Synthesis and Characterization of Spherical Hollow Assembly Composed of Cu Nanoparticles

2007 ◽  
Vol 72 (10) ◽  
pp. 1375-1382 ◽  
Author(s):  
Ming Yang ◽  
Xiao Yang

Hollow spheres of Cu nanoparticles with an average diameter of 300-500 nm have been prepared by a simple reaction of CuCl and hydrazine in suspension in the presence of gelatin at 60 °C. Gelatin played a decisive role as an inhibitor of the direct attack of hydrazine on CuCl surfaces and in coagulation of the growing Cu producing the hollow spheres. The products were characterized by X-ray powder diffraction, transmission electron microscopy, UV-VIS absorption spectroscopy and X-ray photoelectron spectrometry.

2013 ◽  
Vol 347-350 ◽  
pp. 1196-1198
Author(s):  
Ming Yang ◽  
Juan Juan Xia

Nanorods of CuCl with an average length of 100-200 nm have been prepared by a simple reaction between CuO suspension and NH2OH·HCl in the presence of deionized gelatin at room temperature. Gelatin played a decisive role as an inhibitor of the direct attack of NH2OH·HCl to CuO surfaces and coagulation of the growing CuCl in producing the nanorods. The products were characterized by X-ray powder diffraction and transmission electron microscopy.


2020 ◽  
Vol 10 ◽  
pp. 184798042096688
Author(s):  
Galo Cárdenas-Triviño ◽  
Sergio Triviño-Matus

Metal colloids in 2-mercaptoethanol using nanoparticles (NPs) of iron (Fe), cobalt (Co), and nickel (Ni) were prepared by chemical liquid deposition method. Transmission electron microscopy, electron diffraction, UV-VIS spectroscopy, and scanning electron microscopy with electron dispersive X-ray spectroscopy characterized the resulting colloidal dispersions. The NPs exhibited sizes with ranges from 9.8 nm for Fe, 3.7 nm for Co, and 7.2 nm for Ni. The electron diffraction shows the presence of the metals in its elemental state Fe (0), Co (0), and Ni (0) and also some compounds FeO (OH), CoCo2S4, and NiNi2S4.


2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.


2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang

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.


2012 ◽  
Vol 186 ◽  
pp. 212-215
Author(s):  
Jacek Krawczyk ◽  
Włodzimierz Bogdanowicz ◽  
Grzegorz Dercz ◽  
Wojciech Gurdziel

Microstructure of terminal area of Al65Cu32.9Co2.1ingots (numbers indicate at.%), obtained via directional solidification was studied. Scanning Electron Microscopy, Transmission Electron Microscopy and X-ray powder diffraction were applied. Point microanalysis by Scanning Electron Microscope was used for examination of chemical compositions of alloy phases. It was found that tetragonal θ phase of Al2Cu stoichiometric formula was the dominate phase (matrix). Additionally the alloy contained orthogonal set of nanofibres of Al7Cu2Co T phase with the average diameter of 50-500 nm and oval areas of hexagonal Al3(Cu,Co)2H-phase, surrounded by monoclinic AlCu η1phase rim. Inside some areas of H-phase cores of decagonal quasicrystalline D phase were observed.


2000 ◽  
Vol 15 (10) ◽  
pp. 2076-2079
Author(s):  
Chika Nozaki ◽  
Takashi Yamada ◽  
Kenji Tabata ◽  
Eiji Suzuki

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.


2012 ◽  
Vol 568 ◽  
pp. 295-298
Author(s):  
Juan Liao ◽  
Kai Zhang ◽  
Wen Zhong Wang ◽  
Yong Gang Wang ◽  
Li Yu

AgCl microparticle materials, with novel heart-like morphology, were successfully prepared by means of a simple solution phase route, in which a small amount of hydrochloric acid, ethylene and PVP were introduced to the conventional polyol process. The obtained microparticle materials were characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), and UV-Vis absorption spectrum. SEM images show that the obtained AgCl microparticle materials have heart-like morphology with an average diameter of 3 um. The influence of different reaction times on size and morphology of the microparticle materials were also investigated. A possible growth mechanism of AgCl microparticle materials has been proposed on the basis of experimental results and analysis. The as-prepared AgCl microparticle materials would find possible potential applications in photocatalytic fields.


NANO ◽  
2015 ◽  
Vol 10 (05) ◽  
pp. 1550071 ◽  
Author(s):  
Maoquan Xue ◽  
Changsheng Li

In this paper, regularly shaped AlF 3 particles with cubic structure were successfully synthesized via a solvothermal route. The as-prepared products were characterized by X-ray powder diffraction (XRD), energy-dispersive spectroscopy (EDS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The experimental results indicated that reaction temperature and time have significant effects on the morphology of the as-prepared products. A possible formation process has also been investigated on the basis of a series of XRD and SEM studies of the product obtained at different conditions. This well-controlled synthesis approach may be extended to fabricate other metal fluoride materials.


2012 ◽  
Vol 512-515 ◽  
pp. 2019-2022 ◽  
Author(s):  
Xiao Lu Liang ◽  
Xian Hua Wei

Cu2FeSnS4semiconductor nanocrystals with zincblende structure have been successfully synthesized by a hot-injection approach. Cu+, Fe2+, and Sn4+cations have a random distribution in the zincblende unit cell, and the occupancy possibilities are 1/2, 1/4 and 1/4, respectively. Those nanocrystals were characterized by means of X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED), energy dispersive spectroscopy (EDS), and UV-Vis-NIR absorption spectroscopy. The Cu2FeSnS4 nanocrystals have an average size of 7.5 nm and a band gap of 0.92 eV.


2007 ◽  
Vol 121-123 ◽  
pp. 255-258 ◽  
Author(s):  
Young Hwan Kim ◽  
Beong Gi Jo ◽  
Jee Hean Jeong ◽  
Young Soo Kang

A room temperature route for doping silica particles with Cu nanoparticles to achieve hybrid structures is introduced. First, silica nanoparticles were synthesized according to the well-known Stöber method by hydrolysis and condensation of TEOS in a mixture of ethanol with water, using ammonia as catalyst to initiate the reaction. These SiO2 nanoaprticles were dried at 100 oC. We measured the size of these nanoparticles with transmission electron microscopy (TEM). Second, Cu-SiO2 nanoparticles were synthesized by reaction with CuCl2 and SiO2 nanoparticles in presence of catalyst at room temperature for 12 hrs. Results show silica nanoparticles of about 70 nm size with regularly deposited Cu nanoparticles. Cu-SiO2 nanoparticles were investigated with TEM images, energy dispersive X-ray analysis (EDX) spectrum and so on.


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