Electroplating of ZnO Influenced by the Concentration of Aluminum Nitrate in the Bath

2016 ◽  
Vol 863 ◽  
pp. 102-107
Author(s):  
Jing Chie Lin ◽  
Amrita Choudhury ◽  
Yao Tien Tsneg ◽  
Kun Cheng Peng
Keyword(s):  
Photoelectron Spectroscopy ◽  
Dye Sensitized Solar Cells ◽  
Reference Electrode ◽  
Average Diameter ◽  
Aluminum Nitrate ◽  
Maximum Efficiency ◽  
Chemical Compositions ◽  
Axis Orientation ◽  
X Ray ◽  
Ito Glass

Electrochemical deposition of Al-doped ZnO (AZO) on the ITO glass was investigated in baths containing various concentrations of aluminum nitrate. The electrochemical and chemical reactions can be deduced by means of investigating cathodic polarization curves and time/electroplating-current curves for further characterizing structures of ZnO and AZO, and establishing growth mechanism. High-quality AZO nanorods, depositing on ITO substrate that coated with ZnO seed-layer, were utilized the electrochemical method at-1.0 V (against a reference electrode of Ag/AgCl in 3.0M KCl) in the bath of 90 °C. After annealing at 350 °C, ZnO and AZO nanorods were analyzed by field-emission scanning electron microscope (FESEM) to explore the morphology of nanostructure. The SEM image displayed that the lower Al3+ concentrations (20 ~ 60 μM) in the bath, the average diameter of nanorods decreased; while the Al3+ concentrations excessed over 60 μM, the morphology of the AZO nanorods turned into partial-area nanosheets instead of the nanorods spread. The crystal structure of the AZO nanorods were identified by using grazing-incident X-ray diffraction (GIXRD). The patterns of the Al3+ ions in the range of 20 ~ 60 μM in the bath showed that the preferred orientations were along with the [002] direction which confirmed the result of AZO nanorods well aligned in c-axis orientation, and the characterized peak (002) slightly shifted to the right suggested that Al atoms had doped into the ZnO lattice. We also adopted the X-ray photoelectron spectroscopy to characterize the elemental and chemical compositions of the AZO nanorods. XPS spectrums confirmed that the Al atoms successfully doped. Finally, for identifying the optimal boundary condition of Al content in ZnO, the nanorods with various Al concentrations were utilized via dye-sensitized solar cells (DSSC) experiment with the standard solar Simulators (AM1.5G) and J-V Measurement. We found that the AZO nanorods as the photoanode contained 2.84 at.% Al (60 μM aluminum nitrate in the bath) which performed the highest fill-factor (0.53) and the maximum efficiency (0.41%).

scholarly journals Structure and Characterization of TiC/GLC Multilayered Films with Various Bilayers Periods

Coatings ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 787
Author(s):  
Weiqi Wang ◽  
Xiaoming Ling ◽  
Rui Wang ◽  
Wenhao Nie ◽  
Li Ji ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Chemical Compositions ◽  
Closed Field ◽  
Multilayered Structures ◽  
Multilayered Films ◽  
Sputtering Deposition ◽  
X Ray ◽  
Mechanical And Tribological Properties ◽  
Self Organizing

The spontaneously self-organizing multilayered graphite-like carbon (denoted as GLC) /TiC films with various bilayer periods in the range of 13.3–17.5 nm were deposited on silicon and 1Cr18Mn8Ni5N stainless steel substrates using closed field magnetron sputtering deposition facility. The microstructures and chemical compositions of the prepared multilayered films were characterized by scanning electron microscopy, high resolution transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy respectively. The self-organizing multilayered structures in all of the films consisted of titanium carbide layers and sp2-rich carbon layers periodically alternate arrangement. The TiC contents and bilayer periods of the multilayered films can be controlled by means of adjusting of sputtering current of graphite target. Furthermore, the mechanical and tribological performances of the prepared films were appraised by nano-indentor, scratch measures, and ball-on-plate tribometer respectively. The results indicated that multilayer structure endowed the as-deposited TiC/GLC films outstanding mechanical and tribological properties, especially the multilayer film with 15.9 nm bilayer period deposited at 10 A sputtering current showed the excellent adhesion strength and hardness; Simultaneously it also exhibited the lowest average friction coefficient in the humid environment owing to its high content of sp2 hybrid carbon.

X-Ray Photoelectron Spectroscopy Study on Reduction of Graphene Oxide with Hydrazine Hydrate

2011 ◽  
Vol 287-290 ◽  
pp. 539-543 ◽  
Author(s):  
Wen Shi Ma ◽  
Jun Wen Zhou ◽  
Xiao Dan Lin
Keyword(s):  
Graphene Oxide ◽  
Hydrazine Hydrate ◽  
Photoelectron Spectroscopy ◽  
Reduction Rate ◽  
Reduction Reaction ◽  
Chemical Compositions ◽  
Total Oxygen ◽  
Graphene Oxides ◽  
X Ray ◽  
Oxygen Groups

Graphene oxide was prepared through Hummers' method，then different reduced graphenes were prepared via reduction of graphene oxide with hydrazine hydrate for 1h、12h and 24h. X-ray photoelectron spectroscopy (XPS) was used for the characterization of graphene oxide and the reduced graphenes. The variation of the contents of carbon in carbon and oxygen functional groups and chemical compositions of graphene oxides were investigated through analysis the content of different carbon atoms in different reduced graphenes. The results showed that the reduction reaction was very fast in the first 1 h, the content of total oxygen bonded carbon atoms decreased from 83.6% to 22.1%, and then after the reduction rate became very slow. After 12h, the content of total oxygen bonded carbon atom is 19.56%, only 2.54% lower than that of 1h’s. At the same time, C-N was introduced in the graphene oxides; this increased the stereo-hindrance for hydrazine hydrate attacking the C-Oxygen groups, thus reduced the reduction rate. After reduction for 24h, there still exists 16.4% oxygen bonded carbon atoms and the total conversion ratio of graphene approaches 70%.

Characterization of Al65.0Cu32.9Co2.1 Alloy Containing Nanofibres

2012 ◽  
Vol 186 ◽  
pp. 212-215
Author(s):  
Jacek Krawczyk ◽  
Włodzimierz Bogdanowicz ◽  
Grzegorz Dercz ◽  
Wojciech Gurdziel
Keyword(s):  
Electron Microscopy ◽  
Average Diameter ◽  
Chemical Compositions ◽  
X Ray ◽  
Transmission Electron ◽  
Orthogonal Set ◽  
T Phase ◽  
Terminal Area ◽  
Scanning Electron

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.

scholarly journals Ultrasound enhanced heterogeneous activation of peroxymonosulfate by a Co-NiOx catalyst

2017 ◽  
Vol 76 (6) ◽  
pp. 1436-1446 ◽  
Author(s):  
Chenmo Wei ◽  
Jing Zhang ◽  
Yongli Zhang ◽  
Gucheng Zhang ◽  
Peng Zhou ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Maximum Efficiency ◽  
Acid Orange 7 ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Hydroxyl ◽  
Transmission Electron ◽  
Initial Ph ◽  
Reactive Oxidant

Sulfate radical-based advanced oxidation processes have had considerable attention due to the highly oxidizing function of sulfate radicals (SO4−·) resulting in acceleration of organic pollutants degradation in aqueous environments. A Co-Ni mixed oxide nanocatalyst, which was prepared by the sol-gel method, was employed to activate peroxymonosulfate (PMS, HSO5−) to produce SO4−· with Acid Orange 7 (AO7) selected as a radical probe. The catalyst was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). The characterization results indicated that the ingredient of the catalyst had been changed and the amount of surface hydroxyl increased significantly with the addition of Ni. Therefore, it proved that Co-NiOx catalyst was more effective than CoOx to activate PMS. Moreover, ultrasound (US) can increase the degradation rate of AO7 and US/Co-NiOx/PMS system. This study also focused on some synthesis parameters and the system reached the maximum efficiency under the condition when [PMS] = 0.4 mM, [catalyst] = 0.28 g/L, Pus = 200 W. The AO7 removal in these systems follows first order kinetics. Last but not least, quenching studies was conducted which indicated that the amount of hydroxyl radicals (·OH) increases with the increase of initial pH and SO4−· was the primary reactive oxidant for AO7 degradation.

Preparation of PCL/PVP/Ag Nanofiber Membranes by Electrospinning Method

2012 ◽  
Vol 268-270 ◽  
pp. 580-583 ◽  
Author(s):  
Yong Tang Jia ◽  
Cui Wu ◽  
Feng Chun Dong ◽  
Gang Huang ◽  
Xian Hua Zeng
Keyword(s):  
Silver Nanoparticles ◽  
Photoelectron Spectroscopy ◽  
Composite Nanofibers ◽  
Average Diameter ◽  
Vinyl Pyrrolidone ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electrospinning Method ◽  
Nanofiber Membranes ◽  
Poly Vinyl Pyrrolidone

The composite nanofiber membranes of poly (ε-caprolactone)/poly(vinyl pyrrolidone) (PCL/PVP) containing silver nanoparticles were prepared by electrospinning method. The morphology of composite nanofibers was characterized by scanning electron microscopy (SEM). The silver nanoparticles on the electrospun fibers were characterized by X-Ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The contact angle and water uptake of PCL/PVP/Ag nanofiber membranes were measured. The SEM photos indicated that the average diameter of the fibers was significantly decreased with the addition of silver nanoparticles. The X-Ray images showed that Ag nanoparticles were distributed on the surface of nanofiber membranes. When the PVP mole ratio was higher than 15%, the nanofiber membranes showed good hydrophilic property. The PCL/PVP/Ag nanofiber membranes could be applied to prepare wound dressing.

scholarly journals X-Ray Photoelectron Spectroscopy Study of Silane Coupling Agents/Basalt Fiber Interface

2011 ◽  
Vol 236-238 ◽  
pp. 1467-1471 ◽  
Author(s):  
Ya Lan Liu ◽  
Shi Jie Shen ◽  
Li Zhang ◽  
Ling Min Shao
Keyword(s):  
Coupling Agent ◽  
Photoelectron Spectroscopy ◽  
Silane Coupling Agent ◽  
Basalt Fiber ◽  
Fiber Surface ◽  
Chemical Compositions ◽  
Hydroxyl Groups ◽  
Silane Coupling Agents ◽  
X Ray ◽  
Silane Coupling

In this paper, two types of fiber surface treatment methods, namely heat treatment and chemical coupling, were used to improve the basalt fiber surface properties. The basalt fiber surface was heated under 250Celsius degree for 30minites, and then was treated by silane coupling agent ethanol solution with different concentrations. X-ray photoelectron spectroscopy (XPS) was utilized to study the surface chemical compositions of basalt fiber after treatments. The XPS analysis indicated that chemical bonds between basalt fiber and KH-550 have occurred, and silanols were adsorbed to the surface of basalt fibers by an ether linkage between the silanols and the hydroxyl groups of the fibers. When the concentration of KH-550 is 0.8wt%, the optimal bonding condition is formed between basalt fiber and silane coupling agent.

Development of a high-precision XYZ translator and estimation of beam profile of the vacuum ultraviolet and soft X-ray undulator beamline BL-13B at the Photon Factory

2020 ◽  
Vol 27 (4) ◽  
pp. 923-933
Author(s):  
Yoshihiro Aiura ◽  
Kenichi Ozawa ◽  
Kazuhiko Mase ◽  
Makoto Minohara ◽  
Satoshi Suzuki
Keyword(s):  
High Precision ◽  
Photoelectron Spectroscopy ◽  
Vacuum Ultraviolet ◽  
Chemical Compositions ◽  
X Ray ◽  
Measurement Capability ◽  
Photon Factory ◽  
Experimental Apparatus ◽  
Elemental Analyses ◽  
Microscopic Measurement

A high-precision XYZ translator was developed for the microanalysis of electronic structures and chemical compositions on material surfaces by electron spectroscopy techniques, such as photoelectron spectroscopy and absorption spectroscopy, utilizing the vacuum ultraviolet and soft X-ray synchrotron radiation at an undulator beamline BL-13B at the Photon Factory. Using the high-precision translator, the profile and size of the undulator beam were estimated. They were found to strongly depend on the photon energy but were less affected by the polarization direction. To demonstrate the microscopic measurement capability of an experimental apparatus incorporating a high-precision XYZ translator, the homogeneities of an SnO film and a naturally grown anatase TiO2 single crystal were investigated using X-ray absorption and photoemission spectroscopies. The upgraded system can be used for elemental analyses and electronic structure studies at a spatial resolution in the order of the beam size.

Properties Study of Mixed Silane Films on the Surface of Steel

2014 ◽  
Vol 971-973 ◽  
pp. 135-138
Author(s):  
Zhen Dong Sun ◽  
Yan Ning Yang ◽  
Qing Peng Li ◽  
Jian Guo Liu ◽  
Chuan Wei Yan
Keyword(s):  
Photoelectron Spectroscopy ◽  
Salt Spray ◽  
Adhesive Property ◽  
Epoxy Coating ◽  
Chemical Compositions ◽  
Neutral Salt ◽  
X Ray ◽  
Steel Sheets ◽  
Silane Solution ◽  
Scanning Electron

The mixed silane films were obtained on the surface of the Q235 steel sheets by directly immersing in a mixed silane solution containing γ-Glycidoxypropyltriethoxysilane (γ-GPS) and 1, 2-bis (triethoxysilyl) ethane (BTSE), The chemical compositions and microstructures of the films were examined by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Fourier Transform infrared spectroscopy (FTIR).The corrosion resistances were investigated by electrochemical measurements and neutral salt spray (NSS) test. The effects of silane films to the epoxy coating were investigated through the adhesive property test. The results showed that the γ-GPS/BTSE mixed silane film could remarkably improve the corrosion resistance of epoxy coating and prolong its service life.

CHARACTERIZATION OF ALUMINUM SURFACES AFTER DIFFERENT PRETREATMENTS AND EXPOSURE TO SILANE COUPLING AGENTS

2001 ◽  
Vol 08 (01n02) ◽  
pp. 43-50 ◽  
Author(s):  
M. KONO ◽  
X. SUN ◽  
R. LI ◽  
K. C. WONG ◽  
K. A. R. MITCHELL ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Coupling Agents ◽  
Chemical Compositions ◽  
Silane Coupling Agents ◽  
Oh Groups ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Aluminum Surfaces

X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and scanning electron microscopy (SEM) have been used to characterize surfaces of aluminum which have been pretreated by mechanical polishing, acid etching and alkaline etching, as well as given subsequent exposures to air and water. These surfaces can differ markedly with regard to their chemical compositions and topographical structures. Characterizations of these surfaces after exposures to three organosilanes, γ-GPS, BTSE and γ-APS, indicate that the amount of silane adsorbed in each case shows a tendency to increase both with the number of OH groups detected at the oxidized aluminum and with the surface roughness. The XPS data are consistent with the adhesion of γ-APS occurring through H bonding, especially via NH3+ groups.

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