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Diffusion coefficients in swelling polypyrrole: ESCR and Cottrell models.

Reliable diffusion coefficients, D, for the diffusion of perchlorate anions into polypyrrole films during polymeric oxidation were obtained from chronoamperometric results. Two different models were used to calculate D: the Cottrell equation and the electrochemically stimulated conformational relaxation (ESCR) model. As expected, the initial Cottrell hypothesis was far from swelling/shrinking polymeric electrodes and the obtained D range was from 10(-10) to 10(-6) cm(2) s(-1). The ESCR model, based on the internal diffusion that takes place from regions where the steady state of oxidation has already been reached to regions where the oxidation is only just beginning, provided values of D ranging from 0.4 x 10(-9) to 2.2 x 10(-9) cm(2) s(-1), which is close to the values expected for a gel. When a constant amplitude is kept for the potential step, D increases with increasing initial anodic potentials, i.e., from increasingly swollen films. When it is stepped to the same oxidation potential, D decreases when starting from more cathodic potentials, i.e., from a more compact structure. These changes in D can be attributed to (i) swelling processes during oxidation, giving a gel-like structure; (ii) compacting processes at increasing cathodic potentials; (iii) the increasing thickness of the film during oxidation; and (iv) a decrease in film viscosity during the swelling process.

Journal Article↗

On the chemical and electrochemical one-electron reduction of peroxynitrous acid.

Peroxynitrous acid was reduced by cathodic linear sweep voltammetry at a gold electrode and by iodide at pH 3.2 and 5.6. The cathodic reduction wave was identified by measuring its decay in time, which was the same as observed by optical spectroscopy. The iodide oxidation was followed by optical measurement of the triiodide formation. Both reductions show one-electron stoichiometry, with the product n(alpha)alpha = 0.23 +/- 0.04 from the electrochemical experiments, in which alpha is the transfer coefficient and n(alpha) the number of electrons transferred, and an diiodine yield of ca. 0.5 equiv per equivalent of peroxynitrous acid. The voltammetric reduction was irreversible up to scan rates of 80 V s(-1). Both reductions were pH independent in the range studied. The voltammetric reduction is most likely an irreversible elemental reaction followed by a chemical decay that cannot be observed directly. Because of the pH independence, we conclude that both reductions have a common short-lived intermediate, namely [HOONO]*-. We estimate the electrode potential of the likely ONOOH/ONOOH*- couple to be larger than 1 V. The commonly used electrode potential E degrees (ONOOH, H+/NO2*, H2O) does not describe the chemistry of peroxynitrous acid.

Journal Article↗

Electrosynthesis of Cu-Se films on copper electrodes in alkaline media: a voltammetric, electrochemical quartz crystal microbalance and I/t transient study.

The electroformation of Cu-Se phases, obtained by selenizing a thin film of copper deposited on the quartz/gold electrode system, was studied with an electrochemical quartz crystal microbalance (EQCM) and by cyclic voltammetry (CV) in an alkaline solution (0.05 M Na(2)B(4)O(7)) containing selenide ion. Potentiodynamic parameters showed that the formation of the initial Cu-Se phases (Cu(2-x)Se/Cu(3)Se(2)) is ruled by an irreversible diffusion controlled mechanism, where a first electron transfer is the rate-determining step. A CV study was also performed with a bulk copper electrode in 1 M NaOH solution containing selenide ion. The deconvolution of the anodic and cathodic I/E profiles corresponding to the electroformation and electroreduction of the Cu-Se film formed allowed us to establish that, depending on the anodic potential limit of the potentiodynamic scan, the Cu-Se phases formed were either a mixture of Cu(2)(-x)Se/Cu(3)Se(2) or Cu(2-x)Se/Cu(3)Se(2)/CuSe. An EQCM study showed that, during the initial stage of Cu-Se phase electroformation, water molecules were released from the electrode. In advanced stages of the process, when the electrode was completely covered by Cu-Se compounds, selenide anions were adsorbed on the formed phase. When the anodic potential limit was extended to -0.2 V, copper oxide compounds were formed. The analysis of the cathodic charge related to Cu-Se phase electroreduction and Energy Dispersive X-ray Spectroscopy (EDXS) analysis confirmed that when the anodic limit was -0.8 V, a mixture of different Cu-Se phases was formed. A I/t transient study performed with a bulk copper electrode in alkaline solution containing selenide established that the nucleation and growth mechanism (NGM) of the Cu-Se phases takes place through an initial bidimensional-instantaneous nucleation (IN2D), followed by four bidimensional-progressive nucleations (PN2D). These results and atomic force microscopy (AFM) experiences supported that the growth of the Cu-Se films occurs through a layer-by-layer mechanism.

Journal Article↗

Influence of pinning effects on the electrochemical formation of silver patterns in agarose-containing sols and gels.

The formation of silver patterns via electrolysis from aqueous silver sulfate + x% w/v agarose sol and gel media, with and without supporting electrolyte, in a quasi-two-dimensional (2D) cylindrical cell at room temperature, is utilized as a reference system to investigate the complexity of pinning effects. From pattern morphology and electrochemical data, both delocalized and localized pinning in the bulk dominate the drift of the growth front, depending on the concentration of agarose in the heterogeneous media. Delocalized pinning results from mobile, small agarose aggregates at the growth front and from their accumulation by the front drift. For gels, localized pinning comes from their own percolated structure. A depinning/pinning transition is observed in going from sols to gels. The relative contribution of diffusion and advection in mass-transport-controlled silver electrodeposition depends on the plating bath composition. On the other hand, silver ion attachment to the cathode appears to be interfered with by some screening caused by weakly adsorbed, mobile agarose aggregates at the metal surface without slowing down the rate of the electron-transfer step at the cathode. Their relative contribution of a delocalized, localized pinning and screening effect to a great extent determines the morphology and transition in the growth mode of silver patterns in both media. The analysis of charge and current transients and the corresponding silver pattern morphologies for open and dense radial patterns is made. Results are qualitatively simulated with a novel, rather simple cellular automaton algorithm.

Electrochemistry↗

Intercluster reactivity of metalloaromatic and antiaromatic compounds and their applications in molecular electronics: a theoretical investigation.

Local reactivity descriptors, such as the condensed local softness and Fukui function, have been employed to investigate the intercluster reactivity of the metalloaromatic (Al4Li- and Al4Na-) and antiaromatic (Al4Li4 and Al4Na4) compounds. We have used the concept of group softness and group Fukui function to characterize the strength of the nucleophilicity (ability to donate electrons) of the Al4 unit in these compounds. The aim of this work is to understand the enhanced efficiency of the electron injection of the Al-Li cathode in the organic light emitting diode due to the formation of Al-Li clusters at the interface. Our analysis shows that the Al4 unit of the Al4Li- cluster has the highest nucleophilicity compared to the other clusters. Hence, we believe that the formation of the Al4Li- type of metalloaromatic clusters would be responsible for the increase in the efficiency of the electron injection of the Al-Li cathode.

Journal Article↗

In situ FTIR spectroscopy study of the break-in phenomenon observed for PPy/PVS films in acetonitrile.

The in situ Fourier transform infrared (in situ FTIR) technique was used for the first time to investigate the break-in phenomenon observed for polypyrrole/poly(vinyl sulfonate) (PPy/PVS) films in acetonitrile containing 0.1 M LiClO(4). Consecutive potential scans provided a continuous increase of the infrared band intensities, simultaneous to an increase observed in the charge involved in the voltammetric peaks, suggesting a rise in the number of the polymeric chains participating in the infrared signal at the same time as the electroactive participants increase in the redox process. Moreover, in situ FTIR spectra evidence that the new infrared-activated chains in each voltammetric cycle adopt the same polymeric structure achieved by the chains activated in the initial cycles. However, if we achieve a cathodic potential limit of -2.1 V (vs Ag/AgCl), a restructuring of the polymeric morphology is observed. In situ FTIR spectra obtained for PPy/ClO(4) films under the same conditions pointed to a steady-state behavior from the very early voltammetric scans. Moreover, the intensities of FTIR bands obtained for PPy/ClO(4) films in the early voltammetric cycles are much higher than those obtained for PPy/PVS films after several potential scans. Only when high cathodic and high anodic potential limits were used for the consecutive cycles did the FTIR band intensities from PPy/PVS become similar to those obtained from PPy/ClO(4), indicating that in both films a similar number of polymeric chains were infrared active. Polarization at a high anodic potential (+1.3 V vs Ag/AgCl) produced overoxidation of the polymer appearing characteristic 1725 cm(-1) band assigned to the formation of carbonyl groups. Furthermore, the approximately 1540 cm(-1) band shifted to higher wavenumbers, indicating that overoxidation reduced the length of conjugated chains in the polypyrrole.

Journal Article↗

Electronic properties of Si surfaces and side reactions during electrochemical grafting of phenyl layers.

The electrochemical grafting process of 4-nitrobenzene and 4-methoxybenzene (anisole) from diazonium salt solutions has been investigated in situ by monitoring the current density, the band bending, and the nonradiative surface recombination during grafting at different potentials and different concentrations of the diazonium salt in the solution. Ex situ infrared spectroscopic ellipsometry has been used to inspect the Si surface species before and after the grafting process. The band bending decreases with either increasing concentration of diazonium salt or when the redox potential of the diazonium compound (anisole) is nearer to the competing H+/H2 couple. The surface recombination increases at more cathodic potentials if an electron donor group is present at the phenyl ring (nitrobenzene) and vice versa for the electron acceptor group (anisole). The influence of side reactions can be reduced by use of moderate concentration and moderate or strong cathodic potential, depending on the redox potential of the diazonium compound.

Diazonium Compounds↗

Electrochemical formation of a Pt/Zn alloy and its use as a catalyst for oxygen reduction reaction in fuel cells.

The characterization of an electrochemically created Pt/Zn alloy by Auger electron spectroscopy is presented indicating the formation of the alloy, the oxidation of the alloy, and the room temperature diffusion of the Zn into the Pt regions. The Pt/Zn alloy is stable up to 1.2 V/RHE and can only be removed with the oxidation of the base Pt metal either electrochemically or in aqua regia. The Pt/Zn alloy was tested for its effectiveness toward oxygen reduction. Kinetics of the oxygen reduction reaction (ORR) were measured using a rotating disk electrode (RDE), and a 30 mV anodic shift in the potential of ORR was found when comparing the Pt/Zn alloy to Pt. The Tafel slope was slightly smaller than that measured for the pure Pt electrode. A simple procedure for electrochemically modifying a Pt-containing gas diffusion electrode (GDE) with Zn was developed. The Zn-treated GDE was pressed with an untreated GDE anode, and the created membrane electrode assembly was tested. Fuel cell testing under two operating conditions (similar anode and cathode inlet pressures, and a larger cathode inlet pressure) indicated that the 30 mV shift observed on the RDE was also evident in the fuel cell tests. The high stability of the Pt/Zn alloy in acidic environments has a potential benefit for fuel cell applications.

Journal Article↗

Effect of rare-earth component of the RE/Ni catalyst on the formation and nanostructure of single-walled carbon nanotubes.

A systematic experimental study has been carried out on the efficiency of bimetallic catalysts based on Ni and the rare-earth elements Y, La, Ce, Nd, Gd, Tb, Dy, Ho, Er, and Lu (group A) and Eu, Sm, Yb, and Tm (group B) in the synthesis of single-walled carbon nanotubes (SWNTs). The two groups give quite different results when analyzed by a combination of SEM/TEM and Raman and UV-NIR spectroscopies. The elements in group A have an obvious catalytic effect and increase the yield of SWNTs dramatically, whereas those in group B are not efficient catalysts. The diameter distribution of the synthesized SWNTs was also affected by the rare-earth element used. For group A metals, there is a tendency that the fraction of small-diameter tubes decreases with decreasing ionic radius of the rare-earth element used. EDX and X-ray analyses indicate that group A metals deposit on the cathode deposits and form rare-earth carbides, whereas no group B metals are found in cathode deposits, except for a small amount of Tm present in the form of thulium carbide. Further analysis indicates that there is a very strong correlation between the ability to form rare-earth carbides and the catalytic efficiency for the formation of SWNTs.

Journal Article↗

An ultrathin self-humidifying membrane for PEM fuel cell application: fabrication, characterization, and experimental analysis.

An ultrathin poly(tetrafluoroethylene) (PTFE)-reinforced multilayer self-humidifying composite membrane (20 microm, thick) is developed. The membrane is composed of Nafion-impregnated porous PTFE composite as the central layer, and SiO2 supported nanosized Pt particles (Pt-SiO2) imbedded into the Nafion as the two side layers. The proton exchange membrane (PEM) fuel cell employing the self-humidifying membrane (Pt-SiO2/NP) turns out a peak power density of 1.40 W cm(-2) and an open circuit voltage (OCV) of 1.032 V under dry H2/O2 condition. The excellent performance is attributed to the combined result of both the accelerated water back-diffusion in the thin membrane and the adsorbing/releasing water properties of the Pt-SiO2 catalyst in the side layers. Moreover, the inclusion of the hygroscopic Pt-SiO2 catalyst inside the membrane results in an enhanced anode self-humidification capability and also the decreased cathode polarization (accordingly an improved cell OCV). Several techniques, such as transmission electronic microscopy, scanning electronic microscopy, energy dispersive spectroscopy, thermal analysis and electrochemical impedance spectroscopy etc., are employed to characterize the Pt-SiO2/NP membrane. The results are discussed in comparison with the plain Nafion/PTFE membrane (NP). It is established that the reverse net water drag (from the cathode to the anode) across the Pt-SiO2/NP membrane reaches 0.16 H2O/H+. This implies a good hydration of the Pt-SiO2/NP membrane and thus ensures an excellent PEM fuel cell performance under self-humidification operation.

Electric Power Supplies↗

Electrochemical methods for the preparation of gold-coated TiO2 nanoparticles with variable coverages.

We report here the first electrochemical methods to prepare elemental Au0-coated TiO2 nanoparticles with controllable coverages. First, Au substrates were cycled in a deoxygenated aqueous solution containing 0.1 N HCl and 1 mM TiO2 nanoparticles from -0.28 to +1.22 V versus Ag/AgCl at 500 mV/s with different numbers of scans. The durations at the cathodic and anodic vertexes were 10 and 5 s, respectively. After this process, positively charged Au-coated TiO2 nanoparticles were formed in the solutions. Then a cathodic overpotential of 0.6 V from the open circuit potential of ca. 0.82 V versus Ag/AgCl was applied under sonication to synthesize elemental Au0-coated TiO2 nanoparticles. The coverage of Au shells in the elemental Au-coated TiO2 nanoparticles is varied from 10% to 95% by increasing the number of scans from 10 to 50 in preparing the positively charged Au-coated TiO2 nanoparticles. The extremely high coverage of 95% in this study is notable, as compared with other methods to prepare Au-coated TiO2 nanoparticles.

Journal Article↗

Factors affecting the preparation and properties of electrodeposited silica thin films functionalized with amine or thiol groups.

Well-adherent sol-gel-derived silica films functionalized with amine or thiol groups have been electrogenerated on gold electrodes and both the deposition process and the film properties have been studied by various physicochemical techniques. Electrodeposition was achieved by combining the formation of a self-assembled "nanoglue" on the electrode surface, the sol-gel process, and the electrochemical manipulation of pH to catalyze polycondensation of the precursors. Gold electrodes pretreated with mercaptopropyltrimethoxysilane (MPTMS) were immersed in sol solutions containing the selected precursors (tetraethoxysilane, TEOS, in mixture with (3-aminopropyl)triethoxysilane, APTES, or MPTMS) where they underwent a cathodic electrolysis to generate the hydroxyl ions that are necessary to catalyze the formation of the organosilica films on the electrode surface. Special attention was given to analyze the effects of deposition time and applied potential and to compare APTES and MPTMS films. Characterization was made using quartz crystal microbalance, scanning electron microscopy, cyclic voltammetry, and atomic force microscopy (including in situ monitoring). The electrodeposition process was found to occur at two growing rates: a first slow stage giving rise to rather homogeneous, yet rough, films with thickness in the sub-mum range (increasing continuously when increasing the deposition time), which was followed by a faster gelification step resulting in much thicker (>1 microm) and rougher macroporous deposits. These two successive situations were observed independently on the applied potential except that more cathodic values led to narrower sub-microm ranges (as expected from the larger amounts of the electrogenerated hydroxyl catalyst). Thiol-functionalized silica films were deposited more rapidly than the amine ones and, for both of them, permeability to redox probe was found to decrease when increasing the film thickness because of higher resistance to mass transport.

Journal Article↗

Bipolar electrochemical mechanism for the propulsion of catalytic nanomotors in hydrogen peroxide solutions.

Bimetallic nanorods are propelled in aqueous solutions by the catalytic decomposition of hydrogen peroxide to oxygen and water. Several mechanisms (interfacial tension gradients, bubble recoil, viscous Brownian ratchet, self-electrophoresis) have been proposed for the transduction of chemical to mechanical energy in this system. From Tafel plots of anodic and cathodic hydrogen peroxide reactions at various metal (Au, Pt, Rh, Ni, Ru, and Pd) ultramicroelectrodes, we determine the potential at which the anodic and cathodic reaction rates are equal for each metal. These measurements allow one to predict the direction of motion of all possible bimetallic combinations according to the bipolar electrochemical (or self-electrophoretic) mechanism. These predictions are consistent with the observed direction of motion in all cases studied, providing strong support for the mechanism. We also find that segmented nanorods with one Au end and one poly(pyrrole) end containing catalase, an enzyme that decomposes hydrogen peroxide nonelectrochemically, perform the overall catalytic reaction at a rate similar to that of nanorods containing Au and Pt segments. However, in this case there is no observed axial movement, again supporting the bipolar electrochemical propulsion mechanism for bimetallic nanorods.

Catalysis↗

Kelvin probe force microscopy study on conjugated polymer/fullerene bulk heterojunction organic solar cells.

We conducted a comprehensive Kelvin probe force microscopy (KPFM) study on a classical organic solar cell system consisting of MDMO-PPV/PCBM blends. The KPFM method yields the information of topography and local work function at the nanometer scale. Experiments were performed either in the dark or under cw laser illumination at 442 nm. We identified distinct differences in the energetics on the surface of chlorobenzene and toluene cast blend films. Together with high-resolution scanning electron microscopy (SEM) experiments we were able to interpret the KPFM results and to draw some conclusions for the electron transport toward the cathode in the solar cell configuration. The results suggest that surfaces of toluene cast films exhibit a morphologically controlled hindrance for electron propagation toward the cathode, which is usually evaporated on top of the films in the solar cell device configuration.

Electric Power Supplies↗

Saturated saline enhances the effect of electrochemical therapy.

We conducted this experiment to assess the effect of saline injection in electrochemical therapy. Platinum electrodes using direct current were inserted into egg white or liver parenchyma. Pure water or 0.9%, 3%, or 26% sodium chloride were injected into various objects to compare with the control group (no injection). Power was set at 10 V. In the egg-white experiment, gas bubbles and coagulated protein developed around the electrodes. In ex vivo liver, frothy reddish debris developed around the cathodes, while a hardening and shrunken surface occurred around the anodes. The pH was 14 around the cathodes, 0 around the anodes. The electric current, the amount of coagulated protein, and the severity of tissue damage were all in proportion to the concentrations of the injected saline. The volume destroyed in the 26% saline group was 8.1 times larger than that of the control group. Therefore, injected saline, especially saturated saline, can enhance the effect of electrochemical therapy.

Animals↗

Effect of stainless steel on corrosion behavior of copper in a copper-bearing intrauterine device.

Some copper-bearing intrauterine devices (Cu-IUDs) consist of pure copper and stainless steel. Corrosion of copper in the Cu-IUD was anticipated to be affected by galvanic action due to electrical contact between these two metals. Electrochemical measurements were carried out in physiological saline with or without indomethacin, which was introduced for bleeding control. In the copper/stainless steel couple, the open-circuit potential of stainless steel was found to play a decisive role. In most cases, when stainless steel was in the passive state and acted as the cathode, the contact accelerated copper corrosion. In addition, the area ratio of stainless steel to copper altered copper corrosion behavior. The larger the area of stainless steel, the greater the acceleration of copper corrosion. It was noted that the stainless steel surface might be activated due to improper handling of the IUD. In this case, copper became the cathode of the couple and its corrosion was suppressed.

Anti-Inflammatory Agents, Non-Steroidal↗

Visualization and analysis of electroosmotic flow in hairless mouse skin.

PURPOSE: To identify the physiological structures in hairless mouse skin responsible for the generation of electroosmotic flow during iontophoresis. Also, to determine the effects of changing the pH of the contacting solution on the magnitude of electroosmotic flow in these structures. METHODS: Localized diffusive and iontophoretic fluxes of a neutral molecule, hydroquinone (HQ), across hairless mouse skin were quantified using scanning electrochemical microscopy (SECM). The iontophoretic flux was determined as a function of the direction of the applied current and pH of the contacting solution. RESULTS: SECM images of HQ transport recorded during iontophoresis at moderate current densities (+/-0.1 mA/cm2) demonstrate that electroosmotic flow is localized to hair follicles. The direction of flow is from anode to cathode at pH > 3.5 and from cathode to anode at pH <3.5. CONCLUSIONS: Electroosmotic flow through hair follicles is an efficient and controllable means of transporting small, electrically neutral molecules across hairless mouse skin. Transport through the appendages is sensitive to the pH of the solution in contact with the skin. The isoelectric point of hair follicles, pI, is estimated to be 3.5 from the dependence of electroosmotic flow on the solution pH.

Animals↗

Optical transmembrane potential recordings during intracardiac defibrillation-strength shocks.

BACKGROUND: The prolongation of the action potential after defibrillation-strength shocks is believed to be a critical component of defibrillation. The response of the transmembrane potential to the shock may affect this prolongation. We studied the effects of an intracardiac shock on the transmembrane potential and action potential duration at multiple sites on the epicardium using a voltage-sensitive dye and optical mapping system. METHODS AND RESULTS: A laser scanner recorded optical action potentials with voltage-sensitive dye at 63 spots on both the left and right ventricles of six isolated, perfused rabbit hearts. Hearts were paced with epicardial point stimulation followed by the delivery of a 2 A and 20 ms rectangular waveform shock during the relative refractory period. The shock was given between right atrial and right ventricular electrodes. Of 621 total spots analyzed, 241 spots hyperpolarized and 76 spots depolarized with a right ventricular anode, whereas 159 spots hyperpolarized and 145 spots depolarized with a right ventricular cathode (P < 0.05). Both hyperpolarized and depolarized spots exhibited prolonged action potential duration, although prolongation was greater with depolarizing responses (16.7 +/- 9 ms vs. 13.3 +/- 13.4 ms, p<0.001). Hyperpolarized and depolarized spots were not randomly distributed, but clustered into regions. The size of the hyperpolarized regions was larger than the depolarized regions with RV anodal stimulation (27 +/- 20 spots/hyperpolarized region vs. 8.5 +/- 9 spots/depolarized region, p < 0.03) but not with RV cathodal stimulation. With reversal of electrode polarity, spots hyperpolarized near the shocking electrodes frequently did not reverse polarization but remained hyperpolarized. CONCLUSIONS: Distinct regions of either polarization occur during intracardiac defibrillation-strength shocks. Although hyperpolarizing membrane responses were observed more often than depolarizing responses, depolarizing membrane polarization resulted in greater action potential prolongation. The absence of sign change in polarization in some regions with shocks of opposite polarities suggests that nonlinear intrinsic membrane properties are operative during strong electrical stimulation.

Action Potentials↗