WorldWideScience

Sample records for voltammetry electrochemical impedance

  1. Electrochemical characterization of gelatinized starch dispersions: voltammetry and electrochemical impedance spectroscopy on platinum surface.

    Science.gov (United States)

    Hernandez-Jaimes, C; Lobato-Calleros, C; Sosa, E; Bello-Pérez, L A; Vernon-Carter, E J; Alvarez-Ramirez, J

    2015-06-25

    The electrochemical properties of gelatinized starch dispersions (GSD; 5% w/w) from different botanical sources were studied using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) tests over a platinum surface. The phenomenological modelling of EIS data using equivalent circuits indicated that after gelatinization the electrical resistance was determined mainly by the resistance of insoluble material (i.e., ghosts). Sonication of the GSD disrupted the ghost microstructure, and produced an increase in electrical conductivity by reducing the resistance of the insoluble material. The CV data showed three oxidation peaks at potentials where glucose solutions displayed oxidation waves. It is postulated that hydrolysis at the bulk and electrocatalyzed oxidation on the Pt-surface are reactions involved in the starch transformation. Starches peak intensity increased with the amylose content, suggesting that the amylose-rich matrix played an important role in the charge transfer in the electrolytic system. Copyright © 2015 Elsevier Ltd. All rights reserved.

  2. Electrochemical impedance spectroscopy and cyclic voltammetry studies of a proton exchange membrane fuel cell operated at low humidity conditions

    Energy Technology Data Exchange (ETDEWEB)

    Malevich, D. [Fuel Cell Research Centre, Kingston, ON (Canada)

    2007-07-01

    This study investigated water balance issue in polymer electrolyte membrane fuel cells (PEMFCs) using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry. Equivalent PEMFC circuits and microporous layers (MPL) were investigated. Bode and Nyquist plots were presented, and the effect of current density on EIS was explored. Membrane resistance, Warburg resistance, and electron transfer resistance was measured. The study also examined hydrogen underpotential deposition on platinum. Cyclic voltammetry was used to develop curves for electrochemically active surfaces and charge transfer resistance of the MPL. Polarization curves for the anode and cathode MPLs were presented along with impedance diagrams for the PEMFC operating at low humidity conditions. tabs., figs.

  3. Poly(glutamic acid) nanofibre modified glassy carbon electrode: Characterization by atomic force microscopy, voltammetry and electrochemical impedance

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Daniela Pereira; Zanoni, Maria Valnice Boldrin; Bergamini, Marcio Fernando [Departamento de Quimica Analitica, Instituto de Quimica, Universidade Estadual Paulista, Caixa Postal 355, 14800-900 Araraquara, S.P. (Brazil); Chiorcea-Paquim, Ana-Maria; Diculescu, Victor Constantin [Departamento de Quimica, Faculdade de Ciencias e Tecnologia, Universidade de Coimbra, 3004-535 Coimbra (Portugal); Oliveira Brett, Ana-Maria [Departamento de Quimica, Faculdade de Ciencias e Tecnologia, Universidade de Coimbra, 3004-535 Coimbra (Portugal)], E-mail: brett@ci.uc.pt

    2008-04-20

    Glassy carbon electrodes (GCE) were modified with poly(glutamic acid) acid films prepared using three different procedures: glutamic acid monomer electropolymerization (MONO), evaporation of poly(glutamic acid) (PAG) and evaporation of a mixture of poly(glutamic acid)/glutaraldehyde (PAG/GLU). All three films showed good adherence to the electrode surface. The performance of the modified GCE was investigated by cyclic voltammetry and differential pulse voltammetry, and the films were characterized by atomic force microscopy (AFM) and electrochemical impedance spectroscopy (EIS). The three poly(glutamic acid) modified GCEs were tested using the electrochemical oxidation of ascorbic acid and a decrease of the overpotential and the improvement of the oxidation peak current was observed. The PAG modified electrode surfaces gave the best results. AFM morphological images showed a polymeric network film formed by well-defined nanofibres that may undergo extensive swelling in solution, allowing an easier electron transfer and higher oxidation peaks.

  4. VOLTAMMETRY AND ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY OF MEMBRANE SYSTEMS UNDER STABILIZED DIFFUSION LAYER THICKNESS

    Directory of Open Access Journals (Sweden)

    Sharafan M. V.

    2015-11-01

    Full Text Available The current-voltage characteristics and the number of effective ion transfer, as well as the frequency spectrum of the electrochemical impedance of multilayer ion-exchange membranes in a stable and controllable thickness of the diffusion layer were measured, using the of rotating membrane disk complex. The article presents a comparative analysis of the frequency spectra of the electrochemical impedance of the source and a surface-modified monopolar anion exchange membranes in 0.01 M sodium chloride was made. The process of water molecules dissociation at current densities above the limiting one in 0.01 M sodium chloride solution was studied in detail

  5. Probing the electrochemical properties of TiO{sub 2}/graphene composite by cyclic voltammetry and impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Yadav, Pankaj [Department of Physics, Marwadi Education Foundation, Rajkot 360003 (India); Pandey, Kavita; Bhatt, Parth [School of Solar Energy, Pandit Deendayal Petroleum University, Gandhinagar 382007 (India); Tripathi, Brijesh, E-mail: brijesh.tripathi@sse.pdpu.ac.in [School of Technology, Pandit Deendayal Petroleum University, Gandhinagar 382007 (India); Pandey, Manoj Kumar; Kumar, Manoj [School of Technology, Pandit Deendayal Petroleum University, Gandhinagar 382007 (India)

    2016-04-15

    Highlights: • Role of TiO{sub 2}/graphene composite in charge transport within supercapacitors. • DC and AC characterization to investigate voltage dependence of charge transport. • Physical insight into the electrochemistry of electrode–electrolyte interface. - Abstract: This work describes the role of graphene in charge transport and diffusion mechanism at TiO{sub 2}/graphene electrode–electrolyte interface. To explore the mechanism, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used. The CV results depict that TiO{sub 2} and TiO{sub 2}/graphene electrodes behave differently in terms of charge transport and ion adsorption under the steady state conditions. The performance of TiO{sub 2} electrode–electrolyte interface is mainly limited by the charge transport and pseudo-capacitive effects while the response of TiO{sub 2}/graphene electrode–electrolyte interface is mainly dominated by the double layer capacitive effects. The EIS measurement leads to the direct determination of broad range of parameters, i.e. series resistance, charge transport, rate capability and ion diffusion. The experimental results and their analysis will have a significant impact on understanding the role of graphene in the electrochemical response of an electrode–electrolyte interface.

  6. Archaeometric analysis of Roman bronze coins from the Magna Mater temple using solid-state voltammetry and electrochemical impedance spectroscopy.

    Science.gov (United States)

    Di Turo, Francesca; Montoya, Noemí; Piquero-Cilla, Joan; De Vito, Caterina; Coletti, Fulvio; Favero, Gabriele; Doménech-Carbó, Antonio

    2017-02-22

    Voltammetry of microparticles (VMP) and electrochemical impedance spectroscopy (EIS) techniques, complemented by SEM-EDX and Raman spectroscopy, were applied to a set of 15 Roman bronze coins and one Tessera from the temple of Magna Mater (Rome, Italy). The archaeological site, dated back between the second half and the end of the 4th century A.D., presented a complicated stratigraphic context. Characteristic voltammetric patterns for cuprite and tenorite for sub-microsamples of the corrosion layers of the coins deposited onto graphite electrodes in contact with 0.10 M HClO4 aqueous solution yielded a grouping of the coins into three main groups. This grouping was confirmed and refined using EIS experiments of the coins immersed in air-saturated mineral water using the reduction of dissolved oxygen as a redox probe. The electrochemical grouping of coins corroborated the complex stratigraphy of the archaeological site and, above all, the reuse of the coins during the later periods due to the economic issues related to the fall of the Roman Empire.

  7. Electrochemical impedance spectroscopy versus cyclic voltammetry for the electroanalytical sensing of capsaicin utilising screen printed carbon nanotube electrodes.

    Science.gov (United States)

    Randviir, Edward P; Metters, Jonathan P; Stainton, John; Banks, Craig E

    2013-05-21

    Screen printed carbon nanotube electrodes (SPEs) are explored as electroanalytical sensing platforms for the detection of capsaicin in both synthetic capsaicin solutions and capsaicin extracted from chillies and chilli sauces utilising both cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). It is found that the technique which is most applicable to the electroanalytical detection of capsaicin depends upon the analyte concentration: for the case of low capsaicin concentrations, CV is a more appropriate method as capsaicin exhibits characteristic voltammetric waves of peak heights relevant to the capsaicin concentration; but for the case of high capsaicin concentrations where the voltammetric waves merge and migrate out of the potential window, EIS is shown to be a more appropriate technique, owing to the observed linear increases in R(ct) with increasing concentration. Furthermore, we explore different types of screen printed carbon nanotube electrodes, namely single- and multi- walled carbon nanotubes, finding that they are technique-specific: for the case of low capsaicin concentrations, single-walled carbon nanotube SPEs are preferable (SW-SPE); yet for the case of EIS at high capsaicin concentrations, multi-walled carbon nanotube SPEs (MW-SPE) are preferred, based upon analytical responses. The analytical performance of CV and EIS is applied to the sensing of capsaicin in grown chillies and chilli sauces and is critically compared to 'gold standard' HPLC analysis.

  8. Study on surface acid-base property of carboxylic acid-terminated self-assembled monolayers by cyclic voltammetry and electro-chemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    罗立强; 程志亮; 杨秀荣; 汪尔康

    2000-01-01

    Cyclic voltammetry and electrochemical impedance spectroscopy were used to study the surface acid-base property of carboxylic acid-terminated self-assembled monolayers (SAMs). A carboxylic acid-terminated thiol, such as thioctic acid (1,2-dithiolane-3-pentanoic acid), was self-assembled on gold electrodes. Electron transfer between the bulk solution and the SAM modified electrode was studied at different pH using Fe(CN)63 as a probe. The surface pK. of thioctic acid was determined by cyclic voltammetry and electrochemical impedance spectroscopy to be 5.6±0.1 and 5.8±0.1, respectively. The method is compared with other methods of monolayer pK.measurement.

  9. Study on the immobilization of anti-IgG on Au-colloid modified gold electrode via potentiometric immunosensor, cyclic voltammetry, and electrochemical impedance techniques.

    Science.gov (United States)

    Fu, Yingzi; Yuan, Ruo; Tang, Dianping; Chai, Yaqin; Xu, Lan

    2005-01-15

    The immobilization of anti-IgG on Au-colloid modified gold electrodes has been investigated. A cleaned gold electrode was first immersed in a mercaptoethylamine (AET) solution, and then gold nanoparticles were chemisorbed onto the thiol groups of the mercaptoethylamine. Finally, anti-IgG was adsorbed onto the surface of the gold nanoparticles. Potentiometric immunosensor, cyclic voltammetry, and electrochemical impedance techniques were used to investigate the immobilization of anti-IgG on Au colloids. In the impedance spectroscopic study, an obvious difference of the electron transfer resistance between the Au-colloid modified electrode and the bare gold electrode was observed. The cyclic voltammogram tends to be more irreversible with increased anti-IgG concentration. Using the potentiometric immunosensor, the proposed technique is based on that the specific agglutination of antibody-coated gold nanoparticles, averaging 16 nm in diameter, in the presence of the corresponding antigen causes a potential change that is monitored by a potentiometry. It is found that the developed immunoagglutination assay system is sensitive to the concentration of IgG antigen as low as 12 ng mL(-1). Experimental results showed that the developed technique is in satisfactory agreement with the ELISA method, and that gold nanoparticles can be used as a biocompatible matrix for antibody or antigen immobilization.

  10. Cyclic Voltammetry and Impedance Spectroscopy Behavior Studies of Polyterthiophene Modified Electrode

    Directory of Open Access Journals (Sweden)

    Naima Maouche

    2011-01-01

    Full Text Available We present in this work a study of the electrochemical behaviour of terthiophene and its corresponding polymer, which is obtained electrochemically as a film by cyclic voltammetry (CV on platinum electrode. The analysis focuses essentially on the effect of two solvents acetonitrile and dichloromethane on the electrochemical behaviour of the obtained polymer. The electrochemical behavior of this material was investigated by cyclic voltammetry and electrochemical impedance spectroscopy (EIS. The voltammograms show that the film of polyterthiophene can oxide and reduce in two solutions; in acetonitrile, the oxidation current intensity is more important than in dichloromethane. The impedance plots show the semicircle which is characteristic of charge-transfer resistance at the electrode/polymer interface at high frequency and the diffusion process at low frequency.

  11. Voltage biasing, cyclic voltammetry, & electrical impedance spectroscopy for neural interfaces.

    Science.gov (United States)

    Wilks, Seth J; Richner, Tom J; Brodnick, Sarah K; Kipke, Daryl R; Williams, Justin C; Otto, Kevin J

    2012-02-24

    Electrical impedance spectroscopy (EIS) and cyclic voltammetry (CV) measure properties of the electrode-tissue interface without additional invasive procedures, and can be used to monitor electrode performance over the long term. EIS measures electrical impedance at multiple frequencies, and increases in impedance indicate increased glial scar formation around the device, while cyclic voltammetry measures the charge carrying capacity of the electrode, and indicates how charge is transferred at different voltage levels. As implanted electrodes age, EIS and CV data change, and electrode sites that previously recorded spiking neurons often exhibit significantly lower efficacy for neural recording. The application of a brief voltage pulse to implanted electrode arrays, known as rejuvenation, can bring back spiking activity on otherwise silent electrode sites for a period of time. Rejuvenation alters EIS and CV, and can be monitored by these complementary methods. Typically, EIS is measured daily as an indication of the tissue response at the electrode site. If spikes are absent in a channel that previously had spikes, then CV is used to determine the charge carrying capacity of the electrode site, and rejuvenation can be applied to improve the interface efficacy. CV and EIS are then repeated to check the changes at the electrode-tissue interface, and neural recordings are collected. The overall goal of rejuvenation is to extend the functional lifetime of implanted arrays.

  12. Spatially resolved voltage, current and electrochemical impedance spectroscopy measurements

    Energy Technology Data Exchange (ETDEWEB)

    Gerteisen, D.; Kurz, T.; Schwager, M.; Hebling, C. [Fraunhofer Institute for Solar Energy Systems ISE, Freiburg im Breisgau (Germany); Merida, W. [Clean Energy Research Centre, University of British Columbia, Vancouver, BC (Canada); Lupotto, P. [Materials Mates Italia, Milano (Italy)

    2011-04-15

    In this work a 50-channel characterisation system for PEMFCs is presented. The system is capable of traditional electrochemical measurements (e.g. staircase voltammetry, chronoamperometry and cyclic voltammetry), and concurrent EIS measurements. Unlike previous implementations, this system relies on dedicated potentiostats for current and voltage control, and independent frequency response analysers (FRAs) at each channel. Segmented fuel cell hardware is used to illustrate the system's flexibility and capabilities. The results here include steady-state data for cell characterisation under galvanostatic and potentiostatic control as well as spatially resolved impedance spectra. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  13. Electrochemical Impedance Characterization of Nafion-Coated Carbon Film Resistor Electrodes for Electroanalysis

    OpenAIRE

    Gouveia-Caridade, Carla; Brett, Christopher M. A.

    2005-01-01

    Carbon film disk electrodes with Nafion coatings have been characterized by electrochemical impedance spectroscopy (EIS) with a view to a better understanding of their advantages and limitations in electroanalysis, particularly in anodic stripping voltammetry of metal ions. After initial examination by cyclic voltammetry, spectra were recorded over the full potential range in acetate buffer solution at the bare electrodes, electrodes electrochemically pretreated in acid solution, and Nafion-c...

  14. Electrochemical impedance studies of AB{sub 5}-type hydrogen storage alloy

    Energy Technology Data Exchange (ETDEWEB)

    Slepski, Pawel; Darowicki, Kazimierz; Andrearczyk, Karolina [Department of Electrochemistry Corrosion and Materials Engineering, Gdansk University of Technology, 11/12 Narutowicza Street, 80-233 Gdansk (Poland); Kopczyk, Maciej; Sierczynska, Agnieszka [Institute of Non-ferrous Metals, Department in Poznan, Central Laboratory of Batteries and Cells, 12 Forteczna Street, 61-362 Poznan (Poland)

    2010-05-01

    Electrochemical impedance spectroscopy technique was used to describe behavior of AB{sub 5}-type hydrogen storage alloy. Impedance investigations were performed during cyclic voltammetry measurement and charge/discharge cycles. The comprehensive interpretation of instantaneous impedance spectra obtained in potentiostatic mode allowed further to interpret impedance results in galvanostatic mode. Proposed methodology enabled to trace electrical parameters as a function of state of charge (SOC) and depth of discharge (DOD). (author)

  15. Applications of Nonlinear Electrochemical Impedance Spectroscopy (NLEIS)

    KAUST Repository

    Adler, S. B.

    2013-08-31

    This paper reviews the use of nonlinear electrochemical impedance spectroscopy (NLEIS) in the analysis of SOFC electrode reactions. By combining EIS and NLEIS, as well as other independent information about an electrode material, it becomes possible to establish quantitative links between electrochemical kinetics and materials properties, even when systems are unstable with time. After a brief review of the method, this paper summarizes recent results analyzing the effects of Sr segregation in thin-film LSC electrodes. © The Electrochemical Society.

  16. Electrochemical Impedance Spectroscopy Of Metal Alloys

    Science.gov (United States)

    Macdowell, L. G.; Calle, L. M.

    1993-01-01

    Report describes use of electrochemical impedance spectroscopy (EIS) to investigate resistances of 19 alloys to corrosion under conditions similar to those of corrosive, chloride-laden seaside environment of Space Transportation System launch site. Alloys investigated: Hastelloy C-4, C-22, C-276, and B-2; Inconel(R) 600, 625, and 825; Inco(R) G-3; Monel 400; Zirconium 702; Stainless Steel 304L, 304LN, 316L, 317L, and 904L; 20Cb-3; 7Mo+N; ES2205; and Ferralium 255. Results suggest electrochemical impedance spectroscopy used to predict corrosion performances of metal alloys.

  17. Magnetic Effect during Copper Electroplating Using Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Hung, Chi-Cheng; Lee, Wen-Hsi; Chang, Shih-Chieh; Hwang, Gwo-Jen; Wang, Ying-Lang

    2009-07-01

    In this paper, the effect of the intensity of the magnetic field on copper electroplating was investigated. Our results indicate that the variation of the magnetic field on the surface of the cathode electrode affected the electroplating rate of the electroplated copper film. By increasing the intensity of the magnetic field, the copper-electroplating rate increases. However, the magnetic field did not affect the grain sizes or shapes of the copper electroplated films. Electrochemical impedance spectroscopy (EIS) was used to analyze the electrochemical effect of the magnetic field during the copper electroplating process. Cyclic-voltammetry stripping, and cell voltage versus plating time were examined to clarify the acceleration behavior of the magnetic field. The proposed equivalent circuit shows that the magnetic field enhanced the copper-electroplating rate by decreasing the charge-transfer resistance as well as the resistance of the diffusion layer.

  18. Tracking of electrochemical impedance of batteries

    Science.gov (United States)

    Piret, H.; Granjon, P.; Guillet, N.; Cattin, V.

    2016-04-01

    This paper presents an evolutionary battery impedance estimation method, which can be easily embedded in vehicles or nomad devices. The proposed method not only allows an accurate frequency impedance estimation, but also a tracking of its temporal evolution contrary to classical electrochemical impedance spectroscopy methods. Taking into account constraints of cost and complexity, we propose to use the existing electronics of current control to perform a frequency evolutionary estimation of the electrochemical impedance. The developed method uses a simple wideband input signal, and relies on a recursive local average of Fourier transforms. The averaging is controlled by a single parameter, managing a trade-off between tracking and estimation performance. This normalized parameter allows to correctly adapt the behavior of the proposed estimator to the variations of the impedance. The advantage of the proposed method is twofold: the method is easy to embed into a simple electronic circuit, and the battery impedance estimator is evolutionary. The ability of the method to monitor the impedance over time is demonstrated on a simulator, and on a real Lithium ion battery, on which a repeatability study is carried out. The experiments reveal good tracking results, and estimation performance as accurate as the usual laboratory approaches.

  19. The electrochemical impedance of metal hydride electrodes

    DEFF Research Database (Denmark)

    Valøen, Lars Ole; Lasia, Andrzej; Jensen, Jens Oluf

    2002-01-01

    The electrochemical impedance responses for different laboratory type metal hydride electrodes were successfully modeled and fitted to experimental data for AB5 type hydrogen storage alloys as well as one MgNi type electrode. The models fitted the experimental data remarkably well. Several AC......, explaining the experimental impedances in a wide frequency range for electrodes of hydride forming materials mixed with copper powder, were obtained. Both charge transfer and spherical diffusion of hydrogen in the particles are important sub processes that govern the total rate of the electrochemical...... hydrogen absorption/desorption reaction. To approximate the experimental data, equations describing the current distribution in porous electrodes were needed. Indications of one or more parallel reduction/oxidation processes competing with the electrochemical hydrogen absorption/desorption reaction were...

  20. Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin

    Directory of Open Access Journals (Sweden)

    Jennifer Halliwell

    2014-12-01

    Full Text Available The standard method for the detection of botulinum neurotoxin is currently the mouse bioassay which is considered to be the most reliable method for the detection of the active form of this toxin. Despite this it is a time-consuming and expensive assay to run and as such many alternative assays have recently been proposed. Herein we report the development of two electrochemical assays for the detection of active botulinum neurotoxin in a pharmaceutical sample. Gold electrodes were modified with self-assembled monolayers of the SNARE protein SNAP-25 which is selectively cleaved by active botulinum neurotoxin A. Cyclic voltammetry and electrochemical impedance spectroscopy were performed on the modified working electrodes to observe changes to the layer on addition of the toxin. Both methods were able to distinguish the difference between the presence of the active toxin and a placebo containing the excipients of the pharmaceutical product. The electrochemical impedance spectroscopy assay also allowed for detection of the active toxin at concentrations as low as 25 fg/ml, with results being obtained in under an hour outperforming the mouse bioassay.

  1. Alternating current scanning electrochemical microscopy with simultaneous fast-scan cyclic voltammetry.

    Science.gov (United States)

    Koch, Jason A; Baur, Melinda B; Woodall, Erica L; Baur, John E

    2012-11-06

    Fast-scan cyclic voltammetry (FSCV) is combined with alternating current scanning electrochemical microscopy (AC-SECM) for simultaneous measurements of impedance and faradaic current. Scan rates of 10-1000 V s(-1) were used for voltammetry, while a high-frequency (100 kHz), low-amplitude (10 mV rms) sine wave was added to the voltammetric waveform for the ac measurement. Both a lock-in amplifier and an analog circuit were used to measure the amplitude of the resultant ac signal. The effect of the added sine wave on the voltammetry at a carbon fiber electrode was investigated and found to have negligible effect. The combined FSCV and ac measurements were used to provide simultaneous chemical and topographical information about a substrate using a single carbon fiber probe. The technique is demonstrated in living cell culture, where cellular respiration and topography were simultaneously imaged without the addition of a redox mediator. This approach promises to be useful for the topographical and multidimensional chemical imaging of substrates.

  2. Electrochemical impedance spectroscopy of oxidized porous silicon

    Energy Technology Data Exchange (ETDEWEB)

    Mula, Guido, E-mail: guido.mula@unica.it [Dipartimento di Fisica, Università degli Studi di Cagliari, Cittadella Universitaria di Monserrato, S.P. 8 km 0.700, 09042 Cagliari (Italy); Tiddia, Maria V. [Dipartimento di Fisica, Università degli Studi di Cagliari, Cittadella Universitaria di Monserrato, S.P. 8 km 0.700, 09042 Cagliari (Italy); Ruffilli, Roberta [Nanochemistry, Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy); Falqui, Andrea [Nanochemistry, Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy); Dipartimento di Scienze Chimiche e Geologiche, Università degli Studi di Cagliari, Cittadella Universitaria di Monserrato, S.P. 8 km 0.700, 09042 Cagliari (Italy); Palmas, Simonetta; Mascia, Michele [Dipartimento di Ingegneria Meccanica Chimica e dei Materiali, Università degli Studi di Cagliari, Piazza d' Armi, 09126 Cagliari (Italy)

    2014-04-01

    We present a study of the electrochemical oxidation process of porous silicon. We analyze the effect of the layer thickness (1.25–22 μm) and of the applied current density (1.1–11.1 mA/cm{sup 2}, values calculated with reference to the external samples surface) on the oxidation process by comparing the galvanostatic electrochemical impedance spectroscopy (EIS) measurements and the optical specular reflectivity of the samples. The results of EIS were interpreted using an equivalent circuit to separate the contribution of different sample parts. A different behavior of the electrochemical oxidation process has been found for thin and thick samples: whereas for thin samples the oxidation process is univocally related to current density and thickness, for thicker samples this is no more true. Measurements by Energy Dispersive Spectroscopy using a Scanning Electron Microscopy confirmed that the inhomogeneity of the electrochemical oxidation process is increased by higher thicknesses and higher currents. A possible explanation is proposed to justify the different behavior of thin and thick samples during the electrochemical process. - Highlights: • A multidisciplinary approach on porous Si electrochemical oxidation is proposed. • Electrochemical, optical, and structural characterizations are used. • Layer thickness and oxidation current effects are shown. • An explanation of the observed behavior is proposed.

  3. Method for conducting nonlinear electrochemical impedance spectroscopy

    Science.gov (United States)

    Adler, Stuart B.; Wilson, Jamie R.; Huff, Shawn L.; Schwartz, Daniel T.

    2015-06-02

    A method for conducting nonlinear electrochemical impedance spectroscopy. The method includes quantifying the nonlinear response of an electrochemical system by measuring higher-order current or voltage harmonics generated by moderate-amplitude sinusoidal current or voltage perturbations. The method involves acquisition of the response signal followed by time apodization and fast Fourier transformation of the data into the frequency domain, where the magnitude and phase of each harmonic signal can be readily quantified. The method can be implemented on a computer as a software program.

  4. Method for conducting nonlinear electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Adler, Stuart B.; Wilson, Jamie R.; Huff, Shawn L.; Schwartz, Daniel T.

    2015-06-02

    A method for conducting nonlinear electrochemical impedance spectroscopy. The method includes quantifying the nonlinear response of an electrochemical system by measuring higher-order current or voltage harmonics generated by moderate-amplitude sinusoidal current or voltage perturbations. The method involves acquisition of the response signal followed by time apodization and fast Fourier transformation of the data into the frequency domain, where the magnitude and phase of each harmonic signal can be readily quantified. The method can be implemented on a computer as a software program.

  5. Relating cyclic voltammetry and impedance analysis in a viologen electrochromic device

    Energy Technology Data Exchange (ETDEWEB)

    Vergaz, Ricardo; Barrios, David; Sanchez-Pena, Jose-Manuel [Grupo de Displays y Aplicaciones Fotonicas, Department Tecnologia Electronica, Universidad Carlos III de Madrid, C/Butarque, 15, E28911 Leganes, Madrid (Spain); Pozo-Gonzalo, Cristina; Salsamendi, Maitane [Centre for Electrochemical Technologies (CIDETEC), Dept. Nuevos Materiales, Parque Tecnologico de San Sebastian - Paseo Miramon, 196, E-20009, San Sebastian (Spain)

    2009-12-15

    Viologens are electrochromic materials that have a wide range of coloration depending on the radical substituents. The results for a new blue viologen-based device, that has recently been patented, with an active area of 8.5 cm{sup 2} is presented in this paper. The characterization techniques used are based on optical measurements, chronoamperometry, cyclic voltammetry, and impedance spectroscopy analysis. A study of the results obtained from these measurements provides both an overview of the reactions taking place and has allowed an equivalent circuit to be developed which relates the different electrochemical parameters. The transmittance is observed to change from 80% to 15% in 600 nm for input voltages ranging from 0 to 2.5 V. However, increasing voltage beyond 1.8 V shows no optical change, thus, maintaining the voltage below this level optimizes the use of electrical current. Voltages and charges used for each redox reaction have been computed and are seen to be linearly related. The equivalent circuit generated to mimic the process has included parameters based on Warburg diffusion and double-layer capacitances. Results from this model are consistent with measurements for up to 1.8 V. Saturation of reduced species has been deduced for input voltages beyond this level. (author)

  6. Voltammetric and electrochemical impedance spectroscopy characterization of a cathodic and anodic pre-treated boron doped diamond electrode

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, S. Carlos B. [Departamento de Quimica, Faculdade de Ciencias e Tecnologia, Universidade de Coimbra, 3004-535 Coimbra (Portugal); Oliveira-Brett, Ana Maria, E-mail: brett@ci.uc.p [Departamento de Quimica, Faculdade de Ciencias e Tecnologia, Universidade de Coimbra, 3004-535 Coimbra (Portugal)

    2010-06-01

    The effect of boron doped diamond (BDD) surface termination, immediately after cathodic and anodic electrochemical pre-treatments, on the electrochemical response of a BDD electrode in aqueous media and the influence of the different supporting electrolytes utilized in these pre-treatments on the final surface termination was investigated with [Fe(CN){sub 6}]{sup 4-/3-}, as redox probe, by cyclic and differential pulse voltammetry and electrochemical impedance spectroscopy. The cyclic voltammetry results indicate that the electrochemical behavior for the redox couple [Fe(CN){sub 6}]{sup 4-/3-} is very dependent on the state of the BDD surface, and a reversible response was observed after the cathodic electrochemical pre-treatment, whereas a quasi-reversible response occurred after anodic electrochemical pre-treatment. Differential pulse voltammetry in acetate buffer also showed that the potential window is very much influenced by the electrochemical pre-treatment of the BDD surface. Electroactivity of non-diamond carbon surface species (sp{sup 2} inclusions) incorporated into the diamond structure was observed after cathodic and anodic pre-treatments. Electrochemical impedance spectroscopy confirmed the cyclic voltammetry results and indicates that the BDD surface resistance and capacitance vary significantly with the electrolyte and with the electrochemical pre-treatment, caused by different surface terminations of the BDD electrode surface.

  7. Use of cyclic voltammetry and electrochemical impedance spectroscopy for determination of active surface area of modified carbon-based electrodes; Uso da voltametria ciclica e da espectroscopia de impedancia eletroquimica na determinacao da area superficial ativa de eletrodos modificados a base de carbono

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Leticia Lopes de

    2011-07-01

    Carbon-based electrodes as well the ion exchange electrodes among others have been applied mainly in the treatment of industrial effluents and radioactive wastes. Carbon is also used in fuel cells as substrate for the electrocatalysts, having high surface area which surpasses its geometric area. The knowledge of the total active area is important for the determination of operating conditions of an electrochemical cell with respect to the currents to be applied (current density). In this study it was used two techniques to determine the electrochemical active surface area of glassy carbon, electrodes and ion exchange electrodes: cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The experiments were carried out with KNO{sub 3} 0.1 mol.L{sup -1} solutions in a three-electrode electrochemical cell: carbon-based working electrode, platinum auxiliary electrode and Ag/AgCl reference electrode. The glassy carbon and porous carbon electrodes with geometric areas of 3.14 x 10{sup -2} and 2.83 X 10{sup -1} cm{sup 2}, respectively, were used. The ion exchange electrode was prepared by mixing graphite, carbon, ion exchange resin and a binder, and this mixture was applied in three layers on carbon felt, using a geometric area of 1.0 cm{sup 2} during the experiments. The capacitance (Cd) of the materials was determined by EIS using Bode diagrams. The value of 172 {mu}F.cm{sup -2} found for the glassy carbon is consistent with the literature data ({approx} 200 {mu}F.cm'-{sup 2}). By VC, varying the scan rate from 0.2 to 2.0 mV.s-1, the capacitance CdS (S = active surface area) in the region of the electric double layer (EDL) of each material was determined. By EIS, the values of C{sub d}, 3.0 x 10{sup -5} {mu}F.cm'-{sup 2} and 11 x 10{sup 3} {mu}F.cm-2, were found for the porous carbon and ion exchange electrodes, respectively, which allowed the determination of active surface areas as 3.73 x 106 cm{sup 2} and 4.72 cm{sup 2}. To sum up, the

  8. Cyclic voltammetry and impedance studies of electrodeposited polypyrrole nanoparticles doped with 2-acrylamido-2-methyl-1-propanesulfonic acid sodium salt

    Energy Technology Data Exchange (ETDEWEB)

    Ebrahim, Sh. M., E-mail: shebrahim@igsr.alex.edu.e [Department of Materials Science, Institute of Graduate Studies and Research, Alexandria University, Postal Code 21526, Alexandria (Egypt); Latif, M.M. Abd-El [Mubarak City for Scientific Research and Technology Applications, Institute of Advanced Technology and New Materials, Borg El-Arab City, Alexandria (Egypt); Gad, A.M.; Soliman, M.M. [Department of Materials Science, Institute of Graduate Studies and Research, Alexandria University, Postal Code 21526, Alexandria (Egypt)

    2010-05-31

    Electrochemical synthesis of polypyrrole (PPY), doped with 2-acrylamido-2-methyl-1-propanesulfonic acid sodium salt (AMPSNa), was carried out using chronoamperometric technique. Cyclic voltammetry measurements showed that the electroactivity of PPY films, doped with AMPSNa, increases with the film thickness. Scanning electron microscopy photographs revealed that the PPY particles are in the nano-scale range and that their size depends on the potential at which the PPY has formed. Electrochemical impedance spectroscopy (EIS), in the potential range of + 1.0 and - 1.0 V, revealed in the PPY film charge transfer domination with a semicircle at high frequencies, and anion diffusion dominance at low frequencies. EIS also showed that the charge transfer resistance of PPY film at - 1.0 V is lower than what is expected and that on increasing the thickness of the PPY films, the overall impedance decreases. The proposed equivalent circuit model, based on the double layer capacity and the Warburg impedance, was replaced by two constant-phase elements to fit the experimental work of this study. The values of the fractional exponent of the first constant phase element at approximately 0.5 indicate that the processes have a diffusion-limited nature.

  9. Electrochemical impedance characterization of FeSn{sub 2} electrodes for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chamas, M.; Lippens, P-E.; Jumas, J-C. [Institut Charles Gerhardt, Equipe Agregats Interfaces et Materiaux pour l' Energie, UMR 5253 CNRS, Universite Montpellier 2, Place Eugene Bataillon, 34095 Montpellier cedex 5 (France); Hassoun, J., E-mail: jusef.hassoun@uniroma1.it [Dipartemento di Chimica, Universita di Roma, ' La Sapienza' , 00185 Rome (Italy); Panero, S.; Scrosati, B. [Dipartemento di Chimica, Universita di Roma, ' La Sapienza' , 00185 Rome (Italy)

    2011-07-30

    Highlights: > In this paper we study a tin based, FeSn{sub 2}, high capacity lithium-alloying electrode. > The electrochemical performance of this electrode in lithium batteries is remarkably influenced by the current rate. > This aspect is investigated by electrochemical techniques such as galvanostatic cycling and impedance spectroscopy. > The results demonstrated that the good electrochemical behavior of the electrode at the higher currents is due to the formation of a stable solid electrolyte interphase (SEI) film. - Abstract: This work reports the electrochemical characterization of a micro-scale FeSn{sub 2} electrode in a lithium battery. The electrode is proposed as anode material for advanced lithium ion batteries due to its characteristics of high capacity (500 mAh g{sup -1}) and low working voltage (0.6 V vs. Li). The electrochemical alloying process is studied by cyclic voltammetry and galvanostatic cycling while the interfacial properties are investigated by electrochemical impedance spectroscopy. The impedance measurements in combination with the galvanostatic cycling tests reveal relatively low overall impedance values and good electrochemical performance for the electrode, both in terms of delivered capacity and cycling stability, even at the higher C-rate regimes.

  10. Electrochemical Impedance Spectroscopy of Conductive Polymer Coatings

    Science.gov (United States)

    Calle, Luz Marina; MacDowell, Louis G.

    1996-01-01

    Electrochemical impedance spectroscopy (EIS) was used to investigate the corrosion protection performance of twenty nine proprietary conductive polymer coatings for cold rolled steel under immersion in 3.55 percent NaCl. Corrosion potential as well as Bode plots of the data were obtained for each coating after one hour immersion, All coatings, with the exception of one, have a corrosion potential that is higher in the positive direction than the corrosion potential of bare steel under the same conditions. Group A consisted of twenty one coatings with Bode plots indicative of the capacitive behavior characteristic of barrier coatings. An equivalent circuit consisting of a capacitor in series with a resistor simulated the experimental EIS data for these coatings very well. Group B consisted of eight coatings that exhibited EIS spectra showing an inflection point which indicates that two time constants are present. This may be caused by an electrochemical process taking place which could be indicitive of coating failing. These coatings have a lower impedance that those in Group A.

  11. An Electrochemical Impedance Spectroscopy System for Monitoring Pineapple Waste Saccharification

    Science.gov (United States)

    Conesa, Claudia; Ibáñez Civera, Javier; Seguí, Lucía; Fito, Pedro; Laguarda-Miró, Nicolás

    2016-01-01

    Electrochemical impedance spectroscopy (EIS) has been used for monitoring the enzymatic pineapple waste hydrolysis process. The system employed consists of a device called Advanced Voltammetry, Impedance Spectroscopy & Potentiometry Analyzer (AVISPA) equipped with a specific software application and a stainless steel double needle electrode. EIS measurements were conducted at different saccharification time intervals: 0, 0.75, 1.5, 6, 12 and 24 h. Partial least squares (PLS) were used to model the relationship between the EIS measurements and the sugar determination by HPAEC-PAD. On the other hand, artificial neural networks: (multilayer feed forward architecture with quick propagation training algorithm and logistic-type transfer functions) gave the best results as predictive models for glucose, fructose, sucrose and total sugars. Coefficients of determination (R2) and root mean square errors of prediction (RMSEP) were determined as R2 > 0.944 and RMSEP 0.973 and RMSEP < 0.486 for artificial neural networks (ANNs), respectively. Therefore, a combination of both an EIS-based technique and ANN models is suggested as a promising alternative to the traditional laboratory techniques for monitoring the pineapple waste saccharification step. PMID:26861317

  12. An Electrochemical Impedance Spectroscopy System for Monitoring Pineapple Waste Saccharification

    Directory of Open Access Journals (Sweden)

    Claudia Conesa

    2016-02-01

    Full Text Available Electrochemical impedance spectroscopy (EIS has been used for monitoring the enzymatic pineapple waste hydrolysis process. The system employed consists of a device called Advanced Voltammetry, Impedance Spectroscopy & Potentiometry Analyzer (AVISPA equipped with a specific software application and a stainless steel double needle electrode. EIS measurements were conducted at different saccharification time intervals: 0, 0.75, 1.5, 6, 12 and 24 h. Partial least squares (PLS were used to model the relationship between the EIS measurements and the sugar determination by HPAEC-PAD. On the other hand, artificial neural networks: (multilayer feed forward architecture with quick propagation training algorithm and logistic-type transfer functions gave the best results as predictive models for glucose, fructose, sucrose and total sugars. Coefficients of determination (R2 and root mean square errors of prediction (RMSEP were determined as R2 > 0.944 and RMSEP < 1.782 for PLS and R2 > 0.973 and RMSEP < 0.486 for artificial neural networks (ANNs, respectively. Therefore, a combination of both an EIS-based technique and ANN models is suggested as a promising alternative to the traditional laboratory techniques for monitoring the pineapple waste saccharification step.

  13. An Electrochemical Impedance Spectroscopy System for Monitoring Pineapple Waste Saccharification.

    Science.gov (United States)

    Conesa, Claudia; Ibáñez Civera, Javier; Seguí, Lucía; Fito, Pedro; Laguarda-Miró, Nicolás

    2016-02-04

    Electrochemical impedance spectroscopy (EIS) has been used for monitoring the enzymatic pineapple waste hydrolysis process. The system employed consists of a device called Advanced Voltammetry, Impedance Spectroscopy & Potentiometry Analyzer (AVISPA) equipped with a specific software application and a stainless steel double needle electrode. EIS measurements were conducted at different saccharification time intervals: 0, 0.75, 1.5, 6, 12 and 24 h. Partial least squares (PLS) were used to model the relationship between the EIS measurements and the sugar determination by HPAEC-PAD. On the other hand, artificial neural networks: (multilayer feed forward architecture with quick propagation training algorithm and logistic-type transfer functions) gave the best results as predictive models for glucose, fructose, sucrose and total sugars. Coefficients of determination (R²) and root mean square errors of prediction (RMSEP) were determined as R² > 0.944 and RMSEP 0.973 and RMSEP < 0.486 for artificial neural networks (ANNs), respectively. Therefore, a combination of both an EIS-based technique and ANN models is suggested as a promising alternative to the traditional laboratory techniques for monitoring the pineapple waste saccharification step.

  14. Sensing Estrogen with Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Li, Jing; Kim, Byung Kun; Im, Ji-Eun; Choi, Han Nim; Kim, Dong-Hwan; Cho, Seong In

    2016-01-01

    This study demonstrates the application feasibility of electrochemical impedance spectroscopy (EIS) in measuring estrogen (17β-estradiol) in gas phase. The present biosensor gives a linear response (R2 = 0.999) for 17β-estradiol vapor concentration from 3.7 ng/L to 3.7 × 10−4 ng/L with a limit of detection (3.7 × 10−4 ng/L). The results show that the fabricated biosensor demonstrates better detection limit of 17β-estradiol in gas phase than the previous report with GC-MS method. This estrogen biosensor has many potential applications for on-site detection of a variety of endocrine disrupting compounds (EDCs) in the gas phase.

  15. Sensing Estrogen with Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Jing Li

    2016-01-01

    Full Text Available This study demonstrates the application feasibility of electrochemical impedance spectroscopy (EIS in measuring estrogen (17β-estradiol in gas phase. The present biosensor gives a linear response (R2=0.999 for 17β-estradiol vapor concentration from 3.7 ng/L to 3.7 × 10−4 ng/L with a limit of detection (3.7 × 10−4 ng/L. The results show that the fabricated biosensor demonstrates better detection limit of 17β-estradiol in gas phase than the previous report with GC-MS method. This estrogen biosensor has many potential applications for on-site detection of a variety of endocrine disrupting compounds (EDCs in the gas phase.

  16. Electrochemical-Voltammetry Behavior of Several Aromatic Aldehydes in Acid Solution

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The electrochemical-voltammetry behavior of vanillin, heliotropin, anisaldehyde on the surface ofPt, Au electrodes in acid solution has been studied by means of the electrochemical cyclic voltammetry method. I was found that the electrochemical processes of them are irreversible on both Pt and Au elec-trodes. The electrochemical activity of vanillin is stronger than heliotropin's and heliotropin's is stronger than, anisaldehyde's on Pt electrode. While the electrochemical activity of anisaldehyde is stronger than heliotropin's and vanillin's is the weakest on Au. The results indicate that when they are used as additives for electroplating, they must be consumptive, and it will improve the leveling ability of plating solution and brightness of the deposition layer.

  17. Plasmonic-Based Electrochemical Impedance Spectroscopy: Application to Molecular Binding

    Science.gov (United States)

    Lu, Jin; Wang, Wei; Wang, Shaopeng; Shan, Xiaonan; Li, Jinghong; Tao, Nongjian

    2012-01-01

    Plasmonic-based electrochemical impedance spectroscopy (P-EIS) is developed to investigate molecular binding on surfaces. Its basic principle relies on the sensitive dependence of surface plasmon resonance (SPR) signal on surface charge density, which is modulated by applying an AC potential to a SPR chip surface. The AC component of the SPR response gives the electrochemical impedance, and the DC component provides the conventional SPR detection. The plasmonic-based impedance measured over a range of frequency is in quantitative agreement with the conventional electrochemical impedance. Compared to the conventional SPR detection, P-EIS is sensitive to molecular binding taking place on the chip surface, and less sensitive to bulk refractive index changes or non-specific binding. Moreover, this new approach allows for simultaneous SPR and surface impedance analysis of molecular binding processes. PMID:22122514

  18. Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry.

    Science.gov (United States)

    Brycht, Mariola; Nosal-Wiercińska, Agnieszka; Sipa, Karolina; Rudnicki, Konrad; Skrzypek, Sławomira

    2017-01-01

    In this paper, the square-wave adsorptive stripping voltammetric (SWAdSV) determination of the veterinary drug closantel using a renewable silver amalgam film electrode (Hg(Ag)FE) is presented. As observed in SWAdSV, closantel provided one well-shaped reduction peak suitable for analytical purposes at potential ca. -1.4 V in the Britton-Robinson (B-R) buffer at pH 7.0. At optimal conditions, the SWAdSV response of Hg(Ag)FE for determining closantel was linear over two concentration ranges of 5.0 × 10(-8) to 2.0 × 10(-7) mol dm(-3) and 2.0 × 10(-7) to 1.2 × 10(-6) mol dm(-3) with a detection limit of 1.1 × 10(-8) mol dm(-3). In addition, a relevance of the developed SWAdSV method was successfully verified by the quantitative analysis of closantel in the commercial formulation Closamectin Pour-On with satisfactory results (RSD = 5.8%, recovery = 101.8%). The results showed that the developed procedure can be adequate for screening purposes. Also, the electrochemical behavior of closantel was characterized by cyclic voltammetry, and it was found that closantel exhibited a quasi-reversible behavior with cathodic peak on the forward scan at ca. -1.4 V and anodic peak on the reverse scan at ca. -1.35 V vs. Ag/AgCl in B-R buffer, pH 7.0. As the obtained results showed that the electrode mechanism of closantel is controlled by the adsorption, the effect of adsorption was studied using the electrochemical impedance spectroscopy technique.

  19. The Impedance Response of Semiconductors: An Electrochemical Engineering Perspective.

    Science.gov (United States)

    Orazem, Mark E.

    1990-01-01

    Shows that the principles learned in the study of mass transport, thermodynamics, and kinetics associated with electrochemical systems can be applied to the transport and reaction processes taking place within a semiconductor. Describes impedance techniques and provides several graphs illustrating impedance data for diverse circuit systems. (YP)

  20. Electrochemical impedance spectroscopy in solid state ionics: recent advances

    NARCIS (Netherlands)

    Boukamp, Bernard A.

    2004-01-01

    Electrochemical Impedance Spectroscopy (EIS) has become an important research tool in Solid State Ionics. Some new developments are highlighted: new methods of automatic parameter extraction from impedance measurements are briefly discussed. The Kramers–Kronig data validation test presents another p

  1. Characterization of LiFePO4/C Composite Thin Films Using Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Bajars, G.; Kucinskis, G.; Smits, J.; Kleperis, J.; Lusis, A.

    2012-08-01

    The composite LiFePO4/C thin films were prepared on steel substrate by radio frequency (RF) magnetron sputtering. Electrochemical properties of the obtained thin films were investigated by cyclic voltammetry charge-discharge measurements and electrochemical impedance spectroscopy (EIS). The films annealed at 550 °C exhibited a couple of redox peaks at 3.45 V vs. Li/Li+ characteristic for the electrochemical lithium insertion/extraction in LiFePO4. At low current rate such composite thin film showed a discharge capacity of over 110 mAh g-1. The dependence of charge transfer resistance, double layer capacitance and lithium diffusion coefficients on applied electrode potential were calculated from EIS data. Determined values of lithium diffusion coefficient were in the range from 8.3-10-13 cm2 s1 to 1.2-10-13 cm2 s-1 at 3.4 V and 3.7 V, respectively.

  2. Development and Use of a Cyclic Voltammetry Simulator to Introduce Undergraduate Students to Electrochemical Simulations

    Science.gov (United States)

    Brown, Jay H.

    2015-01-01

    Cyclic voltammetry (CV) is a popular technique for the study of electrochemical mechanisms because the method can provide useful information on the redox couple. The technique involves the application of a potential ramp on an unstirred solution while the current is monitored, and then the ramp is reversed for a return sweep. CV is sometimes…

  3. Development and Use of a Cyclic Voltammetry Simulator to Introduce Undergraduate Students to Electrochemical Simulations

    Science.gov (United States)

    Brown, Jay H.

    2015-01-01

    Cyclic voltammetry (CV) is a popular technique for the study of electrochemical mechanisms because the method can provide useful information on the redox couple. The technique involves the application of a potential ramp on an unstirred solution while the current is monitored, and then the ramp is reversed for a return sweep. CV is sometimes…

  4. The Rise of Voltammetry: From Polarography to the Scanning Electrochemical Microscope

    Science.gov (United States)

    Bard, Allen J.

    2007-01-01

    The drooping mercury electrode (DME) was previously used to carry out electrochemical experiments but invention of polarography technique changed this. Voltammetry with DME was given the term polarography and are used in measurement of current as a function of potential at small electrodes.

  5. Simulating cyclic voltammetry under advection for electrochemical cantilevers

    DEFF Research Database (Denmark)

    Adesokan, Bolaji James; Evgrafov, Anton; Sørensen, Mads Peter

    2015-01-01

    We present a mathematical model describing an electrochemical system involving electrode–electrolyte interaction. The model is governed by a system of advection–diffusion equations with a nonlinear reaction term at the boundary. Our calculations based on such model demonstrate the dynamics of ion...

  6. Hydrodynamics studies of cyclic voltammetry for electrochemical micro biosensors

    DEFF Research Database (Denmark)

    Adesokan, Bolaji James; Quan, Xueling; Evgrafov, Anton

    2015-01-01

    We investigate the effect of flow rate on the electrical current response to the applied voltage in a micro electrochemical system. To accomplish this, we considered an ion-transport model that is governed by the Nernst-Planck equation coupled to the Navier-Stokes equations for hydrodynamics. The...

  7. Electrochemical Impedance of a Battery Electrode with Anisotropic Active Particles

    CERN Document Server

    Song, J

    2013-01-01

    Electrochemical impedance spectra for battery electrodes are usually interpreted using models that assume isotropic active particles, having uniform current density and symmetric diffusivities. While this can be reasonable for amorphous or polycrystalline materials with randomly oriented grains, modern electrode materials increasingly consist of highly anisotropic, single-crystalline, nanoparticles, with different impedance characteristics. In this paper, analytical expressions are derived for the impedance of anisotropic particles with tensorial diffusivities and orientation-dependent surface reaction rates and capacitances. The resulting impedance spectrum contains clear signatures of the anisotropic material properties and aspect ratio, as well as statistical variations in any of these parameters.

  8. Electrochemical Impedance Studies of SOFC Cathodes

    DEFF Research Database (Denmark)

    Hjelm, Johan; Søgaard, Martin; Wandel, Marie

    2007-01-01

    impedance of the cathode at intermediate operating temperatures. The perovskite is of the La-Sr-Co-Fe type. The EIS response of symmetrical cells with a thick (similar to 200 mu m) gadolinia doped ceria electrolyte was compared with the impedance contribution of the cathode of a full anode supported cell....... The full cells had a Ni-YSZ anode and anode support, a thin YSZ electrolyte, and a CGO barrier layer. The symmetric and full cell cathode responses were compared at open-circuit voltage. Humidified hydrogen was used as the fuel in the full cell measurements. Differential analysis of the impedance data...

  9. Electrochemical Impedance Spectra of Particulate Matter and Smoke

    Energy Technology Data Exchange (ETDEWEB)

    Osite, A; Katkevich, J; Viksna, A; Vaivars, G, E-mail: agnese.osite@lu.lv [Department of Chemistry, University of Latvia, Riga, Valdemara Street 48, Latvia, LV-1013 (Latvia)

    2011-06-23

    Particularly aerosol particles of fine dimensions are recognized to have a strong impact on the climate change, on the atmospheric energy budget, on the environment and on human health. In this study coarse aerosol particles with different black carbon mass concentrations were investigated by electrochemical impedance spectroscopy. Present work describes preparation of particulate matter samples for impedance measurements, the principles of the structure of electrochemical cell and the relationship between parameters obtained from impedance spectra and black carbon mass concentration. Using complex electrode it is possible to obtain qualitative impedance spectra of particulate matter which were sampled on glass fibre filters. The values of equivalent circuit's elements (R, Q and n) are depending on sampled mass of black carbon and mass of other carbonaceous components which are not black as well as they depend on filter pore packing with solid particles.

  10. Benzene Oxidation on Boron-Doped Diamond Electrode: Electrochemical-Impedance Study of Adsorption Effects

    Directory of Open Access Journals (Sweden)

    Yuri Pleskov

    2012-01-01

    Full Text Available Benzene oxidation at a boron-doped diamond anode in 0.5 M K2SO4 aqueous solution is studied by cyclic voltammetry and electrochemical impedance spectroscopy. It is shown by measurements of differential capacitance and anodic current that in the ideal-polarizability potential region benzene either is not adsorbed at the diamond electrode or the benzene adsorption does not affect its capacitance. At more positive potentials, the adsorption of some intermediate of the benzene oxidation occurs at the electrode. The intermediate partially blocks the electrode surface and lowers the anodic current. The very fact of the electrode surface blocking is reflected in the complex-plane presentation of the impedance-potential plots.

  11. A new monitoring method for electrochemical aggregates by impedance spectroscopy

    Science.gov (United States)

    Kurzweil, P.; Fischle, H.-J.

    A variant of ac impedance spectroscopy is applied to monitor and control electrochemical cells and appliances without need for reference values and knowledge of control points in advance. Electrolyzers, fuels cells, energy stores, sensors and electrochemical reactors are steered to an optimum operating state by continuous evaluation of capacitance and the derivatives thereof. Dry and humid electrode-electrolyte interfaces are distinguished with the aid of the low-frequency impedance. The problem is solved in order to determine electrolyte concentrations unambiguously from electrolyte resistance, although the conductivity of the solution has a maximum and changes nonlinearly with the concentration.

  12. Local resolved electrochemical impedance spectroscopy of PEFC single cells

    Energy Technology Data Exchange (ETDEWEB)

    Schulze, M.; Gulzow, E. [German Aerospace Center, Inst. of Technical Thermodynamics, Stuttgart (Germany)

    2009-07-01

    Experimental data on a spatial resolved level is needed to understand the integral behaviour of fuel cells as well as to validate models describing fuel cell behaviour. This paper described a new tool developed to increase the accuracy of current density measurements. Based on a printed circuit board, the tool integrated local electrochemical impedance spectroscopy techniques in order to determine local membrane resistance, electrochemical reactions, and transport processes. Solutions for locally resolved impedance spectroscopy measurements were presented. It was concluded that the tool will help to provide a more detailed understanding of fuel cell behaviour.

  13. Advanced impedance modeling of solid oxide electrochemical cells

    DEFF Research Database (Denmark)

    Graves, Christopher R.; Hjelm, Johan

    2014-01-01

    Impedance spectroscopy is a powerful technique for detailed study of the electrochemical and transport processes that take place in fuel cells and electrolysis cells, including solid oxide cells (SOCs). Meaningful analysis of impedance measurements is nontrivial, however, because a large number o...... analysis methods and integrates the analysis process in a modular workflow – data validation (Kramers-Kronig), clean-up, visualization (DRT and others), modeling (nonlinear least-squares fitting), and final plotting for publication....

  14. Tunable nanogap devices for ultra-sensitive electrochemical impedance biosensing

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Yong [Department of Chemistry, Wannan Medical College, Wuhu 241002 (China); Guo, Zheng [Nanomaterials and Environmental Detection Laboratory, Institute of Intelligent Machines, Chinese Academy of Sciences, Hefei 230031 (China); Song, Jing-Jing; Huang, Qin-An; Zhu, Si-Wei [Department of Chemistry, Wannan Medical College, Wuhu 241002 (China); Huang, Xing-Jiu [Nanomaterials and Environmental Detection Laboratory, Institute of Intelligent Machines, Chinese Academy of Sciences, Hefei 230031 (China); Wei, Yan, E-mail: yanwei_wnmc@hotmail.com [Department of Chemistry, Wannan Medical College, Wuhu 241002 (China)

    2016-01-28

    A wealth of research has been available discussing nanogap devices for detecting very small quantities of biomolecules by observing their electrical behavior generally performed in dry conditions. We report that a gold nanogapped electrode with tunable gap length for ultra-sensitive detection of streptavidin based on electrochemical impedance technique. The gold nanogap is fabricated using simple monolayer film deposition and in-situ growth of gold nanoparticles in a traditional interdigitated array (IDA) microelectrode. The electrochemical impedance biosensor with a 25-nm nanogap is found to be ultra-sensitive to the specific binding of streptavidin to biotin. The binding of the streptavidin hinder the electron transfer between two electrodes, resulting in a large increase in electron-transfer resistance (R{sub et}) for operating the impedance. A linear relation between the relative R{sub et} and the logarithmic value of streptavidin concentration is observed in the concentration range from 1 pM (picomolar) to 100 nM (nanomolar). The lowest detectable concentration actually measured reaches 1 pM. We believe that such an electrochemical impedance nanogap biosensor provides a useful approach towards biomolecular detection that could be extended to a number of other systems. - Highlights: • A tunable gold nanogap device was used as to electrochemical impedance biosensor. • Linear range from 1 pM to 100 nM with LOD of 1 pM for streptavidin detection was obtained. • The nanogap devices exhibit a satisfactory precision, stability, and reproducibility. • The combination of electrochemical impedance technique and nanogap devices was achieved.

  15. Waste incineration corrosion processes: Oxidation mechanisms by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Perez, F.J.; Hierro, M.P.; Nieto, J. [Departamento de Ciencia de los Materiales. Facultad de Ciencias Quimicas, Grupo de Investigacion de Ingenieria de Superficies, Universidad Complutense de Madrid, 28040 Madrid (Spain)

    2008-07-15

    Molten chloride mixtures are formed in waste incineration plants during waste firing and energy production. These mixtures are responsible for degradation processes like hot corrosion. In order to evaluate the damage of molten salt mixtures in waste incineration environments, the alloys 625 and 617 were exposed beneath a molten KCl-ZnCl{sub 2} mixture at 650 C in air. The corrosion process was monitored by electrochemical impedance spectroscopy (EIS). An extensive microscopy analysis has been done in order to correlate the electrochemical results, and to establish an electrochemical mechanism for such high temperature corrosion processes. (Abstract Copyright [2008], Wiley Periodicals, Inc.)

  16. An approach to the electrochemical activity of poly-(phenothiazines) by complementary electrochemical impedance spectroscopy and Vis-NIR spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Agrisuelas, J. [Departament de Quimica Fisica, Universitat de Valencia, C/Dr Moliner, 50, 46100 Burjassot, Valencia (Spain); Garcia-Jareno, J.J., E-mail: Jose.J.Garcia@uv.e [Departament de Quimica Fisica, Universitat de Valencia, C/Dr Moliner, 50, 46100 Burjassot, Valencia (Spain); Gimenez-Romero, D.; Vicente, F. [Departament de Quimica Fisica, Universitat de Valencia, C/Dr Moliner, 50, 46100 Burjassot, Valencia (Spain)

    2010-08-30

    The electroactivity of two poly-(phenothiazine), the poly-(Azure A) and the poly-(Methylene Blue), has been compared in this work. The spectroelectrochemical results prove clearly the existence of two electroactive moieties integrated in the polymeric lattice, the phenothiazine ring (detected by changes of absorbance at 590 and 685 nm) and the newly formed covalent links which fixes the monomers in the backbone of the polymer (detected by changes of absorbance at 460 and 875 nm). Differences in the electrochemical response of both polymers are due to differences in this covalent link. However in both polymers, the charge balance during electrochemical reactions takes place by the exchange of one anion species and one cation species during the double electronic transference in both types of electroactive centers. Electrochemical impedance analysis together with the spectroelectrochemical (cyclic voltammetry + Vis-Near IR spectroscopy) makes possible to throw light on the mechanistic model of the electrochemical reaction of these polymers taking into account the coupled electronic/ionic transports, the trapped polarons (pinning model), structural configurations and inner water molecules.

  17. Electrochemical Impedance Modeling of a Solid Oxide Fuel Cell Anode

    DEFF Research Database (Denmark)

    Mohammadi, R.; Søgaard, Martin; Ramos, Tania

    2014-01-01

    (TLM), which is suitably modified to account for the electrode microstructural details, is used for modeling the impedance arising from the electrochemical reactions. In order to solve the system of nonlinear equations, an in-house code based on the finite difference method was developed. Some...

  18. Monitoring early zeolite formation via in situ electrochemical impedance spectroscopy.

    Science.gov (United States)

    Brabants, G; Lieben, S; Breynaert, E; Reichel, E K; Taulelle, F; Martens, J A; Jakoby, B; Kirschhock, C E A

    2016-04-01

    Hitherto zeolite formation has not been fully understood. Although electrochemical impedance spectroscopy has proven to be a versatile tool for characterizing ionic solutions, it was never used for monitoring zeolite growth. We show here that EIS can quantitatively monitor zeolite formation, especially during crucial early steps where other methods fall short.

  19. Materials analyses and electrochemical impedance of implantable metal electrodes.

    Science.gov (United States)

    Howlader, Matiar M R; Ul Alam, Arif; Sharma, Rahul P; Deen, M Jamal

    2015-04-21

    Implantable electrodes with high flexibility, high mechanical fixation and low electrochemical impedance are desirable for neuromuscular activation because they provide safe, effective and stable stimulation. In this paper, we report on detailed materials and electrical analyses of three metal implantable electrodes - gold (Au), platinum (Pt) and titanium (Ti) - using X-ray photoelectron spectroscopy (XPS), scanning acoustic microscopy, drop shape analysis and electrochemical impedance spectroscopy. We investigated the cause of changes in electrochemical impedance of long-term immersed Au, Pt and Ti electrodes on liquid crystal polymers (LCPs) in phosphate buffered saline (PBS). We analyzed the surface wettability, surface and interface defects and the elemental depth profile of the electrode-adhesion layers on the LCP. The impedance of the electrodes decreased at lower frequencies, but increased at higher frequencies compared with that of the short-term immersion. The increase of impedances was influenced by the oxidation of the electrode/adhesion-layers that affected the double layer capacitance behavior of the electrode/PBS. The oxidation of the adhesion layer for all the electrodes was confirmed by XPS. Alkali ions (sodium) were adsorbed on the Au and Pt surfaces, but diffused into the Ti electrode and LCPs. The Pt electrode showed a higher sensitivity to surface and interface defects than that of Ti and Au electrodes. These findings may be useful when designing electrodes for long-term implantable devices.

  20. Study of PEM fuel cell performance by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Asghari, Saeed; Mokmeli, Ali; Samavati, Mahrokh [Isfahan Engineering Research Center, 7th kilometer of Imam Khomeini ave., P.O. Box 81395-619, Isfahan (Iran)

    2010-09-15

    Electrochemical impedance spectroscopy is a suitable and powerful diagnostic testing method for fuel cells because it is non-destructive and provides useful information about fuel cell performance and its components. This paper presents the diagnostic testing results of a 120 W single cell and a 480 W PEM fuel cell short stack by electrochemical impedance spectroscopy. The effects of clamping torque, non-uniform assembly pressure and operating temperature on the single cell impedance spectrum were studied. Optimal clamping torque of the single cell was determined by inspection of variations of high frequency and mass transport resistances with the clamping torque. The results of the electrochemical impedance analysis show that the non-uniform assembly pressure can deteriorate the fuel cell performance by increasing the ohmic resistance and the mass transport limitation. Break-in procedure of the short stack was monitored and it is indicated that the ohmic resistance as well as the charge transfer resistance decrease to specified values as the break-in process proceeds. The effect of output current on the impedance plots of the short stack was also investigated. (author)

  1. Characterization of an electrochemical mercury sensor using alternating current, cyclic, square wave and differential pulse voltammetry.

    Science.gov (United States)

    Guerreiro, Gabriela V; Zaitouna, Anita J; Lai, Rebecca Y

    2014-01-31

    Here we report the characterization of an electrochemical mercury (Hg(2+)) sensor constructed with a methylene blue (MB)-modified and thymine-containing linear DNA probe. Similar to the linear probe electrochemical DNA sensor, the resultant sensor behaved as a "signal-off" sensor in alternating current voltammetry and cyclic voltammetry. However, depending on the applied frequency or pulse width, the sensor can behave as either a "signal-off" or "signal-on" sensor in square wave voltammetry (SWV) and differential pulse voltammetry (DPV). In SWV, the sensor showed "signal-on" behavior at low frequencies and "signal-off" behavior at high frequencies. In DPV, the sensor showed "signal-off" behavior at short pulse widths and "signal-on" behavior at long pulse widths. Independent of the sensor interrogation technique, the limit of detection was found to be 10nM, with a linear dynamic range between 10nM and 500nM. In addition, the sensor responded to Hg(2+) rather rapidly; majority of the signal change occurred in <20min. Overall, the sensor retains all the characteristics of this class of sensors; it is reagentless, reusable, sensitive, specific and selective. This study also highlights the feasibility of using a MB-modified probe for real-time sensing of Hg(2+), which has not been previously reported. More importantly, the observed "switching" behavior in SWV and DPV is potentially generalizable and should be applicable to most sensors in this class of dynamics-based electrochemical biosensors. Copyright © 2013 Elsevier B.V. All rights reserved.

  2. Electrical impedance potential mammography for visualization of objects (electrochemical tests)

    Science.gov (United States)

    Karpov, A.; Korotkova, M.; Tsofin, Yu; Tsyplyonkov, V.; Machin, M.

    2010-04-01

    The article presents the result of the electrochemical testing of the potential electric impedance mammograph "MEIK" (version 5.6) which reconstructs the image using the reciprocal projection method. The testing was carried out on several categories: biological objects visualization, definition size, location, depth and shape of the biological objects, concentration and electrical conductivity, resolution capability. The research has been conducted in the original tank filled with homogeneous and heterogeneous medium. The research of the visualization of abiological and bialogical objects, objects dimensions, objects location, objects structure. According to the data of the electrochemical testing, the resolution capability of the objects with high electrical conductivity ranges from 1 to 3 mm and of the objects with low electrical conductivity - from 3 to 5 mm. Due to the given electrochemical testing results potencial electric impedance mammograph "MEIK" (version 5.6) can be rated as the medical visualization device.

  3. Influence of metal oxides on Pt catalysts for methanol electrooxidation using electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Huiping; Qiu, Xinping; Chen, Liquan [Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084 (China); Lab of Advanced Power Sources, Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); Guo, Daojun; Zhu, Wentao [Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084 (China)

    2009-03-01

    Carbon nanotubes used as supports for platinum catalysts deposited with metal oxides (CeO{sub 2}, TiO{sub 2}, and SnO{sub 2}) were prepared for their application as anode catalysts in a direct methanol fuel cell. Cyclic voltammetry, chronoamperometry, and electrochemical impedance spectroscopy measurements were carried out in a solution of 0.5 M CH{sub 3}OH and 0.5 M H{sub 2}SO{sub 4}. Catalysts with the addition of CeO{sub 2}, TiO{sub 2}, and SnO{sub 2} presented higher catalytic activity than pure platinum catalysts, and the catalysts with CeO{sub 2} were the best among them. Electrochemical impedance spectra indicated that methanol electrooxidation on these catalysts had different impedance behaviors at different potential regions. The mechanism of methanol electrooxidation changed with increases of the potential. The promotion effect of the metal oxides lies in the oxidation of intermediate CO{sub ads} on Pt at low potential regions. (author)

  4. Copper-based electrochemical sensor with palladium electrode for cathodic stripping voltammetry of manganese.

    Science.gov (United States)

    Kang, Wenjing; Pei, Xing; Bange, Adam; Haynes, Erin N; Heineman, William R; Papautsky, Ian

    2014-12-16

    In this work, we report on the development of a palladium-based, microfabricated point-of-care electrochemical sensor for the determination of manganese using square wave cathodic stripping voltammetry. Heavy metals require careful monitoring, yet current methods are too complex for a point-of-care system. Voltammetry offers an attractive approach to metal detection on the microscale, but traditional carbon, gold, or platinum electrodes are difficult or expensive to microfabricate, preventing widespread use. Our sensor uses palladium working and auxiliary electrodes and integrates them with a copper-based reference electrode for simple fabrication and compatibility with microfabrication and printed circuit board processing, while maintaining competitive performance in electrochemical detection. Copper electrodes were prepared on glass substrate using a combination of microfabrication procedures followed by electrodeposition of palladium. The disposable sensor system was formed by bonding a poly(dimethylsiloxane) (PDMS) well to the glass substrate. Cathodic stripping voltammetry of manganese using our new disposable palladium-based sensors exhibited 334 nM (18.3 ppb) limit of detection in borate buffer. The sensor was used to demonstrate manganese determination in natural water samples from a pond in Burnet Woods, located in Cincinnati, OH, and the Ohio River.

  5. Electrochemical impedance of poly(9-tosyl-9H-carbazole-co-pyrrole) electrocoated carbon fiber

    Energy Technology Data Exchange (ETDEWEB)

    Ates, Murat; Uludag, Nesimi [Department of Chemistry, Faculty of Arts and Sciences, Namik Kemal University, Degirmenalti Campus, 59030, Tekirdag (Turkey); Sarac, A. Sezai, E-mail: sarac@itu.edu.tr [Department of Chemistry, Polymer Science and Technology, Istanbul Technical University, Maslak, 34469, Istanbul (Turkey)

    2011-05-16

    Research highlights: {yields} Impedance study of poly(9-tosyl-9H-carbazole-co-pyrrole) electrocoated carbon fiber. {yields} Copolymer of 9-tosyl-9H-carbazole and pyrrole were electrocoated on carbon fiber. {yields} Impedance spectroscopy and circuit models of poly(9-tosyl-9H-carbazole-co-pyrrole). - Abstract: In this paper, copolymer of 9-tosyl-9H-carbazole (TCz) and pyrrole (Py) comonomers were electrochemically deposited onto carbon fiber micro electrode (CFME) as an active electrode material. An electrochemical impedance study on the prepared electrodes is reported. Poly(TCz-co-Py)/CFME is characterized by cyclic voltammetry (CV), Fourier transform infrared reflectance-attenuated total reflection spectroscopy (FTIR-ATR), scanning electron microscopy-energy dispersive X-ray analysis (SEM-EDX), and electrochemical impedance spectroscopy (EIS). Capacitive behaviors of modified CFMEs were defined via Nyquist, Bode-magnitude and Bode-phase plots. An examination is made of which equivalent circuits of R(C(R(Q(RW)))) and R(C(R(Q(RW))))(CR) used for modeling the system. The effect of monomer ratio (mole fraction, X{sub TCz} = n{sub TCz}/n{sub TCz} + n{sub Py}) on the formation of copolymer is reported in 0.1 M sodium perchlorate (NaClO{sub 4})/acetonitrile (ACN) solution. The inclusion of TCz in the copolymer structure was also confirmed by FTIR-ATR, SEM, and CV measurements. The highest low frequency capacitance (C{sub LF} = 22.7 for R(C(R(Q(RW)))) and C{sub LF} = 22.6 mF cm{sup -2} for R(C(R(Q(RW))))(CR)) were obtained for X{sub TCz} = 0.91.

  6. Tunable nanogap devices for ultra-sensitive electrochemical impedance biosensing.

    Science.gov (United States)

    Lu, Yong; Guo, Zheng; Song, Jing-Jing; Huang, Qin-An; Zhu, Si-Wei; Huang, Xing-Jiu; Wei, Yan

    2016-01-28

    A wealth of research has been available discussing nanogap devices for detecting very small quantities of biomolecules by observing their electrical behavior generally performed in dry conditions. We report that a gold nanogapped electrode with tunable gap length for ultra-sensitive detection of streptavidin based on electrochemical impedance technique. The gold nanogap is fabricated using simple monolayer film deposition and in-situ growth of gold nanoparticles in a traditional interdigitated array (IDA) microelectrode. The electrochemical impedance biosensor with a 25-nm nanogap is found to be ultra-sensitive to the specific binding of streptavidin to biotin. The binding of the streptavidin hinder the electron transfer between two electrodes, resulting in a large increase in electron-transfer resistance (Ret) for operating the impedance. A linear relation between the relative Ret and the logarithmic value of streptavidin concentration is observed in the concentration range from 1 pM (picomolar) to 100 nM (nanomolar). The lowest detectable concentration actually measured reaches 1 pM. We believe that such an electrochemical impedance nanogap biosensor provides a useful approach towards biomolecular detection that could be extended to a number of other systems.

  7. Reconstruction of relaxation time distribution from linear electrochemical impedance spectroscopy

    Science.gov (United States)

    Zhang, Yanxiang; Chen, Yu; Yan, Mufu; Chen, Fanglin

    2015-06-01

    Linear electrochemical impedance spectroscopy (EIS), and in particular its representation of distribution of relaxation time (DRT), enables the identification of the number of processes and their nature involved in electrochemical cells. With the advantage of high frequency resolution, DRT has recently drawn increasing attention for applications in solid oxide fuel cells (SOFCs). However, the method of DRT reconstruction is not yet presented clearly in terms of what mathematical treatments and theoretical assumptions have been made. Here we present unambiguously a method to reconstruct DRT function of impedance based on Tikhonov regularization. By using the synthetic impedances and analytic DRT functions of RQ element, generalized finite length Warburg element, and Gerischer element with physical quantities representative to those of SOFC processes, we show that the quality of DRT reconstruction is sensitive to the sampling points per decade (ppd) of frequency from the impedance measurement. The robustness of the DRT reconstruction to resist noise imbedded in impedance data and numerical calculations can be accomplished by optimizing the weighting factor λ according to well defined criterion.

  8. Electrochemical impedance analysis of perovskite–electrolyte interfaces

    Energy Technology Data Exchange (ETDEWEB)

    Li, Zhen; Mercado, Candy C.; Yang, Mengjin; Palay, Ethan; Zhu, Kai

    2017-01-01

    Flat band potentials and carrier densities of spin coated and sprayed MAPbI3, FA0.85Cs0.15PbI3, and MAPbBr3 perovskite films were determined using the Mott-Schottky relation. The films developed a space charge layer and exhibited p-type conduction with carrier concentration ~ 1016 cm-3 for spin coated films. Electrochemical impedance spectra showed typical space charge impedance at frequencies > 1 kHz with increasing capacitance < 1 kHz owing to an ion diffusion component.

  9. Dynamic electrochemical impedance spectroscopy reconstructed from continuous impedance measurement of single frequency during charging/discharging

    Science.gov (United States)

    Huang, Jun; Li, Zhe; Zhang, Jianbo

    2015-01-01

    In this study, a novel implementation of dynamic electrochemical impedance spectroscopy (DEIS) is proposed. The method first measures the impedance continuously at a single frequency during one charging/discharging cycle, then repeats the measurement at a number of other selected frequencies. The impedance spectrum at a specific SOC is obtained by interpolating and collecting the impedance at all of the selected frequencies. The charge transfer resistance, Rct, from the DEIS is smaller than that from the steady EIS in a wide state-of-charge (SOC) range from 0.4 to 1.0, the Rct during charging is generally smaller than that during discharging for the battery chemistry used in this study.

  10. Characterization of an electrochemical mercury sensor using alternating current, cyclic, square wave and differential pulse voltammetry

    Energy Technology Data Exchange (ETDEWEB)

    Guerreiro, Gabriela V.; Zaitouna, Anita J.; Lai, Rebecca Y., E-mail: rlai2@unl.edu

    2014-01-31

    Graphical abstract: -- Highlights: •An electrochemical Hg(II) sensor based on T–Hg(II)–T sensing motif was fabricated. •A methylene blue-modified DNA probe was used to fabricate the sensor. •Sensor performance was evaluated using ACV, CV, SWV, and DPV. •The sensor behaves as a “signal-off” sensor in ACV and CV. •The sensor behaves as either a “signal-on” or “signal-off” sensor in SWV and DPV. -- Abstract: Here we report the characterization of an electrochemical mercury (Hg{sup 2+}) sensor constructed with a methylene blue (MB)-modified and thymine-containing linear DNA probe. Similar to the linear probe electrochemical DNA sensor, the resultant sensor behaved as a “signal-off” sensor in alternating current voltammetry and cyclic voltammetry. However, depending on the applied frequency or pulse width, the sensor can behave as either a “signal-off” or “signal-on” sensor in square wave voltammetry (SWV) and differential pulse voltammetry (DPV). In SWV, the sensor showed “signal-on” behavior at low frequencies and “signal-off” behavior at high frequencies. In DPV, the sensor showed “signal-off” behavior at short pulse widths and “signal-on” behavior at long pulse widths. Independent of the sensor interrogation technique, the limit of detection was found to be 10 nM, with a linear dynamic range between 10 nM and 500 nM. In addition, the sensor responded to Hg{sup 2+} rather rapidly; majority of the signal change occurred in <20 min. Overall, the sensor retains all the characteristics of this class of sensors; it is reagentless, reusable, sensitive, specific and selective. This study also highlights the feasibility of using a MB-modified probe for real-time sensing of Hg{sup 2+}, which has not been previously reported. More importantly, the observed “switching” behavior in SWV and DPV is potentially generalizable and should be applicable to most sensors in this class of dynamics-based electrochemical biosensors.

  11. On accurate differential measurements with electrochemical impedance spectroscopy

    CERN Document Server

    Kernbach, S; Kernbach, O

    2016-01-01

    This paper describes the impedance spectroscopy adapted for analysis of small electrochemical changes in fluids. To increase accuracy of measurements the differential approach with temperature stabilization of fluid samples and electronics is used. The impedance analysis is performed by the single point DFT, signal correlation, calculation of RMS amplitudes and interference phase shift. For test purposes the samples of liquids and colloids are treated by fully shielded electromagnetic generators and passive cone-shaped structures. Fluidic samples collected from different geological locations are also analysed. In all tested cases we obtained different results for impacted and non-impacted samples, moreover, a degradation of electrochemical stability after treatment is observed. This method is used in laboratory analysis of weak emissions and ensures a high repeatability of results.

  12. Evaluation of corrosion protection performance of poly(o-ethyl aniline) coated copper by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Shinde, Vandana, E-mail: vda_shinde@yahoo.co [Department of Physics, North Maharashtra University, Jalgaon 425 001 (India); Patil, Pradip P., E-mail: pnmu@yahoo.co.i [Department of Physics, North Maharashtra University, Jalgaon 425 001 (India)

    2010-04-15

    Poly(o-ethylaniline) coatings were synthesized on copper (Cu) by electrochemical polymerization of o-ethylaniline in an aqueous salicylate solution by using cyclic voltammetry. The performance of poly(o-ethylaniline) as protective coating against corrosion of Cu in aqueous 3% NaCl was assessed by the electrochemical impedance spectroscopy (EIS). The results of these studies demonstrate that the poly (o-ethylaniline) coating has ability to protect the Cu against corrosion. The corrosion inhibition efficiency of coating is found to be 97%. The evaluation of the impedance parameters with immersion time was studied and water uptake and delamination area were determined. The variation of the water uptake and delamination area with the immersion time provides further evidence to the protective action of the poly(o-ethylaniline).

  13. Characterization by electrochemical impedance spectroscopy of magnetite nanoparticles supported on carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez-Lopez, A.; Torres-Torres, D.; Mojica-Gomez, J.; Estrada-Arteaga, C. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, S. C., Parque Tecnologico Queretaro - Sanfandila, C.P. 76703, Pedro Escobedo, Queretaro (Mexico); Antano-Lopez, R., E-mail: rantano@cideteq.mx [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, S. C., Parque Tecnologico Queretaro - Sanfandila, C.P. 76703, Pedro Escobedo, Queretaro (Mexico)

    2011-09-30

    Magnetite nanoparticles were supported on carbon paste electrode and characterized by low scan rate voltammetry and electrochemical impedance spectroscopy (EIS) to obtain mechanistic information related to its oxidation and reduction in acid media. The voltammograms showed only one reduction and one oxidation peak for the supported magnetite, which were attributed to formation of ferrous ion and ferric oxide, respectively. Both peaks are fairly wide, indicating complex mechanisms. Using EIS, a mechanism showing up to three time constants, capacitive all of them, was evidenced, both in anodic and cathodic domain. These were attributed to charge transfer at the highest frequencies, adsorption of generated species at intermediate frequencies, and proton adsorption at low frequencies. Discussion about the nature of the adsorbed species and the concerned mechanism for each domain is developed.

  14. Electrochemical characterization of lithium ferrite electrodes through cyclic voltammetry and Raman spectra

    Energy Technology Data Exchange (ETDEWEB)

    Manley, M.; Cook, W. [Univ. of New Brunswick, Dept. of Chemical Engineering, Fredericton, New Brunswick (Canada)

    2013-07-01

    Lithium ferrite, a mixed spinel with the formula, Fe[Li{sub 0.5}Fe{sub 1.5}]O{sub 4} or LiFe{sub 5}O{sub 8}, has been synthesized and characterized in both its ordered (α) and disordered (β) phases. In an effort to scope the electrochemical activity lithium ferrite in lithium hydroxide solutions, the powders produced were compressed into pellets and tested with cyclic voltammetry and the surface of the electrodes were analyzed with laser Raman spectroscopy. Results of the initial electrochemical testing showed good correlation with Nernstian behavior and exhibited quasi-reversible behaviour. The redox mechanism involves the breakdown of lithium ferrite into hematite, a hybrid lithiated-hematite oxide and lithium ions under the alkaline conditions tested. By comparing the equilibrium potential of the redox process with proposed reaction schemes and examining the reaction products using the laser Raman microprobe, the proposed redox mechanism could be verified. (author)

  15. Signal Processing for the Impedance Measurement on an Electrochemical Generator

    Directory of Open Access Journals (Sweden)

    El-Hassane AGLZIM

    2008-04-01

    Full Text Available Improving the life time of batteries or fuel cells requires the optimization of components such as membranes and electrodes and enhancement of the flow of gases [1], [2]. These goals could be reached by using a real time measurement on loaded generator. The impedance spectroscopy is a new way that was recently investigated. In this paper, we present an electronic measurement instrumentation developed in our laboratory to measure and plot the impedance of a loaded electrochemical generator like batteries and fuel cells. Impedance measures were done according to variations of the frequency in a larger band than what is usually used. The electronic instrumentation is controlled by Hpvee® software which allows us to plot the Nyquist graph of the electrochemical generator impedance. The theoretical results obtained in simulation under Pspice® confirm the choice of the method and its advantage. For safety reasons, the experimental preliminary tests were done on a 12 V vehicle battery, having an input current of 330 A and a capacity of 40 Ah and are now extended to a fuel cell. The results were plotted at various nominal voltages of the battery (12.7 V, 10 V, 8 V and 5 V and with two imposed currents (0.6 A and 4 A. The Nyquist diagram resulting from the experimental data enable us to show an influence of the load of the battery on its internal impedance. The similitude in the graph form and in order of magnitude of the values obtained (both theoretical and practical enables us to validate our electronic measurement instrumentation. Different sensors (temperature, pressure were placed around the device under test (DUT. These influence parameters were permanently recorded. Results presented here concern a classic loaded 12 V vehicle battery. The Nyquist diagram resulting from the experimental data confirms the influence of the load of the DUT on its internal impedance.

  16. Impedance spectroscopy study of a catechol-modified activated carbon electrode as active material in electrochemical capacitor

    Science.gov (United States)

    Cougnon, C.; Lebègue, E.; Pognon, G.

    2015-01-01

    Modified activated carbon (Norit S-50) electrodes with electrochemical double layer (EDL) capacitance and redox capacitance contributions to the electric charge storage were tested in 1 M H2SO4 to quantify the benefit and the limitation of the surface redox reactions on the electrochemical performances of the resulting pseudo-capacitive materials. The electrochemical performances of an electrochemically anodized carbon electrode and a catechol-modified carbon electrode, which make use both EDL capacitance of the porous structure of the carbon and redox capacitance, were compared to the performances obtained for the pristine carbon. Nitrogen gas adsorption measurements have been used for studying the impact of the grafting on the BET surface area, pore size distribution, pore volume and average pore diameter. The electrochemical behavior of carbon materials was studied by cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The EIS data were discussed by using a complex capacitance model that allows defining the characteristic time constant, the global capacitance and the frequency at which the maximum charge stored is reached. The EIS measurements were achieved at different dc potential values where a redox activity occurs and the evolution of the capacitance and the capacitive relaxation time with the electrode potential are presented. Realistic galvanostatic charge/discharge measurements performed at different current rates corroborate the results obtained by impedance.

  17. Electrochemical Investigation of Coenzyme Q10 on Silver Electrode in Ethanol Aqueous Solution and Its Determination Using Differential Pulse Voltammetry.

    Science.gov (United States)

    Li, Dan; Deng, Wei; Xu, Hu; Sun, Yinxing; Wang, Yuhong; Chen, Shouhui; Ding, Xianting

    2016-08-01

    The electrochemistry reduction of coenzyme Q10 (CoQ10) on silver electrodes has been investigated in mixed solvent containing 95 vol. % ethanol and 5 vol. % water. A combination of cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) is employed to explore the mechanism of redox processes of CoQ10 in the presence and absence of oxygen, respectively. It has been proved that the redox reaction of CoQ10 is highly dependent on the oxygen in the solution compared with that of CoQ0, which may be attributed to the isoprenoid side chain effect of CoQ10 Moreover, the effects of experimental variables such as electrolyte component, pH, temperature, and sonication time on the amperometric and potentiometric responses of CoQ10 are presented. The differential pulse voltammetry method has been developed for the quantification of the CoQ10 in the complex samples. Under the optimum conditions, the method is linear over the concentration range of 1.00 × 10(-7) to 1.00 × 10(-3) mol/L (8.63 × 10(-2) to 8.63 × 10(2) mg/kg). The limit of detection (3σ/k) is 3.33 × 10(-8) mol/L (2.88 × 10(-2) mg/kg). The recoveries of the spiked samples are between 91% and 108%. The presented method can be applied to the analysis of CoQ10 in real samples without any pretreatment.

  18. Non-conductive nanomaterial enhanced electrochemical response in stripping voltammetry: The use of nanostructured magnesium silicate hollow spheres for heavy metal ions detection.

    Science.gov (United States)

    Xu, Ren-Xia; Yu, Xin-Yao; Gao, Chao; Jiang, Yu-Jing; Han, Dong-Dong; Liu, Jin-Huai; Huang, Xing-Jiu

    2013-08-06

    Nanostructured magnesium silicate hollow spheres, one kind of non-conductive nanomaterials, were used in heavy metal ions (HMIs) detection with enhanced performance for the first time. The detailed study of the enhancing electrochemical response in stripping voltammetry for simultaneous detection of ultratrace Cd(2+), Pb(2+), Cu(2+) and Hg(2+) was described. Electrochemical properties of modified electrodes were characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The operational parameters which have influence on the deposition and stripping of metal ions, such as supporting electrolytes, pH value, and deposition time were carefully studied. The anodic stripping voltammetric performance toward HMIs was evaluated using square wave anodic stripping voltammetry (SWASV) analysis. The detection limits achieved (0.186nM, 0.247nM, 0.169nM and 0.375nM for Cd(2+), Pb(2+), Cu(2+) and Hg(2+)) are much lower than the guideline values in drinking water given by the World Health Organization (WHO). In addition, the interference and stability of the modified electrode were also investigated under the optimized conditions. An interesting phenomenon of mutual interference between different metal ions was observed. Most importantly, the sensitivity of Pb(2+) increased in the presence of certain concentrations of other metal ions, such as Cd(2+), Cu(2+) and Hg(2+) both individually and simultaneously. The proposed electrochemical sensing method is thus expected to open new opportunities to broaden the use of SWASV in analysis for detecting HMIs in the environment. Copyright © 2013 Elsevier B.V. All rights reserved.

  19. Time-domain fitting of battery electrochemical impedance models

    Science.gov (United States)

    Alavi, S. M. M.; Birkl, C. R.; Howey, D. A.

    2015-08-01

    Electrochemical impedance spectroscopy (EIS) is an effective technique for diagnosing the behaviour of electrochemical devices such as batteries and fuel cells, usually by fitting data to an equivalent circuit model (ECM). The common approach in the laboratory is to measure the impedance spectrum of a cell in the frequency domain using a single sine sweep signal, then fit the ECM parameters in the frequency domain. This paper focuses instead on estimation of the ECM parameters directly from time-domain data. This may be advantageous for parameter estimation in practical applications such as automotive systems including battery-powered vehicles, where the data may be heavily corrupted by noise. The proposed methodology is based on the simplified refined instrumental variable for continuous-time fractional systems method ('srivcf'), provided by the Crone toolbox [1,2], combined with gradient-based optimisation to estimate the order of the fractional term in the ECM. The approach was tested first on synthetic data and then on real data measured from a 26650 lithium-ion iron phosphate cell with low-cost equipment. The resulting Nyquist plots from the time-domain fitted models match the impedance spectrum closely (much more accurately than when a Randles model is assumed), and the fitted parameters as separately determined through a laboratory potentiostat with frequency domain fitting match to within 13%.

  20. Electrochemical Impedance Spectroscopy to Characterize Inflammatory Atherosclerotic Plaques

    Science.gov (United States)

    Yu, Fei; Dai, Xiaohu; Beebe, Tyler; Hsiai, Tzung

    2011-01-01

    Despite advances in diagnosis and therapy, atherosclerotic cardiovascular disease remains the leading cause of morbidity and mortality in the Western world. Predicting metabolically active atherosclerotic lesions has remained an unmet clinical need. We hereby developed an electrochemical strategy to characterize the inflammatory states of high-risk atherosclerotic plaques. Using the concentric bipolar microelectrodes, we sought to demonstrate distinct Electrochemical Impedance Spectroscopic (EIS) measurements for unstable atherosclerotic plaques that harbored active lipids and inflammatory cells. Using equivalent circuits to simulate vessel impedance at the electrode-endoluminal tissue interface, we demonstrated specific electric elements to model working and counter electrode interfaces as well as the tissue impedance. Using explants of human coronary, carotid, and femoral arteries at various Stary stages of atherosclerotic lesions (n = 15), we performed endoluminal EIS measurements (n = 147) and validated with histology and immunohistochemistry. We computed the vascular tissue resistance using the equivalent circuit model and normalized the resistance to the lesion-free regions. Tissue resistance was significantly elevated in the oxLDL-rich thin-cap atheromas (1.57±0.40, n = 14, p 0.05). Hence, we demonstrate that the application of EIS strategy was sensitive to detect fibrous cap oxLDL-rich lesions and specific to distinguish oxLDL-absent fibroatheroma. PMID:21959227

  1. Organic electrochemical transistors for cell-based impedance sensing

    Energy Technology Data Exchange (ETDEWEB)

    Rivnay, Jonathan, E-mail: rivnay@emse.fr, E-mail: owens@emse.fr; Ramuz, Marc; Hama, Adel; Huerta, Miriam; Owens, Roisin M., E-mail: rivnay@emse.fr, E-mail: owens@emse.fr [Department of Bioelectronics, Ecole des Mines de St. Etienne, 13541 Gardanne (France); Leleux, Pierre [Department of Bioelectronics, Ecole des Mines de St. Etienne, 13541 Gardanne (France); Microvitae Technologies, Pole d' Activite Y. Morandat, 13120 Gardanne (France)

    2015-01-26

    Electrical impedance sensing of biological systems, especially cultured epithelial cell layers, is now a common technique to monitor cell motion, morphology, and cell layer/tissue integrity for high throughput toxicology screening. Existing methods to measure electrical impedance most often rely on a two electrode configuration, where low frequency signals are challenging to obtain for small devices and for tissues with high resistance, due to low current. Organic electrochemical transistors (OECTs) are conducting polymer-based devices, which have been shown to efficiently transduce and amplify low-level ionic fluxes in biological systems into electronic output signals. In this work, we combine OECT-based drain current measurements with simultaneous measurement of more traditional impedance sensing using the gate current to produce complex impedance traces, which show low error at both low and high frequencies. We apply this technique in vitro to a model epithelial tissue layer and show that the data can be fit to an equivalent circuit model yielding trans-epithelial resistance and cell layer capacitance values in agreement with literature. Importantly, the combined measurement allows for low biases across the cell layer, while still maintaining good broadband signal.

  2. Organic electrochemical transistors for cell-based impedance sensing

    Science.gov (United States)

    Rivnay, Jonathan; Ramuz, Marc; Leleux, Pierre; Hama, Adel; Huerta, Miriam; Owens, Roisin M.

    2015-01-01

    Electrical impedance sensing of biological systems, especially cultured epithelial cell layers, is now a common technique to monitor cell motion, morphology, and cell layer/tissue integrity for high throughput toxicology screening. Existing methods to measure electrical impedance most often rely on a two electrode configuration, where low frequency signals are challenging to obtain for small devices and for tissues with high resistance, due to low current. Organic electrochemical transistors (OECTs) are conducting polymer-based devices, which have been shown to efficiently transduce and amplify low-level ionic fluxes in biological systems into electronic output signals. In this work, we combine OECT-based drain current measurements with simultaneous measurement of more traditional impedance sensing using the gate current to produce complex impedance traces, which show low error at both low and high frequencies. We apply this technique in vitro to a model epithelial tissue layer and show that the data can be fit to an equivalent circuit model yielding trans-epithelial resistance and cell layer capacitance values in agreement with literature. Importantly, the combined measurement allows for low biases across the cell layer, while still maintaining good broadband signal.

  3. Sensorless battery temperature measurements based on electrochemical impedance spectroscopy

    Science.gov (United States)

    Raijmakers, L. H. J.; Danilov, D. L.; van Lammeren, J. P. M.; Lammers, M. J. G.; Notten, P. H. L.

    2014-02-01

    A new method is proposed to measure the internal temperature of (Li-ion) batteries. Based on electrochemical impedance spectroscopy measurements, an intercept frequency (f0) can be determined which is exclusively related to the internal battery temperature. The intercept frequency is defined as the frequency at which the imaginary part of the impedance is zero (Zim = 0), i.e. where the phase shift between the battery current and voltage is absent. The advantage of the proposed method is twofold: (i) no hardware temperature sensors are required anymore to monitor the battery temperature and (ii) the method does not suffer from heat transfer delays. Mathematical analysis of the equivalent electrical-circuit, representing the battery performance, confirms that the intercept frequency decreases with rising temperatures. Impedance measurements on rechargeable Li-ion cells of various chemistries were conducted to verify the proposed method. These experiments reveal that the intercept frequency is clearly dependent on the temperature and does not depend on State-of-Charge (SoC) and aging. These impedance-based sensorless temperature measurements are therefore simple and convenient for application in a wide range of stationary, mobile and high-power devices, such as hybrid- and full electric vehicles.

  4. Characterization of antimicrobial peptide activity by electrochemical impedance spectroscopy

    Science.gov (United States)

    Chang, William K.; Wimley, William C.; Searson, Peter C.; Hristova, Kalina; Merzlyakov, Mikhail

    2008-01-01

    Summary Electrochemical impedance spectroscopy performed on surface-supported bilayer membranes allows for the monitoring of changes in membrane properties, such as thickness, ion permeability, and homogeneity, after exposure to antimicrobial peptides (AMPs). We show that two model cationic peptides, very similar in sequence but different in activity, induce dramatically different changes in membrane properties as probed by impedance spectroscopy. Moreover, the impedance results excluded the “barrel-stave” and the “toroidal pore” models of AMP mode of action, and are more consistent with the “carpet” and the “detergent” models. The impedance data provide important new insights about the kinetics and the scale of the peptide action which currently are not addressed by the “carpet” and the “detergent” models. The method presented not only provides additional information about the mode of action of a particular AMP, but offers a means of characterizing AMP activity in reproducible, well-defined quantitative terms. PMID:18657512

  5. Interpretation of electrochemical impedance spectroscopy (EIS) circuit model for soils

    Institute of Scientific and Technical Information of China (English)

    韩鹏举; 张亚芬; 陈幼佳; 白晓红

    2015-01-01

    Based on three different kinds of conductive paths in microstructure of soil and theory of electrochemical impedance spectroscopy (EIS), an integrated equivalent circuit model and impedance formula for soils were proposed, which contain 6 meaningful resistance and reactance parameters. Considering the conductive properties of soils and dispersion effects, mathematical equations for impedance under various circuit models were deduced and studied. The mathematical expression presents two semicircles for theoretical EIS Nyquist spectrum, in which the center of one semicircle is degraded to simply the equivalent model. Based on the measured parameters of EIS Nyquist spectrum, meaningful soil parameters can easily be determined. Additionally, EIS was used to investigate the soil properties with different water contents along with the mathematical relationships and mechanism between the physical parameters and water content. Magnitude of the impedance decreases with the increase of testing frequency and water content for Bode graphs. The proposed model would help us to better understand the soil microstructure and properties and offer more reasonable explanations for EIS spectra.

  6. Electrochemical Studies of Betti Base and Its Copper(II Complex by Cyclic and Elimination Voltammetry

    Directory of Open Access Journals (Sweden)

    Shardul Bhatt

    2013-01-01

    Full Text Available The electrochemical behavior of Betti base 1-(α-amino benzyl-2-naphthol (BB and its copper(II complex by cyclic and elimination voltammetry (EVLS is reported in the present study. The cyclic voltammetric studies carried out at a glassy carbon working electrode, Ag/Ag+ reference electrode (0.01 M AgNO3 in acetonitrile in DCM at 100 mV/sec, 200 mV/sec, and 400 mV/sec scan rates indicated a preceding chemical oxidation of the adsorbed BB species to form an iminium ion followed by formation of a carbanion via two-step quasireversible reduction. The suggested reaction mechanism has been supported by the elimination voltammetry. The CV and EVLS studies revealed Cu(IIBB complex to undergo a chemical or a surface reaction before electron transfer from the electrode at −0.49 V to form Cu(IBB species. The oxidation of Cu(IBB species has been observed to be CV silent.

  7. Application of Electrochemical Impedance Spectroscopy in the Evaluation of Corrosion and Cathodic Protection in Reinforced Concrete

    NARCIS (Netherlands)

    Koleva, D.A.; Van Breugel, K.; De Wit, J.H.W.; Fraaij, A.L.A.; Boshkov, N.

    2007-01-01

    The electrochemical behavior of steel reinforcement in conditions of corrosion and cathodic protection (CP) was studied, using electrochemical impedance spectroscopy (EIS) and compared to reference (non-corroding) conditions. Polarization resistance (PR) method and potentio-dynamic polarization (PDP

  8. Botulinum Neurotoxin Serotypes Detected by Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Savage, Alison C.; Buckley, Nicholas; Halliwell, Jennifer; Gwenin, Christopher

    2015-01-01

    Botulinum neurotoxin is one of the deadliest biological toxins known to mankind and is able to cause the debilitating disease botulism. The rapid detection of the different serotypes of botulinum neurotoxin is essential for both diagnosis of botulism and identifying the presence of toxin in potential cases of terrorism and food contamination. The modes of action of botulinum neurotoxins are well-established in literature and differ for each serotype. The toxins are known to specifically cleave portions of the SNARE proteins SNAP-25 or VAMP; an interaction that can be monitored by electrochemical impedance spectroscopy. This study presents a SNAP-25 and a VAMP biosensors for detecting the activity of five botulinum neurotoxin serotypes (A–E) using electrochemical impedance spectroscopy. The biosensors are able to detect concentrations of toxins as low as 25 fg/mL, in a short time-frame compared with the current standard methods of detection. Both biosensors show greater specificity for their compatible serotypes compared with incompatible serotypes and denatured toxins. PMID:25954998

  9. Botulinum Neurotoxin Serotypes Detected by Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Alison C. Savage

    2015-05-01

    Full Text Available Botulinum neurotoxin is one of the deadliest biological toxins known to mankind and is able to cause the debilitating disease botulism. The rapid detection of the different serotypes of botulinum neurotoxin is essential for both diagnosis of botulism and identifying the presence of toxin in potential cases of terrorism and food contamination. The modes of action of botulinum neurotoxins are well-established in literature and differ for each serotype. The toxins are known to specifically cleave portions of the SNARE proteins SNAP-25 or VAMP; an interaction that can be monitored by electrochemical impedance spectroscopy. This study presents a SNAP-25 and a VAMP biosensors for detecting the activity of five botulinum neurotoxin serotypes (A–E using electrochemical impedance spectroscopy. The biosensors are able to detect concentrations of toxins as low as 25 fg/mL, in a short time-frame compared with the current standard methods of detection. Both biosensors show greater specificity for their compatible serotypes compared with incompatible serotypes and denatured toxins.

  10. Detection of parathyroid hormone using an electrochemical impedance biosensor based on PAMAM dendrimers.

    Science.gov (United States)

    Özcan, Hakkı Mevlüt; Sezgintürk, Mustafa Kemal

    2015-01-01

    This paper presents a novel hormone-based impedimetric biosensor to determine parathyroid hormone (PTH) level in serum for diagnosis and monitoring treatment of hyperparathyroidism, hypoparathyroidism and thyroid cancer. The interaction between PTH and the biosensor was investigated by an electrochemical method. The biosensor was based on the gold electrode modified by 12-mercapto dodecanoic (12MDDA). Antiparathyroid hormone (anti-PTH) was covalently immobilized on to poly amidoamine dendrimer (PAMAM) which was bound to a 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide/N-hydroxysuccinimide (EDC/NHS) couple, self-assembled monolayer structure from one of the other NH2 sites. The immobilization of anti-PTH was monitored by electrochemical impedance spectroscopy, cyclic voltammetry and scanning electron microscope techniques. After the optimization studies of immobilization materials such as 12MDDA, EDC-NHS, PAMAM, and glutaraldehyde, the performance of the biosensor was investigated in terms of linearity, sensitivity, repeatability, and reproducibility. PTH was detected within a linear range of 10-60 fg/mL. Finally the described biosensor was used to monitor PTH levels in artificial serum samples.

  11. Electrochemical analysis of the alanine phenylthiohydantoin derivative by cathodic stripping voltammetry.

    Science.gov (United States)

    Vilaseca, C; Quintana, M C; Vicente, J; Hernández, P; Hernández, L

    2008-08-01

    A square-wave cathodic stripping voltammetry method for alanine determination as its phenylthiohydantoin (PTH-alanine) derivative is developed. To this end, all the chemical and instrumental variables affecting the determination of PTH-alanine are optimized. From studies of the mechanisms governing the electrochemical response of PTH-alanine, it was concluded that it is an electrochemically irreversible system with a diffusive-adsorptive reduction phenomenon. Under optimal conditions, the variation of analytical signal (I(p)) with PTH-alanine concentration is linear in the 2.4x10(-8)-4.8x10(-7) M range, with a LOD of 1.2x10(-8) M and a LOQ of 4.2x10(-8) M, a RSD (%) less than 11%, and a E(r) (%) less than 10%. The optimized method was applied to the determination of PTH-alanine obtained from a synthetic protein after Edman reaction and the results were corroborated by high-performance liquid chromatography with UV detection.

  12. Electrochemical Impedance Spectroscopy to Assess Vascular Oxidative Stress

    Science.gov (United States)

    Yu, Fei; Li, Rongsong; Ai, Lisong; Edington, Collin; Yu, Hongyu; Barr, Mark; Kim, E. S.; Hsiai, Tzung K.

    2012-01-01

    Vascular inflammatory responses are intimately linked with oxidative stress, favoring the development of pre-atherosclerotic lesions. We proposed that oxidized low density lipoprotein (oxLDL) and foam cell infiltrates in the subendothelial layer engendered distinct electrochemical properties that could be measured in terms of the electrochemical impedance spectroscopy (EIS). Concentric bipolar microelectrodes were applied to interrogate EIS of aortas isolated from fat-fed New Zealand White (NZW) rabbits and explants of human aortas. Frequency-dependent EIS measurements were assessed between 10 kHz and 100 kHz, and were significantly elevated in the pre-atherosclerotic lesions in which oxLDL and macrophage infiltrates were prevalent (At 100 kHz: aortic arch lesion = 26.7 ± 2.7 kΩ vs. control = 15.8 ± 2.4 kΩ; at 10 kHz: lesions = 49.2 ± 7.3 kΩ vs. control = 27.6 ± 2.7 kΩ, n = 10, p<0.001). Similarly, EIS measurements were significantly elevated in the human descending aorta where pre-atherosclerotic lesions or fatty streaks were prominent. EIS measurements remained unchanged in spite of various depths of electrode submersion or orientation of the specimens. Hence, the concentric bipolar microelectrodes provided a reliable means to measure endoluminal electrochemical modifications in regions of pro-inflammatory with high spatial resolution and reproducibility albeit uneven lesion topography and non-uniform current distribution. PMID:20652746

  13. Analysis by electrochemical impedance spectroscopy of new MCFC cathode materials

    Science.gov (United States)

    Pérez, F. J.; Duday, D.; Hierro, M. P.; Gómez, C.; Romero, M.; Casais, M. T.; Alonso, J. A.; Martínez, M. J.; Daza, L.

    The corrosion and electrochemical behaviours of Li 1- xNi 1+ xO 2 and Li 1- x(Ni yCo 1- y) 1+ xO 2 oxides were investigated in a molten carbonate electrolyte at 650°C and compared with a NiO reference cathode material. These oxides are future candidate cathode materials for molten carbonate fuel cell (MCFC) and are divided in two families: monophasic oxides and biphasic oxides. The monophasic oxides show an important dissolution or a lower catalytic activity and are not good candidates for future use in MCFC. The biphasic oxides show a low dissolution and a good catalytic efficiency close to the NiO value. In this first study of new cathode materials by electrochemical impedance spectroscopy (EIS), it appears that the biphasic Li-Ni-Co-O oxides are the best candidates for MCFC. The MCFC electrochemical cathodic mechanism, taking into account the peroxide and the superoxide pathways and the O 2-, CO 2 and H 2O diffusion proposed in the bibliography [I. Uchida, T. Nishina, Y. Mugikura, K. Itaya, J. Electroanal. Chem., 206 (1986) 229; C. Yuh, J.R. Selman, AIChE J., 34(12) (1988) 1949; T. Nishina, I. Uchida, Proc. Symp. Molten Carbonate Fuel Cell Technol., The Electrochem. Soc., PV90-16 (1990) 438; T. Nishina, G. Lindbergh, T. Kudo, I. Uchida, The International Fuel Cell Conference Proceedings, NEDO (1992) 189-192], is used to discuss the EIS results. The limiting rate of the peroxide or/and superoxide reactions of the new oxides was compared with the NiO reference oxide.

  14. Mapping Electrochemical Heterogeneity at Iron Oxide Surfaces: A Local Electrochemical Impedance Study.

    Science.gov (United States)

    Lucas, Marie; Boily, Jean-François

    2015-12-22

    Alternating current scanning electrochemical microscopy (AC-SECM) was used for the first time to map key electrochemical attributes of oriented hematite (α-Fe2O3) single crystal surfaces at the micron-scale. Localized electrochemical impedance spectra (LEIS) of the (001) and (012) faces provided insight into the spatial variations of local double layer capacitance (C(dl)) and charge transfer resistance (R(ad)). These parameters were extracted by LEIS measurements in the 0.4-8000 Hz range to probe the impedance response generated by the redistribution of water molecules and charge carriers (ions) under an applied AC. These were attributed to local variations in the local conductivity of the sample surfaces. Comparison with global EIS measurements on the same samples uncovered highly comparable frequency-resolved processes, that were broken down into contributions from the bulk hematite, the interface as well as the microelectrode/tip assembly. This work paves the way for new studies aimed at mapping electrochemical processes at the mesoscale on this environmentally and technologically important material.

  15. Electrochemical Studies of 1,4-Bis[2-(2-pyridyl)-vinyl] Benzene and 1,4-Bis[2-(4-pyridyl) vinyl] Benzene Laser Dyes via Cyclic Voltammetry, Convolutive Voltammetry and Digital Simulation Methods

    Institute of Scientific and Technical Information of China (English)

    EL-DALY, Samy A; EL-HALLAG,Ibrahirn S; EBEED, Ezeiny M; GHONEIM, Mohamed M

    2009-01-01

    Electrochemical properties of two diolefinic laser dyes namely 1,4-bis[2-(2-pyddyl)-vinyl] benzene (2PVB) and 1,4-bis[2-(4-pyridyl) vinyl] benzene (4PVB) have been investigated using cyclic voltammetry and convolutive voltammetry combined with digital simulation at a platinum electrode in 0.1 mol/L tetrabutyl ammonium perchlo-rate (TBAP) in the two different solvents acetonitrile (CH3CN) and dimethylformamide (DMF). The species were reduced via consumption of two sequential electrons to form radical anion and dianion. In switching the potential to positive direction, the two compounds were oxidized by loss of one electron, which was followed by a fast isomeri-sation process. The electrode reaction pathway and the electrochemical parameters of the investigated compounds were determined using cyclic voltammetry. The extracted electrochemical parameters were verified and confirmed via digital simulation and convolutive voltammetry methods.

  16. Alternating current(AC) corrosion analyzed by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Ha, Tae Hyun; Kim, Dae Kyeong; Bae, Jeong Hyo; Lee, Hyun Goo; Lee, Sung Jin [Korea Electrotechnology Research Institute, Changwon (Korea, Republic of)

    2002-12-15

    So far, many research results on AC corrosion have been reported but each one is not consistent with another. In order to understand the characteristics and factors affecting on AC corrosion, Electrochemical impedance spectroscopy (E.I.S) was used and changes in kinetics and surface properties was analyzed. Generally, E.I.S. test has been used mainly for the diagnosis of the concrete corrosion and coating material. However, considering the outstanding functions of E.I.S. test, it can be adopted as a good method to study AC corrosion. Electrolyte resistance (R{sub sol}), double layer capacitance (C{sub dl}) and polarization resistance (R{sub p}) are the basic circuit elements. Using the model which is consist of these basic elements, various results of E.I.S. test can be interpreted. And through this method the mechanism and characteristics of AC corrosion can be explained

  17. Electrochemical impedance spectroscopy study on corrosion inhibition of benzyltriethylammonium chloride

    Science.gov (United States)

    Idris, Mohd Nazri; Daud, Abdul Razak; Othman, Norinsan Kamil

    2013-11-01

    Electrochemical Impedance Spectroscopy (EIS) was employed to study the corrosion inhibition behavior of benzyltriethylammonium chloride (BTC) for carbon steel corrosion. The inhibition efficiency was investigated in 1.0 M HCl solution at room temperature (25°C) by varying the BTC concentration. EIS results indicated that the double layer capacitance of electrolyte/carbon steel interface decreases with the increasing of BTC concentration and consequently enhances the polarization resistance of equivalence Randles circuit. The results indicated that inhibition efficiency of as high as 65% could be achieved when 10mM BTC was present in 1.0 M HCl solution as compared to inhibitor-free solution. The inhibition process of BTC on the carbon steel corrosion was found to obey Langmuir adsorption isotherm. This study revealed that BTC is suitable to be used as a corrosion inhibitor in acid media.

  18. The application of electrochemical impedance spectroscopy for characterizing the degradation of Ni(OH)2/NiOOH electrodes

    Science.gov (United States)

    Macdonald, D. D.; Pound, B. G.; Lenhart, S. J.

    1989-01-01

    Electrochemical impedance spectra of rolled and bonded and sintered porous nickel battery electrodes were recorded periodically during charge/discharge cycling in concentrated KOH solution at various temperatures. A transmission line model (TLM) was adopted to represent the impedance of the porous electrodes, and various model parameters were adjusted in a curve fitting routine to reproduce the experimental impedances. Degradation processes for rolled and bonded electrodes were deduced from changes in model parameters with electrode cycling time. In developing the TLM, impedance spectra of planar (non-porous) electrodes were used to represent the pore wall and backing plate interfacial impedances. These data were measured over a range of potentials and temperatures, and an equivalent circuit model was adopted to represent the planar electrode data. Cyclic voltammetry was used to study the characteristics of the oxygen evolution reaction on planar nickel electrodes during charging, since oxygen evolution can affect battery electrode charging efficiency and ultimately electrode cycle life if the overpotential for oxygen evolution is sufficiently low. Transmission line modeling results suggest that porous rolled and bonded nickel electrodes undergo restructuring during charge/discharge cycling prior to failure.

  19. Pore Characteristics of Chitosan Scaffolds Studied by Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Tully-Dartez, Stephanie; Cardenas, Henry E.

    2010-01-01

    In this study, a novel approach, electrochemical impedance spectroscopy (EIS), was used to examine the pore characteristics of chitosan scaffolds under aqueous conditions. The EIS was run with a constant current of 0.1 mA with the frequency sweep of 106 to 10−4 Hz. The resulting complex impedance measurement was then used to calculate porosity, which was determined to be 71%. Scanning electron microscopy (SEM) and mercury intrusion porosimetry (MIP), two commonly used methods for scaffold characterization, were used to independently evaluate the pore characteristics and compare with that of EIS. The SEM and MIP were performed and analyzed under standard conditions. The pore diameter values found by SEM and MIP are 107 μm and 82 μm, respectively, indicating that both the image-based (SEM) and pressure-based (MIP) analyses provide similar results. The porosity of 73% calculated by MIP is comparable to that of EIS. From these results, it can be suggested that EIS, a relatively nondestructive test, is able to obtain comparable data on pore characteristics, as compared to SEM and MIP. The advantage of the EIS as an nondestructive test is that it can be performed under physiologically relevant conditions, whereas SEM and MIP require dry samples and vacuum conditions for measurement. These benefits make EIS a viable option for the characterization and long-term observation of tissue-engineered scaffolds. PMID:19580421

  20. Simulating Linear Sweep Voltammetry from First-Principles: Application to Electrochemical Oxidation of Water on Pt(111) and Pt3Ni(111)

    DEFF Research Database (Denmark)

    Viswanathan, Venkatasubramanian; Hansen, Heine Anton; Rossmeisl, Jan

    2012-01-01

    Cyclic voltammetry is a fundamental experimental method for characterizing adsorbates on electrochemical surfaces. We present a model for the electrochemical solid–liquid interface, and we simulate the linear sweep voltammogram of the electrochemical oxidation of H2O on Pt(111) and Pt3Ni(111...

  1. Electrochemical Protease Biosensor Based on Enhanced AC Voltammetry Using Carbon Nanofiber Nanoelectrode Arrays.

    Science.gov (United States)

    Swisher, Luxi Z; Syed, Lateef U; Prior, Allan M; Madiyar, Foram R; Carlson, Kyle R; Nguyen, Thu A; Hua, Duy H; Li, Jun

    2013-02-28

    We report an electrochemical method for measuring the activity of proteases using nanoelectrode arrays (NEAs) fabricated with vertically aligned carbon nanofibers (VACNFs). The VACNFs of ~150 nm in diameter and 3 to 5 μm in length were grown on conductive substrates and encapsulated in SiO2 matrix. After polishing and plasma etching, controlled VACNF tips are exposed to form an embedded VACNF NEA. Two types of tetrapeptides specific to cancer-mediated proteases legumain and cathepsin B are covalently attached to the exposed VACNF tip, with a ferrocene (Fc) moiety linked at the distal end. The redox signal of Fc can be measured with AC voltammetry (ACV) at ~1 kHz frequency on VACNF NEAs, showing distinct properties from macroscopic glassy carbon electrodes due to VACNF's unique interior structure. The enhanced ACV properties enable the kinetic measurements of proteolytic cleavage of the surface-attached tetrapeptides by proteases, further validated with a fluorescence assay. The data can be analyzed with a heterogeneous Michaelis-Menten model, giving "specificity constant" kcat /Km as (4.3 ± 0.8) × 10(4) M(-1)s(-1) for cathepsin B and (1.13 ± 0.38) × 10(4) M(-1)s(-1) for legumain. This method could be developed as portable multiplex electronic techniques for rapid cancer diagnosis and treatment monitoring.

  2. Characterization and evaluation of Pt-Ru catalyst supported on multi-walled carbon nanotubes by electrochemical impedance

    Energy Technology Data Exchange (ETDEWEB)

    Ocampo, A.L.; Miranda-Hernandez, M.; Sebastian, P.J. [Centro de Investigacion en Energia-UNAM, Temixco, 62580 Morelos (Mexico); Morgado, J.; Montoya, J.A. [IMP, Eje Central Lazaro Cardenas 152, 07730 D.F. Mexico (Mexico)

    2006-10-06

    In this work the authors present the results of a systematic characterization and evaluation of the carbon nanotube supported Pt-Ru (Pt-Ru/CNT) for its use as methanol oxidation catalyst. Its activity was compared with that of Pt and Pt-Ru catalysts supported on Vulcan and synthesized from carbonyl precursors, and another commercial Pt-Ru catalyst. The cyclic voltammetry, CO stripping and electrochemical impedance techniques were employed to determine the electrocatalytic activity of the catalysts. The electrochemical studies were performed in 0.5M H{sub 2}SO{sub 4} containing different concentrations of methanol (0.05-1M). The results showed a noticeable influence of the catalyst support (CNT) on the performance of the catalyst for CO oxidation. The electrochemical impedance studies allowed us to separate the different steps in the methanol oxidation reaction and to control these steps or reactions by varying the applied potential and the methanol concentration. At low methanol concentration and potentials the de-hydrogenation of methanol predominated. But, at high potential and methanol concentrations, the CO oxidation predominated. These results allowed us to clearly describe at what potential and concentration ranges the bi-functional effect of Ru becomes evident. Our results indicated that the CO oxidation occurs both on Pt and Ru. Compared to other catalysts, Pt-Ru supported on carbon nanotubes showed superior catalytic activity for CO and methanol oxidation. (author)

  3. Electrochemical Deposition of Si-Ca/P on Nanotube Formed Beta Ti Alloy by Cyclic Voltammetry Method.

    Science.gov (United States)

    Jeong, Yong-Hoon; Choe, Han-Cheol

    2015-08-01

    The purpose of this study was to investigate electrochemical deposition of Si-Ca/P on nanotube formed Ti-35Nb-10Zr alloy by cyclic voltammetry method. Electrochemical deposition of Si substituted Ca/P was performed by pulsing the applied potential on nanotube formed surface. The surface characteristics were observed by field-emission scanning electron microscopy, X-ray diffractometer, and potentiodynamic polarization test. The phase structure and surface morphologies of Si-Ca/P deposition were affected by deposition cycles. From the anodic polarization test, nanotube formed surface at 20 V showed the high corrosion resistance with lower value of Icorr, I300, and Ipass.

  4. Electrochemical impedance spectroscopy on nanostructured carbon electrodes grown by supersonic cluster beam deposition

    Energy Technology Data Exchange (ETDEWEB)

    Bettini, Luca Giacomo; Bardizza, Giorgio; Podesta, Alessandro; Milani, Paolo; Piseri, Paolo, E-mail: piseri@mi.infn.it [Universita degli Studi di Milano, Dipartimento di Fisica and CIMaINa (Italy)

    2013-02-15

    Nanostructured porous films of carbon with density of about 0.5 g/cm{sup 3} and 200 nm thickness were deposited at room temperature by supersonic cluster beam deposition (SCBD) from carbon clusters formed in the gas phase. Carbon film surface topography, determined by atomic force microscopy, reveals a surface roughness of 16 nm and a granular morphology arising from the low kinetic energy ballistic deposition regime. The material is characterized by a highly disordered carbon structure with predominant sp2 hybridization as evidenced by Raman spectroscopy. The interface properties of nanostructured carbon electrodes were investigated by cyclic voltammetry and electrochemical impedance spectroscopy employing KOH 1 M solution as aqueous electrolyte. An increase of the double layer capacitance is observed when the electrodes are heat treated in air or when a nanostructured nickel layer deposited by SCBD on top of a sputter deposited film of the same metal is employed as a current collector instead of a plain metallic film. This enhancement is consistent with an improved charge injection in the active material and is ascribed to the modification of the electrical contact at the interface between the carbon and the metal current collector. Specific capacitance values up to 120 F/g have been measured for the electrodes with nanostructured metal/carbon interface.

  5. A Multilayer MEMS Platform for Single-Cell Electric Impedance Spectroscopy and Electrochemical Analysis

    Science.gov (United States)

    Dittami, Gregory M.; Ayliffe, H. Edward; King, Curtis S.; Rabbitt, Richard D.

    2008-01-01

    The fabrication and characterization of a microchamber electrode array for electrical and electrochemical studies of individual biological cells are presented. The geometry was tailored specifically for measurements from sensory hair cells isolated from the cochlea of the mammalian inner ear. Conventional microelectromechanical system (MEMS) fabrication techniques were combined with a heat-sealing technique and polydimethylsiloxane micromolding to achieve a multilayered microfluidic system that facilitates cell manipulation and selection. The system allowed for electrical stimulation of individual living cells and interrogation of excitable cell membrane dielectric properties as a function of space and time. A three-electrode impedimetric system was incorporated to provide the additional ability to record the time-dependent concentrations of specific biochemicals in microdomain volumes near identified regions of the cell membrane. The design and fabrication of a robust fluidic and electrical interface are also described. The interface provided the flexibility and simplicity of a “cartridge-based” approach in connecting to the MEMS devices. Cytometric measurement capabilities were characterized by using electric impedance spectroscopy (1 kHz–10 MHz) of isolated outer hair cells. Chemical sensing capability within the microchannel recording chamber was characterized by using cyclic voltammetry with varying concentrations of potassium ferricyanide (K3Fe(CN)6). Chronoamperometric recordings of electrically stimulated PC12 cells highlight the ability of the platform to resolve exocytosis events from individual cells. PMID:19756255

  6. Detection of 1,5-Anhydroglucitol by Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Adamson, Teagan L.; Cook, Curtiss B.

    2014-01-01

    Multiple markers are used to assess glycemic control in patients with diabetes mellitus (DM). New technology that permits simultaneous detection of multiple biomarkers combined with those used at the point of care indicative of glycemic control, including glycemic variability determined from 1,5-anhydroglucitol measurement, could provide better management and further insight into the disease. This platform was based on previous research involving glucose detection and uses electrochemical impedance spectroscopy to detect a range of 1,5-anhydroglucitol concentrations at an optimal binding frequency. The enzyme pyranose oxidase was fixed to gold electrodes while a sine wave of sweeping frequencies was induced in purified solutions and in variable presence of whole blood. The optimal binding frequency for the detection of 1,5-anhydroglucitol was found to be 3.71 kHz. The impedance response compared to the concentration of target present was found to have a logarithmic slope of 7.04 with an R-squared value of 0.96. This response includes 2 experimental sets, a single test of a low concentration range and a high concentration range with 5 replicates. The relative standard deviation of the high range varied from 28% to 27% from lowest to highest concentrations. Best detection in complex solutions was found in lower blood concentrations of 0.5% and 1%, but maintained relatively high accuracy in concentrations 5% and 10%. The sensor platform was successfully evaluated at a high dynamic range of 1,5-AG in purified solutions. In the presence of whole blood, lowest percentages yielded the best results indicating that filtering interferents may be necessary in final device architecture. PMID:24876587

  7. Fast voltammetry of metals at carbon-fiber microelectrodes: copper adsorption onto activated carbon aids rapid electrochemical analysis.

    Science.gov (United States)

    Pathirathna, Pavithra; Samaranayake, Srimal; Atcherley, Christopher W; Parent, Kate L; Heien, Michael L; McElmurry, Shawn P; Hashemi, Parastoo

    2014-09-21

    Rapid, in situ trace metal analysis is essential for understanding many biological and environmental processes. For example, trace metals are thought to act as chemical messengers in the brain. In the environment, some of the most damaging pollution occurs when metals are rapidly mobilized and transported during hydrologic events (storms). Electrochemistry is attractive for in situ analysis, primarily because electrodes are compact, cheap and portable. Electrochemical techniques, however, do not traditionally report trace metals in real-time. In this work, we investigated the fundamental mechanisms of a novel method, based on fast-scan cyclic voltammetry (FSCV), that reports trace metals with sub-second temporal resolution at carbon-fiber microelectrodes (CFMs). Electrochemical methods and geochemical models were employed to find that activated CFMs rapidly adsorb copper, a phenomenon that greatly advances the temporal capabilities of electrochemistry. We established the thermodynamics of surface copper adsorption and the electrochemical nature of copper deposition onto CFMs and hence identified a unique adsorption-controlled electrochemical mechanism for ultra-fast trace metal analysis. This knowledge can be exploited in the future to increase the sensitivity and selectivity of CFMs for fast voltammetry of trace metals in a variety of biological and environmental models.

  8. Electrochemical Impedance Spectroscopic Sensing of Methamphetamine by a Specific Aptamer

    Directory of Open Access Journals (Sweden)

    Omid Mashinchian

    2012-05-01

    Full Text Available Introduction: Electrochemical impedance spectroscopy (EIS is a simple and highly sensitive technique that can be used for evaluation of the aptamer-target interaction even in a label-free approach. Methods: To pursue the effectiveness of EIS, in the current study, the folding properties of specific aptamer for methamphetamine (METH (i.e., aptaMETH were evaluated in the presence of METH and amphetamine (Amph. Folded and unfolded aptaMETH was mounted on the gold electrode surface and the electron charge transfer was measured by EIS. Results: The Ret of methamphetamine-aptaMETH was significantly increased in comparison with other folding conditions, indicating specific detection of METH by aptaMETH. Conclusion: Based on these findings, methamphetamine-aptaMETH on the gold electrode surface displayed the most interfacial electrode resistance and thus the most folding situation. This clearly indicates that the aptaMETH can profoundly and specifically pinpoint METH; as a result we suggest utilization of this methodology for fast and cost-effective identification of METH.

  9. Electrochemical Impedance Spectroscopic Sensing of Methamphetamine by a Specific Aptamer

    Science.gov (United States)

    Ebrahimi, Mohsen; Johari-Ahar, Mohammad; Hamzeiy, Hossein; Barar, Jaleh; Mashinchian, Omid; Omidi, Yadollah

    2012-01-01

    Introduction Electrochemical impedance spectroscopy (EIS) is a simple and highly sensitive technique that can be used for evaluation of the aptamer-target interaction even in a label-free approach. Methods To pursue the effectiveness of EIS, in the current study, the folding properties of specific aptamer for methamphetamine (METH) (i.e., aptaMETH) were evaluated in the presence of METH and amphetamine (Amph). Folded and unfolded aptaMETH was mounted on the gold electrode surface and the electron charge transfer was measured by EIS. Results The Ret of methamphetamine-aptaMETH was significantly increased in comparison with other folding conditions, indicating specific detection of METH by aptaMETH. Conclusion Based on these findings, methamphetamine-aptaMETH on the gold electrode surface displayed the most interfacial electrode resistance and thus the most folding situation. This clearly indicates that the aptaMETH can profoundly and specifically pinpoint METH; as a result we suggest utilization of this methodology for fast and cost-effective identification of METH. PMID:23678446

  10. Electrochemical impedance spectroscopy analysis of porous silicon prepared by photo-electrochemical etching: current density effect

    Science.gov (United States)

    Husairi, F. S.; Rouhi, J.; Eswar, K. A.; Zainurul, A. Z.; Rusop, M.; Abdullah, S.

    2014-09-01

    Electrical impedance characteristics of porous silicon nanostructures (PSiNs) in frequency function were studied. PSiNs were prepared through photo-electrochemical etching method at various current densities (15-40 mA/cm2) and constant etching time. The atomic force microscope images of PSiNs show that pore diameter and roughness increase when current density increases to 35 mA/cm2. The surface roughness subsequently decreases because of continuous etching of pillars, and a second etching process occurs. Photoluminescence spectra show blue and red shift with increasing applied current density that is attributed to PSiNs size. Variations of electrical resistance and capacitance values of PSiNs were measured using electrochemical impedance spectroscopy analysis. These results indicate that PSiNs prepared at 20 mA/cm2 current density have uniform porous structures with a large number of pillars. Furthermore, this PSiNs structure influences large values of charge transfer resistance and double layer capacitance, indicating potential application in sensors.

  11. Multiparametric characterisation of metal-chalcogen atomic multilayer assembly by potentiodynamic electrochemical impedance spectroscopy

    NARCIS (Netherlands)

    Ragoisha, G.A.; Bondarenko, A.S.; Osipovich, N.P.; Rabchynski, S.M.; Streltsov, E.A.

    2008-01-01

    An approach to multiparametric characterisation of variable electroactive interfaces based on potentiodynamic electrochemical impedance spectroscopy (PDEIS) [G.A. Ragoisha, A.S. Bondarenko, Electrochim. Acta 50 (2005) 1553] has been extended to atomic multilayer assembly monitoring. The multilayers

  12. Electrochemical study of stainless steels used in an oil company by electrochemical impedance

    Energy Technology Data Exchange (ETDEWEB)

    Boudinar, Y.; Chadli, H. [Laboratory of Physical Metallurgy and Materials Properties (LMPPM), University of Annaba, Annaba (Algeria); Innal, F. [University of Bordeaux/IMS-LAPS, Talence (France); Belmokre, K. [Laboratory of Corrosion and Surface Treatment (LCTS), University of Skikda, Skikda (Algeria)

    2010-07-15

    Localized corrosion is a serious problem for stainless steel exposed in a chloride solution. In this context, the present work concerns the study of electrochemical behavior of 316 (A and B) and 430 (C and D) stainless steels, where A and C are laboratory steels, while steels B and D were taken from heat exchangers tubes (after 10 years of operation). This study has addressed three different aqueous environments: (1) monoethanolamine (MEA) 15%, (2) natural seawater (NSW), and (3) NaCl 3%, using the technique of potentiodynamic polarization curve complemented by electrochemical impedance spectroscopy (EIS). The obtained experimental electrochemical parameters (E{sub corr}, J{sub corr}, E{sub r}, C{sub d}, R{sub tc}, and constant phase element) were used to compare the corrosion resistance of the tested steels. As a result, the nobility of these steels in NaCl 3% and in MEA 15% solutions is established in the following order: 316 (A) > 316 (B) > 430 (C) > 430 (D), where E{sub r} moves increasingly toward the positive direction, indicating a good protection against corrosion. In addition, the results show that the effect of the electrolyte (aggression) is characterized by increased corrosion potential and a decrease in the passivity domain for all samples. The hierarchy of the nobility of steels A and C in these electrolytes can be determined as follows: MEA 15% > NSW > NaCl 3%. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  13. Electrode materials for lithium-ion batteries characterized by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Schweikert, N.; Indris, S. [Karlsruher Institut fuer Technologie (KIT), Karlsruhe (Germany); Krueger, S.; Roling, B. [Marburg Univ. (Germany)

    2010-07-01

    In order to characterize the electrochemical properties of Li{sub 4}Ti{sub 5}O{sub 12} electrochemical impedance spectroscopy (EIS) was used. Long-term measurements were performed in order to identify interfacial reactions, loss mechanisms and degradation processes. By performing impedance measurements at different Li contents, the dependency on the state-of-charge (SOC) of the Li/Li{sub 4+x}Ti{sub 5}O{sub 12} battery was investigated. (orig.)

  14. An Electrochemical Impedance Spectroscopy Investigation of the Overpotentials in Li−O2 Batteries

    DEFF Research Database (Denmark)

    Højberg, Jonathan; McCloskey, Bryan D.; Hjelm, Johan;

    2015-01-01

    Lithium−O2 (Li−O2) batteries are currently limited by a large charge overpotential at practically relevant current densities, and the origin of this overpotential has been heavily debated in the literature. This paper presents a series of electrochemical impedance measurements suggesting...... in this paper are used to develop the understanding of the electrochemical impedance, which will be important for further improvement of the Li−air battery....

  15. Electrochemical impedance study of self-assembled layer-by-layer iron-silicotungstate/poly(ethylenimine) modified electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Fernandes, Diana M. [Department of Chemistry/CICECO, University of Aveiro, 3810-193 Aveiro (Portugal); Ghica, Mariana E. [Department of Chemistry, Faculty of Science and Technology, University of Coimbra, 3004-535 Coimbra (Portugal); Cavaleiro, Ana M.V. [Department of Chemistry/CICECO, University of Aveiro, 3810-193 Aveiro (Portugal); Brett, Christopher M.A., E-mail: brett@ci.uc.p [Department of Chemistry, Faculty of Science and Technology, University of Coimbra, 3004-535 Coimbra (Portugal)

    2011-09-30

    Electrochemical impedance spectroscopy (EIS) has been used to study multilayer films containing anionic iron-substituted silicotungstate [SiW{sub 11}Fe{sup III}(H{sub 2}O)O{sub 39}]{sup 5-} (SiW{sub 11}Fe) and positively charged poly(ethylenimine) self-assembled by the layer-by-layer method on glassy carbon and indium tin oxide electrodes. The effect of the charge of the outermost layer of the multilayer assembly on the electron transfer of soluble species was studied using the redox probes [Fe(CN){sub 6}]{sup 3-} and [Ru(NH{sub 3}){sub 6}]{sup 3+}; cyclic voltammetry indicating that the surface charge has a significant effect on the process. EIS demonstrated that the electrostatic attraction or repulsion between the surface and the redox probes plays a significant role. Analysis of the impedance spectra showed that the charge transfer resistance increases with an increasing number of bilayers for both redox probes and that the porosity of the multilayer film, which varies with the electrode substrate, also has a significant effect on the electrochemical response.

  16. Electrochemical Impedance of Ethanol Oxidation in Alkaline Media

    Institute of Scientific and Technical Information of China (English)

    DANAEE Iman; JAFARIAN Majid; GOBAL Fereydoon; SHARAFI Mahboobeh; MAHJANI Mohammad-ghasem

    2012-01-01

    Nickel modified NiOOH electrodes were used for the electrocatalytic oxidation of ethanol in alkaline solutions.The electro-oxidation of ethanol in a 1 mol/L NaOH solution at different concentrations of ethanol was studied by ac impedance spectroscopy.Electrooxidation of ethanol on Ni shows negative resistance on impedance plots.The impedance shows different patterns at different applied anodic potential.The influence of the electrode potential on impedance was studied and a quantitative explanation for the impedance of ethanol oxidation was given by means of a proposed mathematical model.At potentials higher than 0.52 V(vs.Ag/AgCl),a pseudoinductive behavior was observed,but at those higher than 0.57 V,impedance patterns were reversed to the second and third quadrants.The conditions required for the reversing of impedance pattern were delineated with the impedance model.

  17. Comparison of the stem-loop and linear probe-based electrochemical DNA sensors by alternating current voltammetry and cyclic voltammetry.

    Science.gov (United States)

    Yang, Weiwei; Lai, Rebecca Y

    2011-12-06

    Here we systematically characterized the sensor performance of the stem-loop probe (SLP) and linear probe (LP) electrochemical DNA sensors using alternating current voltammetry (ACV) and cyclic voltammetry (CV), with the goal of generating the set of operational criteria that best suits each sensor architecture, in addition to elucidating the signaling mechanism behind these sensors. Although the LP sensor shows slightly better % signal suppression (SS) upon hybridization with the perfect match target at 10 Hz, our frequency-dependent study suggests that it shows optimal % SS only in a very limited AC frequency range. Similar results are observed in CV studies in which the LP sensor, when compared to the SLP sensor, displays a narrower range of voltammetric scan rates where the optimal % SS can be achieved. More importantly, the difference between the two sensors' performance is particularly pronounced if the change in integrated charge (Q) upon target hybridization, rather than the peak current (I), is measured in CV. The temperature-dependent study further highlights the differences between the two sensors, where the LP sensor, owing to the flexible linear probe architecture, is more readily perturbed by temperature changes. Both SLP and LP sensors, however, show a loss of % SS when operated at elevated temperatures, despite the significant improvement in the hybridization kinetics. In conjunction with the ACV, CV, and temperature-dependent studies, the electron-transfer kinetics study provides further evidence in support of the proposed signaling mechanism of these two sensors, in which the SLP sensor's signaling efficiency and sensor performance is directly linked to the hybridization-induced conformational change in the redox-labeled probe, whereas the performance of the LP sensor relies on the hybridization-induced change in probe dynamics. © 2011 American Chemical Society

  18. An Electrochemical Impedance Study of the Capacity Limitations in Na–O2 Cells

    DEFF Research Database (Denmark)

    Knudsen, Kristian Bastholm; Nichols, Jessica E.; Vegge, Tejs

    2016-01-01

    Electrochemical impedance spectroscopy, pressure change measurements, and scanning electron microscopy were used to investigate the nonaqueous Na–O2 cell potential decrease and rise (sudden deaths) on discharge and charge, respectively. To fit the impedance spectra from operating cells, an equiva...

  19. Direct Electrochemical Evidence of the Dissociation and Adsorption Behavior of Acetonitrile at Gold Electrodes by Ultrafast Voltammetry

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Ultrafast cyclic voltammetry was used to study the redox behavior of a gold electrode in acetonitrile. The direct electrochemical evidence of the dissociation and adsorption behavior of acetonitrile at gold electrodes was found. It could be stated that two consecutive redox paths are involved, each with a special adsorption state acting as the reaction intermediate. The mean value,obtained of the electron-transfer rate constant of the second path, was 1.3 × 105 s-1 with a standard deviation of 0.24 × 105 s-1.

  20. Ageing of electrochromic WO{sub 3} coatings characterized by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Pehlivan, Esat; Niklasson, Gunnar A.; Granqvist, Claes-Goeran [Department of Engineering Sciences, Aangstroem Laboratory, Uppsala University, P. O. Box 534, 751 21 Uppsala (Sweden); Georen, Peter [ChromoGenics AB, Maerstagatan 4, 753 23 Uppsala (Sweden)

    2010-07-15

    We have developed a method for characterization of ageing of electrochromic materials by electrochemical impedance spectroscopy (EIS). Electrochromic WO{sub 3} thin films have been electrochemically cycled in propionic acid electrolyte and probed by EIS and optical measurements. A very small amount of optical degradation was observed in both the bleached and coloured states. The samples exhibited a few hundred times higher impedance in the bleached state than in the coloured state. It was observed that, in the bleached state, impedance values at low frequencies increased significantly with increasing number of cycles. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  1. Electrochemical Dopamine Detection: Comparing Gold and Carbon Fiber Microelectrodes using Background Subtracted Fast Scan Cyclic Voltammetry

    OpenAIRE

    Zachek, Matthew K.; Hermans, Andre; Wightman, R. Mark; McCarty, Gregory S.

    2008-01-01

    Electrochemical detection is becoming increasingly important for the detection of biological species. Most current biological research with electrochemical detection is done with carbon fiber electrodes due to their many beneficial properties. The ability to build electrochemical sensor from noble metals instead of carbon fibers may be beneficial in developing inexpensive multiplexed electrochemical detection schemes. To advance understanding and to test the feasibility of using noble metal e...

  2. Single-Use Disposable Electrochemical Label-Free Immunosensor for Detection of Glycated Hemoglobin (HbA1c) Using Differential Pulse Voltammetry (DPV).

    Science.gov (United States)

    Molazemhosseini, Alireza; Magagnin, Luca; Vena, Pasquale; Liu, Chung-Chiun

    2016-07-01

    A single-use disposable in vitro electrochemical immunosensor for the detection of HbA1c in undiluted human serum using differential pulse voltammetry (DPV) was developed. A three-electrode configuration electrochemical biosensor consisted of 10-nm-thin gold film working and counter electrodes and a thick-film printed Ag/AgCl reference electrode was fabricated on a polyethylene terephthalate (PET) substrate. Micro-fabrication techniques including sputtering vapor deposition and thick-film printing were used to fabricate the biosensor. This was a roll-to-roll cost-effective manufacturing process making the single-use disposable in vitro HbA1c biosensor a reality. Self-assembled monolayers of 3-Mercaptopropionic acid (MPA) were employed to covalently immobilize anti-HbA1c on the surface of gold electrodes. Electrochemical impedance spectroscopy (EIS) and X-ray photoelectron spectroscopy (XPS) confirmed the excellent coverage of MPA-SAM and the upward orientation of carboxylic groups. The hindering effect of HbA1c on the ferricyanide/ferrocyanide electron transfer reaction was exploited as the HbA1c detection mechanism. The biosensor showed a linear range of 7.5-20 µg/mL of HbA1c in 0.1 M PBS. Using undiluted human serum as the test medium, the biosensor presented an excellent linear behavior (R² = 0.999) in the range of 0.1-0.25 mg/mL of HbA1c. The potential application of this biosensor for in vitro measurement of HbA1c for diabetic management was demonstrated.

  3. Insight into the electroreduction of nitrate ions at a copper electrode, in neutral solution, after determination of their diffusion coefficient by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Aouina, Nizar; Cachet, Hubert [Laboratoire Interfaces et Systemes Electrochimiques - UPR15 du CNRS, Universite Pierre et Marie Curie - Paris 6, 4, place Jussieu, F-75005 Paris (France); Debiemme-chouvy, Catherine, E-mail: catherine.debiemme-chouvy@upmc.f [Laboratoire Interfaces et Systemes Electrochimiques - UPR15 du CNRS, Universite Pierre et Marie Curie - Paris 6, 4, place Jussieu, F-75005 Paris (France); Tran, Thi Tuyet Mai [Laboratoire Interfaces et Systemes Electrochimiques - UPR15 du CNRS, Universite Pierre et Marie Curie - Paris 6, 4, place Jussieu, F-75005 Paris (France)

    2010-10-01

    The electrochemical reduction of nitrate ions at a copper electrode in an unbuffered neutral aqueous solution is studied. Using a two compartment electrochemical cell, three stationary cathodic waves, noted P1, P2 and P3, were evidenced by cyclic voltammetry at -0.9, -1.2 and -1.3 V/SCE, respectively. By comparing the electrochemical response of nitrate and nitrite containing solutions, P1 was attributed to the reduction of nitrate to nitrite. In order to assign P2 and P3 features by determining the number of electrons involved at the corresponding potential, rotating disk electrode experiments at various rotation speeds, combined with linear sweep voltammetry, were performed. Current data analysis at a given potential was carried out using Koutecky-Levich treatment taking into account water reduction. Confident values of the diffusion coefficient D of nitrate ions were assessed by electrochemical impedance spectroscopy for nitrate concentrations of 10{sup -3}, 10{sup -2} and 10{sup -1} M. For a nitrate concentration of 10{sup -2} M, D was found to be 1.31 x 10{sup -5} cm{sup 2} s{sup -1} allowing the number of electrons to be determined as 6 for P2 and 8 for P3, in accordance with nitrate reduction into hydroxylamine and ammonia, respectively. The formation of hydroxylamine was confirmed by the observation of its reoxidation at a Pt microelectrode present at the Cu electrode/nitrate solution interface.

  4. An Electrochemical Impedance Spectroscopy Study on a Lithium Sulfur Pouch Cell

    DEFF Research Database (Denmark)

    Stroe, Daniel Loan; Knap, Vaclav; Swierczynski, Maciej Jozef;

    2016-01-01

    The impedance behavior of a 3.4 Ah pouch Lithium-Sulfur cell was extensively characterized using the electrochemical impedance spectroscopy (EIS) technique. EIS measurements were performed at various temperatures and over the entire state-of-charge (SOC) interval without applying a superimposed DC...... current. The obtained results have revealed a high dependency of the pouch cell’s impedance spectrum on the operating conditions. An equivalent electrical circuit was proposed to further analyze the results and to quantify the contributions of different resistances to the total impedance of the Li-S pouch...

  5. 1,4-Di-N-oxide quinoxaline-2-carboxamide: Cyclic voltammetry and relationship between electrochemical behavior, structure and anti-tuberculosis activity

    OpenAIRE

    Moreno-Viguri, E. (Elsa); Perez-Silanes, S. (Silvia); Gouravaram, S. (S.); Macharam, A. (Abinav); Ancizu, S. (Saioa); Torres, E; Aldana, I.; Monge, A; Crawford, P.W. (Philip W.)

    2011-01-01

    To gain insight into the mechanism of action, the redox properties of 37 quinoxaline-2-carboxamide 1,4-di-N-oxides with varying degrees of anti-tuberculosis activity were studied in dimethylformamide (DMF) using cyclic voltammetry and first derivative cyclic voltammetry. For all compounds studied, electrochemical reduction in DMF is consistent with the reduction of the N-oxide functionality to form a radical anion. The influence of molecular structure on reduction potential is addressed and i...

  6. A kinetic study of ferrocenium cation decomposition utilizing an integrated electrochemical methodology composed of cyclic voltammetry and amperometry.

    Science.gov (United States)

    Singh, Archana; Chowdhury, Debarati Roy; Paul, Amit

    2014-11-21

    A novel, easy, quick, and inexpensive integrated electrochemical methodology composed of cyclic voltammetry and amperometry has been developed for the determination of the kinetic stability of higher oxidation states for inorganic complexes. In this study, ferrocene and its derivatives have been used as model systems and the corresponding ferrocenium cations were generated in situ during the electrochemical experiments to determine their kinetic stabilities. The study found that the ferrocenium cations decompose following the first-order kinetics at 27 ± 3 °C in the presence of ambient oxygen and water. The half-lives of the ferrocenium, carboxylate ferrocenium, and decamethyl ferrocenium cations were found to be 1.27 × 10(3), 1.52 × 10(3), and ≫11.0 × 10(3) s, respectively, in acetonitrile solvent having a 0.5 M tetrabutylammonium hexafluorophosphate electrolyte. These results are in agreement with the previous reports, i.e. the ferrocenium cation is unstable whereas the decamethyl ferrocenium cation has superior stability. The new methodology has been established by performing various experiments using different concentrations of ferrocene, variable scan rates in cyclic voltammetry, different time periods for amperometry, and in situ spectroelectrochemical experiments.

  7. The Influence of Nanopore Dimensions on the Electrochemical Properties of Nanopore Arrays Studied by Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Krishna Kant

    2014-11-01

    Full Text Available The understanding of the electrochemical properties of nanopores is the key factor for better understanding their performance and applications for nanopore-based sensing devices. In this study, the influence of pore dimensions of nanoporous alumina (NPA membranes prepared by an anodization process and their electrochemical properties as a sensing platform using impedance spectroscopy was explored. NPA with four different pore diameters (25 nm, 45 nm and 65 nm and lengths (5 μm to 20 μm was used and their electrochemical properties were explored using different concentration of electrolyte solution (NaCl ranging from 1 to 100 μM. Our results show that the impedance and resistance of nanopores are influenced by the concentration and ion species of electrolytes, while the capacitance is independent of them. It was found that nanopore diameters also have a significant influence on impedance due to changes in the thickness of the double layer inside the pores.

  8. The Influence of Nanopore Dimensions on the Electrochemical Properties of Nanopore Arrays Studied by Impedance Spectroscopy

    Science.gov (United States)

    Kant, Krishna; Priest, Craig; Shapter, Joe G.; Losic, Dusan

    2014-01-01

    The understanding of the electrochemical properties of nanopores is the key factor for better understanding their performance and applications for nanopore-based sensing devices. In this study, the influence of pore dimensions of nanoporous alumina (NPA) membranes prepared by an anodization process and their electrochemical properties as a sensing platform using impedance spectroscopy was explored. NPA with four different pore diameters (25 nm, 45 nm and 65 nm) and lengths (5 μm to 20 μm) was used and their electrochemical properties were explored using different concentration of electrolyte solution (NaCl) ranging from 1 to 100 μM. Our results show that the impedance and resistance of nanopores are influenced by the concentration and ion species of electrolytes, while the capacitance is independent of them. It was found that nanopore diameters also have a significant influence on impedance due to changes in the thickness of the double layer inside the pores. PMID:25393785

  9. Electrochemical behaviour of iron in a third-generation ionic liquid: cyclic voltammetry and micromachining investigations.

    Science.gov (United States)

    Moustafa, Essam M; Mann, Olivier; Fürbeth, Wolfram; Schuster, Rolf

    2009-12-07

    The electrochemical behaviour of Fe in 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([Emim](+)Ntf2(-)) and mixtures with Cl(-) is studied with the aim of investigating the applicability of ionic liquids (IL) for the electrochemical machining of iron. Whereas in pure IL iron could not be significantly dissolved, the addition of Cl(-) enables the active dissolution with anodic current densities up to several mA cm(-2). Although several anodic peaks appear in the cyclic voltammograms (CV), the distinct assignment of those electrochemical processes remain difficult. In particular no proof for the formation of FeCl(x) (2-x) complexes during Fe dissolution are deduced from the CV, although such complexes are shown to be stable in the employed electrolyte. In addition, we present electrochemical drilling experiments with short potential pulses, which demonstrate that electrochemical machining of Fe is, in principle, possible in IL based electrolytes, even though hampered by slow machining speed.

  10. A novel immunosensor based on immobilization of hepatitis B surface antibody on platinum electrode modified colloidal gold and polyvinyl butyral as matrices via electrochemical impedance spectroscopy.

    Science.gov (United States)

    Tang, Dianping; Yuan, Ruo; Chai, Yaqin; Dai, Jianyuan; Zhong, Xia; Liu, Yan

    2004-12-01

    Hepatitis B surface antibody (HBsAb) was immobilized to the surface of platinum electrode modified with colloidal gold and polyvinyl butyral (PVB) as matrices to detect hepatitis B surface antigen (HBsAg) via electrochemical impedance spectroscopy (EIS). The electrochemical measurements of cyclic voltammetry and impedance spectroscopy showed that K(4)[Fe(CN)(6)]/K(3)[Fe(CN)(6)] reactions on the platinum electrode surface were blocked due to the procedures of self-assembly of HBsAb-Au-PVB. The binding of a specific HBsAb to HBsAg recognition layer could be detected by measurements of the impedance change. A new strategy was introduced for improving the sensitivity of impedance measurements via the large specific surface area and high surface free energy of Au nanoparticles and the encapsulated effect of polyvinyl butyral. The results showed that this strategy caused dramatic improvement of the detection sensitivity of HBsAg and had good linear response to detect HBsAg in the range of 20-160 ng.ml(-1) with a detection limit of 7.8 ng.ml(-1). Moreover, the studied immunosensor exhibited high sensitivity and long-term stability.

  11. Electrochemical Impedance Spectroscopy Investigation of the Anodic Functionalities and Processes in LSCM-CGO-Ni Systems

    KAUST Repository

    Boulfrad, Samir

    2015-07-17

    Electrochemical impedance spectroscopy was used to characterize anode compositions made of (La0.75Sr0.25)0.97Cr0.5Mn0.5O3 (LSCM) and gadolinia doped ceria (CGO) with and without additional submicron Ni, or exsoluted Ni nanoparticles. In addition, the effects of the anode gas flow rate and the working temperature were investigated. Higher content of the ionic conductor leads to a decrease of the impedance in the frequency range from 100 Hz to 10 Hz. The effect of the catalyst component was investigated while keeping the electronic conductivity unchanged in the tested materials. Enhanced catalytic activity was demonstrated to considerably decrease the impedance especially in the frequency range between 100 Hz to 1 Hz. The change in the gas flow rate affects mainly the impedance bellow 1 Hz. © The Electrochemical Society.

  12. Use of Electrochemical Impedance Spectroscopy (EIS to monitoring the corrosion of reinforced concrete

    Directory of Open Access Journals (Sweden)

    D.V. RIBEIRO

    Full Text Available AbstractElectrochemical techniques are among the most commonly techniques used for the evaluation and study of corrosion in reinforced concrete, including electrochemical impedance spectroscopy (EIS. Electrochemical impedance spectroscopy (EIS is a powerful technique for characterizing a wide variety of electrochemical systems and for determining the contribution of electrode or electrolytic processes in these systems. The analysis of EIS results on samples of concrete is highly complex due to overlapping arcs from simultaneous phenomena and noise measurement, of course, associated with the heterogeneity of the samples and that complicate the analysis considerably. Thus, this paper proposes a new form of analysis based on the characteristic relaxation angular frequency, w, of each phenomenon and associating the typical capacitances and frequencies.

  13. Study on the Carbonation Behavior of Cement Mortar by Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Biqin Dong

    2014-01-01

    Full Text Available A new electrochemical model has been carefully established to explain the carbonation behavior of cement mortar, and the model has been validated by the experimental results. In fact, it is shown by this study that the electrochemical impedance behavior of mortars varies in the process of carbonation. With the cement/sand ratio reduced, the carbonation rate reveals more remarkable. The carbonation process can be quantitatively accessed by a parameter, which can be obtained by means of the electrochemical impedance spectroscopy (EIS-based electrochemical model. It has been found that the parameter is a function of carbonation depth and of carbonation time. Thereby, prediction of carbonation depth can be achieved.

  14. Electrochemical impedance spectroscopy study of a surface confined redox reaction: The reduction of azobenzene on mercury in the absence of diffusion

    Energy Technology Data Exchange (ETDEWEB)

    Prieto, Francisco, E-mail: dapena@us.es [Department of Physical Chemistry, University of Seville, c/Profesor Garcia Gonzalez no 2, 41012 Seville (Spain); Rueda, Manuela; Hidalgo, Jose; Martinez, Elisa; Navarro, Inmaculada [Department of Physical Chemistry, University of Seville, c/Profesor Garcia Gonzalez no 2, 41012 Seville (Spain)

    2011-09-30

    The kinetics of azobenzene reduction on mercury electrodes in the absence of diffussional mass transport is studied by electrochemical impedance spectroscopy (EIS) in acetic acid/acetate buffered solutions at different pH values. Cyclic voltammetry experiments confirm the absence of diffusion effects and provide the values of the surface equilibrium potential. The analysis of the impedance frequency spectrums at every potential within the faradaic region conforms well the model and provides the global rate constant of the process, k{sub f}. The potential dependence of k{sub f} suggests the existence of an EE mechanism, with two electron transfers controlling the overall rate. The kinetic parameters of every step are obtained and their pH dependences clarify the role played by the protonation steps.

  15. Electrochemical Impedance Analysis of β-TITANIUM Alloys as Implants in Ringers Lactate Solution

    Science.gov (United States)

    Bhola, Rahul; Bhola, Shaily M.; Mishra, Brajendra; Olson, David L.

    2010-02-01

    Commercially pure titanium and two β-titanium alloys, TNZT and TMZF, have been characterized using various electrochemical techniques for their corrosion behavior in Ringers lactate solution. The variation of corrosion potential and solution pH with time has been discussed. Electrochemical Impedance Spectroscopy has been used to fit the results into a circuit model. The stability of the oxides formed on the surface of these alloys has been correlated with impedance phase angles. Cyclic Potentiodynamic Polarization has been used to compute the corrosion parameters for the alloys. TMZF is found to be a better β-alloy as compared to TNZT.

  16. Electrochemical Characterization and Degradation Analysis of Large SOFC Stacks by Impedance Spectroscopy

    DEFF Research Database (Denmark)

    Mosbæk, Rasmus Rode; Hjelm, Johan; Barfod, R.;

    2013-01-01

    electrochemical characterization during operation. An experimental stack with low ohmic resistance from Topsoe Fuel Cell A/S was characterized in detail using electrochemical impedance spectroscopy (EIS). An investigation of the optimal geometrical placement of the current feeds and voltage probes was carried out...... with hydrogen as fuel with 52% fuel utilization and constant current load (0.2 A cm–2) at 750 °C. Stack interconnects were coated with six different coatings to prevent chromium poisoning on the cathode side. Four repeating units (RUs) with different coatings were selected for detailed impedance analysis. EIS...

  17. In situ anodization of aluminum surfaces studied by x-ray reflectivity and electrochemical impedance spectroscopy

    Science.gov (United States)

    Bertram, F.; Zhang, F.; Evertsson, J.; Carlà, F.; Pan, J.; Messing, M. E.; Mikkelsen, A.; Nilsson, J.-O.; Lundgren, E.

    2014-07-01

    We present results from the anodization of an aluminum single crystal [Al(111)] and an aluminum alloy [Al 6060] studied by in situ x-ray reflectivity, in situ electrochemical impedance spectroscopy and ex situ scanning electron microscopy. For both samples, a linear increase of oxide film thickness with increasing anodization voltage was found. However, the slope is much higher in the single crystal case, and the break-up of the oxide film grown on the alloy occurs at a lower anodization potential than on the single crystal. The reasons for these observations are discussed as are the measured differences observed for x-ray reflectivity and electrochemical impedance spectroscopy.

  18. Electrochemical impedance spectroscopy in chromatography paper and its application to latex bead detection

    Science.gov (United States)

    Iwahara, Shohei; Miki, Masashi; Hori, Fumitaka; Uno, Shigeyasu

    2014-01-01

    The principle of the quantitative immunochromatographic strip test (IST) is proposed. Electrochemical impedance spectroscopy is shown to be capable of detecting latex beads in chromatography paper, where latex beads can serve as a label in IST. Measurements to examine the impedance changes in the absence and presence of latex beads are conducted. In the presence of latex beads, an increase of 12.5% in the bulk solution resistance is observed. This indicates that the latex-bead-labeled antigen-antibody complex can be detected electrochemically by actual IST.

  19. A cultural evolutionary programming approach to automatic analytical modeling of electrochemical phenomena through impedance spectroscopy

    CERN Document Server

    Arpaia, Pasquale

    2009-01-01

    An approach to automatic analytical modeling of electrochemical impedance spectroscopy data by evolutionary programming based on cultural algorithms is proposed. A solution-search strategy based on a cultural mechanism is exploited for defining the equivalent-circuit model automatically: information on search advance is transmitted to all potential solutions, rather than only to a small inheriting subset, such as in a traditional genetic approach. Moreover, with respect to the state of the art, also specific information related to constraints on the application physics knowledge is transferred. Experimental results of the proposed approach implementation in impedance spectroscopy for general-purpose electrochemical circuit analysis and for corrosion monitoring and diagnosing are presented.

  20. In situ anodization of aluminum surfaces studied by x-ray reflectivity and electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Bertram, F., E-mail: florian.bertram@sljus.lu.se; Evertsson, J.; Messing, M. E.; Mikkelsen, A.; Lundgren, E. [Division of Synchrotron Radiation Research, Lund University, Box 118, 221 00 Lund (Sweden); Zhang, F.; Pan, J. [KTH Royal Institute of Technology, School of Chemical Science and Engineering, Department of Chemistry, Division of Surface and Corrosion Science, Drottning Kristinas väg 51, 10044 Stockholm (Sweden); Carlà, F. [ESRF, B. P. 220, 38043 Grenoble (France); Nilsson, J.-O. [Sapa Technology, Kanalgatan 1, 612 31 Finspång (Sweden)

    2014-07-21

    We present results from the anodization of an aluminum single crystal [Al(111)] and an aluminum alloy [Al 6060] studied by in situ x-ray reflectivity, in situ electrochemical impedance spectroscopy and ex situ scanning electron microscopy. For both samples, a linear increase of oxide film thickness with increasing anodization voltage was found. However, the slope is much higher in the single crystal case, and the break-up of the oxide film grown on the alloy occurs at a lower anodization potential than on the single crystal. The reasons for these observations are discussed as are the measured differences observed for x-ray reflectivity and electrochemical impedance spectroscopy.

  1. New aspects of the electrochemical-catalytic (EC’) mechanism in square-wave voltammetry

    OpenAIRE

    Gulaboski, Rubin; Mirceski, Valentin

    2015-01-01

    Several new theoretical aspects of the electrocatalytic (regenerative) EC’ mechanism under conditions of square-wave (SWV) and staircase cyclic voltammetry (SCV) are presented. Elaborating the effect of the rate of the catalytic reaction in the diffusion-controlled catalytic mechanism (diffusional EC’ mechanism) and surface catalytic mechanism (surface EC’ mechanism), we refer to several phenomena related to the shift of the position and the half-peak width of the net peak in ...

  2. Cyclic voltammetry and scanning electrochemical microscopy studies of methylene blue immobilized on the self-assembled monolayer of n-dodecanethiol

    Energy Technology Data Exchange (ETDEWEB)

    Salamifar, Seyed Ehsan [Department of Chemistry, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of); Mehrgardi, Masoud Ayatollahi [Department of Chemistry, University of Isfahan, Isfahan (Iran, Islamic Republic of); Kazemi, Sayed Habib [Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan (Iran, Islamic Republic of); Mousavi, Mir Fazllollah, E-mail: mousavim@modares.ac.i [Department of Chemistry, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of)

    2010-12-30

    Electron transfer (ET) kinetics through n-dodecanethiol (C{sub 12}SH) self-assembled monolayer on gold electrode was studied using cyclic voltammetry (CV), scanning electrochemical microscopy (SECM) and electrochemical impedance spectroscopy (EIS). An SECM model for compensating pinhole contribution, was used to measure the ET kinetics of solution-phase probes of ferrocyanide/ferricyanide (Fe(CN){sub 6}{sup 4-/3-}) and ferrocenemethanol/ferrociniummethanol (FMC{sup 0/+}) through the C{sub 12}SH monolayer yielding standard tunneling rate constant (k{sub ET}{sup 0}) of (4 {+-} 1) x 10{sup -11} and (3 {+-} 1) x 10{sup -10} cm s{sup -1} for Fe(CN){sub 6}{sup 4-/3-} and FMC{sup 0/+} respectively. Decay tunneling constants ({beta}) of 0.97 and 0.96 A{sup -1} for saturated alkane thiol chains were obtained using Fe(CN){sub 6}{sup 4-} and FMC respectively. Also, it was found that methylene blue (MB) molecules are effectively immobilized on the C{sub 12}SH monolayer and can mediate the ET between the solution-phase probes and underlying gold substrate. SECM-mediated model was used to simultaneously measure the bimolecular ET between the solution-phase probes and the monolayer-immobilized MB molecules, as well as tunneling ET between the monolayer-immobilized MB molecules and the underlying gold electrode, allowing the measurement of k{sub BI} = (5 {+-} 1) x 10{sup 6} and (4 {+-} 2) x 10{sup 7} cm{sup 3} mol{sup -1} s{sup -1} for the bimolecular ET and k{sub ET/MB}{sup 0}=(1{+-}0.3)x10{sup -3} and (7 {+-} 3) x 10{sup -2} s{sup -1} for the standard tunneling rate constant of ET using Fe(CN){sub 6}{sup 4-/3-} and FMC{sup 0/+} probes respectively.

  3. Electrochemical characterisation and anodic stripping voltammetry at mesoporous platinum rotating disc electrodes.

    Science.gov (United States)

    Lozano-Sanchez, Pablo; Elliott, Joanne M

    2008-02-01

    Using the technique of liquid crystal templating a rotating disc electrode (RDE) was modified with a high surface area mesoporous platinum film. The surface area of the electrode was characterised by acid voltammetry, and found to be very high (ca. 86 cm(2)). Acid characterisation of the electrode produced distorted voltammograms was interpreted as being due to the extremely large surface area which produced a combination of effects such as localised pH change within the pore environment and also ohmic drop effects. Acid voltammetry in the presence of two different types of surfactant, namely Tween 20 and Triton X-100, suggested antifouling properties associated with the mesoporous deposit. Further analysis of the modified electrode using a redox couple in solution showed typical RDE behaviour although extra capacitive currents were observed due to the large surface area of the electrode. The phenomenon of underpotential deposition was exploited for the purpose of anodic stripping voltammetry and results were compared with data collected for microelectrodes. Underpotential deposition of metal ions at the mesoporous RDE was found to be similar to that at conventional platinum electrodes and mesoporous microelectrodes although the rate of surface coverage was found to be slower at a mesoporous RDE. It was found that a mesoporous RDE forms a suitable system for quantification of silver ions in solution.

  4. Electrochemical Impedance Study of Schiff Base by Means of Self-assembled Monolayer

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    In this work, the self-assembled monolayer of Schiff base was first investigated using electrochemical impedance spectroscopy (ELS). The complexation of Cu2+ with the Schiff base was also detected with EIS method. The approximate linear relationship between Cu2+ and the reaction resistance (Rr) was observed. All the results suggest that the electrochemical property of Schiff base could be studied conveniently by means of forming self-assembled monolayer.

  5. Characterization and modeling of electrochemical energy conversion systems by impedance techniques

    Energy Technology Data Exchange (ETDEWEB)

    Klotz, Dino

    2012-07-01

    This work introduces (i) amendments to basic electrochemical measurement techniques in the time and frequency domain suitable for electrochemical energy conversion systems like fuel cells and batteries, which enable shorter measurement times and improved precision in both measurement and parameter identification, and (ii) a modeling approach that is able to simulate a technically relevant system just by information gained through static and impedance measurements of laboratory size cells.

  6. The Role of Electrochemical Impedance Spectroscopy in the Characterization of Electrodes and Devices for Energy Conversion and Storage

    Directory of Open Access Journals (Sweden)

    Magdić, K.

    2013-03-01

    Full Text Available This article describes the basic principles of the Electrochemical Impedance Spectroscopy, EIS, technique and its application in the characterization of electrode materials and electrochemical devices for energy conversion and storage. The concept of impedance and the necessary steps of impedance spectra analysis are explained. Basic relations for impedance of particular electro- chemical processes occurring in the system(s are derived. Electrical equivalent circuits as impedance analogues for single-cell units of electrochemical (supercapacitors, galvanic cells (batteries and fuel cells, as well as separate impedance components and parameters describing the system(s are presented and discussed. The advantages and problems in application of the EIS technique for evaluation of operating states and possible failures of these electrochemical devices are described.

  7. Estimation of Parameters Obtained by Electrochemical Impedance Spectroscopy on Systems Containing High Capacities

    Directory of Open Access Journals (Sweden)

    Mirjana Rajčić Vujasinović

    2009-09-01

    Full Text Available Electrochemical systems with high capacities demand devices for electrochemical impedance spectroscopy (EIS with ultra-low frequencies (in order of mHz, that are almost impossible to accomplish with analogue techniques, but this becomes possible by using a computer technique and accompanying digital equipment. Recently, an original software and hardware for electrochemical measurements, intended for electrochemical systems exhibiting high capacities, such as supercapacitors, has been developed. One of the included methods is EIS. In this paper, the method of calculation of circuit parameters from an EIS curve is described. The results of testing on a physical model of an electrochemical system, constructed of known elements (including a 1.6 F capacitor in a defined arrangement, proved the validity of the system and the method.

  8. Estimation of parameters obtained by electrochemical impedance spectroscopy on systems containing high capacities.

    Science.gov (United States)

    Stević, Zoran; Vujasinović, Mirjana Rajčić; Radunović, Milan

    2009-01-01

    Electrochemical systems with high capacities demand devices for electrochemical impedance spectroscopy (EIS) with ultra-low frequencies (in order of mHz), that are almost impossible to accomplish with analogue techniques, but this becomes possible by using a computer technique and accompanying digital equipment. Recently, an original software and hardware for electrochemical measurements, intended for electrochemical systems exhibiting high capacities, such as supercapacitors, has been developed. One of the included methods is EIS. In this paper, the method of calculation of circuit parameters from an EIS curve is described. The results of testing on a physical model of an electrochemical system, constructed of known elements (including a 1.6 F capacitor) in a defined arrangement, proved the validity of the system and the method.

  9. Estimation of Parameters Obtained by Electrochemical Impedance Spectroscopy on Systems Containing High Capacities

    Science.gov (United States)

    Stević, Zoran; Vujasinović, Mirjana Rajčić; Radunović, Milan

    2009-01-01

    Electrochemical systems with high capacities demand devices for electrochemical impedance spectroscopy (EIS) with ultra-low frequencies (in order of mHz), that are almost impossible to accomplish with analogue techniques, but this becomes possible by using a computer technique and accompanying digital equipment. Recently, an original software and hardware for electrochemical measurements, intended for electrochemical systems exhibiting high capacities, such as supercapacitors, has been developed. One of the included methods is EIS. In this paper, the method of calculation of circuit parameters from an EIS curve is described. The results of testing on a physical model of an electrochemical system, constructed of known elements (including a 1.6 F capacitor) in a defined arrangement, proved the validity of the system and the method. PMID:22400000

  10. Quantitative Label-Free Cell Proliferation Tracking with a Versatile Electrochemical Impedance Detection Platform

    DEFF Research Database (Denmark)

    Caviglia, Claudia; Carminati, M; Heiskanen, Arto

    2012-01-01

    optimal detection strategies. Electrochemical Impedance Spectroscopy (EIS) has been used to monitor and compare adhesion of different cell lines. HeLa cells and 3T3 fibroblasts have been cultured for 12 hours on interdigitated electrode arrays integrated into a tailor-made cell culture platform. Both...

  11. A study on the impact of lithium-ion cell relaxation on electrochemical impedance spectroscopy

    Science.gov (United States)

    Barai, Anup; Chouchelamane, Gael H.; Guo, Yue; McGordon, Andrew; Jennings, Paul

    2015-04-01

    Lithium-ion (Li-ion) batteries are of great interest to the automotive industry due to their higher power and energy density, higher cell voltage, longer cycle life and lower self-discharge compared to other battery chemistries. Electrochemical impedance spectroscopy is a powerful tool employed to investigate the fundamental electrochemical reactions within a Li-ion battery cell, which relates to state of charge, internal temperature and state of health. Its effectiveness has established it as a core method to study electrochemical behaviour of batteries in both off-line and on-line applications. In this work it is shown that in addition to state of charge, internal temperature and state of health, the time period between the removal of an electrical load and the impedance measurement affects the results. The study of five commercially available cells of varying capacities and electrode chemistries show that, regardless of cell type, maximum impedance change takes place within the first 4 h of the relaxation period. The root cause of this impedance change has been discussed from an electrochemical perspective.

  12. Modelling of a High Temperature PEM Fuel Cell Stack using Electrochemical Impedance Spectroscopy

    DEFF Research Database (Denmark)

    Andreasen, Søren Juhl; Jespersen, Jesper Lebæk; Kær, Søren Knudsen

    2008-01-01

    This work presents the development of an equivalent circuit model of a 65 cell high temperature PEM (HTPEM) fuel cell stack using Electrochemical Impedance Spectroscopy (EIS). The HTPEM fuel cell membranes used are PBI-based and uses phosphoric acid as proton conductor. The operating temperature...

  13. Label-free electrochemical impedance detection of kinase and phosphatase activities using carbon nanofiber nanoelectrode arrays

    Science.gov (United States)

    Li, Yifen; Syed, Lateef; Liu, Jianwei; Hua, Duy H.; Li, Jun

    2012-01-01

    We demonstrate the feasibility of a label-free electrochemical method to detect the kinetics of phosphorylation and dephosphorylation of surface-attached peptides catalyzed by kinase and phosphatase, respectively. The peptides with a sequence specific to c-Src tyrosine kinase and protein tyrosine phosphatase 1B (PTP1B) were first validated with ELISA-based protein tyrosine kinase assay and then functionalized on vertically aligned carbon nanofiber (VACNF) nanoelectrode arrays (NEAs). Real-time electrochemical impedance spectroscopy (REIS) measurements showed reversible impedance changes upon the addition of c-Src kinase and PTP1B phosphatase. Only a small and unreliable impedance variation was observed during the peptide phosphorylation, but a large and fast impedance decrease was observed during the peptide dephosphorylation at different PTP1B concentrations. The REIS data of dephosphorylation displayed a well-defined exponential decay following the Michaelis-Menten heterogeneous enzymatic model with a specific constant, kcat/Km, of (2.1 ± 0.1) × 107 M−1 s−1. Consistent values of the specific constant was measured at PTP1B concentration varying from 1.2 to 2.4 nM with the corresponding electrochemical signal decay constant varying from 38.5 to 19.1 s. This electrochemical method can be potentially used as a label-free method for profiling enzyme activities in fast reactions. PMID:22935373

  14. Estimation of CO concentration in high temperature PEM fuel cells using electrochemical impedance

    DEFF Research Database (Denmark)

    Jensen, Hans-Christian Becker; Andreasen, Søren Juhl; Kær, Søren Knudsen;

    This work presents the results of using the electrochemical impedance to analyse the behaviour of a BASF Celtec P2100 MEA operated under varying operating conditions with different temperatures and gas concentrations. Figure 1 shows the experimental setup used for these measurements....

  15. An electrochemical impedance model for integrated bacterial biofilms

    Energy Technology Data Exchange (ETDEWEB)

    Ben-Yoav, Hadar, E-mail: benyoav@post.tau.ac.il [Department of Physical Electronics, School of Electrical Engineering, Faculty of Engineering, Tel Aviv University (Israel); Freeman, Amihay [Department of Molecular Microbiology and Biotechnology, Faculty of Life Sciences, Tel Aviv University (Israel); Sternheim, Marek [The Center for Nanoscience and Nanotechnology, Tel Aviv University (Israel); Shacham-Diamand, Yosi [Department of Physical Electronics, School of Electrical Engineering, Faculty of Engineering, Tel Aviv University (Israel)

    2011-09-30

    Bacterial cells attachment onto solid surfaces and the following growth into mature microbial biofilms may result in highly antibiotic resistant biofilms. Such biofilms may be incidentally formed on tissues or implanted devices, or intentionally formed by directed deposition of microbial sensors on whole-cell bio-chip surface. A new method for electrical characterization of the later on-chip microbial biofilm buildup is presented in this paper. Measurement of impedance vs. frequency in the range of 100 mHz to 400 kHz of Escherichia coli cells attachment to indium-tin-oxide-coated electrodes was carried out while using optical microscopy estimating the electrode area coverage. We show that impedance spectroscopy measurements can be interpreted by a simple electrical equivalent model characterizing both attachment and growth of the biofilm. The correlation of extracted equivalent electrical lumped components with the visual biofilm parameters and their dependence on the attachment and growth phases is confirmed.

  16. Potential-dependent adsorption/desorption behavior of perfluorosulfonated ionomer on a gold electrode surface studied by cyclic voltammetry, electrochemical quartz microbalance, and electrochemical atomic force microscopy.

    Science.gov (United States)

    Masuda, Takuya; Ikeda, Kota; Uosaki, Kohei

    2013-02-19

    Potential-dependent adsorption/desorption behavior of perfluorosulfonated ionomer (PFSI) on a gold electrode was investigated by cyclic voltammetry (CV), electrochemical quartz crystal microbalance (EQCM), and electrochemical atomic force microscopy (EC-AFM) in a Nafion (i.e., PFSI) dispersed aqueous solution without any other electrolyte. It was found that PFSI serves as an electrolyte and that electrochemical measurements can be performed in this solution without any significant IR drop. PFSI molecules were adsorbed on the Au surface in the lying-down configuration in the potential range between 0 and 0.45 V, the amount of adsorbed PFSI increased when the potential was made more positive than 0.75 V, and the adsorbed PFSI fully desorbed from the surface at potentials more positive than 1.4 V where gold oxide was formed. Once the gold oxide had been reduced, PFSI readsorbed on the surface, albeit slowly. PFSI desorbed from the surface as the potential was made more negative than 0 V. These processes took place reversibly.

  17. Electrochemical impedance analysis of SOFC cathode reaction using evolutionary programming

    Energy Technology Data Exchange (ETDEWEB)

    Hershkovitz, S.; Baltianski, S.; Tsur, Y. [Department of Chemical Engineering, Technion-Israel Institute of Technology, Haifa (Israel)

    2012-02-15

    Investigation of the cathode reaction in solid oxide fuel cells (SOFC) by impedance spectroscopy (IS) measurements using evolutionary-based programming analysis is demonstrated. In contrast to the conventional analysis methods used for impedance spectroscopy measurements, e.g., equivalent circuits, the impedance spectroscopy genetic programming (ISGP) program seeks for a distribution of relaxation times that has the form of a peak or a sum of several peaks, assuming the Debye kernel. Using this method one finds a functional (parametric) form of the distribution of relaxation times. A symmetric cell configuration of Pt vertical stroke LSCF vertical stroke GDC vertical stroke LSCF vertical stroke Pt was examined using IS measurements combined with I-V measurements. Different samples at different temperatures and different oxygen partial pressures were examined in order to investigate their influence on the oxygen reduction reaction. The resulting IS data was analyzed using the ISGP program and the resulting peaks constructing the distribution of relaxation times were assigned for the different processes that occur at the cathode side. The activation energies as well as the dependence of the processes on the oxygen partial pressure were also evaluated. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  18. Electrochemical impedance immunosensor for the detection of cardiac biomarker Myogobin (Mb) in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Rajesh, E-mail: rajesh_csir@yahoo.com; Sharma, V.; Tanwar, V.K.; Mishra, S.K.; Biradar, A.M.

    2010-11-30

    A label-free, electrochemical impedance immunosensor based on surface modified thin flat gold wire electrode is reported for the quantitative detection of cardiac biomarker Myoglobin in aqueous solution. The protein antibody, ab-Mb, was covalently immobilized through a self assembled monolayer of 11-mercaptoundecanoic acid (MUA) and 3-mercapto propionic acid (MPA) via carbodiimide coupling reaction using N-(3-dimethylaminopropyl)-N'-ethyl carbodiimide hydrochloride (EDC) and N-Hydroxy Succinamide (NHS). The immunosensor (ab-Mb/MUA-MPA/Au) was characterized by electrochemical techniques. The electrochemical performance of the immunosensor was studied by electrochemical impedance spectroscopy. The immunosensor showed an increased electrontransfer resistance on coupling with biomarker protein antigen, ag-Mb, in the presence of a redox probe [Fe (CN){sub 6}]{sup 3-/4-}. The modified Au electrode immunosensor exhibits an electrochemical impedance response to antigen, ag-Mb concentrations in a linear range from 10 ng to 650 ng mL{sup -1} with a lowest detection limit of 5.2 ng mL{sup -1}.

  19. An Electrochemical Impedance Study of AISI 321 Stainless Steel in 0.5 M H2SO4

    Directory of Open Access Journals (Sweden)

    A. Fattah-Alhosseini

    2011-01-01

    Full Text Available The electrochemical behavior of passive films formed on AISI 321 has been examined using electrochemical impedance spectroscopy. AISI 321 is characterized by high interfacial impedance, thereby illustrating its high corrosion resistance. Results showed that the interfacial impedance and the polarization resistance initially increase with applied potential, within the low potential. However, at a sufficiently high potential (>0.6 V, the interfacial impedance and the polarization resistance decrease with increasing potential. The impedance data were adequately represented by an equivalent electrical circuit model based on point defect model, which described the behavior of the passive film on stainless steel more satisfactorily than the proposed models.

  20. Standard practice for verification of algorithm and equipment for electrochemical impedance measurements

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    1989-01-01

    1.1 This practice covers an experimental procedure which can be used to check one's instrumentation and technique for collecting and presenting electrochemical impedance data. If followed, this practice provides a standard material, electrolyte, and procedure for collecting electrochemical impedance data at the open circuit or corrosion potential that should reproduce data determined by others at different times and in different laboratories. This practice may not be appropriate for collecting impedance information for all materials or in all environments. 1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

  1. Electrochemical impedance spectroscopy: A deeper and quantitative insight into the fingermarks physical modifications over time.

    Science.gov (United States)

    Rosa, Roberto; Giovanardi, Roberto; Bozza, Andrea; Veronesi, Paolo; Leonelli, Cristina

    2017-02-24

    The present work is focused on a novel approach for the study and quantification of some of the physical changes to which a fingermark deposited on non-porous substrates is subjected as its ageing proceeds. Particularly, electrochemical impedance spectroscopy (EIS) technique has been applied for the first time in order to monitor the electrochemical behaviour of the system constituted by the fingermark residue and the underlying substrate. The impedance spectra proved to be significantly affected by the presence of the mark residue as well as by its ageing process. Opportune fitting operations performed on the experimental data allowed obtaining quantitative electrochemical parameters used to reach useful information on the fingermarks ageing mechanism as well as to calculate the fingermark ageing curves from which fundamental information could be potentially extrapolated.

  2. Fabrication and Demonstration of Mercury Disc-Well Probes for Stripping-Based Cyclic Voltammetry Scanning Electrochemical Microscopy.

    Science.gov (United States)

    Barton, Zachary J; Rodríguez-López, Joaquín

    2017-03-07

    Scanning electrochemical microscopy (SECM) is a rising technique for the study of energy storage materials. Hg-based probes allow the extension of SECM investigations to ionic processes, but the risk of irreversible Hg amalgam saturation limits their operation to rapid timescales and dilute analyte solutions. Here, we report a novel fabrication protocol for Hg disc-well ultramicroelectrodes (UMEs), which retain access to stripping information but are less susceptible to amalgam saturation than traditional Hg sphere-caps or thin-films. The amalgamation and stripping behaviors of Hg disc-well UMEs are compared to those of traditional Hg sphere-cap UMEs and corroborated with data from finite element simulations. The improved protection against amalgam saturation allows Hg disc-wells to operate safely in highly concentrated environments at long timescales. The utility of the probes for bulk measurements extends also to SECM studies, where the disc geometry facilitates small tip-substrate gaps and improves both spatial and temporal resolution. Because they can carry out slow, high-resolution anodic stripping voltammetry approaches and imaging in concentrated solutions, Hg disc-well electrodes fill a new analytical niche for studies of ionic reactivity and are a valuable addition to the electrochemical toolbox.

  3. Substituent Inductive Effects on the Electrochemical Oxidation of Flavonoids Studied by Square Wave Voltammetry and Ab Initio Calculations.

    Science.gov (United States)

    Arroyo-Currás, Netzahualcóyotl; Rosas-García, Víctor M; Videa, Marcelo

    2016-10-27

    Flavonoids are natural products commonly found in the human diet that show antioxidant, anti-inflammatory and anti-hepatotoxic activities. These nutraceutical properties may relate to the electrochemical activity of flavonoids. To increase the understanding of structure-electrochemical activity relations and the inductive effects that OH substituents have on the redox potential of flavonoids, we carried out square-wave voltammetry experiments and ab initio calculations of eight flavonoids selected following a systematic variation in the number of hydroxyl substituents and their location on the flavan backbone: three flavonols, three anthocyanidins, one anthocyanin and the flavonoid backbone flavone. We compared the effect that the number of -OH groups in the ring B of flavan has on the oxidation potential of the flavonoids considered, finding linear correlations for both flavonols and anthocyanidins ( R 2 = 0.98 ). We analyzed the effects that position and number of -OH substituents have on electron density distributions via ab initio quantum chemical calculations. We present direct correlations between structural features and oxidation potentials that provide a deeper insight into the redox chemistry of these molecules.

  4. A study of gadolinia-doped ceria electrolyte by electrochemical impedance spectroscopy

    Science.gov (United States)

    Zhang, Lei; Liu, Feng; Brinkman, Kyle; Reifsnider, Kenneth L.; Virkar, Anil V.

    2014-02-01

    Samples of Gd2O3-doped CeO2 (GDC) were fabricated by sintering of powder compacts. Impedance spectra were measured from 400 °C to 675 °C in air by electrochemical impedance spectroscopy (EIS). Above ∼500 °C, high frequency arc was not semicircular but could be fitted with a constant phase element (CPE). Above ∼625 °C, high frequency arc could not be resolved due to a significant contribution from the inductive load. The impedance spectra were described using a simple equivalent circuit which included the leads/instrument impedance. The leads/instrument impedance was measured over a range of frequencies and temperatures. The high frequency part of the impedance after subtracting leads/instrument impedance could be resolved even at the highest measurement temperature and was described by a semicircle representative of transport across grain boundaries. From these measurements, grain and grain boundary resistivities were determined. The corresponding activation energies were 0.69 eV and 1.11 eV, respectively. The grain boundary capacitance was nearly independent of temperature. The present results show that grain boundary effects can be described by a resistor and a capacitor. Relevant equivalent circuit parameters were obtained from intercepts, maxima and minima in impedance diagrams.

  5. Highly sensitive electrochemical impedance spectroscopic detection of DNA hybridization based on Au(nano)-CNT/PAN(nano) films.

    Science.gov (United States)

    Zhou, Na; Yang, Tao; Jiang, Chen; Du, Meng; Jiao, Kui

    2009-01-15

    A polyaniline nanofibers (PAN(nano))/carbon paste electrode (CPE) was prepared via dopping PAN(nano) in the carbon paste. The nanogold (Au(nano)) and carbon nanotubes (CNT) composite nanoparticles were bound on the surface of the PAN(nano)/CPE. The immobilization and hybridization of the DNA probe on the Au(nano)-CNT/PAN(nano) films were investigated with differential pulse voltammetry (DPV) and cyclic voltammetry (CV) using methylene blue (MB) as indicator, and electrochemical impedance spectroscopy (EIS) using [Fe(CN)(6)](3-/4-) as redox probe. The voltammetric peak currents of MB increased dramatically owing to the immobilization of the probe DNA on the Au(nano)-CNT/PAN(nano) films, and then decreased obviously owing to the hybridization of the DNA probe with the complementary single-stranded DNA (cDNA). The electron transfer resistance (R(et)) of the electrode surface increased after the immobilization of the probe DNA on the Au(nano)-CNT/PAN(nano) films and rose further after the hybridization of the probe DNA. The remarkable difference between the R(et) value at the DNA-immobilized electrode and that at the hybridized electrode could be used for the label-free EIS detection of the target DNA. The loading of the DNA probe on Au(nano)-CNT/PAN(nano) films was greatly enhanced and the sensitivity for the target DNA detection was markedly improved. The sequence-specific DNA of phosphinothricin acetyltransferase (PAT) gene and the polymerase chain reaction (PCR) amplification of nopaline synthase (NOS) gene from transgenically modified beans were determined with this label-free EIS DNA detection method. The dynamic range for detecting the PAT gene sequence was from 1.0 x 10(-12)mol/L to 1.0 x 10(-6)mol/L with a detection limit of 5.6 x 10(-13)mol/L.

  6. The use of electrochemical impedance spectroscopy (EIS) in the evaluation of the electrochemical properties of a microbial fuel cell.

    Science.gov (United States)

    Manohar, Aswin K; Bretschger, Orianna; Nealson, Kenneth H; Mansfeld, Florian

    2008-04-01

    Electrochemical impedance spectroscopy (EIS) has been used to determine several electrochemical properties of the anode and cathode of a mediator-less microbial fuel cell (MFC) under different operational conditions. These operational conditions included a system with and without the bacterial catalyst and EIS measurements at the open-circuit potential of the anode and the cathode or at an applied cell voltage. In all cases the impedance spectra followed a simple one-time-constant model (OTCM) in which the solution resistance is in series with a parallel combination of the polarization resistance and the electrode capacitance. Analysis of the impedance spectra showed that addition of Shewanella oneidensis MR-1 to a solution of buffer and lactate greatly increased the rate of the lactate oxidation at the anode under open-circuit conditions. The large decrease of open-circuit potential of the anode increased the cell voltage of the MFC and its power output. Measurements of impedance spectra for the MFC at different cell voltages resulted in determining the internal resistance (R(int)) of the MFC and it was found that R(int) is a function of cell voltage. Additionally, R(int) was equal to R(ext) at the cell voltage corresponding to maximum power, where R(ext) is the external resistance that must be applied across the circuit to obtain the maximum power output.

  7. Analysis of bio-anode performance through electrochemical impedance spectroscopy.

    Science.gov (United States)

    ter Heijne, Annemiek; Schaetzle, Olivier; Gimenez, Sixto; Navarro, Lucia; Hamelers, Bert; Fabregat-Santiago, Francisco

    2015-12-01

    In this paper we studied the performance of bioanodes under different experimental conditions using polarization curves and impedance spectroscopy. We have identified that the large capacitances of up to 1 mF·cm(-2) for graphite anodes have their origin in the nature of the carbonaceous electrode, rather than the microbial culture. In some cases, the separate contributions of charge transfer and diffusion resistance were clearly visible, while in other cases their contribution was masked by the high capacitance of 1 mF·cm(-2). The impedance data were analyzed using the basic Randles model to analyze ohmic, charge transfer and diffusion resistances. Increasing buffer concentration from 0 to 50mM and increasing pH from 6 to 8 resulted in decreased charge transfer and diffusion resistances; lowest values being 144 Ω·cm(2) and 34 Ω·cm(2), respectively. At acetate concentrations below 1 mM, current generation was limited by acetate. We show a linear relationship between inverse charge transfer resistance at potentials close to open circuit and saturation (maximum) current, associated to the Butler-Volmer relationship that needs further exploration.

  8. Electrochemical impedance spectroscopy on in-situ analysis of oxide layer formation in liquid metal

    Energy Technology Data Exchange (ETDEWEB)

    Kondo, M., E-mail: kondo.masatoshi@tokai-u.jp [Department of Nuclear Engineering, School of Engineering, Tokai University, 4-1-1 Kitakaname, Hiratsuka-shi, Kanagawa 259-1292 (Japan); Suzuki, N.; Nakajima, Y. [Department of Nuclear Engineering, School of Engineering, Tokai University, 4-1-1 Kitakaname, Hiratsuka-shi, Kanagawa 259-1292 (Japan); Tanaka, T.; Muroga, T. [National Institute for Fusion Science, Toki, Gifu 502-5292 (Japan)

    2014-10-15

    Graphical abstract: Some test materials (i.e. Fe, Cr, Y and JLF-1 steel) were immersed to liquid metal lead (Pb) mainly at 773 K as the working electrode of electrochemical impedance spectroscopy (EIS). Some oxide layers formed on the electrodes in liquid Pb were analyzed by EIS. The impedance response was summarized as semicircular Nyquist plot, and the electrical properties and the thickness of the oxide layers were evaluated in non-destructive manner. Large impedance due to the formation of Y oxide formed in liquid Pb was detected by EIS, though impedance of Fe oxide and Cr oxide could not be detected due to their small electro resistance. The time constant of the oxide layers was evaluated from the impedance information, and this value identified the types of oxides. The change of the time constant with the immersion time indicated the change of the electrical properties determined by the chemical composition and the crystal structure. The thickness of the oxide layer estimated by EIS agreed well with that evaluated by metallurgical analysis. The growth of Y oxide layer in the liquid Pb was successfully detected by EIS in non-destructive manner. - Highlights: • The electrical properties and the thickness of lead oxide layer formed in liquid Pb were obtained by electrochemical impedance spectroscopy (EIS). • The Fe oxide, Cr oxide and Fe–Cr oxide formed on the electrodes in liquid Pb were not detected by EIS due to their small electrical resistance. • The formation and the growth of Y oxide formed in liquid Pb was detected by EIS. - Abstract: Some test materials (i.e. Fe, Cr, Y and JLF-1 steel) were immersed to liquid metal lead (Pb) mainly at 773 K as the working electrode of electrochemical impedance spectroscopy (EIS). Some oxide layers formed on the electrodes in liquid Pb were analyzed by EIS. The impedance response was summarized as Nyquist plot, and the electrical properties and the thickness of the oxide layers were evaluated in non

  9. Electrochemical Genotoxicity Assay Based on a SOS/umu Test Using Hydrodynamic Voltammetry in a Droplet

    OpenAIRE

    Kazuharu Sugawara; Masami Fukushima; Shigeru Taguchi; Noriko Hata; Kazuto Sazawa; Yasuaki Nanayama; Hideki Kuramitz

    2012-01-01

    The SOS/umu genotoxicity assay evaluates the primary DNA damage caused by chemicals from the β-galactosidase activity of S. typhimurium. One of the weaknesses of the common umu test system based on spectrophotometric detection is that it is unable to measure samples containing a high concentration of colored dissolved organic matters, sediment, and suspended solids. However, umu tests with electrochemical detection techniques prove to be a better strategy because it causes less inter...

  10. Impact of adsorption on scanning electrochemical microscopy voltammetry and implications for nanogap measurements

    OpenAIRE

    Tan, Sze-yin; Zhang, Jie; Bond, Alan M.; Macpherson, Julie V.; Unwin, Patrick R.

    2016-01-01

    Scanning electrochemical microscopy (SECM) is a powerful tool that enables quantitative measurements of fast electron transfer (ET) kinetics when coupled with modeling predictions from finite-element simulations. However, the advent of nanoscale and nanogap electrode geometries that have an intrinsically high surface area-to-solution volume ratio realizes the need for more rigorous data analysis procedures, as surface effects such as adsorption may play an important role. The oxidation of fer...

  11. Predicting molecular scale skin-effect in electrochemical impedance due to anomalous subdiffusion mediated adsorption phenomenon

    Science.gov (United States)

    Kushagra, Arindam

    2016-02-01

    Anomalous subdiffusion governs the processes which are not energetically driven, on a molecular scale. This paper proposes a model to predict the response of electrochemical impedance due to such diffusion process. Previous works considered the use of fractional calculus to predict the impedance behaviour in response to the anomalous diffusion. Here, we have developed an expression which predicts the skin-effect, marked by an increase in the impedance with increasing frequency, in this regime. Negative inductances have also been predicted as a consequence of the inertial response of adsorbed species upon application of frequency-mediated perturbations. It might help the researchers in the fields of impedimetric sensors to choose the working frequency and those working in the field of batteries to choose the parameters, likewise. This work would shed some light into the molecular mechanisms governing the impedance when exposed to frequency-based perturbations like electromagnetic waves (microwaves to ionizing radiations) and in charge storage devices like batteries etc.

  12. Evaluation of pitting corrosion with electrochemical impedance spectroscopy (EIS) for alumina/aluminium alloys composites

    Energy Technology Data Exchange (ETDEWEB)

    Odegard, C.; Bronson, A. [Univ. of Texas, El Paso, TX (United States)

    1998-12-31

    The pitting susceptibility of monolithic aluminum 6061 alloy and alumina/aluminum alloy composites has been analyzed by using electrochemical impedance spectroscopy and subsequent comparison with their polarization scans. The composites consisting of 0.10 and 0.15 volume fraction of alumina particles (VFAP) and the monolith as cylindrical electrodes were rotated at 1500 rpm while immersed in NaCl solution. The passive currents of the composites were greater than that of the monolith as per the polarization scans. The impedance spectra were acquired at constant potential increments along the passive region up to the pitting potential. The impedance spectra represented by semicircles on a Nyquist plot acquired above the pitting potential collapsed underneath the spectra obtained in the passive region near the corrosion potential for the monolithic alloy and composites. The impedance spectra modeled with a simplified equivalent circuit indicate that the effective capacitance for the composites is greater than that of the monolithic alloy.

  13. High Temperature PEM Fuel Cell Performance Characterisation with CO and CO2 using Electrochemical Impedance Spectroscopy

    DEFF Research Database (Denmark)

    Andreasen, Søren Juhl; Vang, Jakob Rabjerg; Kær, Søren Knudsen

    2011-01-01

    In this work, extensive electrochemical impedance measurements have been conducted on a 45 cm2 BASF Celtec P2100 high temperature PEM MEA. The fuel cell performance has been examined subject to some of the poisoning effects experienced when running on a reformate gas. The impedance is measured...... at different temperatures, currents, and different content of CO, CO2 and H2 in the anode gas. The impedance spectrum at each operating point is fitted to an equivalent circuit and an analysis to identify the different mechanisms governing the impedance is performed. The trends observed, when varying...... the operating conditions under pure H2, generally show good agreement with results from the literature. When adding CO and CO2 to the anode gas the entire frequency spectrum is affected, and especially the measurements conducted at low temperatures and high CO concentrations reveal undesirable transient effects....

  14. Graphical analysis of electrochemical impedance spectroscopy data in Bode and Nyquist representations

    Science.gov (United States)

    Huang, Jun; Li, Zhe; Liaw, Bor Yann; Zhang, Jianbo

    2016-03-01

    Though it becomes a routine to fit impedance data to an equivalent electric circuit model (EECM) using complex nonlinear least square (CNLS) to extract physical parameters from impedance data, two formidable challenges still remain: to build a physically meaningful EECM and to find good initial estimates for model parameters. In this study, combining graphical analysis of impedance data in both Bode and Nyquist plots, a two-step procedure is proposed to address the challenges: (1) a frequency derivative phase angle method is developed in Bode plot to identify the number of time constants (or electrochemical processes); (2) graphical analysis of impedance data in Nyquist plot is used sequentially for initial parameter determination. Major graphical analysis methods are compared in terms of frequency resolution, accuracy and complexity using synthetic data. The superiority of the proposed procedure is illustrated using the experimental data of a three-electrode lithium-ion cell.

  15. In situ electrochemical impedance and noise measurements of corroding stainless steel in high temperature water

    Energy Technology Data Exchange (ETDEWEB)

    Macak, Jan [Power Engineering Department, Institute of Chemical Technology Prague, Technicka 5, 166 28 Prague 6 (Czech Republic)]. E-mail: macakj@vscht.cz; Sajdl, Petr [Power Engineering Department, Institute of Chemical Technology Prague, Technicka 5, 166 28 Prague 6 (Czech Republic); Kucera, Pavel [Power Engineering Department, Institute of Chemical Technology Prague, Technicka 5, 166 28 Prague 6 (Czech Republic); Novotny, Radek [Institute for Energy, Joint Research Centre, 1755ZG Petten (Netherlands); Vosta, Jan [Power Engineering Department, Institute of Chemical Technology Prague, Technicka 5, 166 28 Prague 6 (Czech Republic)

    2006-04-25

    An in situ corrosion study of austenitic stainless steel 08CH18N10T in high temperature water was performed. The material under study is used in the construction of steam generator of PWR (pressurized water reactor) nuclear power stations and is similar to AISI 321 stainless steel. In situ 300-h tests were performed under autoclave conditions at 280 deg. C and 8 MPa and consisted of impedance measurements, polarization measurements and electrochemical noise measurements. The experiments were performed in deionised water with the pH adjusted to 9.5, in the presence/absence of chlorides. An additional modification of corrosivity was achieved by changing oxygen concentration. A detailed analysis of the impedance data is presented identifying in the impedance spectra contributions of oxide, corrosion reaction, double layer and diffusion process. A good agreement was found between corrosion data from electrochemical impedance spectroscopy (EIS) and that from electrochemical noise (EN) measurements. It was confirmed that the oxide response cannot be attributed to the overall oxide layer but only to the part corresponding to the space charge layer, thus indicating the semi-conductive character of the oxide.

  16. Electrochemical impedance spectroscopy investigation on the clinical lifetime of ProTaper rotary file system.

    Science.gov (United States)

    Penta, Virgil; Pirvu, Cristian; Demetrescu, Ioana

    2014-01-01

    The main objective of the current paper is to show that electrochemical impedance spectroscopy (EIS) could be a method for evaluating and predicting of ProTaper rotary file system clinical lifespan. This particular aspect of everyday use of the endodontic files is of great importance in each dental practice and has profound clinical implications. The method used for quantification resides in the electrochemical impedance spectroscopy theory and has in its main focus the characteristics of the surface titanium oxide layer. This electrochemical technique has been adapted successfully to identify the quality of the Ni-Ti files oxide layer. The modification of this protective layer induces changes in corrosion behavior of the alloy modifying the impedance value of the file. In order to assess the method, 14 ProTaper sets utilized on different patients in a dental clinic have been submitted for testing using EIS. The information obtained in regard to the surface oxide layer has offered an indication of use and proves that the said layer evolves with each clinical application. The novelty of this research is related to an electrochemical technique successfully adapted for Ni-Ti file investigation and correlation with surface and clinical aspects.

  17. Thermal Transitions in Layer-by-Layer Assemblies Observed Using Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Sung, Choonghyun; Hearn, Katelin; Lutkenhaus, Jodie

    2014-03-01

    Layer-by-layer (LbL) assemblies have been of great interest due to their versatile functionality and ease of fabrication. Charge and mass transport in LbL assemblies have been studied for the application of electrochemical devices and ion-conducting membranes. However, there are limited studies on the effect of temperature and of thickness on charge transport in LbL assemblies. Some LbL assemblies are known to have a thermal transition similar to a glass transition when hydrated. Thus, electrochemical properties can be strongly influenced by temperature. In this presentation, we studied the electrochemical impedance spectra of layer-by-layer assemblies of poly(diallyldimethyl ammonium chloride) and poly(styrene sulfonate) as a function of temperature using the ferricyanide/ferrocyanide redox couple. The effect of assembly salt concentration, thickness, and outermost layer on electrochemical properties is studied. Modified Randles circuits were used to quantitatively analyze the impedance spectra. Temperature-dependent impedance data are discussed with respect to the structure and thermal properties of LbL assemblies.

  18. Electrochemical Impedance Spectroscopy Investigation on the Clinical Lifetime of ProTaper Rotary File System

    Science.gov (United States)

    Pirvu, Cristian; Demetrescu, Ioana

    2014-01-01

    The main objective of the current paper is to show that electrochemical impedance spectroscopy (EIS) could be a method for evaluating and predicting of ProTaper rotary file system clinical lifespan. This particular aspect of everyday use of the endodontic files is of great importance in each dental practice and has profound clinical implications. The method used for quantification resides in the electrochemical impedance spectroscopy theory and has in its main focus the characteristics of the surface titanium oxide layer. This electrochemical technique has been adapted successfully to identify the quality of the Ni-Ti files oxide layer. The modification of this protective layer induces changes in corrosion behavior of the alloy modifying the impedance value of the file. In order to assess the method, 14 ProTaper sets utilized on different patients in a dental clinic have been submitted for testing using EIS. The information obtained in regard to the surface oxide layer has offered an indication of use and proves that the said layer evolves with each clinical application. The novelty of this research is related to an electrochemical technique successfully adapted for Ni-Ti file investigation and correlation with surface and clinical aspects. PMID:24605336

  19. Electrochemical Impedance Spectroscopy Investigation on the Clinical Lifetime of ProTaper Rotary File System

    Directory of Open Access Journals (Sweden)

    Virgil Penta

    2014-01-01

    Full Text Available The main objective of the current paper is to show that electrochemical impedance spectroscopy (EIS could be a method for evaluating and predicting of ProTaper rotary file system clinical lifespan. This particular aspect of everyday use of the endodontic files is of great importance in each dental practice and has profound clinical implications. The method used for quantification resides in the electrochemical impedance spectroscopy theory and has in its main focus the characteristics of the surface titanium oxide layer. This electrochemical technique has been adapted successfully to identify the quality of the Ni-Ti files oxide layer. The modification of this protective layer induces changes in corrosion behavior of the alloy modifying the impedance value of the file. In order to assess the method, 14 ProTaper sets utilized on different patients in a dental clinic have been submitted for testing using EIS. The information obtained in regard to the surface oxide layer has offered an indication of use and proves that the said layer evolves with each clinical application. The novelty of this research is related to an electrochemical technique successfully adapted for Ni-Ti file investigation and correlation with surface and clinical aspects.

  20. Anodic oxides on a beta type Nb-Ti alloy and their characterization by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Woldemedhin, Michael Teka; Hassel, Achim Walter [Max Planck Institut fuer Eisenforschung GmbH, Duesseldorf (Germany); Institute for Chemical Technology of Inorganic Materials, Johannes Kepler University, Linz (Austria); Raabe, Dierk [Max Planck Institut fuer Eisenforschung GmbH, Duesseldorf (Germany)

    2010-04-15

    Anodic oxides were grown on the surface of an electropolished (Ti-30 at% Nb) beta-titanium ({beta}-Ti) alloy by cyclic voltammetry. The scan rate was 100 mV s{sup -1} between 0 and 8 V in increments of l V in an acetate buffer of pH 6.0. Electrochemical impedance spectroscopy was carried out right after each anodic oxide growth increment to study the electronic properties of the oxide/electrolyte interface in a wide frequency range from 100 kHz to 10 MHz with an AC perturbation voltage of 10 mV. A film formation factor of 2.4 nm V{sup -1} was found and a relative permittivity number (dielectric constant) of 42.4 was determined for the oxide film formed. Mott-Schottky analysis on a potentiostatically formed 7 nm thick oxide film was performed to assess the semiconducting properties of the mixed anodic oxide grown on the alloy. A flat band potential of -0.47 V (standard hydrogen electrode, SHE) was determined, connected to a donor density of 8.2 x 10{sup 17} cm{sup -3}. {beta}-Ti being highly isotropic in terms of mechanical properties should be superior to the stiffer {alpha}-Ti compound. Its application, however, requires a passivation behaviour comparable or better than {alpha}-Ti which in fact is found. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  1. Electrochemical characteristics of nanostructured platinum electrodes--a cyclic voltammetry study.

    Science.gov (United States)

    Daubinger, P; Kieninger, J; Unmüssig, T; Urban, G A

    2014-05-14

    Platinum surfaces play a decisive role in catalysis in sensors, fuel cells, solar cells and other applications like neuronal stimulation and recording. Technical advances in nanotechnology contributed tremendously to the progress in these fields. A fundamental understanding of the chemical and physical interactions between the nanostructured surfaces and electrolytes is essential, but was barely investigated up to now. In this article, we present a wet-chemical process for the deposition of nanostructures on polycrystalline platinum surfaces. The electrochemically active surface area was increased by a factor of over 1000 times with respect to the geometrical surface. The influence of the nanostructures was examined in different acidic, alkaline, and neutral electrolytes. Comparing cyclic voltammograms of nanostructured and planar polycrystalline platinum revealed new insights into the microenvironment at the electrode-electrolyte interface. The characteristic features of the cyclic voltammograms were altered in their shape and strongly shifted with respect to the applied potential. In neutral buffered and unbuffered electrolytes the water window was expanded from 1.4 V to more than 2 V. The shifts were interpreted as local pH-changes and exhausted buffer capacity in direct proximity of the electrode surface due to the strong release and binding of protons, respectively. These polarized electrodes induce significant changes in the electrochemical potential of the electrolyte due to the high roughness of their surface. The electrochemical phenomena and the observed voltage shifts are crucial for the understanding of the basic mechanism at nanostructured electrodes and mandatory for designing fuel cells, sensors and many other devices.

  2. Simultaneous Impedance Analysis of Three Parallel Piezoelectric Quartz Crystals for Electrochemical Depletion Layer Effect Study

    Institute of Scientific and Technical Information of China (English)

    Hui Yan liu; Qing Ji XIE

    2004-01-01

    Simultaneous impedance analysis of three one-face sealed resonating piezoelectric quartz crystals (PQCs) in parallel is proposed through admittance measurements of the three PQCs on one impedance analyzer and then non-linear fitting according to the parallel combination of three Butterworth-Van Dyke circuits. Responses of each PQC obtained from the three-PQC mode agreed well with those measured separately in series sucrose aqueous solutions. This novel method has been used for the study of depletion-layer effect during ferri-/ferrocyanide electrochemical reactions.

  3. Effects of Nitrogen on Passivity of Nickel-Free Stainless Steels by Electrochemical Impedance Spectroscopy Analysis

    Science.gov (United States)

    Wu, Xinqiang; Fu, Yao; Ke, Wei; Xu, Song; Feng, Bing; Hu, Botao

    2015-09-01

    The effects of different nitrogen contents on the passivity of nickel-free stainless steels in 0.5 M sulfuric acid + 0.5 M sodium chloride solution were investigated by electrochemical impedance spectroscopy in the potential ranges of active dissolution and active-passive transition. A simplified reaction model containing adsorbed intermediates involved dissolution process, and passivation process was proposed to explain the impedance characteristics. Based on both equivalent circuit and mathematical model analysis, the effects of nitrogen on the passivity of stainless steels are discussed.

  4. Flow electrochemical analyses of zinc by stripping voltammetry on graphite felt electrode.

    Science.gov (United States)

    Feier, B; Floner, D; Cristea, C; Bodoki, E; Sandulescu, R; Geneste, F

    2012-08-30

    A flow sensor for trace analysis of zinc, using graphite felt as working electrode is reported here. A flow cell, well-adapted to 3-D porous electrodes and capable to do both the preconcentration step at a cathodic potential and the stripping of the zinc was successfully developed. It was demonstrated that this cell allows to obtain better electrochemical signals for Zn(2+) compared to a standard three-electrodes cell and that the percolation during accumulation increases the kinetics of electrodeposition. The influence on Zn(2+) signal of the deposition potential, the time of deposition and the flow rate was studied. The resulting sensor shows a linear response towards Zn(2+) with a linear range of 10(-6)-10(-4)M and a limit of detection of 5×10(-7) M for an analysis time of 5 min. The interferences study showed that the Cr(3+), Pb(2+), Cd(2+) ions have a small effect on the Zn electrochemical signal, whereas Fe(3+), Cu(2+), Co(2+) and Ni(2+) ions strongly influence it. The electrode was tested on real samples (tap water spiked with Zn(2+), food supplement) with a good recovery by applying the standard addition method. Copyright © 2012 Elsevier B.V. All rights reserved.

  5. A study of the electrochemical processes in lithium-sulphur cells by impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kolosnitsyn, V.S.; Kuzmina, E.V.; Karaseva, E.V.; Mochalov, S.E. [Institution of the Russian Academy of Sciences Institute of Organic Chemistry of Ufa Scientific Center of the Russian Academy of Sciences, Laboratory of Electrochemistry, 71, pr. Oktyabrya, Ufa, Bashkortostan, 450054 (Russian Federation)

    2011-02-01

    The changes in the properties of lithium-sulphur cell components (electrolyte, sulphur and lithium electrodes) during cycling are studied by AC impedance spectroscopy. It is shown that during the charge and discharge of lithium-sulphur cells the conductivity of the electrolyte is changed. We believe that the observed changes in the electrolyte conductivity can be explained by the formation of soluble lithium polysulphides by electrochemical reactions. The properties of the electrolyte significantly influence the rate of the electrochemical processes which occur both on the sulphur and lithium electrodes in lithium-sulphur cells. (author)

  6. Electrochemical impedance spectroscopy based-on interferon-gamma detection

    Science.gov (United States)

    Li, Guan-Wei; Kuo, Yi-Ching; Tsai, Pei-I.; Lee, Chih-Kung

    2014-03-01

    Tuberculosis (TB) is an ancient disease constituted a long-term menace to public health. According to World Health Organization (WHO), mycobacterium tuberculosis (MTB) infected nearly a third of people of the world. There is about one new TB occurrence every second. Interferon-gamma (IFN-γ) is associated with susceptibility to TB, and interferongamma release assays (IGRA) is considered to be the best alternative of tuberculin skin test (TST) for diagnosis of latent tuberculosis infection (LTBI). Although significant progress has been made with regard to the design of enzyme immunoassays for IFN-γ, adopting this assay is still labor-intensive and time-consuming. To alleviate these drawbacks, we used IFN-γ antibody to facilitate the detection of IFN-γ. An experimental verification on the performance of IGRA was done in this research. We developed two biosensor configurations, both of which possess high sensitivity, specificity, and rapid IFN-γ diagnoses. The first is the electrochemical method. The second is a circular polarization interferometry configuration, which incorporates two light beams with p-polarization and s-polarization states individually along a common path, a four photo-detector quadrature configuration to arrive at a phase modulated ellipsometer. With these two methods, interaction between IFN-γ antibody and IFN-γ were explored and presented in detail.

  7. Hydrogen oxidation kinetics on model Pd/C electrodes: Electrochemical impedance spectroscopy and rotating disk electrode study

    Energy Technology Data Exchange (ETDEWEB)

    Pronkin, Sergey N., E-mail: sergey.pronkin@unistra.f [Laboratory of Materials, Surfaces and Catalytic Processes, UMR 7515 of CNRS-UdS-ECPM, 25 rue Becquerel, 67087 Strasbourg (France); Bonnefont, Antoine [Institut de Chimie de Strasbourg, UMR 7177, CNRS-Universite de Strasbourg, 4 rue Blaise Pascal, 67000 Strasbourg (France); Ruvinskiy, Pavel S.; Savinova, Elena R. [Laboratory of Materials, Surfaces and Catalytic Processes, UMR 7515 of CNRS-UdS-ECPM, 25 rue Becquerel, 67087 Strasbourg (France)

    2010-03-30

    This work reports on the kinetics of the hydrogen oxidation reaction (HOR) on model Pd nanoparticles supported on a low surface area carbon substrate. Two Pd/C samples, with the average particle size 2.6 and 4.0 nm were used. The structure of the catalysts was characterized with the ex situ (electron microscopy) and in situ (electrochemical) methods. We utilized the electrochemical impedance spectroscopy (EIS) and the rotating disk electrode (RDE) voltammetry to study the kinetics of the HOR on Pd/C. The relevance of these techniques for elucidating the kinetics and the mechanism of the HOR on Pd/C was explored. The experimental results suggest that the catalytic activity of Pd in the HOR is more than 2 orders of magnitude lower than that of Pt, and does not depend on the particle size in the range from 2.6 to 4.0 nm. Computational modeling of the experimental steady-state (RDE) and non-steady-state (EIS) data shows that the reaction kinetics can be adequately described within Heyrovsky-Volmer mechanism, with the rate constants upsilon{sub 0H} = (8.8 +- 1.5) x 10{sup -10} mol cm{sup -2} s{sup -1} and upsilon{sub 0V} = (1.0 +- 0.3) x 10{sup -8} mol cm{sup -2} s{sup -1}. The model suggests that underpotentially deposited hydrogen H{sub UPD} is unlikely to be the active intermediate H{sub ad} of the HOR. It is concluded that the surface coverage of H{sub ad} deviates from that of H{sub UPD} with increasing overpotential, and the lateral interactions within H{sub ad} adlayer are weak.

  8. Compositional analysis of electrodeposited bismuth telluride thermoelectric thin films using combined electrochemical quartz crystal microgravimetry--stripping voltammetry.

    Science.gov (United States)

    Ham, Sunyoung; Jeon, Soyeon; Lee, Ungki; Park, Minsoon; Paeng, Ki-Jung; Myung, Noseung; Rajeshwar, Krishnan

    2008-09-01

    Bismuth telluride (Bi 2Te 3 ) is a benchmark material for thermoelectric power generation and cooling applications. Electrodeposition is a versatile technique for preparing thin films of this material; however, it affords films of variable composition depending on the preparation history. A simple and rapid assay of electrodeposited films, therefore, has both fundamental and practical importance. In this study, a new protocol for the electroanalysis of Bi 2Te 3 thin films is presented by combining the two powerful and complementary techniques of electrochemical quartz crystal microgravimetry (EQCM) and stripping voltammetry. First, any free (and excess) tellurium in the electrodeposited film was reduced to soluble Te ( 2- ) species by scanning to negative potentials in a 0.1 M Na 2SO 4 electrolyte, and the accompanying frequency increase (mass loss) was used to determine the content of free tellurium. The film was again subjected to cathodic stripping in the same medium (to generate Bi (0) and soluble Te (2-) from the Bi 2 Te 3 film component of interest), and the EQCM frequency change was used to determine the content of chemically bound Te in the Bi 2Te 3 thin film and thereby the compound stoichiometry. Finally, the EQCM frequency change during Bi oxidation to Bi (3+) and the difference between total Bi and Bi in Bi 2Te 3 resulted in the assay of free (excess) Bi in the electrodeposited film. Problems associated with the chemical/electrochemical stability of the free Bi species were circumvented by a flow electroanalysis approach. Data are also presented on the sensitivity of electrodeposited Bi 2Te 3 film composition to the electrodeposition potential. This newly developed method can be used for the compositional analysis of other thermoelectric thin-film material candidates in general.

  9. An improvement to the data processing course of electrochemical impedance technique

    Institute of Scientific and Technical Information of China (English)

    Yinglv Jiang; Yinshun Wu; Hong Chu

    2003-01-01

    For some electrochemical systems the traditional data processing methods can not be met, so it is necessary to develop a new method to deal with these problems. When processing the electrochemical AC impedance data of titanium alloy TA12 in 3% NaC1 solution (at free corrosion potential, room temperature) a new method is developed which can detach the information of the interface resistance demonstrably from the interface capacitance. The results show that the interface resistance and capacitance are all functions of frequency. And the AC impedance of the resistance and capacitance obey the following relations: C(f) = 104.01982 f-0.9292,R(f) =104.80011 (f+0.008)-0.90897, which is completely different from the traditional conception that the interface resistance and capacitance are constants. And this phenomenon is ubiquitous in titanium alloys according to the study. So perhaps it is an innate characteristic of interface.

  10. ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY STUDY OF CORROSION INHIBITION OF MODIFIED LIGNOSULPHONATE FOR CARBON STEEL

    Institute of Scientific and Technical Information of China (English)

    C.H. Yi; X.Q. Qiu; D.J. Yang; H.M. Lou

    2005-01-01

    The corrosion inhibition for carbon steel in circulating cooling water by modified lignosulphonate has been investigated using electrochemical impedance spectroscopy technique. Results show that the inhibition efficiency of modified lignosulphonate GCL2 is a great improvement on that of lignosulphonate. The maximum inhibition efficiency of GCL2 reaches 99.21% at forming adsorption film on the metal surface for the electrochemical impedance spectroscopy in GCL2 solution shows more than one time-constant. Moreover, results also indicate that it is more efficient in stirring solution than in still solution for GCL2 because the constant of adsorption in stirring solution is much larger than that in still solution. The adsorption of inhibitor GCL2 follows Langmuir's adsorption isotherm.

  11. Electrochemical cell design for the impedance studies of chlorine evolution at DSA anodes

    Science.gov (United States)

    Silva, J. F.; Dias, A. C.; Araújo, P.; Brett, C. M. A.; Mendes, A.

    2016-08-01

    A new electrochemical cell design suitable for the electrochemical impedance spectroscopy (EIS) studies of chlorine evolution on Dimensionally Stable Anodes (DSA®) has been developed. Despite being considered a powerful tool, EIS has rarely been used to study the kinetics of chlorine evolution at DSA anodes. Cell designs in the open literature are unsuitable for the EIS analysis at high DSA anode current densities for chlorine evolution because they allow gas accumulation at the electrode surface. Using the new cell, the impedance spectra of the DSA anode during chlorine evolution at high sodium chloride concentration (5 mol dm-3 NaCl) and high current densities (up to 140 mA cm-2) were recorded. Additionally, polarization curves and voltammograms were obtained showing little or no noise. EIS and polarization curves evidence the role of the adsorption step in the chlorine evolution reaction, compatible with the Volmer-Heyrovsky and Volmer-Tafel mechanisms.

  12. Direct immobilization of antibodies on a new polymer film for fabricating an electrochemical impedance immunosensor.

    Science.gov (United States)

    Zhang, Xiangyang; Shen, Guangyu; Shen, Youming; Yin, Dan; Zhang, Chunxiang

    2015-09-15

    A new polymer bearing aldehyde groups was designed and synthesized by grafting 4-pyridinecarboxaldehyde onto poly(epichlorohydrin). Antibodies can be directly immobilized on the surface of the polymer film through the covalent bonding of aldehyde groups of the film with amino groups of antibodies. In this study, human immunoglobulin G (IgG) was used as a model analyte for the fabrication of an electrochemical impedance immunosensor. Using the proposed immunosensor, IgG in the range from 0.1 to 80 ng ml(-1) was detected with a detection limit of 0.07 ng ml(-1) (signal/noise [S/N]=3). In addition, the electrochemical impedance immunosensor displays good stability and reproducibility.

  13. Electrochemical impedance analysis of spray deposited CZTS thin film: Effect of Se introduction

    Science.gov (United States)

    Patil, Swati J.; Lokhande, Vaibhav C.; Lee, Dong-Weon; Lokhande, Chandrakant D.

    2016-08-01

    The present work deals with electrochemical impedance analysis of spray deposited Cu2ZnSnS4 (CZTS) thin films grown on fluorine doped tin oxide (FTO) substrates and effect of post Se introduction. The CZTS thin films are characterized using X-ray diffraction (XRD), X-Ray photo spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM) and UV-Vis spectroscopy techniques. The electrochemical measurements are carried out using impedance analysis spectroscopy. The strong peak in XRD pattern along (112) plane confirms the Kestrite crystal structure of CZTS film. The FE-SEM analysis reveals that nanoflakes contain crack-free surface microstructure changes with post Se introucation. The optical study reveals that absorption increases with Se dipping time and observed lower band gap of 1.31 eV. Introduction of Se in CZTS film results an improvement in the grain size and surface morphology which leads to increased electrical conductivity of CZTS film.

  14. Integration of Faradaic electrochemical impedance spectroscopy into a scalable surface plasmon biosensor for in tandem detection.

    Science.gov (United States)

    Hong, Brandon; Sun, Alexander; Pang, Lin; Venkatesh, A G; Hall, Drew; Fainman, Yeshaiahu

    2015-11-16

    We present an integrated label-free biosensor based on surface plasmon resonance (SPR) and Faradaic electrochemical impedance spectroscopy (f-EIS) sensing modalities, for the simultaneous detection of biological analytes. Analyte detection is based on the angular spectroscopy of surface plasmon resonance and the extraction of charge transfer resistance values from reduction-oxidation reactions at the gold surface, as responses to functionalized surface binding events. To collocate the measurement areas and fully integrate the modalities, holographically exposed thin-film gold SPR-transducer gratings are patterned into coplanar electrodes for tandem impedance sensing. Mutual non-interference between plasmonic and electrochemical measurement processes is shown, and using our scalable and compact detection system, we experimentally demonstrate biotinylated surface capture of neutravidin concentrations as low as 10 nM detection, with a 5.5 nM limit of detection.

  15. Electrochemical cell design for the impedance studies of chlorine evolution at DSA(®) anodes.

    Science.gov (United States)

    Silva, J F; Dias, A C; Araújo, P; Brett, C M A; Mendes, A

    2016-08-01

    A new electrochemical cell design suitable for the electrochemical impedance spectroscopy (EIS) studies of chlorine evolution on Dimensionally Stable Anodes (DSA(®)) has been developed. Despite being considered a powerful tool, EIS has rarely been used to study the kinetics of chlorine evolution at DSA anodes. Cell designs in the open literature are unsuitable for the EIS analysis at high DSA anode current densities for chlorine evolution because they allow gas accumulation at the electrode surface. Using the new cell, the impedance spectra of the DSA anode during chlorine evolution at high sodium chloride concentration (5 mol dm(-3) NaCl) and high current densities (up to 140 mA cm(-2)) were recorded. Additionally, polarization curves and voltammograms were obtained showing little or no noise. EIS and polarization curves evidence the role of the adsorption step in the chlorine evolution reaction, compatible with the Volmer-Heyrovsky and Volmer-Tafel mechanisms.

  16. Potentiodynamic electrochemical impedance spectroscopy of silver on platinum in underpotential and overpotential deposition

    Science.gov (United States)

    Ragoisha, Genady A.; Bondarenko, Alexander S.

    2004-09-01

    Simultaneous monitoring of ac and dc responses of the electrode-electrolyte interface with potentiodynamic electrochemical impedance spectroscopy (PDEIS) in silver underpotential and overpotential deposition on platinum has confirmed the role of intrinsic Pt surface changes in the irreversibility of Ag underpotential deposition and disclosed exceptionally high stability of Ag monolayer on Pt. PDEIS has been demonstrated to be a convenient means for wet surface chemistry monitoring.

  17. Potentiodynamic Electrochemical Impedance Spectroscopy of Silver on Platinum in Underpotential and Overpotential Deposition

    OpenAIRE

    Ragoisha, Genady; Bondarenko, Alexander

    2003-01-01

    Simultaneous monitoring of ac and dc responses of the electrode-electrolyte interface with potentiodynamic electrochemical impedance spectroscopy (PDEIS) in silver underpotential and overpotential deposition on platinum has confirmed the role of intrinsic Pt surface changes in the irreversibility of Ag underpotential deposition and disclosed exceptionally high stability of Ag monolayer on Pt. PDEIS has been demonstrated to be a convenient means for wet surface chemistry monitoring.

  18. Modelling of a High Temperature PEM Fuel Cell Stack using Electrochemical Impedance Spectroscopy

    DEFF Research Database (Denmark)

    Andreasen, Søren Juhl; Jespersen, Jesper Lebæk; Kær, Søren Knudsen

    In designing and controlling fuel cell sys-tems it is advantageous having models predicting the behavior of the fuel cells in steady-state as well as in dynamic ope-ration. This work examines the use of electro-chemical impedance spectroscopy (EIS) for characterizing and developing a model for a ...... for a high temperature PEM (HTPEM) fuel cell stack. A Labview virtual interface has been developed to perform the signal generation and acquisition which is needed to perform EIS....

  19. Lithium-Ion Battery Power Degradation Modelling by Electrochemical Impedance Spectroscopy

    DEFF Research Database (Denmark)

    Stroe, Daniel-Ioan; Swierczynski, Maciej Jozef; Stroe, Ana-Irina

    2017-01-01

    This paper investigates the use of the electrochemical impedance spectroscopy (EIS) technique as an alternative to the DC pulses technique for estimating the power capability decrease of Lithium-ion batteries during calendar ageing. Based on results obtained from calendar ageing tests performed...... at different conditions during one to two years, a generalized model that estimates the battery power capability decrease as function of the resistance Rs increase (obtained from EIS) was proposed and successfully verified....

  20. Characterization by acoustic emission and electrochemical impedance spectroscopy of the cathodic disbonding of Zn coating

    Energy Technology Data Exchange (ETDEWEB)

    Amami, Souhail [Universite de Technologie de Compiegne, Departement de Genie Mecanique, Laboratoire Roberval, UMR 6066 du CNRS, B.P. 20529, 60206 Compiegne Cedex (France)], E-mail: souhail.amami@utc.fr; Lemaitre, Christian; Laksimi, Abdelouahed; Benmedakhene, Salim [Universite de Technologie de Compiegne, Departement de Genie Mecanique, Laboratoire Roberval, UMR 6066 du CNRS, B.P. 20529, 60206 Compiegne Cedex (France)

    2010-05-15

    Galvanized steel has been tested in a synthetic sea water solution under different cathodic overprotection conditions. The generated hydrogen flux caused the damage of the metal-zinc interface and led to a progressive coating detachment. Scanning electron microscopy, electrochemical impedance spectroscopy and acoustic emission technique were used to characterize the damage chronology under different cathodic potentials. A damage mechanism was proposed and the acoustic signature related to the coating degradation was statistically identified using clustering techniques.

  1. Quantitative electrochemical detection of cathepsin B activity in complex tissue lysates using enhanced AC voltammetry at carbon nanofiber nanoelectrode arrays.

    Science.gov (United States)

    Swisher, Luxi Z; Prior, Allan M; Shishido, Stephanie; Nguyen, Thu A; Hua, Duy H; Li, Jun

    2014-06-15

    The proteolytic activity of a cancer-related enzyme cathepsin B is measured with alternating current voltammetry (ACV) using ferrocene (Fc) labeled tetrapeptides attached to nanoelectrode arrays (NEAs) fabricated with vertically aligned carbon nanofibers (VACNFs). This combination enables the use of high AC frequencies (~1kHz) with enhanced electrochemical signals. The specific proteolysis of the Fc-peptide by cathepsin B produces decay in the ACV peak current versus the reaction time. The exponential component of the raw data can be extracted and defined as the "extracted proteolytic signal" which allows consistent quantitative analyses using a heterogeneous Michaelis-Menten model. A "specificity constant" kcat/KM = (3.68 ± 0.50) × 10(4)M(-1)s(-1) for purified cathepsin B was obtained. The detections of cathepsin B activity in different concentrations of whole lysate of human breast tissue, tissue lysate spiked with varied concentrations of cathepsin B, and the tissue lysate after immunoprecipitation showed that there is ~13.4 nM higher cathepsin B concentration in 29.1 µg mL(-1) of whole tissue lysate than the immunoprecipitated sample. The well-defined regular VACNF NEAs by e-beam lithography show a much faster kinetics for cathepsin B proteolysis with kcat/KM = 9.2 × 10(4)M(-1)s(-1). These results illustrate the potential of this technique as a portable multiplex electronic system for cancer diagnosis by rapid protease profiling of serum or blood samples.

  2. Cyclic voltammetry and scanning electrochemical microscopy studies of the heterogeneous electron transfer reaction of some nitrosoaromatic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Bollo, S.; Finger, S.; Sturm, J.C.; Nunez-Vergara, L.J.; Squella, J.A. [Bioelectrochemistry Laboratory, Chemical and Pharmaceutical Sciences Faculty, University of Chile, P.O. Box 233, Santiago 1 (Chile)

    2007-04-20

    The heterogeneous electron transfer reaction for the reduction of some nitroso aromatic derivatives in aqueous-alcoholic medium was studied on both mercury and glassy carbon electrodes (GCE) by using cyclic voltammetry (CV) and scanning electrochemical microscopy techniques (SECM). The nitrosoaromatic derivatives followed a two-electron two-proton mechanism producing a quasi-reversible overall process. This strongly pH dependent mechanism varied from ECCE mechanism at pH < 8.5 to ECEC mechanism at pH > 8.5. The apparent heterogeneous rate constant for the reduction of the nitroso derivatives was calculated using CV or SECM. The rate constant for the electron transfer process depends on the nature of the electrode material. The heterogeneous rate constant on the GCE is almost two orders of magnitude smaller than that on mercury electrode i.e. (3.4 {+-} 0.3) x 10{sup -3} cm s{sup -1} on Hg and (7.0 {+-} 1.0) x 10{sup -5} cm s{sup -1} on GCE, for the same nitroso compound and pH. The heterogeneous rate constant values were checked by comparison between experimental and simulated cyclic voltammograms. (author)

  3. Solid-state voltammetry-based electrochemical immunosensor for Escherichia coli using graphene oxide-Ag nanoparticle composites as labels.

    Science.gov (United States)

    Jiang, Xiaochun; Chen, Kun; Wang, Jing; Shao, Kang; Fu, Tao; Shao, Feng; Lu, Donglian; Liang, Jiangong; Foda, M Frahat; Han, Heyou

    2013-06-21

    A new electrochemical immunosensor based on solid-state voltammetry was fabricated for the detection of Escherichia coli (E. coli) by using graphene oxide-Ag nanoparticle composites (P-GO-Ag) as labels. To construct the platform, Au nanoparticles (AuNPs) were first self-assembled on an Au electrode surface through cysteamine and served as an effective matrix for antibody (Ab) attachment. Under a sandwich-type immunoassay format, the analyte and the probe (P-GO-Ag-Ab) were successively captured onto the immunosensor. Finally, the bonded AgNPs were detected through a solid-state redox process in 0.2 M of KCl solution. Combining the advantages of the high-loading capability of graphene oxide with promoted electron-transfer rate of AuNPs, this immunosensor produced a 26.92-fold signal enhancement compared with the unamplified protocol. Under the optimal conditions, the immunosensor exhibited a wide linear dependence on the logarithm of the concentration of E. coli ranging from 50 to 1.0 × 10(6) cfu mL(-1) with a detection limit of 10 cfu mL(-1). Moreover, as a practical application, the proposed immunosensor was used to monitor E. coli in lake water with satisfactory results.

  4. Characterisation and modelling of a high temperature PEM fuel cell stack using electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Jespersen, J.L. [Danish Technological Institute, Kongsvang Alle 29, DK-8000 Arhus C (Denmark); Schaltz, E.; Kaer, S.K. [Department of Energy Technology, Aalborg University, Pontoppidanstraede 101, DK-9220 Aalborg East (Denmark); Andreasen, S.J.

    2009-08-15

    In designing and controlling fuel cell systems, it is advantageous to have models which predict fuel cell behaviour in steady-state as well as in dynamic operation. This work examines the use of electro-chemical impedance spectroscopy (EIS) for characterising and developing an impedance model for a high temperature PEM (HT-PEM) fuel cell stack. A Labview virtual instrument has been developed to perform the signal generation and data acquisition which is needed to perform EIS. The typical output of an EIS measurement on a fuel cell is a Nyquist plot, which shows the imaginary and real parts of the impedance of the measured system. The full stack impedance depends on the impedance of each of the single cells of the stack. Equivalent circuit models for each single cell can be used to predict the stack impedance at different temperature profiles of the stack. The information available in such models can be used to predict the fuel cell stack performance, e.g. in systems where different electronic components introduce current harmonics. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  5. Electrochemical synthesis and surface characterization of (pyrrole+2-methylfuran) copolymer

    Science.gov (United States)

    Djaouane, Linda; Nessark, Belkacem; Sibous, Lakhdar

    2017-02-01

    Electrochemical copolymerization of pyrrole (Py) and 2-methylfuran (2 MF) was performed on platinum and ITO substrates in acetonitrile/lithium perchlorate solution, using cyclic voltammetry method. The electrochemical behavior of the modified electrode surface by polypyrrole, poly(2-methylfuran) homopolymers and (pyrrole+2-methylfuran) copolymer was characterized by cyclic voltammetry, electrochemical impedance spectroscopy (EIS), UV-visible spectroscopy, atomic force microscopy (AFM) and scanning electron microscopy (SEM). The cyclic voltammetry shows anodic and cathodic peaks which are characteristic of the oxidation and the reduction of the formed films. The electrochemical impedance spectroscopy confirmed the results obtained by cyclic voltammetry. AFM and SEM analyses proved as well that the morphology and the electrochemical properties of the polypyrrole film are modified in the presence of 2-methylfuran.

  6. Electrochemical Impedance Study of Zinc Yellow Polypropylene-Coated Aluminum Alloy

    Directory of Open Access Journals (Sweden)

    Zhi-hua Sun

    2010-01-01

    Full Text Available Performance of zinc yellow polypropylene-coated aluminum alloy 7B04 during accelerated degradation test is studied using electrochemical impedance spectroscopy (EIS. It has been found that the zinc yellow polypropylene paint has few flaw and acts as a pure capacitance before accelerated test. After 336-hour exposure to the test, the impedance spectroscopy shows two time constants, and water has reached to the aluminum alloy/paint interface and forms corrosive microcell. For the scratched samples, the reaction of metal corrosion and the hydrolysis of zinc yellow ion can occur simultaneously. The impedance spectroscopy indicates inductance after 1008-hour exposure to the test, but the inductance disappears after 1344-hour exposure and the passivation film has pitting corrosion.

  7. The theory of cyclic voltammetry of electrochemically heterogeneous surfaces: comparison of different models for surface geometry and applications to highly ordered pyrolytic graphite.

    Science.gov (United States)

    Ward, Kristopher R; Lawrence, Nathan S; Hartshorne, R Seth; Compton, Richard G

    2012-05-28

    The cyclic voltammetry at electrodes composed of multiple electroactive materials, where zones of one highly active material are distributed over a substrate of a second, less active material, is investigated by simulation. The two materials are assumed to differ in terms of their electrochemical rate constants towards any given redox couple. For a one-electron oxidation or reduction, the effect on voltammetry of the size and relative surface coverages of the zones as well as the rate constant of the slower zone are considered for systems where it is much slower than the rate constant of the faster zones. The occurrence of split peak cyclic voltammetry where two peaks are observed in the forward sweep, is studied in terms of the diffusional effects present in the system. A number of surface geometries are compared: specifically the more active zones are modelled as long, thin bands, as steps in the surface, as discs, and as rings (similar to a partially blocked electrode). Similar voltammetry for the band, step and ring models is seen but the disc geometry shows significant differences. Finally, the simulation technique is applied to the modelling of highly-ordered pyrolytic graphite (HOPG) surface and experimental conditions under which it may be possible to observe split peak voltammetry are predicted.

  8. Electrochemical impedance spectroscopy of metal alloys in the space transportation system launch environment

    Science.gov (United States)

    Calle, Luz

    1990-01-01

    AC impedance measurements were performed to investigate the corrosion resistance of 18 alloys under conditions similar to the Space Transportation System (STS) launch environment. The alloys were: (1) zirconium 702; (2) Hastelloy C-22, C-276, C-4, and B-2; (3) Inconel 600 and 825; (4) Ferralium 255; (5) Inco Alloy G-3; (6) 20Cb-3; (7) SS 904L, 304LN, 316L, 317L, and 304L; (8) ES 2205; and (9) Monel 400. AC impedance data were gathered for each alloy at various immersion times in 3.55 percent NaCl-0.1N HCl. Polarization resistance values were obtained for the Nyguist plots at each immersion time using the EQUIVALENT CIRCUIT software package available with the 388 electrochemical impedance software. Hastelloy C-22 showed the highest overall values for polarization resistance while Monel 400 and Inconel 600 had the lowest overall values. There was good general correlation between the corrosion performance of the alloys at the beach corrosion testing site, and the expected rate of corrosion as predicted based on the polarization resistance values obtained. The data indicate that electrochemical impedance spectroscopy can be used to predict the corrosion performance of metal alloys.

  9. Theoretical models for electrochemical impedance spectroscopy and local ζ-potential of unfolded proteins in nanopores

    Science.gov (United States)

    Vitarelli, Michael J.; Talaga, David S.

    2013-01-01

    Single solid-state nanopores find increasing use for electrical detection and/or manipulation of macromolecules. These applications exploit the changes in signals due to the geometry and electrical properties of the molecular species found within the nanopore. The sensitivity and resolution of such measurements are also influenced by the geometric and electrical properties of the nanopore. This paper continues the development of an analytical theory to predict the electrochemical impedance spectra of nanopores by including the influence of the presence of an unfolded protein using the variable topology finite Warburg impedance model previously published by the authors. The local excluded volume of, and charges present on, the segment of protein sampled by the nanopore are shown to influence the shape and peak frequency of the electrochemical impedance spectrum. An analytical theory is used to relate the capacitive response of the electrical double layer at the surface of the protein to both the charge density at the protein surface and the more commonly measured zeta potential. Illustrative examples show how the theory predicts that the varying sequential regions of surface charge density and excluded volume dictated by the protein primary structure may allow for an impedance-based approach to identifying unfolded proteins. PMID:24050368

  10. Electrochemical characteristics and impedance spectroscopy studies of nano-cobalt silicate hydroxide for supercapacitor

    Science.gov (United States)

    Zhang, Guo-Qing; Zhao, Yong-Qing; Tao, Feng; Li, Hu-Lin

    Cobalt silicate hydroxide (Co 3[Si 2O 5] 2[OH] 2) was prepared by chemical method for use in electrochemical capacitors. X-ray diffraction (XRD) and transmission electron microscopy (TEM) tests indicate that the material was pure hexagonal phase with uniform nanometer size distribution. Cyclic voltammeter (CV) and galvanostatic charge/discharge measurements show that the cobalt silicate hydroxide-based electrode has stable electrochemical capacitor properties between potential range of 0.1-0.55 V with a maximum specific capacitance of 237 F g -1 in alkaline solution and 95% of capacity efficiency was reached after 150 cycles. Electrochemical impedance spectra (EIS) investigation illustrates that the capacitance of the test electrode was mainly consisted of pseudo-capacitance, which was caused by underpotential deposition of H 3O + at the electrode surface.

  11. Electrochemical impedance spectroscopy characterization of mercaptopropionic acid capped ZnS nanocrystal based bioelectrode for the detection of the cardiac biomarker--myoglobin.

    Science.gov (United States)

    Mishra, Sujeet K; Kumar, Devendra; Biradar, Ashok M; Rajesh

    2012-12-01

    3-Mercaptopropionic acid (MPA) capped ZnS nanocrystals (ZnS(MPA)) are covalently attached to a self assembled monolayer (SAM) of 3-aminopropyltriethoxysilane (APTES) on an indium-tin-oxide (ITO) coated glass plate. The protein antibody, anti-myoglobin (Ab-Mb), is covalently linked to free carboxyl groups present on ZnS(MPA) nanocrystals via carbodiimide coupling reaction to form a bioelectrode (Ab-Mb(BSA)/ZnS(MPA)/APTES/ITO-glass). This bioelectrode has been characterized using atomic force microscopy (AFM), contact angle measurements, cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The optimal equivalent circuit model that matches the impedimetric responses of the bioelectrode describes three distinct regions: the electrolyte solution resistance (R(s)), the double layer capacitance (C(dl)) and the specific charge transfer resistance (R(et)). The EIS measurements revealed that the R(et) increases considerably with no significant change in C(dl) after immunoreaction with protein specific antigen myoglobin, Ag-Mb, so that the prepared bioelectrode can be used for the detection of Ag-Mb. The bioelectrode exhibits an electrochemical impedance response to Ag-Mb, in a linear range from 10ng to 1μgmL(-1) phosphate buffer solution (pH 7.4) with a R(et) sensitivity of 117.36Ωcm(2) per decade.

  12. Analysis of Different Series-Parallel Connection Modules for Dye-Sensitized Solar Cell by Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Jung-Chuan Chou

    2016-01-01

    Full Text Available The internal impedances of different dye-sensitized solar cell (DSSC models were analyzed by electrochemical impedance spectrometer (EIS with an equivalent circuit model. The Nyquist plot was built to simulate the redox reaction of internal device at the heterojunction. It was useful to analyze the component structure and promote photovoltaic conversion efficiency of DSSC. The impedance of DSSC was investigated and the externally connected module assembly was constructed utilizing single cells on the scaled-up module. According to the experiment results, the impedance was increased with increasing cells connected in series. On the contrary, the impedance was decreased with increasing cells connected in parallel.

  13. A new lithium-ion battery internal temperature on-line estimate method based on electrochemical impedance spectroscopy measurement

    Science.gov (United States)

    Zhu, J. G.; Sun, Z. C.; Wei, X. Z.; Dai, H. F.

    2015-01-01

    The power battery thermal management problem in EV (electric vehicle) and HEV (hybrid electric vehicle) has been widely discussed, and EIS (electrochemical impedance spectroscopy) is an effective experimental method to test and estimate the status of the battery. Firstly, an electrochemical-based impedance matrix analysis for lithium-ion battery is developed to describe the impedance response of electrochemical impedance spectroscopy. Then a method, based on electrochemical impedance spectroscopy measurement, has been proposed to estimate the internal temperature of power lithium-ion battery by analyzing the phase shift and magnitude of impedance at different ambient temperatures. Respectively, the SoC (state of charge) and temperature have different effects on the impedance characteristics of battery at various frequency ranges in the electrochemical impedance spectroscopy experimental study. Also the impedance spectrum affected by SoH (state of health) is discussed in the paper preliminary. Therefore, the excitation frequency selected to estimate the inner temperature is in the frequency range which is significantly influenced by temperature without the SoC and SoH. The intrinsic relationship between the phase shift and temperature is established under the chosen excitation frequency. And the magnitude of impedance related to temperature is studied in the paper. In practical applications, through obtaining the phase shift and magnitude of impedance, the inner temperature estimation could be achieved. Then the verification experiments are conduced to validate the estimate method. Finally, an estimate strategy and an on-line estimation system implementation scheme utilizing battery management system are presented to describe the engineering value.

  14. Cyclic Voltammetry Experiment.

    Science.gov (United States)

    Van Benschoten, James J.; And Others

    1983-01-01

    Describes a three-part experiment designed to introduce cyclic voltammetry to graduate/undergraduate students. Part 1 demonstrates formal reduction potential, redox electron transfer, diffusion coefficient, and electrochemical reversibility. Part 2 investigates electrochemical behavior of acetaminophen. Part 3 examines such experimental variables…

  15. Cyclic Voltammetry Experiment.

    Science.gov (United States)

    Van Benschoten, James J.; And Others

    1983-01-01

    Describes a three-part experiment designed to introduce cyclic voltammetry to graduate/undergraduate students. Part 1 demonstrates formal reduction potential, redox electron transfer, diffusion coefficient, and electrochemical reversibility. Part 2 investigates electrochemical behavior of acetaminophen. Part 3 examines such experimental variables…

  16. Electrochemical Impedance Spectroscopy as a Powerful Analytical Tool for the Study of Microbial Electrochemical Cells

    NARCIS (Netherlands)

    Yoho, R.A.; Popat, S.C.; Fabregat-Santiago, F.; Giménez, S.; Heijne, ter A.; Torres, C.

    2015-01-01

    In microbial electrochemical cells (MXCs), not only classic overpotentials known from other types of fuel cells are encountered, but also overpotentials associated with the metabolic processes and electron-transport pathways in bacteria are encountered. Of the many techniques that can be used to inv

  17. Application of electrochemical impedance spectroscopy for fuel cell characterization: PEFC and oxygen reduction reaction in alkaline solution

    Energy Technology Data Exchange (ETDEWEB)

    Wagner, N.; Friedrich, K.A. [German Aerospace Center, Institute for Technical Thermodynamics, Stuttgart (Germany)

    2009-06-15

    The most common method used to characterise the electrochemical performance of fuel cells is the recording of current/voltage U(i) curves. Separation of electrochemical and ohmic contributions to the U(i) characteristics requires additional experimental techniques like electrochemical impedance spectroscopy (EIS). The application of EIS is an approach to determine parameters which have proved to be indispensable for the characterisation and development of all types of fuel cell electrodes and electrolyte electrode assemblies [1]. In addition to EIS semi-empirical approaches based on simplified mathematical models can be used to fit experimental U(i) curves [2]. By varying the operating conditions of the fuel cell and by the simulation of the measured EIS with an appropriate equivalent circuit, it is possible to split the cell impedance into electrode impedances and electrolyte resistance. Integration in the current density domain of the individual impedance elements enables the calculation of the individual overpotentials in the fuel cell (PEFC) and the assignment of voltage loss to the different processes. In case of using a three electrode cell configuration with a reference electrode, one can directly determine the corresponding overvoltage. For the evaluation of the measured impedance spectra the porous electrode model of Goehr [3] was used. This porous electrode model includes different impedance contributions like impedance of the interface porous layer/pore, interface porous layer/electrolyte, interface porous layer/bulk, impedance of the porous layer and impedance of the pores filled by electrolyte. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  18. Cyclic Voltammetry Probe Approach Curves with Alkali Amalgams at Mercury Sphere-Cap Scanning Electrochemical Microscopy Probes.

    Science.gov (United States)

    Barton, Zachary J; Rodríguez-López, Joaquín

    2017-03-07

    We report a method of precisely positioning a Hg-based ultramicroelectrode (UME) for scanning electrochemical microscopy (SECM) investigations of any substrate. Hg-based probes are capable of performing amalgamation reactions with metal cations, which avoid unwanted side reactions and positive feedback mechanisms that can prove problematic for traditional probe positioning methods. However, prolonged collection of ions eventually leads to saturation of the amalgam accompanied by irreversible loss of Hg. In order to obtain negative feedback positioning control without risking damage to the SECM probe, we implement cyclic voltammetry probe approach surfaces (CV-PASs), consisting of CVs performed between incremental motor movements. The amalgamation current, peak stripping current, and integrated stripping charge extracted from a shared CV-PAS give three distinct probe approach curves (CV-PACs), which can be used to determine the tip-substrate gap to within 1% of the probe radius. Using finite element simulations, we establish a new protocol for fitting any CV-PAC and demonstrate its validity with experimental results for sodium and potassium ions in propylene carbonate by obtaining over 3 orders of magnitude greater accuracy and more than 20-fold greater precision than existing methods. Considering the timescales of diffusion and amalgam saturation, we also present limiting conditions for obtaining and fitting CV-PAC data. The ion-specific signals isolated in CV-PACs allow precise and accurate positioning of Hg-based SECM probes over any sample and enable the deployment of CV-PAS SECM as an analytical tool for traditionally challenging conditions.

  19. Electrochemical impedance spectra of V2O5 xerogel films with intercalation of lithium ion

    Institute of Scientific and Technical Information of China (English)

    ZHANG Yong; LIU Yu-wen; CHENG Yu-shan; HU Xin-guo

    2005-01-01

    Vanadium pentoxide xerogel films used for lithium rechargeable batteries were prepared from crystalline c-V2 O5 by melt quenching method,then the electrochemical process of lithium intercalation into vanadium pentoxide xerogel films was simulated with an equivalent circuit model, which was derived from the mechanism of electrode reactions. Measured electrochemical impedance spectra at various electrode potentials were analyzed by using the complex non-linear least-squares fitting method. The results show that impedance spectra consist of 2 high-to-medium frequency depressed arcs and a low frequency straight line. The high frequency arc is attributed to the absorption reaction of lithium ions into the oxide film, the medium frequency arc is attributed to the charge transfer reaction at the vanadium oxide/electrolyte interface and the low frequency is characterized by a straight line with a phase angle of 45° corresponding to the diffusion of lithium ion through vanadium oxide phase. The experimental and calculated results are compared and discussed focusing on the electrochemical performance and the state of charge of the electrode. Moreover, the high consistence of the fitted values of the model to the experimental data indicates that this mathematical model does give a satisfying description of the intercalation process of vanadium pentoxide xerogel films.

  20. Simultaneous Investigation of the Effect of Advanced Thermomechanical Treatment and Repetitive Cyclic Voltammetry on the Electrochemical Behavior of AISI 430 Ferritic Stainless Steel

    Science.gov (United States)

    Vafaeian, Saeed; Fattah-alhosseini, Arash; Keshavarz, Mohsen K.; Mazaheri, Yousef

    2017-01-01

    In this study, it was revealed that the electrochemical behavior of AISI 430 ferritic stainless steel can be modified and improved to a large extent by the application of repetitive cyclic voltammetry in the anodic polarization branch of the alloy. The efficiency of this method was evaluated on the basis of the alloy grain size which is of great importance in corrosion studies. In fact, a coarse grain structure versus a fine grain structure was the subject of the used surface treatment method. Coarsening and refining of the grain size were conducted through a heat treatment and an advanced thermomechanical process. On the basis of cyclic voltammetry tests and also the electrochemical tests performed after that, it was shown that cyclic voltammetry had a significant improving effect on the passive behavior of both fine- and coarse-grained samples. Moreover, superior behavior of fine-grained sample in comparison with coarse-grained one was distinguished by its smaller cyclic voltammogram loops, more noble free potentials, larger capacitive arcs in the Nyquist plots, and less charge carrier densities within the passive film.

  1. Simultaneous Investigation of the Effect of Advanced Thermomechanical Treatment and Repetitive Cyclic Voltammetry on the Electrochemical Behavior of AISI 430 Ferritic Stainless Steel

    Science.gov (United States)

    Vafaeian, Saeed; Fattah-alhosseini, Arash; Keshavarz, Mohsen K.; Mazaheri, Yousef

    2017-02-01

    In this study, it was revealed that the electrochemical behavior of AISI 430 ferritic stainless steel can be modified and improved to a large extent by the application of repetitive cyclic voltammetry in the anodic polarization branch of the alloy. The efficiency of this method was evaluated on the basis of the alloy grain size which is of great importance in corrosion studies. In fact, a coarse grain structure versus a fine grain structure was the subject of the used surface treatment method. Coarsening and refining of the grain size were conducted through a heat treatment and an advanced thermomechanical process. On the basis of cyclic voltammetry tests and also the electrochemical tests performed after that, it was shown that cyclic voltammetry had a significant improving effect on the passive behavior of both fine- and coarse-grained samples. Moreover, superior behavior of fine-grained sample in comparison with coarse-grained one was distinguished by its smaller cyclic voltammogram loops, more noble free potentials, larger capacitive arcs in the Nyquist plots, and less charge carrier densities within the passive film.

  2. The Influence of Uncompensated Solution Resistance on the Determination and Standard Electrochemical Rate Constants Using Cyclic Voltammetry, and Some Comparisons with AC Voltammetry.

    Science.gov (United States)

    1987-09-25

    rate constants, k2r using cyclic voltametry . The res tss are expressed in terms of systematic deviations oP sapparent measured" rate constants, k~b(app...Classification) The Influence of Uncompensated Solution Resistance on the Determination and Standard Electro- - . chemical Rate Constants Using Cyclic ...Year MonhOy SAGE COUNT FIELD GROUP Sue-GROUP digital simulation analysis, uncompensated solution resis- I A tance, electrochemical rate constants, cyclic

  3. Electrochemical impedance spectroscopy of dodecylsulphate doped polypyrrole films in the dark and under illumination

    Directory of Open Access Journals (Sweden)

    Martini Milena

    2000-01-01

    Full Text Available The morphology, thickness, oxidation and illumination effects in dodecylsulphate doped polypyrrole films can be qualitatively observed by EIS and consist in variations of interfacial and bulk resistances and capacitances of a proposed equivalent circuit. The circuit well with the measured spectra of films obtained with 190 mC cm-2 of synthesis charge density. For thinner films the calculated values observed by electrochemical impedance spectroscopy (EIS deviate probably due to the absence of diffusion effects. The oxidation of the films diminishes the total impedance over the entire frequency range. The morphology effects are also observed in the entire spectra. The illumination effects are reversible and are observed as expected only in the reduced form of the polymer. The illumination reduces the internal resistance and the space-charge capacitance and increases the charge transfer resistance and the double layer capacitance.

  4. Characterisation of proton exchange membrane fuel cell (PEMFC) failures via electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Merida, W. [Clean Energy Research Centre, University of British Columbia, Vancouver, BC (Canada V6T 1Z4); Harrington, D.A. [Institute for Integrated Energy Systems, University of Victoria, Victoria, BC (Canada V8W 3P6); Le Canut, J.M. [Hydrogenics Corporation, 5985 McLaughlin Road, Mississauga, Ont. (Canada L5R 1B8); McLean, G. [Angstrom Power Corporation, 106-980 West 1st Street, North Vancouver, BC (Canada V7P 3N4)

    2006-10-20

    Two PEMFC failure modes (dehydration and flooding) were investigated using in situ electrochemical impedance spectroscopy (EIS) on a four-cell stack under load. The EIS measurements were made at different temperatures (70 and 80{sup o}C), covering the current density range 0.1-1.0Acm{sup -2}, and the frequency range 0.1-2x10{sup 5}Hz. Dehydration and flooding effects were observed in the frequency ranges 0.5-10{sup 5} and 0.5-10{sup 2}Hz, respectively. We propose that impedance measurements at separate frequency ranges (or narrow bands thereof) can be used to distinguish between flooding and dehydration events. Similar approaches may be used to diagnose other important PEMFC failures. (author)

  5. Anticorrosion performance of the coating/metal system by electrochemical impedance spectra

    Institute of Scientific and Technical Information of China (English)

    Yinghuai Zhang; Lining Xu; Minxu Lu; Pu Zhang

    2008-01-01

    In order to investigate the anticorrosion performance of the organic coating/metal system, electrochemical impedance spectra (EIS) were measured in the 3.5wt% NaC1 solution, the chemical component and the formation of corrosion products scale were analyzed by laser Raman microspectroscopy, and the pattern of the organic coating/metal system was observed by scanning electron microscopy (SEM). The characteristics and the delamination process of the organic coating/metal system were investigated systematically, and the emphases were on the transportation of the corrosive medium and the changes of the coating/metal interface. The results show that the impedance decreases at the initial immersion, then increases at the middle-immersion, and again decreases at last, which is related to the corrosion products scale. The concentration of Cl-in the coating, which destroys the corrosion products scale, increases with the immersion time.

  6. Development of electrochemical impedance spectroscopy based sensing system for DEHP detection

    KAUST Repository

    Zia, Asif I.

    2011-11-01

    This research work presents a real time and non invasive technique to detect Di(2-ethylhexyl) phthalate (DEHP)content in purified water and quantify its concentration by Electrochemical Impedance Spectroscopy(E.I.S.). Planar Inter-digital capacitive sensor is employed to evaluate conductivity, permeability and dielectric properties of material under test. This sensor, consisting of inter-digitated microelectrodes, is fabricated on silicon substrate using thin-film Microelectromechanical system (MEMS) based semiconductor device fabrication technology. Impedance spectrums are obtained with various concentrations of DEHP in purified water by using an electric circuit in order to extract sample conductance. Relationship of sample conductance with DEHP concentration is studied in this research work which enables us to show the ability of E.I.S. to detect DEHP concentration in water and hence can be applied in water treatment process for contamination quantification. © 2011 IEEE.

  7. Characterization of photoelectrochemical cells for water splitting by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Lopes, Tania; Andrade, Luisa; Ribeiro, Helena Aguilar; Mendes, Adelio [Laboratorio de Engenharia de Processos, Ambiente e Energia (LEPAE), Faculdade de Engenharia da Universidade do Porto, Rua Roberto Frias, 4200-465 Porto (Portugal)

    2010-10-15

    The photocurrent-voltage characteristic of a photoelectrochemical cell for solar hydrogen production via water splitting, using undoped-hematite as photoanode, was obtained. Photoelectrochemical characteristics of the cell were also investigated by electrochemical impedance spectroscopy. Both techniques were carried out in the dark and under illumination. The analysis of the frequency spectra for the real and imaginary parts of the complex impedance allowed obtaining equivalent electrical analogs for the PEC cell operating in the dark and under 1 sun simulated illumination. Additionally, different electrode configurations were used (two and three-electrode arrangements). The two-electrode configuration allowed the study of the overall charge transfer phenomena occurring at the semiconductor, within the electrolyte and at the counter-electrode side of the cell, whereas the three-electrode configuration gave more detailed information concerning the double charged layer at the semiconductor/electrolyte interface. (author)

  8. Single cells and intracellular processes studied by a plasmonic-based electrochemical impedance microscopy

    Science.gov (United States)

    Wang, Wei; Foley, Kyle; Shan, Xiaonan; Wang, Shaopeng; Eaton, Seron; Nagaraj, Vinay J; Wiktor, Peter; Patel, Urmez; Tao, Nongjian

    2012-01-01

    We report an electrochemical impedance microscope (EIM) based on surface plasmon resonance. The new EIM can resolve local impedance with sub-micron spatial resolution, and monitor dynamics of various processes, such as apoptosis and electroporation of individual cells with millisecond time resolution. The high spatial and temporal resolution images make it possible to not only study individual cells, but also resolve the sub-cellular structures and processes without labels. The detection sensitivity achieved with the current setup is ~2 pS, which is excellent considering the conductance of a single ion channel is in the range of 5–400 pS. We describe also a model that simulates the EIM images of cells based on local dielectric constant and conductivity. PMID:21336333

  9. Electrochemical Impedance and Modelling Studies of the Corrosion of Three Commercial Stainless Steels in Molten Carbonate

    Directory of Open Access Journals (Sweden)

    C. S. Ni

    2014-01-01

    Full Text Available The corrosion induced by molten carbonates on the metallic structure materials is a problem constraining the life span of molten carbonate fuel cell (MCFC at elevated temperatures. The reaction between the outgrowing oxide scale and lithium carbonate in the electrolyte is generally a slow process and very important to the passivation behaviour of the underlying steel. The corrosion behaviour of three commercial alloys (P92, SS304, and SS310 with different Cr contents in molten (0.62Li, 0.38K2CO3 at 650°C was monitored by electrochemical impedance spectroscopy (EIS for 120 hours to investigate the lithiation process. With SEM images and extensive XRD analysis of the oxides, equivalent circuits were proposed to interpret the impedance data and explain the corrosion behaviour of the three alloys at different stage with respect to lithiation process.

  10. Electrochemical Impedance Sensors for Monitoring Trace Amounts of NO3 in Selected Growing Media

    Directory of Open Access Journals (Sweden)

    Seyed Alireza Ghaffari

    2015-07-01

    Full Text Available With the advent of smart cities and big data, precision agriculture allows the feeding of sensor data into online databases for continuous crop monitoring, production optimization, and data storage. This paper describes a low-cost, compact, and scalable nitrate sensor based on electrochemical impedance spectroscopy for monitoring trace amounts of NO3− in selected growing media. The nitrate sensor can be integrated to conventional microelectronics to perform online nitrate sensing continuously over a wide concentration range from 0.1 ppm to 100 ppm, with a response time of about 1 min, and feed data into a database for storage and analysis. The paper describes the structural design, the Nyquist impedance response, the measurement sensitivity and accuracy, and the field testing of the nitrate sensor performed within tree nursery settings under ISO/IEC 17025 certifications.

  11. Investigation of the electroreduction of silver sulfite complexes by means of electrochemical FFT impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Valiuniene, A., E-mail: ausra.valiuniene@chf.vu.lt [Department of Physical Chemistry, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania); Baltrunas, G.; Valiunas, R. [Department of Physical Chemistry, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania); Popkirov, G. [Faculty of Engineering, University of Kiel, Kaiserstr. 2, D-24143 Kiel (Germany)

    2010-08-15

    The electroreduction kinetics of silver sulfite complexes was investigated by electrochemical fast Fourier transform (FFT) impedance spectroscopy (0.061-1500 Hz). The time dependences of the real and imaginary components of impedance were determined in a solution containing 0.05 M Ag (I) and 1 M Na{sub 2}SO{sub 3}. The mean duration of silver ad-atom diffusion on the surface to the nearest crystallization centre was calculated: during the first 210 s of contact with the electrolyte, these values increase from 0.66 up to 1.77 s; thereafter, this variation stabilizes and the mean duration of silver ad-atom diffusion reaches an almost constant value (1.56 s).

  12. Electrochemical Impedance Sensors for Monitoring Trace Amounts of NO3 in Selected Growing Media

    Science.gov (United States)

    Ghaffari, Seyed Alireza; Caron, William-O.; Loubier, Mathilde; Normandeau, Charles-O.; Viens, Jeff; Lamhamedi, Mohammed S.; Gosselin, Benoit; Messaddeq, Younes

    2015-01-01

    With the advent of smart cities and big data, precision agriculture allows the feeding of sensor data into online databases for continuous crop monitoring, production optimization, and data storage. This paper describes a low-cost, compact, and scalable nitrate sensor based on electrochemical impedance spectroscopy for monitoring trace amounts of NO3− in selected growing media. The nitrate sensor can be integrated to conventional microelectronics to perform online nitrate sensing continuously over a wide concentration range from 0.1 ppm to 100 ppm, with a response time of about 1 min, and feed data into a database for storage and analysis. The paper describes the structural design, the Nyquist impedance response, the measurement sensitivity and accuracy, and the field testing of the nitrate sensor performed within tree nursery settings under ISO/IEC 17025 certifications. PMID:26197322

  13. Proton Diffusion Coefficient in Electrospun Hybrid Membranes by Electrochemical Impedance Spectroscopy.

    Science.gov (United States)

    Dos Santos, Leslie; Laberty-Robert, Christel; Maréchal, Manuel; Perrot, Hubert; Sel, Ozlem

    2015-09-15

    Electrochemical Impedance Spectroscopy (EIS) was, for the first time, used to estimate the global transverse proton diffusion coefficient, D(H+)(EHM), in electrospun hybrid conducting membranes (EHMs). In contrast to conventional impedance spectroscopy, EIS measurements were performed at room temperature with a liquid interface. In this configuration, the measure of the bulk proton transport is influenced by the kinetics of the transfer of proton at the solid/liquid interface. We demonstrated that the use of additives in the process of the membrane impacts the organization of the hydrophilic domains and also the proton transport. The D(H+)(EHM) is close to 1.10(-7) cm(2) s(-1) (± 0.1.10(-7) cm(2) s(-1)) for the EHMs without additive, whereas it is 4.10(-6) cm(2) s(-1) (± 0.4.10(-6) cm(2) s(-1)) for EHMs with additives.

  14. Electrochemical Impedance Spectroscopy Study on Corrosion Protection of Acrylate Nanocomposite on Mild Steel Doped Carbon Nanotubes

    Science.gov (United States)

    Mahmud, M. R.; Akhir, M. M.; Shamsudin, M. S.; Afaah, A. N.; Aadila, A.; Asib, N. A. M.; Alrokayan, Salman A. H.; Khan, Haseeb A.; Harun, M. K.; Rusop, M.; Abdullah, S.

    2015-05-01

    Acrylate:carbon nanotubes (A:CNTs) nanocomposite thin film was prepared by sol- gel technique. The corrosion coating protection of acrylate:carbon nanotubes (CNTs) nanocomposite thin film has been coated on mild steel characterised by electrochemical impedance spectrometer (EIS) measurement and equivalent circuit model are employed to analyse coating impedance for corrosion protection. In this study, 3.5 w/v % sodium chloride (NaCl) solution was immersed the acrylate:carbon nanotubes nanocomposite thin film. As the results, the surface morphology were found that there formation of carbon nanotubes with good distribution on acrylate-based coating. From EIS measurement, A:CNTs nanocomposite thin film with 0.4 w/v % contain of CNTs was exhibited the highest coating impedance from Nyquist graph after immersed in sodium chloride solution and may provide the excellent corrosion protection. The Bode plots have shown the impedance is high at the beginning from the time at high frequency and slightly decreases with value of frequency become smaller.

  15. Predicting molecular scale skin-effect in electrochemical impedance due to anomalous subdiffusion mediated adsorption phenomenon

    Directory of Open Access Journals (Sweden)

    Arindam Kushagra

    2016-02-01

    Full Text Available Anomalous subdiffusion governs the processes which are not energetically driven, on a molecular scale. This paper proposes a model to predict the response of electrochemical impedance due to such diffusion process. Previous works considered the use of fractional calculus to predict the impedance behaviour in response to the anomalous diffusion. Here, we have developed an expression which predicts the skin-effect, marked by an increase in the impedance with increasing frequency, in this regime. Negative inductances have also been predicted as a consequence of the inertial response of adsorbed species upon application of frequency-mediated perturbations. It might help the researchers in the fields of impedimetric sensors to choose the working frequency and those working in the field of batteries to choose the parameters, likewise. This work would shed some light into the molecular mechanisms governing the impedance when exposed to frequency-based perturbations like electromagnetic waves (microwaves to ionizing radiations and in charge storage devices like batteries etc.

  16. Interpretation of electrochemical impedance spectroscopy(EIS) circuit model for soils

    Institute of Scientific and Technical Information of China (English)

    韩鹏举; 张亚芬; 陈幼佳; 白晓红

    2015-01-01

    Based on three different kinds of conductive paths in microstructure of soil and theory of electrochemical impedance spectroscopy(EIS), an integrated equivalent circuit model and impedance formula for soils were proposed, which contain 6 meaningful resistance and reactance parameters. Considering the conductive properties of soils and dispersion effects, mathematical equations for impedance under various circuit models were deduced and studied. The mathematical expression presents two semicircles for theoretical EIS Nyquist spectrum, in which the center of one semicircle is degraded to simply the equivalent model. Based on the measured parameters of EIS Nyquist spectrum, meaningful soil parameters can easily be determined. Additionally, EIS was used to investigate the soil properties with different water contents along with the mathematical relationships and mechanism between the physical parameters and water content. Magnitude of the impedance decreases with the increase of testing frequency and water content for Bode graphs. The proposed model would help us to better understand the soil microstructure and properties and offer more reasonable explanations for EIS spectra.

  17. Comparative study of electrolyte additives using electrochemical impedance spectroscopy on symmetric cells

    Science.gov (United States)

    Petibon, R.; Sinha, N. N.; Burns, J. C.; Aiken, C. P.; Ye, Hui; VanElzen, Collette M.; Jain, Gaurav; Trussler, S.; Dahn, J. R.

    2014-04-01

    The effect of various electrolyte additives and additive combinations added to a 1 M LiPF6 EC:EMC electrolyte on the positive and negative electrodes surface of 1 year old wound LiCoO2/graphite cells and Li[Ni0.4Mn0.4Co0.2])O2/graphite cells was studied using electrochemical impedance spectroscopy (EIS) on symmetric cells. The additives tested were: vinylene carbonate (VC), trimethoxyboroxine (TMOBX), fluoroethylene carbonate (FEC), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and H2O alone or in combination. In general, compared to control electrolyte, the additives tested reduced the impedance of the positive electrode and increased the impedance of the negative electrode with the exception of LiTFSI in Li[Ni0.4Mn0.4Co0.2]O2/graphite wound cells. Higher charge voltage led to higher positive electrode impedance, with the exception of 2%VC + 2% FEC, and 2% LiTFSI. In some cases, some additives when mixed with another controlled the formation of the SEI at one electrode, and shared the formation of the SEI at one electrode when mixed with a different additive.

  18. Electrochemical Impedance Spectra of Dye-Sensitized Solar Cells: Fundamentals and Spreadsheet Calculation

    Directory of Open Access Journals (Sweden)

    Subrata Sarker

    2014-01-01

    Full Text Available Electrochemical impedance spectroscopy (EIS is one of the most important tools to elucidate the charge transfer and transport processes in various electrochemical systems including dye-sensitized solar cells (DSSCs. Even though there are many books and reports on EIS, it is often very difficult to explain the EIS spectra of DSSCs. Understanding EIS through calculating EIS spectra on spreadsheet can be a powerful approach as the user, without having any programming knowledge, can go through each step of calculation on a spreadsheet and get instant feedback by visualizing the calculated results or plot on the same spreadsheet. Here, a brief account of the EIS of DSSCs is given with fundamental aspects and their spreadsheet calculation. The review should help one to develop a basic understanding about EIS of DSSCs through interacting with spreadsheet.

  19. Label-Free Toxin Detection by Means of Time-Resolved Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Paul Takhistov

    2010-01-01

    Full Text Available The real-time detection of trace concentrations of biological toxins requires significant improvement of the detection methods from those reported in the literature. To develop a highly sensitive and selective detection device it is necessary to determine the optimal measuring conditions for the electrochemical sensor in three domains: time, frequency and polarization potential. In this work we utilized a time-resolved electrochemical impedance spectroscopy for the detection of trace concentrations of Staphylococcus enterotoxin B (SEB. An anti-SEB antibody has been attached to the nano-porous aluminum surface using 3-aminopropyltriethoxysilane/glutaraldehyde coupling system. This immobilization method allows fabrication of a highly reproducible and stable sensing device. Using developed immobilization procedure and optimized detection regime, it is possible to determine the presence of SEB at the levels as low as 10 pg/mL in 15 minutes.

  20. Interface Design for CMOS-Integrated Electrochemical Impedance Spectroscopy (EIS Biosensors

    Directory of Open Access Journals (Sweden)

    Arjang Hassibi

    2012-10-01

    Full Text Available Electrochemical Impedance Spectroscopy (EIS is a powerful electrochemical technique to detect biomolecules. EIS has the potential of carrying out label-free and real-time detection, and in addition, can be easily implemented using electronic integrated circuits (ICs that are built through standard semiconductor fabrication processes. This paper focuses on the various design and optimization aspects of EIS ICs, particularly the bio-to-semiconductor interface design. We discuss, in detail, considerations such as the choice of the electrode surface in view of IC manufacturing, surface linkers, and development of optimal bio-molecular detection protocols. We also report experimental results, using both macro- and micro-electrodes to demonstrate the design trade-offs and ultimately validate our optimization procedures.

  1. Interface design for CMOS-integrated Electrochemical Impedance Spectroscopy (EIS) biosensors.

    Science.gov (United States)

    Manickam, Arun; Johnson, Christopher Andrew; Kavusi, Sam; Hassibi, Arjang

    2012-10-29

    Electrochemical Impedance Spectroscopy (EIS) is a powerful electrochemical technique to detect biomolecules. EIS has the potential of carrying out label-free and real-time detection, and in addition, can be easily implemented using electronic integrated circuits (ICs) that are built through standard semiconductor fabrication processes. This paper focuses on the various design and optimization aspects of EIS ICs, particularly the bio-to-semiconductor interface design. We discuss, in detail, considerations such as the choice of the electrode surface in view of IC manufacturing, surface linkers, and development of optimal bio-molecular detection protocols. We also report experimental results, using both macro- and micro-electrodes to demonstrate the design trade-offs and ultimately validate our optimization procedures.

  2. Revisiting the electrochemical impedance behaviour of the LiFePO4/C cathode

    Indian Academy of Sciences (India)

    Hua Ju; Jun Wu; Yanhui Xu

    2013-05-01

    In the present work, the electrochemical behaviour of LiFePO4/C electrode has been reported. Specially, the electrochemical impedance spectroscopies (EIS) have been studied in detail. The discharge capacity is more than 120 mAh/g. There are two semicircles being found in the Nyquist plot for the cycled electrode and one semicircle for the as-prepared electrode. It is found that the interface capacitance is in an order of magnitude of 10 F/cm2 for the high-frequency semicircle, while for the second semicircle the interface capacitance is 5.3 ∼ 45.4 × 103 F/cm2. It could be concluded that the high-frequency semicircle is to correspond to the charge transfer process. The function of the carbon layer is also briefly discussed.

  3. Label-Free Toxin Detection by Means of Time-Resolved Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Chai, Changhoon; Takhistov, Paul

    2010-01-01

    The real-time detection of trace concentrations of biological toxins requires significant improvement of the detection methods from those reported in the literature. To develop a highly sensitive and selective detection device it is necessary to determine the optimal measuring conditions for the electrochemical sensor in three domains: time, frequency and polarization potential. In this work we utilized a time-resolved electrochemical impedance spectroscopy for the detection of trace concentrations of Staphylococcus enterotoxin B (SEB). An anti-SEB antibody has been attached to the nano-porous aluminum surface using 3-aminopropyltriethoxysilane/glutaraldehyde coupling system. This immobilization method allows fabrication of a highly reproducible and stable sensing device. Using developed immobilization procedure and optimized detection regime, it is possible to determine the presence of SEB at the levels as low as 10 pg/mL in 15 minutes. PMID:22315560

  4. Interface Design for CMOS-Integrated Electrochemical Impedance Spectroscopy (EIS) Biosensors

    Science.gov (United States)

    Manickam, Arun; Johnson, Christopher Andrew; Kavusi, Sam; Hassibi, Arjang

    2012-01-01

    Electrochemical Impedance Spectroscopy (EIS) is a powerful electrochemical technique to detect biomolecules. EIS has the potential of carrying out label-free and real-time detection, and in addition, can be easily implemented using electronic integrated circuits (ICs) that are built through standard semiconductor fabrication processes. This paper focuses on the various design and optimization aspects of EIS ICs, particularly the bio-to-semiconductor interface design. We discuss, in detail, considerations such as the choice of the electrode surface in view of IC manufacturing, surface linkers, and development of optimal bio-molecular detection protocols. We also report experimental results, using both macro- and micro-electrodes to demonstrate the design trade-offs and ultimately validate our optimization procedures. PMID:23202170

  5. Correlation between Electrochemical Impedance Spectroscopy and Structural Properties of Amorphous Tunisian Metanacrite Synthetic Material

    Directory of Open Access Journals (Sweden)

    Nouha Jaafar

    2014-01-01

    Full Text Available In the present work, we report the structural and electrochemical properties of metanacrite. Metanacrite is a synthetic material originated by heating (550°C of a clay mineral (Tunisian nacrite belonging to the kaolin group. The structure of the amorphous synthetic product was corroborated by X-ray diffraction (disappearing of nacrite peaks and infrared spectroscopy (disappearing of Al–OH and water bands. The decomposition of the silicate framework was confirmed by transmission electron microscope (TEM. The obtained metanacrite synthetic material was also examined by electrochemical impedance spectroscopy (EIS. Accordingly, the electronic conduction is followed by the correlated barrier hopping (C.B.H. model. Therefore, by combining ac and dc electrical conductivity, a semiconductor behavior is evidenced. The dependence of the dielectric constant (ε′ and dielectric loss (ε″ on both temperature and frequency is also discussed.

  6. Modelling of a High Temperature PEM Fuel Cell Stack using Electrochemical Impedance Spectroscopy

    DEFF Research Database (Denmark)

    Andreasen, Søren Juhl; Jespersen, Jesper Lebæk; Kær, Søren Knudsen

    2008-01-01

    This work presents the development of an equivalent circuit model of a 65 cell high temperature PEM (HTPEM) fuel cell stack using Electrochemical Impedance Spectroscopy (EIS). The HTPEM fuel cell membranes used are PBI-based and uses phosphoric acid as proton conductor. The operating temperature...... of the MEA's is 160-180oC, depending on the purity of the hydrogen used, the load pattern and the desired lifetime. The advantages of the HTPEM fuel cell technology include fast response to load changes and high tolerance to CO (1-3%)...

  7. A Study on a Partially Immersed Gold Electrode Using an Electrochemical Quartz Crystal Impedance System

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The electrochemical quartz crystal impedance system (EQCIS) has been used for the study of a partially immersed Au electrode in 0.2 mol/L NaClO4 aqueous solution.The influences of the immersed area and height of the electrode on the EQCIS responses were evaluated,showing the highest response sensitivity to liquid loading at the center of the piezoelectric quartz crystal electrode.The increase in the immersed height of the Au electrode at oxygen reduction potentials during potential cycling was measured by this technique.

  8. Characterization of Formation Kinetics of Self-Assembled Thiol Monolayers on Gold by Electrochemical Impedance Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Self-assembled monolayers of octadecanethiol (ODT) on gold have been studied by electrochemical impedance spectroscopy (EIS). The fractional coverage has been examined as a function of immersion time of Au in ODT deposition solution. The fractional coverage exhibits two distinct adsorption steps: an initial rapid step followed by a slow one. The fractional coverage of ODT monolayer increases sharply from zero to more than 99% of its maximum within the first minute. However, it takes a day for the fractional coverage to approach its final value.

  9. Investigation of Temperature and Aging Effects in Nanostructured Dye Solar Cells Studied by Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Minna Toivola

    2009-01-01

    Full Text Available Effects of aging and cyclically varying temperature on the electrical parameters of dye solar cells were analyzed with electrochemical impedance spectroscopy. Photoelectrode total resistance increased as a function of time due to increasing electron transport resistance in the TiO2 film. On the other hand, photoelectrode recombination resistance was generally larger, electron lifetimes in the TiO2 were film longer, and charge transfer resistance on the counter electrode was smaller after the temperature treatments than before them. These effects correlated with the slower deterioration rate of the temperature-treated cells, in comparison to the reference cells.

  10. Electrochemical impedance spectroscopy based MEMS sensors for phthalates detection in water and juices

    KAUST Repository

    Zia, Asif I

    2013-06-10

    Phthalate esters are ubiquitous environmental and food pollutants well known as endocrine disrupting compounds (EDCs). These developmental and reproductive toxicants pose a grave risk to the human health due to their unlimited use in consumer plastic industry. Detection of phthalates is strictly laboratory based time consuming and expensive process and requires expertise of highly qualified and skilled professionals. We present a real time, non-invasive, label free rapid detection technique to quantify phthalates\\' presence in deionized water and fruit juices. Electrochemical impedance spectroscopy (EIS) technique applied to a novel planar inter-digital (ID) capacitive sensor plays a vital role to explore the presence of phthalate esters in bulk fluid media. The ID sensor with multiple sensing gold electrodes was fabricated on silicon substrate using micro-electromechanical system (MEMS) device fabrication technology. A thin film of parylene C polymer was coated as a passivation layer to enhance the capacitive sensing capabilities of the sensor and to reduce the magnitude of Faradic current flowing through the sensor. Various concentrations, 0.002ppm through to 2ppm of di (2-ethylhexyl) phthalate (DEHP) in deionized water, were exposed to the sensing system by dip testing method. Impedance spectra obtained was analysed to determine sample conductance which led to consequent evaluation of its dielectric properties. Electro-chemical impedance spectrum analyser algorithm was employed to model the experimentally obtained impedance spectra. Curve fitting technique was applied to deduce constant phase element (CPE) equivalent circuit based on Randle\\'s equivalent circuit model. The sensing system was tested to detect different concentrations of DEHP in orange juice as a real world application. The result analysis indicated that our rapid testing technique is able to detect the presence of DEHP in all test samples distinctively.

  11. Electrochemical impedance spectroscopy based MEMS sensors for phthalates detection in water and juices

    Science.gov (United States)

    Zia, Asif I.; Mohd Syaifudin, A. R.; Mukhopadhyay, S. C.; Yu, P. L.; Al-Bahadly, I. H.; Gooneratne, Chinthaka P.; Kosel, Jǘrgen; Liao, Tai-Shan

    2013-06-01

    Phthalate esters are ubiquitous environmental and food pollutants well known as endocrine disrupting compounds (EDCs). These developmental and reproductive toxicants pose a grave risk to the human health due to their unlimited use in consumer plastic industry. Detection of phthalates is strictly laboratory based time consuming and expensive process and requires expertise of highly qualified and skilled professionals. We present a real time, non-invasive, label free rapid detection technique to quantify phthalates' presence in deionized water and fruit juices. Electrochemical impedance spectroscopy (EIS) technique applied to a novel planar inter-digital (ID) capacitive sensor plays a vital role to explore the presence of phthalate esters in bulk fluid media. The ID sensor with multiple sensing gold electrodes was fabricated on silicon substrate using micro-electromechanical system (MEMS) device fabrication technology. A thin film of parylene C polymer was coated as a passivation layer to enhance the capacitive sensing capabilities of the sensor and to reduce the magnitude of Faradic current flowing through the sensor. Various concentrations, 0.002ppm through to 2ppm of di (2-ethylhexyl) phthalate (DEHP) in deionized water, were exposed to the sensing system by dip testing method. Impedance spectra obtained was analysed to determine sample conductance which led to consequent evaluation of its dielectric properties. Electro-chemical impedance spectrum analyser algorithm was employed to model the experimentally obtained impedance spectra. Curve fitting technique was applied to deduce constant phase element (CPE) equivalent circuit based on Randle's equivalent circuit model. The sensing system was tested to detect different concentrations of DEHP in orange juice as a real world application. The result analysis indicated that our rapid testing technique is able to detect the presence of DEHP in all test samples distinctively.

  12. Recent Advances in Voltammetry

    Science.gov (United States)

    Batchelor-McAuley, Christopher; Kätelhön, Enno; Barnes, Edward O; Compton, Richard G; Laborda, Eduardo; Molina, Angela

    2015-01-01

    Recent progress in the theory and practice of voltammetry is surveyed and evaluated. The transformation over the last decade of the level of modelling and simulation of experiments has realised major advances such that electrochemical techniques can be fully developed and applied to real chemical problems of distinct complexity. This review focuses on the topic areas of: multistep electrochemical processes, voltammetry in ionic liquids, the development and interpretation of theories of electron transfer (Butler–Volmer and Marcus–Hush), advances in voltammetric pulse techniques, stochastic random walk models of diffusion, the influence of migration under conditions of low support, voltammetry at rough and porous electrodes, and nanoparticle electrochemistry. The review of the latter field encompasses both the study of nanoparticle-modified electrodes, including stripping voltammetry and the new technique of ‘nano-impacts’. PMID:26246984

  13. Recent Advances in Voltammetry.

    Science.gov (United States)

    Batchelor-McAuley, Christopher; Kätelhön, Enno; Barnes, Edward O; Compton, Richard G; Laborda, Eduardo; Molina, Angela

    2015-06-01

    Recent progress in the theory and practice of voltammetry is surveyed and evaluated. The transformation over the last decade of the level of modelling and simulation of experiments has realised major advances such that electrochemical techniques can be fully developed and applied to real chemical problems of distinct complexity. This review focuses on the topic areas of: multistep electrochemical processes, voltammetry in ionic liquids, the development and interpretation of theories of electron transfer (Butler-Volmer and Marcus-Hush), advances in voltammetric pulse techniques, stochastic random walk models of diffusion, the influence of migration under conditions of low support, voltammetry at rough and porous electrodes, and nanoparticle electrochemistry. The review of the latter field encompasses both the study of nanoparticle-modified electrodes, including stripping voltammetry and the new technique of 'nano-impacts'.

  14. Corrosion protection of copper by polypyrrole film studied by electrochemical impedance spectroscopy and the electrochemical quartz microbalance

    Science.gov (United States)

    Lei, Yanhua; Ohtsuka, Toshiaki; Sheng, Nan

    2015-12-01

    Polypyrrole (PPy) films were synthesized on copper in solution of sodium di-hydrogen phosphate and phytate for corrosion protection. The protection properties of PPy films were comparatively investigated in NaCl solution. During two months immersion, the PPy film doped with phytate anions, working as a cationic perm-selective membrane, inhibited the dissolution of copper to 1% of bare copper. Differently, the PPy film doped with di-hydrogen phosphate anions, possessing anionic perm-selectivity, was gradually reduced, and inhibited the dissolution to 7.8% of bare copper. Degradation of the PPy films was studied by comparing the electrochemical impedance spectroscopy change at different immersion time and Raman spectra change after immersion.

  15. Voltammetry Method Evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Hoyt, N. [Argonne National Lab. (ANL), Argonne, IL (United States); Pereira, C. [Argonne National Lab. (ANL), Argonne, IL (United States); Willit, J. [Argonne National Lab. (ANL), Argonne, IL (United States); Williamson, M. [Argonne National Lab. (ANL), Argonne, IL (United States)

    2016-07-29

    The purpose of the ANL MPACT Voltammetry project is to evaluate the suitability of previously developed cyclic voltammetry techniques to provide electroanalytical measurements of actinide concentrations in realistic used fuel processing scenarios. The molten salts in these scenarios are very challenging as they include high concentrations of multiple electrochemically active species, thereby creating a variety of complications. Some of the problems that arise therein include issues related to uncompensated resistance, cylindrical diffusion, and alloying of the electrodeposited metals. Improvements to the existing voltammetry technique to account for these issues have been implemented, resulting in good measurements of actinide concentrations across a wide range of adverse conditions.

  16. Comprehensive characterization of all-solid-state thin films commercial microbatteries by Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Larfaillou, S.; Guy-Bouyssou, D.; le Cras, F.; Franger, S.

    2016-07-01

    Constant miniaturization of electronic devices opens the way to the development of thin film microbatteries (TFB). For this type of devices, the use of an all-solid-state thin film technology has many advantages over conventional lithium cells. These microbatteries are thin, bendable and can be produced with a customizable shape for integration in microelectronic devices. Moreover, without liquid electrolyte, they are safer. With the aim to support the industrial production of these TFBs, adequate tools for understanding the electrochemical behavior of the complete microbattery and the identification of their possible failures that can occur have to be developed. In this context, the Electrochemical Impedance Spectroscopy seems to be a good compromise for cells characterization. Widely used for the characterization of liquid electrolyte-based batteries, this technique has been less applied to all solid state batteries, mainly because of the difficulty to work with a two-electrode system. There has been no comprehensive study deeply explaining the impedance evolution during the entire life of a microbattery. In this paper, physical characterizations of individual active materials and aging experiments have been performed in order to undoubtedly assign each EIS contributions, and to propose a more comprehensive electrical model for this family of commercial all-solid-state microbatteries.

  17. The Electrochemical Impedance Spectroscopy as a Diagnostic Tool of the Transformer Oil

    Directory of Open Access Journals (Sweden)

    Alexander Cueli Corugedo

    2014-11-01

    Full Text Available The quality of the transformer oil is essential to ensure its right performance in electrical appliances such as transformers and switches, in which oil works as insulating. The necessity toguarantee such condition can be affected due to the law level of pollution, refining, and humidity among others, reason why a systematic evaluation of the oil´s condition must be carried out to avoid the expensive failures in the power´s transmission and distribution. This work deals with the usage of the Electrochemical Impedance Spectroscopy for the first time as a diagnostic of the national new regenerated oils, which helps showing its resistive behavior to corrosive processes and so the preservation of its electrical properties. An electrochemical glass cell with three electrodes is used in this work in order to control the test temperature to a specific determined range (75° C y 95° C. Electrolytic copper was used as work electrode, taking as reference and auxiliary the ones specified for this purpose. The impedance spectrums obtained, confirmed the dielectric properties of the oil tested. With the increase of the temperature, the resistive effect of the oil decreases.

  18. Application of electrochemical impedance spectroscopy: A phase behavior study of babassu biodiesel-based microemulsions

    Science.gov (United States)

    Pereira, Thulio C.; Conceição, Carlos A. F.; Khan, Alamgir; Fernandes, Raquel M. T.; Ferreira, Maira S.; Marques, Edmar P.; Marques, Aldaléa L. B.

    2016-11-01

    Microemulsions are thermodynamically stable systems of two immiscible liquids, one aqueous and the other of organic nature, with a surfactant and/or co-surfactant adsorbed in the interface between the two phases. Biodiesel-based microemulsions, consisting of alkyl esters of fatty acids, open a new means of analysis for the application of electroanalytical techniques, and is advantageous as it eliminates the required pre-treatment of a sample. In this work, the phase behaviours of biodiesel-based microemulsions were investigated through the electrochemical impedance spectroscopy (EIS) technique. We observed thatan increase in the amount of biodiesel in the microemulsion formulation increases the resistance to charge transfer at the interface. Also, the electrical conductivity measurements revealed that a decrease or increase in electrical properties depends on the amount of biodiesel. EIS studies of the biodiesel-based microemulsion samples showed the presence of two capacitive arcs: one high-frequency and the other low-frequency. Thus, the formulation of microemulsions plays an important role in estimating the electrical properties through the electrochemical impedance spectroscopy technique.

  19. Selective detection of endotoxin using an impedance aptasensor with electrochemically deposited gold nanoparticles.

    Science.gov (United States)

    Su, Wenqiong; Kim, Sung-Eun; Cho, MiSuk; Nam, Jae-Do; Choe, Woo-Seok; Lee, Youngkwan

    2013-01-01

    Using a single-stranded DNA (ssDNA) aptamer exhibiting high binding affinity (Kd = 12 nM) to endotoxin as a probe, an impedance sensor where aptamer-conjugated gold nanoparticles (AuNPs) were electrochemically deposited on a gold electrode was fabricated and its performance in regard to endotoxin detection assessed. AuNPs have been employed widely as biosensors because of their unique physical and chemical properties. In order to maximize the performance of the impedance aptasensor on endotoxin detection, some critical factors affecting aptamer conjugation to AuNPs and target recognition ability (i.e. concentrations of aptamer coupled with AuNPs, pH, ion strength and cation effect at the time of aptamer-endotoxin interaction) were optimized. Electrochemical impendence spectroscopy, cyclic voltametry, atomic force microscope, scanning electron microscope and quartz crystal microbalance were employed to characterize all the modification/detection procedures during the sensor fabrication. The developed aptasensor showed a broad linear dynamic detection range (0.01-10.24 ng/ml) with a very low detection limit for endotoxin (0.005 ng/ml), despite the presence of several biomolecules (e.g. plasmid DNA, RNA, serum albumin, Glc and sucrose) known to interfere with other endotoxin assays. The demonstrated aptasensor required a detection time of only 10 min, providing a simple and fast analytical method to specifically detect endotoxin from complex biological liqors.

  20. Energy resolved electrochemical impedance spectroscopy for electronic structure mapping in organic semiconductors

    Energy Technology Data Exchange (ETDEWEB)

    Nádaždy, V., E-mail: nadazdy@savba.sk; Gmucová, K. [Institute of Physics SAS, Dúbravská cesta 9, 845 11 Bratislava (Slovakia); Schauer, F. [Faculty of Education, Trnava University in Trnava, 918 43 Trnava (Slovakia); Faculty of Applied Informatics, Tomas Bata University in Zlin, 760 05 Zlin (Czech Republic)

    2014-10-06

    We introduce an energy resolved electrochemical impedance spectroscopy method to map the electronic density of states (DOS) in organic semiconductor materials. The method consists in measurement of the charge transfer resistance of a semiconductor/electrolyte interface at a frequency where the redox reactions determine the real component of the impedance. The charge transfer resistance value provides direct information about the electronic DOS at the energy given by the electrochemical potential of the electrolyte, which can be adjusted using an external voltage. A simple theory for experimental data evaluation is proposed, along with an explanation of the corresponding experimental conditions. The method allows mapping over unprecedentedly wide energy and DOS ranges. Also, important DOS parameters can be determined directly from the raw experimental data without the lengthy analysis required in other techniques. The potential of the proposed method is illustrated by tracing weak bond defect states induced by ultraviolet treatment above the highest occupied molecular orbital in a prototypical σ-conjugated polymer, poly[methyl(phenyl)silylene]. The results agree well with those of our previous DOS reconstruction by post-transient space-charge-limited-current spectroscopy, which was, however, limited to a narrow energy range. In addition, good agreement of the DOS values measured on two common π-conjugated organic polymer semiconductors, polyphenylene vinylene and poly(3-hexylthiophene), with the rather rare previously published data demonstrate the accuracy of the proposed method.

  1. Energy resolved electrochemical impedance spectroscopy for electronic structure mapping in organic semiconductors

    Science.gov (United States)

    Nádaždy, V.; Schauer, F.; Gmucová, K.

    2014-10-01

    We introduce an energy resolved electrochemical impedance spectroscopy method to map the electronic density of states (DOS) in organic semiconductor materials. The method consists in measurement of the charge transfer resistance of a semiconductor/electrolyte interface at a frequency where the redox reactions determine the real component of the impedance. The charge transfer resistance value provides direct information about the electronic DOS at the energy given by the electrochemical potential of the electrolyte, which can be adjusted using an external voltage. A simple theory for experimental data evaluation is proposed, along with an explanation of the corresponding experimental conditions. The method allows mapping over unprecedentedly wide energy and DOS ranges. Also, important DOS parameters can be determined directly from the raw experimental data without the lengthy analysis required in other techniques. The potential of the proposed method is illustrated by tracing weak bond defect states induced by ultraviolet treatment above the highest occupied molecular orbital in a prototypical σ-conjugated polymer, poly[methyl(phenyl)silylene]. The results agree well with those of our previous DOS reconstruction by post-transient space-charge-limited-current spectroscopy, which was, however, limited to a narrow energy range. In addition, good agreement of the DOS values measured on two common π-conjugated organic polymer semiconductors, polyphenylene vinylene and poly(3-hexylthiophene), with the rather rare previously published data demonstrate the accuracy of the proposed method.

  2. Application of electrochemical impedance spectroscopy: A phase behavior study of babassu biodiesel-based microemulsions.

    Science.gov (United States)

    Pereira, Thulio C; Conceição, Carlos A F; Khan, Alamgir; Fernandes, Raquel M T; Ferreira, Maira S; Marques, Edmar P; Marques, Aldaléa L B

    2016-11-01

    Microemulsions are thermodynamically stable systems of two immiscible liquids, one aqueous and the other of organic nature, with a surfactant and/or co-surfactant adsorbed in the interface between the two phases. Biodiesel-based microemulsions, consisting of alkyl esters of fatty acids, open a new means of analysis for the application of electroanalytical techniques, and is advantageous as it eliminates the required pre-treatment of a sample. In this work, the phase behaviours of biodiesel-based microemulsions were investigated through the electrochemical impedance spectroscopy (EIS) technique. We observed thatan increase in the amount of biodiesel in the microemulsion formulation increases the resistance to charge transfer at the interface. Also, the electrical conductivity measurements revealed that a decrease or increase in electrical properties depends on the amount of biodiesel. EIS studies of the biodiesel-based microemulsion samples showed the presence of two capacitive arcs: one high-frequency and the other low-frequency. Thus, the formulation of microemulsions plays an important role in estimating the electrical properties through the electrochemical impedance spectroscopy technique.

  3. Tuning the physico-electrochemical properties of novel cobalt (II) octa[(3,5-biscarboxylate)-phenoxy] phthalocyanine complex using phenylamine-functionalised SWCNTs

    CSIR Research Space (South Africa)

    Agboola, BO

    2010-03-01

    Full Text Available OBPPc-SWCNT-phenylamine hybrid were evaluated using spectroscopy (IR and UV–vis), field emission scanning electron microscopy and electrochemistry (cyclic voltammetry and electrochemical impedance spectroscopy). Integration of SWCNT-phenylamine resulted in the physical...

  4. The electrochemical impedance of polarized 316L stainless steel: structure-property-adsorption correlation.

    Science.gov (United States)

    Gettens, Robert T T; Gilbert, Jeremy L

    2009-07-01

    Electrochemical (EC) impedance and polarization data were synergistically coupled with AFM micrographs providing insight on the polarized alloy-electrolyte interface. Several regions of oxide topography/ impedance characteristic were apparent on a 316L SS surface. A relatively rough surface with apparent EC reaction products was observed below -500 mV. Smooth surfaces were seen from -500 mV to 200 mV. A transition region which displayed the aggregation of particles on the surface was seen from 200 mV to 600 mV. Above 600 mV these particles disappeared revealing a smooth topography. These topographical observations matched closely with the impedance behavior of the system, particularly the capacitance (C), polarization resistance (R(p)) and current density. The presence of pre-adsorbed Fb had a significant impact on C below approximately -500 mV (increased capacitance). The deviation from ideality of the current response as determined by a KWW empirical dielectric decay function showed significant differences between PBS-immersed and pre-adsorbed Fb cases. Earlier, changes in Fb area coverage, height, and eccentricity were observed between voltages lower and higher than 0 mV. The presence of the flat-band potential around -150 mV as well as high cathodic charge-transfer reactions taking place below -100 mV relate to these observations.

  5. Development of an enrofloxacin immunosensor based on label-free electrochemical impedance spectroscopy.

    Science.gov (United States)

    Wu, Ching-Chou; Lin, Chia-Hung; Wang, Way-Shyan

    2009-06-30

    Enrofloxacin is the most widespread antibiotic in the fluoroquinolone family. As such, the development of a rapid and sensitive method for the determination of trace amounts of enrofloxacin is an important issue in the health field. The interaction of the enrofloxacin antigen to a specific antibody (Ab) immobilized on an 11-mercapto-undecanoic acid-coated gold electrode was quantified by electrochemical impedance spectroscopy. Two equivalent circuits were separately used to interpret the obtained impedance spectra. These circuits included one resistor in series with one parallel circuit comprised of a resistor and a capacitor (1R//C), and one resistor in series with two parallel RC circuits (2R//C). The results indicate that the antigen-antibody reaction analyzed using the 1R//C circuit provided a more sensitive resistance increment against the enrofloxacin concentration than that of the 2R//C circuit. However, the 2R//C circuit provided a better fitting for impedance spectra, and therefore supplies more detailed results of the enrofloxacin-antibody interaction, causing the increase of electron transfer resistance selectively to the modified layer, and not the electrical double layer. The antibody-modified electrode allowed for analysis of the dynamic linear range of 1-1000 ng/ml enrofloxacin with a detection limit of 1 ng/ml. The reagentless and label-free impedimetric immunosensors provide a simple and sensitive detection method for the specific determination of enrofloxacin.

  6. Dynamic Characterization of Dendrite Deposition and Growth in Li-Surface by Electrochemical Impedance Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez-Maya, R; Rosas, O; Saunders, J; Castaneda, H

    2015-01-13

    The evolution of dendrite formation is characterized by DC and AC electrochemical techniques. Interfacial mechanisms for lithium deposition are described and quantified by electrochemical impedance spectroscopy (EIS) between a lithium electrode and a graphite electrode. The initiation and growth of dendrites in the lithium surface due to the cathodic polarization conditions following anodic dissolution emulate long term cycling process occurring in the lithium electrodes. The dendrite initiation at the lithium/organic electrolyte interface is proposed to be performed through a combination of layering and interfacial reactions during different cathodic conditions. The growth is proposed to be performed by surface geometrical deposition. In this work, we use EIS in galvanostatic mode to assess the initiation and growth stages of dendrites by the accumulation of precipitates formed under different current conditions. The lithium/organic solvent experimental system using frequency domain techniques is validated by the theoretical approach using a deterministic model that accounts for the faradaic processes at the interface assuming a coverage fraction of the electrodic surface affected by the dendritic growth. (C) 2015 The Electrochemical Society. All rights reserved.

  7. In Situ Characterization of Ultrathin Films by Scanning Electrochemical Impedance Microscopy.

    Science.gov (United States)

    Estrada-Vargas, Arturo; Bandarenka, Aliaksandr; Kuznetsov, Volodymyr; Schuhmann, Wolfgang

    2016-03-15

    Control over the properties of ultrathin films plays a crucial role in many fields of science and technology. Although nondestructive optical and electrical methods have multiple advantages for local surface characterization, their applicability is very limited if the surface is in contact with an electrolyte solution. Local electrochemical methods, e.g., scanning electrochemical microscopy (SECM), cannot be used as a robust alternative yet because their methodological aspects are not sufficiently developed with respect to these systems. The recently proposed scanning electrochemical impedance microscopy (SEIM) can efficiently elucidate many key properties of the solid/liquid interface such as charge transfer resistance or interfacial capacitance. However, many fundamental aspects related to SEIM application still remain unclear. In this work, a methodology for the interpretation of SEIM data of "charge blocking systems" has been elaborated with the help of finite element simulations in combination with experimental results. As a proof of concept, the local film thickness has been visualized using model systems at various tip-to-sample separations. Namely, anodized aluminum oxide (Al2O3, 2-20 nm) and self-assembled monolayers based on 11-mercapto-1-undecanol and 16-mercapto-1-hexadecanethiol (2.1 and 2.9 nm, respectively) were used as model systems.

  8. Detection of 2D phase transitions at the electrode/electrolyte interface using electrochemical impedance spectroscopy

    Science.gov (United States)

    Tymoczko, Jakub; Colic, Viktor; Bandarenka, Aliaksandr S.; Schuhmann, Wolfgang

    2015-01-01

    The capacitance of the electric double layer, CDL, formed at the electrode/electrolyte interface is generally determined by electrochemical impedance spectroscopy (EIS). However, CDL values obtained using EIS data often depend on the ac frequency of the potential perturbation used in EIS. The reasons for the observed frequency dispersions can be various, and hence extracting valuable information about the status of the electrified interface is not possible with the required certainty. In this work, using well-understood electrochemical systems, namely Pt(111) electrodes in contact with a series of acidic sulfate ions containing electrolytes, we provide strong evidence that 2D phase transitions in the adsorbate layers and, in general, structural effects at the electrode/electrolyte interface are in many cases responsible for the frequency dispersion of the double layer capacitance. These empirical findings open new opportunities for the detection and evaluation of 2D phase transition processes and other structural effects using EIS, even in presence of simultaneously occurring electrochemical processes. However, further theoretical elaboration of this effect is necessary.

  9. Fast and sensitive detection of foodborne pathogen using electrochemical impedance analysis, urease catalysis and microfluidics.

    Science.gov (United States)

    Chen, Qi; Wang, Dan; Cai, Gaozhe; Xiong, Yonghua; Li, Yuntao; Wang, Maohua; Huo, Huiling; Lin, Jianhan

    2016-12-15

    Early screening of pathogenic bacteria is a key to prevent and control of foodborne diseases. In this study, we developed a fast and sensitive bacteria detection method integrating electrochemical impedance analysis, urease catalysis with microfluidics and using Listeria as model. The Listeria cells, the anti-Listeria monoclonal antibodies modified magnetic nanoparticles (MNPs), and the anti-Listeria polyclonal antibodies and urease modified gold nanoparticles (AuNPs) were incubated in a fluidic separation chip with active mixing to form the MNP-Listeria-AuNP-urease sandwich complexes. The complexes were captured in the separation chip by applying a high gradient magnetic field, and the urea was injected to resuspend the complexes and hydrolyzed under the catalysis of the urease on the complexes into ammonium ions and carbonate ions, which were transported into a microfluidic detection chip with an interdigitated microelectrode for impedance measurement to determine the amount of the Listeria cells. The capture efficiency of the Listeria cells in the separation chip was ∼93% with a shorter time of 30min due to the faster immuno-reaction using the active magnetic mixing. The changes on both impedance magnitude and phase angle were demonstrated to be able to detect the Listeria cells as low as 1.6×10(2)CFU/mL. The detection time was reduced from original ∼2h to current ∼1h. The recoveries of the spiked lettuce samples ranged from 82.1% to 89.6%, indicating the applicability of this proposed biosensor. This microfluidic impedance biosensor has shown the potential for online, automatic and sensitive bacteria separation and detection.

  10. Characterization of Molybdate Conversion Coatings for Aluminum Alloys by Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Calle, Luz Marina

    2000-01-01

    Electrochemical impedance spectroscopy (EIS) was used to investigate the corrosion inhibiting properties of newly developed proprietary molybdate conversion coatings on aluminum alloy 2024-T3 under immersion in aerated 5% (w/w) NaCl. Corrosion potential and EIS measurements were gathered for six formulations of the coating at several immersion times for two weeks. Nyquist as well as Bode plots of the data were obtained. The conversion-coated alloy panels showed an increase in the corrosion potential during the first 24 hours of immersion that later subsided and approached a steady value. Corrosion potential measurements indicated that formulations A, D, and F exhibit a protective effect on aluminum 2024-T3. The EIS spectra of the conversion-coated alloy were characterized by an impedance that is higher than the impedance of the bare alloy at all the immersion times. The low frequency impedance, Z(sub lf) (determined from the value at 0.05 Hz) for the conversion-coated alloy was higher at all the immersion times than that of the bare panel. This indicates improvement of corrosion resistance with addition of the molybdate conversion coating. Scanning electron microscopy (SEM) revealed the presence of cracks in the coating and the presence of cubic crystals believed to be calcium carbonate. Energy dispersive spectroscopy (EDS) of the test panels revealed the presence of high levels of aluminum, oxygen, and calcium but did not detect the presence of molybdenum on the test panels. X-ray photoelectron spectroscopy (XPS) indicated the presence of less than 0.01 atomic percent molybdenum on the surface of the coating.

  11. The Estimation of Corrosion Behavior of NiTi and NiTiNb Alloys Using Dynamic Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Georgiana Bolat

    2013-01-01

    Full Text Available Linear anodic potentiodynamic polarization and dynamic electrochemical impedance spectroscopic (DEIS measurements were carried out for NiTi and NiTiNb alloys in physiological 0.9 wt% NaCl solution in order to assess their corrosion resistance. DEIS measurements were performed from open circuit potential to dissolution potential. It was shown that the impedance measurements in potentiodynamic conditions allow simultaneous investigation of changes in passive layer structure. The impedance spectra of various potential regions were fitted and also discussed. The surface morphology of the alloys after linear anodic polarization test was studied using scanning electron microscopy (SEM technique.

  12. Investigation of electrochemical degradation process in polyaniline/polystyrene sulfonated self-assembly films by impedance spectroscopy.

    Science.gov (United States)

    Simões, F R; Pocrifka, L A; Marchesi, L F Q P; Pereira, E C

    2011-09-29

    In this study, the electrochemical degradation of polyaniline/polystyrene sulfonated (PANI/PSS) self-assembly films was investigated by an electrochemical impedance technique using transmission line models to fit the results. The experiments were performed by polarizing the working electrode at a fixed oxidative potential of 0.55 V. The results showed that changes in the electrochemical behavior of the oxidized PANI/PSS film occurred mainly in the polymer/solution interface by an increase in the charge transfer resistance.

  13. Experimentation and numerical modeling of cyclic voltammetry for electrochemical micro-sized sensors under the influence of electrolyte flow

    DEFF Research Database (Denmark)

    Adesokan, Bolaji James; Quan, Xueling; Evgrafov, A.

    2016-01-01

    In this study, we perform experimental studies as well as simulations for cyclic voltammetry(CV) of the redox couple FeIII(CN)63-/FeII(CN)64- on a gold plated ECC biosensor encapsulated by a microfluidic system. We examine the effect of flow rate, scan rate, varying supporting electrolyte, exchan...

  14. Electrochemical impedance-based DNA sensor using a modified single walled carbon nanotube electrode

    Energy Technology Data Exchange (ETDEWEB)

    Weber, Jessica E. [Department of Mechanical Engineering, University of South Florida, Tampa, FL (United States); Nanomaterials and Nanomanufacturing Research Center, University of South Florida, Tampa, FL (United States); Pillai, Shreekumar [Center for NanoBiotechnology Research, Alabama State University, Montgomery, AL (United States); Ram, Manoj Kumar, E-mail: mkram@usf.edu [Department of Mechanical Engineering, University of South Florida, Tampa, FL (United States); Nanomaterials and Nanomanufacturing Research Center, University of South Florida, Tampa, FL (United States); Kumar, Ashok [Department of Mechanical Engineering, University of South Florida, Tampa, FL (United States); Nanomaterials and Nanomanufacturing Research Center, University of South Florida, Tampa, FL (United States); Singh, Shree R. [Center for NanoBiotechnology Research, Alabama State University, Montgomery, AL (United States)

    2011-07-20

    Carbon nanotubes have become promising functional materials for the development of advanced electrochemical biosensors with novel features which could promote electron-transfer with various redox active biomolecules. This paper presents the detection of Salmonella enterica serovar Typhimurium using chemically modified single walled carbon nanotubes (SWNTs) with single stranded DNA (ssDNA) on a polished glassy carbon electrode. Hybridization with the corresponding complementary ssDNA has shown a shift in the impedance studies due to a higher charge transfer in ssDNA. The developed biosensor has revealed an excellent specificity for the appropriate targeted DNA strand. The methodologies to prepare and functionalize the electrode could be adopted in the development of DNA hybridization biosensor.

  15. Corrosion Behavior of Stainless Steels in Neutral and Acidified Sodium Chloride Solutions by Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Calle, L. M.; Kolady, M. R.; Vinje, R. D.

    2004-01-01

    The objective of this work was to evaluate the corrosion performance of three alloys by Electrochemical Impedance Spectroscopy (EIS) and to compare the results with those obtained during a two-year atmospheric exposure study.' Three alloys: AL6XN (UNS N08367), 254SM0 (UNS S32154), and 304L (UNS S30403) were included in the study. 304L was included as a control. The alloys were tested in three electrolyte solutions which consisted of neutral 3.55% NaC1, 3.55% NaC1 in 0.lN HC1, and 3.55% NaC1 in 1.ON HC1. These conditions were expected to be less severe, similar, and more severe respectively than the conditions at NASA's Kennedy Space Center launch pads.

  16. Real-Time Electrochemical Impedance Spectroscopy Diagnosis of the Marine Solid Oxide Fuel Cell

    Science.gov (United States)

    Nakajima, Hironori; Kitahara, Tatsumi

    2016-09-01

    We have investigated the behavior of an operating solid oxide fuel cell (SOFC) with supplying a simulated syngas to develop SOFC diagnosis method for marine SOFC units fueled with liquefied natural gas. We analyse the characteristics of syngas fueled anode of an intermediate temperature microtubular SOFC at 500 °C as a model case by electrochemical impedance spectroscopy (EIS) to find parameters useful for the diagnosis. EIS analyses are performed with an equivalent circuit model consisting of several resistances and capacitances attributed to the anode and cathode processes. The characteristic changes of those circuit parameters by internal reforming and anode degradation show that they can be used for the real-time diagnosis of operating SOFCs.

  17. Protein-G-based human immunoglobulin G biosensing by electrochemical impedance spectroscopy

    Science.gov (United States)

    Tsugimura, Kaiki; Ohnuki, Hitoshi; Endo, Hideaki; Tsuya, Daijyu; Izumi, Mitsuru

    2016-02-01

    A highly sensitive biosensor based on electrochemical impedance spectroscopy (EIS) was developed for the determination of human immunoglobulin G (IgG). Protein G, which specifically binds to IgG, was employed as the molecular receptor. Protein G was covalently immobilized on interdigitated electrodes through a mixed self-assembled monolayer (SAM) composed of 11-mercaptoundecanoic acid (MUA) and 6-mercaptohexanol. It was found that the mixing ratio of the SAM markedly affected the sensor performance. The sample prepared on 25% MUA SAM exhibited a linear behavior in the concentration range of 0.01-10 ng/mL, which is a record low detection for EIS-based IgG sensors. On the other hand, the sample on 100% MUA SAM showed no IgG-sensing action. A possible mechanism of the mixing ratio that affects the sensing performance was proposed.

  18. A bacteriophage endolysin-based electrochemical impedance biosensor for the rapid detection of Listeria cells.

    Science.gov (United States)

    Tolba, Mona; Ahmed, Minhaz Uddin; Tlili, Chaker; Eichenseher, Fritz; Loessner, Martin J; Zourob, Mohammed

    2012-12-21

    The objective of this study was to develop a biosensor using the cell wall binding domain (CBD) of bacteriophage-encoded peptidoglycan hydrolases (endolysin) immobilized on a gold screen printed electrode (SPE) and subsequent electrochemical impedance spectroscopy (EIS) for a rapid and specific detection of Listeria cells. The endolysin was amine-coupled to SPEs using EDC/NHS chemistry. The CBD-based electrode was used to capture and detect the Listeria innocua serovar 6b from pure culture and 2% artificially contaminated milk. In our study, the endolysin functionalized SPEs have been characterized using X-ray photoelectron spectroscopy (XPS). The integration of endolysin-based recognition for specific bacteria and EIS can be used for direct and rapid detection of Listeria cells with high specificity against non-Listeria cells with a limit of detection of 1.1 × 10(4) and 10(5) CFU mL(-1) in pure culture and 2% milk, respectively.

  19. Indirect identification of H{sub ads} relaxation on different metals by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Amokrane, N.; Gabrielli, C. [UPR15 du CNRS ' ' Physique des Liquides et Electrochimie' ' , Universite Pierre et Marie Curie, 75252 Paris Cedex 05 (France); Nogueira, R.P. [Institut National Polytechnique de Grenoble, ENSEEG, UMR5614 and 5631 INPG-CNRS LTPCM, LEPMI, BP 75, 38402 St Martin d' Heres (France)

    2007-03-10

    For the hydrogen evolution reaction, the coverage rate of the electrode surface by adsorbed hydrogen is generally difficult to evidence especially in presence of bubbles. In the present paper, a parallel competing reaction was incorporated to the interface by the addition of ferricyanide to a NaOH solution. This reaction was supposed to take place on the free electrode surface and allowed the relaxation of adsorbed hydrogen to be identified. Models taking into account hydrogen evolution, hydrogen absorption, and ferricyanide reduction were proposed. Three metals were tested: platinum, iron, and palladium, which absorb hydrogen in very different quantities. In these conditions, low frequency loops related to the H{sub ads} surface coverage appeared in the electrochemical impedance diagrams, whose properties depend on the tested metal. Very good agreement was found between the experimental data and model predictions. (author)

  20. Characterization of TiO2-based semiconductors for photocatalysis by electrochemical impedance spectroscopy

    Science.gov (United States)

    Ângelo, Joana; Magalhães, Pedro; Andrade, Luísa; Mendes, Adélio

    2016-11-01

    The photocatalytic activity of a commercial titanium dioxide (P25) and of an in-house prepared P25/graphene composite is assessed according to standard ISO 22197-1:2007. The photoactivity performances of bare and composite TiO2-based materials were further studied by electrochemical impedance spectroscopy (EIS) technique to better understand the function of the graphene in the composite. EIS experiments were performed using a three-electrode configuration, which allows obtaining more detailed information about the complex charge transfer phenomena at the semiconductor/electrolyte interface. The Randles equivalent circuit was selected as the most suitable for modelling the present photocatalysts. The use of the graphene composite allows a more effective charge separation with lower charge transfer resistance and less e-/h+ recombination on the composite photocatalyst, reflected in the higher values of NO conversion.

  1. Studies of the first lithiation of graphite materials by electrochemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    ZHUANG Quanchao; CHEN Zuofeng; DONG Quanfeng; JIANG Yanxia; HUANG Ling; SUN Shigang

    2006-01-01

    First lithiation of graphite electrode in 1mol/L LiPF6-EC:DEC:DMC electrolyte was investigated by electrochemical impedance spectroscopy (EIS). The results illustrated that the first arc in the high-frequency range observed in the Nyquist diagram appears near 0.9 V in the initial lithiation of graphite electrode, and its diameter increases with the decrease of polarization potential. These ElS features were attributed to the formation and growth of SEI film. Appropriate equivalent circuit was proposed to fit the experimental ElS data. The fitting results revealed the process of the formation and growth of SEI film, and evaluated quantitatively the resistance of charge transfer, as well as the capacitance of double layer along with the increase of polarization potentials.

  2. ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY DURING CORROSION PROCESS OF 8090 Al-Li ALLOY IN EXCO SOLUTION

    Institute of Scientific and Technical Information of China (English)

    J.F. Li; Z.Q. Zheng; C.Y. Tan; S.C. Li; Z. Zhang; J.Q. Zhang

    2004-01-01

    The corrosion behavior and electrochemical impedance spectroscopy ( EIS) features of 8090 Al-Li alloys in EXCO solution were investigated, and the EIS was simulated using an equivalent circuit. At the beginning of immersion in EXCO solution, the EIS is comprised by a depressed capacitive arc at high-mediate frequency and an inductive arc at low frequency, and the inductive component decreases and disappears with immersion time. Once exfoliation or severe pitting corrosion is produced, two capacitivearcs appear in the EIS. These two capacitive arcs are originated from the two parts of the corroded alloy surface, the original flat alloy surface and the new inter-face exposed to the aggressive EXCO solution due to the exfoliation or pitting corrosion.Some corrosion development features of 8090 Al-Li alloys in EXCO solution can be obtained through simulated EIS information.

  3. Diagnosis of Lithium-Ion Batteries State-of-Health based on Electrochemical Impedance Spectroscopy Technique

    DEFF Research Database (Denmark)

    Stroe, Daniel Ioan; Swierczynski, Maciej Jozef; Stan, Ana-Irina

    2014-01-01

    Lithium-ion batteries have developed into a popular energy storage choice for a wide range of applications because of their superior characteristics in comparison to other energy storage technologies. Besides modelling the performance behavior of Lithium-ion batteries, it has become of huge...... interest to accurately diagnose their state-of-health (SOH). At present, Lithium-ion batteries are diagnosed by performing capacity or resistance (current pulse) measurements; however, in the majority of the cases, these measurements are time consuming and result in changing the state of the battery...... as well. This paper investigates the use of the electrochemical impedance spectroscopy (EIS) technique for SOH diagnosis of Lithium-ion battery cells, instead of using the aforementioned techniques, since this new method allows for online and direct measurement of the battery cell response in any working...

  4. The corrosion protection mechanism of rust converters: An electrochemical impedance spectroscopy study

    Energy Technology Data Exchange (ETDEWEB)

    Collazo, A. [ENCOMAT Group, ETSEI, Universidade de Vigo, Campus Universitario, 36310 Vigo (Spain); Novoa, X.R., E-mail: rnovoa@uvigo.e [ENCOMAT Group, ETSEI, Universidade de Vigo, Campus Universitario, 36310 Vigo (Spain); Perez, C.; Puga, B. [ENCOMAT Group, ETSEI, Universidade de Vigo, Campus Universitario, 36310 Vigo (Spain)

    2010-08-30

    Oxide converters represent an interesting alternative for the protection of steel surfaces that have some degree of rust. Although the mechanism of these converters is not clear, it is assumed that they react with iron oxides and generate new compounds that may have a passivation effect on the steel surface. This last point is not well established, and several authors have even spoken of an accelerating effect of these compounds. We present here a study of the electrochemical behaviour of iron oxides immersed in the rust converter. The modulus of the impedance increases significantly after a certain time of immersion, suggesting that the electronic conductivity and, consequently, the rate of the cathodic reaction tend to decrease.

  5. Energy Dispersive X-Ray and Electrochemical Impedance Spectroscopies for Performance and Corrosion Analysis of PEMWEs

    Science.gov (United States)

    Steen, S. M., Iii; Zhang, F.-Y.

    2014-11-01

    Proton exchange membrane water electrolyzers (PEMWEs) are a promising energy storage technology due to their high efficiency, compact design, and ability to be used in a renewable energy system. Before they are able to make a large commercial impact, there are several hurdles facing the technology today. Two powerful techniques for both in-situ and ex- situ characterizations to improve upon their performance and better understand their corrosion are electrochemical impedance spectroscopy and energy dispersive x-ray spectroscopy, respectively. In this paper, the authors use both methods in order to characterize the anode gas diffusion layer (GDL) in a PEMWE cell and better understand the corrosion that occurs in the oxygen electrode during electrolysis.

  6. In Situ Representation of Soil/Sediment Conductivity Using Electrochemical Impedance Spectroscopy.

    Science.gov (United States)

    Li, Xiaojing; Wang, Xin; Zhao, Qian; Zhang, Yueyong; Zhou, Qixing

    2016-04-30

    The electrical conductivity (EC) of soil is generally measured after soil extraction, so this method cannot represent the in situ EC of soil (e.g., EC of soils with different moisture contents) and therefore lacks comparability in some cases. Using a resistance measurement apparatus converted from a configuration of soil microbial fuel cell, the in situ soil EC was evaluated according to the Ohmic resistance (Rs) measured using electrochemical impedance spectroscopy. The EC of soils with moisture content from 9.1% to 37.5% was calculated according to Rs. A significant positive correlation (R² = 0.896, p < 0.01) between the soil EC and the moisture content was observed, which demonstrated the feasibility of the approach. This new method can not only represent the actual soil EC, but also does not need any pretreatment. Thus it may be used widely in the measurement of the EC for soils and sediments.

  7. In-situ quantification of solid oxide fuel cell electrode microstructure by electrochemical impedance spectroscopy

    Science.gov (United States)

    Zhang, Yanxiang; Chen, Yu; Chen, Fanglin

    2015-03-01

    Three-dimensional (3D) microstructure of solid oxide fuel cell electrodes plays critical roles in determining fuel cell performance. The state-of-the-art quantification technique such as X-ray computed tomography enables direct calculation of geometric factors by 3D microstructure reconstruction. Taking advantages of in-situ, fast-responding and low cost, electrochemical impedance spectroscopy represented by distribution of relaxation time (DRT) is a novel technique to estimate geometric properties of fuel cell electrodes. In this study, we employed the anode supported cells with the cell configuration of Ni-YSZ || YSZ || LSM-YSZ as an example and compared the tortuosity factor of pores of the anode substrate layer by X-ray computed tomography and DRT analysis. Good agreement was found, validating the feasibility of in-situ microstructural quantification by using the DRT technique.

  8. Detection of methotrexate in a flow system using electrochemical impedance spectroscopy and multivariate data analysis.

    Science.gov (United States)

    Tesfalidet, Solomon; Geladi, Paul; Shimizu, Kenichi; Lindholm-Sethson, Britta

    2016-03-31

    Methotrexate (MTX), a common pharmaceutical drug in cancer therapy and treatment of rheumatic diseases, is known to cause severe adverse side effects at high dose. As the side effect may be life threatening, there is an urgent need for a continuous, bed-side monitoring of the nominal MTX serum level in a patient while the chemical is being administered. This article describes a detection of MTX using a flow system that consists two modified gold electrodes. Interaction of MTX with the antibodies fixed on the electrode surface is detected by electrochemical impedance spectroscopy and evaluated using singular value decomposition (SVD). The key finding of this work is that the change in the electrode capacitance is found to be quantitative with respect to the concentration of MTX. Moreover a calibration curve constructed using the principal component regression method has a linear range of six orders of magnitude and a detection limit of 1.65 × 10(-10) M.

  9. Solid oxide electrolysis cell analysis by means of electrochemical impedance spectroscopy: A review

    Science.gov (United States)

    Nechache, A.; Cassir, M.; Ringuedé, A.

    2014-07-01

    High temperature water electrolysis based on Solid Oxide Electrolysis Cell (SOEC) is a very promising solution to produce directly pure hydrogen. However, degradation issues occurring during operation still represent a scientific and technological barrier in view of its development at an industrial scale. Electrochemical Impedance Spectroscopy (EIS) is a powerful in-situ fundamental tool adapted to the study of SOEC systems. Hence, after a quick presentation of EIS principle and data analysis methods, this review demonstrates how EIS can be used: (i) to characterize the performance and mechanisms of SOEC electrodes; (ii) as a complementary tool to study SOEC degradation processes for different cell configurations, in addition to post-test tools such as scanning electron microscopy (SEM) or X-ray diffraction (XRD). The use of EIS to establish a systematic SOEC analysis is introduced as well.

  10. In Situ Representation of Soil/Sediment Conductivity Using Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Xiaojing Li

    2016-04-01

    Full Text Available The electrical conductivity (EC of soil is generally measured after soil extraction, so this method cannot represent the in situ EC of soil (e.g., EC of soils with different moisture contents and therefore lacks comparability in some cases. Using a resistance measurement apparatus converted from a configuration of soil microbial fuel cell, the in situ soil EC was evaluated according to the Ohmic resistance (Rs measured using electrochemical impedance spectroscopy. The EC of soils with moisture content from 9.1% to 37.5% was calculated according to Rs. A significant positive correlation (R2 = 0.896, p < 0.01 between the soil EC and the moisture content was observed, which demonstrated the feasibility of the approach. This new method can not only represent the actual soil EC, but also does not need any pretreatment. Thus it may be used widely in the measurement of the EC for soils and sediments.

  11. Investigation of exfoliation corrosion of rolled AA8090 Al-Li alloy using electrochemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    李劲风; 张昭; 曹发和; 程英亮; 张鉴清; 曹楚南

    2003-01-01

    The exfoliation morphologies and electrochemical impedance spectroscopy (EIS) features of as-received rolled AA8090 Al-Li alloy in EXCO solution were studied. The EIS was simulated using an equivalent circuit. The results show that once the exfoliation occurs, the EIS is composed of two capacitive arcs at high frequency and mediate-low frequency; among them, the capacitance corresponding to high frequency (C1) is originated from original flat alloy surface, while the capacitance corresponding to mediate-low frequency (C2) from new interface exposed to EXCO solution due to the exfoliation and the ratio of C2 to C1 increases with exfoliation degree. It is advanced that the exfoliation degree can be quantitatively judged through this ratio.

  12. Electrochemical impedance spectroscopy study of the metal hydride alloy/electrolyte junction

    Energy Technology Data Exchange (ETDEWEB)

    Khaldi, Chokri [Laboratoire de Mecanique, Materiaux et Procedes, ESSTT, 5 Avenue Taha Hussein, 1008 Tunis (Tunisia)], E-mail: chokri.khaldi@esstt.rnu.tn; Mathlouthi, Hamadi; Lamloumi, Jilani [Laboratoire de Mecanique, Materiaux et Procedes, ESSTT, 5 Avenue Taha Hussein, 1008 Tunis (Tunisia)

    2009-06-24

    The behaviour of the LaNi{sub 3.55}Mn{sub 0.4}Al{sub 0.3}Co{sub 0.75} alloy, used as a negative electrode in the Ni-MH batteries, was studied by the electrochemical impedance spectroscopy (EIS), measured at different potentials. The modeling of the EIS spectra allows us to model the interface electrolyte/Ni-MH electrode by a succession of interfaces electrolyte/corrosion film/alloy particles. The various processes and the physics parameters of each interface are discussed and evaluated. When the potential shifts to more negative values, two reactions are in competition: the hydrogen molecular evolution and the hydrogen atomic absorption. The hydrogen diffuses in the bulk of the alloy and the diffusion is not the limiting factor for the hydrogen absorption.

  13. A Realtime and Continuous Assessment of Cortisol in ISF Using Electrochemical Impedance Spectroscopy.

    Science.gov (United States)

    Venugopal, Manju; Arya, Sunil K; Chornokur, Ganna; Bhansali, Shekhar

    2011-12-01

    This study describes the functioning of a novel sensor to measure cortisol concentration in the interstitial fluid (ISF) of a human subject. ISF is extracted by means of vacuum pressure from micropores created on the stratum corneum layer of the skin. The pores are produced by focusing a near infrared laser on a layer of black dye material attached to the skin. The pores are viable for approximately three days after skin poration. Cortisol measurements are based on electrochemical impedance (EIS) technique. Gold microelectrode arrays functionalized with Dithiobis (succinimidyl propionate) self-assembled monolayer (SAM) have been used to fabricate an ultrasensitive, disposable, electrochemical cortisol immunosensor. The biosensor was successfully used for in-vitro measurement of cortisol in ISF. Tests in a laboratory setup show that the sensor exhibits a linear response to cortisol concentrations in the range 1 pm to 100 nM. A small pilot clinical study showed that in-vitro immunosensor readings, when compared with commercial evaluation using enzyme-linked immunoassay (ELISA) method, correlated well with cortisol levels in saliva and ISF. Further, circadian rhythm could be established between the subject's ISF and the saliva samples collected over 24 hours time-period. Cortisol levels in ISF were found reliably higher than in saliva. This Research establishes the feasibility of using impedance based biosensor architecture for a disposable, wearable cortisol detector. The projected commercial in-vivo real-time cortisol sensor device, besides being minimally invasive, will allow continuous ISF harvesting and cortisol monitoring over 24 hours even when the subject is asleep. Forthcoming, this sensor could be interfaced to a wireless health monitoring system that could transfer sensor data over existing wide-area networks such as the internet and a cellular phone network to enable real-time remote monitoring of subjects.

  14. A Realtime and Continuous Assessment of Cortisol in ISF Using Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Arya, Sunil K.; Chornokur, Ganna; Bhansali, Shekhar

    2011-01-01

    This study describes the functioning of a novel sensor to measure cortisol concentration in the interstitial fluid (ISF) of a human subject. ISF is extracted by means of vacuum pressure from micropores created on the stratum corneum layer of the skin. The pores are produced by focusing a near infrared laser on a layer of black dye material attached to the skin. The pores are viable for approximately three days after skin poration. Cortisol measurements are based on electrochemical impedance (EIS) technique. Gold microelectrode arrays functionalized with Dithiobis (succinimidyl propionate) self-assembled monolayer (SAM) have been used to fabricate an ultrasensitive, disposable, electrochemical cortisol immunosensor. The biosensor was successfully used for in-vitro measurement of cortisol in ISF. Tests in a laboratory setup show that the sensor exhibits a linear response to cortisol concentrations in the range 1 pm to 100 nM. A small pilot clinical study showed that in-vitro immunosensor readings, when compared with commercial evaluation using enzyme-linked immunoassay (ELISA) method, correlated well with cortisol levels in saliva and ISF. Further, circadian rhythm could be established between the subject's ISF and the saliva samples collected over 24 hours time-period. Cortisol levels in ISF were found reliably higher than in saliva. This Research establishes the feasibility of using impedance based biosensor architecture for a disposable, wearable cortisol detector. The projected commercial in-vivo real-time cortisol sensor device, besides being minimally invasive, will allow continuous ISF harvesting and cortisol monitoring over 24 hours even when the subject is asleep. Forthcoming, this sensor could be interfaced to a wireless health monitoring system that could transfer sensor data over existing wide-area networks such as the internet and a cellular phone network to enable real-time remote monitoring of subjects. PMID:22163154

  15. Correlation of capacity fading processes and electrochemical impedance spectra in lithium/sulfur cells

    Science.gov (United States)

    Risse, Sebastian; Cañas, Natalia A.; Wagner, Norbert; Härk, Eneli; Ballauff, Matthias; Friedrich, K. Andreas

    2016-08-01

    The capacity fading of lithium/sulfur (Li/S) cells is one major challenge that has to be overcome for a successful commercialization of this electrochemical storage system. Therefore it is essential to detect the major fading mechanisms for further improvements of this system. In this work, the processes leading to fading are analyzed in terms of a linear four state model and correlated to the distribution of relaxation times calculated with a modified Levenberg-Marquardt algorithm. Additionally, the Warburg impedance and the solution resistance are also obtained by the same algorithm. The detailed analysis of intermediate states during the first cycle gives the distinction between relaxation processes at the sulfur cathode and at the lithium anode. The influence of the polysulfides on the impedance parameters was evaluated using symmetric cells; this yields a good correlation with the results obtained from the first discharge/charge experiment. A fast and a slow capacity fading process are observed for the charge and the discharge during 50 cycles. The fast fading process can be assigned to Faradaic reactions at the lithium anode.

  16. Surface Characteristics and Electrochemical Impedance Investigation of Spark-Anodized Ti-6Al-4V Alloy

    Science.gov (United States)

    Garsivaz jazi, M. R.; Golozar, M. A.; Raeissi, K.; Fazel, M.

    2014-04-01

    In this study, the surface characteristic of oxide films on Ti-6Al-4V alloy formed by an anodic oxidation treatment in H2SO4/H3PO4 electrolyte at potentials higher than the breakdown voltage was evaluated. Morphology of the surface layers was studied by scanning electron microscope. The results indicated that the diameter of pores and porosity of oxide layer increase by increasing the anodizing voltage. The thickness measurement of the oxide layers showed a linear increase of thickness with increasing the anodizing voltage. The EDS analysis of oxide films formed in H2SO4/H3PO4 at potentials higher than breakdown voltage demonstrated precipitation of sulfur and phosphor elements from electrolyte into the oxide layer. X-ray diffraction was employed to exhibit the effect of anodizing voltage on the oxide layer structure. Roughness measurements of oxide layer showed that in spark anodizing, the Ra and Rz parameters would increase by increasing the anodizing voltage. The structure and Corrosion properties of oxide layers were studied using electrochemical impedance spectroscopy (EIS) techniques, in 0.9 wt.% NaCl solution. The obtained EIS spectra and their interpretation in terms of an equivalent circuit with the circuit elements indicated that the detailed impedance behavior is affected by three regions of the interface: the space charge region, the inner compact layer, and outer porous layer.

  17. Equivalent circuit model analysis on electrochemical impedance spectroscopy of lithium metal batteries

    Science.gov (United States)

    Gao, Peng; Zhang, Cuifen; Wen, Guangwu

    2015-10-01

    Lithium metal electrode is pretreated with 1,3-dioxolane or 1,4-dioxane to improve its properties. The components and morphology of the surface films formed in the above two pretreatment liquids are studied using FTIR and SEM respectively. Li-LiCoO2 coin cells are then fabricated and their cycle and discharge performance are tested. It is found that the battery performance is greatly improved by such pretreatment. Interestingly, the 1,4-dioxane pretreatment is more effective than 1,3-dioxolane in improving the lithium metal electrode performance. To explore the mechanism(s) behind, the electrochemical impedance spectroscopy (EIS) is employed and an equivalent circuit model is designed for EIS analysis. The fitting curves are aligned well with the experimental curves, suggesting that the proposed equivalent circuit model is an ideal model for lithium battery. Next, the corresponding relationship between the impedance components and every individual semicircle in the Nyquist curves is inferred theoretically and the result is satisfying. Based on the analysis using this model, we conclude that the structural stability of SEI film is increased and the interfacial compatibility between the lithium substrate and the SEI film is improved by 1,3-dioxolane or 1,4-dioxane pretreatment.

  18. Electrochemical impedance spectroscopy investigation on indium tin oxide films under cathodic polarization in NaOH solution

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Wenjiao; Cao, Si; Yang, Yanze; Wang, Hao; Li, Jin; Jiang, Yiming, E-mail: corrosion@fudan.edu.cn

    2012-09-30

    The electrochemical corrosion behaviors of indium tin oxide (ITO) films under the cathodic polarization in 0.1 M NaOH solution were investigated by electrochemical impedance spectroscopy. The as-received and the cathodically polarized ITO films were characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy and X-ray diffraction for morphological, compositional and structural studies. The results showed that ITO films underwent a corrosion process during the cathodic polarization and the main component of the corrosion products was body-centered cubic indium. The electrochemical impedance parameters were related to the effect of the cathodic polarization on the ITO specimens. The capacitance of ITO specimens increased, while the charge transfer resistance and the inductance decreased with the increase of the polarization time. The proposed mechanism indicated that the corrosion products (metallic indium) were firstly formed during the cathodic polarization and then absorbed on the surface of the ITO film. As the surface was gradually covered by indium particles, the corrosion process was suppressed. - Highlights: Black-Right-Pointing-Pointer Cathodic polarization of indium tin oxide (ITO) in 0.1 M NaOH. Black-Right-Pointing-Pointer Cathodic polarization studied with electrochemical impedance spectroscopy. Black-Right-Pointing-Pointer ITO underwent a corrosion attack during cathodic polarization, indium was observed. Black-Right-Pointing-Pointer Electrochemical parameters of ITO were obtained using equivalent electrical circuit. Black-Right-Pointing-Pointer A corrosion mechanism is proposed.

  19. Enhancement of corrosion resistance of polypyrrole using metal oxide nanoparticles: Potentiodynamic and electrochemical impedance spectroscopy study.

    Science.gov (United States)

    Hosseini, Marzieh; Fotouhi, Lida; Ehsani, Ali; Naseri, Maryam

    2017-11-01

    We introduce a simple and facile strategy for dispersing of nanoparticles within a p-type conducting polymer matrix by in situ electropolymerization using oxalic acid as the supporting electrolyte. Coatings prepared from polypyrrole-nano-metal oxide particles synthesized by in situ polymerization were found to exhibit excellent corrosion resistance much superior to polypyrrole (Ppy) in aggressive environments. The anti-corrosion behavior of polypyrrole films in different states and the presence of TiO2, Mn2O3 and ZnO nanoparticles synthesized by electropolymerization on Al electrodes have been investigated in corrosive solutions using potentiodynamic polarization and electrochemical impedance spectroscopy. The electrochemical response of the coated electrodes in polymer and nanocomposite state was compared with bare electrodes. The use of TiO2 nanoparticles has proved to be a great improvement in the performances of polypyrrole films for corrosion protection of Al samples. The polypyrrole synthesized in the presence of TiO2 nanoparticles coated electrodes offered a noticeable enhancement of protection against corrosion processes. The exceptional improvement of performance of these coatings has been associated with the increase in barrier to diffusion, prevention of charge transport by the nanosize TiO2, redox properties of polypyrrole as well as very large surface area available for the liberation of dopant due to nano-size additive. Copyright © 2017 Elsevier Inc. All rights reserved.

  20. Stainless steel electrode characterizations by electrochemical impedance spectroscopy for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Kanta, A.-F., E-mail: abdoul.kanta@umons.ac.be [Service de Science des Materiaux, Universite de Mons, Rue de l' Epargne 56, 7000 Mons (Belgium); Decroly, A. [Service de Science des Materiaux, Universite de Mons, Rue de l' Epargne 56, 7000 Mons (Belgium)

    2011-11-30

    Electrochemical impedance spectroscopy (EIS) was used to understand the electrochemical mechanisms which appear in dye-sensitized solar cells (DSSCs). This qualitative and quantitative technique permits identification of the phenomena proceeding within the different elements composing the cell and at their interfaces. In this study, the classical conducting glass substrate was replaced by a protected stainless steel (304 type) substrate as the counter-electrode (cathode) in dye-sensitized solar cells. Platinum was deposited at the substrate surface to optimize the charge transfer resistance of the electrode. After a few days of immersion in the electrolytic solution, stainless steel substrates coated with low thickness of Pt show pitting corrosion due to iodine. Defects in the Pt layer such as discontinuity of the film and micro-cracks may explain the corrosion of the stainless steel substrate. However the Pt layer degradation is retarded for thicker films. On the other hand, polished substrates show a better behaviour probably due to the elimination of the defects on the stainless steel surface. Electrolytic solution was optimized. For this, components such as 1-butyl-3-methylimidazolium iodide (BMII), guanidine thiocyanate (GT) and 4-tert-butylpyridine (TBP) were added. No corrosion phenomena on stainless steel 304 appeared within 3 days when TBP was added. This means that TBP acts as a corrosion inhibitor. A schematic equivalent circuit is also proposed.

  1. Characterisation of nanocarbon-based gas diffusion media by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Gallo Stampino, P.; Omati, L.; Cristiani, C.; Dotelli, G. [Politecnico di Milano, Dipartimento di Chimica, Materiali e Ingegneria Chimica ' ' G. Natta' ' (Italy); INSTM R.U. POLIMI, Milano (Italy)

    2010-04-15

    A multi-wall carbon nanotubes (MWCNTs)-based gas diffusion medium (GDM) was prepared, where carbon black was partially substituted by carbon nanotube (CNT) in the formulation of the micro-porous layer (MPL). A rheological analysis of the ink used to coat the gas diffusion layer (GDL) was previously performed to correlate viscosities with the slurry composition. Shear thinning inks with viscosity of 0.4 (Pas{sup -1}) were obtained for a composition containing 10 wt.-% of CNT and 12 wt.-% of fluorinated polymer. Using the doctor-blade technique, a coating thickness of about 100-150 {mu}m was obtained. Moreover, electrochemical performance of a single cell assembled with the CNT-based GDM was compared with that obtained with a sample without CNTs. In order to better understand the role of CNTs, electrochemical impedance spectroscopy (EIS) of the running fuel cell (FC) was also performed. As a result, it was found that the addition of CNTs sensibly improves single cell performances. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  2. Impedance model of lithium ion polymer battery considering temperature effects based on electrochemical principle: Part I for high frequency

    Science.gov (United States)

    Xiao, Meng; Choe, Song-Yul

    2015-03-01

    Measurement of impedance is one of well-known methods to experimentally characterize electrochemical properties of Li-ion batteries. The measured impedance responses are generally fitted to an equivalent circuit model that is composed of linear and nonlinear electric components that mimic behaviors of different layers of a battery. However, the parameters do not provide quantitative statements on charge dynamics considering material properties. Therefore, electrochemical models are widely employed to study the charge dynamics, but have not included high frequency responses predominantly determined by double layers. Thus, we have developed models for the double layer and bulk that are integrated into the electrochemical model for a pouch type Li-ion battery. The integrated model is validated against the frequency response obtained from EIS equipment at different temperatures as well as the time response. The results show that the proposed model is capable of representing the responses at charging and discharging in time and frequency domain.

  3. Origin of Capacity Fading in Nano-Sized Co3O4Electrodes: Electrochemical Impedance Spectroscopy Study

    Science.gov (United States)

    2008-01-01

    Transition metal oxides have been suggested as innovative, high-energy electrode materials for lithium-ion batteries because their electrochemical conversion reactions can transfer two to six electrons. However, nano-sized transition metal oxides, especially Co3O4, exhibit drastic capacity decay during discharge/charge cycling, which hinders their practical use in lithium-ion batteries. Herein, we prepared nano-sized Co3O4with high crystallinity using a simple citrate-gel method and used electrochemical impedance spectroscopy method to examine the origin for the drastic capacity fading observed in the nano-sized Co3O4anode system. During cycling, AC impedance responses were collected at the first discharged state and at every subsequent tenth discharged state until the 100th cycle. By examining the separable relaxation time of each electrochemical reaction and the goodness-of-fit results, a direct relation between the charge transfer process and cycling performance was clearly observed.

  4. Preparation and Electrochemical Application of Praseodymium Modified TiO2-NTs/SnO2-Sb Anode by Cyclic Voltammetry Method

    Institute of Scientific and Technical Information of China (English)

    王燕; 陈迓宾; 朱怀工; 张旭斌

    2016-01-01

    A Pr-doped TiO2-NTs/SnO2-Sb electrode was prepared by a simple method, cyclic voltammetry(CV). The methyl orange(MO)aqueous solution was selected as a simulated wastewater. The ordered microstructural TiO2-NTs substrate was synthesized by an electrochemical method to obtain large specific surface area and high space utilization. The phase structure, electrode surface morphology and electrochemical properties of electrodes were characterized by XRD, SEM and electrochemical technology, respectively. The results showed that praseo-dymium oxide was successfully doped into the SnO2-Sb film by CV method. Due to the doped Pr, the oxygen evo-lution potential increased from 2.25 V to 2.40 V. The degradation of MO was investigated by UV-vis. TheCt/C0(φ) was studied as a function to obtain the optimal parameters, such as the amount of doped Pr, current density and initial dye concentration. In addition, the degradation process followed pseudo-first-order reaction kinetics and the rate constant was 0.099 3 min-1. The result indicated that the introduction of Pr reduced the formation of oxygen vacancies or enhanced the formation of adsorbed hydroxyl radical groups on the surface, thus leading to better ac-tivity and stability.

  5. Electrochemical Impedance Spectroscopy of Alloys in a Simulated Space Shuttle Launch Environment

    Science.gov (United States)

    Calle, L. M.; Kolody, M. R.; Vinje, R. D.; Whitten, M. C.; Li, D.

    2005-01-01

    Corrosion studies began at NASA/Kennedy Space Center in 1966 during the Gemini/Apollo Programs with the evaluation of long-term protective coatings for the atmospheric protection of carbon steel. An outdoor exposure facility on the beach near the launch pad was established for this purpose at that time. The site has provided over 35 years of technical information on the evaluation of the long-term corrosion performance of many materials and coatings as well as on maintenance procedures. Results from these evaluations have helped NASA find new materials and processes that increase the safety and reliability of our flight hardware, launch structures, and ground support equipment. The launch environment at the Kennedy Space Center (KSC) is extremely corrosive due to the combination of ocean salt spray, heat, humidity, and sunlight. With the introduction of the Space Shuttle in 1981, the already highly corrosive conditions at the launch pad were rendered even more severe by the acidic exhaust from the solid rocket boosters. Over the years, many materials have been evaluated for their corrosion performance under conditions similar to those found at the launch pads. These studies have typically included atmospheric exposure and evaluation with conventional electrochemical methods such as open circuit potential (OCP) measurements, polarization techniques, and electrochemical impedance spectroscopy (EIS). The atmosphere at the Space Shuttle launch site is aggressive to most metals and causes severe pitting in many of the common stainless steel alloys such as type 304L stainless steel (304L SS). A study was undertaken to find a more corrosion resistant material to replace the existing 304L SS tubing. This paper presents the results from atmospheric exposure as well as electrochemical measurements on the corrosion resistance of AL-6XN (UNS N08367) and 254-SMO (UNS S32154). Type 304L SS (UNS S30403) was used as a control. Conditions at the Space Shuttle launch pad were

  6. Pyrolytic carbon microelectrodes for impedance based cell sensing

    DEFF Research Database (Denmark)

    Hassan, Yasmin Mohamed; Caviglia, Claudia; Hemanth, Suhith

    2016-01-01

    Electrically conductive glass-like carbon structures can be obtained from a polymer template through a pyrolysis process. These structures can be used as electrodes for bio sensing applications such as electrochemical evaluation of cell adhesion and proliferation. This study focuses on the optimi...... to decrease the resistivity of the resulting carbon material and improve the performance in cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Finally, EIS was used to monitor adhesion and proliferation of HeLa cells....

  7. Effects of Sodium Sulfate as Electrolyte Additive on Electrochemical Performance of Lead Electrode

    Institute of Scientific and Technical Information of China (English)

    YU Jin-yu; QIAN Zhao-hong; ZHAO Meng; WANG Yu-jie; NIU Lin

    2013-01-01

    Sodium sulfate as an electrolyte additive was studied via electrochemical methods including linear sweep voltammetry(LSV),cyclic voltammetry(CV) and electrochemical impedance spectroscopy(EIS) to deeply understand its effect on the hydrogen evolution current and overpotential as well as the formation and structure of anodic passivation films on lead surface during the redox processes.The results achieved will be valuable to improve the cycle life and maintenance-free properties of lead-acid batteries.

  8. Exploration of Electrochemical Intermediates of the Anticancer Drug Doxorubicin Hydrochloride Using Cyclic Voltammetry and Simulation Studies with an Evaluation for Its Interaction with DNA

    Directory of Open Access Journals (Sweden)

    Partha Sarathi Guin

    2014-01-01

    Full Text Available Electrochemical behavior of the anticancer drug doxorubicin hydrochloride was studied using cyclic voltammetry in aqueous medium using Hepes buffer (pH~7.4. At this pH, doxorubicin hydrochloride undergoes a reversible two-electron reduction with E1/2 value −665±5 mV (versus Ag/AgCl, saturated KCl. Depending on scan rates, processes were either quasireversible (at low scan rates or near perfect reversible (at high scan rates. This difference in behavior of doxorubicin hydrochloride with scan rate studied over the same potential range speaks of differences in electron transfer processes in doxorubicin hydrochloride. Attempt was made to identify and understand the species involved using simulation. The information obtained was used to study the interaction of doxorubicin hydrochloride with calf thymus DNA. Cathodic peak current gradually decreased as more calf thymus DNA was added. The decrease in cathodic peak current was used to estimate the interaction of the drug with calf thymus DNA. Nonlinear curve fit analysis was applied to evaluate the intrinsic binding constant and site size of interaction that was compared with previous results on doxorubicin hydrochloride-DNA interaction monitored by cyclic voltammetry or spectroscopic techniques.

  9. Electrochemical behaviorof carbon paste electrode modified with Carbon Nanofibers: Application to detection of Bisphenol A

    Directory of Open Access Journals (Sweden)

    N.Achargui

    2016-12-01

    Full Text Available The electrochemical behavior of carbon paste electrode modified with carbon nanofibers has been studied using cyclic voltammetry (CV, electrochemical impedance spectroscopy (EIS and scaning electron microscopy. The response of modified electrodein ferroferricyanidesolutionshows reversible behavior and significant increment in current value compared to the bare CPE indicating that CNFs act as efficient electron mediator to catalyze reactions at the surface. The modified electrode has been used to study the electrochemical response of bisphenol Ausing different electrochemical techniques such as cyclic voltammetry, linear sweep voltammetry, differential pulse voltammetry and square wave voltammetry. The oxidation peak of BPA was observed at about 0.53 V in phosphate buffer solution at pH 6.7. The oxidation peak current of BPA varied linearly with concentration over a wide range of 5µmol L-1 to 400 µmol L-1 and the detection limit of this method was found to be 0.55 µmol L-1

  10. Gold Cleaning Methods for Electrochemical Detection Applications

    DEFF Research Database (Denmark)

    Fischer, Lee MacKenzie; Tenje, Maria; Heiskanen, Arto

    2009-01-01

    ; hydrochloric acid potential cycling; dimethylamine borane reducing agent solutions at 25 and 65 degrees C; and a dilute form of Aqua Regia. Peak-current potential-differences obtained from cyclic voltammetry and charge transfer resistance obtained from electrochemical impedance spectroscopy, as well as X...

  11. Influence of temperature and applied potential on the electrochemical behaviour of nickel in LiBr solutions by means of electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Guinon-Pina, V.; Igual-Munoz, A. [Departamento de Ingenieria Quimica y Nuclear, ETSI Industriales, Universidad Politecnica de Valencia, P.O. Box 22012, E-46071 Valencia (Spain); Garcia-Anton, J. [Departamento de Ingenieria Quimica y Nuclear, ETSI Industriales, Universidad Politecnica de Valencia, P.O. Box 22012, E-46071 Valencia (Spain)], E-mail: jgarciaa@iqn.upv.es

    2009-10-15

    The effects of temperature, applied potential and hydrogen generation on the passive behaviour of nickel were investigated in lithium bromide aqueous solution using different electrochemical techniques: open circuit potential (OCP), potentiodynamic and potentiostatic measurements, and electrochemical impedance spectroscopy (EIS). From the polarization curves, it is observed that localised corrosion resistance decreases with temperature, the repassivation of nickel is more difficult at 75 {sup o}C and the hydrogen evolution reaction is favoured with an increase in temperature. Impedance results showed that the most suitable corrosion mechanism of nickel in LiBr solutions includes the double layer and the passive film formed on the nickel surface. The passive film of nickel partially disappears when a low cathodic potential is applied.

  12. Cyclability study of silicon-carbon composite anodes for lithium-ion batteries using electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Guo Juchen; Sun, Ann; Chen Xilin [Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD 20742 (United States); Wang Chunsheng, E-mail: cswang@umd.ed [Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD 20742 (United States); Manivannan, Ayyakkannu [US Department of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 (United States)

    2011-04-15

    Research highlights: {yields} Silicon-carbon anode materials for Li-ion batteries were synthesized. {yields} Carbonization and annealing processes were used in electrode preparation. {yields} Capacity fading mechanism was investigated by electrochemical impedance spectroscopy. {yields} Impedance evolution revealed better stability of the carbonized anode material. - Abstract: The effects of carbonization process and carbon nanofiber/nanotube additives on the cycling stability of silicon-carbon composite anodes were investigated by monitoring the impedance evolution during charge/discharge cycles with electrochemical impedance spectroscopy (EIS). Three types of Si-C anodes were investigated: the first type consisted of Si nanoparticles incorporated into a network of carbon nanofibers (CNFs) and multi-walled carbon nanotubes (MWNTs), with annealed polymer binder. The second type of Si-C anodes was prepared by further heat treatment of the first Si-C anodes to carbonize the polymer binder. The third Si-C anode was as same as the second one except no CNFs and MWNTs being added. Impedance analysis revealed that the carbonization process stabilized the Si-C anode structure and decreased the charge transfer resistance, thus improving the cycling stability. On the other hand, although the MWNTs/CNFs additives could enhance the electronic conductivity of the Si-C anodes, the induced inhomogeneous structure decreased the integrity of the electrode, resulting in a poor long term cycling stability.

  13. Electrochemical impedance spectroscopy as an alternative to determine dielectric constant of potatoes at various moisture contents.

    Science.gov (United States)

    Chee, Grace; Rungraeng, Natthakan; Han, Jung H; Jun, Soojin

    2014-02-01

    The dielectric (DE) properties, specifically the DE constant (ε') and loss factor (ε''), were measured for vacuum-dried and freeze-dried potato samples at a microwave frequency of 2.45 GHz over a range of different moisture contents (MCs) using a DE probe and also a 2-probe electrochemical impedance spectroscopy (EIS). Third-order polynomial models (ε' = f₁(MC); and ε'' = f₂(MC)) at room temperature were developed for regression analysis. Additionally, at various temperatures (T), biphasic 3rd-order polynomial models (ε' = f₁(MC, T); and ε'' = f₂(MC, T)) were obtained to determine ε' and ε'' as a function of MC and T using measured data. The vacuum-dried potato sample showed a good fitness of ε' and ε'' (R² = 0.95 and 0.96, respectively) to the regression model with the range of MCs from 18% to 80% (w/w), while the freeze-dried potato sample showed a good fitness of ε' and ε'' to the 1st-phase regression model with MC 50% w/w (R² = 0.94 to 0.96). EIS measurements were also used to obtain correlation impedances for ε' and ε'' determined by the DE probe method. The resulted regression analysis meets the demands for simple, rapid, and accurate assessment for transient values of ε' and ε'' of food products during dehydration/drying processes. The EIS method was verified to be a successful alternative to direct measurements of ε' and ε''.

  14. Mismatch detection in DNA monolayers by atomic force microscopy and electrochemical impedance spectroscopy

    Directory of Open Access Journals (Sweden)

    Maryse D. Nkoua Ngavouka

    2016-02-01

    Full Text Available Background: DNA hybridization is at the basis of most current technologies for genotyping and sequencing, due to the unique properties of DNA base-pairing that guarantee a high grade of selectivity. Nonetheless the presence of single base mismatches or not perfectly matched sequences can affect the response of the devices and the major challenge is, nowadays, to distinguish a mismatch of a single base and, at the same time, unequivocally differentiate devices read-out of fully and partially matching sequences.Results: We present here two platforms based on different sensing strategies, to detect mismatched and/or perfectly matched complementary DNA strands hybridization into ssDNA oligonucleotide monolayers. The first platform exploits atomic force microscopy-based nanolithography to create ssDNA nano-arrays on gold surfaces. AFM topography measurements then monitor the variation of height of the nanostructures upon biorecognition and then follow annealing at different temperatures. This strategy allowed us to clearly detect the presence of mismatches. The second strategy exploits the change in capacitance at the interface between an ssDNA-functionalized gold electrode and the solution due to the hybridization process in a miniaturized electrochemical cell. Through electrochemical impedance spectroscopy measurements on extended ssDNA self-assembled monolayers we followed in real-time the variation of capacitance, being able to distinguish, through the difference in hybridization kinetics, not only the presence of single, double or triple mismatches in the complementary sequence, but also the position of the mismatched base pair with respect to the electrode surface.Conclusion: We demonstrate here two platforms based on different sensing strategies as sensitive and selective tools to discriminate mismatches. Our assays are ready for parallelization and can be used in the detection and quantification of single nucleotide mismatches in microRNAs or

  15. Detailed dynamic solid oxide fuel cell modeling for electrochemical impedance spectra simulation

    Energy Technology Data Exchange (ETDEWEB)

    Hofmann, Ph. [Laboratory of Steam Boilers and Thermal Plants, School of Mechanical Engineering, Thermal Engineering Section, National Technical University of Athens, Heroon Polytechniou 9, 15780 Athens (Greece); Panopoulos, K.D. [Institute for Solid Fuels Technology and Applications, Centre for Research and Technology Hellas, 4th km. Ptolemais-Mpodosakeio Hospital, Region of Kouri, P.O. Box 95, GR 502, 50200 Ptolemais (Greece)

    2010-08-15

    This paper presents a detailed flexible mathematical model for planar solid oxide fuel cells (SOFCs), which allows the simulation of steady-state performance characteristics, i.e. voltage-current density (V-j) curves, and dynamic operation behavior, with a special capability of simulating electrochemical impedance spectroscopy (EIS). The model is based on physico-chemical governing equations coupled with a detailed multi-component gas diffusion mechanism (Dusty-Gas Model (DGM)) and a multi-step heterogeneous reaction mechanism implicitly accounting for the water-gas-shift (WGS), methane reforming and Boudouard reactions. Spatial discretization can be applied for 1D (button-cell approximation) up to quasi-3D (full size anode supported cell in cross-flow configuration) geometries and is resolved with the finite difference method (FDM). The model is built and implemented on the commercially available modeling and simulations platform gPROMS trademark. Different fuels based on hydrogen, methane and syngas with inert diluents are run. The model is applied to demonstrate a detailed analysis of the SOFC inherent losses and their attribution to the EIS. This is achieved by means of a step-by-step analysis of the involved transient processes such as gas conversion in the main gas chambers/channels, gas diffusion through the porous electrodes together with the heterogeneous reactions on the nickel catalyst, and the double-layer current within the electrochemical reaction zone. The model is an important tool for analyzing SOFC performance fundamentals as well as for design and optimization of materials' and operational parameters. (author)

  16. Electrochemical behavior of folic acid at calixarene based chemically modified electrodes and its determination by adsorptive stripping voltammetry

    Energy Technology Data Exchange (ETDEWEB)

    Vaze, Vishwanath D. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India); Srivastava, Ashwini K. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India)], E-mail: aksrivastava@chem.mu.ac.in

    2007-12-31

    Voltammetric behavior of folic acid at plain carbon paste electrode and electrode modified with calixarenes has been studied. Two peaks for irreversible oxidation were observed. Out of the three calixarenes chosen for modification of the electrodes, p-tert-butyl-calix[6]arene modified electrode (CME-6) was found to have better sensitivity for folic acid. Chronocoulometric and differential pulse voltammetric studies reveal that folic acid can assemble at CME-6 to form a monolayer whose electron transfer rate is 0.00273 s{sup -1} with 2-electron/2-proton transfer for the peak at +0.71 V against SCE. An adsorption equilibrium constant of 5 x 10{sup 3} l/mol for maximum surface coverage of 2.89 x 10{sup -10} mol/cm{sup 2} was obtained. The current is found to be rectilinear with concentration by differential pulse voltammetry. However, linearity in the lower range of concentration 8.79 x 10{sup -12} M to 1.93 x 10{sup -9} M with correlation coefficient of 0.9920 was achieved by adsorptive stripping voltammetry. The limit of detection obtained was found to be 1.24 x 10{sup -12} M. This method was used for the determination of folic acid in a variety of samples, viz. serum, asparagus, spinach, oranges and multivitamin preparations.

  17. Characterization of LSM/CGO Symmetric Cells Modified by NOx Adsorbents for Electrochemical NOx Removal with Impedance Spectroscopy

    DEFF Research Database (Denmark)

    Shao, Jing; Kammer Hansen, Kent

    2013-01-01

    /CGO electrode by selectively trapping NO2 in the form of nitrate over the BaO sites and provided availability for a direct reduction of the stored nitrate. The BaO-Pt-Al2O3 layer enhanced the NOx adsorption and promoted the formation of NO2 due to the NO oxidation ability of the Pt catalyst, but hindered......This study uses electrochemical impedance spectroscopy (EIS) to characterize an LSM/CGO symmetric cell modified by NOx adsorbents for the application of electrochemical NOx reduction. Three cells were prepared and tested: a blank cell, a cell impregnated with BaO, and a cell coated with a Ba...

  18. The accurate use of impedance analysis for the study of microbial electrochemical systems.

    Science.gov (United States)

    Dominguez-Benetton, Xochitl; Sevda, Surajbhan; Vanbroekhoven, Karolien; Pant, Deepak

    2012-11-07

    The present critical review aims to portray the principles and theoretical foundations that have been used for the application of electrochemical impedance spectroscopy (EIS) to study electron-transfer mechanisms, mass transfer phenomena and distribution of the heterogeneous properties of microbial electrochemical systems (MXCs). Over the past eight years, the application of this method has allowed major breakthroughs, especially in the field of microbial fuel cells (MFCs); however, it is still most widely extended only to the calculation of internal resistances. The use and interpretation of EIS should greatly improve since the intrinsic knowledge of this field, and efforts and current trends in this field have already allowed its understanding based on rather meaningful physical properties and not only on fitting electrical analogues. From this perspective, the use, analysis and interpretation of EIS applied to the study of MXCs are critically examined. Together with the revision of more than 150 articles directly devoted to this topic, two examples of the correct and improved analysis of EIS data are extensively presented. The first one focuses on the use of graphical methods for improving EIS analysis and the other one concentrates on the elucidation of the constant phase element (CPE) parameters. CPEs have been introduced in equivalent circuit models, sometimes without solid justification or analysis; the effective capacitance has been obtained from CPE parameters, following an unsuitable theory for the case of microbial-electrochemical interfaces. The use of CPE is reviewed in terms of meaningful physical parameters, such as biofilm thickness. The use of a finite-diffusion element is reviewed throughout estimation of accurate values for obtaining the dimensionless numbers, Schmidt and Sherwood, in the context of a dioxygen-reducing-biocathode, under different flow-rate conditions. The use and analysis of EIS in this context are still emerging, but because of

  19. Analysis of nitroguanidine in Aqueous Solutions by HPLC (High Performance Liquid Chromatography) with electrochemical Detection and Voltammetry

    Science.gov (United States)

    1987-04-01

    The nitroguanidine was analyzed by high performance liquid chromatography (HPLC) with electrochemical detection at a hanging miercury drop electrode...previously reported on the application of solid sorbent collection techniques to the analysis of several explosives in water by high performance liquid chromatography (HPLC

  20. Exfoliation corrosion susceptibility of 8090 Al-Li alloy examined by electrochemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    蔡超; 李劲风; 郑子樵; 张昭

    2004-01-01

    The exfoliation corrosion susceptibility and electrochemical impedance spectroscopy(EIS) of rolled and peak-aged 8090 Al-Li alloys in EXCO solution were studied, and the EIS after exfoliation was simulated. Once exfoliation occurs, two capacitive arcs appear in the EIS at high-mediate frequency and mediate-low frequency respective ly. The exfoliation-attacked alloy surface consists of two parts, an original flat alloy surface and a new inter-face exposed to EXCO solution due to the exfoliation. The capacitance corresponding to the new exfoliation inter-face in creases approximately linearly with time at early exfoliation stage, due to the enlargement of the new inter-face. Then it maintains stable, due to the corrosion product covering on the new inter-face. The exfoliation susceptibility can be judged through the average slope of the capacitance vs time curve of the early exfoliation stage. This average slope of the rolled 8090 alloy is much higher than that of the peak-aged 8090 alloy, accordingly the rolled 8090 alloy is more susceptible to exfoliation than the peak-aged 8090 alloy.

  1. Electrochemical impedance spectroscopy for quantitative interface state characterization of planar and nanostructured semiconductor-dielectric interfaces

    Science.gov (United States)

    Meng, Andrew C.; Tang, Kechao; Braun, Michael R.; Zhang, Liangliang; McIntyre, Paul C.

    2017-10-01

    The performance of nanostructured semiconductors is frequently limited by interface defects that trap electronic carriers. In particular, high aspect ratio geometries dramatically increase the difficulty of using typical solid-state electrical measurements (multifrequency capacitance- and conductance-voltage testing) to quantify interface trap densities (D it). We report on electrochemical impedance spectroscopy (EIS) to characterize the energy distribution of interface traps at metal oxide/semiconductor interfaces. This method takes advantage of liquid electrolytes, which provide conformal electrical contacts. Planar Al2O3/p-Si and Al2O3/p-Si0.55Ge0.45 interfaces are used to benchmark the EIS data against results obtained from standard electrical testing methods. We find that the solid state and EIS data agree very well, leading to the extraction of consistent D it energy distributions. Measurements carried out on pyramid-nanostructured p-Si obtained by KOH etching followed by deposition of a 10 nm ALD-Al2O3 demonstrate the application of EIS to trap characterization of a nanostructured dielectric/semiconductor interface. These results show the promise of this methodology to measure interface state densities for a broad range of semiconductor nanostructures such as nanowires, nanofins, and porous structures.

  2. Salt transport properties of model reverse osmosis membranes using electrochemical impedance spectroscopy

    Science.gov (United States)

    Feldman, Kathleen; Chan, Edwin; Stafford, Gery; Stafford, Christopher

    With the increasing shortage of clean water, efficient purification technologies including membrane separations are becoming critical. The main requirement of reverse osmosis in particular is to maximize water permeability while minimizing salt permeability. Such performance optimization has typically taken place through trial and error approaches. In this work, key salt transport metrics are instead measured in model reverse osmosis membranes using electrochemical impedance spectroscopy (EIS). As shown previously, EIS can provide both the membrane resistance Rm and membrane capacitance Cm, with Rm directly related to salt permeability. The membranes are fabricated in a molecular layer by layer approach, which allows for control over such parameters as thickness, surface and bulk chemistry, and network geometry/connectivity. Rm, and therefore salt permeability, follows the expected trends with thickness and membrane area but shows unusual behavior when the network geometry is systematically varied. By connecting intrinsic material properties such as the salt permeability with macroscopic performance measures we can begin to establish design rules for improving membrane efficiency and facilitate the creation of next-generation separation membranes.

  3. Human haptoglobin phenotypes and concentration determination by nanogold-enhanced electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Tsai-Mu; Lee, Tzu-Cheng; Tseng, Shin-Hua; Chu, Hsueh-Liang; Chang, Chia-Ching [Department of Biological Science and Technology, National Chiao Tung University, Hsinchu 30050, Taiwan (China); Pan, Ju-Pin, E-mail: ccchang01@faculty.nctu.edu.tw [Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei 11217, Taiwan (China)

    2011-06-17

    Haptoglobin (Hp) is an acute phase protein that binds free hemoglobin (Hb), preventing Hb-induced oxidative damage in the vascular system. There are three phenotypes in human Hp, whose heterogeneous polymorphic structures and varying concentrations in plasma have been attributed to the cause of diseases and outcome of clinical treatments. Different phenotypes of Hp may be composed of the same subunits but different copy numbers, rendering their determination difficult by a single procedure. In this study, we have developed a simple, fast, reliable and sensitive method, using label-free nanogold-modified bioprobes coupled with self-development electrochemical impedance spectroscopy (EIS). By this method, probe surface charge transfer resistance is detected. The relative charge transfer resistance ratios for Hp 1-1, Hp 2-1 and Hp 2-2 were characterized. We were able to determine protein size difference within 3 nm, and the linear region of the calibration curve for Hp levels in the range of 90 pg ml{sup -1} and 90 {mu}g ml{sup -1} ({approx}1 fM to 1 pM). We surmise that similar approaches can be used to investigate protein polymorphism and altered protein-protein interaction associated with diseases.

  4. Probing the chemistry of nickel/metal hydride battery cells using electrochemical impedance spectroscopy

    Science.gov (United States)

    Isaac, Bryan J.

    1994-01-01

    Electrochemical Impedance Spectroscopy (EIS) is a valuable tool for investigating the chemical and physical processes occurring at electrode surfaces. It offers information about electron transfer at interfaces, kinetics of reactions, and diffusion characteristics of the bulk phase between the electrodes. For battery cells, this technique offers another advantage in that it can be done without taking the battery apart. This non-destructive analysis technique can thus be used to gain a better understanding of the processes occurring within a battery cell. This also raises the possibility of improvements in battery design and identification or prediction of battery characteristics useful in industry and aerospace applications. EIS as a technique is powerful and capable of yielding significant information about the cell, but it also requires that the many parameters under investigation can be resolved. This implies an understanding of the processes occurring in a battery cell. Many battery types were surveyed in this work, but the main emphasis was on nickel/metal hydride batteries.

  5. Charge Carrier Conduction Mechanism in PbS Quantum Dot Solar Cells: Electrochemical Impedance Spectroscopy Study.

    Science.gov (United States)

    Wang, Haowei; Wang, Yishan; He, Bo; Li, Weile; Sulaman, Muhammad; Xu, Junfeng; Yang, Shengyi; Tang, Yi; Zou, Bingsuo

    2016-07-20

    With its properties of bandgap tunability, low cost, and substrate compatibility, colloidal quantum dots (CQDs) are becoming promising materials for optoelectronic applications. Additionally, solution-processed organic, inorganic, and hybrid ligand-exchange technologies have been widely used in PbS CQDs solar cells, and currently the maximum certified power conversion efficiency of 9.9% has been reported by passivation treatment of molecular iodine. Presently, there are still some challenges, and the basic physical mechanism of charge carriers in CQDs-based solar cells is not clear. Electrochemical impedance spectroscopy is a monitoring technology for current by changing the frequency of applied alternating current voltage, and it provides an insight into its electrical properties that cannot be measured by direct current testing facilities. In this work, we used EIS to analyze the recombination resistance, carrier lifetime, capacitance, and conductivity of two typical PbS CQD solar cells Au/PbS-TBAl/ZnO/ITO and Au/PbS-EDT/PbS-TBAl/ZnO/ITO, in this way, to better understand the charge carriers conduction mechanism behind in PbS CQD solar cells, and it provides a guide to design high-performance quantum-dots solar cells.

  6. Electrochemical Impedance Studies on Tribocorrosion Behavior of Plasma-Sprayed Al2O3 Coatings

    Science.gov (United States)

    Liu, Zhe; Chu, Zhenhua; Chen, Xueguang; Dong, Yanchun; Yang, Yong; Li, Yingzhen; Yan, Dianran

    2015-06-01

    In this paper, the tribocorrosion of plasma-sprayed Al2O3 coatings in simulated seawater was investigated by electrochemical impedance spectroscopy (EIS) technique, complemented by scanning electron microscopy to observe the morphology of the tribocorrosion attack. Base on EIS of plasma-sprayed Al2O3 coatings undergoing long-time immersion in simulated seawater, the corrosion process of Al2O3 coatings can be divided into the earlier stage of immersion (up to 20 h) and the later stage (beyond 20 h). Then, the wear tests were carried out on the surface of Al2O3 coating undergoing different times of immersion to investigate the influence of wear on corrosion at different stages. The coexistence of wear and corrosion condition had been created by a boron nitride grinding head rotating on the surface of coatings corroded in simulated seawater. The measured EIS and the values of the fitting circuit elements showed that wear accelerated corrosion at the later stage, meanwhile, corrosion accelerated wear with the immersion time increasing.

  7. DNA Hybridization Sensors Based on Electrochemical Impedance Spectroscopy as a Detection Tool

    Directory of Open Access Journals (Sweden)

    Jin-Young Park

    2009-11-01

    Full Text Available Recent advances in label free DNA hybridization sensors employing electrochemical impedance spectroscopy (EIS as a detection tool are reviewed. These sensors are based on the modulation of the blocking ability of an electrode modified with a probe DNA by an analyte, i.e., target DNA. The probe DNA is immobilized on a self-assembled monolayer, a conducting polymer film, or a layer of nanostructures on the electrode such that desired probe DNA would selectively hybridize with target DNA. The rate of charge transfer from the electrode thus modified to a redox indicator, e.g., [Fe(CN6]3–/4–, which is measured by EIS in the form of charge transfer resistance (Rct, is modulated by whether or not, as well as how much, the intended target DNA is selectively hybridized. Efforts made to enhance the selectivity as well as the sensitivity of DNA sensors and to reduce the EIS measurement time are briefly described along with brief future perspectives in developing DNA sensors.

  8. Detecting proton exchange membrane fuel cell hydrogen leak using electrochemical impedance spectroscopy method

    Science.gov (United States)

    Mousa, Ghassan; Golnaraghi, Farid; DeVaal, Jake; Young, Alan

    2014-01-01

    When a proton exchange membrane (PEM) fuel cell runs short of hydrogen, it suffers from a reverse potential fault that, when driven by neighboring cells, can lead to anode catalyst degradation and holes in the membrane due to local heat generation. As a result, hydrogen leaks through the electrically-shorted membrane-electrode assembly (MEA) without being reacted, and a reduction in fuel cell voltage is noticed. Such voltage reduction can be detected by using electrochemical impedance spectroscopy (EIS). To fully understand the reverse potential fault, the effect of hydrogen crossover leakage in a commercial MEA is measured by EIS at different differential pressures between the anode and cathode. Then the signatures of these leaky cells were compared with the signatures of a no-leaky cells at different oxygen concentrations with the same current densities. The eventual intent of this early stage work is to develop an on-board diagnostics system that can be used to detect and possibly prevent cell reversal failures, and to permit understanding the status of crossover or transfer leaks versus time in operation.

  9. DNA Hybridization Sensors Based on Electrochemical Impedance Spectroscopy as a Detection Tool

    Science.gov (United States)

    Park, Jin-Young; Park, Su-Moon

    2009-01-01

    Recent advances in label free DNA hybridization sensors employing electrochemical impedance spectroscopy (EIS) as a detection tool are reviewed. These sensors are based on the modulation of the blocking ability of an electrode modified with a probe DNA by an analyte, i.e., target DNA. The probe DNA is immobilized on a self-assembled monolayer, a conducting polymer film, or a layer of nanostructures on the electrode such that desired probe DNA would selectively hybridize with target DNA. The rate of charge transfer from the electrode thus modified to a redox indicator, e.g., [Fe(CN)6]3−/4−, which is measured by EIS in the form of charge transfer resistance (Rct), is modulated by whether or not, as well as how much, the intended target DNA is selectively hybridized. Efforts made to enhance the selectivity as well as the sensitivity of DNA sensors and to reduce the EIS measurement time are briefly described along with brief future perspectives in developing DNA sensors. PMID:22303136

  10. Characterization of electrochemical response of a hybrid micro-nanochannel system using computational impedance spectroscopy (CIS)

    Science.gov (United States)

    Nandigana, Vishal; Aluru, Narayan

    2013-11-01

    Single molecule/particle sensing using micro/nanochannel integrated systems has attracted tremendous interest in recent years. The molecule in an aqueous ionic solution is translocated from the source microchannel towards the drain microchannel across a nanochannel under the influence of an external electric field. The translocated molecules are characterized from the electrical response of the system. In order to develop an efficient design for accurate characterization of single molecules, it is important to first understand the ion-transport dynamics in these integrated systems. To this end, we develop a computationally efficient area-averaged multi-ion transport model (AAM), considering an ion-selective nanochannel integrated with a microchannel on either side. Further, we study the ion transport dynamics both under equilibrium and non-equilibrium regimes. In each regime, the base state is perturbed with an external harmonic electrical disturbance over a wide range of frequency spectrum and the electrochemical impedance response is computed. We correlate each characteristic frequency present in the system to its corresponding physical phenomena and also characterize the microscopic diffusion boundary layer lengths (DBL) observed in the microchannel. This work was supported by the National Science Foundation (NSF) under Grants 0328162 (nano-CEMMS, UIUC), 0852657 and 0915718.

  11. Electrochemical impedance spectroscopy for graphene surface modification and protein translocation through the chemically modified graphene nanopore

    Science.gov (United States)

    Tiwari, Purushottam; Shan, Yuping; Wang, Xuewen; Darici, Yesim; He, Jin

    2014-03-01

    The multilayer graphene surface has been modified using mercaptohexadecanoic acid (MHA) and 1,2-dimyristoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-750] (DPPE-PEG750). The surface modifications are evaluated using electrochemical impedance spectroscopy (EIS). EIS measurements show the better graphene surface passivation with DPPE-PEG750 than with MHA. After modification with ferritin, the MHA modified surface shows greater charge transfer resistance (Rct) change than DPPE-PEG750 modified surface. Based on these results the translocations of ferritin through modified graphene nanopore with diameter 5-20 nm are studied. The translocation is more successful through DPPE-PEG750 modified graphene nanopore. This concludes that that the attachment of ferritin to DPPE-PEG750 modified graphene nanopore is not significant compared to MHA modified pore for the ferritin translocation hindrance. These results nicely correlate with the EIS data for respective Rct change of ferritin modified surfaces. P. Tiwari would like to thank FIU School of Integrated Science & Humanity, College Arts & Sciences for the research assistantship.

  12. Generation of Small Single Domain Nanobody Binders for Sensitive Detection of Testosterone by Electrochemical Impedance Spectroscopy.

    Science.gov (United States)

    Li, Guanghui; Zhu, Min; Ma, Lu; Yan, Junrong; Lu, Xiaoling; Shen, Yanfei; Wan, Yakun

    2016-06-01

    A phage display library of variable domain of the heavy chain only antibody or nanobody (Nb) was constructed after immunizing a bactrian camel with testosterone. With the smaller molecular size (15 kDa), improved solubility, good stability, high affinity, specificity, and lower immunogenicity, Nbs are a promising tool in the next generation of diagnosis and medical applications. Testosterone is a reproductive hormone, playing an important role in normal cardiac function and being the highly predictive marker for many diseases. Herein, a simple and sensitive immunosensor based on electrochemical impedance spectroscopy (EIS) and Nbs was successfully developed for the determination of testosterone. We successfully isolated the antitestosterone Nbs from an immune phage display library. Moreover, one of the Nbs was biotinylated according to in vivo BirA system, which showed the highest production yield and the most stable case. Further, the EIS immunosensor was set up for testosterone detection by applying the biotinylated antitestosterone Nb. As a result, the biosensor exhibited a linear working range from 0.05 to 5 ng mL(-1) with a detection limit of 0.045 ng mL(-1). In addition, the proposed immunosensor was successfully applied in determining testosterone in serum samples. In conclusion, the proposed immunosensor revealed high specificity of testosterone detection and showed as a potential approach for sensitive and accurate diagnosis of testosterone.

  13. Electrochemical impedance immunosensor for rapid detection of stressed pathogenic Staphylococcus aureus bacteria.

    Science.gov (United States)

    Bekir, Karima; Barhoumi, Houcine; Braiek, Mohamed; Chrouda, Amani; Zine, Nadia; Abid, Nabil; Maaref, Abdelrazek; Bakhrouf, Amina; Ouada, Hafedh Ben; Jaffrezic-Renault, Nicole; Mansour, Hedi Ben

    2015-10-01

    In this work, we report the adaptation of bacteria to stress conditions that induce instability of their cultural, morphological, and enzymatic characters, on which the identification of pathogenic bacteria is based. These can raise serious issues during the characterization of bacteria. The timely detection of pathogens is also a subject of great importance. For this reason, our objective is oriented towards developing an immunosensing system for rapid detection and quantification of Staphylococcus aureus. Polyclonal anti-S. aureus are immobilized onto modified gold electrode by self-assembled molecular monolayer (SAM) method. The electrochemical performances of the developed immunosensor were evaluated by impedance spectroscopy through the monitoring of the charge transfer resistance at the modified solid/liquid interface using ferri-/ferrocyanide as redox probe. The developed immunosensor was applied to detect stressed and resuscitate bacteria. As a result, a stable and reproducible immunosensor with sensitivity of 15 kΩ/decade and a detection limit of 10 CFU/mL was obtained for the S. aureus concentrations ranging from 10(1) to 10(7) CFU/mL. A low deviation in the immunosensor response (±10 %) was signed when it is exposed to stressed and not stressed bacteria.

  14. Effects of Operating Conditions on Internal Resistances in Enzyme Fuel Cells Studied via Electrochemical Impedance Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Aaron, D [Georgia Institute of Technology; Borole, Abhijeet P [ORNL; Yiacoumi, Sotira [Georgia Institute of Technology; Tsouris, Costas [ORNL

    2012-01-01

    Enzyme fuel cells (EFCs) offer some advantages over traditional precious-metal-catalyzed fuel cells, such as polymer electrolyte membrane fuel cells (PEMFCs). However, EFCs exhibit far less power output than PEMFCs and have relatively short life spans before materials must be replaced. In this work, electrochemical impedance spectroscopy (EIS) is used to analyze the internal resistances throughout the EFC at a variety of operating conditions. EIS analysis is focused primarily on the resistances of the anode, solution/membrane, and cathode. Increased enzyme loading results in improved power output and reductions in internal resistance. Conditions are identified for which enzyme loading does not limit the EFC performance. EIS experiments are also reported for EFCs operated continuously for 2 days; power output declines sharply over time, while all internal resistances increase. Drying of the cathode and enzyme/mediator degradation are believed to have contributed to this behavior. Finally, experiments are performed at varying air-humidification temperatures. Little effect on internal resistances or power output is observed. However, it is anticipated that increased air humidification can improve longevity by delivering more water to the cathode. Improvements to the enzymatic cathode are needed for EFC development. These improvements need to focus on improving transport rather than increasing enzyme loading.

  15. Aptamer-based biosensor for label-free detection of ethanolamine by electrochemical impedance spectroscopy.

    Science.gov (United States)

    Liang, Gang; Man, Yan; Jin, Xinxin; Pan, Ligang; Liu, Xinhui

    2016-09-14

    A label-free sensing assay for ethanolamine (EA) detection based on G-quadruplex-EA binding interaction is presented by using G-rich aptamer DNA (Ap-DNA) and electrochemical impedance spectroscopy (EIS). The presence of K(+) induces the Ap-DNA to form a K(+)-stabilized G-quadruplex structure which provides binding sites for EA. The sensing mechanism was further confirmed by circular dichroism (CD) spectroscopy and EIS measurement. As a result, the charge transfer resistance (RCT) is strongly increased as demonstrated by using the ferro/ferricyanide ([Fe(CN)6](3-/4-)) as a redox probe. Under the optimized conditions, a linear relationship between ΔRCT and EA concentration was obtained over the range of 0.16 nM and 16 nM EA, with a detection limit of 0.08 nM. Interference by other selected chemicals with similar structure was negligible. Analytical results of EA spiked into tap water and serum by the sensor suggested the assay could be successfully applied to real sample analysis. With the advantages of high sensitivity, selectivity and simple sensor construction, this method is potentially suitable for the on-site monitoring of EA contamination.

  16. Electrochemical Impedance Spectroscopy—A Simple Method for the Characterization of Polymer Inclusion Membranes Containing Aliquat 336

    OpenAIRE

    Michelle O’Rourke; Noel Duffy; Roland De Marco; Ian Potter

    2011-01-01

    Electrochemical impedance spectroscopy (EIS) has been used to estimate the non-frequency dependent (static) dielectric constants of base polymers such as poly(vinyl chloride) (PVC), cellulose triacetate (CTA) and polystyrene (PS). Polymer inclusion membranes (PIMs) containing different amounts of PVC or CTA, along with the room temperature ionic liquid Aliquat 336 and plasticizers such as trisbutoxyethyl phosphate (TBEP), dioctyl sebecate (DOS) and 2-nitrophenyloctyl ether (NPOE) have been in...

  17. Electrochemical investigation of [Co4(μ3-O)4(μ-OAc)4(py)4] and peroxides by cyclic voltammetry.

    Science.gov (United States)

    Clatworthy, Edwin B; Li, Xiaobo; Masters, Anthony F; Maschmeyer, Thomas

    2016-12-13

    Two oxidative redox processes of the neutral cobalt(iii) cubane, [Co4(μ3-O)4(μ-OAc)4(py)4], were investigated by cyclic voltammetry at a glassy carbon electrode in acetonitrile. In addition to the first quasi-reversible one-electron oxidation at E1/2 = 0.283 V vs. Fc(0/+), a second quasi-reversible one-electron oxidation was observed at E1/2 = 1.44 V vs. Fc(0/+). Oxidation at this potential does not facilitate water oxidation. In the presence of tert-butylhydroperoxide the peak current of this second oxidation increases, suggesting oxidation of the peroxide by the doubly oxidised cubane.

  18. Dynamic electrochemical impedance spectroscopy of Pt/C-based membrane-electrode assemblies subjected to cycling protocols

    Science.gov (United States)

    Darab, Mahdi; Dahlstrøm, Per Kristian; Thomassen, Magnus Skinlo; Seland, Frode; Sunde, Svein

    2013-11-01

    A PEM fuel cell membrane-electrode assembly (MEA) was characterized by dynamic electrochemical impedance spectroscopy (dEIS) before and after cycling in a single cell configuration. The cell was subjected to 100 cycles between 0.6 V and 1.5 V vs. RHE in N2/5% H2 and 80 °C and 100% RH. Initially, the impedance-plane plots contained first- and fourth-quadrant behavior, which is resulting from a reaction mechanism at the cathode involving adsorbed intermediates. After the cycling, the impedance spectra changed to display first-quadrant behavior only. This is suggested to be due to particle growth and possibly the formation of edges between agglomerated particles. The results show that dEIS is a sensitive technique to detect even very moderate changes in electrocatalyst structure.

  19. Electrochemical impedance spectroscopy analysis of a thin polymer film-based micro-direct methanol fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Schulz, Tobias; Weinmueller, Christian; Nabavi, Majid; Poulikakos, Dimos [Department of Mechanical and Process Engineering, Laboratory of Thermodynamics in Emerging Technologies, Institute of Energy Technology, ETH Zurich, CH-8092 Zurich (Switzerland)

    2010-11-15

    A single cell micro-direct methanol fuel cell (micro-DMFC) was investigated using electrochemical impedance spectroscopy. The electrodes consisted of thin, flexible polymer (SU8) film microchannel structures fabricated in-house using microfabrication techniques. AC impedance spectroscopy was used to separate contributions to the overall cell polarization from the anode, cathode and membrane. A clear distinction between the different electrochemical phenomena occurring in the micro-DMFC, especially the distinction between double layer charging and Faradaic reactions was shown. The effect of fuel flow rate, temperature, and anode flow channel structure on the impedance of the electrode reactions and membrane/electrode double layer charging were investigated. Analysis of impedance data revealed that the performance of the test cell was largely limited by the presence of intermediate carbon monoxide in the anode reaction. Higher temperatures increase cell performance by enabling intermediate CO to be oxidized at much higher rates. The results also revealed that serpentine anode flow microchannels show a lower tendency to intermediate CO coverage and a more stable cell behavior than parallel microchannels. (author)

  20. Two-Point Stretchable Electrode Array for Endoluminal Electrochemical Impedance Spectroscopy Measurements of Lipid-Laden Atherosclerotic Plaques.

    Science.gov (United States)

    Packard, René R Sevag; Zhang, XiaoXiao; Luo, Yuan; Ma, Teng; Jen, Nelson; Ma, Jianguo; Demer, Linda L; Zhou, Qifa; Sayre, James W; Li, Rongsong; Tai, Yu-Chong; Hsiai, Tzung K

    2016-09-01

    Four-point electrode systems are commonly used for electric impedance measurements of biomaterials and tissues. We introduce a 2-point system to reduce electrode polarization for heterogeneous measurements of vascular wall. Presence of endoluminal oxidized low density lipoprotein (oxLDL) and lipids alters the electrochemical impedance that can be measured by electrochemical impedance spectroscopy (EIS). We developed a catheter-based 2-point micro-electrode configuration for intravascular deployment in New Zealand White rabbits. An array of 2 flexible round electrodes, 240 µm in diameter and separated by 400 µm was microfabricated and mounted on an inflatable balloon catheter for EIS measurement of the oxLDL-rich lesions developed as a result of high-fat diet-induced hyperlipidemia. Upon balloon inflation, the 2-point electrode array conformed to the arterial wall to allow deep intraplaque penetration via alternating current (AC). The frequency sweep from 10 to 300 kHz generated an increase in capacitance, providing distinct changes in both impedance (Ω) and phase (ϕ) in relation to varying degrees of intraplaque lipid burden in the aorta. Aortic endoluminal EIS measurements were compared with epicardial fat tissue and validated by intravascular ultrasound and immunohistochemistry for plaque lipids and foam cells. Thus, we demonstrate a new approach to quantify endoluminal EIS via a 2-point stretchable electrode strategy.

  1. Pulse Voltammetry.

    Science.gov (United States)

    Osteryoung, Janet

    1983-01-01

    Discusses the nature of pulse voltammetry, indicating that its widespread use arises from good sensitivity and detection limits and from ease of application and low cost. Provides analytical and mechanistic applications of the procedure. (JN)

  2. Voltammetry of Medical Biomaterials

    OpenAIRE

    Gulaboski, Rubin; Markovski, Velo

    2015-01-01

    The use of biomaterials in the medicine, dentistry and pharmacy represents probably a major breakthrough in tackling many diseases or disabilities in the last 50 years. We refer to varios techniques that are used for the characterization of the structure and the composition of the biomaterials. Voltammetry is an electrochemical technique that helps mainly in understanding the redox properties of various biomaterials containing some suitable redox centers in their structure. We give in this le...

  3. Nature of the Electrochemical Properties of Sulphur Substituted LiMn2O4 Spinel Cathode Material Studied by Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Monika Bakierska

    2016-08-01

    Full Text Available In this work, nanostructured LiMn2O4 (LMO and LiMn2O3.99S0.01 (LMOS1 spinel cathode materials were comprehensively investigated in terms of electrochemical properties. For this purpose, electrochemical impedance spectroscopy (EIS measurements as a function of state of charge (SOC were conducted on a representative charge and discharge cycle. The changes in the electrochemical performance of the stoichiometric and sulphur-substituted lithium manganese oxide spinels were examined, and suggested explanations for the observed dependencies were given. A strong influence of sulphur introduction into the spinel structure on the chemical stability and electrochemical characteristic was observed. It was demonstrated that the significant improvement in coulombic efficiency and capacity retention of lithium cell with LMOS1 active material arises from a more stable solid electrolyte interphase (SEI layer. Based on EIS studies, the Li ion diffusion coefficients in the cathodes were estimated, and the influence of sulphur on Li+ diffusivity in the spinel structure was established. The obtained results support the assumption that sulphur substitution is an effective way to promote chemical stability and the electrochemical performance of LiMn2O4 cathode material.

  4. Electrochemical impedance spectroscopic measurements of FCCP-induced change in membrane permeability of MDCK cells.

    Science.gov (United States)

    Zhao, Lingzhi; Li, Xianchan; Lin, Yuqing; Yang, Lifen; Yu, Ping; Mao, Lanqun

    2012-05-07

    This study demonstrates a new electrochemical impedance spectroscopic (EIS) method for measurements of the changes in membrane permeability during the process of cell anoxia. Madin-Darby canine kidney (MDCK) cells were employed as the model cells and were cultured onto gelatin-modified glassy carbon (GC) electrodes. EIS measurements were conducted at the MDCK/gelatin-modified GC electrodes with Fe(CN)(6)(3-/4-) as the redox probe. The anoxia of the cells grown onto electrode surface was induced by the addition of carbonycyanide p-(trifluoromethoxy) phenylhydrazone (FCCP) into the cell culture, in which the MDCK/gelatin-modified GC electrodes were immersed for different times. The EIS results show that the presence of FCCP in the cell culture clearly decreases the charge-transfer resistance of the Fe(CN)(6)(3-/4-) redox probe at the MDCK/gelatin-modified GC electrodes, and the charge-transfer resistance decreases with increasing time employed for immersing the MDCK/gelatin-modified GC electrodes into the cell culture containing FCCP. These results demonstrate that the EIS method could be used to monitor the changes in the cell membrane permeability during the FCCP-induced cell anoxia. To simulate the EIS system, a rational equivalent circuit was proposed and the values of ohmic resistance of the electrolyte, charge-transfer resistance and constant phase elements for both the gelatin and the cell layers are given with the fitting error in an acceptable value. This study actually offers a new and simple approach to measuring the dynamic process of cell death induced by anoxia through monitoring the changes in the cell membrane permeability.

  5. Critical View on Electrochemical Impedance Spectroscopy Using the Ferri/Ferrocyanide Redox Couple at Gold Electrodes.

    Science.gov (United States)

    Vogt, Stephan; Su, Qiang; Gutiérrez-Sánchez, Cristina; Nöll, Gilbert

    2016-04-19

    Electrochemical or faradaic impedance spectroscopy (EIS) using the ferri/ferrocyanide couple as a redox probe at gold working electrodes was evaluated with respect to its ability to monitor consecutive surface modification steps. As a model reaction, the reversible hybridization and dehybridization of DNA was studied. Thiol-modified single stranded DNA (ssDNA, 20 bases, capture probe) was chemisorbed to a gold electrode and treated with a solution of short thiols to release nonspecifically adsorbed DNA before hybridization with complementary ssDNA (20 bases, target) was carried out. Reversible dehybridization was achieved by intense rinsing with pure water. The experimental procedures were optimized by kinetic surface plasmon resonance (SPR) and quartz crystal microbalance with dissipation (QCM-D) measurements to maximize the increase in reflectivity or decrease in frequency upon hybridization before hybridization/dehybridization was also monitored by EIS. In contrast to SPR and QCM-D, repeatable EIS measurements were not possible at first. Combined SPR/EIS and QCM-D/EIS measurements revealed that during EIS the gold surface is seriously damaged due to the presence of CN(-) ions, which are released from the ferri/ferrocyanide redox probe. Even at optimized experimental conditions, etching the gold electrodes could not be completely suppressed and the repeatability of the EIS measurements was limited. In three out of four experimental runs, only two hybridization/dehybridization steps could be monitored reversibly by EIS. Thereafter etching the gold electrode significantly contributed to the EIS spectra whereas the QCM-D response was still repeatable. Hence great care has to be taken when this technique is used to monitor surface modification at gold electrodes.

  6. Investigating Water Splitting with CaFe2O4 Photocathodes by Electrochemical Impedance Spectroscopy.

    Science.gov (United States)

    Díez-García, María Isabel; Gómez, Roberto

    2016-08-24

    Artificial photosynthesis constitutes one of the most promising alternatives for harvesting solar energy in the form of fuels, such as hydrogen. Among the different devices that could be developed to achieve efficient water photosplitting, tandem photoelectrochemical cells show more flexibility and offer high theoretical conversion efficiency. The development of these cells depends on finding efficient and stable photoanodes and, particularly, photocathodes, which requires having reliable information on the mechanism of charge transfer at the semiconductor/solution interface. In this context, this work deals with the preparation of thin film calcium ferrite electrodes and their photoelectrochemical characterization for hydrogen generation by means of electrochemical impedance spectroscopy (EIS). A fully theoretical model that includes elementary steps for electron transfer to the electrolyte and surface recombination with photogenerated holes is presented. The model also takes into account the complexity of the semiconductor/solution interface by including the capacitances of the space charge region, the surface states and the Helmholtz layer (as a constant phase element). After illustrating the predicted Nyquist plots in a general manner, the experimental results for calcium ferrite electrodes at different applied potentials and under different illumination intensities are fitted to the model. The excellent agreement between the model and the experimental results is illustrated by the simultaneous fit of both Nyquist and Bode plots. The concordance between both theory and experiments allows us to conclude that a direct transfer of electrons from the conduction band to water prevails for hydrogen photogeneration on calcium ferrite electrodes and that most of the carrier recombination occurs in the material bulk. In more general vein, this study illustrates how the use of EIS may provide important clues about the behavior of photoelectrodes and the main strategies

  7. Tethered bilayer lipid membranes studied by simultaneous attenuated total reflectance infrared spectroscopy and electrochemical impedance spectroscopy

    Science.gov (United States)

    Erbe, Andreas; Bushby, Richard J.; Evans, Stephen D.; Jeuken, Lars J. C.

    2013-01-01

    The formation of tethered lipid bilayer membranes (tBLMs) from unilamelar vesicles of egg yolk phosphatidylcholine (EggPC) on mixed self–assembled monolayers (SAMs) from varying ratios of 6-mercaptohexanol and EO3Cholesteryl on gold has been monitored by simultaneous attenuated total reflectance fourier transform infrared (ATR–FTIR) spectroscopy and electrochemical impedance spectroscopy (EIS). The influence of the lipid orientation (and hence the anisotropy) of lipids on a gold film on the dichroic ratio was studied by simulations of spectra with a matrix method for anisotropic layers. It is shown that for certain tilt angles of the dielectric tensor of the adsorbed anisotropic layer dispersive and negative absorption bands are possible. The experimental data indicates that the structure of the assemblies obtained varies with varying SAM composition. On SAMs with a high content of EO3Cholesteryl, tBLMs with reduced fluidity are formed. For SAMs with high content of 6-mercaptohexanol, the results are consistent with the adsorption of flattened vesicles, while spherical vesicles have been found in a small range of surface compositions. The kinetics of the adsorption process is consistent with the assumption of spherical vesicles as long–living intermediates for surfaces of high 6-mercaptohexanol content. No long–living spherical vesicles have been detected for surfaces with large fraction of EO3Cholesteryl tethers. The observed differences between the surfaces suggest that for the formation of tBLMs (unlike supported BLMs) no critical surface coverage of vesicles is needed prior to lipid bilayer formation. PMID:17388505

  8. Electrochemical impedance spectroscopy of BaCeO{sub 3} modified by Ti and Y

    Energy Technology Data Exchange (ETDEWEB)

    Pasierb, P.; Wierzbicka, M.; Komornicki, S.; Rekas, M. [AGH University of Science and Technology, Faculty of Materials Science and Ceramics, Al. Mickiewicza 30, 30-059 Krakow (Poland)

    2009-10-20

    Barium cerate exhibits high protonic conductivity, especially when modified by trivalent dopant such as Y, Yb, Nd, Sm or Dy. Unfortunately, the poor chemical stability in the presence of CO{sub 2} is the main disadvantage of this material. One of the possible approach to get the stable protonic conductor is the preparation of solid solutions. For example, doping of BaCeO{sub 3} with Zr leads to the improvement of the chemical stability, but the electrical properties are simultaneously corrupted. In the present work the influence of Ti, per analogy to Zr, and Y dopants on electrical properties of BaCeO{sub 3} was investigated using the electrochemical impedance spectroscopy (EIS) technique. BaCe{sub 1-x}Ti{sub x}O{sub 3-{delta}} (0 {<=} x {<=} 0.3) and Ba(Ce{sub 0.95}Ti{sub 0.05}){sub 0.95}Y{sub 0.05}O{sub 3-{delta}} solid electrolytes were prepared by solid-state reaction method. It was found that the changes of electrical properties due to the introduction of Ti into the BaCeO{sub 3} lattice is caused predominantly by the modification of the grain boundary properties. The Ti doping leads to the substantial decrease of grain boundary electrical conductivity, comparing to undoped material. The introduction of yttrium dopant to the BaCe{sub 0.95}Ti{sub 0.05}O{sub 3} lattice has the opposite effect. The total electrical conductivity increases, due to significant modification of grain boundary electrical properties. (author)

  9. Electrochemical Impedance Response of the surface treated FMS in Liquid Sodium Environment

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Jeong Hyeon; Shin, Sang Hun; Kim, Ji Hyun [Ulsan National Institute of Science and Technology, Ulsan (Korea, Republic of)

    2014-05-15

    HT9 and Gr.92 are known as compatible in sodium environment because the usual refueling time of SFRs is designed about 54 months. It is very important to investigate the corrosion-related behavior such as surface corrosion rate, carburization, decarburization and mechanical properties for its operation time. SiC and Si{sub 3}N{sub 4} CVD coating for decarburization barrier on the surface of FMS is considered in this study. The decarburization process where dissolved carbon near the specimen surface disused in to the liquid sodium. This process can originate from the difference between dissolved carbon in the material and liquid sodium. A compatibility test the cladding tube revealed that a decrease of the mechanical property instigated by the aging proves governed the whole mechanical property. To monitor the corrosion behavior of these candidate materials in sodium environment, Electrochemical Impedance Spectroscopy (EIS) method is first introduced and investigated in this study. The compatibility of cladding and structural materials with sodium has to be carefully investigated, as sodium could promote corrosion of cladding and structural materials in two ways. One is produced by the dissolution of alloy constituents into the sodium, and the other is produced through a chemical reaction with impurities (especially oxygen and carbon) in the sodium environment. EIS test with pre-oxidized Gr. 92 specimen in 200 .deg. C liquid sodium environment was carried out in this study. A clear Nyquist and Bode plots were obtained in liquid metal environment and the resistance of sodium and the oxide, and the capacitance of the oxide were measured from this result.

  10. Electrochemical impedance characteristics of LC4 aluminum alloytreated with ZH1 technique

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    ZHI technique was used to form a corrosion resistant layer on LC4 alloy. The composition of the layer was studied by X-ray photoelectron spectroscopy (XPS). It is found that the layer is composed of oxides of metals on the substrate, such as Al2O3, ZnO, MgO2, CuO, and MnO2. The electrochemical impedance spectrums (EIS) of LC4 aluminum alloy specimen were measured in NaCl solutions to study the mechanism of the corrosion resistance of the alloy treated with ZH1 technique. The results show that in NaCl solutions the capacitance of the Helmholtz layer and space charge layer of the oxide coating formed on the surface of LC4 alloy is less than that of a normal metal electrode while its ohmic resistance is relatively greater. At the same time, the thickness of the Helmholtz layer is 1-3 exponentially greater than that of a normal metal electrode. Compared with a normal metal electrode, all these characteristics make it more difficult for charges to transfer between the solution and the surface of the electrode. That is why the polarized current density of LC4 alloy treated with ZH1 technique kept small in 3.5% NaCl solution within a wide range of potential, and why the polarized curves of LC4 alloy treated with ZH1 technique changed a little in 3.5% NaCl solution of different pHi values.Moreover, according to the capacitance of the space charge layer (Csc) obtained at different potentials in 3.5% NaCl solution, I/C2sc-E curve was laid out. It is found that there does not exist a simple linear relation between l/C2sc and the potential. Therefore, the oxide coating formed on LC4 alloy with ZH1 technique is not a semiconductor at room temperature.

  11. Electrochemical characterization of the LiCoO{sub 2}/acetylene carbon ratios for porous electrodes in alkaline lithium aqueous solutions by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Castaneda, H., E-mail: castanedah@battelle.or [Battelle Memorial Institute, 505 King Avenue, Columbus OH, 43201 (United States); Tan, B.; Saunders, J. [Battelle Memorial Institute, 505 King Avenue, Columbus OH, 43201 (United States)

    2010-05-01

    LiCoO{sub 2} electrodes were fabricated with different acetylene carbon (AC) additions and fixed binder content. Subsequent electrochemical testing showed different processes at the interface that are related to pore distribution and electrode composition. Electrochemical impedance spectroscopy characterized the mechanisms close to open circuit conditions. The active state, combined with diffusion mechanisms within the cylindrical pores, contributed to the functionality of the particles according to the LiCoO{sub 2}/AC content, and surface characteristics of the electrode influenced the impedance distribution. The de Levie theory for porous electrode was used to describe the influence of the LiCoO{sub 2}/AC ratios in the impedance distribution when exposed to alkaline aqueous electrolytes (LiOH + Li{sub 2}SO{sub 4}). The pore model helped relate physical properties of the composite material, such as pore count, pore length, and double layer capacitance, with the mechanisms present at the interface. The theoretical model was validated with experimental data and the fitting process resulted in good agreement.

  12. Investigation of cathodic current collection in lithium/manganese dioxide cells by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Merritt, D.R.; Schmidt, C.L. [Medtronic, Inc., Minneapolis, MN (United States)

    1994-12-31

    Contact impedance between pressed composite manganese dioxide cathodes and current collectors has been shown to play an important role in the overall impedance of primary Li/MnO{sub 2} cells. Specifically, this impedance is manifested by an arc in the complex-plane impedance plot, representative of a parallel resistive/capacitive combination, This paper presents the results of a systematic series of experiments designed to better define the relationship between cathodic current collector configuration and cell impedance. A refined equivalent circuit model of the Li/MnO{sub 2} cell is also presented.

  13. Electrochemical investigation of surface area effects on PVD Al-Ni as electrocatalyst for alkaline water electrolysis

    DEFF Research Database (Denmark)

    Kjartansdóttir, Cecilía Kristín; Caspersen, Michael; Egelund, Sune Daaskov;

    2014-01-01

    be manipulated by altering the time interval of the diffusion. In that way the actual electrochemical surface area and, thus, the electrocatalytic activity of the coatings towards HER and OER can be influenced. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) investigations, display...

  14. Electrochemical Removal of NOx-Gasses by Use of LSM-Cathodes Impregnated with a NOx Storage Compound

    DEFF Research Database (Denmark)

    Traulsen, Marie Lund; Kammer Hansen, Kent

    2010-01-01

    different atmospheres: 1000 ppm NO, 10% O2 and 1000 ppm NO + 10% O2. Electrochemical impedance spectroscopy and cyclic voltammetry are used for electrochemical characterization of the electrodes, and the conversion of NO and O2 is measured on a mass-spectrometer. The results show a significant increase...

  15. Characterization of group III–nitride nanowires for bio–electrochemical sensors

    OpenAIRE

    Wallys, Jens Matthias Emil

    2014-01-01

    In the present work, the potential of group III–nitride nanowire (NW) ensembles for application as bio–chemical sensors with optical readout was evaluated. The sample analysis was divided into two main parts. At first, an electrochemical analysis with impedance spectroscopy and cyclic voltammetry was conducted. The second part comprises a photoelectrochemical examination by means of photoluminescence spectroscopy at room temperature. In the electrochemical characterization by impedance spe...

  16. Fabrication of TiO2-NTs and TiO2-NTs covered honeycomb lattice and investigation of carrier densities in I-/I3- electrolyte by electrochemical impedance spectroscopy

    Science.gov (United States)

    Baran, Evrim; Yazıcı, Birgül

    2015-12-01

    The TiO2 nanotubes (NTs) were produced by one-step (1S) and two-step (2S) anodization technique. Effects of various anodization potential and times on the growth of TiO2-NTs were investigated by using Field Emission-Scanning Electron Microscopy (FE-SEM). The crystal structure of the electrodes was determined with X-ray powder diffractometry (XRD). The most suitable potential and time for TiO2-NTs obtained by both of anodization methods were found to be 21 V and 4 h. XRD results indicated that 2S anodization technique provided better crystallinity. The electrochemical behaviors of the electrodes in acetonitrile electrolyte contained I-/I3- were examined by utilizing electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV) techniques. Electrochemical results showed that 2S anodization technique increases the carrier densities (ND) value of TiO2-NTs, and flat band potential is shifted by 50 mV to more negative values.

  17. Deposition of selenium thin layers on gold surfaces from sulphuric acid media: Studies using electrochemical quartz crystal microbalance, cyclic voltammetry and AFM

    Energy Technology Data Exchange (ETDEWEB)

    Cabral, Murilo Feitosa [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, C.P. 780, 13566-590 Sao Carlos, SP (Brazil); Pedrosa, Valber A., E-mail: vzp0002@auburn.ed [Department of Materials Engineering, Samuel Ginn College of Engineering, Auburn University, Auburn, AL 36849 (United States); Spinola Machado, Sergio Antonio [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, C.P. 780, 13566-590 Sao Carlos, SP (Brazil)

    2010-01-01

    In this paper we report here new considerations about the relationship between the mass and charge variations (m/z relationship) in underpotential deposition (UPD), bulk deposition and also in the H{sub 2}Se formation reaction. Nanogravimetric experiments were able to show the adsorption of H{sub 2}SeO{sub 3} on the AuO surface prior to the voltammetric sweep and that, after the AuO reduction, 0.40 monolayer of H{sub 2}SeO{sub 3} remains adsorbed on the newly reduced Au surface, which was enough to gives rise to the UPD layer. The UPD results indicate that the maximum coverage with Se{sub ads} on polycrystalline gold surface corresponds to approximately 0.40 monolayer, in good agreement with charge density results. The cyclic voltammetry experiments demonstrated that the amount of bulk Se obtained during the potential scan to approximately 2 Se monolayers, which was further confirmed by electrochemical quartz crystal microbalance (EQCM) measurements that pointed out a mass variation corresponding of 3 monolayers of Se. In addition, the Se thin films were obtained by chronoamperometric experiments, where the Au electrode was polarized at +0.10 V during different times in 1.0 M H{sub 2}SO{sub 4} + 1.0 mM SeO{sub 2}. The topologic aspects of the electrodeposits were observed in Atomic Force Microscope (AFM) measurements. Finally, in highly negative potential polarizations, the H{sub 2}Se formation was analyzed by voltammetric and nanogravimetric measurements. These finding brings a new light on the selenium electrodeposition and point up to a proposed electrochemical model for molecule controlled surface engineering.

  18. Hampering of the Stability of Gold Electrodes by Ferri-/Ferrocyanide Redox Couple Electrolytes during Electrochemical Impedance Spectroscopy.

    Science.gov (United States)

    Lazar, Jaroslav; Schnelting, Christoph; Slavcheva, Evelina; Schnakenberg, Uwe

    2016-01-01

    In the past decades, numerous measurements have applied electrochemical impedance spectroscopy (EIS) in an electrode-electrolyte system consisting of gold electrodes and the redox couple potassium ferrocyanide/potassium ferricyanide (HCF). Yet these measurements are often hampered by false positive and negative results. Electrochemical impedance signals often display a nonlinear drift in electrolyte systems containing the HCF redox couple, which can mask the accuracy of the analysis. Thus, this Article aims to elucidate the stability and reliability of this particular electrode-electrolyte system. Here, different gold electrode cleaning treatments were compared with respect to adsorption and roughness of the surface of gold electrodes. They show substantial nonlinear long-term drifts of the charge-transfer resistance RD. In particular, the use of HCF-containing electrolytes causes adsorption and corrosion on the gold electrode surface, resulting in a nonlinear impedance behavior that depends on the incubation period as well as on electrolyte composition. Consequently, it is strongly recommended not to use HCF containing electrolytes in combination with gold electrodes.

  19. Resolving Losses at the Negative Electrode in All-Vanadium Redox Flow Batteries Using Electrochemical Impedance Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Che Nan [ORNL; Delnick, Frank M [ORNL; Aaron, D [University of Tennessee, Knoxville (UTK); Mench, Matthew M [ORNL; Zawodzinski, Thomas A [ORNL

    2014-01-01

    We present an in situ electrochemical technique for the quantitative measurement and resolution of the ohmic, charge transfer and diffusion overvoltages at the negative electrode of an all-vanadium redox flow battery (VRFB) using electrochemical impedance spectroscopy (EIS). The mathematics describing the complex impedance of the V+2/V+3 redox reaction is derived and matches the experimental data. The voltage losses contributed by each process have been resolved and quantified at various flow rates and electrode thicknesses as a function of current density during anodic and cathodic polarization. The diffusion overvoltage was affected strongly by flow rate while the charge transfer and ohmic losses were invariant. On the other hand, adopting a thicker electrode significantly changed both the charge transfer and diffusion losses due to increased surface area. Furthermore, the Tafel plot obtained from the impedance resolved charge transfer overvoltage yielded the geometric exchange current density, anodic and cathodic Tafel slopes (135 5 and 121 5 mV/decade respectively) and corresponding transfer coefficients = 0.45 0.02 and = 0.50 0.02 in an operating cell.

  20. Origin of Capacity Fading in Nano-Sized Co3O4Electrodes: Electrochemical Impedance Spectroscopy Study

    Directory of Open Access Journals (Sweden)

    Kang Jin-Gu

    2008-01-01

    Full Text Available Abstract Transition metal oxides have been suggested as innovative, high-energy electrode materials for lithium-ion batteries because their electrochemical conversion reactions can transfer two to six electrons. However, nano-sized transition metal oxides, especially Co3O4, exhibit drastic capacity decay during discharge/charge cycling, which hinders their practical use in lithium-ion batteries. Herein, we prepared nano-sized Co3O4with high crystallinity using a simple citrate-gel method and used electrochemical impedance spectroscopy method to examine the origin for the drastic capacity fading observed in the nano-sized Co3O4anode system. During cycling, AC impedance responses were collected at the first discharged state and at every subsequent tenth discharged state until the 100th cycle. By examining the separable relaxation time of each electrochemical reaction and the goodness-of-fit results, a direct relation between the charge transfer process and cycling performance was clearly observed.

  1. Electrochemical impedance spectroscopy of supercapacitors: A novel analysis approach using evolutionary programming

    Science.gov (United States)

    Oz, Alon; Hershkovitz, Shany; Tsur, Yoed

    2014-11-01

    In this contribution we present a novel approach to analyze impedance spectroscopy measurements of supercapacitors. Transforming the impedance data into frequency-dependent capacitance allows us to use Impedance Spectroscopy Genetic Programming (ISGP) in order to find the distribution function of relaxation times (DFRT) of the processes taking place in the tested device. Synthetic data was generated in order to demonstrate this technique and a model for supercapacitor ageing process has been obtained.

  2. Simultaneous Measurement of Nonlinearity and Electrochemical Impedance for Protein Sensing Using Two-Tone Excitation

    Science.gov (United States)

    Daniels, Jonathan S.; Anderson, Erik P.; Lee, Thomas H.; Pourmand, Nader

    2009-01-01

    Impedance biosensors detect the binding of a target to an immobilized probe by quantifying changes in the impedance of the electrode-electrolyte interface. The interface's I-V relationship is inherently nonlinear, varying with DC bias, and target binding can alter the degree of nonlinearity. We propose and demonstrate a method to simultaneously measure the nonlinearity and conventional small-signal impedance using intermodulation products from a two-tone input. Intermodulation amplitudes accurately reflect the impedance's manually-measured voltage dependence. We demonstrate that changes in nonlinearity can discriminate protein binding. Our measurements suggest that target binding can alter nonlinearity via the voltage dependence of the ionic double layer. PMID:19164024

  3. Electrochemical Study on Corrosion Inhibition of Copper in Hydrochloric Acid Medium and the Rotating Ring-Disc Voltammetry for Studying the Dissolution

    Directory of Open Access Journals (Sweden)

    A. K. Satpati

    2011-01-01

    Full Text Available Dissolution characteristics of copper in hydrochloric acid medium and the effect of 4-amino 1,2,4-triazole (ATA on the corrosion process have been studied using conventional electrochemical techniques and rotating ring-disc electrodes (RRDEs. Corrosion potential (corr and corrosion current density (corr were obtained by Tafel extrapolation methods. Charge transfer resistance (ct and double-layer capacitance (dl were obtained from the electrochemical impedance spectroscopy (EIS. ATA was shown to be an effective inhibitor for the copper-corrosion inhibition in acid medium. The corrosion rate was retarded in presence of inhibitors mainly because of the adsorption of the inhibitor on the electrode surface. Adsorption of the inhibitor on the metal surface was found to follow the Langmuir adsorption isotherm. Standard free energy change of the adsorption process (Δ0ad was calculated to be −54.3 kJ mol−1; such a large negative value of Δ0ad suggests the prescence of a chemisorption process.

  4. Investigation on the origin of diffusion impedance in the porous cathode of a proton exchange membrane fuel cell (PEMFC) via electrochemical impedance spectroscopy (EIS)

    Energy Technology Data Exchange (ETDEWEB)

    Mainka, J.; Maranzana, G.; Dillet, J.; Didierjean, S.; Lottin, O. [Nancy Univ., Centre national de la recherche scientifique, Vandoeuvre les Nancy (France). Laboratoire d' Energetique et de Mecanique Theorique et Appliquee

    2009-07-01

    This study provided a preliminary examination of the impact of gas flow rate on the impedance characteristics of a proton exchange membrane fuel cell (PEMFC). The mass transport phenomena within the porous cathode of PEMFCs can be analyzed through electrochemical impedance spectroscopy (EIS). The geometrical description of the electrodes chosen to complete the EIS interpretations is a form of the agglomerate model, where the agglomerates are a mixture of carbon powder and catalyst particles, whereas the electrolyte is assumed to cover only the pore surfaces. Therefore, the reactants access the active catalyst sites by passing successively through the gas diffusion layer (GDL), the pores of the electrode, and finally through a thin electrolyte layer. The fuel cell equivalent electrical circuit is based on a Butler-Volmer formalism that takes into consideration oxygen diffusion in the pores of the GDL and/or the active layer through a Warburg element. The results reveal that in the cathode, the mass transfer limiting layer is most likely the active layer, provided liquid water is present within the pores. Under normal operating conditions, the mass transport resistance of the gas diffusion layer is negligible, as is the fine electrolyte layer coating the agglomerate.

  5. Electrochemical Impedance Spectroscopic Measurements of Sexithiophene-Effect of the Electrode Nature and the Dopant (CuCl2) Content

    Institute of Scientific and Technical Information of China (English)

    NESSARK,Belkacem; MAOUCHE,Na(i)ma

    2009-01-01

    Electrochemical impedance spectroscopic (EIS) measurements of sexithiophene (6T) were carried out according to the Pt/6T/M sandwich structure configuration,for various electrode materials (M=GC,ITO,Ag,Cu,AI) and for different doping levels of copper chloride (CuCl2).The results demonstrate that two types of charge transport are involved in the redox process at the electrode/6T interface and inside the bulk oligomer.The complex-plane impedance plots obtained for various doping levels of CuCl2 exhibit arc shapes.The charge-transfer resistance measured from the diagrams decreases systematically with the addition of the salt,leading to an increase of the oligothiophene conductivity.

  6. A study of steel bar reinforcement corrosion in concretes with SF and SRH using electrochemical impedance spectroscopy

    Directory of Open Access Journals (Sweden)

    Fernanda Giannotti da Silva

    2006-06-01

    Full Text Available Several electrochemical techniques can be used to monitor corrosion, among them are open circuit potential (OCP and eletrochemical impedance spectroscopy (EIS. Monitoring OCP is the most typical procedure for routine inspection of reinforced concrete structures and can be easily carried out, however it only gives an approximate idea of the corrosion process. EIS is a more complete technique, which supplies information regarding the mechanism and kinetics of reaction electrochemistries, but only used in the laboratory. Based on these two techniques, this study is related to the steel corrosion in high-performance concrete with silica fume and silica from rice husk. The acceleration of the corrosion was carried out using immersion cycles in a 3.5% NaCl solution. As well as high compressive strength values, the addition of silica fume presented low corrosion risks and high impedance module values and significant increases of the concrete resistivity after 22 months of alternate immersion/drying cycles were obtained.

  7. Analysis of dye-sensitized solar cells with current collecting electrodes using electrochemical impedance spectroscopy, with a finite element method

    Science.gov (United States)

    Shitanda, Isao; Inoue, Kazuya; Hoshi, Yoshinao; Itagaki, Masayuki

    2014-02-01

    The internal resistances of dye-sensitized solar cells (DSCs) with and without current collecting electrodes (CCEs) were analyzed using electrochemical impedance spectroscopy (EIS) with a finite element method (FEM). Three different DSC models with or without current collecting electrodes were designed. Theoretical values of the internal resistance were estimated by FEM on changing the position and size of the current collecting electrodes. Large DSCs with current collecting electrodes were fabricated using a screen-printing technique, and experimental values of the internal resistance were analyzed by EIS and compared with the theoretical values. The internal resistances obtained from the impedance measurements were in good agreement with those obtained by simulation. The internal resistance was found to decrease with increasing width and thickness of the CCEs, below a threshold value. EIS was found to be extremely useful for evaluating CCE design for improved DSCs.

  8. Effect of sintering temperature on the microstructure, roughness and electrochemical impedance of electrophoretically deposited YSZ electrolyte for SOFCs

    Energy Technology Data Exchange (ETDEWEB)

    Talebi, Tahereh; Haji, Mohsen; Raissi, Babak [Materials and Energy Research Center, P. Box 14155-4777, Karaj, Tehran (Iran)

    2010-09-15

    In the present work, the microstructures of YSZ electrolyte films, which were sintered at various temperatures in the range of 1300-1600 C, were investigated. First, a suitable and uniform film was deposited on the surface of NiO-YSZ composite by EPD. After the consequence sintering, the surfaces of deposited YSZ films were observed by SEM. In addition, other characteristics of the YSZ electrolyte films such as surface roughness and morphology of the sintered films were investigated by AFM. The ability of ionic transfer and permeability of the YSZ electrolyte was examined by electrochemical impedance spectroscopy at different temperatures. It seems that the YSZ electrolyte sintered at 1400 C was appropriate for SOFCs applications, because this film had the minimum impedance, minimum roughness and the maximum conductivity. Furthermore, the temperature of 1400 C was the minimum temperature in which a dense film of YSZ was formed uniformly on the surface of anode and coated it completely. (author)

  9. Comparative Study by Electrochemical Impedance Spectroscopy (EIS On The Corrosion Resistance of Industrial and Laboratory Zinc Coatings

    Directory of Open Access Journals (Sweden)

    Y. Hamlaoui

    2007-01-01

    Full Text Available In this work, corrosion monitoring of Zn-based coatings is investigated through potentiodynamic and electrochemical impedance spectroscopy (EIS methods. The first part of the study is devoted to galvanised coatings conventionally manufactured in the industry. The second part focuses on the corrosion resistance of a laboratory-made electrolytic coating. For such purpose, the corrosion behaviour is studied in NaCl media under various conditions. The results show that EIS allows to establish the interfacial reactions and the dissolution mechanisms occurring in this media, hence to foresee the protection conferred by these coatings. Moreover, the salted media at different concentrations allow to unambiguously assess the coating quality in terms of porosity. However, others corrosive media can reveal the slowest reaction without having appeal to a very low frenquency scanning. Finally, Zn/NaCl interface is characterised by a specific equivalent circuit giving a similar impedance response.

  10. Exfoliation corrosion of Al-Zn-Mg-Cu-Zr alloy containing Sc examined by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Y.P.; Liu, X.Y.; He, Y.B.; Li, C.L. [School of Materials Science and Engineering, Central South University, Changsha (China); Pan, Q.L. [School of Materials Science and Engineering, Central South University, Changsha (China); The Key Laboratory of Nonferrous Materials Science and Engineering of Ministry of Education, Changsha (China); Li, W.B. [School of Materials Science and Engineering, Central South University, Changsha (China); School of Civil Engineering, Hunan City University, Yiyang (China)

    2012-02-15

    The exfoliation corrosion behavior of an Al-Zn-Mg-Cu-Zr alloy containing Sc artificially aged at 120 C for 24 h is studied by macroscopic observation techniques and electrochemical impedance spectroscopy (EIS) measurements. After 48 h immersion, the blisters start bursting and delamination initiates, along with the appearance of two time constants in the impedance diagrams. According to the simulation by equivalent circuit, the corrosion rate decreases sharply and then reaches a steady state, which is due to the change of the solution pH and oxide layer thickness, as well as the accumulation of corrosion products. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  11. Development of a method to estimate the lifespan of proton exchange membrane fuel cell using electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Ju-hyung; Lee, Jong-Hak; Choi, Woojin [Department of Electrical Engineering, Soongsil University, 1-1 Sangdo-dong, Dongjak-gu, Seoul 156-743 (Korea); Park, Kyung-Won [Department of Chemical/Environmental Engineering, Soongsil University, 1-1 Sangdo-dong, Dongjak-gu, Seoul 156-743 (Korea); Sun, Hee-Young [Samsung Advanced Institute of Technology, Mt. 14-1, Nongseo-dong, Giheung-gu, Yongin-si, Gyeonggi-do 446-712 (Korea); Oh, Jae-Hyuk [Samsung Electronics, 416 Maetan-dong, Youngtong-gu, Suwon-si, Gyeonggi-do 443-370 (Korea)

    2010-09-15

    This paper proposes a new method for estimating the state and lifespan of fuel cells in operation by fuel cell equivalent impedance modeling by electrochemical impedance spectroscopy (EIS) and observing degradation. The performance change of fuel cells takes place in the form of changes in each parameter value comprising an equivalent AC impedance circuit; monitoring such changes allows for the prediction of the state and lifespan of a fuel cell. In the experiments, the AC impedance of high-temperature proton exchange membrane (PEM) fuel cells was measured at constant time intervals during their continuous operation for over 2200 h. The expression for the lifespan of a fuel cell was deduced by curve fitting the changes in each parameter to a polynomial. Electric double layer capacitance and charge transfer resistance, which show the reduction reaction of the cathode, were used as major parameters for judging the degradation; a method of using time constants is proposed to more accurately estimate the degree of degradation. In addition, an algorithm that can evaluate the soundness and lifespan of a fuel cell is proposed; it compares the measured time constant of the fuel cell being tested with that of average lifespan fuel cell. (author)

  12. Cyclic Voltammetry.

    Science.gov (United States)

    Evans, Dennis H.; And Others

    1983-01-01

    Cyclic voltammetry is a simple experiment that has become popular in chemical research because it can provide useful information about redox reactions in a form which is easily obtained and interpreted. Discusses principles of the method and illustrates its use in the study of four electrode reactions. (Author/JN)

  13. Cyclic Voltammetry.

    Science.gov (United States)

    Evans, Dennis H.; And Others

    1983-01-01

    Cyclic voltammetry is a simple experiment that has become popular in chemical research because it can provide useful information about redox reactions in a form which is easily obtained and interpreted. Discusses principles of the method and illustrates its use in the study of four electrode reactions. (Author/JN)

  14. Electrochemical surface modification technique to impede mild steel corrosion using perfluorooctanoic acid

    Directory of Open Access Journals (Sweden)

    Shubha H Natarj

    2016-02-01

    Full Text Available The present work demonstrated that corrosion inhibition efficiency of electrochemically generated organic coat is remarkably effective than self-assembled monolayer (SAM generated by dip coating technique. Perfluorooctanoic Acid (PFOA is used to modify mild steel surface for effective protection. Infrared reflection absorption spectroscopy and contact angle measurements substantiate the modification of mild steel surface and its effect on surface hydrophobicity. A comparison between electrochemical properties of PFOA SAM generated by dip coat method (DC-PFOA and PFOA coat generated by electrochemical method (EC-PFOA is presented. Electrochemical measurements reveal that the corrosion protection efficiency of EC-PFOA (91% is much superior to DC-PFOA (28%.

  15. The platinum microelectrode/Nafion interface - An electrochemical impedance spectroscopic analysis of oxygen reduction kinetics and Nafion characteristics

    Science.gov (United States)

    Parthasarathy, Arvind; Dave, Bhasker; Srinivasan, Supramaniam; Appleby, John A.; Martin, Charles R.

    1992-01-01

    The objectives of this study were to use electrochemical impedance spectroscopy (EIS) to study the oxygen-reduction reaction under lower humidification conditions than previously studied. The EIS technique permits the discrimination of electrode kinetics of oxygen reduction, mass transport of O2 in the membrane, and the electrical characteristics of the membrane. Electrode-kinetic parameters for the oxygen-reduction reaction, corrosion current densities for Pt, and double-layer capacitances were calculated. The production of water due to electrochemical reduction of oxygen greatly influenced the EIS response and the electrode kinetics at the Pt/Nafion interface. From the finite-length Warburg behavior, a measure of the diffusion coefficient of oxygen in Nafion and diffusion-layer thickness was obtained. An analysis of the EIS data in the high-frequency domain yielded membrane and interfacial characteristics such as ionic conductivity of the membrane, membrane grain-boundary capacitance and resistance, and uncompensated resistance.

  16. In situ monitoring of discharge/charge processes in Li-O2 batteries by electrochemical impedance spectroscopy

    Science.gov (United States)

    Landa-Medrano, Imanol; Ruiz de Larramendi, Idoia; Ortiz-Vitoriano, Nagore; Pinedo, Ricardo; Ignacio Ruiz de Larramendi, José; Rojo, Teófilo

    2014-03-01

    Gaining insight into the reaction mechanisms underway during charge and discharge in Li-air batteries is essential to allow the target development of improved power and performance devices. This work reports the in situ monitoring of Li-air cells by electrochemical impedance spectroscopy and, for the first time, the development of an electrochemical model allowing the identification and attribution of the processes involved. The voltage at which each reaction product forms has been identified, including Li2O2 or Li2CO3 during discharge, together with the delithiation of the outer part of Li2O2 and oxidation reactions and electrolyte decomposition. The developed model can be used as a valuable tool for the optimisation of composition and structure of the air electrode through the investigation of the resistance associated with each process.

  17. Influence of the compaction pressure on the electrochemical impedance spectroscopy response of the AB{sub 5}-type electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, J.E.; Castro, E.B.; Visintin, A. [Instituto de Investigaciones Fisicoquimicas Teoricas y Aplicadas (INIFTA), Facultad de Ciencias Exactas, UNLP, CCT La Plata-CONICET, CC 16, Suc. 4 (1900) La Plata (Argentina)

    2010-06-15

    AB5-type alloys are commercially used in electrodes for rechargeable batteries due to their high capacity, good kinetics for the hydriding/dehydriding reactions and long useful life (cycling resistance). The aim of this work is to study, using electrochemical impedance spectroscopy, the influence of the preparation compaction pressure, on the performance of the electrode. The results show the effect of increasing compaction pressure on the interfacial and active areas, and on the reduction of the contact resistance between particles. In this study a pressure range for optimal electrode behavior is determined. These results agree with behavior predicted by the proposed physicochemical model and with experimental results reported in previous works, using others electrochemical techniques. (author)

  18. Electrochemical impedance spectroscopy and corrosion behaviour of Al{sub 2}O{sub 3}-Ni nano composite coatings

    Energy Technology Data Exchange (ETDEWEB)

    Ciubotariu, Alina-Crina [Dunarea de Jos, University of Galati, Metallurgy and Materials Science Faculty, Competences Center Interfaces-Tribocorrosion-Electrochemical Systems, CC-ITES, 47 Domneasca Street, 80008 Galati (Romania)], E-mail: Alina.Ciubotariu@ugal.ro; Benea, Lidia [Dunarea de Jos, University of Galati, Metallurgy and Materials Science Faculty, Competences Center Interfaces-Tribocorrosion-Electrochemical Systems, CC-ITES, 47 Domneasca Street, 80008 Galati (Romania); Lakatos-Varsanyi, Magda [Bay Zoltan Foundation, Institute for Materials Science and Technology, Budapest H-1116 (Hungary); Dragan, Viorel [Dunarea de Jos, University of Galati, Metallurgy and Materials Science Faculty, Competences Center Interfaces-Tribocorrosion-Electrochemical Systems, CC-ITES, 47 Domneasca Street, 80008 Galati (Romania)

    2008-05-20

    In this paper, the results on the electrochemical impedance spectroscopy and corrosion properties of electrodeposited nanostructured Al{sub 2}O{sub 3}-Ni composite coatings are presented. The nanocomposite coatings were obtained by codeposition of alumina nanoparticles (13 nm) with nickel during plating process. The coating thickness was 50 {mu}m on steel support and an average of nano Al{sub 2}O{sub 3} particles inside of coatings at 15 vol.% was present. The structure of the coatings was investigated by scanning electron microscopy (SEM). It has been found that the codeposition of Al{sub 2}O{sub 3} particles with nickel disturbs the nickel coating's regular surface structure. The electrochemical behavior of the coatings in the corrosive solutions was investigated by polarization potentiodynamic and electrochemical impedance spectroscopy methods. As electrochemical test solutions 0.5 M sodium chloride and 0.5 M potassium sulphate were used in a three electrode open cell. The corrosion potential is shifted to more negative values for nanostructured coatings in 0.5 M sodium chloride. The polarization resistance in 0.5 M sodium chloride decreases in 24 h, but after that increases slowly. In 0.5 M potassium sulphate solution the polarization resistance decreases after 2 h and after 30 h of immersion the polarization resistance is higher than that of the beginning value. The corrosion rate calculated by polarization potentiodynamic curves obtained after 30 min from immersion in solution is smaller for nanostructured coatings in 0.5 M potassium sulphate (4.74 {mu}m/year) and a little bit bigger in 0.5 M sodium chloride (5.03 {mu}m/year)

  19. Electrochemical impedance studies of methanol oxidation on GC/Ni and GC/NiCu electrode

    Energy Technology Data Exchange (ETDEWEB)

    Danaee, I.; Jafarian, M.; Forouzandeh, F.; Mahjani, M.G. [Department of Chemistry, K.N. Toosi University of Technology, PO Box 15875-4416, Tehran (Iran); Gobal, F. [Department of Chemistry, Sharif University of Technology, PO Box 11365-9516, Tehran (Iran)

    2009-01-15

    The electro-oxidation of methanol on nickel and nickel-copper alloy modified glassy carbon electrodes (GC/Ni and GC/NiCu) in a 1 M NaOH solution at different concentrations of methanol was studied by the method of ac-impedance spectroscopy. Two semicircles in the first quadrant of a Nyquist diagram were observed for electro-oxidation of methanol on GC/Ni corresponding to charge transfer resistance and adsorption of intermediates. Electro-oxidation of methanol on GC/NiCu shows negative resistance in impedance plots as signified by semi-circles terminating in the second quadrant. The impedance behavior shows different patterns at different applied anodic potential. The influence of the electrode potential on impedance pattern is studied and a mathematical model was put forward to quantitatively account for the impedance behavior of methanol oxidation. At potentials higher than 0.49 V vs. Ag/AgCl, a pseudoinductive behavior is observed but at higher than 0.58 V, impedance patterns terminate in the second quadrant. The conditions required for this behavior are delineated with the use of the impedance model. (author)

  20. Degradation of all-vanadium redox flow batteries (VRFB) investigated by electrochemical impedance and X-ray photoelectron spectroscopy: Part 2 electrochemical degradation

    Science.gov (United States)

    Derr, Igor; Bruns, Michael; Langner, Joachim; Fetyan, Abdulmonem; Melke, Julia; Roth, Christina

    2016-09-01

    Electrochemical degradation (ED) of carbon felt electrodes was investigated by cycling of a flow through all-vanadium redox flow battery (VRFB) and conducting half-cell measurements with two reference electrodes inside the test bench. ED was detected using half-cell and full-cell electrochemical impedance spectroscopy (EIS) at different states of charge (SOC). Reversing the polarity of the battery to recover cell performance was performed with little success. Renewing the electrolyte after a certain amount of cycles restored the capacity of the battery. X-ray photoelectron spectroscopy (XPS) reveals that the amount of surface functional increases by more than a factor of 3 for the negative side as well as for the positive side. Scanning electron microscope (SEM) images show a peeling of the fiber surface after cycling the felts, which leads to a loss of electrochemically active surface area (ECSA). Long term cycling shows that ED has a stronger impact on the negative half-cell [V(II)/V(III)] than the positive half-cell [V(IV)/V(V)] and that the negative half-cell is the rate-determining half-cell for the VRFB.

  1. The Electrochemical Investigation of MEH-PPV in Ionic Liquid

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The electrochemical properties of MEH-PPV were studied in ionic liquid ( [bmim]+[PF6]- ) by cyclic voltammetry, chronoamperometry and AC impedance measurements.Both p- and n-doping of MEH-PPV were observed in the cyclic voltammograms.The chronoamperometric and AC impedance results indicate that the p-doping of MEH-PPV was controlled by the linear diffusion of counterions.

  2. Green-synthesized gold nanoparticles decorated graphene sheets for label-free electrochemical impedance DNA hybridization biosensing.

    Science.gov (United States)

    Hu, Yuwei; Hua, Shucheng; Li, Fenghua; Jiang, Yuanyuan; Bai, Xiaoxue; Li, Dan; Niu, Li

    2011-07-15

    Sensitive electrochemical impedance assay of DNA hybridization by using a novel graphene sheets platform was achieved. The graphene sheets were firstly functionalized with 3,4,9,10-perylene tetracarboxylic acid (PTCA). PTCA molecules separated graphene sheets efficiently and introduced more negatively-charged -COOH sites, both of which were beneficial to the decoration of graphene with gold nanoparticles. Then amine-terminated ionic liquid (NH₂-IL) was applied to the reduction of HAuCl₄ to gold nanoparticles. The green-synthesized gold nanoparticles, with the mean diameter of 3 nm, dispersed uniformly on graphene sheets and its outer layer was positively charged imidazole termini. Due to the presence of large graphene sheets and NH₂-IL protected gold nanoparticles, DNA probes could be immobilized via electrostatic interaction and adsorption effect. Electrochemical impedance value increased after DNA probes immobilization and hybridization, which was adopted as the signal for label-free DNA hybridization detection. Unlike previously anchoring DNA to gold nanoparticles, this label-free method was simple and noninvasive. The conserved sequence of the pol gene of human immunodeficiency virus 1 was satisfactorily detected via this strategy.

  3. Improved electrochemical performances of polyaniline nanotubes-poly-L-lysine composite for label-free impedance detection of DNA hybridization

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    A sensitive label-free DNA hybridization biosensing platform was fabricated based on the synergistic effect of polyaniline nanotubes (PANInt) and poly-L-lysine (pLys).The composite of pLys and PANInt was coated onto the carbon paste electrode (CPE) to form a uniform and very stable nanocomposite membrane.The pLys in the composite film not only acts as a membrane to retain good electron transfer capability of PANInt even at physiological pH,but also possesses fine biocompatibility for bio-analytes.DNA probes with negatively charged phosphate groups were readily linked to the positively charged pLys surface due to the strong electrostatic affinity.The synergistic effect of PANInt and pLys could significantly enhance the sensitivity of DNA hybridization recognition.The phosphinothricin acetyltransferase (PAT) gene fragment from transgenic corn and the polymerase chain reaction amplification of the terminator of nopaline synthase gene from the real sample of a kind of transgenic soybean were detected by this DNA electrochemical biosensor via label-free impedance method.This stable composite gives convenient permselectivity properties as a transducer material for the design of modern electrochemical impedance biosensor using [Fe(CN)6]3-/4as an indicator.

  4. Label-free electrochemical impedance biosensor to detect human interleukin-8 in serum with sub-pg/ml sensitivity.

    Science.gov (United States)

    Sharma, R; Deacon, S E; Nowak, D; George, S E; Szymonik, M P; Tang, A A S; Tomlinson, D C; Davies, A G; McPherson, M J; Wälti, C

    2016-06-15

    Biosensors with high sensitivity and short time-to-result that are capable of detecting biomarkers in body fluids such as serum are an important prerequisite for early diagnostics in modern healthcare provision. Here, we report the development of an electrochemical impedance-based sensor for the detection in serum of human interleukin-8 (IL-8), a pro-angiogenic chemokine implicated in a wide range of inflammatory diseases. The sensor employs a small and robust synthetic non-antibody capture protein based on a cystatin scaffold that displays high affinity for human IL-8 with a KD of 35 ± 10 nM and excellent ligand specificity. The change in the phase of the electrochemical impedance from the serum baseline, ∆θ(ƒ), measured at 0.1 Hz, was used as the measure for quantifying IL-8 concentration in the fluid. Optimal sensor signal was observed after 15 min incubation, and the sensor exhibited a linear response versus logarithm of IL-8 concentration from 900 fg/ml to 900 ng/ml. A detection limit of around 90 fg/ml, which is significantly lower than the basal clinical levels of 5-10 pg/ml, was observed. Our results are significant for the development of point-of-care and early diagnostics where high sensitivity and short time-to-results are essential.

  5. Electrochemical impedance analysis of nanoporous TiO2 electrode at low bias potential

    Institute of Scientific and Technical Information of China (English)

    Sheng Jun Li; Yuan Lin; Zeng Chen; Jing Bo Zhang; Xiao Wen Zhou

    2010-01-01

    TiO2 colloid was prepared by the sol-gel method and was bladed on transparent conduction glass to made nanoporous electrode.The impedance performance of TiO2 electrode was studied at various bias potential.A simplified equivalent circuit was proposed to investigate the charge transport impedance of TiO2 film and good fitting results were obtained.

  6. Electrochemical and spectroscopic characterization of poly (bithiophene + 2-methylfuran) copolymer

    Science.gov (United States)

    Lamiri, Leila; Nessark, Belkacem; Habelhames, Farid; Sibous, Lakhdar

    2017-09-01

    In this work, Poly(bithiophene + 2-methylfuran) copolymer was successfully synthetized by an electrochemical polymerization of two monomers, bithiophene and 2-methylfuran in acetonitrile containing lithium perchlorate. The obtained copolymer was characterized via cyclic voltammetry, impedance spectroscopy, UV-visible, scanning electron microscope, conductivity and photocurrent measurements. The cyclic voltammetry study showed two redox couples characteristic of Poly (bithiophene + 2-methylfuran) copolymer. The impedance spectroscopy study revealed that the resistance of the copolymer film increases with the addition of 2-methylfuran. The photocurrent measurement showed good photoelectrochemical properties, making this copolymer an ideal candidate for photovoltaic cell applications.

  7. Electrochemical impedance based chiral analysis of anti-ascorbutic drug: l-Ascorbic acid and d-ascorbic acid using C-dots decorated conductive polymer nano-composite electrode.

    Science.gov (United States)

    Pandey, Indu; Kant, Rama

    2016-03-15

    Clinical manifestations owing to l-ascorbic acid for scurvy as comparison to d-ascorbic acid and challenges of chiral purity are overcome by using chiral selective conductive polymer nanocomposite which mimics antibodies and enzymes. A novel chiral selective imprinted polyaniline-ferrocene-sulfonic acid film has been electrochemically fabricated on C-dots modified pencil graphite electrode. The performance of the obtained l-ascorbic acid or d-ascorbic acid chiral selective sensor was investigated by electrochemical impedance spectroscopy, cyclic and differential pulse voltammetry. The surface characteristics of the C-dots, chiral sensor before and after the de-doping of chiral d- and l-ascorbic acid were characterized by scanning electron microscopy, Raman spectroscopy and X-ray diffraction spectroscopy. Excellent recognition results were obtained by difference in electron transfer resistance. The proposed chiral sensor is capable of measuring d-ascorbic acid or l-ascorbic acid in aqueous as well as in real and commercial samples within the range of 0.020-0.187 nM and 0.003-0.232 nM with detection limit of 0.00073 nM and 0.00016 nM, respectively. The proposed method has also been examined for the chiral selective recognition of ascorbic acid isomers (d- and l-) quantitatively, in complicated matrices of real samples.

  8. Electrochemical determination of the diffusion coefficient of cations into Chevrel phase-based electrochemical transfer junction by potential step chronoamperometry and impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Seghir, S.; Stein, N. [Institut Jean Lamour - Electrochimie des Materiaux, Nancy-Universite, Universite Paul Verlaine Metz, CNRS, 1 Bd. Arago, F-57078 Metz (France); Boulanger, C., E-mail: clotilde.boulanger@univ-metz.f [Institut Jean Lamour - Electrochimie des Materiaux, Nancy-Universite, Universite Paul Verlaine Metz, CNRS, 1 Bd. Arago, F-57078 Metz (France); Lecuire, J.-M. [Institut Jean Lamour - Electrochimie des Materiaux, Nancy-Universite, Universite Paul Verlaine Metz, CNRS, 1 Bd. Arago, F-57078 Metz (France)

    2011-02-15

    The molybdenum chalcogenides Mo{sub 6}X{sub 8} (X = S, Se) offer the possibility of intercalation/de-intercalation processes by chemical or electrochemical way. Besides the different applications of so-called Chevrel phases, we have proposed an electrochemical transfer junction for selective recovery of metallic cations in the perspective of recycling of industrial liquid mineral wastes. Thus, the knowledge of the diffusion properties of cations in the Chevrel phases is essential. Here we report on the electrochemical determination of diffusion coefficients of Co{sup 2+}, Ni{sup 2+}, Fe{sup 2+}, Cd{sup 2+}, Zn{sup 2+}, Mn{sup 2+} and Cu{sup 2+} for Mo{sub 6}S{sub 8} and Mo{sub 6}Se{sub 8} matrices. Experiments were realized on samples with compactness of 50% and 96-98%. They point out that the lower compactness is unfavorable to the mobility of the cobalt ions. From potential step chronoamperometry and electrochemical impedance spectroscopy, the diffusion coefficients were found around 10{sup -9} cm{sup 2} s{sup -1}, even 10{sup -6} cm{sup 2} s{sup -1} for copper. These results confirm the high mobility of transition metal ions in studied phases and complete the data for Co, Fe or Mn-Mo{sub 6}S{sub 8} system and Mn-Mo{sub 6}Se{sub 8} system. For the sulfide phase, the following sequence for D-tilde is observed Ni < Co < Fe < Cd < Zn < Mn << Cu and can be explained in regards with structural considerations and repulsion effects for copper.

  9. A kinetic study of electrochemical lithium insertion in nanosized rutile {beta}-MnO{sub 2} by impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Bach, S., E-mail: bach@glvt-cnrs.fr [Institut de Chimie et des Materiaux Paris Est, GESMAT, UMR 7182 CNRS-Universite Paris XII, 2 rue Henri Dunant 94320 Thiais (France); Universite d' Evry Val d' Essonne, Bd F.Mitterrand, Departement Chimie, 91025 Evry Cedex (France); Pereira-Ramos, J.P. [Institut de Chimie et des Materiaux Paris Est, GESMAT, UMR 7182 CNRS-Universite Paris XII, 2 rue Henri Dunant 94320 Thiais (France); Willmann, P. [Centre National d' Etudes Spatiales, 118 avenue Edouard Belin, 31401 Toulouse Cedex 9 (France)

    2011-11-30

    The kinetics of the electrochemical lithium insertion reaction in nano-sized rutile {beta}-MnO{sub 2} has been investigated using ac impedance spectroscopy. The experimental kinetic data are obtained for a rutile compound synthesized by ball-milling the powder produced from the heat treatment of manganese nitrate salts. The results are discussed as a function of the Li content for 0 < x < 0.6 and the number of cycles in the 4.1-2 V window. From a comparison with data obtained on the micro-sized oxide, an improved kinetics is found with D{sub Li} values for the apparent chemical diffusion coefficient of lithium much higher by one order of magnitude than in microsized oxide. Impedance behaviour of the ball-milled rutile {beta}-MnO{sub 2}vs cycles demonstrates a new system takes place from the second cycle, characterized by a significant improvement of Li diffusion by a factor 5 and a cathode impedance which decreases by a factor 2, remaining thereafter unchanged during cycling.

  10. Characterization of implant materials in fetal bovine serum and sodium sulfate by electrochemical impedance spectroscopy. II. Coarsely sandblasted samples.

    Science.gov (United States)

    Contu, F; Elsener, B; Böhni, H

    2003-10-01

    Electrochemical impedance spectroscopy is used to investigate the corrosion resistance of coarsely sandblasted implant alloys, commercially pure titanium, Ti6Al4V, Ti6Al7Nb, and CoCrMo in 0.1M sodium sulfate and fetal bovine serum. Coarsely sandblasted samples have a heterogeneous surface constituted by a large number of protrusions and recessions. Impedance spectra collected in sodium sulfate present two time constants (maxima in the phase-angle of the bode plot) associated with the total surface and with the tips, respectively. In bovine serum, the two maxima in the impedance spectra cannot be distinguished because of the formation of an adsorption layer of organic molecules, which causes a decrease in the values of both the total and tips' capacitances as well as an increase in the polarization resistance. Ti6Al4V and Ti6Al7Nb show the highest corrosion rate both in serum and in sodium sulfate. Based on the capacitance values obtained in sodium sulfate, the real surface area of the coarsely sandblasted electrodes has been estimated relative to mechanically polished surfaces. The values of the effective electrode area correlate with the mechanical properties of the samples: in fact, the softest electrode (commercially pure titanium) shows the largest effective electrode area, whereas the hardest material (CoCrMo alloy) shows the smallest surface area.

  11. Stretchable Electrochemical Impedance Sensors for Intravascular Detection of Lipid-Rich Lesions in New Zealand White Rabbits

    Science.gov (United States)

    Cao, Hung; Yu, Fei; Zhao, Yu; Scianmarello, Nick; Lee, Juhyun; Dai, Wangde; Jen, Nelson; Beebe, Tyler; Li, Rongsong; Ebrahimi, Ramin; Chang, Donald S.; Mody, Freny V.; Pacella, John; Tai, Yu-Chong; Hsiai, Tzung

    2014-01-01

    Flexible electronics have enabled catheter-based intravascular sensing. However, real-time interrogation of unstable plaque remains an unmet clinical challenge. Here, we demonstrate the feasibility of stretchable electrochemical impedance spectroscopy (EIS) sensors for endoluminal investigations in New Zealand White (NZW) rabbits on diet-induced hyperlipidemia. A parylene C (PAC)-based EIS sensor mounted on the surface of an inflatable silicone balloon affixed to the tip of an interrogating catheter was deployed 1) on the explants of NZW rabbit aorta for detection of lipid-rich atherosclerotic lesions, and 2) on live animals for demonstration of balloon inflation and EIS measurements. An input peak-to-peak AC voltage of 10 mV and sweeping-frequency from 300 kHz to 100 Hz were delivered to the endoluminal sites. Balloon inflation allowed EIS sensors to be in contact with endoluminal surface. In the oxidized low-density-lipoprotein (oxLDL)-rich lesions from explants of fat-fed rabbits, impedance magnitude increased significantly by 1.5-fold across the entire frequency band, and phase shifted ~5 degrees at frequencies below 10 kHz. In the lesion-free sites of the normal diet-fed rabbits, impedance magnitude increased by 1.2-fold and phase shifted ~5 degrees at frequencies above 30 kHz. Thus, we demonstrate the feasibility of stretchable intravascular EIS sensors for identification of lipid rich lesions, with a translational implication for detecting unstable lesions. PMID:24333932

  12. Effect of sulphate-reducing bacteria on the electrochemical impedance spectroscopy characteristics of 1Cr18Ni9Ti

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The electrochemical characteristics of 1Cr18Ni9Ti in sulphate-reducing bacteria (SRB) solutions and the biofilm of SRB on the surface of the 1Cr18Ni9Ti electrode were studied by electrochemical, microbiological, and surface analysis methods. Electrochemical impedance spectroscopy (EIS) of 1Cr18Ni9Ti was measured in the solutions with and without SRB at the culture time of 2,4, 8 d, respectively. The measurement used two test methods, the nonimmersion electrode method and the immersion electrode method. It was found that the polarization resistance (Rp) of 1Cr18Ni9Ti in the solutions without SRB is the greatest for each test method. When using the nonimmersion electrode method, Rp shifts negatively at first and then positively, and the time constant is only one. Although using the immersion electrode method, the Rp shifts positively at first and then negatively, and the time constant also changes when the biofilm forms. The biofilm observed through SEM is with pores. It was demonstrated that SRB has accelerated corrosion action on 1Cr18Ni9Ti. The protection effect of the biofilm on the electrode depends on the compact degree of the film.

  13. Understanding Long-term Changes in Microbial Fuel Cell Performance Using Electrochemical Impedance Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Borole, Abhijeet P [ORNL; Aaron, D [Georgia Institute of Technology; Hamilton, Choo Yieng [ORNL; Tsouris, Costas [ORNL

    2010-01-01

    Changes in the anode, cathode, and solution/membrane impedances during enrichment of an anode microbial consortium weremeasuredusing electrochemicalimpedancespectroscopy. The consortium was enriched in a compact, flow-through porous electrode chamber coupled to an air-cathode. The anode impedance initially decreased from 296.1 to 36.3 in the first 43 days indicating exoelectrogenic biofilm formation. The external load on the MFC was decreased in a stepwise manner to allow further enrichment. MFC operation at a final load of 50 decreased the anode impedance to 1.4 , with a corresponding cathode and membrane/solution impedance of 12.1 and 3.0 , respectively. An analysis of the capacitive element suggested that most of the three-dimensional anode surface was participating in the bioelectrochemical reaction. The power density of the air-cathode MFC stabilized after 3 months of operation and stayed at 422 ( 42 mW/m2 (33 W/m3) for the next 3 months. The normalized anode impedance for theMFCwas 0.017 k cm2, a 28-fold reduction over that reported previously. This study demonstrates a unique ability of biological systems to reduce the electron transfer resistance in MFCs, and their potential for stable energy production over extended periods of time.

  14. Investigation of the degradation of LSM-YSZ SOFC cathode by electrochemical impedance spectroscopy

    DEFF Research Database (Denmark)

    Torres da Silva, Iris Maura

    conductivity would not be a problem during degradation experiments of the cells. The experiments carried out for this purpose include x-ray diffraction, conductivity and dilatometry. LSM-YSZ/YSZ/LSM-YSZ symmetrical cells were prepared and investigated by means ofelectrochemical impedance spectroscopy...... that at the applied operating conditions the impedance data could not be deconvoluted as anode and cathode processes were overlapping. Nonetheless it appeared that at OCV the degradation of the cathode is similar for symmetrical and single cells. Under current degradation was significantly lower, so real performance...

  15. Evaluation of Thymus vulgaris plant extract as an eco-friendly corrosion inhibitor for stainless steel 304 in acidic solution by means of electrochemical impedance spectroscopy, electrochemical noise analysis and density functional theory.

    Science.gov (United States)

    Ehsani, A; Mahjani, M G; Hosseini, M; Safari, R; Moshrefi, R; Mohammad Shiri, H

    2017-03-15

    Inhibition performance of Thymus vulgaris plant leaves extract (thyme) as environmentally friendly (green) inhibitor for the corrosion protection of stainless steel (SS) type 304 in 1.0molL(-1) HCl solution was studied by potentiodynamic polarization, electrochemical impedance (EIS) and electrochemical noise measurements (EN) techniques. The EN data were analyzed with FFT technique to make the spectral power density plots. The calculations were performed by MATLAB 2014a software. Geometry optimization and calculation of the structural and electronic properties of the molecular system of inhibitor have been carried out using UB3LYP/6-311++G(∗∗) level. Moreover, the results obtained from electrochemical noise analysis were compared with potentiodynamic polarization and electrochemical impedance spectroscopy. All of the used techniques showed positive effect of green inhibitor with increasing inhibitor concentration.

  16. Characterisation and Modelling of a High Temperature PEM Fuel Cell Stack using Electrochemical Impedance Spectroscopy

    DEFF Research Database (Denmark)

    Andreasen, Søren Juhl; Jespersen, Jesper Lebæk; Schaltz, Erik

    2009-01-01

    temperature PEM (HTPEM) fuel cell stack. A Labview virtual instrument has been developed to perform the signal generation and data acquisition which is needed to perform EIS. The typical output of an EIS measurement on a fuel cell, is a Nyquist plot, which shows the imaginary and real part of the impedance...

  17. Characterization of Porous WO3 Electrochromic Device by Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Chien Chon Chen

    2013-01-01

    Full Text Available This paper concerns the microstructure of the anodic tungsten oxide (WO3 and its use in an electrochromic (EC glass device. When voltages between 100 V and 160 V were applied to tungsten film for 1 h under 0.4 wt. % NaF electrolyte, porous WO3 film was formed. The film, which had a large surface area, was used as electrochromic film for EC glass. The average transmittance in a visible region of the spectrum for a 144 cm2 EC device was above 75% in the bleached state and below 40% in the colored state, respectively. Repeatability using of the colored/bleached cycles was tested good by a cyclic voltammograms method. The internal impedance values under colored and bleached states were detected and simulated using an electrical impedance spectra (EIS technique. The EC glass impedance characteristics were simulated using resistors, capacitors, and Warburg impedance. The ITO/WO3, WO3/electrolyte, electrolyte/NiO, and NiO/ITO interfaces can be simulated using a resistance capacitance (RC parallel circuits, and bulk materials such as the indium tin oxide (ITO and conducting wire can be simulated by using a series of resisters.

  18. Transport in fuel cells: Electrochemical impedance spectroscopy and neutron imaging studies

    Science.gov (United States)

    Aaron, Douglas Scott

    This dissertation focuses on two powerful methods of performing in-situ studies of transport limitations in fuel cells. The first is electrochemical impedance spectroscopy (EIS) while the second is neutron imaging. Three fuel cell systems are studied in this work: polymer electrolyte membrane fuel cells (PEMFCs), microbial fuel cells (MFCs) and enzyme fuel cells (EFCs). The first experimental section of this dissertation focuses on application of EIS and neutron imaging to an operating PEMFC. The effects of cathode-side humidity and flow rate, as well as cell temperature and a transient response to cathode-side humidity, were studied for a PEMFC via EIS. It was found that increased air humidity in the cathode resulted in greatly reduced cathode resistance as well as a significant reduction in membrane resistance. The anode resistance was only slightly reduced in this case. Increased air flow rate was observed to have little effect on any resistance in the PEMFC, though slight reductions in both the anode and the cathode were observed. Increased cell temperature resulted in decreased cathode and anode resistances. Finally, the transient response to increased humidity exhibited unstable behavior for both the anode and the cathode resistances and the PEMFC power output. Neutron imaging allowed the calculation of water content throughout the PEMFC, showing a maximum in water content at the cathode gas diffusion layer - membrane interface. The second experimental section of this dissertation delves into the world of microbial fuel cells. Multiple long-term observations of changes in internal resistances were performed and illustrated the reduction in anode resistance as the bacterial community was established. Over this same time period, the cathode resistance was observed to have increased; these two phenomena suggest that the anode improved over time while the cathode suffered from degradation. Increased anode fluid ionic strength and flow rate both led to significant

  19. Discerning the Impact of a Lithium Salt Additive in Thin-Film Light-Emitting Electrochemical Cells with Electrochemical Impedance Spectroscopy.

    Science.gov (United States)

    Bastatas, Lyndon D; Lin, Kuo-Yao; Moore, Matthew D; Suhr, Kristin J; Bowler, Melanie H; Shen, Yulong; Holliday, Bradley J; Slinker, Jason D

    2016-09-20

    Light-emitting electrochemical cells (LEECs) from small molecules, such as iridium complexes, have great potential as low-cost emissive devices. In these devices, ions rearrange during operation to facilitate carrier injection, bringing about efficient operation from simple, single-layer devices. Prior work has shown that the luminance, efficiency, and responsiveness of iridium LEECs is greatly enhanced by the inclusion of small fractions of lithium salts, but much remains to be understood about the origin of this enhancement. Recent work with planar devices demonstrates that lithium additives in iridium LEECs enhance double-layer formation. However, the quantitative influence of lithium salts on the underlying physics of conventional thin-film, sandwich structure LEECs, which beneficially operate at low voltages and generate higher luminance, has yet to be clarified. Here, we use electrochemical impedance spectroscopy to discern the impact of the lithium salt concentration on double-layer formation within the device and draw correlations with performance metrics, such as current, luminance, and external quantum efficiency.

  20. A high-precision approach to reconstruct distribution of relaxation times from electrochemical impedance spectroscopy

    Science.gov (United States)

    Zhang, Yanxiang; Chen, Yu; Li, Mei; Yan, Mufu; Ni, Meng; Xia, Changrong

    2016-03-01

    A new Tikhonov regularization approach without adjusting parameters is proposed for reconstructing distribution of relaxation time (DRT). It is capable of eliminating the pseudo peaks and capturing discontinuities in the DRT, making it feasible to resolve the number and the nature of electrochemical processes without making assumptions.

  1. Rapid Electron Transport Phenomenon in the Bis(terpyridine) Metal Complex Wire: Marcus Theory and Electrochemical Impedance Spectroscopy Study.

    Science.gov (United States)

    Maeda, Hiroaki; Sakamoto, Ryota; Nishihara, Hiroshi

    2015-10-01

    The authors reported previously that bis(terpyiridne)iron(II) complex oligomer wires possess outstanding long-range intrawire electron transport ability. Here, molecular arrays of gold-electrode-bis(terpyridine)iron(II)-ferrocene are constructed by stepwise coordination as simple models of the oligomer wire system. The fast electron transfer between the terminal ferrocene and the gold electrode through the bis(terpyiridne)iron(II) complex unit is studied by potential step chronoamperometry (PSCA) and electrochemical impedance spectroscopy (EIS). Tafel plots derived from PSCA are analyzed based on Marcus theory. The plots reveal greater first-order electron transfer rate constant, weaker electronic coupling between the terminal ferrocene and the gold electrode, and smaller reorganization energy than shown by a conventional ferrocenylalkanethiol self-assembled monolayer. The electron transfer rate constants estimated by EIS agree with the PSCA results.

  2. CORROSION RESISTANCE OF ORGANOMETALLIC COATING APLICATED IN FUEL TANKS USING ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY IN BIOFUEL – PART I

    Directory of Open Access Journals (Sweden)

    Milene Adriane Luciano

    2014-10-01

    Full Text Available Nowadays, the industry has opted for more sustainable production processes, and the planet has also opted for new energy sources. From this perspective, automotive tanks with organometallic coatings as well as a partial substitution of fossil fuels by biofuels have been developed. These organometallic coated tanks have a zinc layer, deposited by a galvanizing process, formed between the steel and the organometallic coating. This work aims to characterize the organometallic coating used in metal automotive tanks and evaluate their corrosion resistance in contact with hydrated ethyl alcohol fuel (AEHC. For this purpose, the resistance of all layers formed between Zinc and EEP steel and also the tin coated steel, which has been used for over thirty years, were evaluated. The technique chosen was the Electrochemical Impedance Spectroscopy. The results indicated an increase on the corrosion resistance when organometallic coatings are used in AEHC medium. In addition to that, these coatings allow an estimated 25% reduction in tanks production costs.

  3. Electrochemical Impedance Spectroscopy and Potentiodynamic Polarization Analysis on Anticorrosive Activity of Thiophene-2-Carbaldehyde Derivative in Acid Medium

    Directory of Open Access Journals (Sweden)

    Nimmy Kuriakose

    2014-01-01

    Full Text Available The corrosion inhibition efficiency of thiophene-2-carbaldehyde tryptophan (T2CTRY on mild steel (MS in 1 M HCl solution has been investigated and compared using weight loss measurements, electrochemical impedance spectroscopy, and potentiodynamic polarization analysis. The Schiff base exhibited very good corrosion inhibition on mild steel in HCl medium and the inhibition efficiency increased with the increase in concentration of the inhibitor. The adsorption of the inhibitor on the surface of the corroding metal obeys Freundlich isotherm. Thermodynamic parameters (Kads, ΔG ads0 were calculated using adsorption isotherm. Polarization studies revealed that T2CTRY acts as a mixed type inhibitor. A maximum of 96.2% inhibition efficiency was achieved by EIS studies at a concentration of 1 mM.

  4. Corrosion of Steel in Concrete – Potential Monitoring and Electrochemical Impedance Spectroscopy during Corrosion Initiation and Propagation

    DEFF Research Database (Denmark)

    Küter, Andre; Mason, Thomas O.; Geiker, Mette Rica;

    2005-01-01

    A reinforced mortar specimen that allows potential measurements and electrochemical impedance spectroscopy (EIS) immediately after preparation was designed and tested. The specimen consists of a mortar cylinder with a central rebar and a concentric arrangement of embedded Ru/Ir activated titanium...... and titanium wires can be monitored immediately after preparation. The wire arrangement also allows investigation of local changes in the bulk mortar by EIS or by measuring the potential development of the titanium wires versus an external standard electrode. The specimen design was evaluated...... in an investigation on the effect of the steel quality and the steel surface properties on initiation and propagation of chloride-induced reinforcement corrosion. Besides untreated (as received) carbon rebars and stainless rebars, selected surface treatments and galvanization were investigated. The surface treatments...

  5. Electrochemical impedance spectroscopy study of high-palladium dental alloys. Part II: behavior at active and passive potentials.

    Science.gov (United States)

    Sun, D; Monaghan, P; Brantley, W A; Johnston, W M

    2002-05-01

    Electrochemical impedance spectroscopic (EIS) analyses were performed on three high-palladium alloys and a gold-palladium alloy at active and passive potentials in five electrolytes that simulated body fluid and oral environmental conditions. All four alloys were previously found to have excellent corrosion resistance in these in vitro environments. Before performing the EIS analyses, alloy specimens were subjected to a clinically relevant heat treatment that simulated the firing cycles for a dental porcelain. It was found that the EIS spectra varied with test potential and electrolyte. Diffusional effects, related to the dealloying and subsequent surface enrichment in palladium of the high-palladium alloys, along with species adsorption and passivation, were revealed at both active and passive potentials, although these effects were more evident at the passive potentials.

  6. Study of caffeine as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    Science.gov (United States)

    Solehudin, Agus; Berman, Ega Taqwali; Nurdin, Isdiriayani

    2015-09-01

    The corrosion behaviour of steel surface in the absence and presence of caffeine in 3.5% NaCl solution containing dissolved H2S gas is studied using electrochemical impedance spectroscopy (EIS). The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H2S at different caffeine concentrations showed that corrosion rate of carbon steel decreases with increasing of caffeine concentrations from 0 to 0,1 mmol/l. Whereas, the corrosion rate increase with increasing of caffeine concentrations from 1 to 10 mmol/l. It is clear that no inhibition efficiency increases with increasing inhibitor concentration. The optimum value of inhibition efficiency was 90% at a caffeine concentration of 0.1 mmol/l. This suggests that caffeine's performance as a corrosion inhibitor is more effective at a concentration of 0.1 mmol/l.

  7. Cationic effect on dye-sensitized solar cell properties using electrochemical impedance and transient absorption spectroscopy techniques

    Science.gov (United States)

    Gupta, Ravindra Kumar; Bedja, Idriss

    2017-06-01

    Redox-couple polymer electrolytes, (poly(ethylene oxide)-succinonitrile) blend/MI-I2, where M  =  Li or K, were prepared by the solution cast method. Owing to the plasticizing property of K+ ions, the K+ ion-based electrolyte exhibited better electrical conductivity than the Li+ ion-based electrolyte, which did however exhibit better photovoltaic properties. Electrochemical impedance spectroscopy revealed faster redox species diffusions and interfacial processes in the Li+ ion-based dye-sensitized solar cells than in the K+ ion-based ones. Transient absorption spectroscopy ascertained faster dye-regeneration by the Li+ ion-based electrolyte than the K+ ion-based electrolyte.

  8. EVALUATION OF THE INHIBITORY EFFECTIVENESS OF THREE FERROCENE DERIVATIVES FOR CORROSION OF STEEL XC70 BY SPECTROSCOPY OF ELECTROCHEMICAL IMPEDANCE

    Directory of Open Access Journals (Sweden)

    O. Rahim

    2015-07-01

    Full Text Available In this work, we studied the efficacy of corrosion inhibition of carbon steel X70 in HCl 1M solution using ferrocenyl compounds prepared in VPRS laboratory, these compounds are: N-(férrocenyl méthyl-2-nitro aniline(Fc12, N-(férrocenyl méthyl-3-nitro aniline(Fc13 and N-(férrocenyl méthyl-4-nitro aniline(Fc14.The inhibitory potency of these compounds was determined by the electrochemical impedance spectroscopy (EIS. The overall results show that these compounds have varying percentages of inhibition. The adsorption of these compounds on the surface of the metal is a chemical adsorption.In HCl 1M, the compound Fc12 had the best ability of inhibition  at a concentration of 70ppm (R = 91.24%.

  9. Characterization of Damp-Heat Degradation of CuInGaSe2 Solar Cell Components and Devices by (Electrochemical) Impedance Spectroscopy: Preprint

    Energy Technology Data Exchange (ETDEWEB)

    Pern, F. J. J.; Noufi, R.

    2011-09-01

    This work evaluated the capability of (electrochemical) impedance spectroscopy (IS, or ECIS as used here) to monitor damp heat (DH) stability of contact materials, CuInGaSe2 (CIGS) solar cell components, and devices. Cell characteristics and its variation of the CIGS devices were also examined by the ECIS.

  10. Impedance Spectroscopic Investigation of Proton Conductivity in Nafion Using Transient Electrochemical Atomic Force Microscopy (AFM

    Directory of Open Access Journals (Sweden)

    Emil Roduner

    2012-06-01

    Full Text Available Spatially resolved impedance spectroscopy of a Nafion polyelectrolyte membrane is performed employing a conductive and Pt-coated tip of an atomic force microscope as a point-like contact and electrode. The experiment is conducted by perturbing the system by a rectangular voltage step and measuring the incurred current, followed by Fourier transformation and plotting the impedance against the frequency in a conventional Bode diagram. To test the potential and limitations of this novel method, we present a feasibility study using an identical hydrogen atmosphere at a well-defined relative humidity on both sides of the membrane. It is demonstrated that good quality impedance spectra are obtained in a frequency range of 0.2–1,000 Hz. The extracted polarization curves exhibit a maximum current which cannot be explained by typical diffusion effects. Simulation based on equivalent circuits requires a Nernst element for restricted diffusion in the membrane which suggests that this effect is based on the potential dependence of the electrolyte resistance in the high overpotential region.

  11. Impedance Spectroscopic Investigation of Proton Conductivity in Nafion Using Transient Electrochemical Atomic Force Microscopy (AFM)

    Science.gov (United States)

    Hink, Steffen; Wagner, Norbert; Bessler, Wolfgang G.; Roduner, Emil

    2012-01-01

    Spatially resolved impedance spectroscopy of a Nafion polyelectrolyte membrane is performed employing a conductive and Pt-coated tip of an atomic force microscope as a point-like contact and electrode. The experiment is conducted by perturbing the system by a rectangular voltage step and measuring the incurred current, followed by Fourier transformation and plotting the impedance against the frequency in a conventional Bode diagram. To test the potential and limitations of this novel method, we present a feasibility study using an identical hydrogen atmosphere at a well-defined relative humidity on both sides of the membrane. It is demonstrated that good quality impedance spectra are obtained in a frequency range of 0.2–1000 Hz. The extracted polarization curves exhibit a maximum current which cannot be explained by typical diffusion effects. Simulation based on equivalent circuits requires a Nernst element for restricted diffusion in the membrane which suggests that this effect is based on the potential dependence of the electrolyte resistance in the high overpotential region. PMID:24958175

  12. Application of electrochemical impedance spectroscopy to monitoring discharging process of nickel/metal hydride battery

    Science.gov (United States)

    Slepski, Pawel; Darowicki, Kazimierz; Janicka, Ewa; Sierczynska, Agnieszka

    2013-11-01

    This paper presents the possibility of applying impedance analysis to cell diagnostics. In order to obtain characteristic curves of both electrodes of a NiMH battery simultaneously, a reference electrode was added into the circuit. The authors analysed the cell under three cases, i.e. when its properties are determined only by the state of the positive electrode, only by the state of the negative electrode, or when both electrodes determine operation of the cell to the same extent. Impedance characteristic curves of the entire cell in the function of variable state of charge do not allow for a conclusion as to which electrode determines cell capacity. This is not possible until an analysis of impedance graphs is carried out for each electrode. In view of the obtained results equivalent circuits for the positive electrode, the negative electrode, and the entire cell were selected. Further, a correlation between charge transfer resistance, calculated for the entire cell, and the values obtained for the positive electrode, as well as the negative one, is presented.

  13. A Novel Application for Low Frequency Electrochemical Impedance Spectroscopy as an Online Process Monitoring Tool for Viable Cell Concentrations

    Science.gov (United States)

    Slouka, Christoph; Wurm, David J.; Brunauer, Georg; Welzl-Wachter, Andreas; Spadiut, Oliver; Fleig, Jürgen; Herwig, Christoph

    2016-01-01

    New approaches in process monitoring during industrial fermentations are not only limited to classical pH, dO2 and offgas analysis, but use different in situ and online sensors based on different physical principles to determine biomass, product quality, lysis and far more. One of the very important approaches is the in situ accessibility of viable cell concentration (VCC). This knowledge provides increased efficiency in monitoring and controlling strategies during cultivations. Electrochemical impedance spectroscopy—EIS—is used to monitor biomass in a fermentation of E. coli BL21(DE3), producing a recombinant protein using a fed batch-based approach. Increases in the double layer capacitance (Cdl), determined at frequencies below 1 kHz, are proportional to the increase of biomass in the batch and fed batch phase, monitored in offline and online modes for different cultivations. A good correlation of Cdl with cell density is found and in order to get an appropriate verification of this method, different state-of-the-art biomass measurements are performed and compared. Since measurements in this frequency range are largely determined by the double layer region between the electrode and media, rather minor interferences with process parameters (aeration, stirring) are to be expected. It is shown that impedance spectroscopy at low frequencies is a powerful tool for cultivation monitoring. PMID:27845720

  14. A Novel Application for Low Frequency Electrochemical Impedance Spectroscopy as an Online Process Monitoring Tool for Viable Cell Concentrations

    Directory of Open Access Journals (Sweden)

    Christoph Slouka

    2016-11-01

    Full Text Available New approaches in process monitoring during industrial fermentations are not only limited to classical pH, dO2 and offgas analysis, but use different in situ and online sensors based on different physical principles to determine biomass, product quality, lysis and far more. One of the very important approaches is the in situ accessibility of viable cell concentration (VCC. This knowledge provides increased efficiency in monitoring and controlling strategies during cultivations. Electrochemical impedance spectroscopy—EIS—is used to monitor biomass in a fermentation of E. coli BL21(DE3, producing a recombinant protein using a fed batch-based approach. Increases in the double layer capacitance (Cdl, determined at frequencies below 1 kHz, are proportional to the increase of biomass in the batch and fed batch phase, monitored in offline and online modes for different cultivations. A good correlation of Cdl with cell density is found and in order to get an appropriate verification of this method, different state-of-the-art biomass measurements are performed and compared. Since measurements in this frequency range are largely determined by the double layer region between the electrode and media, rather minor interferences with process parameters (aeration, stirring are to be expected. It is shown that impedance spectroscopy at low frequencies is a powerful tool for cultivation monitoring.

  15. Heat loss distribution: Impedance and thermal loss analyses in LiFePO4/graphite 18650 electrochemical cell

    Science.gov (United States)

    Balasundaram, Manikandan; Ramar, Vishwanathan; Yap, Christopher; Lu, Li; Tay, Andrew A. O.; Palani, Balaya

    2016-10-01

    We report here thermal behaviour and various components of heat loss of 18650-type LiFePO4/graphite cell at different testing conditions. In this regard, the total heat generated during charging and discharging processes at various current rates (C) has been quantified in an Accelerating Rate Calorimeter experiment. Irreversible heat generation, which depends on applied current and internal cell resistance, is measured under corresponding charge/discharge conditions using intermittent pulse techniques. On the other hand, reversible heat generation which depends on entropy changes of the electrode materials during the cell reaction is measured from the determination of entropic coefficient at various states of charge/discharge. The contributions of irreversible and reversible heat generation to the total heat generation at both high and low current rates are evaluated. At every state of charge/discharge, the nature of the cell reaction is found to be either exothermic or endothermic which is especially evident at low C rates. In addition, electrochemical impedance spectroscopy measurements are performed on above 18650 cells at various states of charge to determine the components of internal resistance. The findings from the impedance and thermal loss analysis are helpful for understanding the favourable states of charge/discharge for battery operation, and designing better thermal management systems.

  16. Electrochemical noise and impedance of Au electrode/electrolyte interfaces enabling extracellular detection of glioma cell populations

    Science.gov (United States)

    Rocha, Paulo R. F.; Schlett, Paul; Kintzel, Ulrike; Mailänder, Volker; Vandamme, Lode K. J.; Zeck, Gunther; Gomes, Henrique L.; Biscarini, Fabio; de Leeuw, Dago M.

    2016-10-01

    Microelectrode arrays (MEA) record extracellular local field potentials of cells adhered to the electrodes. A disadvantage is the limited signal-to-noise ratio. The state-of-the-art background noise level is about 10 μVpp. Furthermore, in MEAs low frequency events are filtered out. Here, we quantitatively analyze Au electrode/electrolyte interfaces with impedance spectroscopy and noise measurements. The equivalent circuit is the charge transfer resistance in parallel with a constant phase element that describes the double layer capacitance, in series with a spreading resistance. This equivalent circuit leads to a Maxwell-Wagner relaxation frequency, the value of which is determined as a function of electrode area and molarity of an aqueous KCl electrolyte solution. The electrochemical voltage and current noise is measured as a function of electrode area and frequency and follow unambiguously from the measured impedance. By using large area electrodes the noise floor can be as low as 0.3 μVpp. The resulting high sensitivity is demonstrated by the extracellular detection of C6 glioma cell populations. Their minute electrical activity can be clearly detected at a frequency below about 10 Hz, which shows that the methodology can be used to monitor slow cooperative biological signals in cell populations.

  17. Characterization of implant materials in fetal bovine serum and sodium sulfate by electrochemical impedance spectroscopy. I. Mechanically polished samples.

    Science.gov (United States)

    Contu, F; Elsener, B; Böhni, H

    2002-12-01

    Electrochemical impedance spectroscopy is used to monitor the long-term stability (up to 150 days) of mechanically polished commercial pure titanium, Ti6Al4V, Ti6Al7Nb, and CoCrMo alloys in 0.1M sodium sulfate and fetal bovine serum. A capacitive spectrum in the frequency range from 10(-3) to 10(5) Hz is always found and the impedance spectra can be fitted by a simple parallel RC circuit with a constant phase element. The open circuit potential observed in serum is always more cathodic and the polarization resistance (R(p)) is higher than that recorded in sodium sulfate solutions. The observed variation of the equivalent capacitance in serum bovine suggests that an adsorption layer of organic molecules develops on the electrode surface and it is responsible for both the decrease in open circuit potential and the higher R(p), because it hinders the oxygen evolution reaction and the charge transfer responsible for the passive film dissolution (or growth). Among the alloys studied, Ti6Al4V displayed the highest steady-state values of R(p) both in serum and in sodium sulfate.

  18. Evaluation of Temper Embrittlement of 30Cr2MoV Rotor Steels Using Electrochemical Impedance Spectroscopy Technique

    Directory of Open Access Journals (Sweden)

    Zhang Shenghan

    2015-01-01

    Full Text Available Temper embrittlement tends to occur in the turbine rotor after long running, which refers to the decrease in notch toughness of alloy steels in a certain temperature range (e.g., 400°C to 600°C. The severity of temper embrittlement must be monitored timely to avoid further damagement, and the fracture appearance transition temperature (FATT50 is commonly used as an indicator parameter to characterize the temper embrittlement. Compared with conventional destructive methods (e.g., small punch test, nondestructive approaches have drawn significant attention in predicting the material degradation in turbine rotor steels without impairing the integrity of the components. In this paper, laboratory experiments were carried out based on a nondestructive method, electrochemical impedance spectroscopy (EIS, with groups of lab-charged specimens for predicting the temper embrittlement (FATT50 of turbine rotor steel. The results show that there was a linear relationship of interfacial impedance of the specimens and their FATT50 values. The predictive error based on the experiment study is within the range of ±15°C, indicating the predicting model is precise, effective, and reasonable.

  19. LiCoO2 electrode/electrolyte interface of Li-ion batteries investigated by electrochemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The storage behavior and the first delithiation of LiCoO2 electrode in 1 mol/L LiPF6-EC:DMC:DEC electrolyte were investigated by electrochemical impedance spectroscopy (EIS). It has found that, along with the increase of storage time, the thickness of SEI film increases, and some organic carbonate lithium compounds are formed due to spontaneous reactions occurring between the LiCoO2 electrode and the electrolyte. When electrode potential is changed from 3.8 to 3.95 V, the reversible breakdown of the resistive SEI film occurs, which is attributed to the reversible dissolution of the SEI film component. With the increase of electrode potential, the thickness of SEI film increases rapidly above 4.2 V, due to overcharge reactions. The inductive loop observed in impedance spectra of the LiCoO2 electrode in Li/LiCoO2 cells is attributed to the formation of a Li1-xCoO2/LiCoO2 concentration cell. Moreover, it has been demonstrated that the lithium-ion insertion-deinsertion in LiCoO2 hosts can be well described by both Langmuir and Frumkin insertion isotherms, and the symmetry factor of charge transfer has been evaluated at 0.5.

  20. Evaluation of corrosion resistance of aluminium coating with and without annealing against molten carbonate using electrochemical impedance spectroscopy

    Science.gov (United States)

    Ni, C. S.; Lu, L. Y.; Zeng, C. L.; Niu, Y.

    2014-09-01

    An arc ion plating (AIP) was used to fabricate a FeAl layer on 310S stainless steel to protect the sealing area being corroded by the molten carbonate in molten carbonate fuel cells (MCFCs). The degradation of aluminide coatings comes from both the corrosion of the coating in contact with the molten carbonate and the aluminium depletion due to the interdiffusion of aluminium and the substrate. The in-situ forming of aluminide in molten carbonate at 650 °C could be a possible way to reduce the inward diffusion of aluminium in the conventional pre-annealing at 850 °C. Electrochemical impedance spectroscopy (EIS) measurements were performed to model the corrosion of this pre-formed FeAl coating in comparison with the one formed in-situ in molten (0.62 Li+0.38 K)2CO3 at 650 °C. Although α-LiAlO2 is the corrosion product in both cases, the impedance spectra show distinct rate-limiting steps; the former is controlled by the charged particles passing through the scale, while the latter by their diffusion in the melt. The microstructure of the scale might be the reason for the difference in corrosion mechanism.

  1. Measurement of Small Molecule Binding Kinetics on a Protein Microarray by Plasmonic-Based Electrochemical Impedance Imaging

    Science.gov (United States)

    2015-01-01

    We report on a quantitative study of small molecule binding kinetics on protein microarrays with plasmonic-based electrochemical impedance microscopy (P-EIM). P-EIM measures electrical impedance optically with high spatial resolution by converting a surface charge change to a surface plasmon resonance (SPR) image intensity change, and the signal is not scaled to the mass of the analyte. Using P-EIM, we measured binding kinetics and affinity between small molecule drugs (imatinib and SB202190) and their target proteins (kinases Abl1 and p38-α). The measured affinity values are consistent with reported values measured by an indirect competitive binding assay. We also found that SB202190 has weak bindings to ABL1 with KD > 10 μM, which is not reported in the literature. Furthermore, we found that P-EIM is less prone to nonspecific binding, a long-standing issue in SPR. Our results show that P-EIM is a novel method for high-throughput measurement of small molecule binding kinetics and affinity, which is critical to the understanding of small molecules in biological systems and discovery of small molecule drugs. PMID:25153794

  2. Sensitivity Enhancement of Bead-based Electrochemical Impedance Spectroscopy (BEIS) biosensor by electric field-focusing in microwells.

    Science.gov (United States)

    Shin, Kyeong-Sik; Ji, Jae Hoon; Hwang, Kyo Seon; Jun, Seong Chan; Kang, Ji Yoon

    2016-11-15

    This paper reports a novel electrochemical impedance spectroscopy (EIS) biosensors that uses magnetic beads trapped in a microwell array to improve the sensitivity of conventional bead-based EIS (BEIS) biosensors. Unloading the previously measured beads by removing the magnetic bar enables the BEIS sensor to be used repeatedly by reloading it with new beads. Despite its recyclability, the sensitivity of conventional BEIS biosensors is so low that it has not attracted much attentions from the biosensor industry. We significantly improved the sensitivity of the BEIS system by introducing of a microwell array that contains two electrodes (a working electrode and a counter electrode) to concentrate the electric field on the surfaces of the beads. We confirmed that the performance of the BEIS sensor in a microwell array using an immunoassay of prostate specific antigen (PSA) in PBS buffer and human plasma. The experimental results showed that a low concentration of PSA (a few tens or hundreds of fg/mL) were detectable as a ratio of the changes in the impedance of the PBS buffer or in human plasma. Therefore, our BEIS sensor with a microwell array could be a promising platform for low cost, high-performance biosensors for applications that require high sensitivity and recyclability.

  3. Electrochemical Behavior of Aluminum in Nitric Acid

    Institute of Scientific and Technical Information of China (English)

    CHEN; Hui; ZHU; Li-yang; LIN; Ru-shan; TAN; Hong-bin; HE; Hui

    2013-01-01

    Aluminum is one of cladding materials for nuclear fuel,it is important to investigate the electrolytic dissolution of aluminum in nitric acid.The electrochemical impedance spectroscopy,polarization curve and cyclic voltammetry cure of anodic aluminum electrode in nitric acid under various conditions were collected(Fig.1).It turns out,under steady state,the thickness of the passivated film of aluminum

  4. Degradation of graphene coated copper in simulated proton exchange membrane fuel cell environment: Electrochemical impedance spectroscopy study

    Science.gov (United States)

    Ren, Y. J.; Anisur, M. R.; Qiu, W.; He, J. J.; Al-Saadi, S.; Singh Raman, R. K.

    2017-09-01

    Metallic materials are most suitable for bipolar plates of proton exchange membrane fuel cell (PEMFC) because they possess the required mechanical strength, durability, gas impermeability, acceptable cost and are suitable for mass production. However, metallic bipolar plates are prone to corrosion or they can passivate under PEMFC environment and interrupt the fuel cell operation. Therefore, it is highly attractive to develop corrosion resistance coating that is also highly conductive. Graphene fits these criteria. Graphene coating is developed on copper by chemical vapor deposition (CVD) with an aim to improving corrosion resistance of copper under PEMFC condition. The Raman Spectroscopy shows the graphene coating to be multilayered. The electrochemical degradation of graphene coated copper is investigated by electrochemical impedance spectroscopy (EIS) in 0.5 M H2SO4 solution at room temperature. After exposure to the electrolyte for up to 720 h, the charge transfer resistance (Rt) of the graphene coated copper is ∼3 times greater than that of the bare copper, indicating graphene coatings could improve the corrosion resistance of copper bipolar plates.

  5. In situ investigation of pore clogging during discharge of a Li/O2 battery by electrochemical impedance spectroscopy

    Science.gov (United States)

    Bardenhagen, Ingo; Yezerska, Olga; Augustin, Matthias; Fenske, Daniela; Wittstock, Arne; Bäumer, Marcus

    2015-03-01

    The behavior of three gas diffusion electrodes (GDE) with macro- and mesopores is investigated by in situ electrochemical impedance spectroscopy (EIS) in the Li/O2 battery system while discharging. Using a three electrode setup the current response from the anode (Li metal) and cathode (GDE) can be separated and the changes of the electrochemical processes at the GDE during discharge can be observed, exclusively. We identify up to four processes with different time constants which we assign to the lithium ion migration through a surface layer, the charge-transfer from the carbon surface to the molecular oxygen, the lithium ion and oxygen diffusion towards the cathode surface and, in case of the mesoporous materials, the lithium ion movement inside the pores, along the pore axis. The latter finding reflects that pore clogging of such is a limiting factor for the discharge of the Li/O2 battery. A large mesopore volume as in the xerogel electrode, however, allows for a high storage capability and a long and constant oxygen reduction. We demonstrate that the three electrode EIS proves to be a powerful in situ diagnostic tool to determine the state and, hence, the reversibility of the reactions at the cathode.

  6. A Label-Free Electrochemical Impedance Cytosensor Based on Specific Peptide-Fused Phage Selected from Landscape Phage Library

    Science.gov (United States)

    Han, Lei; Liu, Pei; Petrenko, Valery A.; Liu, Aihua

    2016-02-01

    One of the major challenges in the design of biosensors for cancer diagnosis is to introduce a low-cost and selective probe that can recognize cancer cells. In this paper, we combined the phage display technology and electrochemical impedance spectroscopy (EIS) to develop a label-free cytosensor for the detection of cancer cells, without complicated purification of recognition elements. Fabrication steps of the cytosensing interface were monitored by EIS. Due to the high specificity of the displayed octapeptides and avidity effect of their multicopy display on the phage scaffold, good biocompatibility of recombinant phage, the fibrous nanostructure of phage, and the inherent merits of EIS technology, the proposed cytosensor demonstrated a wide linear range (2.0 × 102 ‑ 2.0 × 108 cells mL‑1), a low limit of detection (79 cells mL‑1, S/N = 3), high specificity, good inter-and intra-assay reproducibility and satisfactory storage stability. This novel cytosensor designing strategy will open a new prospect for rapid and label-free electrochemical platform for tumor diagnosis.

  7. A Label-Free Electrochemical Impedance Cytosensor Based on Specific Peptide-Fused Phage Selected from Landscape Phage Library.

    Science.gov (United States)

    Han, Lei; Liu, Pei; Petrenko, Valery A; Liu, Aihua

    2016-02-24

    One of the major challenges in the design of biosensors for cancer diagnosis is to introduce a low-cost and selective probe that can recognize cancer cells. In this paper, we combined the phage display technology and electrochemical impedance spectroscopy (EIS) to develop a label-free cytosensor for the detection of cancer cells, without complicated purification of recognition elements. Fabrication steps of the cytosensing interface were monitored by EIS. Due to the high specificity of the displayed octapeptides and avidity effect of their multicopy display on the phage scaffold, good biocompatibility of recombinant phage, the fibrous nanostructure of phage, and the inherent merits of EIS technology, the proposed cytosensor demonstrated a wide linear range (2.0 × 10(2) - 2.0 × 10(8) cells mL(-1)), a low limit of detection (79 cells mL(-1), S/N = 3), high specificity, good inter-and intra-assay reproducibility and satisfactory storage stability. This novel cytosensor designing strategy will open a new prospect for rapid and label-free electrochemical platform for tumor diagnosis.

  8. Impedance Spectroscopic Indication for Solid State Electrochemical Reaction in (CH3NH3)PbI3 Films.

    Science.gov (United States)

    Zohar, Arava; Kedem, Nir; Levine, Igal; Zohar, Dorin; Vilan, Ayelet; Ehre, David; Hodes, Gary; Cahen, David

    2016-01-01

    Halide perovskite-based solar cells still have limited reproducibility, stability, and incomplete understanding of how they work. We track electronic processes in [CH3NH3]PbI3(Cl) ("perovskite") films in vacuo, and in N2, air, and O2, using impedance spectroscopy (IS), contact potential difference, and surface photovoltage measurements, providing direct evidence for perovskite sensitivity to the ambient environment. Two major characteristics of the perovskite IS response change with ambient environment, viz. -1- appearance of negative capacitance in vacuo or post-vacuo N2 exposure, indicating for the first time an electrochemical process in the perovskite, and -2- orders of magnitude decrease in the film resistance upon transferring the film from O2-rich ambient atmosphere to vacuum. The same change in ambient conditions also results in a 0.5 V decrease in the material work function. We suggest that facile adsorption of oxygen onto the film dedopes it from n-type toward intrinsic. These effects influence any material characterization, i.e., results may be ambient-dependent due to changes in the material's electrical properties and electrochemical reactivity, which can also affect material stability.

  9. Electrochemical characterization of an ambient temperature rechargeable Li battery based on low molecular weight polymer electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Bonino, F.; Croce, F.; Panero, S. (Dept. of Chemistry, Univ. of Rome ' La Sapienza' , Rome (Italy))

    1994-06-01

    Preliminary applications of low molecular weight polymer electrolyte (PEG) and lithium salt in lithium rechargeable batteries have been reported. The electrochemical characteristics of these electrolytes have been tested by cyclic voltammetry, charge-discharge cycles and ac impedance methods. Surface layers appear to be present on both electrodes, but they develop upon time with different extension

  10. Amplified DNA Detection Sensitivity Using Streptavidin-Biotinylated Protein Complex: Characterization by Electrochemical Impedance Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    CHENG, Zhi-Liang; YANG, Fan; HUANG, Hai-Zhen; YANG, Xiu-Rong

    2003-01-01

    Thiol-terminated oligonucleotide was immobilized to gold surface by self-assembly method. A novel amplification strategy was introduced for improving the sensitivity of DNA hybridization using biotin labeled protein-streptavidin network complex.This complex can be formed in a cross-linking network of molecules so that the amplification of the response signal will be realized due to the big molecular size of the complex. It could be proved from the impedance technique that this amplification strategy caused dramatic improvement of the detection sensitivity. These results give significant advances in the generality and sensitivity as it is applied to biosensing.

  11. Mechanism of anodic oxidation of molybdenum in nearly-neutral electrolytes studied by electrochemical impedance spectroscopy and X-ray photoelectron spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Petrova, Manuela [University of Chemical Technology and Metallurgy, 8 Kl. Ohridski Blvd., 1756 Sofia (Bulgaria); Bojinov, Martin, E-mail: martin@uctm.edu [University of Chemical Technology and Metallurgy, 8 Kl. Ohridski Blvd., 1756 Sofia (Bulgaria); Zanna, Sandrine; Marcus, Philippe [Laboratoire de Physico-Chimie des Surfaces, CNRS-ENSCP (UMR7045), 11 Rue Pierre et Marie Curie, 75005 Paris (France)

    2011-09-30

    Anodic oxidation of molybdenum in weakly acidic, nearly neutral and weakly alkaline electrolytes was studied by voltammetric and electrochemical impedance spectroscopic measurements in a wide potential and pH range. Current vs. potential curves were found to exhibit two pseudo-Tafel regions suggesting two parallel pathways of the dissolution process. Electrochemical impedance spectra indicated the presence of at least two reaction intermediates. X-ray photoelectron spectroscopic (XPS) results pointed to the formation of an oxide containing Mo(IV), Mo(V) and Mo(VI), the exact ratio between different valence states depending on potential and pH of the solution. A physico-chemical model of the processes is proposed and a set of kinetic equations for the steady-state current vs. potential curve and the impedance response are derived. The model is found to reproduce quantitatively the current vs. potential curves and impedance spectra at a range of potentials and pH and to agree qualitatively with the XPS results. Subject to further improvement, the model could serve as a starting point for the optimization of the electrochemical fabrication of functional molybdenum oxide coatings.

  12. Electrochemical Impedance Spectroscopy (EIS) Characterization of Reformate-operated High Temperature PEM Fuel Cell Stack

    DEFF Research Database (Denmark)

    Sahlin, Simon Lennart; Simon Araya, Samuel; Andreasen, Søren Juhl

    2017-01-01

    their effects on a reformate-operated stack. Polarization curves were also recorded to complement the impedance analysis of the researched phenomena. An equivalent circuit model was used to estimate the different resistances at varying parameters. It showed a significantly higher low frequency resistance...... at lower stoichiometry. Both anode and cathode stoichiometric ratios had significant effects on the stack performance during the dry hydrogen and reformate operation modes. In both cases the effects faded away when sufficient mass transport was achieved, which took place at λanode= 1.3 for dry hydrogen......, λanode= 1.6 for reformate operation and λcathode= 4.The work also compared dry hydrogen, steam reforming and autothermal reforming gas feeds at160 ◦Cand showed appreciably lower performance in the case of autothermal reforming at the same stoichiometry, mainly attributable to mass transport related...

  13. Equivalent Circuits Applied in Electrochemical Impedance Spectroscopy and Fractional Derivatives with and without Singular Kernel

    Directory of Open Access Journals (Sweden)

    J. F. Gómez-Aguilar

    2016-01-01

    Full Text Available We present an alternative representation of integer and fractional electrical elements in the Laplace domain for modeling electrochemical systems represented by equivalent electrical circuits. The fractional derivatives considered are of Caputo and Caputo-Fabrizio type. This representation includes distributed elements of the Cole model type. In addition to maintaining consistency in adjusted electrical parameters, a detailed methodology is proposed to build the equivalent circuits. Illustrative examples are given and the Nyquist and Bode graphs are obtained from the numerical simulation of the corresponding transfer functions using arbitrary electrical parameters in order to illustrate the methodology. The advantage of our representation appears according to the comparison between our model and models presented in the paper, which are not physically acceptable due to the dimensional incompatibility. The Markovian nature of the models is recovered when the order of the fractional derivatives is equal to 1.

  14. Elevated Electrochemical Impedance in the Endoluminal Regions with High Shear Stress: Implication for Assessing Lipid-Rich Atherosclerotic Lesions

    Science.gov (United States)

    Yu, Fei; Lee, Juhyun; Jen, Nelson; Li, Xiang; Zhang, Qian; Tang, Rui; Zhou, Qifa; Kim, Eun. S.; Hsiai, Tzung K.

    2012-01-01

    Background Identifying metabolically active atherosclerotic lesions remains an unmet clinical challenge during coronary intervention. Electrochemical impedance (EIS) increased in response to oxidized low density lipoprotein (oxLDL)-laden lesions. We hereby assessed whether integrating EIS with intravascular ultrasound (IVUS) and shear stress (ISS) provided a new strategy to assess oxLDL-laden lesions in the fat-fed New Zealand White (NZW) rabbits. Methods and Results A micro-heat transfer sensor was deployed to acquire the ISS profiles at baseline and post high-fat diet (HD) in the NZW rabbits (n=8). After 9 weeks of HD, serum oxLDL levels (mg/dL) increased by 140-fold, accompanied by a 1.5-fold increase in kinematic viscosity (cP) in the HD group. Time-averaged ISS (ISSave) in the thoracic aorta also increased in the HD group (baseline: 17.61±0.24 vs. 9 weeks: 25.22±0.95 dyne/cm2, n=4), but remained unchanged in the normal diet group (baseline: 22.85±0.53 dyne/cm2 vs. 9 weeks: 22.37±0.57 dyne/cm2, n=4). High-frequency Intravascular Ultrasound (IVUS) revealed atherosclerotic lesions in the regions with augmented ISSave, and concentric bipolar microelectrodes demonstrated elevated EIS signals, which were correlated with prominent anti-oxLDL immuno-staining (oxLDL-free regions: 497±55 Ω, n = 8 vs. oxLDL-rich lesions: 679±125 Ω, n = 12, P < 0.05). The equivalent circuit model for tissue resistance between the lesion-free and ox-LDL-rich lesions further validated the experimental EIS signals. Conclusions By applying electrochemical impedance in conjunction with shear stress and high-frequency ultrasound sensors, we provided a new strategy to identify oxLDL-laden lesions. The study demonstrated the feasibility of integrating EIS, ISS, and IVUS for a catheter-based approach to assess mechanically unstable plaque. PMID:23318546

  15. Two-dimensional modeling of a polymer electrolyte membrane fuel cell with long flow channel. Part II. Physics-based electrochemical impedance analysis

    Science.gov (United States)

    Bao, Cheng; Bessler, Wolfgang G.

    2015-03-01

    The state-of-the-art electrochemical impedance spectroscopy (EIS) calculations have not yet started from fully multi-dimensional modeling. For a polymer electrolyte membrane fuel cell (PEMFC) with long flow channel, the impedance plot shows a multi-arc characteristic and some impedance arcs could merge. By using a step excitation/Fourier transform algorithm, an EIS simulation is implemented for the first time based on the full 2D PEMFC model presented in the first part of this work. All the dominant transient behaviors are able to be captured. A novel methodology called 'configuration of system dynamics', which is suitable for any electrochemical system, is then developed to resolve the physical meaning of the impedance spectra. In addition to the high-frequency arc due to charge transfer, the Nyquist plots contain additional medium/low-frequency arcs due to mass transfer in the diffusion layers and along the channel, as well as a low-frequency arc resulting from water transport in the membrane. In some case, the impedance spectra appear partly inductive due to water transport, which demonstrates the complexity of the water management of PEMFCs and the necessity of physics-based calculations.

  16. Electrochemical impedance study and performance of PdNi nanoparticles as cathode catalyst in a polymer electrolyte membrane fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Ramos-Sanchez, G.; Santana-Salinas, A.; Vazquez-Huerta, G.; Solorza-Feria, O. [Inst. Politenico Nacional, Centro de Investigacion y de Estudios Avanzados, Mexico City (Mexico). Dept. de Quimica

    2010-07-15

    Polymer electrolyte membrane fuel cells (PEMFC) convert the energy stored in hydrogen and oxygen molecules directly into electricity. However, technical and economic challenges must be overcome to address cost, performance and stability issues associated with membrane electrode assemblies (MEA). The oxygen reduction reaction (ORR) which takes place in the cathode is the limiting reaction due to the slow kinetics of ORR on metals, including platinum (Pt). For that reason, much research has gone into finding catalyst materials with a similar or greater performance than Pt. Bimetallic palladium (Pd) based catalysts have been considered as alternative materials for ORR. In this study, a carbon-dispersed bimetallic PdNi was prepared by borohydride reduction using PdCl{sub 2} and NiCl{sub 2} as precursors in a tetrahydrofuran (THF) solution. The PdNi loading and weight percentage were optimized using the Simplex method. The MEA performance was evaluated at optimum conditions using the PdNi electrocatalyst as the cathode and a Pt-Etek carbon cloth as the anode. The maximum power density of 122 mW per cm{sup 2} was reached with 45 percent of PdNi wt percent at 30 psi and 80 degrees C. The catalytic activity and the mechanism of the ORR on PdNi, in 0.5M H{sub 2}SO{sub 4} was investigated using electrochemical impedance spectroscopy. The Tafel slope and the charge transfer coefficient were obtained from the impedance spectra at optimum condition of PdNi loading and PdNi wt percent. 24 refs., 2 tabs., 5 figs.

  17. Evaluation of Metals (Al, Fe, Zn) in Alternative Fuels by Electrochemical Impedance Spectroscopy in Two Electrode Cell

    Energy Technology Data Exchange (ETDEWEB)

    Song, Yon Kyun [POSCO Technical Research Laboratories, Gwnagyang (Korea, Republic of); Lim, Geun Woong; Kim, Hee San [Hongik University, Chochiwon (Korea, Republic of)

    2010-04-15

    Many kinds of alternative fuels such as biodiesel, ethanol, methanol, and natural gas have been developed in order to overcome the limited deposits in fossil fuels. In some cases, the alternative fuels have been reported to cause degrade materials. The corrosion rates of metals were measured by immersion test, a kind of time consuming test because low conductivity of these fuels was not allowed to employ electrochemical tests. With twin two-electrode cell newly designed for the study, however, electrochemical impedance spectroscopy (EIS) test was successfully applied to evaluation of the corrosion resistance (R{sub p}) of zinc, iron, aluminum, and its alloys in an oxidized biodiesel and gasoline/ethanol solutions and the corrosion resistance from EIS was compared with the corrosion rate from immersion test. In biodiesel, R{sub p} increased in the order of zinc, iron, and aluminum, which agreed with the corrosion resistance measured from immersion test. In addition, on aluminum showing the best corrosion resistance (R{sub p}), the effect of magnesium as an alloying element was evaluated in gasoline/ethanol solutions as well as the oxidized biodiesel. R{sub p} increased with addition of magnesium in gasoline/ethanol solutions containing chloride and the oxidized biodiesel. In the mean while, in gasoline/ethanol solutions containing formic acid, Al-Mg alloy added 1% magnesium had the highest R{sub p} and the further addition of magnesium decreased R{sub p}. It can be explained with the fact that the addition of more than 1% magnesium increases the passive current density of Al-Mg alloys.

  18. An Electrochemical Impedance Spectroscopy Study on the Effects of the Surface- and Solution-Based Mechanisms in Li-O2Cells

    DEFF Research Database (Denmark)

    Knudsen, Kristian Bastholm; Vegge, Tejs; McCloskey, Bryan D.;

    2016-01-01

    + will activate the formation of toroidal shaped Li2O2, thereby dramatically increasing cell capacity. Here we apply porous electrode theory to electrochemical impedance measured at the Li-O2 cathode to investigate changes in the surface- and ionic resistance within the pores under conditions where either...... the surface-mechanism or the solution-mechanism is favored. Our experimental observations show that (i) an additional charge transfer process is observed in the impedance spectrum where the solution-based mechanism is favored; (ii) that the changes in the ionic resistance in the cathode during discharge...

  19. Sensitivity improvement of a miniaturized label-free electrochemical impedance biosensor by electrode edge effect

    Science.gov (United States)

    Kuo, Yi-Ching; Chen, Ching-Sung; Chang, Ku-Ning; Lin, Chih-Ting; Lee, Chih-Kung

    2014-07-01

    Point-of-care (PoC) biosensors continue to gain popularity because of the desire to improve cost performance in today's health care industry. As cardiovascular disease (CVD) remains one of the top three leading causes of death in Asia, a tool that can help to detect CVDs is highly sought after. We present a high-sensitivity PoC biosensor that can be used to detect CVD biomarkers. To meet the requirements of a PoC biosensor, we adopted electrochemical methods as the basis of the detection. A more stable three-electrode configuration was miniaturized and put onto a biochip. To improve the detection sensitivity associated with the reduced size in the biochip, computer simulation was used to investigate several potential effective possibilities. We found that the electrolyte current density on the edge near the working electrode (WE) and counter electrode (CE) was higher. This was verified using an atomic force microscope to measure the surface potential. We then experimented with the configuration by lengthening the edge of the WE and CE without changing the area of the WE and CE and maintained the gap between the two electrodes. We found improved measurement efficiency with our newly developed biochip.

  20. Immobilization and hybridization of DNA based on magnesium ion modified 2,6-pyridinedicarboxylic acid polymer and its application for label-free PAT gene fragment detection by electrochemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    JIAO Kui; YANG Tao; YANG Jie; FENG YuanYuan

    2007-01-01

    A new approach for a simple electrochemical detection of PAT gene fragment is described. Poly(2,6-pyridinedicarboxylic acid) (PDC) modified glassy carbon electrode (GCE) was prepared by potential scan electropolymerization in an aqueous solution. Mg2+ ions were incorporated by immersion of the modified electrode in 0.5 mol/L aqueous solution of MgCl2 to complete the preparation of a generic "activated" electrode ready for binding the probe DNA. The ssDNA was linked to the conducting polymer by forming a bidentate complex between the carboxyl groups on the polymer and the phosphate groups of DNA via Mg2+. DNA immobilization and hybridization were characterized with differential pulse voltammetry (DPV) by using methylene blue (MB) as indicator and electrochemical impedance spectroscopy (EIS). The EIS was of higher sensitivity for DNA detection as compared with voltammetric methods in our strategy. The electron transfer resistance (Ret) of the electrode surface in EIS in [Fe(CN)6]3-/4- solution increased after the immobilization of the DNA probe on the Mg/PDC/GCE electrode. The hybridization of the DNA probe with complementary DNA (cDNA) made Ret increase further. The difference between the Ret at ssDNA/Mg/PDC/GCE and that at hybridization DNA modified electrode (dsDNA/Mg/PDC/GCE) was applied to determine the specific sequence related to the target PAT gene with the dynamic range comprised between 1.0×10-9 and 1.0×10-5 mol/L. A detection limit of 3.4×10-10 mol/L of oligonucleotides can be estimated.

  1. Immobilization and hybridization of DNA based on magnesium ion modified 2,6-pyridinedicarboxylic acid polymer and its application for label-free PAT gene fragment detection by electrochemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A new approach for a simple electrochemical detection of PAT gene fragment is described. Poly(2,6-pyridinedicarboxylic acid) (PDC) modified glassy carbon electrode (GCE) was prepared by potential scan electropolymerization in an aqueous solution. Mg2+ ions were incorporated by immer-sion of the modified electrode in 0.5 mol/L aqueous solution of MgCl2 to complete the preparation of a generic "activated" electrode ready for binding the probe DNA. The ssDNA was linked to the conduct-ing polymer by forming a bidentate complex between the carboxyl groups on the polymer and the phosphate groups of DNA via Mg2+. DNA immobilization and hybridization were characterized with dif-ferential pulse voltammetry (DPV) by using methylene blue (MB) as indicator and electrochemical im-pedance spectroscopy (EIS). The EIS was of higher sensitivity for DNA detection as compared with voltammetric methods in our strategy. The electron transfer resistance (Ret) of the electrode surface in EIS in [Fe(CN)6]3-/4- solution increased after the immobilization of the DNA probe on the Mg/PDC/GCE electrode. The hybridization of the DNA probe with complementary DNA (cDNA) made Ret increase further. The difference between the Ret at ssDNA/Mg/PDC/GCE and that at hybridization DNA modified electrode (dsDNA/Mg/PDC/GCE) was applied to determine the specific sequence related to the target PAT gene with the dynamic range comprised between 1.0 × 10-9 and 1.0 × 105 mol/L. A detection limit of 3.4 × 10-10 mol/L of oligonucleotides can be estimated.

  2. Applications of electrochemical techniques in mineral analysis.

    Science.gov (United States)

    Niu, Yusheng; Sun, Fengyue; Xu, Yuanhong; Cong, Zhichao; Wang, Erkang

    2014-09-01

    This review, covering reports published in recent decade from 2004 to 2013, shows how electrochemical (EC) techniques such as voltammetry, electrochemical impedance spectroscopy, potentiometry, coulometry, etc., have made significant contributions in the analysis of minerals such as clay, sulfide, oxide, and oxysalt. It was discussed based on the classifications of both the types of the used EC techniques and kinds of the analyzed minerals. Furthermore, minerals as electrode modification materials for EC analysis have also been summarized. Accordingly, research vacancies and future development trends in these areas are discussed.

  3. Electrochemical impedance spectroscopy analysis with a symmetric cell for LiCoO2 cathode degradation correlated with Co dissolution

    Directory of Open Access Journals (Sweden)

    Hiroki Nara

    2016-04-01

    Full Text Available Static degradation of LiCoO2 cathodes is a problem that hinders accurate analysis using our developed separable symmetric cell. Therefore, in this study we investigate the static degradation of LiCoO2 cathodes in separable symmetric cells by electrochemical impedance spectroscopy (EIS and inductively coupled plasma analyses. EIS measurements of LiCoO2 cathodes are conducted in various electrolytes, with different anions and with or without HF and/or H2O. This allows us to determine the static degradation of LiCoO2 cathodes relative to their increase of charge transfer resistance. The increase of the charge transfer resistance of the LiCoO2 cathodes is attributed to cobalt dissolution from the active material of LiCoO2. Cobalt dissolution from LiCoO2 is revealed to occur even at low potential in the presence of HF, which is generated from LiPF6 and H2O. The results indicate that avoidance of HF generation is important for the analysis of lithium-ion battery electrodes by using the separable cell. These findings reveal the condition to achieve accurate analysis by EIS using the separable cell.

  4. Electrochemical Impedance Spectroscopy study in micro-grain structured amorphous silicon anodes for lithium-ion batteries

    Science.gov (United States)

    Paloukis, Fotis; Elmasides, Costas; Farmakis, Filippos; Selinis, Petros; Neophytides, Stylianos G.; Georgoulas, Nikolaos

    2016-11-01

    In this paper, a study of the lithiation mechanism of micro-grain structured silicon anode is presented. Micro-grain amorphous silicon was deposited on special copper foil and it is shown that after several decades of galvanostatic cycles, it preserves its granular nature with minor degradation. In order to shed light on the lithiation mechanisms of the micro-grain silicon, Electrochemical Impedance Spectroscopy (EIS) was conducted on silicon half-cells at various State-of-Charge (SoC) and various discharging current values and the Solid-Electrolyte Interphase (SEI) RSEI and polarization resistance Rpol were determined. Results reveal that Rpol highly increases for cell voltages lower than 0.2 V and it strongly depends on the discharging C-rate. From X-ray Photoelectron Spectroscopy (XPS) measurements combined with surface sputtering, the existence of a LixSiyOz interlayer between SEI and silicon is confirmed, which is believed to play an important role to the lithium kinetics. Finally, combining our results, a lithiation mechanism of the micro-grain silicon anode is proposed.

  5. Raman and electrochemical impedance studies of sol-gel titanium oxide and single walled carbon nanotubes composite films.

    Science.gov (United States)

    Rincón, M E; Trujillo-Camacho, M E; Miranda-Hernández, M; Cuentas-Gallegos, A K; Orozco, G

    2007-01-01

    Titanium oxide grown by a sol-gel route on single-walled carbon nanotubes was studied by Raman and Electrochemical Impedance techniques and compared with mixtures obtained by mechanical grinding. In spite of the superior dispersion of single-walled carbon nanotubes bundles in sol-gel composites, the lost of the small-diameter carbon nanotubes in the oxidizing sol-gel bath was inferred from their Raman spectra and the lower capacitive current of the voltammograms in 0.1 M H2SO4. We proposed proton electrosorption as the main charge storage mechanism for sol-gel composites, favoured by the hydroxylation and n-type conductivity of the oxide, while electrodes based on mixtures were dominated by double-layer charging, developing some pseudocapacitance with potential cycling due to the reversible oxidation of carbon nanotubes. Comparsion with TiO2/Carbon Blacks composites shows the effective role of single-walled carbon nanotubes as templates to control the mesoporous nature of sol-gel composite electrodes.

  6. An electrochemical impedance spectroscopic study of the electronic and ionic transport properties of LiCoO2 cathode

    Institute of Scientific and Technical Information of China (English)

    ZHUANG QuanChao; XU JinMei; FAN XiaoYong; DONG QuanFeng; JIANG YanXia; HUANG Ling; SUN ShiGang

    2007-01-01

    The storage behavior and process of the first delithiation-lithiation of LiCoO2 cathode were investigated by electrochemical impedance spectroscopy (EIS). The electronic and ionic transport properties of LiCoO2 cathode along with variation of electrode potential were obtained in 1 mol.L-1 LiPF6-EC: DMC:DEC electrolyte solution. It was found that after 9 h storage of the LiCoO2 cathode in electrolyte solutions, a new arc appears in the medium frequency range in Nyquist plots of ElS, which increases with increasing the storage time. In the charge/discharge processes, the diameter of the new arc is reversibly changed with electrode potential. Such variation coincides well with the electrode potential dependence of electronic conductivity of the LiCoO2. Thus this new ElS feature is attributed to the change of electronic conductivity of LixCoO2 during storage of the LiCoO2 cathode in electrolyte solutions, as well as in processes of intercalation-deintercalationtion of lithium ions. It has been revealed that the reversible increase and decrease of the resistance of SEI film in charge-discharge processes can be also ascribed to the variation of electronic conductance of active materials of the LiCoO2 cathode.

  7. The electrochemical impedance spectroscopy of silver doped hydroxyapatite coating in simulated body fluid used as corrosive agent

    Directory of Open Access Journals (Sweden)

    Mišković-Stanković Vesna

    2012-01-01

    Full Text Available Titanium is a key biomedical material due its good biocompatibility, mechanical properties and corrosion stability, but infections of the implantation site still pose serious threat. One approach to prevent infection is to improve antimicrobial ability of the coating material. Silver doped hydroxyapatite (Ag/HAP nanoparticles were synthesized by new modified precipitation method. The synthesized powder was used for preparation of Ag/HAP coating on titanium by electrophoretic deposition. The coating was characterized in terms of phase composition and structure by Attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR and X-ray diffraction (XRD; surface morphology and chemical composition was assessed using scanning electron microscopy (SEM and energy dispersive spectroscopy (EDS. Research focused on evaluation of the corrosion behaviour of Ag/HAP coating in simulated body fluid (SBF at 37 ºC during prolonged immersion time by electrochemical impedance spectroscopy (EIS. Silver doped HAP coating provided good corrosion protection in SBF solution. [Acknowledgements. This research was financed by the Ministry of Education, Science and Technological Development of the Republic of Serbia, contracts No. III 45019 and by National Sciences and Engineering Research Council of Canada (NSERC. Dr Ana Jankovic was financed by the FP7 Nanotech FTM Grant Agreement 245916

  8. An Electrochemical Impedance Spectroscopy-Based Technique to Identify and Quantify Fermentable Sugars in Pineapple Waste Valorization for Bioethanol Production

    Directory of Open Access Journals (Sweden)

    Claudia Conesa

    2015-09-01

    Full Text Available Electrochemical Impedance Spectroscopy (EIS has been used to develop a methodology able to identify and quantify fermentable sugars present in the enzymatic hydrolysis phase of second-generation bioethanol production from pineapple waste. Thus, a low-cost non-destructive system consisting of a stainless double needle electrode associated to an electronic equipment that allows the implementation of EIS was developed. In order to validate the system, different concentrations of glucose, fructose and sucrose were added to the pineapple waste and analyzed both individually and in combination. Next, statistical data treatment enabled the design of specific Artificial Neural Networks-based mathematical models for each one of the studied sugars and their respective combinations. The obtained prediction models are robust and reliable and they are considered statistically valid (CCR% > 93.443%. These results allow us to introduce this EIS-based technique as an easy, fast, non-destructive, and in-situ alternative to the traditional laboratory methods for enzymatic hydrolysis monitoring.

  9. An Electrochemical Impedance Spectroscopy-Based Technique to Identify and Quantify Fermentable Sugars in Pineapple Waste Valorization for Bioethanol Production.

    Science.gov (United States)

    Conesa, Claudia; García-Breijo, Eduardo; Loeff, Edwin; Seguí, Lucía; Fito, Pedro; Laguarda-Miró, Nicolás

    2015-09-11

    Electrochemical Impedance Spectroscopy (EIS) has been used to develop a methodology able to identify and quantify fermentable sugars present in the enzymatic hydrolysis phase of second-generation bioethanol production from pineapple waste. Thus, a low-cost non-destructive system consisting of a stainless double needle electrode associated to an electronic equipment that allows the implementation of EIS was developed. In order to validate the system, different concentrations of glucose, fructose and sucrose were added to the pineapple waste and analyzed both individually and in combination. Next, statistical data treatment enabled the design of specific Artificial Neural Networks-based mathematical models for each one of the studied sugars and their respective combinations. The obtained prediction models are robust and reliable and they are considered statistically valid (CCR% > 93.443%). These results allow us to introduce this EIS-based technique as an easy, fast, non-destructive, and in-situ alternative to the traditional laboratory methods for enzymatic hydrolysis monitoring.

  10. Electrochemical impedance spectroscopy-a simple method for the characterization of polymer inclusion membranes containing aliquat 336.

    Science.gov (United States)

    O'Rourke, Michelle; Duffy, Noel; Marco, Roland De; Potter, Ian

    2011-06-23

    Electrochemical impedance spectroscopy (EIS) has been used to estimate the non-frequency dependent (static) dielectric constants of base polymers such as poly(vinyl chloride) (PVC), cellulose triacetate (CTA) and polystyrene (PS). Polymer inclusion membranes (PIMs) containing different amounts of PVC or CTA, along with the room temperature ionic liquid Aliquat 336 and plasticizers such as trisbutoxyethyl phosphate (TBEP), dioctyl sebecate (DOS) and 2-nitrophenyloctyl ether (NPOE) have been investigated. In this study, the complex and abstract method of EIS has been applied in a simple and easy to use way, so as to make the method accessible to membrane scientists and engineers who may not possess the detailed knowledge of electrochemistry and interfacial science needed for a rigorous interpretation of EIS results. The EIS data reported herein are internally consistent with a percolation threshold in the dielectric constant at high concentrations of Aliquat 336, which illustrates the suitability of the EIS technique since membrane percolation with ion exchangers is a well-known phenomenon.

  11. Electrochemical Impedance Spectroscopy—A Simple Method for the Characterization of Polymer Inclusion Membranes Containing Aliquat 336

    Directory of Open Access Journals (Sweden)

    Michelle O’Rourke

    2011-06-01

    Full Text Available Electrochemical impedance spectroscopy (EIS has been used to estimate the non-frequency dependent (static dielectric constants of base polymers such as poly(vinyl chloride (PVC, cellulose triacetate (CTA and polystyrene (PS. Polymer inclusion membranes (PIMs containing different amounts of PVC or CTA, along with the room temperature ionic liquid Aliquat 336 and plasticizers such as trisbutoxyethyl phosphate (TBEP, dioctyl sebecate (DOS and 2-nitrophenyloctyl ether (NPOE have been investigated. In this study, the complex and abstract method of EIS has been applied in a simple and easy to use way, so as to make the method accessible to membrane scientists and engineers who may not possess the detailed knowledge of electrochemistry and interfacial science needed for a rigorous interpretation of EIS results. The EIS data reported herein are internally consistent with a percolation threshold in the dielectric constant at high concentrations of Aliquat 336, which illustrates the suitability of the EIS technique since membrane percolation with ion exchangers is a well-known phenomenon.

  12. Electrochemical impedance spectroscopy study of high-palladium dental alloys. Part I: behavior at open-circuit potential.

    Science.gov (United States)

    Sun, D; Monaghan, P; Brantley, W A; Johnston, W M

    2002-05-01

    Electrochemical impedance spectroscopy (EIS) was used to study the in vitro corrosion of three representative high-palladium alloys and a gold-palladium alloy for comparison. The corrosion resistances (measured as the charge transfer resistance R(CT) from an equivalent circuit) of the high-palladium alloys and the gold-palladium alloy were comparable in simulated body fluid and oral environments, and under simulated dental plaque. The great similarity in corrosion behavior for the three high-palladium alloys is largely attributed to their substantial palladium content and passivity in the laboratory test media, and possibly to their similar structure at the submicron level. Differences in composition and microstructure at the micron level and greater, including the effects of heat treatment simulating the firing cycles for dental porcelain, do not have noteworthy effects on the in vitro corrosion of the three high-palladium alloys. Good accuracy and convenience of extracting corrosion characteristics from equivalent circuit modeling, along with the capability of providing intrinsic information about the corrosion mechanism, enable EIS to be an excellent alternative method to conventional potentiodynamic polarization for evaluating the corrosion behavior of noble dental alloys.

  13. Polylactic acid coating on a biodegradable magnesium alloy: An in vitro degradation study by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Alabbasi, Alyaa; Liyanaarachchi, S.; Kannan, M. Bobby, E-mail: bobby.mathan@jcu.edu.au

    2012-09-30

    Polylactic acid (PLA) was coated on a biodegradable magnesium alloy, AZ91, using spin coating technique for temporary implant applications. The degradation behaviour of the coated alloy samples was evaluated using electrochemical impedance spectroscopy (EIS) method in simulated body fluid (SBF). EIS results suggested that the PLA coating enhanced the degradation resistance of the alloy significantly. Increase in the PLA coating thickness was found to increase the degradation resistance, but resulted in poor adhesion. Long-term EIS experiments of the PLA coated samples suggested that their degradation resistance gradually decreased with increase in SBF exposure time. However, the degradation resistance of the PLA coated samples was significantly higher than that of the bare metal even after a 48 h exposure to SBF. - Highlights: Black-Right-Pointing-Pointer Polylactic acid (PLA) was coated on a magnesium-based alloy. Black-Right-Pointing-Pointer PLA coating enhanced the in vitro degradation resistance of the alloy. Black-Right-Pointing-Pointer Increase in the PLA coating thickness improved the alloy degradation resistance. Black-Right-Pointing-Pointer Thin film PLA coating exhibited both good degradation resistance and adhesion.

  14. Position dependent analysis of membrane electrode assembly degradation of a direct methanol fuel cell via electrochemical impedance spectroscopy

    Science.gov (United States)

    Hartmann, Peter; Zamel, Nada; Gerteisen, Dietmar

    2013-11-01

    The performance of a direct methanol fuel cell MEA degraded during an operational period of more than 3000 h in a stack is locally examined using electrochemical impedance spectroscopy. Therefore, after disassembling the MEA is cut into small pieces and analyzed in a 1 cm2 test cell. Using a reference electrode, we were capable of measuring the anode and cathode spectra separately. The spectra of the segments at different positions do not follow a specified trend from methanol inlet to outlet of the stack flow field. The anode spectra were analyzed with an equivalent circuit simulation. The conductance of the charge transfer was found to increase with current density up to a point where a raising limitation process of the complex methanol oxidation dominates, which is not a bottleneck at low current density. Further, an increase of the double layer capacitance with current density was observed. The diffusion resistance was calculated as an effective diffusion coefficient in the order of 10-10 m2 s-1; implying that the diffusion limitation is not the bulk diffusion in the backing layer. Finally, the degree of poisoning of the catalysts by carbon monoxide was measured as a pseudo inductive arc and decreases with increasing current.

  15. Study of benzotriazole as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    Energy Technology Data Exchange (ETDEWEB)

    Solehudin, Agus, E-mail: asolehudin@upi.edu [Department of Mechanical Engineering Education, Indonesia University of Education (UPI), Bandung, West Java (Indonesia); Nurdin, Isdiriayani [Department of Chemical Engineering, Bandung Institute of Technology, Bandung, West Java (Indonesia)

    2014-03-24

    Corrosion and inhibition studies on API 5LX65 carbon steel in chloride solution containing various concentrations of benzotriazole has been conducted at temperature of 70°C using Electrochemical Impedance Spectroscopy (EIS). Corroded carbon steel surface with and without inhibitor have been observed using X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Energy Dispersive Spectroscopy (EDS). The objectives of this research are to study the performance of benzotriazole as corrosion inhibitors. The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H{sub 2}S at different BTAH concentrations showed that corrosion rate of carbon steel decreases with increasing of BTAH concentrations from 0 to 10 mmol/l. The inhibition efficiency of BTAH was found to be affected by its concentration. The optimum efficiency obtained of BTAH is 93% at concentration of 5 mmol/l. The result of XRD and EDS analysis reveal the iron sulfide (FeS) formation on corroded carbon steel surface without inhibitor. The EDS spectrum show the Nitrogen (N) bond on carbon steel surface inhibited by BTAH.

  16. Marine bio-fouling of different alloys exposed to continuous flowing fresh seawater by electrochemical impedance spectroscopy

    Directory of Open Access Journals (Sweden)

    Khalid Al-Muhanna

    2016-07-01

    Full Text Available The petroleum industry and desalination plants suffer from marine bio-fouling problems that have a major role in the stimulation of the corrosion process. Thus, the aim of this study was to investigate the effect of the micro and the macro-organisms, on the corrosion behavior of different alloys used in Kuwait’s industries. The alloys used in this study were; sanicro 28, stainless steel 316L, Cu–Ni 70–30, and titanium. The electrochemical impedance spectroscopy was used in this study in order to determine the corrosion susceptibility of different alloys exposed to continuous fresh seawater. This was achieved by calculating the charge transfer resistance of the metal surface and the resistance of the solution. The total exposure time of the tests was about 180 days. The visual inspection of the tested samples, showed a bio-film formation on the surface of these samples. Also, it was observed that the stainless steel 316, sanicro 28, Cu–Ni 70–30, and titanium alloys exhibited good corrosion resistance.

  17. Single domain antibody coated gold nanoparticles as enhancer for Clostridium difficile toxin detection by electrochemical impedance immunosensors

    Science.gov (United States)

    Zhu, Zanzan; Shi, Lianfa; Feng, Hanping; Zhou, H. Susan

    2016-01-01

    This work presents a sandwich-type electrochemical impedance immunosensor for detecting Clostridium difficile toxin A (TcdA) and toxin B (TcdB). Single domain antibody conjugated gold nanoparticles were applied to amplify the detection signal. Gold nanoparticles (Au NPs) were characterized by transmission electron microscopy and UV–vis spectra. The electron transfer resistance (Ret) of the working electrode surface was used as a parameter in the measurement of the biosensor. With the increase of the concentration of toxins from 1 pg/mL to 100 pg/mL, a linear relationship was observed between the relative electron transfer resistance and toxin concentration. In addition, the detection signal was enhanced due to the amplification effect. The limit of detection for TcdA and TcdB was found to be 0.61 pg/mL and 0.60 pg/mL respectively at a signal-to-noise ratio of 3 (S/N = 3). This method is simple, fast and ultrasensitive, thus possesses a great potential for clinical applications in the future. PMID:25460611

  18. Exfoliation corrosion of 7150 Al alloy with various tempers and its electrochemical impedance spectroscopy in EXCO solution

    Energy Technology Data Exchange (ETDEWEB)

    Li, J.F. [School of Materials Science and Engineering, Central South University, Changsha (China); The Key Laboratory of Nonferrous Metal Materials Science and Engineering, Ministry of Education, Changsha (China); Jia, Z.Q.; Li, C.X. [School of Materials Science and Engineering, Central South University, Changsha (China); Birbilis, N. [Department of Materials Engineering, ARC Centre of Excellence for Design in Light Metals, Monash University, Monash, Victoria (Australia); Cai, C. [School of Chemistry and Chemical Engineering, Ningxia University, Yinchuan (China)

    2009-06-15

    The exfoliation corrosion susceptibility and electrochemical impedance spectroscopy (EIS) of 7150 Al alloys with T6, T73, and RRA (retrogression at 175 C for 3 h) tempers in EXCO solution were investigated. The anodic equilibrium precipitate {eta}(MgZn{sub 2}) is continuous or closely spaced at the grain boundaries in the 7150-T6 Al alloy, resulting in its greatest susceptibility to exfoliation corrosion. The grain boundary {eta} precipitates in the RRA and T73 treated 7150 Al alloys are coarsened and show a clear discontinuous nature; they possess similar exfoliation corrosion sensitivity and their exfoliation corrosion resistance is greatly increased. At the beginning of immersion in EXCO solution, the EIS plot of the 7150 Al alloys is composed of a capacitive arc in the high to medium frequency range and an inductive component in the medium to low frequency range. As immersion time is increased, exfoliation corrosion with different corrosion ratings occurs on the surface of the 7150 Al alloy with various tempers, two capacitive arcs appear in the high to medium and medium to low frequency ranges, respectively. The fitted medium to low frequency capacitance C{sub 2} of 7150-T6 Al alloy, corresponding to the new surface caused by the exfoliation corrosion, is much greater than that of the T73 and RRA treated 7150 Al alloy, which is consistent with the greatest exfoliation corrosion susceptibility of the 7150-T6 Al alloy. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  19. An Electrochemical Impedance Spectroscopy-Based Technique to Identify and Quantify Fermentable Sugars in Pineapple Waste Valorization for Bioethanol Production

    Science.gov (United States)

    Conesa, Claudia; García-Breijo, Eduardo; Loeff, Edwin; Seguí, Lucía; Fito, Pedro; Laguarda-Miró, Nicolás

    2015-01-01

    Electrochemical Impedance Spectroscopy (EIS) has been used to develop a methodology able to identify and quantify fermentable sugars present in the enzymatic hydrolysis phase of second-generation bioethanol production from pineapple waste. Thus, a low-cost non-destructive system consisting of a stainless double needle electrode associated to an electronic equipment that allows the implementation of EIS was developed. In order to validate the system, different concentrations of glucose, fructose and sucrose were added to the pineapple waste and analyzed both individually and in combination. Next, statistical data treatment enabled the design of specific Artificial Neural Networks-based mathematical models for each one of the studied sugars and their respective combinations. The obtained prediction models are robust and reliable and they are considered statistically valid (CCR% > 93.443%). These results allow us to introduce this EIS-based technique as an easy, fast, non-destructive, and in-situ alternative to the traditional laboratory methods for enzymatic hydrolysis monitoring. PMID:26378537

  20. Evaluation of polymer electrolyte membrane fuel cells by electrochemical impedance spectroscopy under different operation conditions and corrosion

    Energy Technology Data Exchange (ETDEWEB)

    Kumagai, Masanobu [Taiyo Stainless Spring Co., Ltd., 2-8-6 Shakujiicho, Nerimaku, Tokyo 177-0041 (Japan); Myung, Seung-Taek; Ichikawa, Takuma; Yashiro, Hitoshi [Department of Chemical Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate 020-8551 (Japan)

    2010-09-01

    Electrochemical impedance spectroscopy (EIS) was employed for in situ diagnosis for polymer electrolyte membrane fuel cells during operation. First, EIS was measured as a function of operation parameters such as applied current density, gas flow rates and gas humidification temperature. The resistance that correlated with conductivity of the membrane and the contact resistance between bipolar plate and gas diffusion layer (GDL) was set as R{sub m} in the assumed equivalent circuit. The charge transfer resistances were considered for cathode (R{sub ct}(C)). The value of R{sub ct}(C) was sensitive to the parameters that affected cell voltage. Additionally, the diffusion resistance (R{sub d}) was ascribed to the effect of oxygen supply and drainage of generated water. Second, the influence of corrosion of type 430 stainless steel bipolar plates was evaluated by EIS method during operation. Corrosion of the stainless steel bipolar plates resulted in an increase in the value of R{sub d}. (author)

  1. Electrochemical Impedance Spectroscopy—A Simple Method for the Characterization of Polymer Inclusion Membranes Containing Aliquat 336

    Science.gov (United States)

    O'Rourke, Michelle; Duffy, Noel; De Marco, Roland; Potter, Ian

    2011-01-01

    Electrochemical impedance spectroscopy (EIS) has been used to estimate the non-frequency dependent (static) dielectric constants of base polymers such as poly(vinyl chloride) (PVC), cellulose triacetate (CTA) and polystyrene (PS). Polymer inclusion membranes (PIMs) containing different amounts of PVC or CTA, along with the room temperature ionic liquid Aliquat 336 and plasticizers such as trisbutoxyethyl phosphate (TBEP), dioctyl sebecate (DOS) and 2-nitrophenyloctyl ether (NPOE) have been investigated. In this study, the complex and abstract method of EIS has been applied in a simple and easy to use way, so as to make the method accessible to membrane scientists and engineers who may not possess the detailed knowledge of electrochemistry and interfacial science needed for a rigorous interpretation of EIS results. The EIS data reported herein are internally consistent with a percolation threshold in the dielectric constant at high concentrations of Aliquat 336, which illustrates the suitability of the EIS technique since membrane percolation with ion exchangers is a well-known phenomenon. PMID:24957616

  2. Electrochemical impedance spectroscopy to study photo - induced effects on self-organized TiO{sub 2} nanotube arrays

    Energy Technology Data Exchange (ETDEWEB)

    Pu, P.; Cachet, H. [CNRS, UPR15, Laboratoire Interfaces et Systemes Electrochimiques, F-75005 Paris (France); UPMC Univ Paris 06, UPR15, LISE, 4 place Jussieu, F-75005 Paris (France); Sutter, E.M.M., E-mail: eliane-sutter@upmc.f [CNRS, UPR15, Laboratoire Interfaces et Systemes Electrochimiques, F-75005 Paris (France); UPMC Univ Paris 06, UPR15, LISE, 4 place Jussieu, F-75005 Paris (France)

    2010-08-01

    Two different morphologies of nano-structured titanium dioxide-a nanotubular layer and a compact layer - were obtained by anodization of titanium in fluoride-based baths, and the photo-induced effects of these layers were investigated by electrochemical impedance spectroscopy (EIS). The first layer showed long-lasting photo-induced modifications after UV illumination, whereas, in the case of the compact layer, no long-lasting UV-induced modifications were observed. Before light exposure, in the nanotubular layer, only the bottom of the tubes were electro-active and contributed to the conduction of the layer. Moreover an exponential distribution of surface states could be evidenced. After UV exposure, the surface states were filled by the photo-generated electrons, leading to activation of the walls of the tubes by inserted hydrogen, and to a hundred fold increase in the space charge layer capacitance. This capacitance increase was attributed to an increase in the active surface of the layer, but also to an increase in the charge carrier density.

  3. The Application of Electrochemical Impedance Techniques in Analyzing the AC Response of Some Two-electron Transfer Dye Systems

    Directory of Open Access Journals (Sweden)

    Farouk Rashwan

    2005-01-01

    Full Text Available The Electrochemical Impedance Spectroscopic techniques (EIS were used to investigate the behavior of some dye compounds (quinoid systems characterized with 2e-transfer processes. For this purpose, Alizarin Red S (ARS, Alizarin Cyanine (AC, Alizarin Viridin (AV and carminic acid were chosen for the measurements. The EIS experiments were performed using a small AC amplitude (10 mV p-p in addition to a relatively wide frequency range (0.01 Hz ≤ f ≤ 105 Hz. The investigations were carried out at room temperature in aqueous media (HClO4, NaClO4 and KNO3 on the Hanging Mercury Drop Electrode (HMDE and for comparison one experiment only was measured in aprotic solvent (DMF on the Pt-disc electrode. The EIS diagrams of these systems were characterized in the complex plane by two fundamental observations, the first of which is a straight line crossing the real axis at an angle of 45° (or at least nearly so and the second one is two semicircles beside each other corresponding to high-frequency and low-frequency regions, which are implying the presence of well-separated time constants. The EIS characteristic parameters for these dye systems were calculated and discussed.

  4. Study of benzotriazole as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    Science.gov (United States)

    Solehudin, Agus; Nurdin, Isdiriayani

    2014-03-01

    Corrosion and inhibition studies on API 5LX65 carbon steel in chloride solution containing various concentrations of benzotriazole has been conducted at temperature of 70°C using Electrochemical Impedance Spectroscopy (EIS). Corroded carbon steel surface with and without inhibitor have been observed using X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Energy Dispersive Spectroscopy (EDS). The objectives of this research are to study the performance of benzotriazole as corrosion inhibitors. The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H2S at different BTAH concentrations showed that corrosion rate of carbon steel decreases with increasing of BTAH concentrations from 0 to 10 mmol/l. The inhibition efficiency of BTAH was found to be affected by its concentration. The optimum efficiency obtained of BTAH is 93% at concentration of 5 mmol/l. The result of XRD and EDS analysis reveal the iron sulfide (FeS) formation on corroded carbon steel surface without inhibitor. The EDS spectrum show the Nitrogen (N) bond on carbon steel surface inhibited by BTAH.

  5. Electrochemical impedance spectroscopy and X-ray photoelectron spectroscopy study of the corrosion behaviour of galvanized steel and electroplating steel

    Energy Technology Data Exchange (ETDEWEB)

    Lebrini, M., E-mail: mlebrini@yahoo.fr [Laboratoire des Procedes d' Elaboration des Revetements Fonctionnels, PERF-LSPES UMR CNRS 8008, ENSCL, BP 90108, F-59652 Villeneuve d' Ascq Cedex (France); Traisnel, M. [Laboratoire des Procedes d' Elaboration des Revetements Fonctionnels, PERF-LSPES UMR CNRS 8008, ENSCL, BP 90108, F-59652 Villeneuve d' Ascq Cedex (France); Gengembre, L. [Unite de Catalyse et Chimie du solide UMR 8181 Bat C3, USTL, F-59655, Villeneuve d' Ascq Cedex (France); Fontaine, G. [Laboratoire des Procedes d' Elaboration des Revetements Fonctionnels, PERF-LSPES UMR CNRS 8008, ENSCL, BP 90108, F-59652 Villeneuve d' Ascq Cedex (France); Lerasle, O.; Genet, N. [TOTAL France, Centre de Recherche de Solaize, Chemin du canal, BP 22, F-69360 Solaize (France)

    2011-02-01

    The efficiency of a formula containing 2-{l_brace}(2-hydroxyethyl)[(4-methyl-1H-1,2,3-benzotriazol-1-yl)methyl] amino{r_brace}ethanol (tolyltriazole) and decanoic acid as corrosion inhibitor for galvanized steel and electroplating steel in aqueous solution have been determined by electrochemical impedance spectroscopy (EIS) techniques. The experimental data obtained from this method show a frequency distribution and therefore a modelling element with frequency dispersion behaviour, a constant phase element (CPE) has been used. The corrosion behaviour in the presence of different concentration of decanoic acid (DA) in the formula was also investigated by EIS. Results obtained reveal that, the formula is a good inhibitor for galvanized steel and electroplating steel in aqueous solution, the better performance was obtained in the case of galvanized steel. The ability of the inhibitor to be adsorbed on the surface was dependent on the nature of metal. X-ray photoelectron spectroscopy surface analysis with inhibitor shows that it's chemisorbed at the galvanized and electroplating steel/aqueous solution interface.

  6. Electrochemical impedance study on the corrosion of Al-Pure in hydrochloric acid solution using Schiff bases

    Indian Academy of Sciences (India)

    A S Patel; V A Panchal; N K Shah

    2012-04-01

    The inhibition effect of newly synthesized Schiff bases -benzylidene benzylamine (A) and benzenemethanamine--methyl--(phenylmethylene) (B) on the corrosion behaviour of Al-Pure in 1.0 M HCl was studied using galvanostatic polarization and electrochemical impedance spectroscopy (EIS) and adsorption studies. The effects of inhibitor concentration, temperature and surface coverage are investigated. The effect of inhibitor concentration and other parameters are evaluated for different inhibitor concentrations and the probable mechanism was also proposed. The results show that (A) and (B) possess excellent inhibiting effect for the corrosion of Al-Pure and the inhibitors act as mixed type inhibitors. The inhibitors do not affect the mechanism of the electrode processes and inhibit corrosion by blocking the reaction sites. The high inhibition efficiency of (A) and (B) were due to the adsorption of inhibitor molecules on the metal surface. The decrease of surface area available for electrode reactions to take place is due to the formation of a protective film. Activation energy and free energy of adsorption have been calculated.

  7. On the sensitivity improvement of a miniaturized label-free electrochemical impedance biosensor

    Science.gov (United States)

    Kuo, Yi-Ching; Chou, Shin-Ting; Tsai, Pei-I.; Li, Guan-Wei; Lin, Chih-Ting; Lee, Chih-Kung

    2014-03-01

    Development of point-of-care biosensors continues to gain popularity due to the demand of improving the cost performance in today's health care. As cardiovascular disease induced death remains on the top 3 death causes for most Asian countries, this paper is to present a high-sensitivity point-of-care biosensor for the detection of cardiovascular disease biomarkers. To meet the point-of-care biosensors requirements, which include characteristics such as small size, low cost, and ease of operation, we adopted electrochemical methods as the basis of detection. The 4-aminothiophenol was adopted as the bio-linkers to facilitate the antibody-antigen interaction. A more stable three-electrode configuration was miniaturized and laid out onto a biochip. A microfluidics subsystem based on opto-piezoelectronic technology was also integrated to create the microfluidic biochip system. To improve the detection sensitivity associated with the reduction in biochip size, electrochemistry simulation was used to investigate several potentially effective means. We found that the electric field on the edge near working electrode and counter electrode was higher, which was verified by using atomic force microscopy to measure the surface potential. With the successful verification, we explored the configuration, i.e., lengthened the edge of working electrode and counter electrode without changing the areas of working electrode and counter electrode and the gap between these two electrodes, so as to evaluate the possibility of improving the measurement efficiency in our newly developed biochips. Detailed design, simulation and experimental results, improved design identified, etc. were all presented in detail.

  8. Electrochemical impedance analysis of electrodeposited Si-O-C composite thick film on Cu microcones-arrayed current collector for lithium ion battery anode

    Science.gov (United States)

    Hang, Tao; Mukoyama, Daikichi; Nara, Hiroki; Yokoshima, Tokihiko; Momma, Toshiyuki; Li, Ming; Osaka, Tetsuya

    2014-06-01

    The impedance behaviors of Si-O-C composite film electrodeposited on Cu microcones-arrayed current collector have been investigated to understand the electrochemical process kinetics that influences the cycling performance when used as a highly-durable anode in a lithium battery. The impedance was measured by using impedance spectroscopy in equilibrium conditions at various depths of discharge and during several hundred charge-discharge cycles. The measured impedance was interpreted with an equivalent circuit composed of solid electrolyte interphase (SEI) film, charge transfer and solid state diffusion. The impedance analysis shows that the change of charge transfer resistance is the main contribution to the total resistance change during discharge, but an abrupt augmentation of diffusive resistance at high depth of discharge is also observed which cannot be explained very well by the presented model. The impedance evolution of this electrode during charge-discharge cycles suggests that the slow growth of the SEI film as well as the increase of the electrode density are responsible for the capacity fading after long term cycling.

  9. Localized Electrochemical Impedance Spectroscopy Study on the Corrosion Behavior of Fe-Cr Alloy in the Solution with Cl- and SO42-

    Institute of Scientific and Technical Information of China (English)

    XIAO Kui; ZHANG Xin; DONG Chaofang; WEI Dan; WANG Chen; LI Xiaogang

    2012-01-01

    The corrosion behaviors of Fe-Cr alloy under three different pH values solutions with Cl-and SO42- were investigated by localized electrochemical impedance spectroscopy (LEIS) measurements and the corrosion products were analyzed by laser Raman spectrometry.The results show that the high corrosion resistance of Fe-Cr Alloy is attributed to a passive film which is formed more easily when the alloy contains a large quantity of Cr element.However,its corrosion resistance varies in the solutions with different pH values,especially in the initial corrosion.The average impedance values in neutral and alkaline solution are much higher than that in acidic solution because the passive film is more likely to dissolve in the acidic condition.Moreover,the destructive effect of Cl- and SO42+ ions on the passive film is also demonstrated in corrosion process through the change of the impedance value with the steeping time.

  10. Measurement of surface resistivity/conductivity of different organic thin films by a combination of optical shearography and electrochemical impedance spectroscopy

    Science.gov (United States)

    Habib, Khaled

    2013-11-01

    Shearography techniques were applied again to measure the surface resistivity/conductivity of different organic thin films on a metallic substrate. The coatings were ACE premium-grey enamel (spray coating), a yellow Acrylic lacquer, and a gold nail polish on a carbon steel substrate. The investigation was focused on determining the in-plane displacement of the coatings by shearography between 20 and 60 °C. Then, the alternating current (AC) impedance (resistance) of the same coated samples was determined by electrochemical impedance spectroscopy (EIS) in 3.0% NaCl solution at room temperature. As a result, the proportionality constant (resistivity or conductivity = 1/surface resistivity) between the determined AC impedance and the in-plane displacement was obtained. The obtained resistivity of all investigated coatings, 40:15 × 106-24:6 × 109Ωcm, was found in the insulator range.

  11. Assessment of the Effects of Flow Rate and Ionic Strength on Microbial Fuel Cell Performance Using Electrochemical Impedance Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Aaron, D [Georgia Institute of Technology; Tsouris, Costas [ORNL; Hamilton, Choo Yieng [ORNL; Borole, Abhijeet P [ORNL

    2010-01-01

    Impedance changes of the anode, cathode and solution were examined for a microbial fuel cell (MFC) under varying conditions in order to improve its performance. An MFC inoculated with a pre-enriched microbial culture resulted in a startup time of ten days. Over this period, the anode impedance decreased below the cathode impedance, suggesting a cathode limited power output. Decreasing the anode flow rate did not impact the anode impedance significantly, while it increased the cathode impedance by 65% . Reducing the anode-medium ionic strength from 100% to 10% increased the cathode impedance by 48%.

  12. Experimental investigation of the effect of indium content on the CuIn{sub 5}S{sub 8} electrodes using electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Gannouni, M., E-mail: gm_mounir@yahoo.fr; Assaker, I. Ben; Chtourou, R.

    2015-01-15

    This paper reports on the use of electrochemical impedance spectroscopy to investigate the electrochemical behavior of spinel CuIn{sub 5}S{sub 8}/electrolyte interface. The CuIn{sub 5}S{sub 8} spinel films have been potentiostatically deposited onto indium tin oxide (ITO)-coated glass substrate. CuCl{sub 2} and InCl{sub 3} mixed solutions with different [Cu]/[In] ratios were used as cation precursor and Na{sub 2}S{sub 2}O{sub 3} as the anion precursor in acidic solution and at room temperature. The effect of the [Cu]/[In] ratio in the precursor solution on the structural, chemical stoichiometry, and morphological properties of prepared samples, as well as the electrochemical behavior of the CuIn{sub 5}S{sub 8}/electrolyte interface was investigated. The electrochemical impedance spectroscopy data have been modeled using an equivalent circuit approach. Several parameters such as, flat-band potential and free carrier concentration were determined by the change in the Mott–Schottky plots.

  13. Study on Electrochemical Copolymerization of Aniline and 3-Methylthiophene in HMIMBF4 Ionic Liquid and Its Properties

    Institute of Scientific and Technical Information of China (English)

    ZHANG Ai-Jian; ZHANG Gui-Rong; YANG Guang-Da; AO Feng-Guo; LU Jia-Xing

    2007-01-01

    Electrochemical polymerization of aniline and 3-methylthiophene has been accomplished in 1-methylimidazium tetrafluoroborate (HMIMBF4) ionic liquid. Homopolymer and copolymers of aniline and 3-methylthiophene were obtained successfully. The copolymer was studied by cyclic voltammetry and electrochemical impedance spectroscopy. The formation of copolymer has been confirmed by FT-IR and UV spectra. The atomic force microscope (AFM) was used for microstructural analysis. Both the homopolymer and the copolymer had the catalytic activity for the hydroquinone.

  14. An electrochemical study of the formation of Benzotriazole surface films on Copper, Zinc and a Copper-Zinc alloy

    OpenAIRE

    Fenelon, Anna M.; Breslin, Carmel B.

    2001-01-01

    The electrochemical behaviour of Cu, Cu–37Zn and Zn in benzotriazole (BTA) containing chloride solutions was studied and compared using potentiodynamic, cyclic voltammetry and electrochemical impedance spectroscopy. The presence of BTA in the chloride-containing solutions gave rise to higher breakdown potentials, significantly higher polarisation resistances and inhibited the formation of CuCl2 and zinc-containing corrosion products. These effects were observed for pure Cu, Cu–Zn and to a som...

  15. Synthesis and characterization of the structural and electrochemical properties of Nd-Al codoped amorphous nickel hydroxide

    Institute of Scientific and Technical Information of China (English)

    刘长久; 陈世娟; 李延伟

    2010-01-01

    Nd-Al codoped amorphous nickel hydroxide powders were synthesized by microemulsion precipitation method combined with rapid freezing technique.The microstructure of the prepared samples was analyzed with X-ray diffractometer(XRD),scanning electron microscopy(SEM),and Raman spectroscopy.The electrochemical performances of the prepared samples were characterized with charge/discharge test,cyclic voltammetry,and electrochemical impedance spectra.The results showed that the codoping of Nd-Al resulted in more st...

  16. Cyclic voltammetry and near edge X-ray absorption fine structure spectroscopy at the Ag L3-edge on electrochemical halogenation of Ag layers on Au(111)

    Science.gov (United States)

    Endo, Osamu; Nakamura, Masashi

    2011-05-01

    One to three layers of Ag grown on a Au(111) electrode were studied by cyclic voltammetry in chloride and bromide solutions and by ex-situ near-edge X-ray absorption fine structure spectroscopy at the Ag L3-edge (Ag L3-NEXAFS). The one and two layers obtained by underpotential deposition exhibited reduced intensity at the absorption edge in the Ag L3-NEXAFS spectra, which suggests the gain of d-electrons in these layers. The cyclic voltammograms and the Ag L3-NEXAFS spectra indicate that the second and third layers of Ag halogenated at positive potentials, whereas the first layer remained in metallic form.

  17. Regioselective electrochemical reduction of 2,4-dichlorobiphenyl - Distinct standard reduction potentials for carbon-chlorine bonds using convolution potential sweep voltammetry

    Science.gov (United States)

    Muthukrishnan, A.; Sangaranarayanan, M. V.; Boyarskiy, V. P.; Boyarskaya, I. A.

    2010-04-01

    The reductive cleavage of carbon-chlorine bonds in 2,4-dichlorobiphenyl (PCB-7) is investigated using the convolution potential sweep voltammetry and quantum chemical calculations. The potential dependence of the logarithmic rate constant is non-linear which indicates the validity of Marcus-Hush theory of quadratic activation-driving force relationship. The ortho-chlorine of the 2,4-dichlorobiphenyl gets reduced first as inferred from the quantum chemical calculations and bulk electrolysis. The standard reduction potentials pertaining to the ortho-chlorine of 2,4-dichlorobiphenyl and that corresponding to para chlorine of the 4-chlorobiphenyl have been estimated.

  18. Electrochemical impedance spectroscopy study of carbon electrodes prepared from date pits and fibers of oil palm empty fruit bunches

    Science.gov (United States)

    Hamdan, E.; Deraman, M.; Suleman, M.; Nor, N. S. M.; Basri, N. H.; Hanappi, M. F. Y. M.; Sazali, N. E. S.; Tajuddin, N. S. M.; Omar, R.; Othman, M. A. R.; Shamsudin, S. A.

    2016-11-01

    In this study, we produced pre-carbonized date pits (PDP) and self-adhesive carbon grains (SACGs) from oil palm empty fruit bunches (EFB) by a low temperature (200°C for DP and 280°C for SACGs, respectively) carbonization method followed by KOH treatment to obtain KOH treated PDP (T-PDP) and KOH treated SACGs (T-SACGs). Four sets of green monolith (GMs) denoted as GM-A, GM-B, GM-C and GM-D were prepared respectively from SACGs (100 wt. %), mixture of PDP and SACGs (50:50 wt. %), T-SACGs (100 wt. %), and mixture of T-SACGs and T-PDP (50:50 wt. %), respectively. From these GMs the respective activated carbon monolith (ACMs) electrodes namely ACM-A, ACM-B, ACM-C and ACM-D were prepared via carbonization (N2 carbonization) and activation (CO2 environment). These ACMs electrodes were used to fabricate the corresponding EDLC cells: Cell-A, Cell-B, Cell-C and Cell-D, respectively. The electrochemical impedance spectroscopy tests conducted on the cells found that the Cell-D showed the maximum value of specific capacitance, Csp (˜ 135 F g-1) whereas the Cell-A showed the minimum values of ESR and characteristic response time, respectively, ˜ 2.14 Ω and ˜ 46 s. Therefore, it can be concluded that the KOH treatment can improve the capacitance but caused the increase in the ESR and response time.

  19. Investigating the role of atomic hydrogen on chloroethene reactions with iron using tafel analysis and electrochemical impedance spectroscopy.

    Science.gov (United States)

    Wang, Jiankang; Farrell, James

    2003-09-01

    Metallic iron filings are commonly employed as reducing agents in permeable barriers used for remediating groundwater contaminated by chlorinated solvents. Reactions of trichloroethylene (TCE) and tetrachloroethylene (PCE) with zerovalent iron were investigated to determine the role of atomic hydrogen in their reductive dechlorination. Experiments simultaneously measuring dechlorination and iron corrosion rates were performed to determine the fractions of the total current going toward dechlorination and hydrogen evolution. Corrosion rates were determined using Tafel analysis, and dechlorination rates were determined from rates of byproduct generation. Electrochemical impedance spectroscopy (EIS) was used to determine the number of reactions that controlled the observed rates of chlorocarbon disappearance, as well as the role of atomic hydrogen in TCE and PCE reduction. Comparison of iron corrosion rates with those for TCE reaction showed that TCE reduction occurred almost exclusively via atomic hydrogen at low pH values and via atomic hydrogen and direct electron transfer at neutral pH values. In contrast, reduction of PCE occurred primarily via direct electron transfer at both low and neutral pH values. At low pH values and micromolar concentrations, TCE reaction rates were faster than those for PCE due to more rapid reduction of TCE by atomic hydrogen. At neutral pH values and millimolar concentrations, PCE reaction rates were faster than those for TCE. This shift in relative reaction rates was attributed to a decreasing contribution of the atomic hydrogen reaction mechanism with increasing halocarbon concentrations and pH values. The EIS data showed that all the rate limitations for TCE and PCE dechlorination occurred during the transfer of the first two electrons. Results from this study show that differences in relative reaction rates of TCE and PCE with iron are dependent on the significance of the reduction pathway involving atomic hydrogen.

  20. A sensitive electrochemical impedance immunosensor for determination of malachite green and leucomalachite green in the aqueous environment.

    Science.gov (United States)

    Zhu, Dan; Li, Qiangqiang; Pang, Xiumei; Liu, Yue; Wang, Xue; Chen, Gang

    2016-08-01

    Application of malachite green (MG) and leucomalachite green (LMG) in fish farm water causes an environmental problem. This study proposes for the first time a sensitive and convenient electrochemical impedance spectroscopy (EIS) method for determining MG and LMG by a bovine serum albumin-decorated gold nanocluster (BSA-AuNC)/antibody composite film-based immunosensor. In order to improve the analytical performance, the glassy carbon electrode (GCE) was modified with 1, 4-phenylenediamine to form a stable layer, and then, BSA-AuNCs were covalently bound to the GCE. An adequate quantity of the polyclonal antibody of LMG was immobilized onto the surface of the BSA-AuNCs by the chemical reaction of EDC/NHS. The sensors can respond to the specific target based on specific covalent bonding. The experimental parameters, such as the pH, incubating concentration, and time, have been investigated and optimized. The calibration curve for LMG was linear in the range of 0.1~10.0 ng/mL with the limit of detection (LOD) 0.03 ng/mL. Furthermore, the sum of MG and LMG was detected in fish farm water by MG reduction. The recovery was between 89.7 % and 99.2 % in spiked samples. The EC sensor method was also compared with the ELISA method and validated by the LC-MS/MS method, which proves its great promise as a field instrument for the rapid monitoring of MG and LMG pollution. Graphical abstract 1, 4-Phenylenediamine and BSA-AuNC/antibody-decorated glassy carbon electrodes have been used for the impedimetric detection of the sum of malachite green and leucomalachite green via specific immuno-binding.

  1. Electrochemical determination of resveratrol in dietary supplements at a boron-doped diamond electrode in the presence of hexadecyltrimethylammonium bromide using square-wave adsorptive stripping voltammetry

    Directory of Open Access Journals (Sweden)

    Yardim Yavuz

    2017-01-01

    Full Text Available A sensitive electroanalytical methodology for the determination of resveratrol is presented for the first time using adsorptive stripping voltammetry at a bare boron-doped diamond (BDD electrode. In cyclic voltammetry, resveratrol shows one irreversible and an adsorption-controlled oxidation peak at a BDD electrode. The voltammetric results indicated that in the presence of hexadecyl trimethyl ammonium bromide, the BDD electrode remarkably enhanced the oxidation of resveratrol, which leads to an improvement in the peak current with a shift of the peak potential to more positive values. Using the square-wave stripping mode, the compound yielded a well-defined voltammetric response in 0.1 M nitric acid solution containing 100 μmol L-1 hexadecyl trimethyl ammonium bromide at 0.74 V (vs. Ag/AgCl, after 60 s accumulation at the open-circuit condition. A linear calibration graph was obtained in the concentration range 0.025 to 60.0 μg mL-1, with a detection limit of 0.0063 μg mL-1. The applicability of the proposed method was verified by analysis of resveratrol in commercial dietary supplements.

  2. A ladder network modelling the electrochemical impedance of the diffusion and reaction processes in semi-infinite space.

    Science.gov (United States)

    Moya, A A

    2016-02-01

    The Gerischer impedance, i.e., the diffusion-reaction impedance of an ionic species in semi-infinite space, has been modelled by means of a novel simple equivalent ladder electric circuit constituted by a finite number of resistors and capacitors, which corresponds to the Cauer structure obtained from development into continued fractions. The Nyquist plots of the impedance of the ladder network or Cauer circuit and the deviation with respect to the Gerischer impedance have been originally analysed as a function of the number of circuit elements. From the Cauer equivalent circuit, a new and simple expression modelling the Gerischer impedance at the limit of the lowest frequencies has been derived.

  3. Detailed electrochemical studies of the tetraruthenium polyoxometalate water oxidation catalyst in acidic media: identification of an extended oxidation series using Fourier transformed alternating current voltammetry.

    Science.gov (United States)

    Lee, Chong-Yong; Guo, Si-Xuan; Murphy, Aidan F; McCormac, Timothy; Zhang, Jie; Bond, Alan M; Zhu, Guibo; Hill, Craig L; Geletii, Yurii V

    2012-11-05

    The electrochemistry of the water oxidation catalyst, Rb(8)K(2)[{Ru(4)O(4)(OH)(2)(H(2)O)(4)}(γ-SiW(10)O(36))(2)] (Rb(8)K(2)-1(0)) has been studied in the presence and absence of potassium cations in both hydrochloric and sulfuric acid solutions by transient direct current (dc) cyclic voltammetry, a steady state dc method in the rotating disk configuration and the kinetically sensitive technique of Fourier transformed large-amplitude alternating current (ac) voltammetry. In acidic media, the presence of potassium ions affects the kinetics (apparent rate of electron transfer) and thermodynamics (reversible potentials) of the eight processes (A'/A to H/H') that are readily detected under dc voltammetric conditions. The six most positive processes (A'/A to F/F'), each involve a one electron ruthenium based charge transfer step (A'/A, B'/B are Ru(IV/V) oxidation and C/C' to F/F' are Ru(IV/III) reduction). The apparent rate of electron transfer of the ruthenium centers in sulfuric acid is higher than in hydrochloric acid. The addition of potassium cations increases the apparent rates and gives rise to a small shift of reversible potential. Simulations of the Fourier transformed ac voltammetry method show that the B'/B, E/E', and F/F' processes are quasi-reversible, while the others are close to reversible. A third Ru(IV/V) oxidation process is observed just prior to the positive potential limit via dc methods. Importantly, the ability of the higher harmonic components of the ac method to discriminate against the irreversible background solvent process allows this (process I) as well as an additional fourth reversible ruthenium based process (J) to be readily identified. The steady-state rotating disk electrode (RDE) method confirmed that all four Ru-centers in Rb(8)K(2)-1(0) are in oxidation state IV. The dc and ac data indicate that reversible potentials of the four ruthenium centers are evenly spaced, which may be relevant to understanding of the water oxidation

  4. One-Step Electrosynthesis of Graphene Oxide-Doped Polypyrrole Nanocomposite as a Nanointerface for Electrochemical Impedance Detection of Cell Adhesion and Proliferation Using Two Approaches

    Directory of Open Access Journals (Sweden)

    Yuan Li

    2016-01-01

    Full Text Available A novel nanointerface of graphene oxide-doped polypyrrole (GO/PPy is prepared on the surface of an indium tin oxide (ITO electrode for electrochemical impedance detection of cell adhesion and proliferation through a facile one-step electropolymerization. The prepared GO/PPy nanocomposite had a robust surface and provided a biocompatible substrate for A549 cells adhesion and proliferation. The adhesion and proliferation of A549 cells on the surface of the GO/PPy modified ITO electrode directly increased the electron transfer resistance of [Fe(CN6]3−/4− redox probe and influenced the impedance properties of the GO/PPy modified ITO electrode system. Based on these results, the adhesion and proliferation of A549 cells could be detected by electrochemical impedance technology using two approaches. Therefore, the present paper confirms that the GO/PPy nanocomposite film provides an excellent biological-electrical interface for cell immobilization and offers advantages of simple, low-cost fabrication and multiparameter detection and possesses potential application in cytological studies.

  5. Electrochemical impedance spectroscopy for lithium-ion cells: Test equipment and procedures for aging and fast characterization in time and frequency domain

    Science.gov (United States)

    Lohmann, Nils; Weßkamp, Patrick; Haußmann, Peter; Melbert, Joachim; Musch, Thomas

    2015-01-01

    New test equipment and characterization methods for aging investigations on lithium-ion cells for automotive applications are presented in this work. Electrochemical impedance spectroscopy (EIS) is a well-established method for cell characterization and analyzing electrochemical processes. In order to integrate this method into long-term aging studies with real driving currents, new test equipment is mandatory. The presented test equipment meets the demands for high current, wide bandwidth and precise measurement. This allows the cells to be cycled and characterized without interruption for changing the test device. The characterization procedures must be of short duration and have a minimum charge-throughput for negligible influence on the aging effect. This work presents new methods in the time and the frequency domain for obtaining the impedance spectrum which allow a flexible trade-off between measurement performance, time consumption and charge-throughput. In addition to sinusoidal waveforms, rectangular, Gaussian and sin(x)/x pulses are applied for EIS. The performance of the different methods is discussed. Finally, the time domain analysis is applied with real driving currents which provides impedance spectra for state of charge estimation considering aging effects in the car.

  6. Estimation of kinetic parameters of the passive state of carbon steel in mildly alkaline solutions from electrochemical impedance spectroscopic and X-ray photoelectron spectroscopic data

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, X.; Wren, J.C. [Department of Chemistry, University of Western Ontario, 1151 Richmond St, London, Ontario, N6A 5B7 (Canada); Betova, I. [Department of Chemistry, Technical University of Sofia, 1000 Sofia (Bulgaria); Bojinov, M., E-mail: martin@uctm.edu [Department of Physical Chemistry, University of Chemical Technology and Metallurgy, 1756 Sofia (Bulgaria)

    2011-07-01

    Highlights: > The passive state of carbon steel is described using the Mixed-Conduction Model for oxide films. > Kinetic parameters are estimated by comparison of the model to EIS and XPS data. > The passive film is intermediate between magnetite and maghemite. > Relevance of film growth and dissolution reactions for corrosion is discussed. - Abstract: The unambiguous interpretation of electrochemical impedance spectra of complex systems such as passive metals and alloys in terms of an unique kinetic model is often hampered by the large number of adjustable modeling parameters. In this paper, a combination of in situ electrochemical data and ex situ surface analytical information is employed to validate the estimates of kinetic and transport parameters of the passive state of carbon steel. For the purpose, electrochemical impedance spectroscopic and X-ray photoelectron spectroscopic data for the oxidation of carbon steel in mildly alkaline solutions are quantitatively compared with the predictions of the Mixed-Conduction Model for oxide films that represent the passive oxide as an intermediate phase between magnetite and maghemite. Estimates of the kinetic rate constants at the film interfaces, as well as the diffusion coefficients and field strength in the film are obtained and their relevance for the corrosion mechanism of carbon steel is discussed.

  7. Cyclic Voltammetry And Linear Sweep Voltammetry Study Of Cyclic Tertiary Amines

    Institute of Scientific and Technical Information of China (English)

    ZHAO Ping; TIAN JinPing; YIN YingWu

    2001-01-01

    @@ Cyclic six membered a-aminonitrile have proved to be very versatile synthetic intermediates and have been widely used in the construction of a large number of indole alkaloids. In order to obtain some information about the mechanisn of electrochemical synthesis of aaminonitrile. Electrochemistry behaviors that include cyclic voltammetry and linear sweep voltammetry of cyclic tertiary amines which including N-benzylpiperidine (NBP), 1-(l-Methoxycarbonyl ethyl) piperidine (MCEP), N-methylcarbonylppiperidine (NMCP), Nethylpiperidine(NEP) was studied.

  8. Cyclic Voltammetry And Linear Sweep Voltammetry Study Of Cyclic Tertiary Amines

    Institute of Scientific and Technical Information of China (English)

    ZHAO; Ping

    2001-01-01

    Cyclic six membered a-aminonitrile have proved to be very versatile synthetic intermediates and have been widely used in the construction of a large number of indole alkaloids. In order to obtain some information about the mechanisn of electrochemical synthesis of aaminonitrile. Electrochemistry behaviors that include cyclic voltammetry and linear sweep voltammetry of cyclic tertiary amines which including N-benzylpiperidine (NBP), 1-(l-Methoxycarbonyl ethyl) piperidine (MCEP), N-methylcarbonylppiperidine (NMCP), Nethylpiperidine(NEP) was studied.……

  9. Investigation of the self-healing properties of shape memory polyurethane coatings with the 'odd random phase multisine' electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Jorcin, Jean-Baptiste, E-mail: jb.jorcin@gmail.co [Research Group Electrochemical and Surface Engineering, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels (Belgium); Scheltjens, Gill [Research Group Electrochemical and Surface Engineering, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels (Belgium)] [Research Group Physical Chemistry and Polymer Science, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels (Belgium); Van Ingelgem, Yves; Tourwe, Els [Research Group Electrochemical and Surface Engineering, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels (Belgium); Van Assche, Guy [Research Group Physical Chemistry and Polymer Science, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels (Belgium); De Graeve, Iris [Research Group Electrochemical and Surface Engineering, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels (Belgium); Van Mele, Bruno [Research Group Physical Chemistry and Polymer Science, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels (Belgium); Terryn, Herman; Hubin, Annick [Research Group Electrochemical and Surface Engineering, Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels (Belgium)

    2010-08-30

    The aim of this work is to study the physical self-healing properties of shape memory polyurethanes (SMPUs) with cerium ions on top of a pure aluminum substrate. To achieve this, the 'odd random phase multisine' electrochemical impedance spectroscopy (EIS) is used. The additional information given by this technique (stochastic noise, non-linear and non-stationary behavior of the sample during the measurement) has been useful to verify the quality of the measurement. Moreover, combined with a fitting algorithm weighted by the stochastic noise, these elements of information proved powerful in rejecting, accepting or improving electrical equivalent circuit models used to fit the impedance spectra. These SMPU consist of two parts: a soft matrix in caprolactone and a hard part in polyurethane. SMPU with 12, 30 and 41% of hard phase were investigated. The results showed that a physical self-healing can be observed for the coating with 12% of hard phase.

  10. Electrochemical growth of Co nanowires in ultra-high aspect ratio InP membranes: FFT-impedance spectroscopy of the growth process and magnetic properties

    Science.gov (United States)

    2014-01-01

    The electrochemical growth of Co nanowires in ultra-high aspect ratio InP membranes has been investigated by fast Fourier transform-impedance spectroscopy (FFT-IS) in the frequency range from 75 Hz to 18.5 kHz. The impedance data could be fitted very well using an electric circuit equivalent model with a series resistance connected in series to a simple resistor-capacitor (RC) element and a Maxwell element. Based on the impedance data, the Co deposition in ultra-high aspect ratio InP membranes can be divided into two different Co deposition processes. The corresponding share of each process on the overall Co deposition can be determined directly from the transfer resistances of the two processes. The impedance data clearly show the beneficial impact of boric acid on the Co deposition and also indicate a diffusion limitation of boric acid in ultra-high aspect ratio InP membranes. The grown Co nanowires are polycrystalline with a very small grain size. They show a narrow hysteresis loop with a preferential orientation of the easy magnetization direction along the long nanowire axis due to the arising shape anisotropy of the Co nanowires. PMID:25050088

  11. Electrochemical growth of Co nanowires in ultra-high aspect ratio InP membranes: FFT-impedance spectroscopy of the growth process and magnetic properties

    Science.gov (United States)

    Gerngross, Mark-Daniel; Carstensen, Jürgen; Föll, Helmut

    2014-06-01

    The electrochemical growth of Co nanowires in ultra-high aspect ratio InP membranes has been investigated by fast Fourier transform-impedance spectroscopy (FFT-IS) in the frequency range from 75 Hz to 18.5 kHz. The impedance data could be fitted very well using an electric circuit equivalent model with a series resistance connected in series to a simple resistor-capacitor ( RC) element and a Maxwell element. Based on the impedance data, the Co deposition in ultra-high aspect ratio InP membranes can be divided into two different Co deposition processes. The corresponding share of each process on the overall Co deposition can be determined directly from the transfer resistances of the two processes. The impedance data clearly show the beneficial impact of boric acid on the Co deposition and also indicate a diffusion limitation of boric acid in ultra-high aspect ratio InP membranes. The grown Co nanowires are polycrystalline with a very small grain size. They show a narrow hysteresis loop with a preferential orientation of the easy magnetization direction along the long nanowire axis due to the arising shape anisotropy of the Co nanowires.

  12. Electrochemical impedance spectroscopy study on the corrosion of the weld zone of 3Cr steel welded joints in CO2 environments

    Science.gov (United States)

    Xu, Li-ning; Zhu, Jin-yang; Lu, Min-xu; Zhang, Lei; Chang, Wei

    2015-05-01

    The welded joints of 3Cr pipeline steel were fabricated with commercial welding wire using the gas tungsten arc welding (GTAW) technique. Potentiodynamic polarization curves, linear polarization resistance (LPR), electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and energy-dispersive spectrometry (EDS) were used to investigate the corrosion resistance and the growth of a corrosion film on the weld zone (WZ). The changes in electrochemical characteristics of the film were obtained through fitting of the EIS data. The results showed that the average corrosion rate of the WZ in CO2 environments first increased, then fluctuated, and finally decreased gradually. The formation of the film on the WZ was divided into three stages: dynamic adsorption, incomplete-coverage layer formation, and integral layer formation.

  13. Electrochemical impedance spectroscopic investigation of the role of alkaline pre-treatment in corrosion resistance of a silane coating on magnesium alloy, ZE41

    Energy Technology Data Exchange (ETDEWEB)

    Chakraborty Banerjee, P. [Department of Chemical Engineering, Monash University, Clayton, VIC-3800 (Australia); CAST Cooperative Research Centre, Hawthorn, VIC-3122 (Australia); Singh Raman, R.K., E-mail: raman.singh@eng.monash.edu.a [Department of Chemical Engineering, Monash University, Clayton, VIC-3800 (Australia); Department of Mechanical and Aerospace Engineering, Monash University, Clayton, VIC-3800 (Australia)

    2011-04-15

    The protective performance of the coatings of bis-1,2-(triethoxysilyl) ethane (BTSE) on ZE41 magnesium alloy with different surface pre-treatments were evaluated using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) in 0.1 M sodium chloride solution. Electrical equivalent circuits were developed based upon hypothetical corrosion mechanisms and simulated to correspond to the experimental data. The morphology and cross section of the alloy subjected to different pre-treatments and coatings were characterized using scanning electron microscope. A specific alkaline pre-treatment of the substrate prior to the coating has been found to improve the corrosion resistance of the alloy.

  14. Optimisation of the hot conditioning of carbon steel surfaces of primary heat transport system of Pressurized Heavy Water Reactors using electrochemical impedance spectroscopy

    Science.gov (United States)

    Kiran Kumar, M.; Gaonkar, Krishna; Ghosh, Swati; Kain, Vivekanand; Bojinov, Martin; Saario, Timo

    2010-06-01

    Hot conditioning operation of the primary heat transport system is an important step prior to the commissioning of Pressurized Heavy Water Reactors. One of the major objectives of the operation is to develop a stable and protective magnetite layer on the inner surfaces of carbon steel piping. The correlation between stable magnetite film growth on carbon steel surfaces and the period of exposure to hot conditioning environment is generally established by a combination of weight change measurements and microscopic/morphological observations of the specimens periodically removed during the operation. In the present study, electrochemical impedance spectroscopy (EIS) at room temperature is demonstrated as an alternate, quantitative technique to arrive at an optimal duration of the exposure period. Specimens of carbon steel were exposed for 24, 35 and 48 h during hot conditioning of primary heat transport system of two Indian PHWRs. The composition and morphology of oxide films grown during exposure was characterized by X-ray diffraction and optical microscopy. Further, ex situ electrochemical impedance spectra of magnetite films formed after each exposure were measured, in 1 ppm Li + electrolyte at room temperature as a function of potential in a range of -0.8 to +0.3 VSCE. The defect density of the magnetite films formed after each exposure was estimated by Mott-Schottky analysis of capacitances extracted from the impedance spectra. Further the ionic resistance of the oxide was also extracted from the impedance spectra. Defect density was observed to decrease with increase in exposure time and to saturate after 35 h, indicating stabilisation of the barrier layer part of the magnetite film. The values of the ionic transport resistance start to increase after 35-40 h of exposure. The quantitative ability of EIS technique to assess the film quality demonstrates that it can be used as a supplementary tool to the thickness and morphological characterizations of samples

  15. Optimisation of the hot conditioning of carbon steel surfaces of primary heat transport system of Pressurized Heavy Water Reactors using electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kiran Kumar, M., E-mail: mkiran@barc.gov.i [Materials Science Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Gaonkar, Krishna; Ghosh, Swati; Kain, Vivekanand [Materials Science Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Bojinov, Martin [Department of Physical Chemistry, University of Chemical Technology and Metallurgy, Kl. Ohridski Blvd. 8, 1756 Sofia (Bulgaria); Saario, Timo [VTT Materials and Building, VTT Technical Research Centre of Finland, P.O. Box 1000, Kemistintie 3, FIN-02044 VTT, Espoo (Finland)

    2010-06-15

    Hot conditioning operation of the primary heat transport system is an important step prior to the commissioning of Pressurized Heavy Water Reactors. One of the major objectives of the operation is to develop a stable and protective magnetite layer on the inner surfaces of carbon steel piping. The correlation between stable magnetite film growth on carbon steel surfaces and the period of exposure to hot conditioning environment is generally established by a combination of weight change measurements and microscopic/morphological observations of the specimens periodically removed during the operation. In the present study, electrochemical impedance spectroscopy (EIS) at room temperature is demonstrated as an alternate, quantitative technique to arrive at an optimal duration of the exposure period. Specimens of carbon steel were exposed for 24, 35 and 48 h during hot conditioning of primary heat transport system of two Indian PHWRs. The composition and morphology of oxide films grown during exposure was characterized by X-ray diffraction and optical microscopy. Further, ex situ electrochemical impedance spectra of magnetite films formed after each exposure were measured, in 1 ppm Li{sup +} electrolyte at room temperature as a function of potential in a range of -0.8 to +0.3 V{sub SCE}. The defect density of the magnetite films formed after each exposure was estimated by Mott-Schottky analysis of capacitances extracted from the impedance spectra. Further the ionic resistance of the oxide was also extracted from the impedance spectra. Defect density was observed to decrease with increase in exposure time and to saturate after 35 h, indicating stabilisation of the barrier layer part of the magnetite film. The values of the ionic transport resistance start to increase after 35-40 h of exposure. The quantitative ability of EIS technique to assess the film quality demonstrates that it can be used as a supplementary tool to the thickness and morphological characterizations of

  16. Electrochemical impedance spectroscopy for analytical determination of paraquat in meconium samples using an immunosensor modified with fullerene, ferrocene and ionic liquid

    Energy Technology Data Exchange (ETDEWEB)

    Sun Xiulan [State Key Laboratory of Food Science and Technology, Wuxi 214122 (China); Li Zaijun, E-mail: zaijunli@263.ne [School of Chemical and Materials Engineering, Jiangnan University, Lihu Road 1800, Wuxi 214122 (China); Cai, Yan; Wei, Zhilei [School of Chemical and Materials Engineering, Jiangnan University, Lihu Road 1800, Wuxi 214122 (China); Fang Yinjun; Ren Guoxiao; Huang Yaru [Zhejiang Zanyu Technology Limited Corporation, Hangzhou 311215 (China)

    2011-01-01

    The paper reports a highly sensitive electrochemical immunosensor for the detection of paraquat. The immunosensor bases on glassy carbon electrode modified with a composite made from fullerene, ferrocene and the ionic liquid. The components were immobilized on the electrode surface by chitosan. The antibody of paraquat was covalently conjugated to the surface which was then blocked with bovine serum albumin. Analytical characteristics of the immunosensor were investigated by electrochemical impedance spectroscopy. It offers good repeatability (RSD = 1.5%), a stability of more than 150 days, an impedimetric response to paraquat in the range from 3.89 x 10{sup -11} to 4.0 x 10{sup -8} mol L{sup -1}, and a detection limit (S/N = 3) of 9.0 x 10{sup -12} mol L{sup -1}. The effects of omitting fullerene and the ionic liquid were well tested. The results indicated that sensitivity of the immunosensor is 3.7-fold better if fullerene and ionic liquid are used. This demonstrates that fullerene facilitates electron transfer on surface of the electrode due to unique electrochemical properties, while the ionic liquid provides biocompatible microenvironment for the antibody, which results in the enhanced sensitivity and stability. Moreover, surface morphology feature and electrochemical properties of the electrode were also examined. The method was satisfactorily applied to the determination of paraquat in meconium.

  17. Negative resistance for methanol electro-oxidation on platinum/carbon (Pt/C) catalyst investigated by an electrochemical impedance spectroscopy

    Science.gov (United States)

    Cai, Guang-Xu; Guo, Jian-Wei; Wang, Jia; Li, Song

    2015-02-01

    The poisoning of Pt-based catalyst occurs generally during methanol electro-oxidation. Though traditional electrochemical techniques have probed these issues intensively, it is amazing to find that the negative resistance presents in the intermediate potential zone during an electrochemical impedance spectroscopy (EIS) measurement. Based on the chemical reaction analysis, we establish an EIS model and make some numerical analyses, thus determining the specific EIS shapes and equivalent circuits relating to various potential zones. These results not only compensate the drawback for traditional electrochemical approaches, but also reveal the dynamic adsorption of CO and OH species on Pt surfaces, providing a chance for understanding bifunctional mechanism towards quantitative manners. Significantly, we clarify that the negative resistance begins from the maximum catalysis of methanol electro-catalysis and ends in the initial passive state on Pt surfaces, offering a tool for further improvement. Interestingly, our discovery for negative resistance is consistent with that in general electrochemical system, facilitating its extension and direction in future.

  18. Compositional Analysis of Electrodeposited Cu-Se Compound Semiconductor Thin Films Using Combined Voltammetry and Flow-Electrochemical Quartz Crystal Microgravimetry

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Wooju; Jeong, Seonghan; Myung, Noseung [Konkuk Univ., Chungju (Korea, Republic of); Rajeshwar, Krishnan [Univ. of Texas at Arlington, Arlington (United States); Lee, Chiwoo [Korea Univ., Seoul (Korea, Republic of)

    2013-10-15

    A novel method which is species selective for the compositional analysis of electrodeposited Cu-Se semiconductor films was developed using combined voltammetry and flow-EQCM. The amounts of free Se and Se in Cu{sub 2}Se were obtained from the frequency changes at constant potentials of -0.8 V and -3 V, respectively. Potential steps to -0.8 V and -1.3 V were employed to reduce free Se to Se{sub 2}{sup -} and Cu{sub 2}Se to Cu + Se{sub 2}{sup -}, respectively. Resultant total Cu was anodically stripped at +0.8 V and the free Cu content was calculated using the difference in frequency changes observed during the stripping of total Cu and Se in Cu{sub 2}Se. The results showed that the amounts of free Se, free Cu and the targeted Cu{sub 2}Se varied with deposition potential as well as film thickness. The ternary compound semiconductor CuInSe{sub 2} (CIS) has attracted great interest due to its unique properties and wide applications.

  19. Optimization of the use of carbon paste electrodes (CPE for electrochemical study of the chalcopyrite

    Directory of Open Access Journals (Sweden)

    Daniela G. Horta

    2009-01-01

    Full Text Available The use of carbon paste electrodes (CPE of mineral sulfides can be useful for electrochemical studies to overcome problems by using massive ones. Using CPE-chalcopyrite some variables were electrochemically evaluated. These variables were: (i the atmosphere of preparation (air or argon of CPE and elapsed time till its use; (ii scan rate for voltammetric measurements and (iii chalcopyrite concentration in the CPE. Based on cyclic voltammetry, open-circuit potential and electrochemical impedance results the recommendations are: oxygen-free atmosphere to prepare and kept the CPE until around two ours, scan rates from 10 to 40 mV s-1, and chalcopyrite concentrations > 20%.

  20. Effects of surface modification on electrochemical performance of MnO2

    Institute of Scientific and Technical Information of China (English)

    LIU Li-qing; WANG Jjan-ming; FAN Yu-kai; WANG Guo-guang; ZHANG Jian-qing

    2005-01-01

    The MnO2 samples coated with Ca(OH)2 were prepared by a liquid-phase surface treatment method.The physical properties of the samples were examined by SEM, EDAX and chemical analysis, and their electrochemical performances were investigated by means of galvanostatic charge-discharge, cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The SEM results show that the samples coated with Ca(OH)2 display a porous surface structure. The electrochemical experiments indicate that the surface modification decreases the polarization of MnO2 electrodes and improves their discharge potentials and discharge capacities.