Synthesis of Trilaminar Core–Shell Au/α-Fe2O3@SnO2Nanocomposites and their Application for Nonenzymatic Dopamine Electrochemical Sensing

NANO ◽  
2019 ◽  
Vol 14 (11) ◽  
pp. 1950138 ◽  
Author(s):  
Sai Zhang ◽  
Shijun Yue ◽  
Jiajia Li ◽  
Jianbin Zheng ◽  
Guojie Gao
Keyword(s):  
Electron Microscopy ◽  
High Sensitivity ◽  
Electrochemical Sensing ◽  
Synthesis Process ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Long Term Stability ◽  
Transmission Electron

Au nanoparticles anchored on core–shell [Formula: see text]-Fe2O3@SnO2 nanospindles were successfully constructed through hydrothermal synthesis process and used for fabricating a novel nonenzymatic dopamine (DA) sensor. The structure and morphology of the Au/[Formula: see text]-Fe2O3@SnO2 trilaminar nanohybrid film were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The electrochemical properties of the sensor were investigated by cyclic voltammetry and amperometry. The experimental results suggest that the composites have excellent catalytic property toward DA with a wide linear range from 0.5[Formula: see text][Formula: see text]M to 0.47[Formula: see text]mM, a low detection limit of 0.17[Formula: see text][Formula: see text]M (S/[Formula: see text]) and high sensitivity of 397.1[Formula: see text][Formula: see text]A[Formula: see text]mM[Formula: see text][Formula: see text]cm[Formula: see text]. In addition, the sensor exhibits long-term stability, good reproducibility and anti-interference.

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.

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.

Growth and characterization of type II ZnO/ZnSe core/shell nanowire arrays

2010 ◽  
Vol 25 (7) ◽  
pp. 1272-1277 ◽  
Author(s):  
Jinjian Zheng ◽  
Zhiming Wu ◽  
Weihuang Yang ◽  
Shuping Li ◽  
Junyong Kang
Keyword(s):  
Electron Microscopy ◽  
Chemical Vapor ◽  
Band Alignment ◽  
Nanowire Arrays ◽  
Core Shell ◽  
Type Ii ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Potential Applications

Type II ZnO/ZnSe core/shell nanowire arrays were grown by a two-step chemical vapor deposition. The nanowire arrays with dense nanoislands on the surface are well aligned and normal to the substrate imaged by scanning electron microscopy. The core/shell structure of nanowires was identified by a high-resolution transmission electron microscopy. The structure and composition of the shell were confirmed to be wurtzite ZnSe by x-ray diffraction, Raman scattering and energy-dispersive x-ray spectroscopy. Moreover, an intense emission was observed at 1.89 eV smaller than the band gaps of core and shell materials by photoluminescence, indicating the achievement of the type II band alignment at the interface. This study is expected to contribute to the potential applications in novel photovoltaic devices.

Silica/Polyurea Composite: Preparation, Characterization and Study of Dielectric Constant

2016 ◽  
Vol 13 (10) ◽  
pp. 7234-7237
Author(s):  
Botong Wang ◽  
Zebo Xu ◽  
Zhiqiang Wang
Keyword(s):  
Electron Microscopy ◽  
Dielectric Constant ◽  
Hydrogen Bonds ◽  
Ultraviolet Spectroscopy ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Modified Silica ◽  
X Ray ◽  
Transmission Electron ◽  
Core Shell Structure

Silica/polyurea composite was prepared after surface modification of silica nanoparticles. Silica/polyurea composite was characterized by Fourier-transform infrared spectroscopy, ultraviolet spectroscopy, X-ray diffraction and transmission electron microscopy. The results indicate that the helical polyurea has been successfully grafted onto the surfaces of the modified silica. Silica/polyurea composite exhibits clearly core–shell structure. The ultraviolet absorption and crystallizability of silica/polyurea are changed due to the shell of helical polyurea, which possesses regular singlehanded conformation and interchain hydrogen bonds. The dielectric constant of silica/polyurea was also investigated. The result indicates that the interfacial interactions between organic shell and inorganic core increase the dielectric constant value being increased to 6.42 for silica/polyurea. The interchain hydrogen bonds of helical polyurea could also be the reason for the increasing of dielectric constant.

Formation of Structurally Complex U-Phase in Al72Pd12.8Co15.2 Alloy

2013 ◽  
Vol 592-593 ◽  
pp. 517-520
Author(s):  
Ivona Černičková ◽  
Peter Švec ◽  
Emília Illeková ◽  
Dusan Janickovic ◽  
Pavol Priputen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Annealing Conditions ◽  
Transmission Electron ◽  
Compositional Homogeneity ◽  
Scanning Electron

The U-phase in the Al72Pd12.8Co15.2alloy was studied under non-equilibrium (casting, differential thermal analysis) and near-equilibrium (long-term annealing) conditions to consider its compositional homogeneity. In the investigation, scanning electron microscopy including energy dispersive X-ray spectroscopy, X-ray diffraction, transmission electron microscopy, and differential thermal analysis were used. Contrary to the finding reported for the Al69.8Pd13.8Co16.4alloy, the results obtained for the investigated Al72Pd12.8Co15.2alloy did not confirm the compositional heterogeneity of the near-equilibrium U-phase after annealing at 700°C for 2000 h and at 850°C for 500 h.

Preparation and characterization of a copper@polyimide core–shell structure via an in situ induction/imidization route

2016 ◽  
Vol 29 (5) ◽  
pp. 569-574
Author(s):  
Haoran Zhou ◽  
Dexin Wang ◽  
Chunyan Qu ◽  
Changwei Liu ◽  
Shanshan Mao
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Amic Acid ◽  
Core Shell ◽  
Oxidation Reactions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Pure Cu

Based on the combination of an in situ induction and imidization method for improving the interface bonding of an inorganic material and a polymer, copper@polyimide (Cu@PI) core–shell composite particles have been successfully prepared from poly(amic acid) ammonium salts (PAAS) and a Cu complex via a simple solvothermal process. The structures and the morphologies of the samples were characterized by X-ray photoelectron spectroscopy, X-ray diffraction, scanning electron microscopy and transmission electron microscopy (TEM), respectively. It was found that PAAS formed PI via a thermal imidization and subsequently precipitated in the solvent. Through crystallization induction, it then successfully coated on the surface of the formed Cu particles. Based on thermo gravimetric analyses curves and due to no Cu oxidation reactions taking place in the core coated with high-temperature-resistant PI, the weight increase was determined to be 106.4%, instead of up to 124.0% in samples consisting of pure Cu.

Electrospun CuO Nanofibre Assemblies for H2S Sensing

2018 ◽  
Vol 233 (1) ◽  
pp. 105-116
Author(s):  
Christoph Seitz ◽  
Sebastian Werner ◽  
Roland Marschall ◽  
Bernd M. Smarsly
Keyword(s):  
Electron Microscopy ◽  
Linear Sweep Voltammetry ◽  
X Ray Diffraction ◽  
Linear Sweep ◽  
X Ray ◽  
Transmission Electron ◽  
Before And After ◽  
Volumetric Stress ◽  
Scanning Electron

Abstract Copper oxide (CuO) nanofibres are utilised to sense the toxic and abrasive gas hydrogen sulfide (H2S) in the ppm (parts per million) range. The detection by CuO is based on a significant increase in the conductance upon the formation of CuS, and is thereby selective and sensitive towards H2S. Nanofibres outperform thin films of CuO by compensating the volumetric stress which occurs during sensing. Here, sensors are presented exhibiting up to 600 cycles of sensing and regeneration. To get further insights into the degradation of the fibres upon the reaction with H2S the sensors were analysed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), resistance and linear sweep voltammetry (LSV) measurements before and after cycling. SEM and TEM revealed a drastic change in morphology of the CuO fibres resulting in an undefined aggregate of nanoparticles after 600 cycles. Resistance and LSV measurements showed that the contacting and the measurement process itself are crucial factors for optimising long-term use of CuO-based H2S sensors.

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.

scholarly journals Crystallization of BaF2 from droplets of phase separated glass – evidence of a core–shell structure by ASAXS

CrystEngComm ◽  
2020 ◽  
Vol 22 (30) ◽  
pp. 5031-5039
Author(s):  
Armin Hoell ◽  
Vikram Singh Raghuwanshi ◽  
Christian Bocker ◽  
Andreas Herrmann ◽  
Christian Rüssel ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Small Angle ◽  
Shell Structure ◽  
Core Shell ◽  
X Ray Diffraction ◽  
X Ray ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Core Shell Structure

Glasses with the mol% compositions 1.88 Na2O·15.04 K2O·7.52 Al2O3·69.56 SiO2·6.00 BaF2 and 1.88 Na2O·15.03 K2O·7.52 Al2O3·69.52 SiO2·6.00 BaF2·0.05 SmF3 were studied using X-ray diffraction, transmission electron microscopy, and anomalous small-angle X-ray scattering.

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