Search

Ni–Zr0.82Y0.18O1.91 (YSZ) and Ni–La0.90Sr0.10ScO2.95 (LSS) cermets for solid oxide and protonic ceramic electrochemical cells were studied by means of H/D isotope exchange with the gas phase equilibration method for the first time. The experiments were carried out at 2 mbar of dry hydrogen in the temperature range of 400–800 ᵒC. The three parallel channels of hydrogen surface exchange were found to exist in both Ni-YSZ and Ni-LSS cermets. The mechanism of hydrogen isotope exchange for Ni-YSZ was found to be temperature independent, while, in the case of Ni-LSS, the mechanism changed with temperature and was more complicated at lower temperatures (400–600 °C). It was revealed that hydrogen spillover was the rate-determining step for both cermets. The electrochemical kinetics of hydrogen oxidation were studied on symmetric cells with a YSZ supported electrolyte and Ni-YSZ electrodes and with an LSS supported electrolyte and Ni-LSS electrodes in a wet (3 vol % H 2O) hydrogen atmosphere at 1 atm. The mechanism of hydrogen oxidation on the Ni-LSS electrode differs from that of the Ni-YSZ electrode. It changes with temperature and is also more complicated at a lower temperature range. © 2021 Elsevier B.V.

We report the synthesis and electrochemical characterization of octahydroxytetraazapentacenedione (OHTAPQ). The potassium batteries using OHTAPQ as electrode material delivered the specific capacity of 190 mAh g−1 at the current density of 0.6 A g−1. The use of the concentrated (2.2 M KPF6) diglyme-based electrolyte suppressed significantly the capacity fading of the potassium half-cells with OHTAPQ electrodes thus enabling their stable operation for 1200 charge-discharge cycles. Furthermore, OHTAPQ delivered the specific discharge capacity of 82–103 mAh g−1 at high current densities of 9–21 A g−1, which leads to high power densities approaching 41000 W kg−1. Thus, we demonstrate that the rationally designed organic electrode material enables high-capacity and high-power potassium batteries, which can be considered as a more environment-friendly and scalable alternative to the mainstream lithium-ion battery technology. © 2021 Elsevier B.V.

The high conductivity of graphene material (or its derivatives) and its very large surface area enhance the direct electron transfer, improving non-enzymatic electrochemical sensors sensitivity and its other characteristics. The offered large pores facilitate analyte transport enabling glucose detection even at very low concentration values. In the current review paper we classified the enzymeless graphene-based glucose electrocatalysts’ synthesis methods that have been followed into the last few years into four main categories: (i) direct growth of graphene (or oxides) on metallic substrates, (ii) in-situ growth of metallic nanoparticles into graphene (or oxides) matrix, (iii) laser-induced graphene electrodes and (iv) polymer functionalized graphene (or oxides) electrodes. The increment of the specific surface area and the high degree reduction of the electrode internal resistance were recognized as their common targets. Analyzing glucose electrooxidation mechanism over Cu-Co-and Ni-(oxide)/graphene (or derivative) electrocatalysts, we deduced that glucose electrochemical sensing properties, such as sensitivity, detection limit and linear detection limit, totally depend on the route of the mass and charge transport between metal(II)/metal(III); and so both (specific area and internal resistance) should have the optimum values. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.

Advancing the lithium-ion battery technology requires the understanding of electrochemical processes in electrode materials with high resolution, accuracy, and sensitivity. However, most techniques today are limited by their inability to separate the complex signals from slurry-coated composite electrodes. Here, we use a three-dimensional “Swiss-roll” microtubular electrode that is incorporated into a micrometer-sized lithium battery. This on-chip platform combines various in situ characterization techniques and precisely probes the intrinsic electrochemical properties of each active material due to the removal of unnecessary binders and additives. As an example, it helps elucidate the critical role of Fe substitution in a conversion-type NiO electrode by monitoring the evolution of Fe2O3 and solid electrolyte interphase layer. The markedly enhanced electrode performances are therefore explained. Our approach exposes a hitherto unexplored route to tracking the phase, morphology, and electrochemical evolution of electrodes in real time, allowing us to reveal information that is not accessible with bulk-level characterization techniques.

Prostate cancer (PCa) is the second most common cancer amongst men worldwide; hence its early and accurate diagnosis is crucial. Due to the lacking current diagnostic approaches, an urgent need arises for an alternating analytical platform targeting selective PCa biomarkers while testing in body fluids, such as urine and serum. With this motivation, we established a disposable and label-free electrochemical immunosensor for sensitive detection of the selective PCa biomarker, prostate-specific membrane antigen (PSMA). A screen-printed gold electrode (SPGE), with its working electrode functionalized by cysteamine-modified gold nanoparticles (Cys-AuNPs), served as the sensor platform. The PSMA was detected by introducing PSMA protein/PSMA-expressing PCa cells with various concentrations and performing differential pulse voltammetry (DPV) measurements. The established biosensor has detection limits of 0.47 ng/mL for PSMA proteins (0–5 ng/mL range) and 5 cells/mL (0–100 cells/mL range) for PSMA-expressing PCa cells. The corresponding limit of quantification (LOQ) and detection sensitivities were calculated as 2.20 ng/mL and 4 cells/mL; 1.71 ?A·mL/ng and 0.15 ?A·mL/cell, respectively. The selectivity studies confirmed that the DPV signals exerted by PSMA (+) cells were statistically significant in comparison to the PSMA (-) groups (p = 0.012, p * 0.05). The developed immunosensor platform offers a feasible alternative to facilitate PCa diagnosis. Also, to the best of our knowledge, it displayed the highest analytical performance for PSMA-expressing PCa cells detection amongst its peers. Therefore, it can be adapted for different proteins, particularly for cell detection, to facilitate other types of cancerous cells’ diagnosis soon. © 2022 Elsevier B.V., The authors would like to acknowledge the support from the Scientific and Technological Research Council of Turkey (TUBITAK) (Project number: 1059B141800294 ) and Hacettepe University, Medical School, Scientific Research Projects (BAP), Turkey (Grant number: THD-2018-16793 ). Also, the authors would like to present their gratitude to Prof. Dr. A. Kevser Ozden for providing support throughout the studies., 1059B141800294; Türkiye Bilimsel ve Teknolojik Araştirma Kurumu, TÜBITAK; Hacettepe Üniversitesi: THD-2018-16793

Prostate cancer (PCa) is the second most common cancer amongst men worldwide; hence its early and accurate diagnosis is crucial. Due to the lacking current diagnostic approaches, an urgent need arises for an alternating analytical platform targeting selective PCa biomarkers while testing in body fluids, such as urine and serum. With this motivation, we established a disposable and label-free electrochemical immunosensor for sensitive detection of the selective PCa biomarker, prostate-specific membrane antigen (PSMA). A screen-printed gold electrode (SPGE), with its working electrode functionalized by cysteamine-modified gold nanoparticles (Cys-AuNPs), served as the sensor platform. The PSMA was detected by introducing PSMA protein/PSMA-expressing PCa cells with various concentrations and performing differential pulse voltammetry (DPV) measurements. The established biosensor has detection limits of 0.47 ng/mL for PSMA proteins (0–5 ng/mL range) and 5 cells/mL (0–100 cells/mL range) for PSMA-expressing PCa cells. The corresponding limit of quantification (LOQ) and detection sensitivities were calculated as 2.20 ng/mL and 4 cells/mL; 1.71 ?A·mL/ng and 0.15 ?A·mL/cell, respectively. The selectivity studies confirmed that the DPV signals exerted by PSMA (+) cells were statistically significant in comparison to the PSMA (-) groups (p = 0.012, p * 0.05). The developed immunosensor platform offers a feasible alternative to facilitate PCa diagnosis. Also, to the best of our knowledge, it displayed the highest analytical performance for PSMA-expressing PCa cells detection amongst its peers. Therefore, it can be adapted for different proteins, particularly for cell detection, to facilitate other types of cancerous cells’ diagnosis soon. © 2022 Elsevier B.V., The authors would like to acknowledge the support from the Scientific and Technological Research Council of Turkey (TUBITAK) (Project number: 1059B141800294 ) and Hacettepe University, Medical School, Scientific Research Projects (BAP), Turkey (Grant number: THD-2018-16793 ). Also, the authors would like to present their gratitude to Prof. Dr. A. Kevser Ozden for providing support throughout the studies., 1059B141800294; Türkiye Bilimsel ve Teknolojik Araştirma Kurumu, TÜBITAK; Hacettepe Üniversitesi: THD-2018-16793

A molecular [Ru(bda)]-type (bda = 2,2’-bipyridine-6,6’-dicarboxylate) water oxidation catalyst with 4-vinylpyridine as the axial ligand (Complex 1) was immobilized or co-immobilized with 1-(trifluoromethyl)-4-vinylbenzene (3F) or styrene (St) blocking units on the surface of glassy carbon (GC) electrodes by electrochemical polymerization, in order to prepare the corresponding poly-1@GC, poly-1+P3F@GC, and poly-1+PSt@GC functional electrodes. Kinetic measurements of the electrode surface reaction revealed that [Ru(bda)] triggers the O–O bond formation via (1) the radical coupling interaction between the two metallo-oxyl radicals (I2M) in the homo-coupling polymer (poly-1), and (2) the water nucleophilic attack (WNA) pathway in poly-1+P3F and poly-1+PSt copolymers. The comparison of the three electrodes revealed that the second coordination sphere of the water oxidation catalysts plays vital roles in stabilizing their reaction intermediates, tuning the O–O bond formation pathways and improving the water oxidation reaction kinetics without changing the first coordination structures., QC 20201123

Electrolytic deposition (ELD) and electrophoretic deposition (EPD) are relevant methods for creating functional layers of solid oxide fuel cells (SOFCs). This review discusses challenges, new findings and prospects for the implementation of these methods, with the main emphasis placed on the use of the ELD method. Topical issues concerning the formation of highly active SOFC electrodes using ELD, namely, the electrochemical introduction of metal cations into a porous electrode backbone, the formation of composite electrodes, and the electrochemical synthesis of perovskite-like electrode materials are considered. The review presents examples of the ELD formation of the composite electrodes based on porous platinum and silver, which retain high catalytic activity when used in the low-temperature range (400–650 °C). The features of the ELD/EPD co-deposition in the creation of nanostructured electrode layers comprising metal cations, ceramic nanoparticles, and carbon nanotubes, and the use of EPD to create oriented structures are also discussed. A separate subsection is devoted to the electrodeposition of CeO2-based film structures for barrier, protective and catalytic layers using cathodic and anodic ELD, as well as to the main research directions associated with the deposition of the SOFC electrolyte layers using the EPD method. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Several types of electrode materials have been developed for high–performance supercapacitors. Most of the relevant studies have focused on the discovery of new atomic structures and paid limited attention to the effect of heterostructures in supercapacitor electrodes, which has long hindered the fundamental understanding of the use of hybrid materials in supercapacitors. In this study, a novel heterostructure based on perovskite oxide (LaNiO3) nanosheets and polyazulene was synthesized. The as–prepared heterostructure–based supercapacitor exhibited a specific capacitance of up to 464 F g−1 at a high current density of 2 A g−1 in 1–ethyl–3–methylimidazolium tetrafluoroborate. In a symmetric supercapacitor, this heterostructure delivered an energy density of up to 56.4 Wh kg−1 at a power density of 1100 W kg−1. Both LaNiO3 and polyazulene contributed pseudocapacitance and dominated the performance. Unexpectedly, electric double–layer capacitance was found to contribute in this system. Density functional theory calculations indicated that the advantage of the high electrical conductivity of the heterostructure benefited the supercapacitor operation. Electrochemical quartz crystal microbalance analysis revealed that the fast ion flux and adsorption boosted performance. The high intrinsic electrical conductivity and improved stability make this heterostructure a promising electrode material candidate for supercapacitors., QC 20220314

The SARS-CoV-2 virus is still causing a dramatic loss of human lives worldwide, constituting an unprecedented challenge for the society, public health and economy, to overcome. The up-to-date diagnostic tests, PCR, antibody ELISA and Rapid Antigen, require special equipment, hours of analysis and special staff. For this reason, many research groups have focused recently on the design and development of electrochemical biosensors for the SARS-CoV-2 detection, indicating that they can play a significant role in controlling COVID disease. In this review we thoroughly discuss the transducer electrode nanomaterials investigated in order to improve the sensitivity, specificity and response time of the as-developed SARS-CoV-2 electrochemical biosensors. Particularly, we mainly focus on the results appeard on Au-based and carbon or graphene-based electrodes, which are the main material groups recently investigated worldwidely. Additionally, the adopted electrochemical detection techniques are also discussed, highlighting their pros and cos. The nanomaterial-based electrochemical biosensors could enable a fast, accurate and without special cost, virus detection. However, further research is required in terms of new nanomaterials and synthesis strategies in order the SARS-CoV-2 electrochemical biosensors to be commercialized. © 2021 Elsevier B.V.

Structural carbon fibre composite batteries are a type of multifunctional batteries that combine the energy storage capability of a battery with the load-carrying ability of a structural material. To extract the current from the structural battery cell, current collectors are needed. However, current collectors are expensive, hard to connect to the electrode material and add mass to the system. Further, attaching the current collector to the carbon fibre electrode must not affect the electrochemical properties negatively or requires time-consuming, manual steps. This paper presents a proof-of-concept method for screen-printing of current collectors for structural carbon fibre composite batteries using silver conductive paste. Current collectors are screen-printed directly on spread carbon fibre tows and a polycarbonate carrier film. Experimental results show that the electrochemical performance of carbon fibre vs lithium metal half-cells with the screen-printed collectors is similar to reference half-cells using metal foil and silver adhered metal-foil collectors. The screen-printed current collectors fulfil the requirements for electrical conductivity, adhesion to the fibres and flexible handling of the fibre electrode. The screen-printing process is highly automatable and allows for cost-efficient upscaling to large scale manufacturing of arbitrary and complex current collector shapes. Hence, the screen-printing process shows a promising route to realization of high performing current collectors in structural batteries and potentially in other types of energy storage solutions., QC 20220510

An electrocoagulation process was used for the treatment of oily wastewater generated from an automotive industry in Medellin (Colombia). An electrochemical cell consisting of four parallel electrodes (Fe and Al) in bipolar configuration was implemented. A multifactorial experimental design was used for evaluating the influence of several parameters including: type and arrangement of electrodes, pH, and current density. Oil and grease removal was defined as the response variable for the statistical analysis. Additionally, the BOD(5), COD, and TOC were monitored during the treatment process. According to the results, at the optimum parameter values (current density = 4.3 mA/cm(2), distance between electrodes = 1.5 cm, Fe as anode, and pH = 12) it was possible to reach a c.a. 95% oils removal, COD and mineralization of 87.4% and 70.6%, respectively. A final biodegradability (BOD(5)/COD) of 0.54 was reached.

Supercapacitors (SCs) are considered promising energy storage systems because of their high power output and long-term cycling stability; however, they usually exhibit poor energy density. The hybrid supercapacitor (HSC) is an emerging concept in which two dissimilar electrodes with different charge storage mechanisms are paired to deliver high energy without sacrificing power output. This Perspective highlights the features of transition-metal phosphides (TMPs) as the positive electrode in HSCs. In particular, bimetallic nickel cobalt phosphide (NiCoP) with multiple redox sites, excellent electrochemical reversibility, and stability is discussed. We outline how the rational heterostructures, elemental variations, and nanocomposite morphologies tune the electrochemical properties of NiCoP as the positive electrode in HSCs. The Perspective further sheds light on NiCoP-based composites that help in improving the overall performance of HSCs in terms of energy density and cycling stability. The key scientific challenges and perspectives on building efficient and stable HSCs for future applications are discussed. © 2021 American Chemical Society. All rights reserved.

Herein, excellent non-volatile memory and aqueous battery properties of solution-processable nickel ferrite (NFO) nanomaterial were demonstrated. In the case of non-volatile memory property, the device operates on ±2 V resistive switching voltage and shows double valued charge-magnetic flux characteristics. Excellent endurance (103) and retention (104 s) non-volatile memory properties with a good memory window (103) were observed for NFO memristive device. The conduction and resistive switching mechanisms based on experimental data are provided. Furthermore, the present work investigates the electrochemical performance of the NFO thin film electrode in the different electrolytes (viz. Na2SO4, Li2SO4, and Na2SO4: Li2SO4). It was revealed that the NFO thin film shows improved electrochemical performance in Na2SO4 electrolyte with a high specific capacity of 18.56 mAh/g at 1 mA/cm2 current density. The electrochemical impedance spectroscopic results reveal that the NFO thin film electrode shows low series and charge transfer resistance values for Na2SO4 electrolyte than other electrolytes. The diffusion coefficient of different ions (DNa+, DLi+ and DNa+:Li+) were found to be 9.975 × 10−10 cm2 s−1, 3.292 × 10−11 cm2 s−1, 2 × 10−10 cm2 s−1, respectively. A high diffusion coefficient was found for Na+ ions, indicating rapid Na+ transport with NFO thin-film electrodes © 2021 The Authors, f

The authors aimed to impart hydroxyapatite formation ability to ultra-high molecular weight polyethylene (UHMWPE) by deposition of apatite nuclei (ApN) by the following two methods. The first method was electrophoretic deposition (EPD). A porous UHMWPE was placed between electrodes in the ApN-dispersed ethanol and constant voltage was applied. By this treatment, the ApN were migrated from anode-side surface to the cathode one through the pores by an electric field in the pores of the UHMWPE and deposited inside the pores. The second method was direct precipitation (DP) of the ApN. A porous UHMWPE was soaked in a simulated body fluid (1.0SBF) with higher pH than the physiological one and subsequently, its temperature was raised. By this treatment, the ApN were precipitated in the pores of the UHMWPE directly in the reaction solution. For both methods, the ApN-deposited UHMWPE showed HAp formation ability not only on the top surface but also inside the pores near the surface of the porous UHMWPE in 1.0SBF although the adhesion strength of thus-formed HAp layer was higher in the case of the EPD in comparison with the DP, oxygen plasma treatment before the DP enabled to achieve a similar level of the HAp layer adhesion to the EPD.

The paper presents the results of an investigation into thin single- and triple-layer ZrO2-Sc2O3-based electrolytes prepared using the tape-casting technique in combination with promising electrodes based on La2NiO4+δ and Ni-Ce0.8Sm0.2O2-δ materials. It is shown that pressing and joint sintering of single electrolyte layers allows multilayer structures to be obtained that are free of defects at the layer interface. Electrical conductivity measurements of a triple-layer electrolyte carried out in longitudinal and transverse directions with both direct and alternating current showed resistance of the interface between the layers on the total resistance of the electrolyte to be minimal. Long-term tests have shown that the greatest degradation in resistance over time occurs in the case of an electrolyte with a tetragonal structure. Symmetrical electrochemical cells with electrodes fabricated using a screen-printing method were examined by means of electrochemical impedance spectroscopy. The polarization resistance of the electrodes was 0.45 and 0.16 Ohm∙cm2 at 800 °C for the fuel and oxygen electrodes, respectively. The distribution of relaxation times method was applied for impedance data analysis. During tests of a single solid oxide fuel cell comprising a supporting triple-layer electrolyte having a thickness of 300 microns, a power density of about 160 mW/cm2 at 850 °C was obtained using wet hydrogen as fuel and air as an oxidizing gas. © 2020 by the authors.

Combined organic (molecular adsorption) and inorganic (TiO2 passivation) modifications for enhancing water splitting efficiency of porous bismuth vanadate electrodes are tested. The catalytic activity of BiVO4 is increased after adsorption of a newly prepared ruthenium catalyst. TiO2 passivation and sensitization with RuP dye does not show straightforward improvements to the complex photocatalytic behaviour depending on the configuration of the (two- or three-electrode) photoelectrochemical cell, type of the experiment and sample aging. The time constant for electron transport in BiVO4 electrodes (in the range of seconds, revealed by electrochemical impedance measurements) was found to correlate with the stable photocurrent of the cells. The femtosecond transient absorption studies confirm the negligible effects of RuP on the population of the photoexcited carriers in BiVO4. The transient absorption studies also show that the processes responsible for the differences in photocurrents of the modified BiVO4 samples occur on a time scale longer than the first nanoseconds., QC 20200706

Carbon steel is an important industrial material, but it usually suffers from serious corrosion in the service environment. Using corrosion inhibitors is an effective approach to mitigate corrosion. The synergistic inhibition behavior of sodium dodecyl sulfonate (SDS) and potassium iodide (KI) on carbon steel corrosion in hydrochloric acid medium was investigated by electrochemical test, surface morphology analysis, and molecular simulation approaches. Results show that the corrosion inhibition performance is significantly enhanced after the two substances are compounded, and the inhibition efficiency can reach approximately 96% at small doses. The Tafel polarization curves suggest that the mixtures can be classified as anodic corrosion inhibitors. Impedance tests indicate that the inhibitor molecules are adsorbed on the steel surface, resulting in an increase of charge transfer resistance but a decrease of electric double layer capacitance. The adsorption process follows the Langmuir adsorption isotherm. Molecular simulation calculations further reveal the active sites of SDS and the stabilizing effect that I- plays in the inhibition process. The present research offers an economic, environmentally friendly and efficient measure of corrosion control, and provides theoretical guidance for the efficient use of carbon steels and the development of novel corrosion inhibitors. This journal is, QC 20200714

The design of new electrode materials for solid oxide electrochemical cells, which are stable against redox processes as well as exhibiting carbon/sulphur tolerance and high electronic conductivity, is a matter of considerable current interest as a means of overcoming the disadvantages of traditional Ni-containing cermets. In the present work, composite materials having the general formula (1−x)Sr2Mg0.25Ni0.75MoO6−δ + xNiO (where x = 0, 15, 30, 50, 70 and 85 mol.%) were successfully prepared to be utilised in solid oxide fuel cells. A detailed investigation of the thermal, electrical, and microstructural properties of these composites, along with their phase stability in oxidising and reducing atmospheres, was carried out. While possessing low thermal expansion coefficient (TEC) values, the composites having low Ni content (15 mol.%-70 mol.%) did not satisfy the requirement of high electronic conductivity. Conversely, the 15Sr2Mg0.25Ni0.75MoO6−δ + 85NiO samples demonstrated very high electrical conductivity (489 S sm−1 at 850 ◦C in wet H2) due to well-developed Ni-based networks, and no deterioration of thermal properties (TEC values of 15.4 × 10−6 K−1 in air and 14.5 × 10−6 K−1 in 50%H2/Ar; linear expansion behaviour in both atmospheres). Therefore, this material has potential for use as a component of a fuel cell electrode system. © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

The design of a suitable electrode is an essential and fundamental research challenge in the field of electrochemical energy storage because the electronic structures and morphologies determine the surface redox reactions. Calcium molybdate (CaMoO4) was synthesized by a combustion route at 300 °C and 500 °C. We describe new findings on the behaviour of CaMoO4 and evaluate the influence of crystallinity on energy storage performance. A wide range of characterization techniques was used to obtain detailed information about the physical and morphological characteristics of CaMoO4. The characterization results enable the phase evolution as a function of the electrode synthesis temperature to be understood. The crystallinity of the materials was found to increase with increasing temperature but with no second phases observed. Molecular dynamics simulation of electronic structures correlated well with the experimental findings. These results show that to enable faster energy storage and release for a given surface area, amorphous CaMoO4 is required, while larger energy storage can be obtained by using crystalline CaMoO4. CaMoO4 has been evaluated as a cathode material in classical lithium-ion batteries recently. However, determining the surface properties in a sodium-ion system experimentally, combined with computational modelling to understand the results has not been reported. The superior electrochemical properties of crystalline CaMoO4 are attributed to its morphology providing enhanced Na+ ion diffusivity and electron transport. However, the presence of carbon in amorphous CaMoO4 resulted in excellent rate capability, suitable for supercapacitor applications., QC 20200903

Reversible protonic ceramic cells (rPCCs) combine two different operation regimes, fuel cell and electrolysis cell modes, which allow reversible chemical-to-electrical energy conversion at reduced temperatures with high efficiency and performance. Here we present novel technological and materials science approaches, enabling a rPCC with symmetrical functional electrodes to be prepared using a single sintering step. The response of the cell fabricated on the basis of P-N- BCZD|BCZD|PBN-BCZD (where BCZD = BaCe0.5Zr0.3Dy0.2O3-δ, PBN = Pr1.9Ba0.1NiO4+δ, P = Pr2O3, N = Ni) is studied at different temperatures and water vapor partial pressures (pH2O) by means of volt-ampere measurements, electrochemical impedance spectroscopy and distribution of relaxation times analyses. The obtained results demonstrate that symmetrical electrodes exhibit classical mixed-ionic/electronic conducting behavior with no hydration capability at 750 °C; therefore, increasing the pH2O values in both reducing and oxidizing atmospheres leads to some deterioration of their electrochemical activity. At the same time, the electrolytic properties of the BCZD membrane are improved, positively affecting the rPCC's efficiency. The electrolysis cell mode of the rPCC is found to be more appropriate than the fuel cell mode under highly humidified atmospheres, since its improved performance is determined by the ohmic resistance, which decreases with pH2O increasing. © 2018 by the authors.

Colloidal quantum dot (CQD) solar cells with a ZnO/PbS-TBAI/PbS-EDT/carbon structure were prepared using a solution processing technique. A commercially available carbon paste that was processed at low-temperatures was used as a counter electrode in place of expensive noble metals, such as Au or Ag, which are used in traditional PbS CQD solar cells. These CQD solar cells exhibited remarkable photovoltaic performance with a short circuit density (Jsc) of 25.6 mA/cm2, an open circuit voltage (Voc) of 0.45 V, a fill factor (FF) of 51.8% and a power conversion efficiency (PCE) as high as 5.9%. A reference device with an Au counter electrode had a PCE of 6.0%. The PCE of the carbon-containing CQD solar cell remained stable for 180 days when tested in ambient atmosphere, while the PCE of the Au-containing CQD solar cell lost 48.3% of its original value. Electrochemical impedance spectroscopy (EIS) demonstrated that holes within the PbS CQD were effectively transported to the carbon counter electrode., QC 20171129

type:Journal Article, A transparent conductive oxide less dye-sensitized solar cell (TCO-less DSC) consisting of a glass/a floating electrode (FE)/a stained nanoporous titania layer/a gel electrolyte sheet/a Pt layer/a Ti sheet is reported. The FE is composed of a stainless mesh sheet covered with a gradient TiOx layer, which suppressed back-electron transfers from the stainless to electrolytes. The efficiency increased from 2.87% to 4.68% by replacing a conventional dense TiO2 blocking layer with the gradient TiOx layer. The cell in this architecture gave the efficiency of 5.56% after optimization.

Asymmetric multiplex ligation-dependent probe amplification (MLPA) was developed for the amplification of seven breast cancer related mRNA markers and the MLPA products were electrochemically detected via hybridization. Seven breast cancer genetic markers were amplified by means of the MLPA reaction, which allows for multiplex amplification of multiple targets with a single primer pair. Novel synthetic MLPA probes were designed to include a unique barcode sequence in each amplified gene. Capture probes complementary to each of the barcode sequences were immobilized on each electrode of a low-cost electrode microarray manufactured on standard printed circuit board (PCB) substrates. The functionalised electrodes were exposed to the single-stranded MLPA products and following hybridization, a horseradish peroxidase (HRP)-labelled DNA secondary probe complementary to the amplified strand completed the genocomplex, which was electrochemically detected following substrate addition. The electrode arrays fabricated using PCB technology exhibited an excellent electrochemical performance, equivalent to planar photolithographically-fabricated gold electrodes, but at a vastly reduced cost (>50 times lower per array). The optimised system was demonstrated to be highly specific with negligible cross-reactivity allowing the simultaneous detection of the seven mRNA markers, with limits of detections as low as 25 pM. This approach provides a novel strategy for the genetic profiling of tumour cells via integrated "amplification-to-detection"., QC 20160524

A novel, unconventional thermal treatment employing borax for preparing porous carbon materials is presented. The new method was used to prepare carbon felt electrodes for use in lithium-air batteries. The etching of the carbon fiber surface was found to be highly controllable by the amount of borax. The resulting felts were characterized by cyclic voltammetry (CV), secondary electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). The borax treatment resulted in a change of the size, shape and orientation of the Li2O2 crystals formed during discharge. © 2016 The Royal Society of Chemistry.

The restricted lifetime of Fe-N-C based catalysts is often assumed to be connected to the operating temperature. This study will investigate how the cell performance, electrode structure and composition vary over time, at different cell temperatures. At lower temperature, one may expect an increase in radical's stability, but a decrease in reactivity. Results show that the electrode degenerates over time, and that the electrochemical performance decay is similar for 40, 60, and 80° C. However, the loss of active sites is higher at higher temperature. This suggests that indirect production of radicals via H2O2 production during ORR is higher at higher temperatures and is a key degradation mechanism for this Fe-N-C catalyst., QC 20170307

We present a reproducible fast prototyping procedure based on micro-drilling to produce homogeneous tubular ultramicroelectrode arrays made from poly(3,4-ethylenedioxythiophene) (PEDOT), a conductive polymer. Arrays of Ø 100 μm tubular electrodes each having a height of 0.37 ± 0.06 μm were reproducibly fabricated. The electrode dimensions were analyzed by SEM after deposition of silver dendrites to visualize the electroactive electrode area. The electrochemical applicability of the electrodes was demonstrated by voltammetric and amperometric detection of ferri-/ferrocyanide. Recorded signals were in agreement with results from finite element modelling of the system. The tubular PEDOT ultramicroelectrode arrays were modified by prussian blue to enable the detection of hydrogen peroxide. A linear sensor response was demonstrated for hydrogen peroxide concentrations from 0.1 mM to 1 mM.

The electrochemical characteristics and compatibility of components of the electrode-electrolyte system, where the electrolyte is chosen to be γ-BIFEVOX compositions crystallizing in a stable tetragonal phase and the cathode material is chosen to be composite electrodes of composition La 0.7Sr0.3CoO3 + Bi4V 1.7Fe0.3O11-δ, were studied. © 2013 Pleiades Publishing, Ltd.

[EN] Three-dimensional (3D) porous nickel structures were fabricated via a double-template electrochemical deposition process. The construction of the foam structures was achieved by means of a hydrogen bubble dynamic template, prepared from Cu electrodeposition at high current densities. Subsequently, a Ni layer was electrodeposited on the Cu 3D template. During the nickel coating, the typical finger-like microstructure of the Cu foam becomes denser and changes to a cauliflower microstructure. The hydrogen evolution reaction (HER) on these macroporous Ni electrodes was evaluated in 30 wt.% KOH solution by means of polarization curves and electrochemical impedance spectroscopy (EIS). Results demonstrate greater apparent activity of the developed electrodes towards HER in comparison with commercial smooth Ni electrode. The 3D porous Ni electrocatalyst obtained from Cu templates synthesized at the lowest current density and the highest electrodeposition time yielded the best electrochemical activity for HER. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

[EN] Three-dimensional (3D) porous nickel structures were fabricated via a double-template electrochemical deposition process. The construction of the foam structures was achieved by means of a hydrogen bubble dynamic template, prepared from Cu electrodeposition at high current densities. Subsequently, a Ni layer was electrodeposited on the Cu 3D template. During the nickel coating, the typical finger-like microstructure of the Cu foam becomes denser and changes to a cauliflower microstructure. The hydrogen evolution reaction (HER) on these macroporous Ni electrodes was evaluated in 30 wt.% KOH solution by means of polarization curves and electrochemical impedance spectroscopy (EIS). Results demonstrate greater apparent activity of the developed electrodes towards HER in comparison with commercial smooth Ni electrode. The 3D porous Ni electrocatalyst obtained from Cu templates synthesized at the lowest current density and the highest electrodeposition time yielded the best electrochemical activity for HER. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

[EN] Hydrogen is considered to be the most promising candidate as a future energy carrier. One of the most used technologies for the electrolytic hydrogen production is alkaline water electrolysis. However, due to the high energy requirements, the cost of hydrogen produced in such a way is high. In continuous search to improve this process using advanced electrocatalytic materials for the hydrogen evolution reaction (HER), high area NiCo/Zn electrodes were prepared on AISI 304 stainless steel substrates by electrodeposition. After preparing, the alloys were leached of to remove part of the zinc and generate a porous layer (type Raney electrodes). The presence of a thin Ni layer between the substrate and the Raney coating favour the adherence of the latter. The porous NiCo/Zn electrode was characterized by SEM, EDX, confocal laser microscopy, and electrochemical impedance spectroscopy. HER on this electrode was evaluated in 30 wt.% KOH solution by means of polarization curves, hydrogen discharge curves, and galvanostatic tests. Results show that the developed electrode presents a most efficient behaviour for HER when comparing with the smooth Ni cathode. The high electrode activity was mainly attributed to the high surface area of the developed electrode. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

Direct current electrokinetic systems generally require Faradaic reactions to occur at a pair of electrodes to maintain an electric field in an electrolyte connecting them. The vast majority of such systems, e. g. electrophoretic separations (capillary electrophoresis) or electroosmotic pumps (EOPs), employ electrolysis of the solvent in these reactions. In many cases, the electrolytic products, such as H+ and OH- in the case of water, can negatively influence the chemical or biological species being transported or separated, and gaseous products such as O-2 and H-2 can break the electrochemical circuit in microfluidic devices. This article presents an EOP that employs the oxidation/reduction of the conjugated polymer poly(3,4-ethylenedioxythiophene), rather than electrolysis of a solvent, to drive flow in a capillary. Devices made with poly(3,4-ethylenedioxythiophene) electrodes are compared with devices made with Pt electrodes in terms of flow and local pH change at the electrodes. Furthermore, we demonstrate that flow is driven for applied potentials under 2 V, and the electrodes are stable for potentials of at least 100 V. Electrochemically active electrodes like those presented here minimize the disadvantage of integrated EOP in, e. g. lab-on-a-chip applications, and may open new possibilities, especially for battery-powered disposable point-of-care devices.

Direct current electrokinetic systems generally require Faradaic reactions to occur at a pair of electrodes to maintain an electric field in an electrolyte connecting them. The vast majority of such systems, e. g. electrophoretic separations (capillary electrophoresis) or electroosmotic pumps (EOPs), employ electrolysis of the solvent in these reactions. In many cases, the electrolytic products, such as H+ and OH- in the case of water, can negatively influence the chemical or biological species being transported or separated, and gaseous products such as O-2 and H-2 can break the electrochemical circuit in microfluidic devices. This article presents an EOP that employs the oxidation/reduction of the conjugated polymer poly(3,4-ethylenedioxythiophene), rather than electrolysis of a solvent, to drive flow in a capillary. Devices made with poly(3,4-ethylenedioxythiophene) electrodes are compared with devices made with Pt electrodes in terms of flow and local pH change at the electrodes. Furthermore, we demonstrate that flow is driven for applied potentials under 2 V, and the electrodes are stable for potentials of at least 100 V. Electrochemically active electrodes like those presented here minimize the disadvantage of integrated EOP in, e. g. lab-on-a-chip applications, and may open new possibilities, especially for battery-powered disposable point-of-care devices.

[EN] Hydrogen is considered to be the most promising candidate as a future energy carrier. One of the most used technologies for the electrolytic hydrogen production is alkaline water electrolysis. However, due to the high energy requirements, the cost of hydrogen produced in such a way is high. In continuous search to improve this process using advanced electrocatalytic materials for the hydrogen evolution reaction (HER), high area NiCo/Zn electrodes were prepared on AISI 304 stainless steel substrates by electrodeposition. After preparing, the alloys were leached of to remove part of the zinc and generate a porous layer (type Raney electrodes). The presence of a thin Ni layer between the substrate and the Raney coating favour the adherence of the latter. The porous NiCo/Zn electrode was characterized by SEM, EDX, confocal laser microscopy, and electrochemical impedance spectroscopy. HER on this electrode was evaluated in 30 wt.% KOH solution by means of polarization curves, hydrogen discharge curves, and galvanostatic tests. Results show that the developed electrode presents a most efficient behaviour for HER when comparing with the smooth Ni cathode. The high electrode activity was mainly attributed to the high surface area of the developed electrode. © 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

The work focuses on the degradation of performance induced by both water and oxygen in an inverted geometry organic photovoltaic device with emphasis on the accumulated barrier effect of the layers comprising the layer stack. By studying the exchange of oxygen in the zinc oxide (ZnO) layer, the barrier effect is reported in both a dry oxygen atmosphere and an oxygen-free humid atmosphere. The devices under study are comprised of a bulk heterojunction formed by poly(3-hexylthiophene) and [6,6]-phenyl-C61-butyric acid methyl ester sandwiched between a layer of zinc oxide (electron transporting layer) and a layer of poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (hole transport layer) and the two electrodes indium tin oxide and silver. Time-of-flight secondary ion mass spectrometry is employed to characterize the accumulated barrier effect. A pronounced barrier effect is observed in the humid atmosphere, correlating well with a long observed lifetime in the same atmosphere.© 2011 Society of Photo-Optical Instrumentation Engineers.

This paper describes the synthesis of copper/copper oxide nanoparticles via a solution plasma, in which the effect of the electrolyte and electrolysis time on the morphology of the products was mainly examined. In the experiments, a copper wire as a cathode was immersed in an electrolysis solution of a K2CO3 with the concentration from 0.001 to 0.50 M or a citrate buffer (pH = 4.8), and was melted by the local-concentration of current. The results demonstrated that by using the K2CO3 solution, we obtained CuO nanoflowers with many sharp nanorods, the size of which decreased with decreasing the concentration of the solution. Spherical particles of copper with/without pores formed when the citrate buffer was used. The pores in the copper nanoparticles appeared when the applied voltage changed from 105 V to 130 V, due to the dissolution of Cu2O.

This study presents the results on the investigation of the corrosion behavior of carbon steel in model alkaline medium in the presence of very low concentration of polymeric nanoaggregates [0.0024 wt % polyethylene oxide (PEO)113-b-PS70 micelles]. The steel electrodes were investigated in chloride free and chloride-containing cement extracts. The electrochemical measurements (electrochemical impedance spectroscopy and potentiodynamic polarization) indicate that the presence of micelles alters the composition of the surface layers (i.e., micelles were indeed absorbed to the steel surface) and influences the electrochemical behavior of the steel, i.e., the micelles lead to an initially increased corrosion resistance of the steel whereas no significant improvement was observed within longer immersion periods. Surface analysis, performed by environmental scanning electronic microscopy, energy-dispersive x-ray analysis, and x-ray photoelectron spectroscopy, supports and elucidates the corrosion performance. The product layers in the micelles-containing specimens are more homogenous and compact, presenting protective ?-Fe2O3 and/or Fe3O4, whereas the product layers in the micelles-free specimens exhibit mainly FeOOH, FeO, and FeCO3, which are prone to chloride attack. Therefore, the increased “barrier effects” along with the layers composition and altered surface morphology denote for the initially increased corrosion resistance of the steel in chloride-containing alkaline medium in the presence of micelles., Design and Construction, Civil Engineering and Geosciences

This paper describes the synthesis of copper/copper oxide nanoparticles via a solution plasma, in which the effect of the electrolyte and electrolysis time on the morphology of the products was mainly examined. In the experiments, a copper wire as a cathode was immersed in an electrolysis solution of a K2CO3 with the concentration from 0.001 to 0.50 M or a citrate buffer (pH = 4.8), and was melted by the local-concentration of current. The results demonstrated that by using the K2CO3 solution, we obtained CuO nanoflowers with many sharp nanorods, the size of which decreased with decreasing the concentration of the solution. Spherical particles of copper with/without pores formed when the citrate buffer was used. The pores in the copper nanoparticles appeared when the applied voltage changed from 105 V to 130 V, due to the dissolution of Cu2O.

Transport of electrons, protons, and oxygen are necessary for the cathode reactions in polymer electrolyte membrane fuel cells, and achieving the optimum structure of the electrode catalyst layer and the efficient transport of reactants is an effective avenue to reduce the use of platinum catalyst. This study applied three-phase boundary and cathode catalyst layer models to understand details of optimally efficient structures for the transport of reaction components. The factors dominating the effects of the catalyst layer structure and the properties identified in this manner are investigated using the models. Additionally, equations of evaluation are developed to evaluate the effects of the structure and the properties on the cell performance, and the effectiveness of the developed equations is confirmed by a comparison of the results calculated by the equations with the model simulations. From these results, the structure of the porosity, the catalyst layer, and the polymer electrolyte thicknesses, that are optimum for the gas transport and proton conduction, are determined. It is found that the solubility of oxygen in the polymer is one of the dominant factors in the processes of the cathode catalyst layer, and that increasing the solubility is highly effective to reduce the need for platinum.

Novel thin film fuel cell based on the 100 nm-thick electrolyte of amorphous ZrP2.6Ox, working at 400℃, was demonstrated. The hydrogen permeable membrane fuel cell (HMFC) using a Pd foil as a nonporous solid anode was fabricated. Ni interlayer of several hundreds nm thickness was introduced between the Pd anode and the ZrP2.6Ox electrolyte in order to suppress the deterioration of the electrolyte nanofilm by the deformation of the Pd anode during hydrogen absorption. In the ZrP2.6Ox electrolyte the transport number of proton was unity at 400℃ as determined by an EMF measurement. The modification of the Ni anode surface by an ultrathin Pt or Pd layer effectively decreased the anode/electrolyte interfacial polarization. Consequently, the HMFC revealed the OCV of 1.0 V and the maximum power density of 1.8 mW cm^[-2] at 400℃.

This paper describes the synthesis of copper/copper oxide nanoparticles via a solution plasma, in which the effect of the electrolyte and electrolysis time on the morphology of the products was mainly examined. In the experiments, a copper wire as a cathode was immersed in an electrolysis solution of a K2CO3 with the concentration from 0.001 to 0.50 M or a citrate buffer (pH = 4.8), and was melted by the local-concentration of current. The results demonstrated that by using the K2CO3 solution, we obtained CuO nanoflowers with many sharp nanorods, the size of which decreased with decreasing the concentration of the solution. Spherical particles of copper with/without pores formed when the citrate buffer was used. The pores in the copper nanoparticles appeared when the applied voltage changed from 105 V to 130 V, due to the dissolution of Cu2O.

Direct current electrokinetic systems generally require Faradaic reactions to occur at a pair of electrodes to maintain an electric field in an electrolyte connecting them. The vast majority of such systems, e. g. electrophoretic separations (capillary electrophoresis) or electroosmotic pumps (EOPs), employ electrolysis of the solvent in these reactions. In many cases, the electrolytic products, such as H+ and OH- in the case of water, can negatively influence the chemical or biological species being transported or separated, and gaseous products such as O-2 and H-2 can break the electrochemical circuit in microfluidic devices. This article presents an EOP that employs the oxidation/reduction of the conjugated polymer poly(3,4-ethylenedioxythiophene), rather than electrolysis of a solvent, to drive flow in a capillary. Devices made with poly(3,4-ethylenedioxythiophene) electrodes are compared with devices made with Pt electrodes in terms of flow and local pH change at the electrodes. Furthermore, we demonstrate that flow is driven for applied potentials under 2 V, and the electrodes are stable for potentials of at least 100 V. Electrochemically active electrodes like those presented here minimize the disadvantage of integrated EOP in, e. g. lab-on-a-chip applications, and may open new possibilities, especially for battery-powered disposable point-of-care devices.

Novel thin film fuel cell based on the 100 nm-thick electrolyte of amorphous ZrP2.6Ox, working at 400℃, was demonstrated. The hydrogen permeable membrane fuel cell (HMFC) using a Pd foil as a nonporous solid anode was fabricated. Ni interlayer of several hundreds nm thickness was introduced between the Pd anode and the ZrP2.6Ox electrolyte in order to suppress the deterioration of the electrolyte nanofilm by the deformation of the Pd anode during hydrogen absorption. In the ZrP2.6Ox electrolyte the transport number of proton was unity at 400℃ as determined by an EMF measurement. The modification of the Ni anode surface by an ultrathin Pt or Pd layer effectively decreased the anode/electrolyte interfacial polarization. Consequently, the HMFC revealed the OCV of 1.0 V and the maximum power density of 1.8 mW cm^[-2] at 400℃.

Transport of electrons, protons, and oxygen are necessary for the cathode reactions in polymer electrolyte membrane fuel cells, and achieving the optimum structure of the electrode catalyst layer and the efficient transport of reactants is an effective avenue to reduce the use of platinum catalyst. This study applied three-phase boundary and cathode catalyst layer models to understand details of optimally efficient structures for the transport of reaction components. The factors dominating the effects of the catalyst layer structure and the properties identified in this manner are investigated using the models. Additionally, equations of evaluation are developed to evaluate the effects of the structure and the properties on the cell performance, and the effectiveness of the developed equations is confirmed by a comparison of the results calculated by the equations with the model simulations. From these results, the structure of the porosity, the catalyst layer, and the polymer electrolyte thicknesses, that are optimum for the gas transport and proton conduction, are determined. It is found that the solubility of oxygen in the polymer is one of the dominant factors in the processes of the cathode catalyst layer, and that increasing the solubility is highly effective to reduce the need for platinum.

This paper describes the synthesis of copper/copper oxide nanoparticles via a solution plasma, in which the effect of the electrolyte and electrolysis time on the morphology of the products was mainly examined. In the experiments, a copper wire as a cathode was immersed in an electrolysis solution of a K2CO3 with the concentration from 0.001 to 0.50 M or a citrate buffer (pH = 4.8), and was melted by the local-concentration of current. The results demonstrated that by using the K2CO3 solution, we obtained CuO nanoflowers with many sharp nanorods, the size of which decreased with decreasing the concentration of the solution. Spherical particles of copper with/without pores formed when the citrate buffer was used. The pores in the copper nanoparticles appeared when the applied voltage changed from 105 V to 130 V, due to the dissolution of Cu2O.

We present a versatile method for the preparation of mesoporous tin-doped indium oxide (ITO) thin films via dip-coating. Two poly(isobutylene)-b- poly(ethyleneoxide) (PIB-PEO) copolymers of significantly different molecular weight (denoted as PIB-PEO 3000 and PIB-PEO 20000) are used as templates and are compared with non-templated films to clarify the effect of the template size on the crystallization and, thus, on the electrochemical properties of mesoporous ITO films. Transparent, mesoporous, conductive coatings are obtained after annealing at 500 °C; these coatings have a specific resistance of 0.5 cm at a thickness of about 100 nm. Electrical conductivity is improved by one order of magnitude by annealing under a reducing atmosphere. The two types of PIB-PEO block copolymers create mesopores with in-plane diameters of 20-25 and 35-45 nm, the latter also possessing correspondingly thicker pore walls. Impedance measurements reveal that the conductivity is significantly higher for films prepared with the template generating larger mesopores. Because of the same size of the primary nanoparticles, the enhanced conductivity is attributed to a higher conduction path cross section. Prussian blue was deposited electrochemically within the films, thus confirming the accessibility of their pores and their functionality as electrode material.

This study presents the results on the investigation of the corrosion behavior of carbon steel in model alkaline medium in the presence of very low concentration of polymeric nanoaggregates [0.0024 wt % polyethylene oxide (PEO)113-b-PS70 micelles]. The steel electrodes were investigated in chloride free and chloride-containing cement extracts. The electrochemical measurements (electrochemical impedance spectroscopy and potentiodynamic polarization) indicate that the presence of micelles alters the composition of the surface layers (i.e., micelles were indeed absorbed to the steel surface) and influences the electrochemical behavior of the steel, i.e., the micelles lead to an initially increased corrosion resistance of the steel whereas no significant improvement was observed within longer immersion periods. Surface analysis, performed by environmental scanning electronic microscopy, energy-dispersive x-ray analysis, and x-ray photoelectron spectroscopy, supports and elucidates the corrosion performance. The product layers in the micelles-containing specimens are more homogenous and compact, presenting protective ?-Fe2O3 and/or Fe3O4, whereas the product layers in the micelles-free specimens exhibit mainly FeOOH, FeO, and FeCO3, which are prone to chloride attack. Therefore, the increased “barrier effects” along with the layers composition and altered surface morphology denote for the initially increased corrosion resistance of the steel in chloride-containing alkaline medium in the presence of micelles., Design and Construction, Civil Engineering and Geosciences

Direct current electrokinetic systems generally require Faradaic reactions to occur at a pair of electrodes to maintain an electric field in an electrolyte connecting them. The vast majority of such systems, e. g. electrophoretic separations (capillary electrophoresis) or electroosmotic pumps (EOPs), employ electrolysis of the solvent in these reactions. In many cases, the electrolytic products, such as H+ and OH- in the case of water, can negatively influence the chemical or biological species being transported or separated, and gaseous products such as O-2 and H-2 can break the electrochemical circuit in microfluidic devices. This article presents an EOP that employs the oxidation/reduction of the conjugated polymer poly(3,4-ethylenedioxythiophene), rather than electrolysis of a solvent, to drive flow in a capillary. Devices made with poly(3,4-ethylenedioxythiophene) electrodes are compared with devices made with Pt electrodes in terms of flow and local pH change at the electrodes. Furthermore, we demonstrate that flow is driven for applied potentials under 2 V, and the electrodes are stable for potentials of at least 100 V. Electrochemically active electrodes like those presented here minimize the disadvantage of integrated EOP in, e. g. lab-on-a-chip applications, and may open new possibilities, especially for battery-powered disposable point-of-care devices.