Relevant bibliographies by topics / Electrochemical Impedance Spectroscopy

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Electrochemical Impedance Spectroscopy'

Author: Grafiati
Published: 4 June 2021
Last updated: 5 October 2024

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Journal articles on the topic "Electrochemical Impedance Spectroscopy"

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Chang, Byoung-Yong, and Su-Moon Park. "Electrochemical Impedance Spectroscopy." Annual Review of Analytical Chemistry 3, no. 1 (June 2010): 207–29. http://dx.doi.org/10.1146/annurev.anchem.012809.102211.

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Sacci, Robert L., and David Harrington. "Dynamic Electrochemical Impedance Spectroscopy." ECS Transactions 19, no. 20 (December 18, 2019): 31–42. http://dx.doi.org/10.1149/1.3247564.

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Ciucci, Francesco. "Modeling electrochemical impedance spectroscopy." Current Opinion in Electrochemistry 13 (February 2019): 132–39. http://dx.doi.org/10.1016/j.coelec.2018.12.003.

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Ragoisha, G. A., and A. S. Bondarenko. "Potentiodynamic electrochemical impedance spectroscopy." Electrochimica Acta 50, no. 7-8 (February 2005): 1553–63. http://dx.doi.org/10.1016/j.electacta.2004.10.055.

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Park, Su-Moon, Jung-Suk Yoo, Byoung-Yong Chang, and Eun-Shil Ahn. "Novel instrumentation in electrochemical impedance spectroscopy and a full description of an electrochemical system." Pure and Applied Chemistry 78, no. 5 (January 1, 2006): 1069–80. http://dx.doi.org/10.1351/pac200678051069.

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The evolution of impedance measurement methods into the current state of the art is reviewed briefly, and recent efforts to develop new instruments to make electrochemical impedance spectroscopy (EIS) measurements faster and more accurate are described. The most recent approach for impedance measurement uses a multichannel detection technique, which is analogous to a spectroscopic measurement such as in Fourier transform infrared spectroscopy. This method, which is capable of making impedance measurements in real time during an electrochemical experiment, allows us to come up with a new integrated equation that makes a full description of an electrochemical system possible.
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Fasmin, Fathima, and Ramanathan Srinivasan. "Review—Nonlinear Electrochemical Impedance Spectroscopy." Journal of The Electrochemical Society 164, no. 7 (2017): H443—H455. http://dx.doi.org/10.1149/2.0391707jes.

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Vereecken, Jean. "Book Review - Electrochemical Impedance Spectroscopy." Electrochemical Society Interface 18, no. 2 (June 1, 2009): 19–20. http://dx.doi.org/10.1149/2.006092if.

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Mukhopadhyay, Rajendrani. "Electrochemical impedance spectroscopy says “cheese!”." Analytical Chemistry 82, no. 21 (November 2010): 8756. http://dx.doi.org/10.1021/ac102467a.

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Tarola, Alessandro, Danilo Dini, Elisabetta Salatelli, Franco Andreani, and Franco Decker. "Electrochemical impedance spectroscopy of polyalkylterthiophenes." Electrochimica Acta 44, no. 24 (July 1999): 4189–93. http://dx.doi.org/10.1016/s0013-4686(99)00133-4.

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Talaga, David S., and Michael J. Vitarelli. "Electrochemical Impedance Spectroscopy of Nanopores." Biophysical Journal 104, no. 2 (January 2013): 521a. http://dx.doi.org/10.1016/j.bpj.2012.11.2882.

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Dissertations / Theses on the topic "Electrochemical Impedance Spectroscopy"

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Ocaña, Tejada Cristina. "Aptasensors based on electrochemical impedance spectroscopy." Doctoral thesis, Universitat Autònoma de Barcelona, 2015. http://hdl.handle.net/10803/305103.

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En els últims anys, a causa de la necessitat de diàgnostics ràpids i de millores en sensat, s’han utilitzat nous elements de reconeixement en biosensors. Un tipus d’aquests nous elements de reconeixement són els aptàmers. Els aptàmers són cadenes sintètiques de ADN o ARN les quals són seleccionades in vitro i tenen la capacitat d’unir-se a proteïnes, ions, cèl.lules, fàrmacs i lligands de baix pes molecular, reconeixent les seves molècules diana amb alta afinitat i especificitat. Diversos biosensors basats en aptàmers, també anomenats aptasensors, han sigut desenvolupats recentment. D’entre totes les tècniques de transducció utilitzades en biosensors, l’Espectrocòpia Electroquímica d’Impedància ha sigut àmpliament emprada como a eina per caracteritzar la superficies de sensors i estudiar esdeveniments en el biosensat en la superficie d’elèctrodes. La característica més important que presenta aquesta tècnica és que no requereix cap espècie marcada per a la transducció, per tant, aquesta tècnica de detecció pot utilitzar-se per dissenyar protocols de detecció directa sense marcatge, evitant assajos més cars i laboriosos. El principal objectiu d’aquesta tesi doctoral va ser el desenvolupament d’aptasensors utilitzant la tècnica electroquímica d’impedància esmentada anteriorment. Per a això, diferents tipus d’elèctrodes van ser utilitzats, tals com elèctrodes de compòsit grafit-epoxi, elèctrodes de biocompòsit grafit-epoxi modificats amb molècules d’avidina i elèctrodes comercials serigrafiats de nanotubs de carboni de paret múltiple. El treball es va dividir principalmente en dues parts d'acord amb la detecció de dues proteïnes diferents. La primera part es va focalitzar en la detecció de trombina. Primer de tot, es van comparar i avaluar diversos aptasensors de detecció directa sense marcatge basat en diferents tècniques d'immobilització dels aptàmers, tals com: adsorció física humida, afinitat avidina-biotina i enllaç covalent mitjançant activació electroquímica de la superfície de l'elèctrode i mitjançant inserció electroquímica. Posteriorment, els elèctrodes de biocompòsit van ser comparats com a plataformes en genosensat i aptasensat. Amb la finalitat d'amplificar el senyal impedimètric obtingut utilitzant elèctrodes de biocompòsit, un protocol sàndwich va ser emprat incloent nanopartícules d'or modificades amb estreptavidina i tractament amplificador de plata. La segona part de l'estudi es va basar en la detecció de citocrom c. Primerament, es va realitzar un simple aptasensor de detecció directa sense marcatge per a la detecció d'aquesta proteïna utilitzant la tècnica d'immobilització d'adsorció física humida. Finalment, i amb l'objectiu d'amplificar el señal impedimètric, es va desenvolupar un assaig tipus sándwich híbrid d’aptàmer i anticòs utilitzant elèctrodes serigrafiats de nanotubs de carboni de paret múltiple. D'aquesta manera, la tesi explora i compara una àmplia gamma de procediments d'immobilització, l'ús de detecció directa sense marcatge o nanomaterial modificat amb biomolècules en diferents protocols directes o d'amplificació, i l'ús de reconeixement directe i sándwich per amplificar la sensibilitat i/o la selectivitat de l'assaig.
In the recent years, due to the need for rapid diagnosis and improvements in sensing, new recognition elements are employed in biosensors. One kind of these new recognition elements are aptamers. Aptamers are synthetic strands of DNA or RNA which are selected in vitro and have the ability to bind to proteins, ions, whole cells, drugs and low molecular weight ligands recognizing their target with high affinity and specificity. Several aptamer-based biosensors, also called aptasensors, have been recently developed. Among all the transduction techniques employed in biosensors, Electrochemical Impedance Spectroscopy has widely used as a tool for characterizing sensor platforms and for studying biosensing events at the surface of the electrodes. The important feature presented by this technique is that it does not require any labelled species for the transduction; thus, this detection technique can be used for designing label-free protocols thus avoiding more expensive and time-consuming assays. The main aim of this PhD work was the development of aptasensors using the electrochemical impedance technique previously mentioned for protein detection. For that, different types of electrodes were used, such as Graphite Epoxy Composite electrodes (GECs), Avidin Graphite Epoxy Composite electrodes (AvGECs) and commercial Multi-Walled carbon nanotubes screen printed electrodes (MWCNT-SPE). The work was divided in two main parts according to the detection of the two different proteins. The first part was focused on thrombin detection. First of all, different impedimetric label-free aptasensors based on several aptamer immobilization techniques such as wet physical adsorption, avidin-biotin affinity and covalent bond via electrochemical activation of the electrode surface and via electrochemical grafting were developed and evaluated. Then, AvGECs electrodes were compared as a platform for genosensing and aptasensing. With the aim to amplying the obtained impedimetric signal using AvGECs, an aptamer sandwich protocol for thrombin detection was used including streptavidin gold-nanoparticles (Strep-AuNPs) and silver enhancement treatment. The second part of the study was based on cytochrome c detection. Firstly, a simple label-free aptasensor for the detection of this protein using a wet physical adsorption immobilization technique was performed. Finally, with the goal to amplify the impedimetric signal, a hybrid aptamer-antibody sandwich assay using MWCNT-SPE for the detection of the target protein was carried out. In this way, the thesis explores and compares a wide scope of immobilization procedures, the use of label-free or nanocomponent modified biomolecules in different direct or amplified protocols, and the use of direct recognition and sandwich alternatives to enhance sensitivity and/or selectivity of the assay
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Barton, Raymond Terence. "Characterisation of nickel electrodes by electrochemical impedance spectroscopy." Thesis, Loughborough University, 1995. https://dspace.lboro.ac.uk/2134/12219.

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The thesis describes an electrochemical investigation of different types of nickel electrode used in nickel-cadmium cells, which are available commercially or currently under development. Impedance spectroscopy has been used to determine the electrochemical characteristics of these electrodes. The electrochemistry of the nickel electrodes was modelled by the electrical analogue method. Allowance was made within the model for porosity and adsorption effects. Component values were initially estimated by graphical techniques and the computer fitting procedure was then completed by an iterative process to provide kinetic parameters which were used to compare and contrast the characteristics of the nickel sintered, pocket and plastic bonded electrodes. The technological target of this work was establish a possible method by which the residual capacity remaining within nickel-cadmium cells could be determined. The kinetic parameters generated by the electrical analogue technique have provided data on which to base a measurement for the prediction of the state of charge in nickel-cadmium cells.
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Ma, Hongshen 1978. "Electrochemical Impedance Spectroscopy using adjustable nanometer-gap electrodes." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/42240.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2007.
Includes bibliographical references (p. 151-154).
Electrochemical Impedance Spectroscopy (EIS) is a simple yet powerful chemical analysis technique for measuring the electrical permittivity and conductivity of liquids and gases. Presently, the limiting factor for using EIS as a portable chemical detection technology is the lack of absolute accuracy stemming from uncertainties in the geometrical factor used to convert measurable quantities of capacitance and conductance into the intrinsic parameters of permittivity and conductivity. The value of this geometrical conversion factor can be difficult to predict since it is easily affected by fringing electric fields, manufacturing variations, and surface chemistry. Existing impedance test cells typically address this problem using a calibration liquid with known permittivity and conductivity, however, this correction is not feasible in many applications since the calibration liquid may irreversibly contaminate the test electrodes. This thesis presents a technique for accurately measuring the permittivity and conductivity of liquids and gases without requiring the use of calibration liquids. This technique is made possible by precisely controlling the separation between two spherical electrodes to measure capacitance and conductance of the sample medium as a function of electrode separation. By leveraging the geometrical accuracy of the spherical electrodes and precise control of the electrode separation, the permittivity and conductivity of the sample can be determined without wet calibration. The electrode separation is adjusted using a flexure stage and a servomechanical actuator, which enables control the electrode separation with 0.25 nm resolution over a range of 50 gm. The nanometer smooth surfaces of the spherical electrodes also enable electrode gaps of less than 20 nm to be created.
(cont.) The technique for measuring permittivity and conductivity presented in this thesis could eventually be adapted to make miniaturized disposable impedance test cells for chemical analysis. Such systems could take advantage of conductivity assays to determine the presence and concentration of specific substances. The adjustable nanometer electrode gap can also be used to study the properties of chemical and biological systems in highly confined states. These studies are fundamentally important for understanding biochemical processes in natural systems where reactions often take place inside confined structures such as cells, organelles, and the intercellular matrix.
by Hongshen Ma.
Ph.D.
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Zheng, Linan. "DETECTION OF CHLAMYDIA TRACHOMATIS BY ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY." OpenSIUC, 2016. https://opensiuc.lib.siu.edu/theses/1966.

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Chlamydia trachomatis is detected by electrochemical impedance spectroscopy using a mouse monoclonal IgG2a anti-MOMP antibody immobilized onto a Si electrode. Two types of electrochemical cells are used in this study, one with the electrode at the bottom and the other will the electrode on the side. Control experiments with Escherichia coli demonstrate this biosensor is not selective to Chlamydia trachomatis. Another control experiment with Chlamydia trachomatis immobilized onto mouse monoclonal IgG2a isotype antibody coated electrode obtains an increased charge transfer resistance (Rct) which is inversely proportional to the rate of electron transfer. These results demonstrate further investigations are needed to develop the Chlamydia trachomatis impedance biosensor.
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Foley, John J. "Microfluidic Electrical Impedance Spectroscopy." DigitalCommons@CalPoly, 2018. https://digitalcommons.calpoly.edu/theses/1950.

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The goal of this study is to design and manufacture a microfluidic device capable of measuring changes in impedance valuesof microfluidic cell cultures. Tocharacterize this, an interdigitated array of electrodes was patterned over glass, where it was then bonded to a series of fluidic networks created in PDMS via soft lithography. The device measured ethanol impedance initially to show that values remain consistent over time. Impedance values of water and 1% wt. saltwater were compared to show that the device is able to detect changes in impedance, with up to a 60% reduction in electrical impedance in saltwater. Cells were introduced into the device, where changes in impedance were seen across multiple frequencies, indicating that the device is capable of detecting the presence of biologic elements within a system. Cell measurements were performed using NIH-3T3 fibroblasts.
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Xu, Mengyun. "Optimised label-free biomarker assays with electrochemical impedance spectroscopy." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:e527a06b-25e5-48fe-8be5-3c0c10210b74.

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There is huge academic interest and clinical need associated with the development of biomarker immunoassays where general aims are the generation of highly specific, convenient and sensitive sensing formats. In this project, a powerful electrochemical technique, electrochemical impedance spectroscopy (EIS), is applied in the establishment of powerful biomarker detecting protocols. Firstly, ultrasensitive, label-free and reusable insulin sensors, based on an antibody-PEGylated thiol self-assembly monolayer (PEG thiol SAM) interface, were produced and characterised via Faradaic EIS, presenting a detection limit (LOD) of 1.2 pM, a linear range across four orders of magnitude, and high sensitivity in even 50 % serum. By applying similar surface chemistry, a label-free biosensor, specific for the detection of α-synuclein antibodies, was fabricated. The α-synuclein interfaces used enabled the reliable detecting of this biomarker in patient sample serum. The concentration levels in the control and a patient group were determined to be significantly different, and, significantly, this difference was consistently across two different cohorts. Strikingly, this could potentially underpin an entirely new means of early Parkinson’s disease (PD) diagnosis. Non-Faradaic EIS methods were additionally applied to label-free insulin assays at both PEG thiol SAM and zwitterionic polymer film interfaces. The latter presented not only an exceptionally non-fouling interface, but also one seemingly both highly biocompatible and facilitating enhanced receptor: target binding. Finally, impedance assays, though potent, generally, operate by sampling only one of a limited number of available experimental variables, typically, Rct for Faradaic EIS, or C or Z for non-Faradaic EIS. Work carried out herein also explores the generation and utility of a portfolio of mathematically derived immittance functions all obtained from the same raw data sets. A particular focus was the examination of whether these were capable of increasing assay sensitivity and efficiency above normal impedance treatments.
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Formisano, Nello. "A study on the optimisation of electrochemical impedance spectroscopy biosensors." Thesis, University of Bath, 2016. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.687325.

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Electrochemical impedance spectroscopy (EIS) has been one of the most intensively studied electrochemical techniques for biosensing in recent decades. However, despite its great potential, real applications of EIS sensors still remain not as widely spread as other techniques because there are many factors that govern impedimetric signals. In particular, features such as the probe coverage density on the sensor surface, as well as the target size, charge and conformation, can assume significant importance. The aim of this study was to analyse both the limitations and the potential solutions for maximizing the EIS signals in certain possible systems which are characterised by having different types of target to detect. In order to reproduce different conditions, four types of molecular targets have been taken in consideration. These provided example systems where the approach for the development of an EIS sensor varied considerably. In the first system the importance of the surface conditions of an aptasensor for prostate specific antigen (PSA) using Faradaic processes was reported. It was demonstrated that the effect of the target binding combined with the relative surface charge modification can diminish the EIS signals. In the second system, a strategy for improving the sensitivity and selectivity of the assay for drug discovery applications was demonstrated. This was obtained by adopting ferrocene-crowned gold nanoparticles that specifically bind to the molecular targets and induced a transition from non-Faradaic to Faradaic processes. In the last two example systems, particular attention has also been given to non-Faradaic processes which are the least exploited in EIS systems although the technique can be simpler to implement compared to Faradaic EIS. Moreover, with non-Faradaic processes more effective results can be achieved under some specific conditions, such as exploiting the size and charge of molecular targets. On such premises, the current work wants to serve as a reference for overcoming the limitations met in several EIS systems and hopefully contribute as a support for enhancing the fields of applications of EIS sensors.
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Valenzuela, Jorge Ignacio. "Electrochemical impedance spectroscopy options for proton exchange membrane fuel cell diagnostics." Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/266.

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Electrochemical impedance spectroscopy (EIS) has been exploited as a rich source of Proton Exchange Membrane Fuel Cell (PEMFC) diagnostic information for many years. Several investigators have characterized different failure modes for PEMFCs using EIS and it now remains to determine how this information is to be obtained and used in a diagnostic or control algorithm for an operating PEMFC. This work utilizes the concept of impedance spectral fingerprints (ISF) to uniquely identify between failure modes in an operating PEMFC. Three well documented PEMFC failure modes, carbon monoxide (CO) poisoning, dehydration, and flooding were surveyed, modelled, and simulated in the time domain and the results were used to create a database of ISFs. The time domain simulation was realized with a fractional order differential calculus state space approach. A primary goal of this work was to develop simple and cost effective algorithms that could be included in a PEMFC on-board controller. To this end, the ISF was discretized as coarsely as possible while still retaining identifying spectral features using the Goertzel algorithm in much the same way as in dual tone multi-frequency detection in telephony. This approach generated a significant reduction in computational burden relative to the classical Fast Fourier Transform approach. The ISF database was used to diagnose simulated experimental PEMFC failures into one of five levels of failure: none (normal operation), mild, moderate, advanced, and extreme from one of the three catalogued failure modes. The described ISF recognition algorithm was shown to correctly identify failure modes to a lower limit of SNR = 1dB.
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Aaron, Douglas Scott. "Transport in fuel cells: electrochemical impedance spectroscopy and neutron imaging studies." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/34699.

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Current environmental and energy sustainability trends have instigated considerable interest in alternative energy technologies that exhibit reduced dependence on fossil fuels. The advantages of such a direction are two-fold: reduced greenhouse gas emissions (notably CO2) and improved energy sustainability. Fuel cells are recognized as a potential technology that achieves both of these goals. However, improvements to fuel cell power density and stability must be realized to make them economically competitive with traditional, fossil-based technologies. The work in this dissertation is largely focused on the use of analytical tools for the study of transport processes in three fuel cell systems toward improvement of fuel cell performance. Polymer electrolyte membrane fuel cells (PEMFCs) are fueled by hydrogen and oxygen to generate electrical current. Microbial fuel cells (MFCs) use bacteria to degrade carbon compounds, such as those found in wastewaters, and simultaneously generate an electric current. Enzyme fuel cells (EFCs) operate similarly to PEMFCs but replace precious metal catalysts, such as platinum, with biologically-derived enzymes. The use of enzymes also allows EFCs to utilize simple carbon compounds as fuel. The operation of all three fuel cell systems involves different modes of ion and electron transport and can be affected negatively by transport limitations. Electrochemical impedance spectroscopy (EIS) was used in this work to study the distribution of transport resistances in all three fuel cell systems. The results of EIS were used to better understand the transport resistances that limited fuel cell power output. By using this technique, experimental conditions (including operating conditions, construction, and materials) were identified to develop fuel cells with greater power output and longevity. In addition to EIS, neutron imaging was employed to quantify the distribution of water in PEMFCs and EFCs. Water content is an integral aspect of providing optimal power output from both fuel cell systems. Neutron imaging contributed to developing an explanation for the loss of water observed in an operating EFC despite conditions designed to mitigate water loss. The findings of this dissertation contribute to the improvement of fuel cell technology in an effort to make these energy devices more economically viable.
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Bhatnagar, Purva. "A microcontroller-based Electrochemical Impedance Spectroscopy Platform for Health Monitoring Systems." University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439307617.

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Books on the topic "Electrochemical Impedance Spectroscopy"

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Orazem, Mark E., and Bernard Tribollet. Electrochemical Impedance Spectroscopy. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119363682.

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Orazem, Mark E., and Bernard Tribollet. Electrochemical Impedance Spectroscopy. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470381588.

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Boškoski, Pavle, Andrej Debenjak, and Biljana Mileva Boshkoska. Fast Electrochemical Impedance Spectroscopy. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-53390-2.

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Srinivasan, Ramanathan, and Fathima Fasmin. An Introduction to Electrochemical Impedance Spectroscopy. First edition. | Boca Raton : CRC Press, 2021.: CRC Press, 2021. http://dx.doi.org/10.1201/9781003127932.

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Lasia, Andrzej. Electrochemical Impedance Spectroscopy and its Applications. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-8933-7.

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Yuan, Xiao-Zi, Chaojie Song, Haijiang Wang, and Jiujun Zhang. Electrochemical Impedance Spectroscopy in PEM Fuel Cells. London: Springer London, 2010. http://dx.doi.org/10.1007/978-1-84882-846-9.

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Stoĭnov, Z. B. Differential impedance analysis. Sofia: Marin Drinov Academic Publishing House, 2005.

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Cottis, Robert. Electrochemical impedance and noise. Huston, TX: NACE International, 1999.

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Thomas, D. L. Testing and analysis of electrochemical cells using frequency response. [Marshall Space Flight Center, Ala.]: National Aeronautics and Space Administration, George C. Marshall Space Flight Center, 1992.

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B, Stoĭnov Z., and Institut ėlektrokhimii im. A.N. Frumkina., eds. Ėlektrokhimicheskiĭ impedans. Moskva: "Nauka", 1991.

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Book chapters on the topic "Electrochemical Impedance Spectroscopy"

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Azzarello, E., E. Masi, and S. Mancuso. "Electrochemical Impedance Spectroscopy." In Plant Electrophysiology, 205–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29119-7_9.

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González-Cortés, Araceli. "Electrochemical Impedance Spectroscopy." In Agricultural and Food Electroanalysis, 381–419. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118684030.ch14.

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Sharifi-Asl, Samin, and Digby D. Macdonald. "Electrochemical Impedance Spectroscopy." In Developments in Electrochemistry, 349–65. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118694404.ch19.

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Retter, Utz, and Heinz Lohse. "Electrochemical Impedance Spectroscopy." In Electroanalytical Methods, 159–77. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-02915-8_8.

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Retter, Utz, and Heinz Lohse. "Electrochemical Impedance Spectroscopy." In Electroanalytical Methods, 149–66. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/978-3-662-04757-6_8.

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Zhang, Jianbo, Shangshang Wang, and Kei Ono. "Electrochemical Impedance Spectroscopy." In Microscopy and Microanalysis for Lithium-Ion Batteries, 301–50. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003299295-11.

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Boškoski, Pavle, Andrej Debenjak, and Biljana Mileva Boshkoska. "Fast Electrochemical Impedance Spectroscopy." In Fast Electrochemical Impedance Spectroscopy, 9–22. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-53390-2_2.

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Naumann, Renate L. C. "Electrochemical Impedance Spectroscopy (EIS)." In Functional Polymer Films, 791–807. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527638482.ch25.

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Boškoski, Pavle, Andrej Debenjak, and Biljana Mileva Boshkoska. "Introduction." In Fast Electrochemical Impedance Spectroscopy, 1–7. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-53390-2_1.

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Boškoski, Pavle, Andrej Debenjak, and Biljana Mileva Boshkoska. "Statistical Properties." In Fast Electrochemical Impedance Spectroscopy, 23–30. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-53390-2_3.

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Conference papers on the topic "Electrochemical Impedance Spectroscopy"

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Helias, Valentin, Julie Zhang, Serge Picaud, Julie Degardin, Patrick Poulichet, Lionel Rousseau, and Olivier Francais. "Using Electrochemical Impedance Spectroscopy to Study the in vivo Evolution of the Electrochemical Properties of Neural Implants." In 2021 International Workshop on Impedance Spectroscopy (IWIS). IEEE, 2021. http://dx.doi.org/10.1109/iwis54661.2021.9711822.

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Raghav, Jyoti, and Soumyendu Roy. "Electrochemical Properties of Ternary Metal Oxides for Supercapacitor." In 2023 International Workshop on Impedance Spectroscopy (IWIS). IEEE, 2023. http://dx.doi.org/10.1109/iwis61214.2023.10302793.

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Hossain, Md Kamal, and S. M. Rakiul Islam. "Battery Impedance Measurement Using Electrochemical Impedance Spectroscopy Board." In 2017 2nd International Conference on Electrical & Electronic Engineering (ICEEE). IEEE, 2017. http://dx.doi.org/10.1109/ceee.2017.8412902.

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Han, H., N. B. Sabani, F. Takei, K. Nobusawa, and I. Yamashita. "DNA detection by Electrochemical Impedance Spectroscopy." In 2019 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2019. http://dx.doi.org/10.7567/ssdm.2019.a-3-01.

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Thiel, Susanne, Volker Seis, and Maik Eichelbaum. "Scanning electrochemical microscopy for the characterization of fuel cell components." In 2022 International Workshop on Impedance Spectroscopy (IWIS). IEEE, 2022. http://dx.doi.org/10.1109/iwis57888.2022.9975128.

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Fortes-Martín, Rebeca, Sebastian Risse, and Rafael Müller. "Drift Correction in Operando Electrochemical Impedance Spectroscopy for Batteries Research." In 2023 International Workshop on Impedance Spectroscopy (IWIS). IEEE, 2023. http://dx.doi.org/10.1109/iwis61214.2023.10302755.

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Castro-Ruiz, Sergio, and Jorge Garcia-Canadas. "Impedance Spectroscopy Analysis of a Thermo-Electrochemical Cell Under Operating Conditions." In 2022 International Workshop on Impedance Spectroscopy (IWIS). IEEE, 2022. http://dx.doi.org/10.1109/iwis57888.2022.9975126.

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Nasraoui, Salem, Ammar Al-Hamry, Sami Ameur, Mounir Ben Ali, and Olfa Kanoun. "Electrochemical Sensor for 4-Aminophenol Based on Flexible Laser Induced Graphene." In 2021 International Workshop on Impedance Spectroscopy (IWIS). IEEE, 2021. http://dx.doi.org/10.1109/iwis54661.2021.9711859.

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Yang, En-Chi, Suz-Ting Wang, Kusn-Lin Liu, Wen-Ho Juang, Ming-Hwa Sheu, How-Chiun Wu, and Shin-Chi Lai. "Fast Measurement of Impedance Calculation for Electrochemical Impedance Spectroscopy." In 2023 20th International SoC Design Conference (ISOCC). IEEE, 2023. http://dx.doi.org/10.1109/isocc59558.2023.10396167.

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Olarte, Oscar, Kurt Barbe, Wendy Van Moer, and Yves Van Ingelgem. "Glucose characterization based on electrochemical impedance spectroscopy." In 2014 IEEE International Instrumentation and Measurement Technology Conference (I2MTC). IEEE, 2014. http://dx.doi.org/10.1109/i2mtc.2014.6860860.

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Reports on the topic "Electrochemical Impedance Spectroscopy"

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Rivera, Rimi, and Narinder Mehta. Electrochemical Impedance Spectroscopy Evaluation of Primed BMI-Graphite/Aluminum Galvanic System. Fort Belvoir, VA: Defense Technical Information Center, July 2001. http://dx.doi.org/10.21236/ada390067.

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Hu, Hongqiang, Claire Xiong, Mike Hurley, and Ju Li. Establishing New Capability of High Temperature Electrochemical Impedance Spectroscopy Techniques for Equilibrium and Kinetic Experiments. Office of Scientific and Technical Information (OSTI), December 2017. http://dx.doi.org/10.2172/1468632.

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Olaes, Christopher, Richard Lampo, Lawrence Clark, Susan Drozdz, and Jeffrey Ryan. Demonstration and validation of portable electrochemical impedance spectroscopy technology : final report on Project F11-AR08. Construction Engineering Research Laboratory (U.S.), June 2018. http://dx.doi.org/10.21079/11681/27349.

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D. Zagidulin, P. Jakupi, J.J. Noel, and D.W. Shoesmith. Evaluation of an Oxide Layer on NI-CR-MO-W Alloy Using Electrochemical Impedance Spectroscopy and Surface Analysis. Office of Scientific and Technical Information (OSTI), December 2006. http://dx.doi.org/10.2172/899320.

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Hosbein, Kathryn. The Application of Electrochemical Impedance Spectroscopy to Immediately Diagnose the Protective Quality of Coatings on Artistic and Architectural Metalwork. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.3305.

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Bastawros, Ashraf. DTPH56-16H-CAP01 Mechanochemistry-Based Detection of Early Stage Corrosion Degradation of Pipeline Steels. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), May 2020. http://dx.doi.org/10.55274/r0011990.

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Abstract:
The aim of the work is to provide measurable precursor signals associated with the initiation stage of near-surface damage and cracking, as depicted in Fig. 1.1. We have identified many salient features during the early stage of the SCC process (Stages 1, 2 on Fig. 1.1), including residual stress build-up, near-surface (within few microns) defect percolation, and changes of dislocation dynamics and measurable changes of the surface osmic resistance. We developed a model-based prediction of the onset and progression of SCC subsurface damage and assessed the electrochemical impedance spectroscopy (EIS) to measure the extent of surface damage. Such a framework would enable the development of appropriate field-deployable NDE technology with the needed spatial and temporal resolutions.
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Hu, Hongqiang, Yanhao Dong, Ju Li, Claire Xiong, and Mike Hurley. (M4CT-18IN0707093) Investigating Electrochemical Impedance Spectroscopic (EIS) Measurement of Surrogate Oxide at High Temperatures. Office of Scientific and Technical Information (OSTI), March 2018. http://dx.doi.org/10.2172/1468637.

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