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Electrochemical Response (electrochemical + response)

Distribution by Scientific Domains

Chemistry	77%
Life Sciences	9%
3 Other Domains	14%

Selected Abstracts

Electrochemical evaluation of cellular physiological status under stress in Escherichia coli with the rpoS-lacZ reporter gene

BIOTECHNOLOGY & BIOENGINEERING, Issue 4 2005
Hisakage Funabashi
Abstract We developed an electrochemical detection method for evaluating cellular physiological status based on the stringent response as a means to monitor cell viability. A reporter plasmid was constructed by inserting the ,-galactosidase gene (lacZ) under the control of the rpoS promoter, and then used to transform E. coli cells. Electrochemical responses from the products catalyzed by ,-galactosidase expressed by these E. coli cells were detected using the chronoamperometric technique in a nondestructive manner. Comparisons of response currents between the relA -positive strain and relA -negative strain revealed that increases in these currents were caused by the stringent response due to the stressful alcoholic environment, and thus as a model of stressful cultivating conditions. The current was proportional to the ,-galactosidase activity assayed by a conventional method that required the destruction of cells. The cellular physiological status, which depends on the stringent response as a viability marker, therefore, could then be evaluated online with a current using the rpoS-lacZ reporter gene in the relA -positive strain without pretreatment. © 2005 Wiley Periodicals, Inc. [source]

The Influence of the Cathodic Pretreatment on the Electrochemical Detection of Dopamine by Poly(1-aminoanthracene) Modified Electrode

ELECTROANALYSIS, Issue 19 2010
Estela de Pieri Troiani
Abstract In this study we demonstrated the influence of the cathodic pretreatment of poly(1-aminoanthracene) (PAA) electropolymerized on a platinum electrode for determination of dopamine (DA). The DA electrochemical response was obtained after a cathodic pretreatment of the PAA electrode which consisted of applying a potential of ,0.7,V (vs. Ag/AgCl) for 3,s before each measurement. The pretreatment of the electrode changed the PAA electrocatalytic properties so that the electrode began to present electrochemical response to DA without interference of ascorbic acid (AA). The anodic peak currents determined by differential pulse voltammetry using pretreated PAA showed a linear dependence on the DA concentration from 0.56 to 100,µM with a detection limit of 0.13,µM and a correlation coefficient of 0.9986. The electrode exhibits a relative standard deviation of 1.2,% for ten successive measurements of a 0.5,mM DA solution. The analysis by scanning electron microscopy and atomic force microscopy show a homogeneous and nanostructured film with globular structures with diameter of about 20,nm. The analytical results obtained for DA determination at a pretreated PAA electrode in pharmaceutical formulation sample were in good agreement with those obtained by a comparative procedure at a 95,% confidence level. PAA electrode after the pretreatment showed electrochemical responses to DA with excellent selectivity, sensitivity, and high stability without interference of AA. [source]

A New Amperometric Hydrazine Sensor Based on Prussian Blue/Single-walled Carbon Nanotube Nanocomposites

ELECTROANALYSIS, Issue 16 2010
Cong Wang
Abstract A slow reaction process has been successfully used to synthesize Prussian blue/single-walled carbon nanotubes (PB/SWNTs) nanocomposites. Electrochemical and surface characterization by cyclic voltammetry (CV), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-vis absorption spectroscopy, Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) confirmed the presence of PB nanocrystallites on SWNTs. PB/SWNTs modified glassy carbon electrode (GCE) exhibits efficient electron transfer ability and high electrochemical response towards hydrazine. The fabricated hydrazine sensor showed a wide linear range of 2.0×10,6,6.0×10,3,M with a response time less than 4,s and a detection limit of 0.5,,M. PB/SWNTs modified electrochemical sensors are promising candidates for cost-effective in the hydrazine assays. [source]

Directly Heated Bismuth Film Electrodes Based on Gold Microwires

ELECTROANALYSIS, Issue 13 2010
Martin Jacobsen
Abstract As a nontoxic substitute for mercury electrodes, bismuth electrodes attained a lot of attention during the last years. In this report we describe for the first time the preparation of two different directly heatable bismuth-modified microwire electrodes. We characterized the electrochemical behaviour using cyclic voltammetry in acetate buffer and alkaline tartrate solution. The bismuth electrodes show a significantly wider potential window compared with bare gold wires. In the presence of picric acid as one example for the detection of explosives, the bismuth electrodes deliver higher signals. By applying heat during the measurements, the signals can be enhanced further. We used the temperature pulse amperometry (TPA) technique to improve the electrochemical response at the different types of electrodes. In this preliminary study, we were able to detect 3,ppm traces of picric acid. [source]

Synthesis and Characterization of MWNTs/Au NPs/HS(CH2)6Fc Nanocomposite: Application to Electrochemical Determination of Ascorbic Acid

ELECTROANALYSIS, Issue 16 2008
Jian-Ding Qiu
Abstract In this article, a detailed electrochemical study of a novel 6-ferrocenylhexanethiol (HS(CH2)6Fc) self-assembled multiwalled carbon nanotubes-Au nanoparticles (MWNTs/Au NPs) composite film was demonstrated. MWNTs/Au NPs were prepared by one-step in situ synthesis using linear polyethyleneimine (PEI) as bifunctionalizing agent. HS(CH2)6Fc, which acted as the redox mediator, was self-assembled to MWNTs/Au NPs via Au-S bond. Transmission electron microscopy (TEM), energy-dispersive X-ray analysis (EDX), Fourier transformed infrared absorption spectroscopy (FT-IR), UV-visible absorption spectroscopy, and cyclic voltammetry were used to characterize the properties of the MWNTs/Au NPs/HS(CH2)6Fc nanocomposite. The preparation of the nanocomposite was very simple and effectively prevented the leakage of the HS(CH2)6Fc mediator during measurements. The electrooxidation of AA could be catalyzed by Fc/Fc+ couple as a mediator and had a higher electrochemical response due to the unique performance of MWNTs/Au NPs. The nanocomposite modified electrode exhibited excellent catalytic efficiency, high sensitivity, good stability, fast response (within 3,s) and low detection limit toward the oxidation of AA at a lower potential. [source]

The Mediated Electrochemical Method for Rapid Fermentation Ability Assessment

ELECTROANALYSIS, Issue 14 2008
Jinsheng Zhao
Abstract The mediated electrochemical method characterized by the combinational utilization of two double mediator systems was proposed to assess the fermentation efficiency of three yeasts. The mediator systems selected were the menadione/ferricyanide system and the 2,6-dichlorophenolindophenol (DCPIP)/ferricyanide system. Both the electrochemical responses and succinate dehydrogenase assay suggested that the menadione/ferricyanide system made the yeasts switch to anaerobic respiration and, the DCPIP/ferricyanide system let the yeasts remain in theirs fermentative mode. The ethanol yields (g ethanol/g glucose) and the RD/RM (RD and RM refer to the electrochemical response from the menadione/ferricyanide system and the DCPIP/ferricyanide system, respectively) values are 0.47 and 0.38, 0.24 and 0.75, 0.23 and 0.81, respectively, for Saccharomyces cerevisiae, Pachysolen tannophilus and Pichia stipitis. The results showed that there was a negative correlation between the ethanol yields and the RD/RM values of the three yeasts, which showed the feasibility of the mediated electrochemical method in rapid fermentation ability assay. [source]

Facilitated Transfer of Alkali Metal Ions by a Tetraester Derivative of Thiacalix[4]arene at the Liquid,Liquid Interface

ELECTROANALYSIS, Issue 12 2008
Akgemci, Emine Guler
Abstract The facilitated transfer of alkali metal ions (Na+, K+, Rb+, and Cs+) by 25,26,27,28-tetraethoxycarbonylmethoxy-thiacalix[4]arene across the water/1,2-dichloroethane interface was investigated by cyclic voltammetry. The dependence of the half-wave transfer potential on the metal and ligand concentrations was used to formulate the stoichiometric ratio and to evaluate the association constants of the complexes formed between ionophore and metal ions. While the facilitated transfer of Li+ ion was not observed across the water/1,2-dichloroethane interface, the facilitated transfers were observed by formation of 1,:,1 (metal:ionophore) complex for Na+, K+, and Rb+ ions except for Cs+ ion. In the case of Cs+ a 1,:,2 (metal:ionophore) complex was obtained from its special electrochemical response to the variation of ligand concentrations in the organic phase. The logarithms of the complex association constants, for facilitated transfer of Na+, K+, Rb+, and Cs+, were estimated as 6.52, 7.75, 7.91 (log ,1°), and 8.36 (log ,2°), respectively. [source]

Investigation of the Role of Ionic Liquids in Imparting Electrocatalytic Behavior to Carbon Paste Electrode

ELECTROANALYSIS, Issue 21 2007
Norouz Maleki
Abstract In this paper, a survey has been undertaken to clarify the possible reasons for the electrocatalytic activity obtained by the presence of ionic liquid in carbon paste electrode (CPE). For this purpose, the effect of the addition of traces of ionic liquid to conventional CPE was investigated. Fe(CN)63,/4, was used as a probe and two ionic liquids, namely n -octylpyridinum hexafluorophosphate and 1-octyl-3-methylimidazolium hexaflourophosphate were tested for their electrocatalytic activity. The reasons for this electrocatalytic behavior were evaluated and it was found that different factors such as increase in the ionic conduction of the binder, decrease in the resistance of the modified electrode, increase in ion exchange properties of the electrode and the inherent catalytic activity of ionic liquids are responsible for the considerable improved electrochemical response obtained in the presence of traces of ionic liquid. [source]

Chitosan Incorporating Cetyltrimethylammonium Bromide Modified Glassy Carbon Electrode for Simultaneous Determination of Ascorbic Acid and Dopamine

ELECTROANALYSIS, Issue 17 2007
Xuelian Zou
Abstract Simultaneous determination of a neurotransmitter, dopamine (DA), and ascorbic acid (AA) is achieved at neutral pH on a chitosan incorporating cetyltrimethylammonium bromide (CTAB) modified glassy carbon (GC) electrode. Differential pulse voltammetry (DPV) technique was used to investigate the electrochemical response of DA and AA at a glassy carbon electrode modified with chitosan incorporating CTAB. An optimum 6.0,mmol L,1 of CTAB together with 0.5 wt% of chitosan was used to improve the resolution and the determination sensitivity. In 0.1,mol L,1 aqueous phosphate buffer solution of pH,6.8, the chitosan-CTAB modified electrode showed a good electrocatalytic response towards DA and AA. The anodic peak potential of DA shifted positively, while that of AA shifted negatively. Thus, the difference of the anodic peaks of DA and AA reached 0.23,V, which was enough to separate the two anodic peaks very well. The presented method herein could be applied to the direct simultaneous determination of DA and AA without prior treatment. The anodic peak currents (Ipa) of DPV are proportional to DA in the concentration range of 8,,M to 1000,,M, to that of AA 10,,M to 2000,,M, with correlation coefficients of 0.9930 and 0.9945, respectively. The linear range is much wider than previously reported. [source]

Study of the Responses of a Sonogel-Carbon Electrode Towards Phenolic Compounds

ELECTROANALYSIS, Issue 9 2005
Cordero-Rando, Ma del
Abstract The electrochemical behavior of a sonogel-carbon electrode towards nine phenolic compounds (chloro-, nitro- and alkyl-phenols) was studied; one of them (4-chloro-3-methylphenol) was used to evaluate characteristics of the electrode, such as accumulation and cleaning procedure of the electrode surface, reproducibility of the measurements, and influence of time from fabrication on electrochemical response. A polyethyleneglycol-modified sonogel-carbon electrode was found to improve the electrochemical response towards the analyte. A linear relationship between peak height and concentration in the range 0.005,0.5,mg L,1 was obtained, with a detection limit of 2.8,,g L,1. The studies of electrochemical parameters, as well as interferences, are also included. [source]

Microchip electrophoresis with wall-jet electrochemical detector: Influence of detection potential upon resolution of solutes

ELECTROPHORESIS, Issue 24 2006
Martin Pumera Dr.
Abstract This report studies the electrochemical response of wall-jet detector for microchip electrophoresis (µCE). It shows that in wall-jet configuration, the electrochemical detector operates in coulometric mode and that there is an influence of detection potential upon peak width and therefore upon the resolution of solutes. Upon raising the detection potential from +0.3 to +0.9,V, the resolution between model analytes, dopamine and catechol, increases from 0.63 to 2.90. The reasons for this behavior originate in wall-jet detector design and in its typically significant higher detector volume than the volume of injected sample. The conversion efficiency of the wall-jet electrochemical detection cell was found to be 97.4% for dopamine and 98.0% for catechol. The paper brings deeper understanding of operations of wall-jet electrochemical detectors for microchip devices, and it explains previously reported significantly sharper peaks when electrocatalytic electrodes (i.e., palladium and carbon nanotube) were used in µCE-electrochemistry wall-jet detector. [source]

Modulation of the Communication between Redox Centers in a Tris(ferrocene)-tren Ligand by Complexation of Lanthanide Ions

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 23 2003
Marie Heitzmann
The tripodal ligand L built on the tren platform and bearing three chemically equivalent ferrocene units was prepared and characterized. Electrochemical investigations indicate that electrostatic communication occurs between the three ferrocene groups in L, which leads to the observation of two distinct voltammetric waves. The electrochemical communication between the three ferrocene moieties is disrupted in 1:1 (L:M3+) type complexes formed between L and Y3+ or Eu3+ metal cations and their electrochemical response tends towards that of a single three-independent-electrons oxidation wave. Modulation of the electrochemical properties of L in the presence of lanthanide ions might be exploited with a view to their electrochemical sensing in organic and aqueous media. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003) [source]

Synthesis and Anion-Binding Properties of Novel Redox-Active Calixarene Receptors

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 25 2008
Estelle Métay
Abstract A novel synthetic approach towards redox-active calixarene-based receptors is described in which ferrocene fragments were introduced at the lower rim through anion-binding urea or amide connections. These derivatives were prepared in one pot by treating an amine-containing calixarene with ferrocenecarboxylic acid in the presence of diphenylphosphoryl azide and diisopropylethylamine. This method allows a convergent approach to these receptors and is readily adaptable to the introduction of other urea substituents. The anion-binding properties of these artificial receptors have been revealed by NMR spectroscopy and thoroughly investigated by electrochemical methods. We have assessed the importance of the urea,phosphate bonds in the observed electrochemical response by studying receptors in which the ferrocene reporters and binding fragments are closely associated or fully disconnected through a long alkyl chain. The experimental results clearly show the utmost importance of ion-pairing effects in the electrochemical recognition process, which account for most of the transduction signal in organic apolar media. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source]

Molecular Dynamics Simulations of the Orientation and Reorientational Dynamics of Water and Polypyrrole Rings as a Function of the Oxidation State of the Polymer

MACROMOLECULAR THEORY AND SIMULATIONS, Issue 1 2005
Jose J. López Cascales
Abstract Summary: Polypyrrole is one of the most widely-studied conducting polymers due to its steady electrochemical response and good chemical stability in different solvents, including organic and inorganic ones. In this work, we provide for the first time valuable information in atomic detail concerning the steady and dynamic properties of pyrrole rings as a function of the oxidation state of the polymer. The study was carried out by Classical molecular dynamics simulation, where the system was modelled by 256 polypyrrole chains of 10 pyrrole rings each. Water was explicitly introduced in our simulations. Besides the uncharged or reduced state, two steady oxidation states of the polymer have been simulated by introducing a net charge (+1) on 85 and 256 of the polypyrrole chains. To balance the charges emerging in these oxidised states, 85 and 256 chloride ions (Cl,1) respectively, were introduced into the system. From an analysis of the simulated trajectories, the orientation and relaxation times of water and pyrrole rings were evaluated for the different oxidation states of the polymer across the polypyrrole/water interface. The calculated densities for different oxidation states describe the swelling or shrinking process during electrochemical oxidation or reduction respectively. The rotational relaxation times calculated for the polypyrrole rings decrease with increasing oxidation of the polymer, which is in a good agreement with experimental electrochemical data. Almost no variation in pyrrole ring orientation was measured for the different oxidation states of the polymer, even compared with polypyrrole bulk. As regards the water structure in the vicinity of the polypyrrole/water interface, both the orientation and orientation relaxation time were strongly affected by the presence of charges in the polymer. Thus, the water dipole was strongly orientated in the vicinity of the water/polypyrrole interface and its orientational relaxation time increased by one order of magnitude compared with bulk water, even when only one-third of the total polymer chains were oxidised. The results attained in this work were validated with experimental results, when they were available. Polypyrrole ring orientation and water orientation at the polypyrrole/water interface. (a) 256 rPPy and (b)171 rPPy,+,85 oPPy. [source]

Synthesis, stability and electrocatalytic activity of polymer-stabilized monometallic Pt and bimetallic Pt/Cu core,shell nanoparticles

PHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 6 2008
D. N. Muraviev
Abstract In this paper we report the results obtained for inter-matrix synthesis (IMS) and characterization of monometallic and bimetallic polymer-stabilized metal nanoparticles (PSMNPs). The IMS procedure is based on the use of appropriately functionalized polymeric membranes as nanoreactors, which allows both synthesis and characterization of the composition and morphology of PSMNPs inside the membranes. The membranes were prepared by using noncrosslinked sulfonated poly(etherether ketone) (SPEEK) of desired degree of sulfonation, which provided insolubility of the polymer in water and solubility in some organic solvents (e.g. dimethylformamide). The IMS of PSMNPs involved loading of the membrane with metal ions or complexes followed by metal reduction inside the membrane resulting in the formation of either monometallic (Cu or Pt) or bimetallic (Pt/Cu) PSMNPs with core,shell structure. The electrocatalytic activity of the PSMNPs was estimated by measuring the electrochemical response of amperometric sensors prepared by using SPEEK-Pt-PSMNP and SPEEK-Pt/Cu-PSMNP nanocomposite membranes as sensing elements to detect H2O2. At the same values of Pt loading the response of Pt/Cu-PSMNP-based sensors appeared to be far higher than that of sensors modified with Pt-PSMNP membranes. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]

Nanoparticle-Based Electrochemical Immunosensor for the Detection of Phosphorylated Acetylcholinesterase: An Exposure Biomarker of Organophosphate Pesticides and Nerve Agents

CHEMISTRY - A EUROPEAN JOURNAL, Issue 32 2008
Guodong Liu Dr.
Abstract A nanoparticle-based electrochemical immunosensor has been developed for the detection of phosphorylated acetylcholinesterase (AChE), which is a potential biomarker of exposure to organophosphate (OP) pesticides and chemical warfare nerve agents. Zirconia nanoparticles (ZrO2 NPs) were used as selective sorbents to capture the phosphorylated AChE adduct, and quantum dots (ZnS@CdS, QDs) were used as tags to label monoclonal anti-AChE antibody to quantify the immunorecognition events. The sandwich-like immunoreactions were performed among the ZrO2 NPs, which were pre-coated on a screen printed electrode (SPE) by electrodeposition, phosphorylated AChE and QD-anti-AChE. The captured QD tags were determined on the SPE by electrochemical stripping analysis of its metallic component (cadmium) after an acid-dissolution step. Paraoxon was used as the model OP insecticide to prepare the phosphorylated AChE adducts to demonstrate proof of principle for the sensor. The phosphorylated AChE adduct was characterized by Fourier transform infrared spectroscopy (FTIR) and mass spectroscopy. The binding affinity of anti-AChE to the phosphorylated AChE was validated with an enzyme-linked immunosorbent assay. The parameters (e.g., amount of ZrO2 NP, QD-anti-AChE concentration,) that govern the electrochemical response of immunosensors were optimized. The voltammetric response of the immunosensor is highly linear over the range of 10,pM to 4,nM phosphorylated AChE, and the limit of detection is estimated to be 8.0,pM. The immunosensor also successfully detected phosphorylated AChE in human plasma. This new nanoparticle-based electrochemical immunosensor provides an opportunity to develop field-deployable, sensitive, and quantitative biosensors for monitoring exposure to a variety of OP pesticides and nerve agents. [source]

The Influence of the Cathodic Pretreatment on the Electrochemical Detection of Dopamine by Poly(1-aminoanthracene) Modified Electrode

The Mediated Electrochemical Method for Rapid Fermentation Ability Assessment

Zinc Oxide/Zinc Hexacyanoferrate Hybrid Film-Modified Electrodes for Guanine Detection

ELECTROANALYSIS, Issue 18 2007
Hung-Wei Chu
Abstract An electroactive polynuclear hybrid films of zinc oxide and zinc hexacyanoferrate (ZnO/ZnHCF) have been deposited on electrode surfaces from H2SO4 solution containing Zn(NO3)2 and K3[Fe(CN)6] by repetitive potential cycling method. Simultaneous cyclic voltammetry and electrochemical quartz crystal microbalance (EQCM) measurements demonstrate the steady growth of hybrid film. There are two redox couples present in the voltammograms of hybrid film and it is obvious in the case of pH,2. Surface morphology of hybrid film was investigated using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Energy dispersive spectrometer (EDS) data confirm existence of zinc oxide in the hybrid film. The effect of type of monovalent cations on the redox behavior of resulting film was investigated. In pure supporting electrolyte, electrochemical responses of modified electrode resemble with that of a surface immobilized redox couple. The electrocatalytic activity of ZnO/ZnHCF hybrid film was investigated towards guanine using cyclic voltammetry and rotating disc electrode (RDE) techniques. Finally, feasibility of using ZnO/ZnHCF hybrid film-coated electrodes for guanine estimation in flow injection analysis (FIA) was also investigated. [source]

Amperometric Nitrite Sensor Based on PVP-Os Entrapped in Titania Sol-Gel Matrix

ELECTROANALYSIS, Issue 19 2004
Yancai Li
Abstract A novel nitrite sensor was developed based on the immobilization of a partially quaternized poly(4-vinylpyridine) complexed with [Os(bpy)2Cl]+/2+ (PVP-Os) in a porous TiO2 sol-gel matrix by a vapor deposition method. The preparation process simplified the traditional sol-gel process and prevented the cracking of conventional sol-gel derived glasses. Electrochemical behavior of the sensor was characterized by cyclic voltammetry and shows excellent electrocatalytic response for the reduction of nitrite. Effect of operating potential on electrochemical responses of the sensor was explored for optimum analytical performance by using the amperometric method. The stability of the sensor was also evaluated. [source]

Sensitive Electrochemical Detection of Native and Aggregated ,-Synuclein Protein Involved in Parkinson's Disease

ELECTROANALYSIS, Issue 13-14 2004
Michal Masa
Abstract The aggregation of ,-synuclein, a 14,kDa protein, is involved in several human neurodegenerative disorders, including Parkinson's disease. We studied native and in vitro aggregated ,-synuclein by circular dichroism (CD), atomic force microscopy (AFM) and electrochemical methods. We used constant current chronopotentiometric stripping analysis (CPSA) to measure hydrogen evolution catalyzed by ,-synuclein (peak H) at hanging mercury drop electrodes (HMDE) and square-wave stripping voltammetry (SWSV) to monitor tyrosine oxidation at carbon paste electrodes (CPE). To decrease the volume of the analyte, most of the electrochemical measurements were performed by adsorptive transfer (medium exchange) from 3,6,,L drops of ,-synuclein samples. With both CPE and HMDE we observed changes in electrochemical responses of ,-synuclein corresponding to protein fibrillization detectable by CD, fluorescence and AFM. Aggregation-induced changes in peak H at HMDE were relatively large in strongly aggregated samples, suggesting that this electrochemical signal may find use in the analysis of early stages of ,-synuclein aggregation. This assumption was documented by marked changes in the peak H potential and height in samples withdrawn at the end of the lag and the beginning of the elongation phase. Native ,-synuclein can be detected down to subnanomolar concentrations by CPSA. [source]

Recent advances in microdevices for electrochemical energy conversion and storage

INTERNATIONAL JOURNAL OF ENERGY RESEARCH, Issue 6-7 2007
Gerardo Jose La O'
Abstract The application of silicon microfabrication technologies to electrochemical devices allows reduction of overall device package to potentially increase volumetric power densities. This review first focuses on some exciting developments in microfuel cells, in particular, solid oxide fuel cells (SOFCs) and proton exchange membrane fuel cells (PEMFCs). The emphasis is given to innovative 2D processing methods, novel 2D architectures of microfuel cells, and demonstrated performance in terms of area power densities. Emerging 3D fabrication techniques that are potentially promising to produce 3D electrochemical devices such as 3D cell and stack architectures on the micrometer scale will then be discussed. Lastly this paper highlights some new opportunities in electrode kinetics studies enabled by microfabricated devices,investigation of scaling relationship between microelectrodes and electrochemical responses, which has led to improved fundamental understanding of electrode reactions and rate-limiting steps. Copyright © 2007 John Wiley & Sons, Ltd. [source]