scholarly journals Pentacyanoammineferrate-Based Non-Enzymatic Electrochemical Biosensing Platform for Selective Uric Acid Measurement

Sensors ◽  
2021 ◽  
Vol 21 (5) ◽  
pp. 1574
Author(s):  
Won-Yong Jeon ◽  
Chang-Jun Lee ◽  
Tun Naw Sut ◽  
Hyug-Han Kim ◽  
Young-Bong Choi
Keyword(s):  
Uric Acid ◽  
Indium Tin Oxide ◽  
High Selectivity ◽  
Electrochemical Impedance ◽  
Nickel Ions ◽  
Electrochemical Biosensing ◽  
Sensing Platforms ◽  
Amine Groups ◽  
Eis Measurements ◽  
And Function

The electrochemical-based detection of uric acid (UA) is widely used for diagnostic purposes. However, various interfering species such as ascorbic acid, dopamine, and glucose can affect electrochemical signals, and hence there is an outstanding need to develop improved sensing platforms to detect UA with high selectivity. Herein, we report a pentagonal mediator-based non-enzymatic electrochemical biosensing platform to selectively measure UA in the presence of interfering species. The working electrode was fabricated by electrodepositing polymerized 1-vinylimidazole (PVI), which has an imidazole ligand, onto indium tin oxide (ITO), and then conjugating nickel ions to the PVI-coated ITO electrode. Electrode performance was characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements and integrated together with pentacyanoammineferrate, which can bind to the amine groups of UA and function as an electron transferring mediator. The experimental results showed a wide linear range of UA concentration-dependent responses and the multi-potential step (MPS) technique facilitated selective detection of UA in the presence of physiologically relevant interfering species. Altogether, these findings support that pentacyanoammineferrate-based non-enzymatic electrodes are suitable biosensing platforms for the selective measurement of UA, and such approaches could potentially be extended to other bioanalytes as well.

Electrochemical Performance Optimization of Li2NixFe1−xSiO4 Cathode Materials for Lithium-Ion Batteries

2017 ◽  
Vol 14 (2) ◽  
Author(s):  
Atef Y. Shenouda ◽  
M. M. S. Sanad
Keyword(s):  
Performance Optimization ◽  
Electrochemical Impedance ◽  
Coulombic Efficiency ◽  
Sol Gel ◽  
Lithium Ion ◽  
Electrochemical Impedance Spectra ◽  
Cell Parameters ◽  
Sol Gel Process ◽  
Eis Measurements ◽  
And Function

Li2NixFe1−xSiO4 (x = 0, 0.2, 0.4, 0.6, 0.8, and 1) samples were prepared by sol–gel process. The crystal structure of prepared samples of Li2NixFe1−xSiO4 was characterized by XRD. The different crystallographic parameters such as crystallite size and lattice cell parameters have been calculated. Scanning electron microscope (SEM) and Fourier transform infrared spectroscopy (FTIR) investigations were carried out explaining the morphology and function groups of the synthesized samples. Furthermore, electrochemical impedance spectra (EIS) measurements are applied. The obtained results indicated that the highest conductivity is achieved for Li2Ni0.4Fe0.6SiO4 electrode compound. It was observed that Li/Li2Ni0.4Fe0.6SiO4 battery has initial discharge capacity of 164 mAh g−1 at 0.1 C rate. The cycle life performance of all Li2NixFe1−xSiO4 batteries was ranged between 100 and 156 mAh g−1 with coulombic efficiency range between 70.9% and 93.9%.

scholarly journals Influence of Monomer Concentration on the Morphologies and Electrochemical Properties of PEDOT, PANI, and PPy Prepared from Aqueous Solution

2016 ◽  
Vol 2016 ◽  
pp. 1-12 ◽  
Author(s):  
Shalini Kulandaivalu ◽  
Zulkarnain Zainal ◽  
Yusran Sulaiman
Keyword(s):  
Electron Microscopy ◽  
Electrochemical Properties ◽  
Tin Oxide ◽  
Indium Tin Oxide ◽  
Electrochemical Impedance ◽  
Monomer Concentration ◽  
Lithium Perchlorate ◽  
Sem Images ◽  
Eis Measurements ◽  
Scanning Electron

Poly(3,4-ethylenedioxyhiophene) (PEDOT), polyaniline (PANI), and polypyrrole (PPy) were prepared on indium tin oxide (ITO) substrate via potentiostatic from aqueous solutions containing monomer and lithium perchlorate. The concentration of monomers was varied between 1 and 10 mM. The effects of monomer concentration on the polymers formation were investigated and compared by using Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, scanning electron microscopy (SEM), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) measurements. FTIR and Raman spectra showed no changes in the peaks upon the increment of the concentration. Based on the SEM images, the increment in monomer concentration gives significant effect on morphologies and eventually affects the electrochemical properties. PEDOT electrodeposited from 10 mM solution showed excellent electrochemical properties with the highest specific capacitance value of 12.8 mF/cm2.

scholarly journals Oxidation Behavior of an Austenitic Steel (Fe, Cr and Ni), the 310 H, in a Deaerated Supercritical Water Static System

Metals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 571
Author(s):  
Aurelia Elena Tudose ◽  
Ioana Demetrescu ◽  
Florentina Golgovici ◽  
Manuela Fulger
Keyword(s):  
Stainless Steel ◽  
Supercritical Water ◽  
Nuclear Reactor ◽  
Electrochemical Impedance ◽  
Electrochemical Methods ◽  
Metallographic Analysis ◽  
Gravimetric Analysis ◽  
Static System ◽  
Eis Measurements ◽  
Supercritical Temperature

The aim of this work was to study the corrosion behavior of a Fe-Cr-Ni alloy (310 H stainless steel) in water at a supercritical temperature of 550 °C and a pressure of 250 atm for up to 2160 h. At supercritical temperature, water is a highly aggressive environment, and the corrosion of structural materials used in a supercritical water-cooled nuclear reactor (SCWR) is a critical problem. Selecting proper candidate materials is one key issue for the development of SCWRs. After exposure to deaerated supercritical water, the oxides formed on the 310 H SS surface were characterized using a gravimetric analysis, a metallographic analysis, and electrochemical methods. Gravimetric analysis showed that, due to oxidation, all the tested samples gained weight, and oxidation of 310H stainless steel at 550 °C follows parabolic rate, indicating that it is driven by a diffusion process. The data obtained by microscopic metallography concord with those obtained by gravimetric analysis and show that the oxides layer has a growing tendency in time. At the same time, the results obtained by electrochemical impedance spectroscopy (EIS) measurements indicate the best corrosion resistance of Cr, and (Fe, Mn) Cr2O4 oxides developed on the samples surface after 2160 h of oxidation. Based on the results obtained, a strong correlation between gravimetric analysis, metallographic analysis, and electrochemical methods was found.

scholarly journals Experimental, DFT and MD Assessments of Bark Extract of Tamarix aphylla as Corrosion Inhibitor for Carbon Steel Used in Desalination Plants

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3679
Author(s):  
Ismat H. Ali
Keyword(s):  
Corrosion Inhibitor ◽  
Potentiodynamic Polarization ◽  
Inhibition Efficiency ◽  
Electrochemical Impedance ◽  
Effect Of Temperature ◽  
Bark Extract ◽  
Plant Sample ◽  
Gravimetric Analysis ◽  
Sample Collection ◽  
Eis Measurements

This study aimed to examine the extract of barks of Tamarix aphylla as a corrosion inhibitor. The methodology briefly includes plant sample collection, extraction of the corrosion inhibitor, gravimetric analysis, plotting potentiodynamic polarization plots, electrochemical impedance spectroscopic measurements, optimization of conditions, and preparation of the inhibitor products. The results show that the values of inhibition efficiency (IE%) increased as the concentrations of the inhibitor increased, with a maximum achievable inhibition efficiency of 85.0%. Potentiodynamic polarization (PP) tests revealed that the extract acts as a dual-type inhibitor. The results obtained from electrochemical impedance spectroscopy (EIS) measurements indicate an increase in polarisation resistance, confirming the inhibitive capacity of the tested inhibitor. The adsorption of the inhibitor on the steel surface follows the Langmuir adsorption isotherm model and involves competitive physio-sorption and chemisorption mechanisms. The EIS technique was utilized to investigate the effect of temperature on corrosion inhibition within the 298–328 K temperature range. Results confirm that the inhibition efficiency (IE%) of the inhibitor decreased slightly as the temperature increased. Lastly, the thermodynamic parameters for the inhibitor were calculated.

scholarly journals Organosilane-functionalization of nanostructured indium tin oxide films

2016 ◽  
Vol 6 (6) ◽  
pp. 20160056 ◽  
Author(s):  
R. Pruna ◽  
F. Palacio ◽  
M. Martínez ◽  
O. Blázquez ◽  
S. Hernández ◽  
...  
Keyword(s):  
Surface Area ◽  
Indium Tin Oxide ◽  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Annealing Treatment ◽  
Electrochemical Analysis ◽  
Cyclic Voltammograms ◽  
X Ray ◽  
Chip Technology ◽  
Significant Difference

Fabrication and organosilane-functionalization and characterization of nanostructured ITO electrodes are reported. Nanostructured ITO electrodes were obtained by electron beam evaporation, and a subsequent annealing treatment was selectively performed to modify their crystalline state. An increase in geometrical surface area in comparison with thin-film electrodes area was observed by atomic force microscopy, implying higher electroactive surface area for nanostructured ITO electrodes and thus higher detection levels. To investigate the increase in detectability, chemical organosilane-functionalization of nanostructured ITO electrodes was performed. The formation of 3-glycidoxypropyltrimethoxysilane (GOPTS) layers was detected by X-ray photoelectron spectroscopy. As an indirect method to confirm the presence of organosilane molecules on the ITO substrates, cyclic voltammetry and electrochemical impedance spectroscopy (EIS) were also carried out. Cyclic voltammograms of functionalized ITO electrodes presented lower reduction-oxidation peak currents compared with non-functionalized ITO electrodes. These results demonstrate the presence of the epoxysilane coating on the ITO surface. EIS showed that organosilane-functionalized electrodes present higher polarization resistance, acting as an electronic barrier for the electron transfer between the conductive solution and the ITO electrode. The results of these electrochemical measurements, together with the significant difference in the X-ray spectra between bare ITO and organosilane-functionalized ITO substrates, may point to a new exploitable oxide-based nanostructured material for biosensing applications. As a first step towards sensing, rapid functionalization of such substrates and their application to electrochemical analysis is tested in this work. Interestingly, oxide-based materials are highly integrable with the silicon chip technology, which would permit the easy adaptation of such sensors into lab-on-a-chip configurations, providing benefits such as reduced size and weight to facilitate on-chip integration, and leading to low-cost mass production of microanalysis systems.

scholarly journals Electrochemical Impedance of Hydrogenated Phases of ZnO and CuO Nanoparticles for Electrode Applications

2020 ◽  
pp. 1-6
Author(s):  
L. I. Menegbo ◽  
J. L. Konne ◽  
N. Boisa
Keyword(s):  
Electrochemical Impedance ◽  
Sol Gel ◽  
Low Frequency ◽  
High Gain ◽  
High Frequency Region ◽  
Nyquist Plots ◽  
Eis Measurements ◽  
Xrd Patterns ◽  
Straight Lines ◽  
First Time

The Electrochemical Impedance Spectroscopy (EIS) measurements of Sol-gel synthesized ZnO, CuO and their respective hydrogenated phases (ZnO:H and CuO:H) for  a proton-type battery model has been reported for the first time. The XRD patterns confirmed that CuO and ZnO were phase pure with minor impurities. However, that of CuO:H showed mixed phases of CuO and Cu2O with the later  appearing prominent. The estimated particle sizes of ZnO, ZnO:H, CuO and CuO:H obtained using Scherrers’ equation were 17.83, 17.75, 21.63 and 15.42 nm respectively, showing remarkable particle size reductions upon hydrogenation as oxygen vacancies were substituted with smaller hydrogen ions. Nyquist plots from the EIS experimental data recorded over a frequency range of 100 kHz – 5 mHz showed expected flat semicircles at the high frequency region and straight lines at the low frequency regions while resistance estimations from the intercepts of the Bode plots were 12.10, 7.80, 16.00 and 10.80 Ω for ZnO, ZnO:H, CuO and CuO:H respectively. It also indicated high gain margins suggesting impressive electrochemical properties for battery applications.

scholarly journals Electrochemical properties of Fe2O3/AB based composite electrodes in alkaline solution

2019 ◽  
Vol 35 (3) ◽  
Author(s):  
Trinh Tuan Anh ◽  
Bui Thi Hang
Keyword(s):  
Iron Oxide ◽  
Alkaline Solution ◽  
Electrochemical Impedance ◽  
Passive Layer ◽  
Composite Electrodes ◽  
Iron Oxide Particles ◽  
Electrochemical Behaviors ◽  
Suitable Material ◽  
Oxide Electrodes ◽  
Eis Measurements

To find a suitable material for Fe-air battery anode, Fe2O3 nanoparticles (nm) and microparticles (µm) were used as active materials and Acetylene Black carbon (AB) as additive to prepare Fe2O3/AB composites. The effect of grain size of iron oxide particles and additives on the electrochemical behavior of Fe2O3/AB composite electrodes in alkaline solution have been investigated using cyclic voltammetry (CV), galvanostatic cycling and electrochemical impedance spectroscopy (EIS) measurements. Iron oxide nanoparticles provided better cyclability than iron oxide microparticles. Impedance of electrode increased during cycling but the nm-Fe2O3/AB electrode gave smaller resistance than µm-Fe2O3/AB one. The additives showed strongly effects on the electrochemical behaviors of iron oxide electrodes. The AB additive enhanced the electric conductivity of Fe2O3/AB electrode and thus increased the redox reaction rate of iron oxide while K2S interacted and broke down the passive layer leading to improved cyclability and giving higher capacity for Fe2O3/AB electrodes.

scholarly journals Synthesis, Characterization and Corrosion Protective Efficiency of 2[2-Oxo-phenyl hydrazinyl ethyl] benzamide on Mild Steel in Sulphuric Acid Medium

2010 ◽  
Vol 7 (2) ◽  
pp. 331-340
Author(s):  
Rinki Goel ◽  
Weqar A. Siddiqi ◽  
V. M. Chaubey ◽  
Bahar Ahmed
Keyword(s):  
Mild Steel ◽  
Acid Medium ◽  
Electrochemical Impedance ◽  
Protective Efficiency ◽  
Inhibitor Molecule ◽  
Protection Efficiency ◽  
Langmuir Isotherm Model ◽  
Eis Measurements ◽  
Increasing Temperature ◽  
Good Agreement

2[2-Oxo-phenyl hydrazinyl ether] benzamide (2BA) was synthesized, characterized and tested effective for corrosion inhibition of mild steel in 1 N H2SO4solution using galvanodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques. Polarization resistances calculated from the EIS measurements are in good agreement with those obtained from alternating current (AC) polarization measurements. The mild steel samples were also analyzed by Scanning Electron Microscopy (SEM). The result showed that 2BA is an excellent inhibitor for mild steel in acid medium. The inhibition was assumed to occurviaadsorption of the inhibitor molecule on the metal surface. In the 303-323K temperature range, the 2BA adsorption follows Langmuir isotherm model. The protection efficiency increases with increasing the inhibitor concentration in the range of 250-1000 ppm but slightly decreases with increasing temperature.

Size-Dependent Effect of Cu2O Nanocubes in Electrochemical and Photocatalytic Properties

2018 ◽  
Vol 18 (12) ◽  
pp. 8282-8288 ◽  
Author(s):  
Yuanyuan Tang ◽  
Yinlong Xu ◽  
Caiyu Qi ◽  
Xianyang Li ◽  
Enming Xing ◽  
...  
Keyword(s):  
Methyl Orange ◽  
Visible Light ◽  
Electrochemical Impedance ◽  
Linear Sweep Voltammetry ◽  
Absorption Capacity ◽  
Electrochemical Impedance Spectra ◽  
Size Dependent ◽  
Eis Measurements ◽  
20 Nm ◽  
Degradation Of Methyl Orange

Cu2O nanocubes with different size (ranging from 20 nm to 400 nm) were prepared by a seed-mediated method to systematically explore the strong size-dependent properties in photocatalytic degradation of methyl orange (MO). Cu2O nanotubes were characterized by TEM, XRD, UV-Vis measurements. The size-dependent photocatalytic efficiency of the Cu2O nanocubes was evaluated by degradation of methyl orange (MO) in water under visible light (λ > 420 nm) irradiation. Furthermore, the photocurrent, linear sweep voltammetry (LSV) and electrochemical impedance spectra (EIS) measurements were applied to elucidate the size-dependent properties of Cu2O nanocubes, which demonstrated that smaller Cu2O nanocubes with certain length (30 nm) showed higher current density, faster electron transfer and lower rate of charge recombination in their exposed (100) facet. Therefore, 30 nm Cu2O nanocubes showed stronger visible light absorption capacity and higher photocatalytic activity in MO degradation among a series of nanocubes (20, 30, 100, 130, 200 and 400 nm) and their corresponding photocatalytic activities decreased with increasing the particles sizes.

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