Fabrication of Mesoporous Cerium Dioxide Films by Cathodic Electrodeposition

2007 ◽  
Vol 7 (11) ◽  
pp. 4198-4201 ◽  
Author(s):  
Young-Soo Kim ◽  
Jin-Kyu Lee ◽  
Jae-Hoon Ahn ◽  
Eun-Kyung Park ◽  
Gil-Pyo Kim ◽  
...  

Mesoporous cerium dioxide (Ceria, CeO2) thin films have been successfully electrodeposited onto ITO-coated glass substrates from an aqueous solution of cerium nitrate using CTAB (Cetyltrimethylammonium Bromide) as a templatingagent. The synthesized films underwent detailed characterizations. The crystallinity of synthesized CeO2 film was confirmed by XRD analysis and HR-TEM analysis, and surface morphology was investigated by SEM analysis. The presence of mesoporosity in fabricated films was confirmed by TEM and small angle X-ray analysis. As-synthesized film was observed from XRD analysis and HR-TEM image to have well-crystallized structure of cubic phase CeO2. Transmission electron microscopy and small angle X-ray analysis revealed the presence of uniform mesoporosity with a well-ordered lamellar phase in the CeO2 films electrodeposited with CTAB templating.

2016 ◽  
Vol 23 (06) ◽  
pp. 1650057
Author(s):  
N. M. ABD-ALGHAFOUR ◽  
NASER M. AHMED ◽  
Z. HASSAN ◽  
D. ABUBAKAR ◽  
M. BOUOUDINA

This paper deals with the investigation of annealing effects on the structural, morphological and optical properties of V2O5 nanorods (NRs) grown on the glass substrates by using chemical spray pyrolysis technique. The as-prepared samples were annealed at [Formula: see text] for 40, 60 and 120 min in a quartz tube furnace. The high resolution X-ray diffraction (XRD) analysis revealed V2O5 NRs with preferred orientation along (001) plane. The crystallite size of the V2O5 NRs was increased by increasing the annealing duration. The morphological observations using field emission scanning electron microscope (FESEM) displayed NRs structures whose diameter and length were found to increase with increase of the annealing duration. The transmission electron microscopy (TEM) analysis confirmed the orthorhombic structures of the NRs. The AFM measurements indicated an increase of the average surface roughness by increasing the annealing time. The Raman spectroscopy revealed V–O–V phonon mode in the NRs annealed for 120 min. The optical bandgap was found in the range 2.6–2.58[Formula: see text]eV and observed to decrease with various duration annealed.


2021 ◽  
Author(s):  
Gamaralalage R. A. Kumara ◽  
Herath Mudiyanselage G. T. A. Pitawala ◽  
Buddika Karunarathne ◽  
Mantilaka Mudiyanselage M. G. P. G. Mantilaka ◽  
Rajapakse Mudiyanselage G. Rajapakse ◽  
...  

Abstract A novel and simple flotation technique has been developed to prepare high-purity graphite from impure graphite. In this method, a suspension of powdered graphite (PG) is dispersed and stirred in water without adding froth formers or supportive chemicals. This makes fine particles of graphite to move upwards and float on water. X-ray diffraction (XRD) analysis reveals that the floated graphite (FG) has a lower c-axis parameter, indicating the removal of interlayer impurities. A notable increase in the intensity ratio of the D band to G band in the Raman spectra indicates that the FG has more edge defects due to their smaller crystallite sizes. Transmission electron microscopic (TEM) analysis shows the number of layers in FG has been reduced to 16 from 68 in PG. The absence of C = O vibration of Fourier Transformed Infrared (FT-IR) spectroscopy in treated and untreated samples suggests that layers of them are not significantly oxidized. However, X-ray photoelectron spectroscopic (XPS) analysis shows the presence of C-O-C ether functionalities, possibly on edge planes. Further, the product has higher purity with increased carbon content. Therefore, the technique is useful in the value enhancement of graphite, the reduction of the chemical cost of the conventional techniques, environmental friendliness, and improvement of its applications.


2013 ◽  
Vol 873 ◽  
pp. 164-167
Author(s):  
Xiao Ming Fu

ZrO2 nanoparticles with a diameter range of less than 10 nm are successfully synthesized with zirconium nitrate as zirconium source and stronger ammonia water as precipitant at 210 °C for 48 h via the easy hydrothermal method. The phase, the morphologies and optical absorption properties of the samples have been characterized and analyzed by X-ray diffraction (XRD), field-emission transmission electron microscopy (TEM) and ultraviolet-visible absorption spectroscopy (UV-VIS), respectively. XRD analysis shows that the phase of as obtained samples is ZrO2. TEM analysis confirms that using stronger ammonia water as precipitant instead of NaOH and the increase of the reaction temperature are in favor of the synthesis of ZrO2 nanoparticles. And UV-VIS measurements show that ZrO2 nanoparticles have a good optical absorption property.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Gamaralalage R. A. Kumara ◽  
Herath Mudiyanselage G. T. A. Pitawala ◽  
Buddika Karunarathne ◽  
Mantilaka Mudiyanselage M. G. P. G. Mantilaka ◽  
Rajapakse Mudiyanselage G. Rajapakse ◽  
...  

AbstractA novel and simple flotation technique has been developed to prepare high-purity graphite from impure graphite. In this method, a suspension of pristine powdered graphite (PG) is dispersed and stirred in water without adding froth formers or supportive chemicals. This makes fine particles of graphite move upwards and float on water. X-ray diffraction (XRD) analysis reveals that the floated graphite (FG) has a lower c-axis parameter, indicating the removal of interlayer impurities. A notable increase in the intensity ratio of the D band to G band in the Raman spectra indicates that the FG has more edge defects due to their smaller crystallite sizes. Transmission electron microscopic (TEM) analysis shows the number of layers in FG has been reduced to 16 from 68 in PG. The absence of C=O vibration of Fourier Transformed Infrared (FT-IR) spectroscopy in treated and untreated samples suggests that their layers are not significantly oxidized. However, X-ray photoelectron spectroscopic (XPS) analysis shows the presence of C–O–C ether functionalities, possibly on edge planes. Further, the product has higher purity with increased carbon content. Therefore, the technique is helpful for the value enhancement of graphite, the reduction of the chemical cost of the conventional techniques, environmental friendliness, and improvement of its applications.


2013 ◽  
Vol 320 ◽  
pp. 11-14
Author(s):  
Xiao Ming Fu

M-ZrO2 nanoparticles with a diameter range of about 10 nm are successfully synthesized with zirconium nitrate as zirconium source and stronger ammonia water as precipitant at 210 °C for 48 h via the easy hydrothermal method. The phase, the morphologies and optical absorption properties of the samples have been characterized and analyzed by X-ray diffraction (XRD), field-emission transmission electron microscopy (TEM) and ultraviolet-visible absorption spectroscopy (UV-VIS), respectively. XRD analysis shows that the phase of as obtained samples is M-ZrO2. TEM analysis confirms that the increase of the reaction temperature is in favor of the synthesis of M-ZrO2 nanoparticles. And UV-VIS measurements show that M-ZrO2 nanoparticles have a good optical absorption property.


Biology ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 473
Author(s):  
Prabu Kumar Seetharaman ◽  
Rajkuberan Chandrasekaran ◽  
Rajiv Periakaruppan ◽  
Sathishkumar Gnanasekar ◽  
Sivaramakrishnan Sivaperumal ◽  
...  

To develop a benign nanomaterial from biogenic sources, we have attempted to formulate and fabricate silver nanoparticles synthesized from the culture filtrate of an endophytic fungus Penicillium oxalicum strain LA-1 (PoAgNPs). The synthesized PoAgNPs were exclusively characterized through UV–vis absorption spectroscopy, Fourier Transform Infra-Red spectroscopy (FT-IR), X-ray powder diffraction (XRD), and Transmission Electron Microscopy (TEM) with energy dispersive X-ray spectroscopy (EDX). The synthesized nanoparticles showed strong absorbance around 430 nm with surface plasmon resonance (SPR) and exhibited a face-centered cubic crystalline nature in XRD analysis. Proteins presented in the culture filtrate acted as reducing, capping, and stabilization agents to form PoAgNPs. TEM analysis revealed the generation of polydispersed spherical PoAgNPs with an average size of 52.26 nm. The PoAgNPs showed excellent antibacterial activity against bacterial pathogens. The PoAgNPs induced a dose-dependent cytotoxic activity against human adenocarcinoma breast cancer cell lines (MDA-MB-231), and apoptotic morphological changes were observed by dual staining. Additionally, PoAgNPs demonstrated better larvicidal activity against the larvae of Culex quinquefasciatus. Moreover, the hemolytic test indicated that the as-synthesized PoAgNPs are a safe and biocompatible nanomaterial with versatile bio-applications.


Soft Matter ◽  
2021 ◽  
Vol 17 (11) ◽  
pp. 3096-3104
Author(s):  
Valeria Castelletto ◽  
Jani Seitsonen ◽  
Janne Ruokolainen ◽  
Ian W. Hamley

A designed surfactant-like peptide is shown, using a combination of cryogenic-transmission electron microscopy and small-angle X-ray scattering, to have remarkable pH-dependent self-assembly properties.


2022 ◽  
Author(s):  
Sunita Kumari ◽  
Dhirendra Singhal ◽  
Rinku Walia ◽  
Ajay Rathee

Abstract The present project proposes to utilize rice husk and maize cob husk ash in the cement to mitigate the adverse impact of cement on environment and to enhance the disposal of waste in a sustainable manner. Ternary concrete / MR concrete was prepared by using rise husk and maize cob ash with cement. For the present project, five concrete mixes MR-0 (Control mix), MR-1 (Rice husk ash 10% and MR-2.5%), MR-2 (Rice husk ash 10% and MR-5%), MR-3 (Rice husk ash 10% and MR-2.5%), MR-4 (Rice husk ash 10% and MR-2.5%) were prepared. M35 concrete mix was designed as per IS 10262:2009 for low slump values 0-25mm. The purpose is to find the optimum replacement level of cement in M35 grade ternary concrete for I – Shaped paver blocks.In order to study the effects of these additions, micro-structural and structural properties test of concretes have been conducted. The crystalline properties of control mix and modified concrete are analyzed by Fourier Transform Infrared Spectroscope (FTIR), Scanning Electron Microscopy (SEM), and X-Ray Diffraction (XRD). The results indicated that 10% Rice husk ash and 5% maize cob ash replaced with cement produce a desirable quality of ternary concrete mix having good compressive strength. The results of SEM analysis indicated that the morphology of both concrete were different, showing porous structure at 7 days age and become unsymmetrical with the addition of ashes. After 28 day age, the control mix contained more quantity of ettringite and became denser than ternary concrete. XRD analysis revealed the presence of portlandite in large quantity in controlled mix concrete while MR concrete had the partially hydrated particle of alite.


MRS Advances ◽  
2016 ◽  
Vol 1 (6) ◽  
pp. 433-439 ◽  
Author(s):  
Asghar Ali ◽  
Patrick Morrow ◽  
Redhouane Henda ◽  
Ragnar Fagerberg

AbstractThis study reports on the preparation of cobalt doped zinc oxide (Co:ZnO) films via pulsed electron beam ablation (PEBA) from a single target containing 20 w% Co on sapphire (0001) and silicon (100) substrates. The films have been deposited at various temperatures (350оC, 400оC, 450оC) and pulse frequencies (2 Hz, 4 Hz), under a background argon (Ar) pressure of about 3 mtorr, and an accelerating voltage of 14 kV. The surface morphology has been examined by atomic force microscopy (AFM) and scanning electron microscopy (SEM). According to SEM analysis, the films consist of nano-globules whose size is in the range of 80-178 nm. Energy dispersive x-ray spectroscopy (EDX) reveals that deposition is congruent and the prepared films contain ∼20±5 w% cobalt. It has been found that the nano-globules in the deposited films are cobalt-rich zones containing ∼70 w% Co. From x-ray photoelectron spectroscopy (XPS) analysis, Co 2p3/2 peaks indicate that the deposited films contain CoO (binding energy = 780.5 eV) as well as metallic Co (binding energy = 778.1-778.5 eV). X-ray diffraction (XRD) analysis supports the presence of metallic Co hcp phase (2ϴ = 44.47° and 47.43°) in the films.


2021 ◽  
pp. 889-896
Author(s):  
Hanan J. Mustafa ◽  
Tagreed M. Al-Saadi

To study the removal of lead (Pb) ions from aqueous solutions, novel magnetite nanoparticles (NPs) of Ni0.31Mg0.15Ag0.04Fe2.5O4 were synthesized by coprecipitation synthesis using metal sulfates, and then coated with Gum Arabic (GA). The prepared NPs were analyzed using various spectroscopic and analytical methods, such as X-Ray diffraction analysis (XRD), Field Emission Scanning Electron Microscopy (FE-SEM), Energy Dispersive X-ray spectroscopy (EDX), Fourier Transform Infra-Red spectroscopy (FT-IR), and Atomic Absorption Spectrophotometer (AAS). By using XRD analysis, the cubic inverse spinel structure of the prepared NPs was proven, showing average values of crystallite size, lattice constant, and density of 28.57nm, 8.32582Å, and 5.2890 g/cm3, respectively. FE-SEM analysis revealed the sphere-like shape of the nanoparticles with a measured crystallite size of 25.93nm. The existence of constituent elements was evidenced by EDX. FT-IR test proved the success of the coating process of magnetite NPs by the presence of the main characteristic absorption bands of GA in the FT-IR spectrum of GA-magnetite NPs. The adsorption of Pb ions by GA- magnetite NPs was shown by AAS analysis, where the concentration of Pb ions decreased from 25ppm to 6.6ppm, reaching 1.1ppm at the time of 25min. The porosity of the NPs and the carboxyl groups in GA played an important role in the process.


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