Synthesis and Characteristic of NiFe/NiFe2O4 Core-Shell Magnetic Nanocomposite Particles

2012 ◽  
Vol 486 ◽  
pp. 65-69
Author(s):  
Jun Hu ◽  
Ai Min Chen
Keyword(s):  
Structural Evolution ◽  
Treatment Temperature ◽  
Oxide Shell ◽  
Core Shell ◽  
Nanocomposite Particles ◽  
X Ray ◽  
The Core ◽  
Transmission Electron ◽  
Diffraction Patterns ◽  
Feni Alloy

NiFe/NiFe2O4 core-shell bimagnetic nanocomposite particles were successfully synthesized by colloidal chemical method combined with H2 reduction. The whole structural evolution process has been well studied through analysis of X-ray diffraction patterns and Infrared spectra. It has been found that FeNi alloy concentrated in the ferrite phase. The core/shell structure, a FeNi alloy core surrounded by NiFe2O4 spinel oxide shell were verified by X-ray powder diffraction (XRD), fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). The influence of post H2 heat treatment temperature on nanoparticles was investigated. The core-shell NiFe/ NiFe2O4 nanoparticles was about 100 nm after reduced at 727 K, The powders exhibited paramagnetic properties and the magnetization was 29.9 emu·g-1.

The Preparation and Characteristic of Superparamagnetic Core/Shell Nanoparticles

2013 ◽  
Vol 274 ◽  
pp. 432-435
Author(s):  
Hong Xia Shen ◽  
Zheng Zhi Yin ◽  
Qiong Cheng
Keyword(s):  
Biomedical Applications ◽  
Superparamagnetic Nanoparticles ◽  
Bioactive Molecules ◽  
Core Shell ◽  
Shell Nanoparticles ◽  
X Ray ◽  
Transmission Electron ◽  
Vibration Sample Magnetometer ◽  
Diffraction Patterns ◽  
Core Shell Nanoparticles

Superparamagnetic core/shell nanoparticles have been prepared successfully by the reduction of Au3+ onto the surface of superparamagnetic nanoparticles. The core/shell nanoparticles were characterized by Transmission electron microscopy (TEM), X-ray powder diffraction patterns (XRD), UV–vis spectrophotometer, Vibration Sample Magnetometer(VSM) and micro-confocal Raman system. The results revealed that the prepared core/shell nanoparticles were covered by Au shell. These superparamagnetic nanoparticles can be highly sensitively detected and afford new opportunities for biomedical applications through chemical bonding of bioactive molecules with the Au shell of nanoparticles.

Preparation of Carbon-Encapsulated Fe Core-Shell Nanostructures by Confined Arc Plasma

2011 ◽  
Vol 688 ◽  
pp. 245-249 ◽  
Author(s):  
Zhi Qiang Wei ◽  
Xiao Yun Wang ◽  
Hua Yang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Particle Size ◽  
Specific Surface ◽  
Surface Area ◽  
Core Shell ◽  
Arc Plasma ◽  
X Ray ◽  
The Core ◽  
Transmission Electron

Special carbon encapsulated Fe core-shell nanoparticles with a size range of 15–40 nm were successfully prepared via confined arc plasma method. The composition, morphology, microstructure, specific surface area, particle size of the product by this process were characterized via X-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), X-ray energy dispersive spectrometry (XEDS) and BET N2adsorption. The experiment results shown that the carbon encapsulated Fe nanoparticles with clear core-shell structure, the core of the particles is body centered cubic (BCC) structure Fe, and the shell of the particles is disorder carbons. The particle size of the nanocapsules ranges from 15 to 40nm，with an averaged value about 30nm, the particles diameter of the core is about 16nm and the thickness of the shells is about 6-8 nm, and the specific surface area is 24 m2/g.

scholarly journals Synthesis and high-resolution structural and chemical analysis of iron-manganese-oxide core-shell nanocubes

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Aladin Ullrich ◽  
Mohammad Mostafizar Rahman ◽  
Paolo Longo ◽  
Siegfried Horn
Keyword(s):  
High Resolution ◽  
Core Shell ◽  
Bright Field ◽  
X Ray ◽  
The Core ◽  
Transmission Electron ◽  
High Boiling Solvent ◽  
Iron Manganese ◽  
Electron Energy Loss ◽  
Shell Region

AbstractWe have investigated the structure and chemical composition of nanoparticles synthesized by thermal decomposition of a mixture of iron oleate and manganese oleate in a high-boiling solvent in the presence of Na-oleate and oleic acid as surfactants by analytical transmission electron microscopy (TEM). The particles appear core-shell like in bright field TEM images. Higher spatial resolution TEM (HRTEM) analysis reveals a FeO/MnO like structure in the core and a spinel like structure in the shell. With high-resolution analytical methods like energy dispersive x-ray spectroscopy (EDS) and electron energy loss spectroscopy (EELS), the distribution of the metals Mn and Fe was investigated. Differences in the oxidation state of these metals were found between the core and the shell region. The presence of sodium from the used surfactant (Na-oleate) on the surface of the particles has been proved.

scholarly journals Luminescence Nanothermometry Based on Pr3+ : LaF3 Single Core and Pr3+ : LaF3/LaF3 Core/Shell Nanoparticles

2019 ◽  
Vol 2019 ◽  
pp. 1-14 ◽  
Author(s):  
M. S. Pudovkin ◽  
D. A. Koryakovtseva ◽  
E. V. Lukinova ◽  
S. L. Korableva ◽  
R. Sh. Khusnutdinova ◽  
...  
Keyword(s):  
Coherent Scattering ◽  
Core Shell ◽  
Fluorescence Intensity Ratio ◽  
X Ray Diffraction ◽  
Shell Nanoparticles ◽  
X Ray ◽  
The Core ◽  
Transmission Electron ◽  
Means Of Transmission ◽  
Core Shell Nanoparticles

Core Pr3+ : LaF3 (CPr = 1%) plate-like nanoparticles (nanoplates), core/shell Pr3+ : LaF3 (CPr = 1%)/LaF3 nanoplates, core Pr3+ : LaF3 (CPr = 1%) sphere-like nanoparticles (nanospheres), and core/shell Pr3+ : LaF3 (CPr = 1%)/LaF3 nanospheres were synthesized via the coprecipitation method of synthesis. The nanoparticles (NPs) were characterized by means of transmission electron microscopy, X-ray diffraction, and optical spectroscopy. The formation of the shell was proved by detecting the increase in physical sizes, sizes of coherent scattering regions, and luminescence lifetimes of core/shell NPs comparing with single core NPs. The average physical sizes of core nanoplates, core/shell nanoplates, core nanospheres, and core/shell nanospheres were 62.2 ± 0.9, 74.7 ± 1.2, 13.8 ± 0.9 and 22.0 ± 1.2 nm, respectively. The formation of the NP shell led to increasing of effective luminescence lifetime τeff of the 3P0 state of Pr3+ ions for the core nanoplates, core/shell nanoplates, core nanospheres, and core/shell nanospheres the values of τeff were 2.3, 3.6, 3.2, and 4.7 μsec, respectively (at 300 K). The values of absolute sensitivity Sa for fluorescence intensity ratio (FIR) thermometry was 0.01 K−1 at 300 K for all the samples. The FIR sensitivity can be attributed to the fact that 3P1 and 3P0 states share their electronic populations according to the Boltzmann process. The values of Sa for lifetime thermometry for core nanoplates, core/shell nanoplates, core nanospheres, and core/shell nanospheres were (36.4 ± 3.1) · 10−4, (70.7 ± 5.9) · 10−4, (40.7 ± 2.6) · 10−4, and (68.8 ± 2.4) · 10−4 K−1, respectively.

Preparation and Characterization of Gold-Loaded Magnetite/Silica Core-Shell Composites

2016 ◽  
Vol 42 ◽  
pp. 47-52
Author(s):  
Dan Dan Huang ◽  
Zhao Dai ◽  
Kun Yang ◽  
Yuan Yuan Chu
Keyword(s):  
Room Temperature ◽  
Solvothermal Reaction ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Core ◽  
Transmission Electron ◽  
Silica Core ◽  
Shell Particles

The fabrication of gold-loaded magnetite/silica core-shell particles was presented in this paper. First, 250 nm of magnetic Fe3O4 nanoparticles were prepared by solvothermal reaction. Then, the Fe3O4 particles were coated by SiO2, and Au nanoparticles (AuNPs), respectively. The core-shell structure of these microspheres was confirmed by transmission electron microscopy (TEM) and Power X-ray diffraction (XRD). The magnetic property of the core-shell microspheres was investigated at room temperature. The results indicated that the core-shell composites had a well-retained high magnetic intensity, thus it can be easily separated from the mixture in less than a few minutes by simply using a magnet.

Synthesis and Optical Properties of CdSe and CdSe/ZnS Core/Shell Quantum Dots

2015 ◽  
Vol 1085 ◽  
pp. 176-181
Author(s):  
Puspendu Barik ◽  
Arup Ratan Mandal ◽  
Denis V. Kuznetsov ◽  
Anna Yu. Godymchuk
Keyword(s):  
Electron Microscopy ◽  
Quantum Dots ◽  
Excitation Wavelength ◽  
Core Shell ◽  
Shell Material ◽  
X Ray Diffraction ◽  
Chemical Route ◽  
X Ray ◽  
The Core ◽  
Transmission Electron

In this work, we have synthesized homogeneous, ordered CdSe and CdSe/ZnS core/shell quantum dots (QDs) by chemical route and characterized them using X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), and Photoluminescence (PL) spectroscopy. Coating with shell material was confirmed by red shift as well as enhancement in the PL peak compared to bare QDs. DLS data showed QDs and core/shell to be stable. PL spectra are red shifted relative to the excitation wavelength. Bare QDs and the core/shell material shows a Stoke-shift of 16 and 18 meV respectively.

RAPET (Reaction under Autogenic Pressure at Elevated Temperatures) Technique Assisted Synthesis of Encapsulated CdE@C [E= S, Se and Te] Nanocrystallites

2016 ◽  
Vol 16 (03) ◽  
pp. 1650032
Author(s):  
P. P. George ◽  
I. Genish ◽  
Shirly ben-david Maklouf ◽  
Y. Koltypin ◽  
A. Gedanken
Keyword(s):  
Electron Microscopy ◽  
Elevated Temperatures ◽  
Carbon Matrix ◽  
Average Diameter ◽  
Core Shell ◽  
Synthetic Method ◽  
X Ray ◽  
Cds Nanocrystals ◽  
The Core ◽  
Transmission Electron

We present an easy synthetic method for the fabrication of encapsulated nanosized semiconductor CdE [E [Formula: see text] S, Se and Te] within the core of carbon capsule. We also discuss the growth of CdSC and neat CdS nanocrystals on stainless steel coupons (SSC) by a reaction under autogenic pressure at elevated temperature (RAPET) technique. The thermal decomposition of mixture of Cd(acetate)2 and sulfur, selenium and tellurium was carried out at 750[Formula: see text]C under air for 3[Formula: see text]h. The synthesized products were systematically characterized by X-ray powder diffraction, scanning electron microscopy (SEM) and transmission electron microscopy. Carbon matrix, with an average diameter of 250[Formula: see text]nm, encapsulated several nanometric-sized CdS nanocrystals, as evidenced from high resolution SEM (HRSEM). We examined the optical properties of this core/shell CdS@C and nonencapsulated CdS nanocrystals and found that both core shell and neat CdS nanocrystals show emission in the pohotoluminescence (PL) spectrum.

scholarly journals Stability of a Bifunctional Cu-Based Core@Zeolite Shell Catalyst for Dimethyl Ether Synthesis Under Redox Conditions Studied by Environmental Transmission Electron Microscopy andIn SituX-Ray Ptychography

2017 ◽  
Vol 23 (3) ◽  
pp. 501-512 ◽  
Author(s):  
Sina Baier ◽  
Christian D. Damsgaard ◽  
Michael Klumpp ◽  
Juliane Reinhardt ◽  
Thomas Sheppard ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Dimethyl Ether ◽  
Core Shell ◽  
X Ray ◽  
Environmental Transmission ◽  
The Core ◽  
Transmission Electron ◽  
The Stability

AbstractWhen using bifunctional core@shell catalysts, the stability of both the shell and core–shell interface is crucial for catalytic applications. In the present study, we elucidate the stability of a CuO/ZnO/Al2O3@ZSM-5 core@shell material, used for one-stage synthesis of dimethyl ether from synthesis gas. The catalyst stability was studied in a hierarchical manner by complementary environmental transmission electron microscopy (ETEM), scanning electron microscopy (SEM) andin situhard X-ray ptychography with a specially designedin situcell. Both reductive activation and reoxidation were applied. The core–shell interface was found to be stable during reducing and oxidizing treatment at 250°C as observed by ETEM andin situX-ray ptychography, although strong changes occurred in the core on a 10 nm scale due to the reduction of copper oxide to metallic copper particles. At 350°C,in situX-ray ptychography indicated the occurrence of structural changes also on theµm scale, i.e. the core material and parts of the shell undergo restructuring. Nevertheless, the crucial core–shell interface required for full bifunctionality appeared to remain stable. This study demonstrates the potential of these correlativein situmicroscopy techniques for hierarchically designed catalysts.

scholarly journals Synthesis of TiO2/SnO2 core shell nanocomposite via sol-gel method

2012 ◽  
Vol 05 ◽  
pp. 251-256 ◽  
Author(s):  
SORAIA KHOBY-SHENDY ◽  
MOHAMMAD REZA VAEZI ◽  
TORAJ EBADZADEH
Keyword(s):  
Sol Gel ◽  
Titanium Isopropoxide ◽  
Core Shell ◽  
Hydrothermal Processing ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Core ◽  
Transmission Electron ◽  
Diffraction Peaks ◽  
Hydrolysis Of

The particles of TiO 2 core/ SnO 2 shell nanocomposite were prepared by hydrolysis of SnCl 4.5 H 2 O in the presence of titania nanoparticle after drying and calcinations treatments. TiO 2 particle were produced from titanium isopropoxide sol by hydrothermal processing. X-ray diffraction (XRD), Fourier transformed infrared (FTIR), and transmission electron microscopy (TEM) were used to characterize the TiO 2/ SnO 2 core shell nanocomposites. The obtained results from XRD show that the SnO 2 nanoparticles coated on TiO 2 yields diffraction peaks correspond to the crystalline SnO 2 phase. Also, TEM results show that the nanocomposite particles have a spherical morphology and a narrow size distribution. The thickness of SnO 2 shell on the surface of TiO 2 particles were about 8 nm. Moreover, the results obtained from EDX analysis show that the core-shell structured nanocomposites have crystalline structure.

Cetyltrimethylammonium bromide- and ethylene glycol-assisted preparation of mono-dispersed indium oxide nanoparticles using hydrothermal method

2014 ◽  
Vol 68 (8) ◽  
Author(s):  
Selvakumar Dhanasingh ◽  
Dharmaraj Nallasamy ◽  
Saravanan Padmanapan ◽  
Vinod Padaki
Keyword(s):  
Ethylene Glycol ◽  
Hydrothermal Method ◽  
Indium Oxide ◽  
Cetyltrimethylammonium Bromide ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
X Ray ◽  
Transmission Electron ◽  
Diffraction Patterns

AbstractThe influence of cetyltrimethylammonium bromide and ethylene glycol on the size and dispersion of indium oxide nanoparticles prepared under hydrothermal conditions was investigated. The precursor compound, indium hydroxide, obtained by the hydrothermal method in the absence as well as the presence of cetyltrimethylammonium bromide, was converted to indium oxide by sintering at 400°C. The formation of nanoscale indium oxide upon sintering was ascertained by the characteristic infrared adsorption bands and X-ray diffraction patterns of indium oxide. Transmission electron microscopy and band gap values confirmed that the cetyltrimethylammonium bromide facilitated the formation of indium oxide nanoparticles smaller in size and narrower in distribution than those prepared without the assistance of cetyltrimethylammonium bromide.

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