during liquid-phase synthesis was attempted. The magnetization, morphology, crystal structure, and chemical species of as-prepared samples were characterized by vibrating sample magnetometer (VSM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray energy-dispersive spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). The experimental results showed that the surface of the γ-Fe2O3 nanoparticles can be modified by adding ZnCl2 to form composite nanoparticles with a γ-Fe2O3/ZnFe2O4 ferrite core coated with Zn (OH)2 and absorbed FeCl36H2O; this modification can be enhanced by additional NaOH.

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