Search

Interfacing photosynthetic protein complexes with electrodes is frequently used for the identification of electron transfer mechanisms and the fabrication of biosensors. Binding of herbicide compounds to the terminal plastoquinone Q B at photosystem II (PSII) causes disruption of electron flow that is associated with a diminished performance of the associated biodevice. Thus, the principle of electron transport inhibition at PSII can be used for herbicide detection and has inspired the fabrication of several biosensors for this purpose. However, the biosensor performance may reveal a more complex behavior than generally expected. As we present here for a photobioelectrode constituted by PSII embedded in a redox polymer matrix, the effect caused by inhibitors does not only impact the electron transfer from PSII but also the properties of the polymer film used for immobilization and electrical wiring of the protein complexes. Incorporation of phenolic inhibitors into the polymer film surprisingly translates into enhanced photocurrents and, in particular cases, in a higher stability of the overall electrode architecture. The achieved results stress the importance to evaluate first the possible influence of analytes of interest on the biosensor architecture as a whole and provide important insights for consideration in future design of bioelectrochemical devices., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

The fabrication and electrochemical evaluation of transparent photoelectrodes consisting of Photosystem I (PSI) or Photosystem II (PSII) is described, which are embedded and electrically wired by a redox polymer. The fabrication process is performed by an automated airbrush-type spray coating system, which ensures controlled and scalable electrode preparation. As proof of concept, electrodes with a surface area of up to 25 cm 2 were prepared. The macro-porous structure of the indium tin oxide electrodes allows a high loading of the photoactive protein complexes leading to enhanced photocurrents, which are essential for potentially technologically relevant solar-powered devices. In addition, we show that unpurified crude PSII extracts, which can be provided in comparatively high yields for electrode modification, are suitable for photoelectrode fabrication with comparable photocurrent densities., (© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.)

In the development of biofuel cells great effort is dedicated to achieving outstanding figures of merit, such as high stability, maximum power output, and a large open circuit voltage. Biofuel cells with immobilized redox mediators, such as redox polymers with integrated enzymes, show experimentally a substantially higher open circuit voltage than the thermodynamically expected value. Although this phenomenon is widely reported in the literature, there is no comprehensive understanding of the potential shift, the high open circuit voltages have not been discussed in detail, and hence they are only accepted as an inherent property of the investigated systems. We demonstrate that this effect is the result of a Nernstian shift of the electrode potential when catalytic conversion takes place in the absence or at very low current flow. Experimental evidence confirms that the immobilization of redox centers on the electrode surface results in the assembled biofuel cell delivering a higher power output because of charge storage upon catalytic conversion. Our findings have direct implications for the design and evaluation of (bio)fuel cells with pseudocapacitive elements., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The measurement of key molecules in individual cells with minimal disruption to the biological milieu is the next frontier in single-cell analyses. Nanoscale devices are ideal analytical tools because of their small size and their potential for high spatial and temporal resolution recordings. Here, we report the fabrication of disk-shaped carbon nanoelectrodes whose radius can be precisely tuned within the range 5-200 nm. The functionalization of the nanoelectrode with platinum allowed the monitoring of oxygen consumption outside and inside a brain slice. Furthermore, we show that nanoelectrodes of this type can be used to impale individual cells to perform electrochemical measurements within the cell with minimal disruption to cell function. These nanoelectrodes can be fabricated combined with scanning ion conductance microscopy probes, which should allow high resolution electrochemical mapping of species on or in living cells.

Newly synthesised osmium complex-modified redox polymers were tested for potential application as mediators in glucose oxidising enzyme electrodes for application to biosensors or biofuel cells. Coupling of osmium complexes containing amine functional groups to epoxy-functionalised polymers of variable composition provides a range of redox polymers with variation possible in redox potential and physicochemical properties. Properties of the redox polymers as mediators for glucose oxidation were investigated by co-immobilisation onto graphite with glucose oxidase or FAD-dependent glucose dehydrogenase using a range of crosslinkers and in the presence and absence of multiwalled carbon nanotubes. Electrodes prepared by immobilising [P20-Os(2,2'-bipyridine)2(4-aminomethylpyridine)Cl].PF6, carbon nanotubes and glucose oxidase exhibit glucose oxidation current densities as high as 560μAcm(-2) for PBS containing 100mM glucose at 0.45V vs. Ag/AgCl. Films prepared by crosslinking [P20-Os(4,4'-dimethoxy-2,2'-bipyridine)2(4-aminomethylpyridine)Cl].PF6, an FAD-dependent glucose dehydrogenase, and carbon nanotubes achieve current densities of 215μAcm(-2) in 5mM glucose at 0.2V vs. Ag/AgCl, showing some promise for application to glucose oxidising biosensors or biofuel cells., (Copyright © 2012 Elsevier B.V. All rights reserved.)

A bioanode with high current density and coulombic efficiency was developed by co-immobilization of pyranose dehydrogenase from Agaricus meleagris (AmPDH) with the dehydrogenase domain of cellobiose dehydrogenase from Corynascus thermophiles (recDHCtCDH) expressed recombinantly in Escherichia coli. The two enzymes were entrapped in Os-complex modified electrodeposition polymers (Os-EDPs) with specifically adapted redox potential by means of chemical co-deposition. AmPDH oxidizes glucose at both the C2 and C3 positions whereas recDHCtCDH oxidizes glucose only at the C1 position. Electrochemical measurements reveal that maximally 6 electrons can be harvested from one glucose molecule at the two-enzyme anode via a cascade reaction, as AmPDH oxidizes the products formed from of the recDHCtCDH catalyzed substrate oxidation and vice versa. Furthermore, a significant increase in current density can be obtained by combining AmPDH and recDHCtCDH in a single modified electrode. We propose the use of this bioanode in biofuel cells with increased current density and coulombic efficiency., (Copyright © 2012 Elsevier B.V. All rights reserved.)

Platinum electrodes modified with Mn(II) 5-(N-(8-pyrrole-yl-3,6-dioxa-1-aminooctane)phenylamide-10,15,20-trimethoxyphenylporphyrin (Mn(II)triOMeTCPPyP) using multi-sweep cyclic voltammetry and differential pulse amperometry were evaluated as electrocatalytic surfaces for the oxidation of nitric oxide. The electrodes modified using the pulse amperometric approach were more sensitive towards the detection of nitric oxide. The increased sensitivity led to the attainment of a wider linear dynamic range for the quantification of nitric oxide.

An automated flow-injection system with an integrated biosensor array using bacterial cells for the selective and simultaneous determination various mono- and disaccharides is described. The selectivity of the individually addressable sensors of the array was achieved by the combination of the metabolic response, measured as the O(2) consumption, of bacterial mutants of Escherichia coli K12 lacking different transport systems for individual carbohydrates. Kappa-carrageenan was used as immobilization matrix for entrapment of the bacterial cells in front of 6 individually addressable working electrodes of a screen-printed sensor array. The local consumption of molecular oxygen caused by the metabolic activity of the immobilized cells was amperometrically determined at the underlying screen-printed gold electrodes at a working potential of -600 mV vs. Ag/AgCl. Addition of mono- or disaccharides for which functional transport systems exist in the used transport mutant strains of E. coli K12 leads to an enhanced metabolic activity of the immobilized bacterial cells and to a concomitant depletion of oxygen at the electrode. Parallel determination of fructose, glucose, and sucrose was performed demonstrating the high selectivity of the proposed analytical system.

The integrity of the solid electrolyte interphase (SEI) formed on the negative electrode of lithium‐ion batteries (LIB) is especially critical for the performance of next‐generation LIBs comprising silicon‐carbon based electrode materials. The protecting character of the SEI is compromised due to volume expansion and shrinking during de/intercalation of Li ions leading to irreversible changes upon long‐term cycling. Scanning electrochemical microscopy (SECM) is proposed as local electrochemical technique to investigate the degradation mechanisms of advanced negative electrodes. The impact of charge/discharge cycling on the SEI properties on Si−C electrodes was investigated, and the sensitivity of SECM successfully reveals inhomogeneities at an early stage of the cycling already at about 5 cycles. Macroscopic EIS measurements and evaluation of the coulombic efficiency may result in misleading interpretations of degradation. SECM is demonstrated to be a powerful and complementary technique for revealing μm‐heterogeneities in the SEI surface reactivity after a few charge/discharge cycles. [ABSTRACT FROM AUTHOR]

Hydrogen generated in electrolyzers is discussed as a key element in future energy scenarios, but oxygen evolution as the standard anode reaction is a complex multi‐step reaction requiring a high overpotential. At the same time,it does not add value‐the oxygen is typically released into the atmosphere. Alternative anode reactions which can proceed at similar current densities as the hydrogen evolution are, therefore, of highest interest. We have discovered a high‐performance electrode based on earth‐abundant elements synthesized in the presence of H2O2, which is able to sustain current densities of close to 1 A cm−2 for the oxidation of many organic molecules, which are partly needed at high production volumes. Such anode reactions could generate additional revenue streams, which help to solve one of the most important problems in the transition to renewable energy systems, i.e. the cost of hydrogen electrolysis. [ABSTRACT FROM AUTHOR]

Gas diffusion electrodes (GDEs) in CO2 reduction reaction (CO2RR) alleviate the mass transfer limitation of gaseous reagents, which is beneficial for reducing CO2 into valuable chemicals. GDEs offer higher current densities compared to electrodes immersed in the electrolyte. Disclosing the roles of different structural parameters in tuning the performance of the GDEs is essential to exert the potential of catalysts and to meet potential large‐scale industrial applications of the CO2RR. A novel layer structure for the airbrush‐type spray fabrication of GDEs was designed and optimised, comprising a carbon‐based gas‐diffusion layer, a PEEK fabric, a Ni mesh, a carbon‐integrated catalyst layer, and a PTFE top layer. It was shown that adjusting the carbon material in the gas diffusion and the catalyst layer impacts the selectivity of the CO2RR due to the modulation of the pore network. This work disclosed a practical and scalable but also an easily transferable pathway for preparing GDEs and offered an idea of how to tune the significant parameters of GDEs for optimising their CO2RR performance. [ABSTRACT FROM AUTHOR]

An enzymatic biofuel cell is integrated on a screen‐printed electrode as a basis for a self‐powered biosensor. A glucose/O2 biofuel cell consisting of a pyrroloquinoline quinone‐dependent glucose dehydrogenase embedded within an Os‐complex modified redox polymer bioanode to oxidize glucose and a non‐limiting bilirubin oxidase‐based gas diffusion biocathode in the direct‐electron transfer regime for the reduction of O2 showed a glucose‐dependent current and power output. For full integration on a single screen‐printed electrode, a miniaturized agar salt bridge was introduced between the two bioelectrodes to ensure operation of the assembly in a two‐compartment configuration with each electrode operating at optimal conditions. [ABSTRACT FROM AUTHOR]

Bimetallic tandem catalysts have emerged as a promising strategy to locally increase the CO flux during electrochemical CO2 reduction, so as to maximize the rate of conversion to C−C‐coupled products. Considering this, a novel Cu/C−Ag nanostructured catalyst has been prepared by a redox replacement process, in which the ratio of the two metals can be tuned by the replacement time. An optimum Cu/Ag composition with similarly sized particles showed the highest CO2 conversion to C2+ products compared to non‐Ag‐modified gas‐diffusion electrodes. Gas chromatography and in‐situ Raman measurements in a CO2 gas diffusion cell suggest the formation of top‐bound linear adsorbed *CO followed by consumption of CO in the successive cascade steps, as evidenced by the increasingνC−H bands. These findings suggest that two mechanisms operate simultaneously towards the production of HCO2H and C−C‐coupled products on the Cu/Ag bimetallic surface. [ABSTRACT FROM AUTHOR]

Although highly desired and studied for decades, direct methane functionalization to liquid products remains a challenge. We report an electrochemical system using a boron‐doped diamond (BDD) anode in concentrated sulfuric acid that is able to convert methane to methyl bisulfate and methanesulfonic acid without the use of a catalyst by indirect electrochemical oxidation. Due to its high material stability, BDD can be operated at high current densities. High temperature (140 °C) and pressure (70 bar) support the formation of methyl bisulfate to concentrations as high as 160 mM in 3 h and methanesulfonic acid to concentrations of up to 750 mM in 8 h. We present a novel way of catalyst‐free electrochemical methane oxidation and show general trends and limitations of this reaction. [ABSTRACT FROM AUTHOR]

Bimetallic silver‐copper electrocatalysts are promising materials for electrochemical CO2 reduction reaction (CO2RR) to fuels and multi‐carbon molecules. Here, we combine Ag core/porous Cu shell particles, which entrap reaction intermediates and thus facilitate the formation of C2+ products at low overpotentials, with gas diffusion electrodes (GDE). Mass transport plays a crucial role in the product selectivity in CO2RR. Conventional H‐cell configurations suffer from limited CO2 diffusion to the reaction zone, thus decreasing the rate of the CO2RR. In contrast, in the case of GDE‐based cells, the CO2RR takes place under enhanced mass transport conditions. Hence, investigation of the Ag core/porous Cu shell particles at the same potentials under different mass transport regimes reveals: (i) a variation of product distribution including C3 products, and (ii) a significant change in the local OH‐ activity under operation. [ABSTRACT FROM AUTHOR]

Electroreduction of CO2 to multi‐carbon products has attracted considerable attention as it provides an avenue to high‐density renewable energy storage. However, the selectivity and stability under high current densities are rarely reported. Herein, B‐doped Cu (B‐Cu) and B‐Cu‐Zn gas diffusion electrodes (GDE) were developed for highly selective and stable CO2 conversion to C2+ products at industrially relevant current densities. The B‐Cu GDE exhibited a high Faradaic efficiency of 79 % for C2+ products formation at a current density of −200 mA cm−2 and a potential of −0.45 V vs. RHE. The long‐term stability for C2+ formation was substantially improved by incorporating an optimal amount of Zn. Operando Raman spectra confirm the retained Cu+ species under CO2 reduction conditions and the lower overpotential for *OCO formation upon incorporation of Zn, which lead to the excellent conversion of CO2 to C2+ products on B‐Cu‐Zn GDEs. [ABSTRACT FROM AUTHOR]

Discerning the influence of electrochemical reactions on the electrode microenvironment is an unavoidable topic for electrochemical reactions that involve the production of OH− and the consumption of water. That is particularly true for the carbon dioxide reduction reaction (CO2RR), which together with the competing hydrogen evolution reaction (HER) exert changes in the local OH− and H2O activity that in turn can possibly affect activity, stability, and selectivity of the CO2RR. We determine the local OH− and H2O activity in close proximity to a CO2‐converting Ag‐based gas diffusion electrode (GDE) with product analysis using gas chromatography. A Pt nanosensor is positioned in the vicinity of the working GDE using shear‐force‐based scanning electrochemical microscopy (SECM) approach curves, which allows monitoring changes invoked by reactions proceeding within an otherwise inaccessible porous GDE by potentiodynamic measurements at the Pt‐tip nanosensor. We show that high turnover HER/CO2RR at a GDE lead to modulations of the alkalinity of the local electrolyte, that resemble a 16 m KOH solution, variations that are in turn linked to the reaction selectivity. [ABSTRACT FROM AUTHOR]

A light-controlled multiplexing platform has been developed on the basis of a quantum dot-sensitized inverse opal TiO2 electrode with integrated biocatalytic reactions. Spatially resolved illumination enables multiplexed sensing and imaging of enzymatic oxidation reactions at relatively negative applied potentials. [ABSTRACT FROM AUTHOR]

Simultaneous anodic adsorptive stripping voltammetry was applied for selective and sensitive electrochemical determination of the flavones luteolin (LU) and the basic flavone core 3‐hydroxyflavone (3HF) using a renewable pencil graphite electrode (PGE). The increased separation of the anodic peak potential of LU and 3HF on a PGE surface together with the increased sensitivity renders their simultaneous determination feasible by square wave anodic adsorptive stripping voltammetry (SWAASV). The electrochemical parameters such as surface concentration (Γ), electron transfer coefficient (α), and the standard rate constant (ks) of both LU and 3HF at a PGE were calculated. For simultaneous detection of both compounds by synchronous change of the concentration of LU and 3HF, the detection limits were 1.34 nM and 5.15 nM, respectively. The proposed procedure was successfully applied for the simultaneous detection of LU and 3HF in human serum and urine samples with satisfactory results. [ABSTRACT FROM AUTHOR]

Engineering stable electrodes using highly active catalyst nanopowders for electrochemical water splitting remains a challenge. We report an innovative and general approach for attaining highly stable catalyst films with self-healing capability based on the in situ self-assembly of catalyst particles during electrolysis. The catalyst particles are added to the electrolyte forming a suspension that is pumped through the electrolyzer. Particles with negatively charged surfaces stick onto the anode, while particles with positively charged surfaces stick to the cathode. The self-assembled catalyst films have self-healing properties as long as sufficient catalyst particles are present in the electrolyte. The proof-of-concept was demonstrated in a non-zero gap alkaline electrolyzer using NiFe-LDH and Ni xB catalyst nanopowders for anode and cathode, respectively. Steady cell voltages were maintained for at least three weeks during continuous electrolysis at 50-100 mA cm−2. [ABSTRACT FROM AUTHOR]

An intrinsic self-charging biosupercapacitor built on a unique concept for the fabrication of biodevices based on redox polymers is presented. The biosupercapacitor consists of a high-potential redox polymer based bioanode and a low-potential redox polymer based biocathode in which the potentials of the electrodes in the discharged state show an apparent potential mismatch Eanode>Ecathode and prevent the use of the device as a conventional biofuel cell. Upon charging, the potentials of the electrodes are shifted to more positive (cathode) and more negative (anode) values because of a change in the aox-to-aredratio within the redox polymer matrix. Hence, a potential inversion occurs in the charged state (Eanodecathode) and an open circuit voltage of >0.4 V is achieved and the biodevice acts as a true biosupercapacitor. The bioanode consists of a novel specifically designed high-potential Os complex modified polymer for the efficient immobilization and electrical wiring of glucose converting enzymes, such as glucose oxidase and flavin adenine dinucleotide (FAD)-dependent glucose dehydrogenase. The cathodic side is constructed from a low-potential Os complex modified polymer integrating the O2 reducing enzyme, bilirubin oxidase. The large potential differences between the redox polymers and the prosthetic groups of the biocatalysts ensure fast and efficient charging of the biodevice. [ABSTRACT FROM AUTHOR]

Co-based layered double hydroxide (LDH) catalysts with Fe and Al contents in the range of 15 to 45 at % were synthesized by an efficient coprecipitation method. In these catalysts, Fe3+ or Al3+ ions play an essential role as trivalent species to stabilize the LDH structure. The obtained catalysts were characterized by a comprehensive combination of surface- and bulk-sensitive techniques and were evaluated for the oxygen evolution reaction (OER) on rotating disk electrodes. The OER activity decreased upon increasing the Al content for the Co- and Al-based LDH catalysts, whereas a synergistic effect in Co- and Fe-based LDHs was observed, which resulted in an optimal Fe content of 35 at %. This catalyst was spray-coated on Ni foam electrodes and showed very good stability in a flow-through cell with a potential of approximately 1.53 V at 10 mA cm−2 in 1 m KOH for at least 48 h. [ABSTRACT FROM AUTHOR]

The growth of metal-organic framework (ZIF-67) nanocrystals on nickel foam (NF), followed by carbonization in diluted H2, leads to a nitrogen-doped carbon-nanotube-grafted cobalt/carbon polyhedra film on NF. The obtained material serves as a highly active binder-free electrocatalyst for both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER), enabling high-performance alkaline (0.1 m KOH) water electrolysis with potentials of 1.62 and 0.24 V, respectively, at OER and HER current densities of 10 mA cm−2. [ABSTRACT FROM AUTHOR]

Frontispiece: A Novel Electrode for Value-Generating Anode Reactions in Water Electrolyzers at Industrial Current Densities Keywords: Anodic Oxidation; FDCA; H2O2; High Current Density; NiFe Electrode EN Anodic Oxidation FDCA H2O2 High Current Density NiFe Electrode 1 1 1 02/07/23 20230206 NES 230206 B Electrooxidation b . A novel electrode for value-generating anode reactions in water electrolyzers at industrial current densities is reported by Yufeng Wu, Ferdi Schüth et al. in their Communication (e202215804). [Extracted from the article]

We propose a potential-pulse-assisted method for the formation of highly compact thiol self-assembled monolayers (SAMs), ensuring fully covered surfaces within minutes. By pulsing between potentials that are more positive and more negative with respect to the potential of zero charge, kinetics of SAM formation is substantially enhanced. The formation of the SAM is followed by using real-time impedance measurements by superimposing the applied potential-pulse profile with a high-frequency AC signal that allows for calculation of the interfacial capacitance and provides information about the compactness of the formed layers. A systematic study of the influence of the pulse potential intensity, the pulse duration, and the nature of the thiol derivative on the potential-pulse-assisted SAM formation is performed. We show that compact thiol monolayers are obtained much faster with the suggested technique, as compared to SAM formation performed at the open-circuit potential or by applying a constant potential. [ABSTRACT FROM AUTHOR]

As surface-enhanced Raman scattering (SERS) crucially depends on the morphology of nanostructured metal surfaces, we developed a convenient approach to produce a size gradient of truncated spherical Au nanovoids on a single bipolar electrode. The continuous potential drop in solution implies a linearly changing interfacial potential difference at the wireless electrode, leading to a linearly changing rate of Au electrodeposition. Such a structural gradient enables fast and reproducible screening for those structures, evoking high SERS intensity in a particular experiment. The optimal Au deposition potential with respect to the highest SERS amplification was determined and applied for the fabrication of highly active SERS substrates. [ABSTRACT FROM AUTHOR]

Today's society relies on energy storage on a day-to-day basis, e.g. match energy production and demand from renewable sources, power a variety of electronics, and enable emerging technologies. As a result, a vast range of energy storage technologies has emerged in the last decades. Among them, rechargeable Zn–Air batteries have held great promises for a long time. However, the severe challenges related to the reversible O 2 reactions and poor cyclability at the positive and negative electrodes, respectively, have severely hindered the success of this technology. Herein, electrically-conducting and semi-flowable Zn semi-solid electrodes are proposed to revive the appealing concept of a mechanically–rechargeable alkaline Zn–Air battery, in which the spent negative electrodes are easily substituted at the end of the discharge process (refillable primary battery). In this proof-of-concept study energy densities of ca. 1500 Wh L−1 (1350 Ah L electrode − 1 and utilization rate of 85%) are achieved thanks to the compromised flowability of the proposed Zn semi-solid electrodes. In this way, semi-solid Zn electrodes become a type of green energy carrier having intrinsic advantages over gas and liquid fuels. Zn semi-flowable electrode can be generated elsewhere using renewable sources, easily stored, transported, and used to produce electricity. [Display omitted] • A new type of mechanically rechargeable Zn-Air batteries is demonstrated. • Electrically conducting Zn slurries enable easy replacement of spent electrodes. • Energy density of 1500 Wh L-1 is achieved. • Zn semi-solid electrodes become a new green energy carrier. • Semi-solid electrodes present distinct advantages over gas and liquid fuels. [ABSTRACT FROM AUTHOR]

Benzoxazine-based redox polymers bearing Os complexes are synthesized and used as an immobilization matrix for glucose oxidase (GOx) as a model system for a reagentless biosensor. The polymers are formed by electrochemically induced anodic polymerization of the corresponding benzoxazine monomers modified with Os complexes. The precursors are synthesized in a Mannich-type reaction between bisphenol A, formaldehyde, and the corresponding Os complexes or ligands, which contain free amino groups. The Os complexes are redox active within the polymer films, and thus, can be used as redox relays for the electron transfer between the electrode surface and the prosthetic group within the enzyme. Entrapment of GOx within the poly(benzoxazine) film is achieved successfully, as shown by the biocatalytic activity of the poly(benzoxazine)/ GOx films upon the addition of glucose. [ABSTRACT FROM AUTHOR]

Powder catalysts were deposited as thin films on transparent conductive oxides (TCO) by means of an airbrush spray coating technique. Photoelectrocatalytic properties of the powder catalysts were characterized using photocurrent spectroscopy at different wavelengths demonstrating on the one hand the stability of the films and on the other hand the electrical connection with the electrode surface. The morphology and thickness of the deposited powder catalyst films on TCO were characterized using scanning electron microscopy. Aiming at photocatalytic water splitting, semiconductor powders like gallium oxide (Ga2O3) and zinc oxide (ZnO) were used as test samples to optimize the deposition technique resulting in thin homogeneous layers and good adhesion on the conductive substrate. The proposed airbrush deposition technique of powder catalysts allows closing an experimental gap between microheterogeneous systems and modified electrodes for finding suitable materials for photoelectrochemical water splitting. [ABSTRACT FROM AUTHOR]

Cavity microelectrodes were used as a binder-free platform to evaluate oxygen evolution reaction (OER) electrocatalysts with respect to gas bubble formation and departure. Electrochemical noise measurements were performed by using RuO2 as a benchmark catalyst and the perovskite La0.58Sr0.4Fe0.8Co0.2O3 as a non-noble metal OER catalyst with lower intrinsic conductivity. Changes in the current during the OER originate from variations in electrolyte resistance during the formation of the gas phase and partial coverage of the active area. Fluctuations observed in current and conductance transients were used to establish the contribution from the ohmic overpotential and to determine the characteristic frequency of oxygen evolution. The proposed quantitative determination of gas bubble growth and departure opens up the route for a rational interface design by considering gas bubble growth and departure as a main contributing factor to the overall electrocatalytic activity at high current densities. [ABSTRACT FROM AUTHOR]

A variety of Os-complex modified redox polymers were synthesized and optimized for an improved bioelectrochemical communication with PQQ-sGDH. The properties of the polymers were varied by changing the monomers composition leading to improved immobilization and increased enzyme loading. Three Os-complexes were designed exhibiting different ligands but similar redox potentials adapted for efficient electron transfer with PQQ-sGDH. Effects of the ligand sphere, polymer backbone and length of the tether chain between Os-complex and polymer backbone as well as the impact of different bifunctional crosslinkers on the catalytic current were evaluated. The optimized bioelectrodes exhibited significantly improved catalytic currents and stability. [ABSTRACT FROM AUTHOR]

The majority of efforts on microbial and photosynthetic microbial fuel cells are both curiosity driven and made to possibly meet the future growing demand for sustainable energy. The most metabolically versatile purple bacteria Rhodobacter capsulatus is a potential candidate for this purpose. However, utilizing bacteria in such systems requires efficient electronic transfer communication between the microbial cells and the electrodes, which is one of the greatest challenges. Previous studies demonstrated that osmium redox polymers (ORPs) could be used for extracellular electron transfer between the cells and electrodes. Recently, heterotrophically grown R. capsulatus has been wired with ORP modified electrodes. Here in this communication, we report electron transfer from R. capsulatus grown under heterotrophic as well as under photoheterotrophic conditions to electrodes. The cells, immobilized on bare graphite and ORP modified graphite electrodes, were excited with visible light and subsequent photosynthetic electron transfer was recorded using cyclic voltammetric and chronoamperometric measurements. Photoheterotrophically grown R. capsulatus cells on bare graphite generate a significant photocurrent density of 3.46 µA cm−2, whereas on an ORP modified electrode the current density increases to 8.46 µA cm−2. Furthermore, when 1 mM p-benzoquinone is added to the electrolyte the photocurrent density reaches 12.25 µA cm−2. Our results could have significant implications in photosynthetic energy conversion and in development of photobioelectrochemical devices. [ABSTRACT FROM AUTHOR]

A new concept for the localized characterization of gas evolving electrodes based on scanning electrochemical microscopy (SECM) is suggested. It offers information about the spatial distribution of the predominant locations, which represent the most active catalytic sites, and dynamic characteristics of gas-bubble departure. The knowledge about gas-bubble departure is critical for the assessment and development of new electrode materials for energy applications. [ABSTRACT FROM AUTHOR]

Improving the chemical diffusion of Li ions in anatase TiO2 is essential to enhance its rate capability as a negative electrode for Li-ion batteries. Ammonia annealing has been used to improve the rate capability of Li4Ti5O12. Similarly, ammonia annealing improves the Li-ion storage performance of anatase TiO2 in terms of the stability upon cycling and the C-rate capability. In order to distinguish whether N doping or oxygen deficiencies, both introduced upon ammonia annealing, are more relevant for the observed improvement, a systematic electrochemical study was performed. The results suggest that the creation of oxygen vacancies upon ammonia annealing is the main reason for the improvement of the stability and C-rate capability. [ABSTRACT FROM AUTHOR]

An electrochemical anodic adsorptive stripping procedure for ultra-trace assay of 3-hydroxyflavone (3HF) and Morin at a renewable pencil electrode (PGE) in bulk form and in biological fluids is described. The nature of the oxidation process of 3HF and Morin taking place at the PGE was characterized by cyclic voltammetry. The results show that the determination of the oxidation peak current is the basis of a simple, accurate and rapid method for quantification of 3HF by square-wave anodic stripping voltammetry. Determination of Morin was achieved by square-wave anodic adsorptive stripping voltammetry of the formed MorinCu(II) complex at a PGE. Factors influencing the trace measurements of 3HF and the MorinCu (II) complex at a PGE are assessed. The limits of detection and quantitation for the determination of 3HF and Morin in bulk form and in biological fluids were determined. The statistical analysis and the calibration curve data for trace determination of 3HF and Morin are reported. [ABSTRACT FROM AUTHOR]

Abstract: Using one of the most understood and well-characterized electrochemical systems, Pt(111) surface in contact with H2SO4, we provide evidences that specific adsorption, 2D phase transitions in the adsorbate layers and, in general, structural effects in the double layer are largely responsible for the so-called frequency dispersion of the double layer. The results also show promise that parameters of the constant phase element (which is used in impedance spectroscopy to account for the frequency dispersion) obtained as a function of the electrode potential can be reasonably used to detect 2D phase transitions at the electrode/electrolyte interfaces. This would provide a better insight into the interface, increasing the impact of measurements made by electrochemical impedance spectroscopy. [Copyright &y& Elsevier]

Electrocatalytic NADH oxidation was investigated at an electrode architecture involving an electropolymerized layer of poly(methylene blue) (pMB) or poly(methylene green) (pMG) in combination with specifically designed toluidine blue or nile blue modified methacrylate-based electrodeposition polymers. Either NAD-dependent lactate dehydrogenase or NAD-dependent glucose dehydrogenase were entrapped between the primary electropolymerized layer of pMB or pMG and the methacrylate-based redox polymer. The composition of the polymer backbone and the polymer-bound redox dye was evaluated and it could be demonstrated that the combination of the electropolymerized pMB or pMG layer together with the dye modified methacrylate-based redox polymer shows superior properties as compared with either of the components alone. NADH was oxidized at an applied potential of 0 mV vs Ag/AgCl/KCl 3 M and current densities of 17 μA·cm and 28 μA·cm were obtained for modified electrodes based on lactate dehydrogenase and glucose dehydrogenase, respectively, at substrate saturation. [Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]

n electrochemical method for the detection of Epstein-Barr virus (EBV) infections is described. The method relies on an immunoassay with electrochemical read-outs based on recombinant antigens. The antigens are immobilised on an Au electrode surface and used to complementarily bind antibodies from serum samples found during different stages of infection with EBV. Thiol chemistry under formation of self-assembled monolayers functions as a means to immobilise the antigens at the Au electrodes. A reporter system consisting of a secondary antibody labelled with alkaline phosphatase is used for electrochemical detection. The feasibility of the assay design is demonstrated and the assay performance is tested against the current gold standard in EBV detection. Close correlation is obtained for the results found for the developed electrochemical immunoassay and a standard line assay. Moreover, the electrochemical immunoassay is combined with a nanoporous electrode system allowing signal amplification by means of redox recycling. An amplification factor of 24 could be achieved. [Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]

An electrode structure consisting of two separately addressable electrodes with 200 nm inter-electrode spacing in a layered nanoporous electrode/insulator/electrode configuration was used as transducer for redox-amplified biosensors. Nanopores were selectively modified with two different enzymes, namely glucose oxidase and alkaline phosphatase by means of electrochemically induced precipitation of electrodeposition paints. Both commercially available and specifically synthesized redox-active electrodeposition paints were used. Selectivity of modification was proven by electrochemical methods and atomic force microscopy. The principle feasibility to amplify the measured current in a model sensor based on alkaline phosphatase could be demonstrated. Signal amplification by a factor of two with respect to the non-amplified response was achieved. [ABSTRACT FROM AUTHOR]

An electrochemical robotic system using standard microtiter plates as reaction wells for potentiostatic and galvanostatic electrosynthesis and high-throughput electroanalysis was conceived and realized using stepmotor driven positioning stages in combination with a flexible software. Electrode bundles specifically adapted to the experimental needs are accurately positioned in the wells of a microtiter plate followed by the automatic performance of sequences of electrosynthetic or electroanalytical techniques. The system allows us to work under inert-gas atmosphere, in aqueous and organic solvents, and to add or remove solutions by means of integrated syringe pumps. A specifically developed script language permits the user to perform very complex experimental sequences in the different wells of the microtiter plate. The hardware and software features of the developed electrochemical robotic system, the design of suitable electrode arrangements for electrosynthesis and electroanalytical techniques, as well as the reproducibility in aqueous and organic electrolytes are described. The performance of the system is demonstrated by redox screening of a Ru-complex library and by electrosynthesis with in situ analysis of a compound library. [ABSTRACT FROM AUTHOR]

Scanning electrochemical microscopy (SECM) has been performed in the restricted space of nanolitre droplets with a robust and easy-to-handle coaxial electrode assembly centring a Pt microdisk in a circular Ag electrode. Straightforward and reproducible fabrication of the specially designed probe tips was achieved by using Tollens’ reaction to chemically deposit a uniform and well-adhering layer of silver on the body of a glass-insulated Pt microdisk electrode. The suitability of the novel dual-electrode SECM tip for measurement in small volumes was evaluated by imaging an array of four Pt band microelectrodes in 500 nL electrolyte. [ABSTRACT FROM AUTHOR]

Ni tetra(4-N-methyl pyridyl)porphyrin was electrochemically entrapped within a polymer matrix formed by an anodic electrodeposition paint on the surface of Pt electrodes. Due to positive charges from the quaternised pyridinium side chains, the metalloporphyrin is soluble in water. By means of charge interactions between the positively charged metalloporphyrin and the negatively charged polymer backbone of the applied anodic electrodeposition paint, the entrapment of the metalloporphyrin in an insoluble polymer “capsule” prevents it from rapidly leaking off the electrode surface. The chemically modified electrodes obtained could be successfully applied to the sensitive determination of nitric oxide, and they displayed satisfactory stability for multiple nitric oxide measurements. The modified electrodes were employed for monitoring the decomposition of methylamine hexamethylene methylamine NONOate by continuous detection of the liberated nitric oxide. [ABSTRACT FROM AUTHOR]

Heated electrodes were applied for the non-isothermal operation of amperometric glucose biosensors based on glucose oxidase immobilised on the electrode surface by entrapment within a polymer layer. The localised deposition of the polymer film under simultaneous entrapment of the enzyme was achieved by an electrochemically induced pH-modulation in the diffusion zone in front of the electrode, thus altering the solubility of the polymer chains. This non-manual sensor preparation protocol could be successfully used for the modification of a novel indirectly heated electrode. The non-isothermal operating mode allows working at the optimum temperature of the enzyme sensors without any thermal distortion of the bulk solution. Increased surface temperature of the sensor thus accelerates transport as well as kinetic processes, resulting in an enhanced amperometric signal. In the presence of interfering compounds such as ascorbic acid, the proposed technique allows use of the diverging thermal impact on the sensing process, for different electrochemically active compounds, for a deconvolution of the amperometric signal at different electrode temperatures. A calculation method for determination of glucose in the presence of one interfering compound is presented as a basis for a calculative interference elimination. [ABSTRACT FROM AUTHOR]

In a preliminary study aimed at developing strategies for the simultaneous detection of various biologically important molecules, a procedure is described that allows the electrochemical detection of nitric oxide (NO) released by a population of human umbilical vein endothelial cells (HUVEC) by using an array of electrodes comprising three individually addressable electrodes. Each electrode in the array was modified with a different NO-sensitive electrocatalyst, thereby demonstrating the possibility of modifying the individual electrodes in an array with different sensing chemistries. This study opens a doorway to the development of arrays of electrodes for the simultaneous detection of multiple analytes in a complex environment by suitably tailoring the sensitivity and selectivity of each electrode in the array to a specific analyte in the test medium. [ABSTRACT FROM AUTHOR]

Nitric oxide (NO) plays multiple roles in the nervous system. It is produced as a result of damage or injury of the retina as a part of the central nervous system. Detailed knowledge of the extent and the time course of NO production is of great importance for the understanding of pathological processes and their appropriate medical treatment. Sections of rat retina were stained with antibodies against the three isoforms of NO synthase (NOS) at several time points after a lesion of the optic nerve. No significant changes of NOS expression could be seen at any of the checked time points. For the electrochemical detection of NO production, we modified small platinum electrodes with a NO-sensitive nickel porphyrin by electrochemical polymerisation. Compared to other substances, electrochemically polymerised eugenol was found to be most suitable for protection against interferences. For the measurements, differential pulse amperometry was used. The response to nitric oxide was linear. NO production of adult rat retinas was measured post axotomy after different time points with electrochemical electrodes ex vivo. With non-treated retinas, an NO concentration of approximately 15 μM was measured. NO concentration is elevated after an axotomy reaching its highest value of up to 30 μM 5 days after the lesion. The NO concentration is decreased below the initial value after 9–14 days post axotomy. [ABSTRACT FROM AUTHOR]

Scanning electrochemical microscopy (SECM) inside a glove box was used for the in situ visualization of solid electrolyte interphase (SEI) formation as well as Li-ion intercalation and de-intercalation on anatase TiO2 based paste electrodes. [ABSTRACT FROM AUTHOR]

If the analyte does not only change the electrochemical but also the optical properties of the electrode/solution interface, the spatial resolution of an electrochemical sensor can be substantially enhanced by combining the electrochemical sensor with optical microscopy. In order to demonstrate this, electrochemical biosensors for the detection of hydrogen peroxide and glucose were developed by drop casting enzyme and redox polymer mixtures onto planar, optically transparent electrodes. These biosensors generate current signals proportional to the analyte concentration via a reaction sequence which ultimately changes the oxidation state of the redox polymer. Images of the interface of these biosensors were acquired using bright field reflected light microscopy (BFRLM). Analysis showed that the intensity of these images is higher when the redox polymer is oxidized than when it is reduced. It also revealed that the time needed for the redox polymer to change oxidation state can be assayed optically and is dependent on the concentration of the analyte. By combining the biosensor for hydrogen peroxide detection with BFRLM, it was possible to determine hydrogen peroxide in concentrations as low as 12.5 µM with a spatial resolution of 12 µm × 12 µm, without the need for the fabrication of microelectrodes of these dimensions. [ABSTRACT FROM AUTHOR]

Abstract: Electrochemically induced crosslinking is suggested to stabilize electrodeposition polymer/enzyme films selectively on an electrode surface. 4 different protected diamine or dithiol based bi-functional crosslinkers have been synthesized, which can be activated by a pH-shift invoked by electrochemical water oxidation or proton reduction. Deprotection occurs either simultaneously or sequentially to the deposition of specifically designed redox electrodeposition polymers. The stability of the resulting polymer films was substantially enhanced as evaluated using continuous potentiodynamic cycling alternated by difference pulse voltammetry. Electrochemically induced crosslinking is compatible with biological recognition elements using Trametes hirsuta laccase or glucose oxidase entrapped within specifically adapted Os-complex modified or phenothiazine-modified redox polymers. [Copyright &y& Elsevier]

Abstract: A CNTs–TiO2−δ composite consisting of carbon nanotubes (CNTs) grown by catalytic chemical vapor deposition on oxygen-deficient titanium dioxide (TiO2−δ) nanoparticles was synthesized and investigated as high-rate negative electrode material for Li-ion batteries. An initial reversible capacity of 185mAhg−1 was obtained at C/2, with an initial irreversible loss of 15%. The composite showed a high stability upon cycling, with 92% retention of the capacity after 37cycles, and good high rate capability, with a capacity of 102mAhg−1 at 10C. The performance of the CNTs–TiO2−δ composite was compared to that of pristine commercial TiO2 and to that of oxygen-deficient TiO2−δwith the aim of identifying the source of the improvement. Both TiO2−δ and CNTs network were found to contribute to the enhanced electrochemical performance of CNTs–TiO2−δ composite. [Copyright &y& Elsevier]