scholarly journals Cu-Ag core-shell nanoparticles: A direct correlation between micro-Raman and electron microscopy

2006 ◽  
Vol 73 (11) ◽  
Author(s):  
M. Cazayous ◽  
C. Langlois ◽  
T. Oikawa ◽  
C. Ricolleau ◽  
A. Sacuto
2021 ◽  
Author(s):  
Anna Frank ◽  
Thomas Gänsler ◽  
Stefan Hieke ◽  
Simon Fleischmann ◽  
Samantha Husmann ◽  
...  

This work presents the synthesis of MoO2/MoS2 core/shell nanoparticles within a carbon nanotube network and their detailed electron microscopy investigation in up to three dimensions. The triple-hybrid core/shell material was...


Nanoscale ◽  
2018 ◽  
Vol 10 (19) ◽  
pp. 9186-9191 ◽  
Author(s):  
Nathalie Claes ◽  
Ramesh Asapu ◽  
Natan Blommaerts ◽  
Sammy W. Verbruggen ◽  
Silvia Lenaerts ◽  
...  

Using electron microscopy, polymer encapsulated silver nanoparticles were visualized and their coverage, molecular structure and plasmonic properties could be investigated.


Author(s):  
Natalia Fernández-Delgado ◽  
Miriam Herrera-Collado ◽  
Pedro Rodríguez-Cantó ◽  
Rafael Abargues ◽  
E Moya López ◽  
...  

2012 ◽  
Vol 531 ◽  
pp. 211-214 ◽  
Author(s):  
Jun Jie Jing ◽  
Ji Min Xie ◽  
Hui Ru Qin ◽  
Wen Hua Li ◽  
Ming Mei Zhang

Nickel(Ni)-silver(Ag) core-shell nanoparticles with different shell thickness were synthesized with Ni nanoparticles by liquid phase reduction technique form water solution. The product was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and inductively coupled plasma spectroscopy (ICP). The results showed that the Ni nanoparticles are in sphere shape and the average diameter is 104nm , the nickel(Ni)-silver(Ag) core-shell nanoparticles has good crystallinity and the thinkness of Ag nanoshells could be effectively controlled by changing the concentration of silver nitrate. The product can be used for nickel-based conductive paste preparation because of the surface character of Ag and the magnetic property of Ni


Catalysts ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 755 ◽  
Author(s):  
Nkosinathi Goodman Dlamini ◽  
Albertus Kotze Basson ◽  
Shandu Jabulani Siyabonga Emmanuel ◽  
Viswanadha Srirama Rajasekhar Pullabhotla

Green synthesis of core–shell nanoparticles is gaining importance nowadays as it is viewed as being environmental friendly and cost effective. The present study aimed to synthesize iron@copper core–shell nanoparticles using a polysaccharide-based bioflocculant from Alcalegenis faecalis and to evaluate its efficiency in dye removal and river water and domestic wastewater treatment. The synthesized samples were characterized by Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, thermogravimetric analysis, transmission electron microscopy, and UV-Vis spectroscopy analysis. To optimize the best concentration for core–shell formation, different ratios of iron to copper were prepared. Sample 1 (S1) contained 1:3 iron to copper (Fe 25%–Cu 75%), sample 2 (S2) contained 1:1 iron to copper (Fe 50%–Cu 50%), and the third sample (S3) contained 3:1 iron to copper (Fe 75%–Cu 25%). The flocculation activity (FA) was above 98% at 0.2 mg/mL for all the samples and the samples flocculated well under acidic, alkaline, and neutral pH conditions. Sample 3 was shown to be thermostable, with flocculation activity above 90%, and samples 2 and 1 were also thermostable, but the flocculation decreased to 87 at 100 °C. All three samples revealed some remarkable properties for staining dye removal as the removal efficiency was above 89% for all dyes tested. The synthesized core–shell nanoparticles could remove nutrients such as total nitrogen and phosphate in both domestic wastewater and Mzingazi river water. Furthermore, high removal efficiency for chemical oxygen demand (COD) and biological oxygen demand (BOD) was also observed.


Nanoscale ◽  
2019 ◽  
Vol 11 (21) ◽  
pp. 10486-10492 ◽  
Author(s):  
Fu-Chun Chen ◽  
Jui-Yuan Chen ◽  
Ya-Hsuan Lin ◽  
Ming-Yu Kuo ◽  
Yung-Jung Hsu ◽  
...  

The formation of different shapes Au–Cu2O core–shell nanoparticles was investigated by in situ liquid cell transmission electron microscopy (LCTEM).


MRS Advances ◽  
2018 ◽  
Vol 3 (47-48) ◽  
pp. 2899-2904
Author(s):  
Ning Bian ◽  
Robert A. Mayanovic ◽  
Mourad Benamara

ABSTRACTThe mixed-valence oxide Co3O4 nanoparticles, having the normal spinel structure, possess large surface area, active-site surface adsorption properties, and fast ion diffusivities. Consequently, they are widely used in lithium-ion batteries, as well as for gas sensing and heterogeneous catalysis applications. In our research, we use a two-step method to synthesize Co3O4–based core-shell nanoparticles (CSNs). Cobalt oxide (Co3O4) nanoparticles were successfully synthesized using a wet synthesis method employing KOH and cobalt acetate. Manganese was incorporated into the Co3O4 structure to synthesize inverted Co3O4@MnxCo3-xO4 CSNs using a hydrothermal method. By adjustment of pH value, we obtained two different morphologies of CSNs, one resulting in pseudo-spherical and octahedron-shaped nanoparticles (PS type) whereas the second type predominantly have a nanoplate (NP type) morphology. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and x-ray photoelectron spectroscopy (XPS) have been performed in order to determine the morphological and structural properties of our CSNs, whereas the magnetic properties have been characterized using a superconducting quantum interference device (SQUID) magnetometer. XRD and TEM results show that the CSNs have the same spinel crystal structure throughout the core and shell with an average particle size of ∼19.8 nm. Our Co3O4 nanoparticles, as measured prior to CSN formation, are shown to be antiferromagnetic (AFM) in nature as shown by the magnetization data. Our SQUID data indicate that the core-shell nanoparticles have both AFM (due to the Co3O4 core) and ferrimagnetic properties (of the shell) with a coercivity field of 300 Oe and 150 Oe at 5 K for the PS and NP samples, respectively. The magnetization vs temperature data show a spin order-disorder transition at ∼33 K and a superparamagnetic blocking temperature of ∼90 K for both batches.


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