Comparative study on the supercapacitive properties of PANI nanofibers, nanotubes, and nanospheres

2019 ◽  
Vol 32 (5) ◽  
pp. 600-608 ◽  
Author(s):  
Shanxin Xiong ◽  
Yong Zhang ◽  
Yuyun Wang ◽  
Bohua Wu ◽  
Jia Chu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Interfacial Polymerization ◽  
Electrochemical Impedance ◽  
Rate Capability ◽  
Electrochemical Performances ◽  
Synthesis Methods ◽  
Chemical Structures ◽  
Transmission Electron ◽  
Current Densities ◽  
Adsorption Desorption

In this study, polyaniline (PANI) nanostructures with different morphologies (nanofibers, nanotubes, and nanospheres) were obtained via interfacial polymerization, rapid mixing reaction, and hydrothermal method. The influences of the synthesis methods on the morphologies and supercapacitive properties of PANI nanostructures were investigated. The chemical structures of materials were characterized by Fourier-transform infrared and Raman spectroscopies. Scanning electron microscopy and transmission electron microscopy images were used to explore the morphologies of PANI nanostructures. N2 adsorption–desorption isotherm, cyclic voltammetry, charge–discharge test, and electrochemical impedance spectroscopy were used to characterize the pore distribution, electrochemical, and supercapacitive properties of PANI nanostructures. The results show that PANI nanotubes (PANI-T) exhibit the best electrochemical performances among three kinds of PANI nanostructures. The PANI-T exhibits high specific capacitances of 648 and 290 F g−1 at current densities of 0.5 and 10 A g−1, respectively, indicating its good supercapacitive property and rate capability. The enhanced electrochemical and supercapacitive performances can be attributed to its hollow nanotube structure.

scholarly journals Impact of incorporation of chromium on electrochemical properties of LiFePO4/C for Li-ion batteries

2015 ◽  
Vol 33 (4) ◽  
pp. 742-750 ◽  
Author(s):  
Amol Naik ◽  
Jian Zhou ◽  
Chao Gao ◽  
Guizhen Liu ◽  
Lin Wang
Keyword(s):  
Electron Microscopy ◽  
Electrochemical Properties ◽  
Electrochemical Impedance ◽  
Single Mode ◽  
X Ray Diffraction ◽  
Raman Spectroscopic ◽  
Transmission Electron ◽  
Specific Discharge ◽  
One Step ◽  
Current Densities

AbstractLiFe0.95Cr0.05PO4/C was successfully synthesized by one-step solid-state reaction using a single mode microwave reactor. The effect of incorporation of chromium on LiFePO4 lattice parameters was systematically investigated by X-ray diffraction. Surface analysis was done by scanning electron microscopy and transmission electron microscopy. The ratio of amorphous to graphitic carbon was determined from Raman spectroscopic data. The influence of chromium incorporation on electrochemical properties was studied by recording charge/discharge cycles combined with electrochemical impedance spectroscopy (EIS) and cyclic voltammetry. It was found that Cr incorporation significantly enhanced the electrochemical performance of LiFePO4 at all current densities up to 10 C. LiFe0.95Cr0.05PO4/C prepared exhibited the best performance with an initial specific discharge capacity of 157.7, 144.8, 138.3, 131.0, 124.1 and 111.1 mAh·g−1 at 0.1 C, 0.5 C, 1.0 C, 2.0 C, 5 C and 10 C, respectively. The doped sample displayed excellent capacity retention, which was substantially superior than that of pristine LiFePO4/C at a higher current rate.

scholarly journals ELECTROCHEMICAL PERFORMANCES AND CORROSION INHIBITION OF AA6061 IN TROPICAL SEAWATER

2017 ◽  
Vol 25 (2) ◽  
pp. 251-259
Author(s):  
R. Rosliza ◽  
H.B. Senin ◽  
W.B. Wan Nik
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Electrochemical Impedance ◽  
Corrosion Current ◽  
Electrochemical Performances ◽  
Double Layer Capacitance ◽  
Sem Images ◽  
Corrosion Rates ◽  
Current Densities ◽  
Scanning Electron

The corrosion performances of AA6061 aluminum alloy in tropical seawater was investigated using potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) and their morphology was characterized by the scanning electron microscopy (SEM). The results showed that the presence of sodium benzoate as an inhibitor significantly decrease the corrosion current densities (i corr ), corrosion rates and double layer capacitance (C dl ), whilst increasing the polarization resistance (R p ). The scanning electron microscopy (SEM) images indicated that the mechanism of charge transfer and the formation of thin film have been taken place on the specimens. 

scholarly journals Electro-Oxidation of Ammonia at Novel Ag2O−PrO2/γ-Al2O3 Catalysts

Coatings ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 257
Author(s):  
Mariam Khan ◽  
Naveed Kausar Janjua ◽  
Safia Khan ◽  
Ibrahim Qazi ◽  
Shafaqat Ali ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Electrochemical Impedance ◽  
Precipitation Method ◽  
Impregnation Method ◽  
X Rays ◽  
Kinetic And Thermodynamic Parameters ◽  
Catalytic Support ◽  
Transmission Electron ◽  
Electro Oxidation ◽  
Oxidation Of Ammonia

An Ag2O(x)−PrO2(y)/γ-Al2O3 electrocatalyst series (X:Y is for Ag:Pr from 0 to 10) was synthesized, to use synthesized samples in electrochemical applications, a step in fuel cells advancements. Ag2O(x)−PrO2(y)/γ-Al2O3/Glassy-Carbon was investigated for electrochemical oxidation of ammonia in alkaline medium and proved to be highly effective, having high potential utility, as compared to commonly used Pt-based electrocatalysts. In this study, gamma alumina as catalytic support was synthesized via precipitation method, and stoichiometric wt/wt.% compositions of Ag2O−PrO2 were loaded on γ-Al2O3 by co-impregnation method. The desired phase of γ-Al2O3 and supported nanocatalysts was obtained after heat treatment at 800 and 600 °C, respectively. The successful loadings of Ag2O−PrO2 nanocatalysts on surface of γ-Al2O3 was determined by X-rays diffraction (XRD), Fourier-transform Infrared Spectroscopy (FTIR), and energy dispersive analysis (EDX). The nano-sized domain of the sample powders sustained with particle sizes was calculated via XRD and scanning electron microscopy (SEM). The surface morphology and elemental compositions were examined by SEM, transmission electron microscopy (TEM) and EDX. The conductive and electron-transferring nature was investigated by cyclic voltammetry and electrochemical impedance (EIS). Cyclic voltammetric profiles were observed, and respective kinetic and thermodynamic parameters were calculated, which showed that these synthesized materials are potential catalysts for ammonia electro-oxidation. Ag2O(6)−PrO2(4)/γ-Al2O3 proved to be the most proficient catalyst among all the members of the series, having greater diffusion coefficient, heterogeneous rate constant and lesser Gibbs free energy for this system. The catalytic activity of these electrocatalysts is revealed from electrochemical studies which reflected their potentiality as electrode material in direct ammonia fuel cell technology for energy production.

Preparation of α-Ni(OH)2 with Flowerlike Hierarchical Architectures via Homogeneous Precipitation Method

2011 ◽  
Vol 284-286 ◽  
pp. 684-687
Author(s):  
Chang Yu Li ◽  
Li Li Liu ◽  
Shou Xin Liu
Keyword(s):  
Electron Microscopy ◽  
Precipitation Method ◽  
Homogeneous Precipitation ◽  
X Ray ◽  
Homogeneous Precipitation Method ◽  
Α Phase ◽  
Transmission Electron ◽  
Hierarchical Architectures ◽  
Flowerlike Structure ◽  
Adsorption Desorption

Without using any templates or surfactants, flowerlike α-nickel hydroxide (Ni(OH)2) was successfully synthesized by homogeneous precipitation method. The prepared products were characterized by X-ray powder diffraction (XRD), high-resolution transmission electron microscopy (HRTEM) and N2 adsorption-desorption. The prepared Ni(OH)2 is α-phase with specific surface area of 245.0 m2/g and shows flowerlike structure with 4-6 um in diameter.

scholarly journals Solvothermal Synthesis of Mn3O4Nanoparticle/Graphene Sheet Composites and Their Supercapacitive Properties

2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Y. F. Liu ◽  
G. H. Yuan ◽  
Z. H. Jiang ◽  
Z. P. Yao
Keyword(s):  
Electron Microscopy ◽  
Graphene Sheet ◽  
Low Cost ◽  
High Specific Capacitance ◽  
Ethanol Solution ◽  
Diffraction Field ◽  
Electrochemical Performances ◽  
One Pot ◽  
Long Term Stability ◽  
Transmission Electron

Mn3O4nanoparticle/graphene sheet (GM) composites were synthesized via a one-pot and low-cost solvothermal process in an ethanol solution. The as-prepared materials were characterized by X-ray diffraction, field emission scanning electron microscopy, and transmission electron microscopy. Results showed that the nanosized Mn3O4particles had tetragonal hausmannite structure and were successfully loaded on the graphene sheets. Moreover, the electrochemical performances of GM composites produced by different mass percents of Mn2+/graphite oxide (GO) were evaluated by means of cyclic voltammetry and galvanostatic charge-discharge studies. The composite prepared with Mn2+/GO mass percent of 10 : 90 showed a high specific capacitance of 245 F/g at 5 mV/s in the 6 M KOH solution and better long-term stability along with 81% of its initial capacitance after 1200 cycles at 0.5 A/g.

Few-Layered MoS2 Nanostructures for Highly Efficient Visible Light Photocatalysis

NANO ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. 1650114 ◽  
Author(s):  
Dan Li ◽  
Jianwei Li ◽  
Caiqin Han ◽  
Xinsheng Zhao ◽  
Haipeng Chu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Electrochemical Impedance ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
Electrochemical Impedance Spectra ◽  
X Ray ◽  
Transmission Electron ◽  
Electron Hole Pair

Few-layered MoS2 nanostructures were successfully synthesized by a simple hydrothermal method without the addition of any catalysts or surfactants. Their morphology, structure and photocatalytic activity were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, electrochemical impedance spectra and UV-Vis absorption spectroscopy, respectively. These results show that the MoS2 nanostructures synthesized at 180[Formula: see text]C exhibit an optimal visible light photocatalytic activity (99%) in the degradation of Rhodamine B owing to the relatively easier adsorption of pollutants, higher visible light absorption and lower electron–hole pair recombination.

Preparation of yolk–shell structured Ag@Cu particles and their application in high performance electrochemical sensing of p-aminobenzoic acid

2019 ◽  
Vol 97 (2) ◽  
pp. 140-146
Author(s):  
Tian Gan ◽  
Zhikai Wang ◽  
Mengru Chen ◽  
Wanqiu Fu ◽  
Haibo Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
High Performance ◽  
Electrochemical Impedance ◽  
High Sensitivity ◽  
Differential Pulse ◽  
Electrochemical Sensing ◽  
High Catalytic Activity ◽  
Aminobenzoic Acid ◽  
Transmission Electron

In this work, the Ag@Cu particles with yolk–shell nanostructure was prepared by facile solvothermal method, which was modified on glassy carbon electrode (GCE) to fabricate electrochemical sensor for the convenient and fast determination of p-aminobenzoic acid (PABA). The surface morphology and electrochemical properties of the as-prepared Ag@Cu nanocomposite modified electrode were characterized by scanning electron microscopy, transmission electron microscopy, chronocoulometry, and electrochemical impedance spectroscopy. Further, the electrochemical sensing of PABA was performed on the Ag@Cu/GCE using cyclic voltammetry and differential pulse voltammetry techniques, showing high catalytic activity. Under the optimal conditions, the sensor exhibited a wide linear range, high sensitivity, and low detection limit of 0.315 μmol/L for PABA. The developed sensor was also successfully applied for PABA detection in anesthetic and cosmetics with satisfactory results.

Study of Corrosion Behavior of Conventional and Nanostructured WC-Co HVOF Sprayed Coats

2010 ◽  
Vol 64 ◽  
pp. 13-18 ◽  
Author(s):  
Shahin Khameneh Asl ◽  
Mohammad Reza Saghi Beyragh ◽  
Mahdi Ghassemi Kakroudi
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Corrosion Resistance ◽  
Electrochemical Impedance ◽  
Heat Treating ◽  
Crystalline Phases ◽  
Chemical Test ◽  
Transmission Electron ◽  
Hvof Spray ◽  
Wear And Corrosion Resistance

Interest in nanomaterials has increased in recent years. This is due to the potential of size reduction to nanometric scale to provide properties of materials such as hardness, toughness, wear, and corrosion resistance. The current study is focused on WC-Co cermet coats, materials that are extensively used in applications requiring wear resistance. In this work, WC-17Co powder was thermally sprayed onto mild steel using High Velocity Oxy Fuel (HVOF) spray technique. The nanostructured specimen was produced from sprayed sample by heat-treating at 1100°C in a vacuum chamber. Their structures were studied by using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Polarization and electrochemical impedance spectroscopy (EIS) tests were performed on the both types of coated samples in 3.5% NaCl solution. The amorphous phase in WC-17Co coating was transformed to crystalline phases by heat treatment at high temperatures. The heat treatment of these coatings at high temperature also resulted in partially dissolution of WC particles and formation of new crystalline phases. Generation of these phases produced the nanostructured coating with better mechanical properties. Comparative electro chemical test results showed that, the heat treatment could improve corrosion resistance of the nanostructured WC-17Co coat than the as sprayed coats.

Synthesis of Nanosized HMS Mesoporous Molecular Sieve in an Ionic Liquid-Water Mixture

2011 ◽  
Vol 236-238 ◽  
pp. 2110-2113
Author(s):  
Hong Liu ◽  
Meng Yang Wang ◽  
Wei Ran Cao
Keyword(s):  
Electron Microscopy ◽  
Ionic Liquid ◽  
Sol Gel ◽  
Mesoporous Molecular Sieve ◽  
Nano Particles ◽  
Water Mixture ◽  
X Ray ◽  
Transmission Electron ◽  
Adsorption Desorption ◽  
Synthesized Materials

The hexagonal mesoporous silica (HMS) nano-particles were prepared in mixture of 1-butyl-3-methyl-imidazolium tetrafluoroborate (BMIM+BF4-) ionic liquid and water by a sol-gel method. The structure and morphology of obtained materials were characterized by X-ray powder diffraction (XRD), N2adsorption-desorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and dynamic light scattering (DLS). The influence of the amount of BMIM+BF4-was investigated. It was shown that the synthesized materials have discrete and uniform spherical morphology with the size in the range of 68-177 nm (obtained from DLS measurements), and the particle size of HMS can be controlled by varying the amount of BMIM+BF4-.

scholarly journals Characterization and Electrochemical Behavior of Graphene-Based Anode for Li-Ion Batteries

2011 ◽  
Vol 5 (1) ◽  
pp. 236-241 ◽  
Author(s):  
Wei-Ren Liu ◽  
Shin-Liang Kuo ◽  
Chia-Yi Lin ◽  
Yi-Chen Chiu ◽  
Ching-Yi Su ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Graphene Nanosheets ◽  
Rate Capability ◽  
Reversible Capacity ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Li Ion ◽  
Synthetic Graphite ◽  
Lower Impedance ◽  
Enhanced Electrochemical Performance

In this study, we investigate the characteristics and electrochemical properties of graphene nanosheets derived from chemical-thermal exfoliation processes of SFG44 synthetic graphite (SFG44-GNS). The characterizations and electrochemical measurements were carried out by means of X-ray diffraction, scanning electron microscopy, transmission electron microscopy, cyclic voltammetry, BET, Raman, rate capability as well as cycling tests and AC impedance. The as-synthesized SFG44-GNS with larger d-spacing of 0.3407 nm exhibits reversible capacity of 626 mAh/g and good rate capability of ~ 300 mAh/g at 2C rate, which are superior to those of graphite anode. The enhanced electrochemical performance of GNS anode was resulted from larger d-spacing, lower impedance in the interface and enhanced pore volume. The results indicate that graphene-based material is a good candidate for HEV/EV application.

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