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Electrochemical Impedance Spectroscopy (electrochemical + impedance_spectroscopy)

Distribution by Scientific Domains

Polymers and Materials Science	47%
Chemistry	46%
2 Other Domains	7%

Selected Abstracts

Label-Free and Ultra-Low Level Detection of Salmonella enterica Serovar Typhimurium Using Electrochemical Impedance Spectroscopy

ELECTROANALYSIS, Issue 20 2009
Jeffrey
Abstract An immunosensor for rapid and low level detection of the bacterial pathogen Salmonella enterica Serovar Typhimurium was designed and developed based upon label-free electrochemical impedance spectroscopy and correlated to viable cell counts. The immunosensor was fabricated by electroplating gold onto a disposable printed circuit board (PCB) electrode by immobilizing monoclonal antibody (MAb) specific against Salmonella typhimurium cell surface lipopolysaccharide (LPS) onto the surface of the electrode. Use of mass-fabricated and electroplated PCB electrodes allowed for disposable, highly sensitive, and rapid detection of Salmonella in an aqueous environment. Results demonstrate that in purified solution, Salmonella can be detected as low as 10 CFU in a 100,,L volume and label-free and rapid manner in fewer than 90,s. The cost effective approach described here can be used for detection of pathogens with relevance for healthcare, food, and environmental applications. [source]

Detecting Biorecognition Events at Blocked Interface Polymeric Membrane Ion-Selective Electrodes Using Electrochemical Impedance Spectroscopy and Atomic Force Microscopy

ELECTROANALYSIS, Issue 3 2008
Marco, Roland De
Abstract Immobilization of a biorecognition element onto a polymeric membrane ion-selective electrode (ISE) using a self-assembly approach may provide scope for a novel biosensor technology platform based on the altered potentiometric response at the blocked ISE interface. In this paper, the authors have investigated the influence of solution adsorption of the model biorecognition element, avidin-biotin, on the electrode kinetics of a conventional polymeric membrane Ca2+ ISE using atomic force microscopy (AFM) coupled with electrochemical impedance spectroscopy (EIS). It is demonstrated that solution adsorption of avidin followed by biotin incorporation leads to a demonstrable biorecognition event characterized by an impediment in the Ca2+ ion transfer kinetics of the modified ISE surface. This kinetic principle is amenable to biosensing using pulsed chronopotentiometric polymeric ISEs, which is an established dynamic electrode technique for use with polymeric membrane ISEs. [source]

Disposable Gold Electrode Array for Simultaneous Electrochemical Studies

ELECTROANALYSIS, Issue 1 2008
Graciela Priano
Abstract An efficient and inexpensive eight gold electrode array has been manufactured by a combination of screen printing and gold electrodeposition techniques. Gold electrodeposition was performed in potentiostatic and galvanostatic conditions. Different treatments, involving temperature and polishing control, led to electrodes with different roughness. The electrochemical behavior of the generated gold surface was studied by cyclic voltammetry showing the characteristic response of polycrystalline gold, in contrast with disposable gold electrodes fabricated by screen printing from gold inks. The electrodes were chemically modified through the adsorption of alkanethiols self-assembled monolayers and the coupling of a model protein. Both reactions were followed by cyclic voltammetry and Electrochemical Impedance Spectroscopy (EIS). The electrodes have shown high reproducibility in their electrochemical behavior as well as in their modifications. [source]

Application of Electrochemical Impedance Spectroscopy for Fuel Cell Characterization: PEFC and Oxygen Reduction Reaction in Alkaline Solution,

FUEL CELLS, Issue 3 2009
N. Wagner
Abstract 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 Göhr [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. [source]

Electrochemical Reduction of Oxygen on Carbon Supported Pt and Pt/Ru Fuel Cell Electrodes in Alkaline Solutions

FUEL CELLS, Issue 4 2003
E.H. Yu
Abstract A study of O2 reduction in 1 M NaOH solution at gas diffusion electrodes made from carbon supported Pt and Pt/Ru catalysts is reported. Two Tafel regions were observed for both the Pt and Pt/Ru electrodes. Although the same mechanism was suggested for oxygen reduction on both Pt and Pt/Ru catalysts, the O2 reduction activity was lower on Ru. Electrochemical Impedance Spectroscopy (EIS) analysis was carried out at different potentials and showed the significant contribution of diffusion on the reaction process and kinetics. The effect of methanol on O2 reduction was investigated in solutions containing various concentrations of methanol. The electrode performance deteriorated with increasing methanol concentration because of a mixed cathode potential. The methanol tolerance, i. e., the methanol concentration which polarises the O2 reduction reaction for O2 reduction, at the Pt/C electrode with a Pt loading of 1.2 mg cm,2 is 0.2 M methanol in 1 M NaOH. [source]

Impedance measurements on oxide films on aluminium obtained by pulsed tensions

MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 1 2003
K. Belmokre
Anodisation; Elektrochemische Impedanzspektroskopie (EIS); pulsierende Spannung; Alterung von Oxidfilmen Abstract We have performed this study on oxide films sealed or not in boiling water. The films are first obtained on type 1050 A aluminium substrat by pulsed tensions anodizing technique, in a sulfuric acid solution. Afterwards the, Electrochemical Impedance Spectroscopy (EIS) is employed to appreciate the films behaviour in a neutral solution of 3.5% K2SO4, in which the interface processes interest only the ageing phenomenon of the oxide films and not their corrosion. We have also attempted a correlation between pulse parameters of anodization and the electrical parameters characterizing these films. The sealing influence on ageing has been studied as well. For all films, ageing is appreciated using impedance diagrams evolution versus time. The results show: , the existence of two capacitive loops confirming the presence of two oxide layers characteristic of oxide films obtained in a sulfuric acid medium. The first loop, at high frequencies, is related to the external porous layer and the second one, at lower freqencies, is related to the internal barrier layer. , the thickness of the barrier layer varies between 25 and 40 nm in relation with the electrical pulse parameters. , the sealing acts favorably against anodic oxide films ageing. Impedanzmessungen an durch pulsierende Spannung erzeugten Oxidfilmen auf Aluminium Die vorliegenden Untersuchungen wurden an versiegelten und nicht versiegelten Oxidfilmen in kochendem Wasser durchgeführt. Die Filme wurden zuerst auf Aluminiumsubstrat des Typs 1050A durch anodische Technik mit pulsierender Spannung in einer Schwefelsäurelösung erzeugt. Anschließend wurde die elektrochemische Impedanzspektroskopie eingesetzt, um das Filmverhalten in einer neutralen 3,5% K2SO4 -Lösung zu beurteilen, wobei bezüglich der Grenzflächenprozesse nur das Alterungsphänomen der Oxidfilme und nicht ihr Korrosionsverhalten interessierte. Es wurde versucht, eine Korrelation zwischen den Pulsparametern der Anodisierung und den elektrischen Parametern, die diese Filme charakterisieren, zu finden. Ebenfalls wurde der Versiegelungseinfluss auf die Alterung untersucht. Für alle Filme wurde die Alterung mit Hilfe der Entwicklung von Impedanzdiagrammen über die Zeit beurteilt. Die Ergebnisse zeigen: , die Existenz von zwei kapazitiven Schleifen, die die Anwesenheit von zwei Oxidschichten bestätigen, was charakteristisch ist für Oxidfilme, die in einer Schwefelsäurelösung erzeugt wurden. Die erste Schleife, bei hohen Frequenzen, bezieht sich auf die äußere poröse Schicht und die zweite, bei niedrigeren Frequenzen, bezieht sich auf die innere Barriereschicht , die Dicke der Barriereschicht variiert zwischen 25 und 40 nm, abhängig von den elektrischen Pulsparametern , die Versiegelung wirkt günstig gegenüber der Alterung des anodischen Oxidfilms. [source]

Impedance Spectroscopy: A Powerful Tool for Rapid Biomolecular Screening and Cell Culture Monitoring

ELECTROANALYSIS, Issue 23 2005
Isaac
Abstract Dielectric spectroscopy or Electrochemical impedance spectroscopy (EIS) is traditionally used in corrosion monitoring, coatings evaluation, batteries, and electrodeposition and semiconductor characterization. However, in recent years, it is gaining widespread application in biotechnology, tissue engineering, and characterization of biological cells, disease diagnosis and cell culture monitoring. This article discusses the principles and implementation of dielectric spectroscopy in these bioanalytical applications. It provides examples of EIS as label-free, mediator-free strategies for rapid screening of biocompatible surfaces, monitoring pathogenic bacteria, as well as the analysis of heterogeneous systems, especially biological cells and tissues. Descriptions are given of the application of nanoparticles to improve the analytical sensitivities in EIS. Specific examples are given of the detection of base pair mismatches in the DNA sequence of Hepatitis B disease, TaySach's disease and Microcystis spp. Others include the EIS detection of viable pathogenic bacteria and the influence of nanomaterials in enhancing biosensor performance. Expanding applications in tissue engineering such as adsorption of proteins onto thiolated hexa(ethylene glycol)-terminated (EG6) self-assembled monolayer (SAM) are discussed. [source]

Enhancement of photocurrent of polymer-gelled dye-sensitized solar cell by incorporation of exfoliated montmorillonite nanoplatelets

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 1 2008
Chi-Wei Tu
Abstract Poly(n -isopropylacrylamide) (PNIPAAm) and its nanocomposite with exfoliated montmorillonite (MMT) were prepared by soap-free emulsion polymerization and individually applied to gel the electrolyte systems for the dye-sensitized solar cells (DSSCs). Each exfoliated MMT nanoplatelet had a thickness of , 1 nm, carried , 1.8 cation/nm2, and acted like a two-dimensional electrolyte. The DSSC with the LiI/I2/tertiary butylpyridine electrolyte system gelled by this polymer nanocomposite had higher short-circuit current density (Jsc) compared to that gelled by the neat PNIPAAm. The former has a Jsc of 12.6 mA/cm2, an open circuit voltage (Voc) of 0.73 V, and a fill factor (FF) of 0.59, which harvested 5.4% electricity conversion efficiency (,) under AM 1.5 irradiation at 100 mW/cm2, whereas the latter has Jsc = 7.28 mA/cm2, Voc = 0.72 V, FF = 0.60, and , = 3.17%. IPCE of the nanocomposite-gelled DSSC were also improved. Electrochemical impedance spectroscopy of the DSSCs revealed that the nanocomposite-gelled electrolytes significantly decreased the impedances in three major electric current paths of DSSCs, that is, the resistance of electrolytes and electric contacts, impedance across the electrolytes/dye-coated TiO2 interface, and Nernstian diffusion within the electrolytes. The results were also consistent with the increased molar conductivity of nanocomposite-gelled electrolytes. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 47,53, 2008 [source]

Novel repair method for technical enamels based on sol,gel and sol-dispersion coatings,

MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 2 2008
S. Benfer
The aim of the work presented here is the development of a novel repair method for technical enamels by using chemical nanotechnology. Good adhesion of coatings requires good wettability of the substrate by the repair solution. This was achieved by different pre-treatments of the steel substrates. Low sintering temperatures of the coatings can be ensured by the use of nanoparticle-based systems. Based on liquid metal alkoxides, a colloidal alumina sol and metal salts homogeneous sols with up to seven enamel compounds were prepared. The sols were brush coated onto plain and partly enamelled steel substrates and sintered in a furnace, by inductive heating or an IR emitter. Thin (single layer,,,1µm) crack-free layers were obtained on nearly all substrates independent of the sintering conditions investigated. The local sintering methods (IR emitter, inductive heating) allow to produce multiple coating systems in short times. Electrochemical impedance spectroscopy (EIS) provides evidence of the protective effect of these layers compared to the bare substrate, but as a result of their chemical composition the layers are not stable in the electrolytic environment for longer times. The thickness of such multiple coatings (20 layers, ,,8 µm) is still small compared to that of a technical enamel. Therefore, sol dispersion systems containing powder particles and sol components are applied on top of the sol,gel layers to increase the thickness of the sintered layers. [source]

Evaluation of different sealing methods for anodized aluminum-silicon carbide (Al/SiC) composites using EIS and SEM techniques

MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 11 2007
H. Herrera-Hernandez
Electrochemical impedance spectroscopy (EIS) and the scanning electron microscope (SEM) have been used in an investigation of the effectiveness of various sealing methods that can be used to improve the corrosion resistance of an anodized aluminum-silicon carbide (Al/SiC) composite. Anodic oxide films were grown on Al7075-T6 and the Al/SiC composite by sulfuric acid anodizing and sealing in a cold saturated solution of nickel acetate. Other samples were sealed using the traditional method of boiling water or hot nickel acetate for comparison. The results revealed a uniform anodized layer on Al7075-T6 that resisted pitting corrosion for more than 2,weeks exposure to NaCl, whereas a cracked oxide film with variations in thickness was observed on the composite material. Pit initiation occurred in less than 5,days on the anodized Al/SiC that was sealed in the hot solutions. This study suggests that the traditional hot sealing methods did not provide sufficient corrosion protection for aluminum metal,matrix composites (MMCs) because the reinforcing SiC particles deteriorated the surface film structure. However, this defective film can be repaired by nickel hydrate precipitation during cold sealing or by applying a thick polyurethane coating. [source]

Electrochemical impedance spectroscopy analysis on aluminum alloys in EXCO solution

MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 5 2005
F.-H. Cao
Abstract Electrochemical impedance spectroscopy (EIS) of Al-Zn-Mg-Cu alloy in EXCO solution has been investigated. The results show that the impedance spectroscopy of the investigated electrode consists of two capacitive loops in the high and middle frequency domain respectively and an inductive loop in the low frequency domain at the first 30 h of immersion; the inductive arc disappears between 30 h and 60 h while it takes on at the low frequency domain at the last 36 h of the immersion time. A model based on the corrosion mechanism of the aluminum alloy and corroding morphology was proposed and applied to analyze the EIS results. [source]

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

PHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 4 2010
Michael Teka Woldemedhin
Abstract Anodic oxides were grown on the surface of an electropolished (Ti,30,at% Nb) beta-titanium (,-Ti) alloy by cyclic voltammetry. The scan rate was 100,mV,s,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,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,×,1017,cm,3. ,-Ti being highly isotropic in terms of mechanical properties should be superior to the stiffer ,-Ti compound. Its application, however, requires a passivation behaviour comparable or better than ,-Ti which in fact is found. [source]

Impedance spectroscopy as a tool for non-intrusive detection of extracellular mediators in microbial fuel cells

BIOTECHNOLOGY & BIOENGINEERING, Issue 5 2009
Ramaraja P. Ramasamy
Abstract Endogenously produced, diffusible redox mediators can act as electron shuttles for bacterial respiration. Accordingly, the mediators also serve a critical role in microbial fuel cells (MFCs), as they assist extracellular electron transfer from the bacteria to the anode serving as the intermediate electron sink. Electrochemical impedance spectroscopy (EIS) may be a valuable tool for evaluating the role of mediators in an operating MFC. EIS offers distinct advantages over some conventional analytical methods for the investigation of MFC systems because EIS can elucidate the electrochemical properties of various charge transfer processes in the bio-energetic pathway. Preliminary investigations of Shewanella oneidensis DSP10-based MFCs revealved that even low quantities of extracellular mediators significantly influence the impedance behavior of MFCs. EIS results also suggested that for the model MFC studied, electron transfer from the mediator to the anode may be up to 15 times faster than the electron transfer from bacteria to the mediator. When a simple carbonate membrane separated the anode and cathode chambers, the extracellular mediators were also detected at the cathode, indicating diffusion from the anode under open circuit conditions. The findings demonstrated that EIS can be used as a tool to indicate presence of extracellular redox mediators produced by microorganisms and their participation in extracellular electron shuttling. Biotechnol. Bioeng. 2009; 104: 882,891. © 2009 Wiley Periodicals, Inc. [source]

The Influence of Charge Transport and Recombination on the Performance of Dye-Sensitized Solar Cells

CHEMPHYSCHEM, Issue 1 2009
Mingkui Wang Dr.
Abstract Electrochemical impedance spectroscopy (EIS) and transient voltage decay measurements are applied to compare the performance of dye sensitized solar cells (DSCs) using organic electrolytes, ionic liquids and organic-hole conductors as hole transport materials (HTM). Nano-crystalline titania films sensitized by the same heteroleptic ruthenium complex NaRu(4-carboxylic acid-4,-carboxylate) (4,4,-dinonyl-2,2,-bipyridyl)(NCS)2,, coded Z-907Na are employed as working electrodes. The influence of the nature of the HTM on the photovoltaic figures of merit, that is, the open circuit voltage, short circuit photocurrent and fill factor is evaluated. In order to derive the electron lifetime, as well as the electron diffusion coefficient and charge collection efficiency, EIS measurements are performed in the dark and under illumination corresponding to realistic photovoltaic operating conditions of these mesoscopic solar cells. A theoretical model is established to interpret the frequency response off the impedance under open circuit conditions, which is conceptually similar to photovoltage transient decay measurements. Important information on factors that govern the dynamics of electron transport within the nanocrystalline TiO2 film and charge recombination across the dye sensitized heterojunction is obtained. [source]

Simultaneous Determination of Ascorbic Acid, Dopamine and Uric Acid at Pt Nanoparticles Decorated Multiwall Carbon Nanotubes Modified GCE

ELECTROANALYSIS, Issue 10 2010
Zekerya Dursun
Abstract A modified electrode was fabricated by electrochemically deposition of Pt nanoparticles on the multiwall carbon nanotube covered glassy carbon electrode (Pt nanoparticles decorated MWCNT/GCE). A higher catalytic activity was obtained to electrocatalytic oxidation of ascorbic acid, dopamine, and uric acid due to the enhanced peak current and well-defined peak separations compared with both, bare and MWCNT/GCE. The electrode surfaces were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and electrochemical impedance spectroscopy (EIS). Individual and simultaneous determination of AA, DA, and UA were studied by differential pulse voltammetry. The detection limits were individually calculated for ascorbic acid, dopamine, and uric acid as being 1.9×10,5,M, 2.78×10,8,M, and 3.2×10,8,M, respectively. In simultaneous determination, LODs were calculated for AA, DA, and UA, as of 2×10,5,M, 4.83×10,8,M, and 3.5×10,7,M, respectively. [source]

Mediated Electron Transfer Across Supported Bilayer Lipid Membrane with TCNQ-Based Organometallic Compounds

ELECTROANALYSIS, Issue 4 2010
Meili Qu
Abstract Supported bilayer lipid membrane (s-BLM) containing one-dimensional compound 1, TCNQ-based (TCNQ=7,7,8,8-tetracyanoquinodimethane) organometallic compound {(Cu2(,-Cl)(,-dppm)2)(,2 -TCNQ)},, was prepared and characterized on the self-assembled monolayer (SAM) of 1-octadecylmercaptan (C18H37SH) deposited onto Au electrode. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) results showed that the compound 1, dotted inside s-BLM, can act as mediator for electron transfer across the membrane. Two redox peaks and the charge-transfer resistance of 400,k, were observed for compound 1 inside s-BLM. The mechanism of the electron transfer across s-BLM by TCNQ is by electron hopping while TCNQ-based organometallic compound is by conducting. Further conclusion drawn from this finding is that the TCNQ-based organometallic compound embedded inside s-BLM exhibits excellent electron transfer ability than that of free TCNQ. This opens a new path for the development of s-BLM sensor and/or biosensor by incorporation with TCNQ-based organometallic compounds. [source]

Label-Free and Ultra-Low Level Detection of Salmonella enterica Serovar Typhimurium Using Electrochemical Impedance Spectroscopy

Direct Electrochemistry and Electrocatalysis of Hemoglobin in Lipid Film Incorporated with Room-Temperature Ionic Liquid

ELECTROANALYSIS, Issue 20 2008
Gaiping Li
Abstract A facile phospholipid/room-temperature ionic liquid (RTIL) composite material based on dimyristoylphosphatidylcholine (DMPC) and 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim]PF6) was exploited as a new matrix for immobilizing protein. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were adopted to characterize this composite film. Hemoglobin (Hb) was chosen as a model protein to investigate the composite system. UV-vis absorbance spectra showed that Hb still maintained its heme crevice integrity in this composite film. By virtue of the Hb/DMPC/[bmim]PF6 composite film-modified glassy carbon electrode (GCE), a pair of well-defined redox peaks of Hb was obtained through the direct electron transfer between protein and underlying GCE. Moreover, the reduction of O2 and H2O2 at the Hb/DMPC/[bmim]PF6 composite film-modified GCE was dramatically enhanced. [source]

Some Properties of Sodium Dodecyl Sulfate Functionalized Multiwalled Carbon Nanotubes Electrode and Its Application on Detection of Dopamine in the Presence of Ascorbic Acid

ELECTROANALYSIS, Issue 16 2008
Dan Zheng
Abstract A sodium dodecyl sulfate (SDS) functionalized multiwalled carbon nanotubes (MWNTs) electrode (SDS/MWNTs) was successfully constructed in this study. The electrochemical property of the SDS/MWNTs electrode has been characterized by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Nyquist plots suggest that the immersion time of SDS affects the resistances of the MWNTs electrodes. The thickness of adsorbed SDS on MWNTs surface is estimated to be 1.23,nm, which is close to the value of SDS monolayer. CV results demonstrate a 5-fold enhanced response for dopamine (DA) at the SDS/MWNTs electrode compared to the bare MWNTs one. DPV results illustrate that DA can be selectively determined in the presence of high concentration ascorbic acid (AA) with a linear range from 20,,M to 0.20,mM and a sensitivity of 0.024,,A ,M,1 at the SDS/MWNTs electrode. [source]

Paste Electrode Based on Short Single-Walled Carbon Nanotubes and Room Temperature Ionic Liquid: Preparation, Characterization and Application in DNA Detection

ELECTROANALYSIS, Issue 12 2008
Xuzhi Zhang
Abstract A paste electrode (SWNT&RTIL PE) has been prepared using carboxylic group-functionalized short single-walled carbon nanotubes (SWNTs) mixed with 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6, one kind of room temperature ionic liquid, RTIL). Its electrochemical behavior was investigated by cyclic voltammetry and electrochemical impedance spectroscopy in comparison with the paste electrode using mineral oil as a binder. Results highlighted the advantages of the paste electrode: not only higher conductivity, but also lower potential separation (,Ep), higher peak current (ip) and better reversibility towards dopamine (DA), methylene blue (MB) and K3[Fe(CN)6]. The SWNT&RTIL PE could be used to detect the number of guanine bases and adenine bases contents in per mol oligonucleotides according to the current response in the range of 0.05,2.0,nM. Based on the current response of guanine bases, oligonucleotides could be detected sensitively in the B,R buffer solution with a detection limit of 9.9,pM. The heterogeneous electron transfer rate constant (ks) of guanine bases contents in the oligonucleotides was investigated and its value was 0.90,s,1. In essence the SWNT&RTIL PE showed high sensitivity, reliability, stability and reproducibility for the detection of DNA. [source]

Fabrication and Application of a Novel Modified Electrode Based on Multiwalled Nanotubes/Cerium(III) 12-Tungstophosphoric Acid Nanocomposite

ELECTROANALYSIS, Issue 11 2008
Bin Fang
Abstract A novel multiwalled nanotubes (MWNTs)/Cerium(III) 12 - tungstophosphoric acid (CePW) nanocomposite film glassy carbon electrode was prepared in this paper. Electrochemical behaviors of the CePW/MWNTs modified electrode were investigated by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). This modified electrode brought new capabilities for electrochemical devices by combining the advantages of carbon nanotubes, rare-earth, and heteropoly-acids. The results demonstrated that the CePW/MWNTs modified electrode exhibited enhanced electrocatalytic behavior and good stability for the detection of guanine and adenine in 0.1,M PBS (pH,7.0). The experimental parameters were optimized and a direct electrochemical method for the simultaneous determination of guanine and adenine was proposed. The detection limit (S/N=3) for guanine and adenine was 2.0×10,8,M and 3.0×10,8,M, respectively. Further, the acid-denatured calf thymus DNA was also detected and the result was satisfied. [source]

Electrochemical Characterization of In Situ Functionalized Gold Cysteamine Self-Assembled Monolayer with 4-Formylphenylboronic Acid for Detection of Dopamine

ELECTROANALYSIS, Issue 5 2008
Karimi Shervedani
Abstract Functionalization of gold cysteamine (AuCA) self-assembled monolayer with 4-formylphenylboronic acid (BA) via Schiff's base formation, through in situ method to fabricate Au-CA-BA electrode is presented and described. The fabricated electrode was used as a novel sensor for accumulation and determination of dopamine (DA). The accumulation of DA as a diol on the topside of Au-CA-BA as a Lewis acid, was performed via esterification (AuCABADA), and followed for determination of DA. Functionalization, characterization, and determination steps were probed by electrochemical methods like cyclic voltammetry and electrochemical impedance spectroscopy. The data will be presented and discussed from which a new sensor for DA is introduced. [source]

Detecting Biorecognition Events at Blocked Interface Polymeric Membrane Ion-Selective Electrodes Using Electrochemical Impedance Spectroscopy and Atomic Force Microscopy

Development of Novel Glucose and Pyruvate Biosensors at Poly(Neutral Red) Modified Carbon Film Electrodes.

ELECTROANALYSIS, Issue 8 2006
Application to Natural Samples
Abstract Amperometric biosensors based on the corresponding oxidase enzyme with poly(neutral red) redox mediator have been developed for the determination of glucose and pyruvate. The enzymes have been immobilized on top of poly(neutral red) modified carbon film electrodes with glutaraldehyde as the cross-linking agent. The biosensors were characterized by cyclic voltammetry and by electrochemical impedance spectroscopy. The glucose biosensor exhibited a linear response in the range 90,,M to 1.8,mM with a detection limit of 22,,M and the pyruvate biosensor in the range 90 to 600,,M with a detection limit of 34,,M. The relative standard deviations were found to be 2.1% (n=3) and 2.8% (n=4) respectively. The interference effects of various compounds were also studied. The glucose content of several types of wine and the amount of pyruvate in onion and garlic were determined and the results were compared with those obtained by standard spectrophotometric methods. [source]

Direct and Rapid Detection of Diphtherotoxin via Potentiometric Immunosensor Based on Nanoparticles Mixture and Polyvinyl Butyral as Matrixes

ELECTROANALYSIS, Issue 24 2005
Dianping Tang
Abstract In this paper a novel potentiometric immunosensor for direct and rapid detection of diphtherotoxin (D-Ag) has been developed by means of self-assembly of monoclonal diphtheria antibody (D-Ab) onto a platinum electrode based on nanoparticles mixture (containing gold nanoparticles and silica nanoparticles) and polyvinyl butyral (PVB) as matrixes. At first, D-Ab was absorbed onto the surface of nanoparticles mixture, and then they were entrapped into polyvinyl butyral sol-gel network on a platinum electrode. The detection is based on the change in the potentiometric response before and after the antigen-antibody reaction in a phosphate buffer solution (pH,7.0). The immobilized D-Ab exhibited direct potentiometric response toward D-Ag. In comparison to the conventional applied methods, this strategy could allow antibodies immobilized with higher loading amount and better retained immunoactivity, as demonstrated by potentiometric response, cyclic voltammetry and electrochemical impedance spectroscopy of the immunosensor. The immunosensor with nanoparticles mixture exhibited much higher sensitivity, better reproducibility, and long-term stability than that with gold nanoparticles or silica nanoparticles alone. The linear range was from 5.0×10,3 to 1.2,,g,mL,1 with a detection limit of 1.1×10,3,,g,mL,1. Up to 16 successive assay cycles with retentive sensitivity were achieved for the probes regenerated with in 0.2,mol,L,1 glycine-hydrochloric acid (Gly-HCl) buffer solution and 0.25,mol,L,1 NaCl. Moreover, the immunosensor with nanoparticles mixture was applied to evaluate a number of practical specimens with potentiometric results in acceptable agreement with those given by the ELISA method, implying a promising alternative approach for detecting diphtherotoxin in the clinical diagnosis. [source]

Performance of Impedimetric Biosensors Based on Anodically Formed Ti/TiO2 Electrodes

ELECTROANALYSIS, Issue 20 2005
Aikaterini
Abstract The advantages and limitations of impedimetric sensors based on Ti/TiO2 architectures are described. Titanium dioxide (titania) was potentiostatically formed onto titanium electrodes of 2,mm diameter, at 10 and 30,V in 1,M H2SO4. The thickness of the titania layers was ellipsometrically determined to be 30 and 86,nm respectively and they are highly insulating with charge-transfer resistances in the M, range, as they were measured with electrochemical impedance spectroscopy under specific experimental conditions. Low voltage anodization (<10,V) results to amorphous TiO2, whereas at higher applied voltages (>25,V), anatase is the predominant form. SEM images are indicative of quite smooth, compact coatings without any severe cracks. [source]

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

ELECTROANALYSIS, Issue 7 2005
Carla Gouveia-Caridade
Abstract 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-coated pretreated electrodes in the presence and absence of dissolved oxygen. EIS equivalent circuit analysis clearly demonstrated the changes between these electrode assemblies. In order to simulate anodic stripping voltammetry conditions, spectra were also obtained in the presence of cadmium and lead ions in solution at Nafion-coated electrodes, both after metal ion deposition and following re-oxidation. Permanent changes to the structure of the Nafion film occurred, which has implications for use of these electrode assemblies in anodic stripping voltammetry at relatively high trace metal ion concentrations. [source]

High-Performance Carbon-LiMnPO4 Nanocomposite Cathode for Lithium Batteries

ADVANCED FUNCTIONAL MATERIALS, Issue 19 2010
Seung-Min Oh
Abstract A cathode material of an electrically conducting carbon-LiMnPO4 nanocomposite is synthesized by ultrasonic spray pyrolysis followed by ball milling. The effect of the carbon content on the physicochemical and electrochemical properties of this material is extensively studied. A LiMnPO4 electrode with 30 wt% acetylene black (AB) carbon exhibits an excellent rate capability and good cycle life in cell tests at 55 and 25 °C. This electrode delivers a discharge capacity of 158 mAh g,1 at 1/20 C, 126 mAh g,1 at 1 C, and 107 mAh g,1 at 2 C rate, which are the highest capacities reported so far for this type of electrode. Transmission electron microscopy and Mn dissolution results confirm that the carbon particles surrounding the LiMnPO4 protect the electrode from HF attack, and thus lead to a reduction of the Mn dissolution that usually occurs with this electrode. The improved electrochemical properties of the C-LiMnPO4 electrode are also verified by electrochemical impedance spectroscopy. [source]

Power Generation and Electrochemical Analysis of Biocathode Microbial Fuel Cell Using Graphite Fibre Brush as Cathode Material

FUEL CELLS, Issue 5 2009
S.-J. You
Abstract To improve cathodic efficiency and sustainability of microbial fuel cell (MFC), graphite fibre brush (GFB) was examined as cathode material for power production in biocatalysed-cathode MFC. Following 133-h mixed culturing of electricity-producing bacteria, the MFC could generate a reproducible voltage of 0.4,V at external resistance (REX) of 100,,. Maximum volumetric power density of 68.4,W,m,3 was obtained at a current density of 178.6,A,m,3. Upon aerobic inoculation of electrochemically active bacteria, charge transfer resistance of the cathode was decreased from 188 to 17,, as indicated by electrochemical impedance spectroscopy (EIS) analysis. Comparing investigations of different cathode materials demonstrated that biocatalysed GFB had better performance in terms of half-cell polarisation, power and Coulombic efficiency (CE) over other tested materials. Additionally, pH deviation of electrolyte in anode and cathode was also observed. This study provides a demonstration of GFB used as biocathode material in MFC for more efficient and sustainable electricity recovery from organic substances. [source]