Characterisation of 3D-GaN/InGaN core-shell nanostructures by transmission electron microscopy

2014 ◽  
Vol 11 (3-4) ◽  
pp. 425-427 ◽  
Author(s):  
Ian Griffiths ◽  
David Cherns ◽  
Xue Wang ◽  
Hergo-Heinrich Wehman ◽  
Martin Mandl ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Core Shell ◽  
Shell Nanostructures ◽  
Transmission Electron

Formation of bismuth iron oxide based core–shell structures and their dielectric, ferroelectric and magnetic properties

2019 ◽  
Vol 7 (5) ◽  
pp. 1280-1291 ◽  
Author(s):  
Alaka Panda ◽  
R. Govindaraj ◽  
R. Mythili ◽  
G. Amarendra
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Magnetic Properties ◽  
Iron Oxide ◽  
Shell Structures ◽  
Core Shell ◽  
Bismuth Iron Oxide ◽  
The Core ◽  
Shell Nanostructures ◽  
Transmission Electron

Bismuth and iron oxides subjected to ball milling followed by controlled annealing treatments showed the formation of core–shell nanostructures with Bi2Fe4O9 as the core and a shell of BiFeO3 and Bi25FeO40 phases as deduced based on the analysis of transmission electron microscopy results.

Microheterogeneities of core-shell latexes probed by 1H spin diffusion and transmission electron microscopy

1995 ◽  
Vol 196 (4) ◽  
pp. 985-993 ◽  
Author(s):  
Stefan Spiegel ◽  
Katharina Landfester ◽  
Günter Lieser ◽  
Christine Boeffel ◽  
Hans Wolfgang Spiess ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Spin Diffusion ◽  
Core Shell ◽  
Transmission Electron

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.

Enhancement of durability of NIR emission of Ag2S@ZnS QDs in water

2017 ◽  
Vol 31 (32) ◽  
pp. 1750297 ◽  
Author(s):  
M. Karimipour ◽  
M. Bagheri ◽  
M. Molaei
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Xrd Analysis ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Nir Emission ◽  
Core Shell Structure ◽  
Phase Transmission

Stability of Ag2S@ZnS QDs in water is a crucial concern for their application in biology. In this work, both physical sustainability and emission stability of Ag2S QDs were enhanced using parameter optimization of a pulsed microwave irradiation (MI) method up to 105 days after their preparation. UV–Vis and photoluminescence spectroscopies depicted an absorption and emission about 817 nm and 878 nm, respectively. X-ray diffraction (XRD) analysis showed a growth of Ag2S acanthite phase. Transmission Electron Microscopy (TEM) images revealed a clear formation of Ag2S@ZnS core–shell structure.

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.

Fast Synthesis of Rutile/Apatite Core/Shell Structured Photocatalyst in Simulated Body Fluid

2012 ◽  
Vol 465 ◽  
pp. 66-71 ◽  
Author(s):  
Fu Zhi Shi ◽  
Yao Gang Li ◽  
Hong Zhi Wang ◽  
Qing Hong Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Simulated Body Fluid ◽  
Body Fluid ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Soaking Time ◽  
X Ray ◽  
Transmission Electron ◽  
Tio2 Microspheres

The core/shell structured rutile/apatite was prepared by soaking rutile TiO2 (R-TiO2) microspheres into a simulated body fluid (SBF) only for 1 day. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), energy dispersive X-ray (EDX) and N2 adsorption measurements. XRD showed that the apatite content increased with prolonging the soaking time or increasing the SBF concentration. TEM and EDX demonstrated that apatite had been coated on the surface of R-TiO2 microspheres successfully. HRTEM indicated that the lattice spacings of 0.27 nm and 0.32 nm were assigned to (211) plane of apatite and (101) plane of R-TiO2, respectively.

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