CHARACTERISTICS OF CdS NANOPARTICLES SYNTHESIZED BY SOLVOTHERMAL ROUTE WITH DIFFERENT RATIOS OF ETHYLENEDIAMINE/WATER

2005 ◽  
Vol 04 (04) ◽  
pp. 659-665
Author(s):  
JIANXI YAO ◽  
LI HONG ◽  
GAOLING ZHAO ◽  
WENJIAN WENG ◽  
GAORONG HAN
Keyword(s):  
Electron Microscopy ◽  
Cds Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Solvothermal Route ◽  
Cds Nanorods ◽  
Transmission Electron ◽  
Coordination Ability ◽  
The Difference ◽  
Xrd Patterns

CdS nanoparticles with various size and shape were synthesized through solvothermal route using different ratios of ethylenediamine/water. X-ray diffraction and transmission electron microscopy results revealed that CdS nanorods were formed by using ethylenediamine and the mixture of ethylenediamine and water as solvents. The CdS nanorods had [002] preferential orientation. When water was used as the solvent, irregular shape particles and typical XRD patterns of hexagonal CdS were observed. The produced nanoparticles displayed interesting photoluminescence feature, which were found to be sensitive to the ratio of ethylenediamine/water. It is suggested that the different coordination ability with Cd 2+ and dielectric constant of ethylenediamine and water caused different formation mechanism of CdS and led to the difference in the shape, crystallinity and optical properties of produced CdS particles.

Preparation and comparison of YBa2Cu4O8 films on MgO(100) and SrTiO3(100) by MOCVD

1993 ◽  
Vol 8 (9) ◽  
pp. 2143-2148 ◽  
Author(s):  
H. Sakai ◽  
Y. Shiohara ◽  
S. Tanaka
Keyword(s):  
Electron Microscopy ◽  
Lattice Mismatch ◽  
Film Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron ◽  
The Difference ◽  
Xrd Patterns

The thin films (Y/Ba/Cu = 1.0/2.7/4.7) which have a strong intensity corresponding to the c-axis peaks of the 124 phase (YBa2Cu4O8) in x-ray diffraction (XRD) patterns were prepared. The film structure and surface morphology of these films were observed by scanning electron microscopy (SEM), energy dispersive x-ray (EDX), transmission electron microscopy (TEM), and atomic force microscopy (AFM). It was found that the film on MgO(100) clearly has grain boundaries with many a-axis oriented grains of the 123 phase (YBa2Cu3O7−x). However, the film on SrTiO3(100) had a smooth surface, and a-axis oriented grains of the 123 phase couldn't be observed. This difference could not be explained by only the difference in the lattice mismatch.

Nanoporous Ni and Ni-Cu Fabricated by Dealloying

2009 ◽  
Vol 1228 ◽  
Author(s):  
Masataka Hakamada ◽  
Yasumasa Chino ◽  
Mamoru Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Noble Metals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
The Difference ◽  
20 Nm ◽  
Good Workability ◽  
Scanning Electron

AbstractMetallic nanoporous architecture can be spontaneously attained by dealloying of a binary alloy. The nanoporous architecture can be often fabricated in noble metals such as Au and Pt. In this study, nanoporous Ni, Ni-Cu are fabricated by dealloying rolled Ni-Mn and Cu-Ni-Mn alloys, respectively. Unlike conventional Raney nickel composed of brittle Ni-Al or Cu-Al intermetallic compounds, the initial alloys had good workability probably because of their fcc crystal structures. After the electrolysis of the alloys in (NH4)2SO4 aqueous solution, nanoporous architectures of Ni and Ni-Cu with pore and ligament sizes of 10–20 nm were confirmed by scanning electron microscopy and transmission electron microscopy. X-ray diffraction analyses suggested that Ni and Cu atoms form a homogeneous solid solution in the Ni-Cu nanoporous architecture. The ligament sizes of nanoporous Ni and Ni-Cu were smaller than that of nanoporous Cu, reflecting the difference between diffusivities of Ni and Cu at solid/electrolyte interface. Ni can reduce the pore and ligament sizes of resulting nanoporous architecture when added to initial Cu-Mn alloys.

Clay minerals in the Namacotche Pegmatite Group from Zambezia Province, Mozambique: main constituents of late-stage secondary paragenesis

Clay Minerals ◽  
2008 ◽  
Vol 43 (4) ◽  
pp. 597-613 ◽  
Author(s):  
M. A. Sequeira Braga ◽  
C. Leal Gomes ◽  
J. Duplay ◽  
H. Paquet
Keyword(s):  
Electron Microscopy ◽  
Clay Minerals ◽  
Late Stage ◽  
Polarized Light ◽  
Chemical Analyses ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Close Relationship ◽  
Xrd Patterns

AbstractNamacotche gem-bearing pegmatites of Alto Ligonha pegmatite district are heterogeneous, strongly fractionated, and have large Li and Ta and extremely large Cs contents. Clay samples were collected in fracture infillings and dilation cavities with gemstones and were studied using X-ray diffraction (XRD), polarized light microscope, scanning electron microscopy-energy dispersive spectroscopy, high-resolution transmission electron microscopy and chemical analyses. The <2 μm fraction contains cookeite, illite, illite-smectite and suggested irregular mixed-layer cookeite-smectite, beidellite, montmorillonite, kaolinite and goethite.The XRD patterns of chlorite and their d values suggest the presence of ‘di-trioctahedral chlorite’ similar to cookeite-Ia polytype. Cookeite chemical analyses show that Li contents range from 0.82 to 1.08 atoms per half unit cell.A close relationship has been established between occurrences of gemstones and clay minerals. Some important textures and crystal chemistry are discussed.The main gemstones related to the Namacotche Pegmatite are: morganite (pink cesian beryl), kunzite (spodumene) and elbaite tourmaline. As the mechanisms responsible for the gemstone formation take place at low temperature, the clay minerals paragenesis cookeite ± cookeite-smectite interstratification ± beidellite + montmorillonite ± illite-smectite interstratification, represents a late-stage secondary paragenesis, generated by hydrothermal alteration.

scholarly journals Synthesis of Flower-Like Cu2ZnSnS4Nanoflakes via a Microwave-Assisted Solvothermal Route

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Fei Long ◽  
Shuyi Mo ◽  
Yan Zeng ◽  
Shangsen Chi ◽  
Zhengguang Zou
Keyword(s):  
Electron Microscopy ◽  
Raman Scattering ◽  
Zinc Acetate Dihydrate ◽  
X Ray Diffraction ◽  
One Pot ◽  
X Ray ◽  
Transmission Electron ◽  
Direct Band ◽  
Xrd Patterns ◽  
Average Size

Flower-like Cu2ZnSnS4(CZTS) nanoflakes were synthesized by a facile and fast one-pot solution reaction using copper(II) acetate monohydrate, zinc acetate dihydrate, tin(IV) chloride pentahydrate, and thiourea as starting materials. The as-synthesized samples were characterized by X-ray diffraction (XRD), Raman scattering analysis, field emission scanning electron microscopy (FESEM) equipped with an energy dispersion X-ray spectrometer (EDS), transmission electron microscopy (TEM), and UV-Vis absorption spectra. The XRD patterns shown that the as-synthesized particles were kesterite CZTS and Raman scattering analysis and EDS confirmed that kesterite CZTS was the only phase of product. The results of FESEM and TEM show that the as-synthesized particles were flower-like morphology with the average size of 1~2 μm which are composed of 50 nm thick nanoflakes. UV-Vis absorption spectrum revealed CZTS nanoflakes with a direct band gap of 1.52 eV.

Initial formation mechanisms of (Ga1−xMnx)N nanorods grown on Al2O3 (0001) substrates

2008 ◽  
Vol 23 (12) ◽  
pp. 3275-3280 ◽  
Author(s):  
K.H. Lee ◽  
J.Y. Lee ◽  
H.C. Jeon ◽  
T.W. Kang ◽  
H.Y. Kwon ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Molecular Beam ◽  
Formation Mechanisms ◽  
X Ray Diffraction ◽  
Initial Formation ◽  
X Ray ◽  
Transmission Electron ◽  
High Resolution Tem ◽  
Xrd Patterns ◽  
Scanning Electron

The (Ga1−xMnx)N nanorods were grown on Al2O3 (0001) substrates by using rf-associated molecular beam epitaxy. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and selected-area diffraction pattern (SADP) results showed that the (Ga1−xMnx)N nanorods had (0001) preferential orientations. XRD patterns showed that the (Ga1−xMnx)N nanorods contained a small number of grains with different preferred orientations. High-resolution TEM (HRTEM) images showed that the (Ga1−xMnx)N nanorods consisted of different preferentially oriented grains. The initial formation mechanisms for the (Ga1−xMnx)N nanorods grown on Al2O3 (0001) substrates are described on the basis of the XRD, the TEM, the SADP, and the HRTEM results.

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.

SYNTHESIS AND PHOTOLUMINESCENCE PROPERTIES OF MICRON-ALUMINA

2014 ◽  
Vol 21 (02) ◽  
pp. 1450031
Author(s):  
SHIHUA ZHAO ◽  
ZHENG WANG ◽  
MINGQUAN WANG ◽  
YUTING CUI ◽  
QUANLIN LIU
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Electronic Transitions ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
Preparation Methods ◽  
X Ray ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Many Particles

Micron-alumina is expected to be of new properties and applications owing to its different morphology structures, which is prepared by the conventional preparation methods. X-ray diffraction (XRD) patterns present that the micron-alumina has poly-crystalline structure. Scanning electron microscopy (SEM) shows that the micron-alumina looks like a bouquet of flowers and its surface is covered with much micron-strips. Transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM) show that the micron-alumina is composed of many particles, which has polycrystalline structure. PL spectra display that emission peak of the micron-alumina centers at 301 nm, which attributes to the F + centers. A schematic drawing for electronic transitions in the excitation and emission processes is proposed.

Solvothermal Synthesis of Mn-Doped CdS Nanorods Using Single-Source Molecular Precursors

2011 ◽  
Vol 284-286 ◽  
pp. 667-670
Author(s):  
Zhen Ni Du ◽  
Zhi You Xu ◽  
Yong Cai Zhang ◽  
Ming Zhang
Keyword(s):  
Electron Microscopy ◽  
Solvothermal Synthesis ◽  
Hexagonal Phase ◽  
Single Source ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molecular Precursors ◽  
Cds Nanorods ◽  
Transmission Electron ◽  
Mn Doped

The synthesis of hexagonal phase Mn-doped CdS (Cd1-xMnxS) nanorods was achieved by solvothermal treatment of a class of easily obtained, air-stable single-source molecular precursors (cadmium manganese diethyldithiocarbamates, Cd1-xMnx-(DDTC)2) in ethylenediamine at 180 °C for 12 h. The structures and compositions of the as-synthesized products were characterized by X-ray diffraction, energy dispersive X-ray spectroscopy and transmission electron microscopy.

Facile Sol-Gel Synthesis of Mesoporous TiO2 in Ionic Liquids

2013 ◽  
Vol 389 ◽  
pp. 53-56
Author(s):  
Shu Guo ◽  
Sheng Xu Lu ◽  
Hui Ding ◽  
Zai Feng Shi
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Sol Gel ◽  
Rutile Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carboxylate Groups ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Sol Gel Synthesis

The mesoporous TiO2 particles was conveniently prepared in a room temperature ionic liquid (RTILs) of 1, 3-di-(3-propionyloxy) imdazolium tetrafluoroborate [DiprCOOBF4 system. The obtained materials were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and N2 adsorptiondesorption analysis. XRD patterns revealed that only rutile phase is formed in the RTILs. The TEM micrographs as well as N2 adsorptiondesorption measurements show that the prepared products exhibited wormlike pore structures. The FTIR (Fourier Transform Infrared Spectra) demonstrate the carboxylate groups attach via bidentate or bridging coordination to the TiO2 surface.

scholarly journals Characterization of Enhanced Antibacterial Effects of Silver Loaded Cerium Oxide Catalyst

2018 ◽  
Vol 34 (6) ◽  
pp. 2895-2901
Author(s):  
Gusliani Eka Putri ◽  
Syukri Arief ◽  
Novesar Jamarun ◽  
Feni Rahayu Gusti ◽  
Annisa Novita Sary
Keyword(s):  
Electron Microscopy ◽  
Silver Nanoparticles ◽  
Sol Gel ◽  
Nitrate Hexahydrate ◽  
X Ray Diffraction ◽  
Tem Analysis ◽  
X Ray ◽  
Transmission Electron ◽  
The Difference

Silver-cerium nanoparticles had been successfully synthesized using the sol-gel method by silver nitrate as a source of silver and cerium nitrate hexahydrate as a source of cerium. The synthesized silver-cerium nanoparticles had been characterized by X-ray diffraction,transmission electron microscopy, and scanning electron microscopy-energy dispersive X-ray. Based on the results of XRD and TEM analysis showed silver-cerium nanoparticles were spherical with the dominant size range of 8.9 -12.73 nm. SEM-EDX analysis showed silver nanoparticles covered by cerium nanoparticles that were known as the core-shell structure. Silver nanoparticles doped with cerium nanoparticles (CeONP) showed an increase in inhibitory with an increase a zone of inhibition after being doped with cerium nanoparticles. The disinfection effect of Ag-doped CeONP was more pronounced on Staphylococcus aureus than Escherichia coli, although the difference was not wide.

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