Studies on plasma-nitrided iron by scanning electron microscopy, glancing angle x-ray diffraction, and x-ray photoelectron spectroscopy

2000 ◽  
Vol 18 (6) ◽  
pp. 2733-2737 ◽  
Author(s):  
Eduardo J. Miola ◽  
Sylvio D. de Souza ◽  
Pedro A. P. Nascente ◽  
Maristela Olzon-Dionysio ◽  
Carlos A. Olivieri ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Glancing Angle ◽  
Scanning Electron

scholarly journals Preparation of Cerium Dioxide Layers on Titanium by Electrodeposition with Organic Solution

2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Vaijayanti Namdeo Nande ◽  
Diana Kostyukova ◽  
Jeonghee Choi ◽  
Yong Hee Chung
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Cerium Dioxide ◽  
Average Crystallite Size ◽  
X Ray Diffraction ◽  
Organic Solution ◽  
X Ray ◽  
Titanium Foils ◽  
Scanning Electron

Layers of cerium dioxide nanoparticles were prepared on titanium by electrodeposition with organic solution. Three concentrations of cerium ions were used at 31.6 V. The organic solution was isobutanol and titanium foils were used as anodes and cathodes. Currents were monitored during the electrodeposition. Deposition times ranged from 0.5 to 8 h. Deposited Deposited layers were calcined at 700 K for 30 min. The morphology and composition of the deposited layers were examined by scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). As-prepared and calcined deposition layers were assayed to be cerium dioxide. The average crystallite size increased from 4 to 7 nm through calcination at 700 K. Sizes of calcined cerium oxide agglomerates were ranging from 73 to 146 nm for 30 min deposition and 209 to 262 nm for 8 h deposition. The electrodeposition efficiencies of 0.5 h deposition at three concentrations were measured to be highest.

Fabrication of g-C3N4/Y-TiO2 Z-scheme heterojunction photocatalysts for enhanced photocatalytic activity

2021 ◽  
Author(s):  
SongSik Pak ◽  
KwangChol Ri ◽  
Chenmin Xu ◽  
Qiuyi Ji ◽  
Dunyu Sun ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Photocatalytic Activity ◽  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

The g-C3N4/Y-TiO2 Z-scheme heterojunction photocatalysts were successfully synthesized. The powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscope, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy were used for...

Magnetic and Structural Properties of Nanocomposite ZnO-Fe3O4 Films Prepared by Solid-State Synthesis

2014 ◽  
Vol 215 ◽  
pp. 158-162
Author(s):  
Liudmila E. Bykova ◽  
V.G. Myagkov ◽  
I.A. Tambasov ◽  
O.A. Bayukov ◽  
Victor S. Zhigalov ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Solid State ◽  
Photoelectron Spectroscopy ◽  
Magnetic Measurements ◽  
X Ray Diffraction ◽  
Simple Method ◽  
Physical Methods ◽  
X Ray ◽  
Scanning Electron

A simple method for obtaining ZnO-Fe3O4 nanocomposites using solid-state reaction Zn + 3Fe2O3 ZnO + 2Fe3O4 is suggested. An analysis of the characteristics and properties of ZnO-Fe3O4 nanocomposites was carried out by a combination of structural and physical methods (X-ray diffraction, scanning electron microscopy, photoelectron spectroscopy, Mössbauer measurements, X-ray fluorescent analysis, and magnetic measurements). The magnetization of the hybrid ZnO-Fe3O4 films is equal to 440 emu/cm3. The resulting Fe3O4 nanoparticles are surrounded by a ZnO shell and have sizes ranging between 20 and 40 nm.

Uranium(VI) interaction with pyrite (FeS2): Chemical and spectroscopic studies

2006 ◽  
Vol 94 (9-11) ◽  
Author(s):  
Noelle Eglizaud ◽  
F. Miserque ◽  
E. Simoni ◽  
M. Schlegel ◽  
M. Descostes
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Spectroscopic Studies ◽  
Solution Chemistry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Natural Pyrite ◽  
Scanning Electron

The mechanism of uranium(VI) interaction with pyrite was studied by solution chemistry and X-ray Photoelectron Spectroscopy (XPS). Natural pyrite was characterized by X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). After equilibration in 10

scholarly journals Electrochemistry, Electrodeposition, and Photoluminescence of Eu (III)/Lanthanides (III) on Terpyridine-Functionalized Ti Nanospikes

Metals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 977
Author(s):  
Min Hee Joo ◽  
So Jeong Park ◽  
Hye Ji Jang ◽  
Sung-Min Hong ◽  
Choong Kyun Rhee ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Cyclic Voltammetry ◽  
Photoelectron Spectroscopy ◽  
Oxidation States ◽  
Complex Structures ◽  
X Ray Diffraction ◽  
Decay Kinetics ◽  
X Ray ◽  
Scanning Electron

Terpyridine-functionalized Ti nanospike electrodes (TiNS-SiTpy) were developed and applied to cyclic voltammetry and amperometry of Ln (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Yb) ions and mixed Eu (III) + Ln (III) ions in a 0.1 M NaClO4 electrolyte. Electrodeposition was successfully performed over TiNS-SiTpy electrodes, which were fully examined by scanning electron microscopy, X-ray diffraction crystallography, Fourier-transform infrared spectroscopy, energy dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, photoluminescence (PL), and PL decay kinetics. The Gd and Tb ions were found to increase PL intensities with 10× longer lifetimes of 1.32 μs and 1.03 μs, respectively, compared with that of the electrodeposited Eu sample. The crystal phase and the oxidation states were fully examined for the mixed Ln (Eu + Gd and Eu + Tb) complex structures.

Hydrothermal Synthesis of Tetragonal Phase CuInS2 Nanoparticles

2012 ◽  
Vol 557-559 ◽  
pp. 489-492
Author(s):  
Zhi Xin Chen ◽  
Ya Zhen Ye ◽  
Han Jie Huang ◽  
Guang Can Xiao ◽  
Yun Hui He
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Photoelectron Spectroscopy ◽  
Tetragonal Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

The tetragonal phase CuInS2 nanoparticles were synthesized by the reaction of Cu(Ac)2, InCl3·4H2O and thioacetamide by hydrothermal method at 200 °C for 6 h in pH 1. The products were characterized by X-ray diffraction, energy-dispersive X-ray spectrum, X-ray photoelectron spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. Experimental results indicate that reaction temperature and the pH of solution are the important factors in the formation of CuInS2. The SEM and TEM results illuminated that the CuInS2 was composed of so many nanoparticles.

Stability and deactivation research of RuO2-PdO/Ti electrode in dye water degradation

2014 ◽  
Vol 70 (5) ◽  
pp. 757-762 ◽  
Author(s):  
Lin Du ◽  
Jin Wu ◽  
Guiying Li ◽  
Changwei Hu
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Coating Layer ◽  
Titanium Substrate ◽  
Catalytic Degradation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Water Degradation ◽  
Scanning Electron

RuO2-PdO/Ti electrode was prepared and used for the electro-catalytic degradation of Active Red K-2BP. It was found that the electrode was very stable in the process. A discoloration rate of 96.2% could still be achieved on the electrode after being used for 100 runs. X-ray photoelectron spectroscopy, X-ray diffraction, and scanning electron microscopy characterizations of the electrode were carried out. Results showed that the deactivation of the electrode was caused by the reconstruction and oxidation of titanium substrate as well as by the coverage of the active phases on the surface of the electrode by silicon. The cracks on the coating layer also contributed to the deactivation.

Bio-Inspired Mineralization from Aqueous Solutions of Zinc Nitrate Directed by Building Blocks of DNA

2007 ◽  
Vol 1008 ◽  
Author(s):  
Micha Jost ◽  
Peter Gerstel ◽  
Joachim Bill ◽  
Fritz Aldinger
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Building Blocks ◽  
Zinc Nitrate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dna And Rna ◽  
Scanning Electron

AbstractIn this paper, the suitability of DNA- and RNA-bases, nucleosides and nucleotides, and DNA itself as structure-directing agents for the mineralization of ZnO-based materials is discussed. Those bioorganic molecules are able to trigger the morphology of mineralization products ranging from smooth, homogenous thin films to sponge-like, sheet-like and fibrous products. Besides the investigation of morphological features by scanning electron microscopy, the structural characterization of these materials by X-ray diffraction, vibrational spectroscopy, photoluminescence spectroscopy and photoelectron spectroscopy is discussed.

XPS Research on SrTiO3-Based Voltage-Sensitive Material

2008 ◽  
Vol 368-372 ◽  
pp. 535-537
Author(s):  
Yu Xing Xu ◽  
Zi Long Tang ◽  
Zhong Tai Zhang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Xps Analysis ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Sensitive Material ◽  
X Ray ◽  
Average Grain Size ◽  
Scanning Electron

SrTiO3-based voltage-sensitive material was prepared successfully. The structure and properties were investigated using scanning electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. It was observed that the average grain size was greater than 3μm and a cubic perovskite structure was obtained. XPS analysis of oxygen indicated that there existed multiform chemical state oxygen at the surface of the grain. Further researches shown that there were a few [AO12] polyhedrons and many cation vacancies in the material discussed, which demonstrated that a lot of oxygen volatilized and a well-known semiconductivity level was achieved.

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