scholarly journals X-ray powder diffraction to analyse bimetallic core–shell nanoparticles (gold and palladium; 7–8 nm)

RSC Advances ◽  
2019 ◽  
Vol 9 (46) ◽  
pp. 26628-26636 ◽  
Author(s):  
A. Rostek ◽  
K. Loza ◽  
M. Heggen ◽  
M. Epple

A comparative X-ray powder diffraction study on poly(N-vinyl pyrrolidone) (PVP)-stabilized palladium and gold nanoparticles and bimetallic Pd–Au nanoparticles (both types of core–shell nanostructures) was performed.

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 730
Author(s):  
Erik Sarnello ◽  
Tao Li

Enzyme immobilization techniques are widely researched due to their wide range of applications. Polymer–protein core–shell nanoparticles (CSNPs) have emerged as a promising technique for enzyme/protein immobilization via a self-assembly process. Based on the desired application, different sizes and distribution of the polymer–protein CSNPs may be required. This work systematically studies the assembly process of poly(4-vinyl pyridine) and bovine serum albumin CSNPs. Average particle size was controlled by varying the concentrations of each reagent. Particle size and size distributions were monitored by dynamic light scattering, ultra-small-angle X-ray scattering, small-angle X-ray scattering and transmission electron microscopy. Results showed a wide range of CSNPs could be assembled ranging from an average radius as small as 52.3 nm, to particles above 1 µm by adjusting reagent concentrations. In situ X-ray scattering techniques monitored particle assembly as a function of time showing the initial particle growth followed by a decrease in particle size as they reach equilibrium. The results outline a general strategy that can be applied to other CSNP systems to better control particle size and distribution for various applications.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Chin-Wei Lin ◽  
Jian-Ming Chen ◽  
You-Jun Lin ◽  
Ling-Wei Chao ◽  
Sin-Yi Wei ◽  
...  

Abstract Recently, gold-coated magnetic nanoparticles have drawn the interest of researchers due to their unique magneto-plasmonic characteristics. Previous research has found that the magneto-optical Faraday effect of gold-coated magnetic nanoparticles can be effectively enhanced because of the surface plasmon resonance of the gold shell. Furthermore, gold-coated magnetic nanoparticles are ideal for biomedical applications because of their high stability and biocompatibility. In this work, we synthesized Fe3O4@Au core-shell nanoparticles and coated streptavidin (STA) on the surface. Streptavidin is a protein which can selectively bind to biotin with a strong affinity. STA is widely used in biotechnology research including enzyme-linked immunosorbent assay (ELISA), time-resolved immunofluorescence (TRFIA), biosensors, and targeted pharmaceuticals. The Faraday magneto-optical characteristics of the biofunctionalized Fe3O4@Au nanoparticles were measured and studied. We showed that the streptavidin-coated Fe3O4@Au nanoparticles still possessed the enhanced magneto-optical Faraday effect. As a result, the possibility of using biofunctionalized Fe3O4@Au nanoparticles for magneto-optical biomedical assays should be explored.


2011 ◽  
Vol 306-307 ◽  
pp. 410-415
Author(s):  
Li Sun ◽  
Fu Tian Liu ◽  
Qi Hui Jiang ◽  
Xiu Xiu Chen ◽  
Ping Yang

Core/shell type nanoparticles with an average diameter of 20nm were synthesized by chemical precipitation method. Firstly, Monodisperse Fe3O4 nanoparticles were synthesized by solvethermal method. FeSO4ž7H2O and NaBH4 were respectively dissolved in distilled water, then moderated Fe3O4 particles and surfactant(PVP) were ultrasonic dispersed into the FeSO4ž7H2O solution. The resulting solution was stirred 2 h at room temperature. Fe could be deposited on the surface of monodispersed Fe3O4 nanoparticles to form core-shell particles. The particles were characterized by using various experimental techniques, such as transmission electron microscopy (TEM), X-ray diffraction (XRD), AGM and DTA. The results suggest that the saturation magnetization of the nanocomposites is 100 emu/g. The composition of the samples show monodisperse and the sides of the core/shell nanoparticles are 20-30nm. It is noted that the formation of Fe3O4/Fe nanocomposites magnetite nanoparticles possess superparamagnetic property.


2018 ◽  
Vol 8 (3) ◽  
pp. 411 ◽  
Author(s):  
Mehrdad Khatami ◽  
Hajar Alijani ◽  
Meysam Nejad ◽  
Rajender Varma

Among an array of hybrid nanoparticles, core-shell nanoparticles comprise of two or more materials, such as metals and biomolecules, wherein one of them forms the core at the center, while the other material/materials that were located around the central core develops a shell. Core-shell nanostructures are useful entities with high thermal and chemical stability, lower toxicity, greater solubility, and higher permeability to specific target cells. Plant or natural products-mediated synthesis of nanostructures refers to the use of plants or its extracts for the synthesis of nanostructures, an emerging field of sustainable nanotechnology. Various physiochemical and greener methods have been advanced for the synthesis of nanostructures, in contrast to conventional approaches that require the use of synthetic compounds for the assembly of nanostructures. Although several biological resources have been exploited for the synthesis of core-shell nanoparticles, but plant-based materials appear to be the ideal candidates for large-scale green synthesis of core-shell nanoparticles. This review summarizes the known strategies for the greener production of core-shell nanoparticles using plants extract or their derivatives and highlights their salient attributes, such as low costs, the lack of dependence on the use of any toxic materials, and the environmental friendliness for the sustainable assembly of stabile nanostructures.


2021 ◽  
Vol 19 (10) ◽  
pp. 82-88
Author(s):  
Duaa A. Uamran ◽  
Qasim Hassan Ubaid ◽  
Hammad R. Humud

Core-shell nanoparticles (SiO2/Ag) were manufactured by using a two-step process: Electric detonation of Ag. Wire in colloidal solution particles then by using laser pulses, nanoparticles are released. The structural features of these nanoparticles were checked by using X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). The (XRD) study showed the progressive coverage of SiO2/Ag by nanoparticles according to the energies of the laser pulse. Measurements of morphology and EDX confirmed the Core/shell structure with particle size at the nano level. It confirmed that preliminary analysis consists of a SiO2 core and an Ag shell from FESEM. The surface of the microscopic balls (SiO2) has been covered completely and homogeneously with Ag nanoparticles, Moreover, Ultraviolet-Visible, and by optical absorption spectroscopy, the Nanoparticles with core crust SiO2/Ag showed excellent photocatalytic activities at various concentrations and laser pulse energy.


Nanoscale ◽  
2019 ◽  
Vol 11 (37) ◽  
pp. 17471-17477 ◽  
Author(s):  
Jiaqi Chen ◽  
Dejing Meng ◽  
Hui Wang ◽  
Haiyun Li ◽  
Yinglu Ji ◽  
...  

Using DMAB as the Raman internal reference, the spatial trajectory of modulating 4-ATP molecules was tracked during the shell growth process.


RSC Advances ◽  
2017 ◽  
Vol 7 (13) ◽  
pp. 7469-7475 ◽  
Author(s):  
Ryeri Lee ◽  
Yogeenth Kumaresan ◽  
Sei Young Yoon ◽  
Soong Ho Um ◽  
Il Keun Kwon ◽  
...  

In this study, we designed core/shell nanostructures (CSNs) of silicon dioxide (SiO2)/titanium dioxide (TiO2), which were decorated with gold (Au) nanoparticles (NPs), to activate the visible light-driven photocatalytic reaction.


Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 672
Author(s):  
Marin Cernea ◽  
Roxana Radu ◽  
Harvey Amorín ◽  
Simona Gabriela Greculeasa ◽  
Bogdan Stefan Vasile ◽  
...  

Herein we report on novel multiferroic core–shell nanostructures of cobalt ferrite (CoFe2O4)–bismuth, sodium titanate doped with barium titanate (BNT–BT0.08), prepared by a two–step wet chemical procedure, using the sol–gel technique. The fraction of CoFe2O4 was varied from 1:0.5 to 1:1.5 = BNT–BT0.08/CoFe2O4 (molar ratio). X–ray diffraction confirmed the presence of both the spinel CoFe2O4 and the perovskite Bi0.5Na0.5TiO3 phases. Scanning electron microscopy analysis indicated that the diameter of the core–shell nanoparticles was between 15 and 40 nm. Transmission electron microscopy data showed two–phase composite nanostructures consisting of a BNT–BT0.08 core surrounded by a CoFe2O4 shell with an average thickness of 4–7 nm. Cole-Cole plots reveal the presence of grains and grain boundary effects in the BNT–BT0.08/CoFe2O4 composite. Moreover, the values of the dc conductivity were found to increase with the amount of CoFe2O4 semiconductive phase. Both X-ray photoelectron spectroscopy (XPS) and Mössbauer measurements have shown no change in the valence of the Fe3+, Co2+, Bi3+ and Ti4+ cations. This study provides a detailed insight into the magnetoelectric coupling of the multiferroic BNT–BT0.08/CoFe2O4 core–shell composite potentially suitable for magnetoelectric applications.


MRS Advances ◽  
2017 ◽  
Vol 2 (49) ◽  
pp. 2675-2681 ◽  
Author(s):  
Constanza Y. Flores ◽  
Estefania Achilli ◽  
Mariano Grasselli

ABSTRACTGold/albumin core/shell nanoparticles (Au/AlbNPs) was prepared by a novel aggregation/crosslinking technique and characterized by several spectroscopic and microscopy methods. Albumin, in presence of gold nanoparticles (AuNPs), is aggregated by the addition of ethanol and further stabilized by radiation-induced crosslinking using a 60Co source. Nanoconstructs are characterized to determine size, morphology and optical characteristics. The Au/AlbNPs were prepared in different ethanol and albumins concentrations. Results showed that it is possible to obtain Au/AlbNPs using ethanol 30 %v/v, albumin in different concentrations and an irradiation dose of 10 kGy. Au/AlbNP plasmon peak shifted to 530 nm, keeping the typical plasmon peak shape. The size of Au/AlbNPs is approximately double respect to the naked AuNPs and they show core/shell type morphology. The main amide peaks of albumin in FTIR spectrum can be found in the spectrum of nanoconstructs.


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