scholarly journals Performance Enhancement of Modified 3D SWCNT/RVC Electrodes Using Microwave-Irradiated Graphene Oxide

2019 ◽  
Vol 14 (1) ◽  
Author(s):  
Ali Aldalbahi ◽  
Mostafizur Rahaman ◽  
Mohammed Almoiqli
Keyword(s):  
Graphene Oxide ◽  
Structural Changes ◽  
Performance Enhancement ◽  
Photoelectron Spectra ◽  
Composite Electrodes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Layers ◽  
Electrode Surfaces ◽  
Porous Architecture

Abstract The goal of this article is to increase the electrode performance of 3D CNT/RVC electrodes by improving the ease of ion adsorption to and ion desorption from the electrode surfaces. This achievement was done by preparing different composites of synthesized microwave-irradiated graphene oxide (mwGO) with CNT and coated on RVC. The morphology of GO was examined by field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD) study. Its surface property was checked by energy-dispersive X-ray spectra (EDX), and Fourier transform infrared spectra; whereas, for mwGO by XRD, Raman spectra, and X-ray photoelectron spectra (XPS), which revealed some structural changes of GO after irradiation, where CNTs, being sandwiched between graphene layers, built 3D highly porous architecture inside the electrodes. The electrochemical test of composite electrodes showed increased electrodes conductivity and afforded rapid ions diffusion. It is observed that the 9-CNT/mwGO/RVC composite electrode performed as the best electrode, which showed 29% increment in specific capacitance value compared to the normal CNT/RVC electrode. This best electrode also showed very high cyclic stability in its cyclic voltammetry test that maintained 97% current stability after 2000 cycles, indicating that the electrode can be an effective material for water purification technology. Graphical Abstract

Graphene Oxide/Fe3O4 Composites Prepared via In Situ Precipitation

2014 ◽  
Vol 904 ◽  
pp. 150-154
Author(s):  
Zhe Wei Yang ◽  
Xin Fan ◽  
Li Ang Guo ◽  
Wei Ting Wei
Keyword(s):  
Graphene Oxide ◽  
Specific Capacitance ◽  
Precipitation Method ◽  
Electrochemical Performances ◽  
Composite Electrodes ◽  
X Ray Diffraction ◽  
Bonding Force ◽  
X Ray

The graphene oxide/Fe3O4 composites were prepared by in situ precipitation method in this article. The microstructure and surface morphology of composites were characterized by Fourier transform infrared spectrum, X-ray diffraction and scanning electron microscopy, respectively. Cyclic voltammetry was employed for the determination of specific capacitance and other electrochemical performances. It was shown that there was the chemical bonding force between GO and Fe3O4 particles. And the surfaces of GO were wrapped by the Fe3O4 particles precipitated on the surfaces of GO sheets and no impurities were detected. Furthermore, the specific capacitance of GO/Fe3O4 composite electrodes decreased as Fe3O4 particles reduced and the redox peaks became weaker owing to the addition of nonconductive Fe3O4 particles.

The Preparation and Characterization of Fluorinated Graphene Oxide with Different Degrees of Oxidation

2018 ◽  
Vol 792 ◽  
pp. 89-97
Author(s):  
Xiao Feng Zhao ◽  
Zi Li Yu ◽  
Cong Li Fu ◽  
Xiu Li Wang
Keyword(s):  
Graphene Oxide ◽  
Photoelectron Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Structure And Property ◽  
Graphene Derivatives ◽  
Ft Ir ◽  
Fluorinated Graphene ◽  
Fluorinated Graphene Oxide

For many excellent graphene derivatives, tailoring the material properties is crucial to get a broader application. In the present work, a series of fluorinated graphene oxide (FGO) with various oxidation degree were synthesized using a modified Hummers method at different reaction temperatures. The structure and property of FGO were analyzed by X-ray diffraction (XRD), Fourier transform infra-red spectra (FT-IR), X-ray photoelectron spectra (XPS) and Zeta potential analysis. The results indicate that the oxygen contents range from 5.61 % to 21.96 % in FGO can be tuned by altering the reaction temperatures. The oxygen in FGO is presented mainly in the form of epoxide and carboxyl groups. With increasing reaction temperature from 50 °C to 90 °C, the oxygen content in FGO decreases and thicker multilayered FGO is formed with lower dispersibility.

scholarly journals ELECTROCHEMICAL DISPERSION OF GRAPHITE IN 58% NITRIC ACID TO PRODUCE MULTILAYER GRAPHENE OXIDE

2021 ◽  
Vol 64 (3) ◽  
pp. 59-65
Author(s):  
Elena V. Yakovleva ◽  
Andrey V. Yakovlev ◽  
Ivan N. Frolov ◽  
Anton S. Mostovoy ◽  
Vitaly N. Tseluikin
Keyword(s):  
Graphene Oxide ◽  
Graphite Powder ◽  
Multilayer Graphene ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Layers ◽  
Intercalated Compounds ◽  
Fold Reduction ◽  
Electrochemical Dispersion ◽  
Oxidized Graphite

Electrochemical oxidation of graphite powder in 58% HNO3 was studied. Samples of oxidized graphite were obtained with a imparting of the amount of electricity 500, 700, 1500 mAh g-1. The character of the galvanostatic dependencies allows to select a region of the formation of intercalated compounds of graphite prior to the accumulation of quantity of electricity of 500 mA h g-1. It was found that when the quantity of electricity of over 700 mA h g-1 the process of electrochemical peroxidation of intercalated graphite begins with the formation of multilayer graphene oxide, as confirmed by comprehensive studies using X-ray diffraction, scanning electron microscopy, FTIR spectroscopy, laser diffraction. The synthesized multilayer graphene oxide is characterized by the presence of a spectrum of oxygen-containing functional groups, mainly hydroxyl, as well as carboxyl, epoxy and alkoxyl. X-ray images show a peak at 2θ = 11.45° which intensity increases for re-oxidized graphite compounds and also indicate the formation of a multilayer graphene oxide with an interlayer distance of 7.8 Å. The synthesized material in aqueous suspensions under the action of ultrasound is dispersed with a 7-11-fold reduction in particle size. Graphene layers remains layered structure but the degree of their deformation increases, and the thickness of the layers decreases with an increase in the imparted amount of electricity. 

X-Ray Diffraction Evaluation of the Average Number of Layers in Thermal Reduced Graphene Powder for Supercapacitor Nanomaterial

2019 ◽  
Vol 958 ◽  
pp. 117-122 ◽  
Author(s):  
Quezia de Aguiar Cardoso ◽  
Julio César Serafim Casini ◽  
Luzinete Pereira Barbosa ◽  
Marilene Morelli Serna ◽  
Eguiberto Galego ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Thermal Treatment ◽  
Low Cost ◽  
Reduction Process ◽  
Thermal Reduction ◽  
Processing Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Layers ◽  
Number Of Layers

Graphene oxide (GO) can be partially reduced to graphene-like sheets by removing the oxygen-containing groups and recovering the conjugated structure. In this work, the thermal reduction of GO powder has been carried out using back pumping vacuum pressures and investigated employing X-ray diffraction analysis. The experimental results of estimating the number of graphene layers on the reduced powder at various temperatures (200 – 1000 °C) have been reported. Electrical changes have been produced in a graphene oxide with the vacuum reduction process. This study has shown that the ideal processing temperature for reducing graphene oxide nanomaterial was about 400 °C. It has also been shown that at 600 °C the number of layers in the reduced nanomaterial increased. The internal series equivalent resistance (ESR) has been improved substantially with the vacuum thermal treatment even at temperatures above 400 °C. ESR was reduced from 95.0 to about 13.8 Ω cm2 with this processing. These results showed that the process can be applied to the reduction of graphene oxide to produce supercapacitor nanomaterials. The advantage of employing this method is that the processing is a straightforward and low cost thermal treatment that might be used for large amount of nanocomposite material.

scholarly journals Impact of high temperatures on aluminoceladonite studied by Mössbauer, Raman, X-ray diffraction and X-ray photoelectron spectroscopy

2021 ◽  
Author(s):  
Mariola Kądziołka-Gaweł ◽  
Maria Czaja ◽  
Mateusz Dulski ◽  
Tomasz Krzykawski ◽  
Magdalena Szubka
Keyword(s):  
Photoelectron Spectroscopy ◽  
Integral Intensity ◽  
Photoelectron Spectra ◽  
X Ray Diffraction ◽  
Structural Reorganization ◽  
Oh Groups ◽  
X Ray ◽  
Al Content ◽  
Integral Intensity Ratio ◽  
Higher Temperature

AbstractMössbauer, Raman, X-ray diffraction and X-ray photoelectron spectroscopies were used to examine the effects of temperature on the structure of two aluminoceladonite samples. The process of oxidation of Fe2+ to Fe3+ ions started at about 350 °C for the sample richer in Al and at 300 °C for the sample somewhat lower Al-content. Mössbauer results show that this process may be associated with dehydroxylation or even initiate it. The first stage of dehydroxylation takes place at a temperature > 350 °C when the adjacent OH groups are replaced with a single residual oxygen atom. Up to ~500 °C, Fe ions do not migrate from cis-octahedra to trans-octahedra sites, but the coordination number of polyhedra changes from six to five. This temperature can be treated as the second stage of dehydroxylation. The temperature dependence on the integral intensity ratio between bands centered at ~590 and 705 cm−1 (I590/I705) clearly reflects the temperature at which six-coordinated polyhedra are transformed into five-coordinated polyhedra. X-ray photoelectron spectra obtained in the region of the Si2p, Al2p, Fe2p, K2p and O1s core levels, highlighted a route to identify the position of Si, Al, K and Fe cations in a structure of layered silicates with temperature. All the measurements show that the sample with a higher aluminum content and a lower iron content in octahedral sites starts to undergo a structural reorganization at a relatively higher temperature than the less aluminum-rich sample does. This suggests that iron may perform an important role in the initiation of the dehydroxylation of aluminoceladonites.

scholarly journals High temperature structural study of decagonal Al-Cu-Rh quasicrystal.

2014 ◽  
Vol 70 (a1) ◽  
pp. C94-C94
Author(s):  
Pawel Kuczera ◽  
Walter Steurer
Keyword(s):  
Structural Changes ◽  
Configurational Entropy ◽  
Lattice Vibrations ◽  
X Ray Diffraction ◽  
Stabilization Mechanism ◽  
X Ray ◽  
Comparative Structure ◽  
The Stability

The structure of d(ecagonal)-Al-Cu-Rh has been studied as a function of temperature by in-situ single-crystal X-ray diffraction in order to contribute to the discussion on energy or entropy stabilization of quasicrystals (QC) [1]. The experiments were performed at 293 K, 1223 K, 1153 K, 1083 K, and 1013 K. A common subset of 1460 unique reflections was used for the comparative structure refinements at each temperature. The results obtained for the HT structure refinements of d-Al-Cu-Rh QC seem to contradict a pure phasonic-entropy-based stabilization mechanism [2] for this QC. The trends observed for the ln func(I(T1 )/I(T2 )) vs.|k⊥ |^2 plots indicate that the best on-average quasiperiodic order exists between 1083 K and 1153 K, however, what that actually means is unclear. It could indicate towards a small phasonic contribution to entropy, but such contribution is not seen in the structure refinements. A rough estimation of the hypothetic phason instability temperature shows that it would be kinetically inaccessible and thus the phase transition to a 12 Å low T structure (at ~800 K) is most likely not phason-driven. Except for the obvious increase in the amplitude of the thermal motion, no other significant structural changes, in particular no sources of additional phason-related configurational entropy, were found. All structures are refined to very similar R-values, which proves that the quality of the refinement at each temperature is the same. This suggests, that concerning the stability factors, some QCs could be similar to other HT complex intermetallic phases. The experimental results clearly show that at least the ~4 Å structure of d-Al-Cu-Rh is a HT phase therefore entropy plays an important role in its stabilisation mechanism lowering the free energy. However, the main source of this entropy is probably not related to phason flips, but rather to lattice vibrations, occupational disorder unrelated to phason flips like split positions along the periodic axis.

Investigations of Actinide Metals and Compounds under Pressure Provide Important Insights into Bonding and Chemistry

2003 ◽  
Vol 802 ◽  
Author(s):  
R. G. Haire ◽  
S. Heathman ◽  
T. Le Bihan ◽  
A. Lindbaum ◽  
M. Iridi
Keyword(s):  
Structural Changes ◽  
Chemical Properties ◽  
X Ray Diffraction ◽  
Interatomic Distances ◽  
X Ray ◽  
Effect Of Pressure ◽  
Electronic Configurations ◽  
5F Electrons ◽  
Actinide Series ◽  
Alloys And Compounds

ABSTRACTOne effect of pressure on elements and compounds is to decease their interatomic distances, which can bring about dramatic perturbations in their electronic nature and bonding, which can be reflected in changes in physical and/or chemical properties. One important issue in the actinide series of elements is the effect of pressure on the 5f-electrons. We have probed changes in electronic behavior with pressure by monitoring structure by X-ray diffraction, and have studied several actinide metals and compounds from thorium through einsteinium. These studies have employed angle dispersive diffraction using synchrotron radiation, and energy dispersive techniques via conventional X-ray sources. The 5f-electrons of actinide metals and their alloys are often affected significantly by pressure, while with compounds, the structural changes are often not linked to the involvement of 5 f-electron. We shall present some of our more recent findings from studies of selected actinide metals, alloys and compounds under pressure. A discussion of the results in terms of the changes in electronic configurations and bonding with regard to the element's position in the series is also addressed.

scholarly journals Attached β-cyclodextrin/γ-(2,3-epoxypropoxy) propyl trimethoxysilane to graphene oxide and its application in copper removal

2017 ◽  
Vol 75 (10) ◽  
pp. 2403-2411 ◽  
Author(s):  
Zongxue Yu ◽  
Qi Chen ◽  
Liang Lv ◽  
Yang Pan ◽  
Guangyong Zeng ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
High Surface ◽  
High Surface Area ◽  
Esterification Reaction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cavity Structure ◽  
Optimum Ph ◽  
Exchange Adsorption ◽  
Langmuir Isotherm Model

The environmental applications of graphene oxide and β-cyclodextrin (β-CD) have attracted great attention since their first discovery. Novel nanocomposites were successfully prepared by using an esterification reaction between β-cyclodextrin/γ-(2,3-epoxypropoxy) propyl trimethoxysilane grafted graphene oxide (β-CD/GPTMS/GO). The β-CD/GPTMS/GO nanocomposites were used to remove the Cu2+ from aqueous solutions. The characteristics of β-CD/GPTMS/GO were detected by scanning electron microscopy (SEM), Fourier transform infrared, X-ray diffraction (XRD), thermogravimetric analysis (TG) and energy dispersive X-ray (EDX). The dispersibility of graphene oxide was excellent due to the addition of β-CD. The adsorption isotherms data obtained at the optimum pH 7 were fitted by Langmuir isotherm model. The excellent adsorption properties of β-CD/GPTMS/GO for Cu2+ ions could be attributed to the apolar cavity structure of β-CD, the high surface area and abundant functional groups on the surface of GO. The adsorption patterns of β-CD/GPTMS/GO were electrostatic attraction, formation of host-guest inclusion complexes and the ion exchange adsorption. The efficient adsorption of β-CD/GPTMS/GO for Cu2+ ions suggested that these novel nanocomposites may be ideal candidates for removing other cation pollutants from waste water.

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