Search results for "Chronoamperometry"
showing 8 items of 18 documents
Graphene electrochemical responses sense surroundings
2012
Abstract Graphite oxide (GO) paper, obtained by direct filtration of exfoliated GO in water over PTFE membrane filters, was reduced by using hydrazine vapours. The graphene-paper thus obtained was characterized by the combination of different techniques. The electrochemical characterization by cyclic voltammetry, chronoamperometry and chronopotentiometry presents a strong influence of the working conditions: temperature, electrolyte concentration and current on the electrochemical responses, indicating a good ability of the material to sense ambient and working conditions. Electrochemical devices based on graphene are expected to work as dual, and simultaneous, sensing-actuators.
Photoelectrocatalysis of paracetamol on Pd–ZnO/ N-doped carbon nanofibers electrode
2021
Abstract The presence of pharmaceuticals in water bodies has become a major concern in recent years. An efficient and innovative way of eliminating these pollutants is through photoelectrocatalytic (PEC) degradation owing to its environmental sustainability and its ability to remove recalcitrant pollutants. In this study, palladium loaded zinc oxide/carbon nanofibers (CZnO–Pd) were employed as a novel photoanode for PEC degradation of paracetamol. The CZnO–Pd composite was prepared through electrospinning and atomic layer deposition (ALD). The obtained materials were characterized. Photoelectrochemical studies were carried out with linear sweep voltammetry and chronoamperometry. The removal…
Low angle bending detection semi-transparent piezoresistive sensor
2022
We designed, fabricated, and validated a piezoresistive bending sensor, a fundamental component of wearable electronic devices for monitoring human motion. The most diffused opaque carbon-based resistance flex sensors suffer from low detection for small bending angles. The sensor we here present is based on a semi-transparent active material (fulleropyrrolidine bisadducts polymer) and has the remarkable advantage of good electrical properties for low bending angles. The fabrication steps are effective since a pre-patterned ITO/PET surface is functionalized by chronoamperometric deposition, and the silver electrical contacts are inkjet printed. We propose a fitting function of the measured t…
Quantification of electrochromic kinetics by analysis of RGB digital video images
2018
A new, rapid, and practical procedure to obtain quantitative kinetic information of electrochromic materials is proposed. When the transition between two colors on a colored electrode surface is monitorized by digital video, the analysis of pixel color intensity (I) in sequential RGB digital images allows us to precise the half-life time (t1/2) of the color change since a maximum value of the standard deviation of the pixel intensity (σ(I)) is reached. We simulated and analyzed the evolution of standard deviation during an electrochromic transition in different circumstances (kinetic and diffusion control). As an example of application, electrochromic transitions of a thin film model, the P…
Chronoamperometry of prussian blue films on ITO electrodes: Ohmic drop and film thickness effect
1999
Abstract The chronoamperograms associated with the reduction of prussian blue films deposited onto indium tin oxide (ITO) electrodes to the Everitt’s salt form, are influenced by the ohmic drop effect. These chronoamperometric curves have been simulated by means of a numerical finite difference model which is able to explain their shape and their dependence on the thickness of the film and on the uncompensated resistance. An analytical expression which describes the dependence of current against time at initial times considering the ohmic drop effect has also been proved when applied to these chronoamperometric curves at short times.
Electron transfer mechanism in Shewanella loihica PV-4 biofilms formed at graphite electrode
2012
Abstract Electron transfer mechanisms in Shewanella loihica PV-4 viable biofilms formed at graphite electrodes were investigated in potentiostat-controlled electrochemical cells poised at oxidative potentials (0.2 V vs. Ag/AgCl). Chronoamperometry (CA) showed a repeatable biofilm growth of S. loihica PV-4 on graphite electrode. CA, cyclic voltammetry (CV) and its first derivative shows that both direct electron transfer (DET) mediated electron transfer (MET) mechanism contributes to the overall anodic (oxidation) current. The maximum anodic current density recorded on graphite was 90 μA cm − 2 . Fluorescence emission spectra shows increased concentration of quinone derivatives and riboflavi…
Acid versus base peptization of mesoporous nanocrystalline TiO2 films: functional studies in dye sensitized solar cells
2005
We report an analysis of the influence of acid/base conditions employed in the synthesis of TiO2 nanoparticles upon the performance of dye sensitised photoelectrochemical solar cells fabricated from these particles. The functional properties of the TiO2 nanoparticles in these devices are investigated by potential step chronoamperometry, transient laser spectroscopy, and photovoltaic device characterisation. We find that base peptization conditions employed in the sol–gel fabrication of the TiO2 nanoparticles result in a reduction in film electron density under negative applied bias, correlated with slower interfacial recombination losses and a higher device open circuit voltage.
Coupling of proton translocation through ATPase incorporated into supported lipid bilayers to an electrochemical process
1997
Abstract H+-ATPase is incorporated into solid-supported lipid bilayers separated from the gold support by a peptide spacer. The translocation of protons across the lipid film to the inner side is coupled to the discharge of protons at the gold surface. The overall process is investigated by square wave voltammetry (SWV) and double potential-pulse chronoamperometry (CA). As a result, the formation of a proton gradient is monitored by SWV whereas currents measured by CA monitor the stationary state when the enzyme activity is directly coupled to the charge transfer at the electrode. These currents markedly depend on the number of ATPases present in the bilayer.