scholarly journals Effect of Different Mediated Agents on Morphology and Crystallinity of Synthesized Silver Nanowires Prepared by Polyol Process

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Mohammad Taghi Satoungar ◽  
Hamed Azizi ◽  
Saeid Fattahi ◽  
Mohammad Khajeh Mehrizi ◽  
Hedieh Fallahi
Keyword(s):  
Electron Microscopy ◽  
Silver Nanowires ◽  
Vinyl Pyrrolidone ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Solution Field ◽  
Poly Vinyl Pyrrolidone ◽  
Xrd Patterns ◽  
Structural Characterizations

Synthesis and characterization of multiple crystalline silver nanowires (NWs) with uniform diameters were carried out by using 1,2-propandiol and ethylene glycol (EG) as comediated solvents and FeCl3as mediated agent in the presence of poly(vinyl pyrrolidone) (PVP). Experimental data and structural characterizations revealed that AgNWs have evolved from the multiple crystalline seeds initially generated by reduction of AgNO3with EG and 1,2-propandiol followed by reducing Fe(III) to Fe(II) which in turn reacts with and removes adsorbed atomic oxygen from the surfaces of silver seeds. In addition, uniform silver nanowires were obtained by using FeCl2and AlCl3as mediated agents in EG solution. Field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) showed uniform nanowires in both diameter and length. UV-Vis spectra showed adsorption peaks confirming the formation of nanowires. X-ray diffraction (XRD) patterns displayed the final product with high crystallinity and purity. In this study, a growth mechanism for forming AgNWs was proposed and a comparison between different mediated agents was carried out.

Synthesis and Characterization of a New Amino-Functionalized PMO Material

2013 ◽  
Vol 712-715 ◽  
pp. 271-279
Author(s):  
Fei Ding ◽  
Shuang Xi Liu
Keyword(s):  
Electron Microscopy ◽  
Solid State Nmr ◽  
Alkyl Chain ◽  
Reaction System ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Xrd Patterns

A new organic silicane which is bridged by a long amino-functionalized alkyl chain was prepared and used as the precursor in the synthesis of a series of PMO materials. The organic silicane was added into the reaction system in CH2Cl2and the PMO materials were prepared by a simple stirring method under acidic condition, with a nonionic surfactantBrij 76 as template. To find the proper synthesis condition, the time of stirring and the proportion of organic silicane and TEOS were varied. Liquid and solid state NMR, X-ray diffraction (XRD) patterns, thermogravimetric analysis (TGA), transmission electron microscopy (TEM) and N2-physisorption properties were used to characterize the structures.

scholarly journals Synthesis and Characterization of Birnessite and Cryptomelane Nanostructures in Presence of Hoffmeister Anions

2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Marcos A. Cheney ◽  
Robin Jose ◽  
Arghya Banerjee ◽  
Pradip K. Bhowmik ◽  
Shizhi Qian ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Manganese Dioxide ◽  
Chloride Ion ◽  
Reduction Reaction ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
Transmission Electron ◽  
Xrd Patterns

The effect of Hoffmeister anions , , and on the structure and morphology of birnessite and cryptomelane-type manganese dioxide nanostructures, produced by the reduction reaction of and in aqueous acidic media, was studied. The syntheses were based on the decomposition of aqueous in presence of HCl for birnessite-type and acidified for cryptomelane-type manganese dioxide under soft hydrothermal conditions. They were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM) techniques. XRD patterns show the formation of birnessite for the first synthesis and a mixture of cryptomelane and birnessite-types for the second synthesis. XRD data revealed that the Hoffmeister anions have a significant effect on the nanostructures of birnessite. The sulphate ion-treated birnessite has the smallest crystals, whereas the chloride ion-treated birnessite has the largest crystals. Their TEM and HRTEM studies revealed a transformation from nanoplatelet morphology for chloride-treated samples to nanofibrous morphology for sulphate-treated birnessite. For the cryptomelane nanostructures, Hoffmeister anions also show a profound effect on their crystalline structures as determined by XRD analyses revealing a transformation of the cryptomelane phase to birnessite phase of . This transformation is also supported by TEM and HRTEM studies.

Structural and Magnetic Characterization of LaFe1-xAlxO3 (x = 0 and 0.2) Orthoferrites Synthesized by Gelatin Method

2017 ◽  
Vol 899 ◽  
pp. 227-231 ◽  
Author(s):  
Patrícia Mendonça Pimentel ◽  
J.L.S. Dutra ◽  
A.C. Lima ◽  
J.H. Araújo ◽  
Osmar Bagnato ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Treatment Temperature ◽  
Ferromagnetic Behavior ◽  
X Ray Diffraction ◽  
Magnetic Characterization ◽  
Organic Precursor ◽  
Transmission Electron ◽  
Heat Treated ◽  
Xrd Patterns

The rare-earth orthoferrites (LnFeO3) are promising materials for various applications, such as chemical sensors, cathode for SOFC, catalysts, among others. In general, these oxides are synthesized at temperatures higher than 700 °C. In this work, nanocrystalline LaFe1-xAlxO3 (x=0, x=0.2) powders were synthesized by a method that uses gelatin as organic precursor and heat treated at 400, 600 and 800 °C. The structural and magnetic characterization of powders was carried out by X-ray diffraction (XRD) and vibrating sample magnetometry (VSM). Morphological analysis was performed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The XRD patterns revealed the formation of orthoferrites single phase since 400°C. The powders exhibited weak ferromagnetic behavior at room temperature where the values of saturation magnetization, remanence and coercivity varied with the doping and heat treatment temperature.

Growth and Characterization of Well-Aligned RuO2/R-TiO2 Heteronanostructures on Sapphire (100) Substrates by Reactive Magnetron Sputtering

2011 ◽  
Vol 170 ◽  
pp. 78-82
Author(s):  
Hung Pin Hsu ◽  
Ying Sheng Huang ◽  
Chien Nan Yeh ◽  
Yi Min Chen ◽  
Dah Shyang Tsai ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Magnetron Sputtering ◽  
Reactive Magnetron Sputtering ◽  
Reactive Magnetron ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Vertically Aligned ◽  
Xrd Patterns ◽  
Electron Diffractometry

We report the growth of well-aligned RuO2/R-TiO2 heteronanostructures on sapphire (100) substrates by reactive magnetron sputtering using Ti and Ru metal targets under different conditions. The surface morphology and structural properties of the as-deposited heteronanostructures were characterized using field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), transmission electron microscopy (TEM) and selected-area electron diffractometry (SAED). The FESEM micrographs and XRD patterns indicated the growth of vertically aligned RuO2(001) nanotubes and twinned V-shaped RuO2(101) nanowedges (NWs) on top of R-TiO2 nanorods under different sputtering pressures. TEM and SAED characterizations of the V-shaped RuO2 NWs showed that the NWs are crystalline RuO2 with twin planes of (101) and twin direction of [ 01] at the V-junction.

Detonation Synthesis of Nano-Size Materials

1995 ◽  
Vol 418 ◽  
Author(s):  
J. Forbes ◽  
J. Davis ◽  
C. Wong
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Nucleation And Growth ◽  
Detonation Synthesis ◽  
X Ray Diffraction ◽  
Crystalline Materials ◽  
X Ray ◽  
Transmission Electron ◽  
Nano Size

AbstractThe detonation of explosives typically creates 100's of kbar pressures and 1000's K temperatures. These pressures and temperatures last for only a fraction of a microsecond as the products expand. Nucleation and growth of crystalline materials can occur under these conditions. Recovery of these materials is difficult but can occur in some circumstances. This paper describes the detonation synthesis facility, recovery of nano-size diamond, and plans to synthesize other nano-size materials by modifying the chemical composition of explosive compounds. The characterization of nano-size diamonds by transmission electron microscopy and electron diffraction, X-ray diffraction and Raman spectroscopy will also be reported.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

Microstructure Characterization of Metal Mixed Oxides

MRS Advances ◽  
2017 ◽  
Vol 2 (64) ◽  
pp. 4025-4030 ◽  
Author(s):  
T. Kryshtab ◽  
H. A. Calderon ◽  
A. Kryvko
Keyword(s):  
Mixed Oxides ◽  
Profile Analysis ◽  
Atomic Resolution ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Reconstruction Procedure ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Co Precipitation

ABSTRACTThe microstructure of Ni-Mg-Al mixed oxides obtained by thermal decomposition of hydrotalcite-like compounds synthesized by a co-precipitation method has been studied by using X-ray diffraction (XRD) and atomic resolution transmission electron microscopy (TEM). XRD patterns revealed the formation of NixMg1-xO (x=0÷1), α-Al2O3 and traces of MgAl2O4 and NiAl2O4 phases. The peaks profile analysis indicated a small grain size, microdeformations and partial overlapping of peaks due to phases with different, but similar interplanar spacings. The microdeformations point out the presence of dislocations and the peaks shift associated with the presence of excess vacancies. The use of atomic resolution TEM made it possible to identify the phases, directly observe dislocations and demonstrate the vacancies excess. Atomic resolution TEM is achieved by applying an Exit Wave Reconstruction procedure with 40 low dose images taken at different defocus. The current results suggest that vacancies of metals are predominant in MgO (NiO) crystals and that vacancies of Oxygen are predominant in Al2O3 crystals.

L-cysteine functionalized graphene quantum dots for sub-ppb detection of As (III)

2021 ◽  
Author(s):  
Md. Farhan Naseh ◽  
Neelam Singh ◽  
Jamilur R. Ansari ◽  
Ashavani Kumar ◽  
Tapan Sarkar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Quantum Dots ◽  
Room Temperature ◽  
Graphene Quantum Dots ◽  
Optical Characterization ◽  
Functionalized Graphene ◽  
Transmission Electron ◽  
Sensitivity And Selectivity ◽  
Structural Characterizations

Abstract Here, we report functionalized graphene quantum dots (GQDs) for the optical detection of arsenic at room temperature. GQDs with the fluorescence of three fundamental colors (red, green, and blue) were synthesized and functionally capped with L-cysteine (L-cys) to impart selectively towards As (III) by exploiting the affinity of L-cys towards arsenite. The optical characterization of GQDs was carried out using UV-Vis absorption spectroscopy, Fourier transform infrared spectroscopy, and fluorescence spectrometry and the structural characterizations were performed using transmission electron microscopy. The fluorescence results showed instantaneous quenching in intensity when the GQDs came in contact with As (III) for all test concentrations over a range from 0.025 ppb to 25 ppb, which covers the permissible limit of arsenic in drinking water. The experimental results suggested excellent sensitivity and selectivity towards As (III).

scholarly journals Preparation and Characterization of Polyhydroxybutyrate/Polycaprolactone Nanocomposites

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Cha Ping Liau ◽  
Mansor Bin Ahmad ◽  
Kamyar Shameli ◽  
Wan Md Zin Wan Yunus ◽  
Nor Azowa Ibrahim ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Basal Spacing ◽  
Cooh Group ◽  
Physical Interaction ◽  
X Ray Diffraction ◽  
Ion Exchange Reaction ◽  
Transmission Electron ◽  
Matrix Enhancement ◽  
Double Hydroxide

Polyhydroxybutyrate (PHB)/polycaprolactone (PCL)/stearate Mg-Al layered double hydroxide (LDH) nanocomposites were prepared via solution casting intercalation method. Coprecipitation method was used to prepare the anionic clay Mg-Al LDH from nitrate salt solution. Modification of nitrate anions by stearate anions between the LDH layers via ion exchange reaction. FTIR spectra showed the presence of carboxylic acid (COOH) group which indicates that stearate anions were successfully intercalated into the Mg-Al LDH. The formation of nanocomposites only involves physical interaction as there are no new functional groups or new bonding formed. X-ray diffraction (XRD) and transmission electron microscopy (TEM) indicated that the mixtures of nanocomposites are intercalated and exfoliated types. XRD results showed increasing of basal spacing from 8.66 to 32.97 Å in modified stearate Mg-Al LDH, and TEM results revealed that the stearate Mg-Al LDH layers are homogeneously distributed in the PHB/PCL polymer blends matrix. Enhancement in 300% elongation at break and 66% tensile strength in the presence of 1.0 wt % of the stearate Mg-Al LDH as compare with PHB/PCL blends. Scanning electron microscopy (SEM) proved that clay improves compatibility between polymer matrix and the best ratio 80PHB/20PCL/1stearate Mg-Al LDH surface is well dispersed and stretched before it breaks.

Synthesis and characterization of homogeneous lead-substituted tin oxide with the (110) face of rutile structure

2000 ◽  
Vol 15 (10) ◽  
pp. 2076-2079
Author(s):  
Chika Nozaki ◽  
Takashi Yamada ◽  
Kenji Tabata ◽  
Eiji Suzuki
Keyword(s):  
Electron Microscopy ◽  
Tin Oxide ◽  
Photoelectron Spectroscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Rutile Structure ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Synthesis of a rutile-type lead-substituted tin oxide with (110) face was investigated. The characterization was performed by x-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive x-ray spectroscopy, infrared spectroscopy, x-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area measurements. The homogeneous rutile-type lead-substituted tin oxide was obtained until 4.1 mol% of tin was substituted with lead. The surface of obtained oxide had a homogeneously lead-substituted (110) face.

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