Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Discussion on Microwave-Matter Interaction Mechanisms by In Situ Observation of "Core-Shell" Microstructure during Microwave Sintering.

ABSTRACT: This research aims to deepen the understanding of the interaction mechanisms between microwave and matter in a metal-ceramic system based on in situ synchrotron radiation computed tomography. A special internal "core-shell" microstructure was discovered for the first time and used as an indicator for the interaction mechanisms between microwave and matter. Firstly, it was proved that the microwave magnetic field acted on metal particles by way of inducing an eddy current in the surface of the metal particles, which led to the formation of a "core-shell" microstructure in the metal particles. On this basis, it was proposed that the ceramic particles could change the microwave field and open a way for the microwave, thereby leading to selective heating in the region around the ceramic particles, which was verified by the fact that all the "core-shell" microstructure was located around ceramic particles. Furthermore, it was indicated that the ceramic particles would gather the microwaves, and might lead to local heating in the metal-ceramic contact region. The focusing of the microwave was proved by the quantitative analysis of the evolution rate of the "core-shell" microstructure in a different region. This study will help to reveal the microwave-matter interaction mechanisms during microwave sintering.

SUBMITTER: Liu W

PROVIDER: S-EPMC5456654 | biostudies-other | 2016 Feb

REPOSITORIES: biostudies-other

ACCESS DATA

Json Xml

Similar Datasets

In situ atomic-scale observation of oxygen-driven core-shell formation in Pt3Co nanoparticles.

Project description:The catalytic performance of core-shell platinum alloy nanoparticles is typically superior to that of pure platinum nanoparticles for the oxygen reduction reaction in fuel cell cathodes. Thorough understanding of core-shell formation is critical for atomic-scale design and control of the platinum shell, which is known to be the structural feature responsible for the enhancement. Here we reveal details of a counter-intuitive core-shell formation process in platinum-cobalt nanoparticles at elevated temperature under oxygen at atmospheric pressure, by using advanced in situ electron microscopy. Initial segregation of a thin platinum, rather than cobalt oxide, surface layer occurs concurrently with ordering of the intermetallic core, followed by the layer-by-layer growth of a platinum shell via Ostwald ripening during the oxygen annealing treatment. Calculations based on density functional theory demonstrate that this process follows an energetically favourable path. These findings are expected to be useful for the future design of structured platinum alloy nanocatalysts.Core-shell platinum alloy nanoparticles are promising catalysts for oxygen reduction, however a deeper understanding of core-shell formation is still required. Here the authors report oxygen-driven formation of core-shell Pt3Co nanoparticles, seen at the atomic scale with in situ electron microscopy at ambient pressure.

| S-EPMC5547122 | biostudies-literature

Thermoresponsive Core-Shell Nanoparticles: Does Core Size Matter?

Project description:Nanoparticles grafted with a dense brush of hydrophilic polymers exhibit high colloidal stability. However, reversible aggregation can be triggered by an increase in temperature if the polymer is thermoresponsive, as the polymer shell partly loses its hydration. We investigate the role of nanoparticle curvature on the critical solution temperature (CST) of grafted poly(2-isopropyl-2-oxazoline) (PiPOx) and critical flocculation temperature (CFT) of the core-shell nanoparticle dispersion. Cores with diameters ranging from 5 to 21 nm were studied by temperature-cycled dynamic light scattering and differential scanning calorimetry over a large range of concentrations. We show that core size and curvature only have a minor influence on particle aggregation (CFT and cluster size), while they have major influence on the CST of the polymer shell. The densely grafted shells exhibit three distinct solvation transitions, the relative contributions of each is controlled by the core curvature. We link these transitions to different polymer density regimes within the spherical brush and demonstrate that the CST of the innermost part of the brush coincides with the CFT of the particle dispersion.

| S-EPMC6163620 | biostudies-literature

Facile synthesis, microstructure and photophysical properties of core-shell nanostructured (SiCN)/BN nanocomposites.

Project description:Increasing structural complexity at nanoscale can permit superior control over photophysical properties in the precursor-derived semiconductors. We demonstrate here the synthesis of silicon carbonitride (SiCN)/boron nitride (BN) nanocomposites via a polymer precursor route wherein the cobalt polyamine complexes used as the catalyst, exhibiting novel composite structures and photophysical properties. High Resolution Transmission Electron Microscopy (HRTEM) analysis shows that the diameters of SiCN-BN core-shell nanocomposites and BN shells are 50‒400 nm and 5‒25 nm, respectively. BN nanosheets (BNNSs) are also observed with an average sheet size of 5‒15 nm. The photophysical properties of these nanocomposites are characterized using the UV-Vis and photoluminescence (PL) analyses. The as-produced composites have emission behavior including an emission lifetime of 2.5 ns (±20 ps) longer observed in BN doped SiCN than that seen for SiC nanoparticles. Our results suggest that the SiCN/BN nanocomposites act as semiconductor displaying superior width photoluminescence at wavelengths spanning the visible to near-infrared (NIR) spectral range (400‒700 nm), owing to the heterojunction of the interface between the SiC(N) nanowire core and the BN nanosheet shell.

| S-EPMC5233973 | biostudies-literature

Enhanced Microwave Absorption Bandwidth in Graphene-Encapsulated Iron Nanoparticles with Core-Shell Structure.

Project description:Graphene-encapsulated iron nanoparticles (Fe(G)) hold great promise as microwave absorbers owing to the combined dielectric loss of the graphene shell and the magnetic loss of the ferromagnetic metal core. Transmission electron microscopy (TEM) revealed transition metal nanoparticles encapsulated by graphene layers. The microwave electromagnetic parameters and reflection loss (R) of the Fe(G) were investigated. Graphene provided Fe(G) with a distinctive dielectric behavior via interfacial polarizations taking place at the interface between the iron cores and the graphene shells. The R of Fe(G)/paraffin composites with different Fe(G) contents and coating thickness was simulated according to the transmit-line theory and the measured complex permittivity and permeability. The Fe(G)/paraffin composites showed an excellent microwave absorption with a minimum calculated R of -58 dB at 11 GHz and a 60 wt% Fe(G) loading. The composites showed a wide bandwidth (the bandwidth of less than -10 dB was about 11 GHz). The R of composites with 1-3 mm coating thickness was measured using the Arch method. The absorption position was in line with the calculated results, suggesting that the graphene-coated iron nanoparticles can generate a suitable electromagnetic match and provide an intense microwave absorption. Excellent Fe(G) microwave absorbers can be obtained by selecting optimum layer numbers and Fe(G) loadings in the composites.

| S-EPMC7279258 | biostudies-literature

Discussion on Local Spark Sintering of a Ceramic-Metal System in an SR-CT Experiment during Microwave Processing.

Project description:In this paper, local spark sintering of a ceramic-metal system (SiO₂-Sn) during microwave processing was examinedby means of synchrotron-radiation-computed tomography technology. From the reconstructed 3-D and cross-section images of the specimen, adensification process was observed below the melting point of Sn, and then the specimen came into a rapid densification stage. These results may be due to the local spark sintering induced by the high-frequency alternating microwave electric fields. As the metallic particles Sn were introduced, the microstructure of "ceramic-metal" will lead to a non-uniform distribution and micro-focusing effect from electric fields in some regions (e.g., the neck). This will result in high-intensity electric fields and then induce rapid spark sintering within the micro-region. However, in the subsequent stage, the densification rate declined even when the specimen was not dense enough. The explanation for this is that as the liquid Sn permeated the gaps between SiO₂, the specimen became dense and the micro-focusing effect of electric fields decreased. This may result in the decrease or disappearance of spark sintering. These results will contribute to the understanding of microwave sintering mechanisms and the improvement of microwave processing methods.

| S-EPMC5456684 | biostudies-other

Direct observation of catalytic oxidation of particulate matter using in situ TEM.

Project description:The ability to observe chemical reactions at the molecular level convincingly demonstrates the physical and chemical phenomena occurring throughout a reaction mechanism. Videos obtained through in situ transmission electron microscopy (TEM) revealed the oxidation of catalytic soot under practical reaction conditions. Carbon oxidation reactions using Ag/SiO2 or Cs2CO3/nepheline catalysts were performed at 330?°C under an O2 flow of 0.5?Pa in the TEM measurement chamber. Ag/SiO2 catalyzed the reaction at the interface of the mobile Ag species and carbon, while the Cs species was fixed on the nepheline surface during the reaction. In the latter case, carbon particles moved, remained attached to the Cs2CO3/nepheline surface, and were consumed at the interface by the oxidation reaction. Using this technique, we were able to visualize such mobile and immobile catalysis according to different mechanisms.

| S-EPMC4495604 | biostudies-literature

Water-assisted and controllable synthesis of core/shell/shell structured carbon-based nanohybrids, and their magnetic and microwave absorption properties.

Project description:By controlling the pyrolysis temperature, core/shell/shell structured Fe/Fe5C2/carbon nanotube bundles (Fe/Fe5C2/CNTBs), Fe/Fe3C/helical carbon nanotubes (Fe/Fe3C/HCNTs) and Fe/Fe3C/chain-like carbon nanospheres (Fe/Fe3C/CCNSs) with high encapsulation efficiency could be selectively synthesized in large-scale by water-assisted chemical vapor deposition method. Water vapor was proved to play an important role in the growth process. Because of ?-Fe nanoparticles tightly wrapped by two layers, the obtained core/shell/shell structured nanohybrids showed high stabilities and good magnetic properties. The minimum reflection loss values of the as-prepared nanohybrids reached approximately -15.0, -46.3 and -37.1?dB, respectively. The excellent microwave absorption properties of the as-prepared core/shell/shell structured nanohybrids were considered to the quarter-wavelength matching model. Moreover, the possible enhanced microwave absorption mechanism of the as-prepared Fe/Fe3C/HCNTs and Fe/Fe3C/CCNSs were discussed in details. Therefore, we proposed a simple, inexpensive and environment-benign strategy for the synthesis of core/shell/shell structured carbon-based nanohybrids, exhibiting a promising prospect as high performance microwave absorbing materials.

| S-EPMC5575045 | biostudies-literature

Understanding the microstructure of a core-shell anode catalyst layer for polymer electrolyte water electrolysis.

Project description:Reducing precious metal loading in the anodic catalyst layer (CL) is indispensable for lowering capital costs and enabling the widespread adoption of polymer electrolyte water electrolysis. This work presents the first three-dimensional reconstruction of a TiO2-supported IrO2 based core shell CL (3 mgIrO2/cm2), using high-resolution X-ray ptychographic tomography at cryogenic temperature of 90 K. The high data quality and phase sensitivity of the technique have allowed the reconstruction of all four phases namely pore space, IrO2, TiO2 support matrix and the ionomer network, the latter of which has proven to be a challenge in the past. Results show that the IrO2 forms thin nanoporous shells around the TiO2 particles and that the ionomer has a non-uniform thickness and partially covers the catalyst. The TiO2 particles do not form a percolating network while all other phases have high connectivity. The analysis of the CL ionic and electronic conductivity shows that for a dry CL, the ionic conductivity is orders of magnitudes lower than the electronic conductivity. Varying the electronic conductivity of the support phase by simulations, reveals that the conductivity of the support does not have a considerable impact on the overall CL electrical conductivity.

| S-EPMC10017760 | biostudies-literature

Observation of polarity-switchable photoconductivity in III-nitride/MoS<sub>x</sub> core-shell nanowires.

Project description:III-V semiconductor nanowires are indispensable building blocks for nanoscale electronic and optoelectronic devices. However, solely relying on their intrinsic physical and material properties sometimes limits device functionalities to meet the increasing demands in versatile and complex electronic world. By leveraging the distinctive nature of the one-dimensional geometry and large surface-to-volume ratio of the nanowires, new properties can be attained through monolithic integration of conventional nanowires with other easy-synthesized functional materials. Herein, we combine high-crystal-quality III-nitride nanowires with amorphous molybdenum sulfides (a-MoSx) to construct III-nitride/a-MoSx core-shell nanostructures. Upon light illumination, such nanostructures exhibit striking spectrally distinctive photodetection characteristic in photoelectrochemical environment, demonstrating a negative photoresponsivity of -100.42 mA W-1 under 254 nm illumination, and a positive photoresponsivity of 29.5 mA W-1 under 365 nm illumination. Density functional theory calculations reveal that the successful surface modification of the nanowires via a-MoSx decoration accelerates the reaction process at the electrolyte/nanowire interface, leading to the generation of opposite photocurrent signals under different photon illumination. Most importantly, such polarity-switchable photoconductivity can be further tuned for multiple wavelength bands photodetection by simply adjusting the surrounding environment and/or tailoring the nanowire composition, showing great promise to build light-wavelength controllable sensing devices in the future.

| S-EPMC9296537 | biostudies-literature

Enhanced Microwave Absorption Properties of Intrinsically Core/shell Structured La(0.6)Sr(0.4)MnO(3) Nanoparticles.

Project description:The intrinsically core/shell structured La(0.6)Sr(0.4)MnO(3) nanoparticles with amorphous shells and ferromagnetic cores have been prepared. The magnetic, dielectric and microwave absorption properties are investigated in the frequency range from 1 to 12 GHz. An optimal reflection loss of -41.1 dB is reached at 8.2 GHz with a matching thickness of 2.2 mm, the bandwidth with a reflection loss less than -10 dB is obtained in the 5.5-11.3 GHz range for absorber thicknesses of 1.5-2.5 mm. The excellent microwave absorption properties are a consequence of the better electromagnetic matching due to the existence of the protective amorphous shells, the ferromagnetic cores, as well as the particular core/shell microstructure. As a result, the La(0.6)Sr(0.4)MnO(3) nanoparticles with amorphous shells and ferromagnetic cores may become attractive candidates for the new types of electromagnetic wave absorption materials. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11671-009-9374-y) contains supplementary material, which is available to authorized users.

| S-EPMC2894104 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data