scholarly journals Selective Cation Exchange in the Core Region of Cu2–xSe/Cu2–xS Core/Shell Nanocrystals

2015 ◽  
Vol 137 (38) ◽  
pp. 12195-12198 ◽  
Author(s):  
Karol Miszta ◽  
Graziella Gariano ◽  
Rosaria Brescia ◽  
Sergio Marras ◽  
Francesco De Donato ◽  
...  
Keyword(s):  
Cation Exchange ◽  
Core Region ◽  
Core Shell ◽  
The Core

scholarly journals Nanoscale Mapping of Heterogeneous Strain and Defects in Individual Magnetic Nanocrystals

Crystals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 658
Author(s):  
Xiaowen Shi ◽  
Ross Harder ◽  
Zhen Liu ◽  
Oleg Shpyrko ◽  
Eric Fullerton ◽  
...  
Keyword(s):  
Uniform Distribution ◽  
Displacement Field ◽  
Density Functional ◽  
Core Region ◽  
Outer Shell ◽  
Core Shell ◽  
Diffractive Imaging ◽  
The Core ◽  
Partial Dislocations ◽  
Distribution Of Magnetization

We map the three-dimensional strain heterogeneity within a single core-shell Ni nanoparticle using Bragg coherent diffractive imaging. We report the direct observation of both uniform displacements and strain within the crystalline core Ni region. We identify non-uniform displacements and dislocation morphologies across the core–shell interface, and within the outer shell at the nanoscale. By tracking individual dislocation lines in the outer shell region, and comparing the relative orientation between the Burgers vector and dislocation lines, we identify full and partial dislocations. The full dislocations are consistent with elasticity theory in the vicinity of a dislocation while the partial dislocations deviate from this theory. We utilize atomistic computations and Landau–Lifshitz–Gilbert simulation and density functional theory to confirm the equilibrium shape of the particle and the nature of the (111) displacement field obtained from Bragg coherent diffraction imaging (BCDI) experiments. This displacement field distribution within the core-region of the Ni nanoparticle provides a uniform distribution of magnetization in the core region. We observe that the absence of dislocations within the core-regions correlates with a uniform distribution of magnetization projections. Our findings suggest that the imaging of defects using BCDI could be of significant importance for giant magnetoresistance devices, like hard disk-drive read heads, where the presence of dislocations can affect magnetic domain wall pinning and coercivity.

scholarly journals Microstructural Evolution from Dendrites to Core-Shell Equiaxed Grain Morphology for CoCrFeNiVx High-Entropy Alloys in Metallic Casting Mold

Metals ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 1172 ◽  
Author(s):  
Leigang Cao ◽  
Lin Zhu ◽  
Hongde Shi ◽  
Zerui Wang ◽  
Yue Yang ◽  
...  
Keyword(s):  
Grain Morphology ◽  
Core Region ◽  
Core Shell ◽  
High Entropy Alloys ◽  
Σ Phase ◽  
High Entropy ◽  
The Core ◽  
Interdendrite Region ◽  
Fcc Phase ◽  
Equiaxed Grain

The CoCrFeNiVx (x = 0, 0.25, 0.5, 0.7, 0.8, 0.9, and 1.0) high-entropy alloys (HEAs) were fabricated by the copper mold casting process. The microstructure, phase constitution, and mechanical properties were investigated by using X-ray diffraction, scanning electron microscopy, transmission electron microscopy analyses and compressive testing. It revealed that, when x ≤ 0.25, the alloys solidified into a single fcc phase. When 0.5 ≤ x ≤ 0.8, the alloys solidified into a dendritic structure of the fcc phase with the formation of the σ phase in the interdendrite region. Interestingly, when x exceeded 0.9, the alloys presented a typical core-shell equiaxed grain morphology. The core region consisting of a mixture of fcc + σ phases was surrounded by the shell of the single σ phase and the interdendrite region solidified into the single fcc phase. The dual-phase “eutectiod” structure in the core region of the equiaxed grain might be formed from the decomposition of the unidentified metastable phase. As the V fraction increased, the compressive yield strength of the CoCrFeNiVx alloys gradually increased from 164 MPa (x = 0) to 458 MPa (x = 0.8), and then sharply increased to 722 MPa (x = 0.9) and 1493 MPa (x = 1.0).

Intramitochondrial Viruses of Reptilian Cell Origin

1972 ◽  
Vol 30 ◽  
pp. 318-319
Author(s):  
Philip D. Lunger ◽  
H. Fred Clark
Keyword(s):  
Particle Production ◽  
Outer Zone ◽  
Density Variation ◽  
Core Region ◽  
Mitochondrial Membranes ◽  
Virus Particles ◽  
The Core ◽  
Vipera Russelli ◽  
Maturation Stages ◽  
Type Particle

In the course of fine structure studies of spontaneous “C-type” particle production in a viper (Vipera russelli) spleen cell line, designated VSW, virus particles were frequently observed within mitochondria. The latter were usually enlarged or swollen, compared to virus-free mitochondria, and displayed a considerable degree of cristae disorganization.Intramitochondrial viruses measure 90 to 100 mμ in diameter, and consist of a nucleoid or core region of varying density and measuring approximately 45 mμ in diameter. Nucleoid density variation is presumed to reflect varying degrees of condensation, and hence maturation stages. The core region is surrounded by a less-dense outer zone presumably representing viral capsid.Particles are usually situated in peripheral regions of the mitochondrion. In most instances they appear to be lodged between loosely apposed inner and outer mitochondrial membranes.

Magnetic Properties of Fe3O4/CoFe2O4 Composite Nanoparticles with Core/Shell Architecture

2020 ◽  
Vol 65 (10) ◽  
pp. 904
Author(s):  
V. O. Zamorskyi ◽  
Ya. M. Lytvynenko ◽  
A. M. Pogorily ◽  
A. I. Tovstolytkin ◽  
S. O. Solopan ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Spinel Ferrite ◽  
Composite Nanoparticles ◽  
Core Shell ◽  
Cofe2o4 Nanoparticles ◽  
Core Diameter ◽  
The Core ◽  
Shell Particles ◽  
Interface Parameters ◽  
Shell Composite

Magnetic properties of the sets of Fe3O4(core)/CoFe2O4(shell) composite nanoparticles with a core diameter of about 6.3 nm and various shell thicknesses (0, 1.0, and 2.5 nm), as well as the mixtures of Fe3O4 and CoFe2O4 nanoparticles taken in the ratios corresponding to the core/shell material contents in the former case, have been studied. The results of magnetic research showed that the coating of magnetic nanoparticles with a shell gives rise to the appearance of two simultaneous effects: the modification of the core/shell interface parameters and the parameter change in both the nanoparticle’s core and shell themselves. As a result, the core/shell particles acquire new characteristics that are inherent neither to Fe3O4 nor to CoFe2O4. The obtained results open the way to the optimization and adaptation of the parameters of the core/shell spinel-ferrite-based nanoparticles for their application in various technological and biomedical domains.

scholarly journals Iron Based Core-Shell Structures as Versatile Materials: Magnetic Support and Solid Catalyst

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 72
Author(s):  
Christian Zambrzycki ◽  
Runbang Shao ◽  
Archismita Misra ◽  
Carsten Streb ◽  
Ulrich Herr ◽  
...  
Keyword(s):  
Water Purification ◽  
Functional Materials ◽  
Core Material ◽  
Solid Catalyst ◽  
Core Shell ◽  
Shell Nanoparticles ◽  
The Core ◽  
Shell Nanostructures ◽  
Sio2 Shell ◽  
Iron Based

Core-shell materials are promising functional materials for fundamental research and industrial application, as their properties can be adapted for specific applications. In particular, particles featuring iron or iron oxide as core material are relevant since they combine magnetic and catalytic properties. The addition of an SiO2 shell around the core particles introduces additional design aspects, such as a pore structure and surface functionalization. Herein, we describe the synthesis and application of iron-based core-shell nanoparticles for two different fields of research that is heterogeneous catalysis and water purification. The iron-based core shell materials were characterized by transmission electron microscopy, as well as N2-physisorption, X-ray diffraction, and vibrating-sample magnetometer measurements in order to correlate their properties with the performance in the target applications. Investigations of these materials in CO2 hydrogenation and water purification show their versatility and applicability in different fields of research and application, after suitable individual functionalization of the core-shell precursor. For design and application of magnetically separable particles, the SiO2 shell is surface-functionalized with an ionic liquid in order to bind water pollutants selectively. The core requires no functionalization, as it provides suitable magnetic properties in the as-made state. For catalytic application in synthesis gas reactions, the SiO2-stabilized core nanoparticles are reductively functionalized to provide the catalytically active metallic iron sites. Therefore, Fe@SiO2 core-shell nanostructures are shown to provide platform materials for various fields of application, after a specific functionalization.

scholarly journals Light-Scattering Simulations from Spherical Bimetallic Core–Shell Nanoparticles

Micromachines ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 359
Author(s):  
Francesco Ruffino
Keyword(s):  
Optical Properties ◽  
Light Scattering ◽  
Bimetallic Nanoparticles ◽  
Dominant Role ◽  
Scattered Light ◽  
Specific Interaction ◽  
Surface Enhanced Raman Spectroscopy ◽  
Localized Surface Plasmon ◽  
Core Shell ◽  
The Core

Bimetallic nanoparticles show novel electronic, optical, catalytic or photocatalytic properties different from those of monometallic nanoparticles and arising from the combination of the properties related to the presence of two individual metals but also from the synergy between the two metals. In this regard, bimetallic nanoparticles find applications in several technological areas ranging from energy production and storage to sensing. Often, these applications are based on optical properties of the bimetallic nanoparticles, for example, in plasmonic solar cells or in surface-enhanced Raman spectroscopy-based sensors. Hence, in these applications, the specific interaction between the bimetallic nanoparticles and the electromagnetic radiation plays the dominant role: properties as localized surface plasmon resonances and light-scattering efficiency are determined by the structure and shape of the bimetallic nanoparticles. In particular, for example, concerning core-shell bimetallic nanoparticles, the optical properties are strongly affected by the core/shell sizes ratio. On the basis of these considerations, in the present work, the Mie theory is used to analyze the light-scattering properties of bimetallic core–shell spherical nanoparticles (Au/Ag, AuPd, AuPt, CuAg, PdPt). By changing the core and shell sizes, calculations of the intensity of scattered light from these nanoparticles are reported in polar diagrams, and a comparison between the resulting scattering efficiencies is carried out so as to set a general framework useful to design light-scattering-based devices for desired applications.

Tuning and understanding the electronic effect of Co-Mo-O sties in bifunctional electrocatalysts for ultralong-lasting rechargable zinc-air battery

2021 ◽  
Author(s):  
Yi Guan ◽  
Nan Li ◽  
Jiao He ◽  
Yongliang Li ◽  
Lei Zhang ◽  
...  
Keyword(s):  
Electronic Effect ◽  
Metal Organic Frameworks ◽  
Core Shell ◽  
Zeolitic Imidazolate Frameworks ◽  
Assembly Strategy ◽  
The Core ◽  
Bifunctional Electrocatalysts ◽  
Metal Organic ◽  
Air Battery

Herein, we report a post-assembly strategy by growing the bimetallic Co/Zn zeolitic imidazolate frameworks (BIMZIF) on the surface of the customized Mo metal-organic frameworks (MOFs) (Mo-MOF) to prepare the core-shell...

scholarly journals Solubilization of Charged Porphyrins in Interpolyelectrolyte Complexes: A Computer Study

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 502
Author(s):  
Karel Šindelka ◽  
Zuzana Limpouchová ◽  
Karel Procházka
Keyword(s):  
Dissipative Particle Dynamics ◽  
Water Soluble ◽  
Coarse Grained ◽  
Core Shell ◽  
Computer Study ◽  
Interpolyelectrolyte Complex ◽  
The Core ◽  
Porphyrin Derivatives ◽  
Oppositely Charged ◽  
Positively Charged

Using coarse-grained dissipative particle dynamics (DPD) with explicit electrostatics, we performed (i) an extensive series of simulations of the electrostatic co-assembly of asymmetric oppositely charged copolymers composed of one (either positively or negatively charged) polyelectrolyte (PE) block A and one water-soluble block B and (ii) studied the solubilization of positively charged porphyrin derivatives (P+) in the interpolyelectrolyte complex (IPEC) cores of co-assembled nanoparticles. We studied the stoichiometric mixtures of 137 A10+B25 and 137 A10−B25 chains with moderately hydrophobic A blocks (DPD interaction parameter aAS=35) and hydrophilic B blocks (aBS=25) with 10 to 120 P+ added (aPS=39). The P+ interactions with other components were set to match literature information on their limited solubility and aggregation behavior. The study shows that the moderately soluble P+ molecules easily solubilize in IPEC cores, where they partly replace PE+ and electrostatically crosslink PE− blocks. As the large P+ rings are apt to aggregate, P+ molecules aggregate in IPEC cores. The aggregation, which starts at very low loadings, is promoted by increasing the number of P+ in the mixture. The positively charged copolymers repelled from the central part of IPEC core partially concentrate at the core-shell interface and partially escape into bulk solvent depending on the amount of P+ in the mixture and on their association number, AS. If AS is lower than the ensemble average ⟨AS⟩n, the copolymer chains released from IPEC preferentially concentrate at the core-shell interface, thus increasing AS, which approaches ⟨AS⟩n. If AS>⟨AS⟩n, they escape into the bulk solvent.

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