Direct Preparation of Ce0.8Sm0.2O1.9 Powders Oxidized With H2O2 for Low Temperature SOFCs Application

2005 ◽  
Author(s):  
Jianbing Huang ◽  
Zongqiang Mao ◽  
Bin Zhu ◽  
Lizhai Yang ◽  
Ranran Peng ◽  
...  
Keyword(s):  
Single Phase ◽  
Fluorite Structure ◽  
X Ray Diffraction ◽  
Composite Electrolyte ◽  
Xrd Pattern ◽  
Transmission Electron ◽  
Direct Preparation ◽  
Novel Method ◽  
Power Densities

A novel method was developed to prepare fine doped ceria (DCO) powders directly. Ceria doped with 20 mol. % of samarium (Ce0.8Sm0.2O1.9, SDC) was prepared by in-situ oxidization of hydroxide precipitates with H2O2 in the solutions. The resultant powder desiccated at 85°C overnight was characterized by X-ray diffraction (XRD), thermogravimetry /differential thermal analysis (TG/DTA), and transmission electron microscopy (TEM). The XRD pattern showed that the as-dried SDC powder is single phase with a cubic fluorite structure like that of pure CeO2. An anode-supported SOFC was also fabricated based on SDC and 20wt. % (62mol. %Li2CO3–38 mol. %K2CO3) composite electrolyte, LiNiO2 as cathode and NiO as anode, by cold pressing. Using hydrogen as the fuel and air as the oxidant, the I-V and I-P characteristics exhibit excellent performances and the maximum power densities are about 696, 469, 377 and 240 mWcm−2 at 650, 600, 550 and 500°C, respectively.

Synthesis of Ce0.8Gd0.05Y0.15O1.9 Nanopowders

2007 ◽  
Vol 336-338 ◽  
pp. 2005-2007
Author(s):  
Xiang Feng Guan ◽  
Zhi Hui Liu ◽  
He Ping Zhou
Keyword(s):  
Electron Microscopy ◽  
Solid Oxide Fuel Cells ◽  
Single Phase ◽  
Fluorite Structure ◽  
Solid Oxide ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Mean Size ◽  
The Mean

Nanosized Ce0.8Gd0.05Y0.15O1.9 powders were synthesized using glycine nitrate process for use as the electrolyte of intermediate temperature solid oxide fuel cells. The powders were characterized by simultaneous thermogravimetry analysis (TGA) and differential thermal analysis (DTA), X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The XRD pattern indicated that the powders exhibited a single phase with cubic fluorite structure. The TEM studies showed that the calcined powders exhibited an almost spherical morphology and the mean size of the particles was 30nm, which is in agreement with the calculated result of XRD.

A Facile One-Step Hydrothermal Synthesis of Graphene/CeO2 Nanocomposite and its Catalytic Properties

2013 ◽  
Vol 747 ◽  
pp. 242-245 ◽  
Author(s):  
Manish Srivastava ◽  
Ashok Kumar Das ◽  
Partha Khanra ◽  
Nam Hoon Kim ◽  
Joong Hee Lee
Keyword(s):  
Catalytic Activity ◽  
Ammonium Bromide ◽  
X Ray Diffraction ◽  
Cetyltrimethyl Ammonium Bromide ◽  
Xrd Pattern ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Cetyltrimethyl Ammonium

Graphene/CeO2 nanocomposite has been successfully prepared by directly growing CeO2 nanoparticles on graphene sheets via in-situ reduction of graphene oxide containing the metal precursor. The presence of cetyltrimethyl ammonium bromide (CTAB) results the formation of CeO2 nanoparticles with a narrow size distribution. The structural, morphological, particles size and optical properties of the synthesized products were investigated through X-ray diffraction (XRD), transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FT-IR) and UVvis absorbance spectroscopy, respectively. The XRD pattern shows that graphene/CeO2 nanocomposite is highly crystalline in nature. Growth of CeO2 nanoparticles with size in range of 5-18 nm on the graphene sheet were observed by TEM measurement. Optical energy band gap was calculated to be ~3.30 eV corresponding to direct transition. The catalytic activity of the synthesized nanocomposite was investigated taking hydrazine hydrate as a model system. Significant enhancement in the peak current with respect to CeO2 was observed on graphene/CeO2 nanocomposite-based electrode demonstrating the higher catalytic activity of graphene/CeO2 nanocomposite-based electrode.

Facile Synthesis of ZnO Nanoparticles Using Mechanochemical Route and their Structural, Morphological and Thermal Properties

2013 ◽  
Vol 378 ◽  
pp. 220-224 ◽  
Author(s):  
Sung Jae Kim ◽  
Faheem Ahmed ◽  
Nishat Arshi ◽  
M.S. Anwar ◽  
Rehan Danish ◽  
...  
Keyword(s):  
Zno Nanoparticles ◽  
Single Phase ◽  
Synthesis Method ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
Transmission Electron ◽  
Average Grain Size ◽  
Ft Ir ◽  
20 Nm ◽  
Grinding Time

In the present work, we have prepared ZnO nanoparticles by a two-step mechanochemical synthesis method. The reaction was carried out in a paste state at room temperature with a short grinding time of 20 min. The prepared ZnO nanoparticles were characterized by using x-ray diffraction (XRD), transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FT-IR), and thermogravimetric analysis-differential thermal analysis (TGA/DTA). XRD and TEM results demonstrated that ZnO have a single phase nature with wurtzite structure with high crystallinity. The lattice parameters calculated from XRD pattern are a= 3.25 Å and c= 5.248 Å and the average grain size of the ZnO nanoparticles was found to be ~ 20 nm (TEM) or ~22 nm (XRD). FTIR spectra demonstrated the peak at ~455 cm-1 which correspond to stretching mode of ZnO.

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

Epitaxy and texture analysis of Bi-Sr-Ca-Cu-O thin films on (100) MgO using Transmission Electron Microscopy

1990 ◽  
Vol 48 (4) ◽  
pp. 68-69
Author(s):  
J. T. Sizemore ◽  
D. G. Schlom ◽  
Z. J. Chen ◽  
J. N. Eckstein ◽  
I. Bozovic ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Transmission Electron Microscopy ◽  
Critical Currents ◽  
Unit Cell ◽  
X Ray Diffraction ◽  
Cell Axis ◽  
Transmission Electron ◽  
Synthesis Procedure

Investigators observe large critical currents for superconducting thin films deposited epitaxially on single crystal substrates. The orientation of these films is often characterized by specifying the unit cell axis that is perpendicular to the substrate. This omits specifying the orientation of the other unit cell axes and grain boundary angles between grains of the thin film. Misorientation between grains of YBa2Cu3O7−δ decreases the critical current, even in those films that are c axis oriented. We presume that these results are similar for bismuth based superconductors and report the epitaxial orientations and textures observed in such films.Thin films of nominally Bi2Sr2CaCu2Ox were deposited on MgO using molecular beam epitaxy (MBE). These films were in situ grown (during growth oxygen was incorporated and the films were not oxygen post-annealed) and shuttering was used to encourage c axis growth. Other papers report the details of the synthesis procedure. The films were characterized using x-ray diffraction (XRD) and transmission electron microscopy (TEM).

Devitrification products of rapidly solidified Ni-Nb amorphous alloys.

1990 ◽  
Vol 48 (4) ◽  
pp. 950-951
Author(s):  
G. A. Bertero ◽  
W.H. Hofmeister ◽  
N.D. Evans ◽  
J.E. Wittig ◽  
R.J. Bayuzick
Keyword(s):  
Electron Microscopy ◽  
Amorphous Structure ◽  
Sulphuric Acid Solution ◽  
X Ray Diffraction ◽  
High Fracture ◽  
Transmission Electron ◽  
Xrd Techniques ◽  
Rapidly Solidified ◽  
Electromagnetically Levitated

Rapid solidification of Ni-Nb alloys promotes the formation of amorphous structure. Preliminary results indicate promising elastic properties and high fracture strength for the metallic glass. Knowledge of the thermal stability of the amorphus alloy and the changes in properties with temperature is therefore of prime importance. In this work rapidly solidified Ni-Nb alloys were analyzed with transmission electron microscopy (TEM) during in-situ heating experiments and after isothermal annealing of bulk samples. Differential thermal analysis (DTA), scanning electron microscopy (SEM) and x-ray diffraction (XRD) techniques were also used to characterize both the solidification and devitrification sequences.Samples of Ni-44 at.% Nb were electromagnetically levitated, melted, and rapidly solidified by splatquenching between two copper chill plates. The resulting samples were 100 to 200 μm thick discs of 2 to 3 cm diameter. TEM specimens were either ion-milled or alternatively electropolished in a methanol-10% sulphuric acid solution at 20 V and −40°C.

scholarly journals Microstructure and properties of nano-laminated Y3Si2C2 ceramics fabricated via in situ reaction by spark plasma sintering

2021 ◽  
Vol 10 (3) ◽  
pp. 578-586
Author(s):  
Lin-Kun Shi ◽  
Xiaobing Zhou ◽  
Jian-Qing Dai ◽  
Ke Chen ◽  
Zhengren Huang ◽  
...  
Keyword(s):  
Spark Plasma Sintering ◽  
Atomic Scale ◽  
Max Phase ◽  
X Ray Diffraction ◽  
Selected Area Electron Diffraction ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Spark Plasma ◽  
Diffraction Patterns

AbstractA nano-laminated Y3Si2C2 ceramic material was successfully synthesized via an in situ reaction between YH2 and SiC using spark plasma sintering technology. A MAX phase-like ternary layered structure of Y3Si2C2 was observed at the atomic-scale by high resolution transmission electron microscopy. The lattice parameters calculated from both X-ray diffraction and selected area electron diffraction patterns are in good agreement with the reported theoretical results. The nano-laminated fracture of kink boundaries, delamination, and slipping were observed at the tip of the Vickers indents. The elastic modulus and Vickers hardness of Y3Si2C2 ceramics (with 5.5 wt% Y2O3) sintered at 1500 °C were 156 and 6.4 GPa, respectively. The corresponding values of thermal and electrical conductivity were 13.7 W·m-1·K-1 and 6.3×105 S·m-1, respectively.

Photoluminescence Enhancement of CdS Nanocrystals Fabricated on Dithiocarbamate Functionalized PET Substrates

2012 ◽  
Vol 512-515 ◽  
pp. 1511-1515
Author(s):  
Chun Lin Zhao ◽  
Li Xing ◽  
Xiao Hong Liang ◽  
Jun Hui Xiang ◽  
Fu Shi Zhang ◽  
...  
Keyword(s):  
Room Temperature ◽  
Hexagonal Structure ◽  
Diffraction Measurement ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
X Ray ◽  
Cds Nanocrystals ◽  
Morphological Studies ◽  
Transmission Electron

Cadmium sulfide (CdS) nanocrystals (NCs) were self-assembled and in-situ immobilized on the dithiocarbamate (DTCs)-functionalized polyethylene glycol terephthalate (PET) substrates between the organic (carbon disulfide diffused in n-hexane) –aqueous (ethylenediamine and Cd2+ dissolved in water) interface at room temperature. Powder X-ray diffraction measurement revealed the hexagonal structure of CdS nanocrystals. Morphological studies performed by scanning electron microscopy (SEM) and high-resolution transmission electron microscope (HRTEM) showed the island-like structure of CdS nanocrystals on PET substrates, as well as energy-dispersive X-ray spectroscopy (EDS) confirmed the stoichiometries of CdS nanocrystals. The optical properties of DTCs modified CdS nanocrystals were thoroughly investigated by ultraviolet-visible absorption spectroscopy (UV-vis) and fluorescence spectroscopy. The as-prepared DTCs present intrinsic hydrophobicity and strong affinity for CdS nanocrystals.

scholarly journals Fracture in Bulk Amorphous Alloys

1998 ◽  
Vol 554 ◽  
Author(s):  
J. A. Horton ◽  
J. L. Wright ◽  
J. H. Schneibel
Keyword(s):  
Crack Propagation ◽  
Crack Growth ◽  
Shear Bands ◽  
Bulk Amorphous Alloy ◽  
In Situ Tem ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Crack Tips ◽  
Temperature Fracture

AbstractThe fracture behavior of a Zr-based bulk amorphous alloy, Zr-10 Al-5 Ti-17.9 Cu-14.6Ni (at.%), was examined by transmission electron microscopy (TEM) and x-ray diffraction forany evidence of crystallization preceding crack propagation. No evidence for crystallizationwas found in shear bands in compression specimens or at the fracture surface in tensile specimens.In- situ TEM deformation experiments were performed to more closely examine actualcrack tip regions. During the in-situ deformation experiment, controlled crack growth occurredto the point where the specimen was approximately 20 μm thick at which point uncontrolledcrack growth occurred. No evidence of any crystallization was found at the crack tips or thecrack flanks. Subsequent scanning microscope examination showed that the uncontrolledcrack growth region exhibited ridges and veins that appeared to have resulted from melting. Performing the deformations, both bulk and in-situ TEM, at liquid nitrogen temperatures (LN2) resulted in an increase in the amount of controlled crack growth. The surface roughness of the bulk regions fractured at LN2 temperatures corresponded with the roughness of the crack propagation observed during the in-situ TEM experiment, suggesting that the smooth-appearing room temperature fracture surfaces may also be a result of localized melting.

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