Search results for "Electrochemical"

Solution Processed Micro- and Nano-Bioarrays for Multiplexed Biosensing

2012

This Feature article reports on solution dispensing methodologies which enable the realization of multiplexed arrays at the micro- and nanoscale for relevant biosensing applications such as drug screening or cellular chips.

Cover Picture: Bis(2,2′‐biphenoxy)borates for Electrochemical Double‐Layer Capacitor Electrolytes (Chem. Eur. J. 11/2011)

2011

Light-emitting electrochemical cells based on a supramolecularly-caged phenanthroline-based iridium complex.

2011

The complex [Ir(ppy)(2)(pphen)][PF(6)] (Hppy = 2-phenylpyridine, pphen = 2-phenyl-1,10-phenanthroline) has been prepared and evaluated as an electroluminescent component for light-emitting electrochemical cells (LECs). Like in analogous LECs using bpy-based iridium(III) complexes a significant enhancement of the device stability is observed.

Single Molecule Solid State Light Emitting Electrochemical Cells with Lifetimes Superior to 3000 Hours

2008

ELECTROCHEMICAL CONVERSION OF DICHLOROACETIC ACID TO CHLOROACETIC ACID IN A MICROFLUIDIC STACK AND IN A SERIES OF MICROFLUIDIC REACTORS

2015

The electrochemical conversion of dichloroacetic acid to chloracetic acid was performed in three different micro devices: a simple micro fluidic cell; a microfluidic stack equipped with various electrode chambers in series and three micro fluidic cells in series. The electrochemical synthesis of chloracetic acid was performed successfully with high yields and selectivity under a single-pass mode without supporting electrolyte at low cell voltages. An increase of the productivity and of the final concentration of the target product was achieved by using a stack with two or three electrode chambers in series. The utilization of three micro reactors in series open interesting new perspectives,…

Transduction of redox Gibbs free energy into modulated electrochemical work

1988

Abstract This work supplies an electrochemical model in order to account for some oscillatory phenomena. The model can be applied both to living bodies and to electrochemical cells. We suppose that one of the products of an electrochemical reaction in solution has a high vapour pressure and study the influence of its mass transfers on its oscillations and on that of the current,induced by the former ones. Mass transfers that we consider are either that from the solution to theatmosphere above it or both that due to bubble nucleation and that from the solution to the bubbles alreadynucleated. Two different oscillation conditions are determined. One derives from the resistance due to theinter…

Channel flow at an immobilised liquid|liquid interface

2000

A novel rectangular channel flow electrochemical cell for the study of liquid | liquid interfaces is presented. The organic phase is immobilised by the use of a gelling agent, while the aqueous phase flows past the interface. This creates an asymmetric setup that allows us to establish diagnostic criteria to determine, for example, the direction of the ion transfer. The effects of varying flow rate and sweep rate have been considered both theoretically and experimentally. By comparison with two-dimensional simulations, it is demonstrated that a simple one-dimensional theory can be used to describe the cyclic voltammetry response of the channel flow cell.

Ion-exchange voltammetry at a surfactant-doped electrode: model of mass transfer kinetics to an anionic surface-charged electrode and its application…

2000

cited By 10; International audience; A theoretical model of mass transfer kinetics was developed for investigating the accumulation of cationic compounds at an anionic surfactant-doped screen-printed electrode. It was extended to an enzyme-generated cationic product for the indirect determination of alkaline phosphatase (AP). The model takes into account the analyte depletion, the kinetics of the ion-exchange reaction-diffusion and the kinetics of the enzymatic reaction. The relationship between the ion-exchange voltammetric anodic peak current and the enzyme incubation/accumulation time for a given concentration of AP was established and the validity of the theoretical model was verified e…

Two are not always better than one: ligand optimisation for long-living light-emitting electrochemical cells

2009

The complex [Ir(ppy)2(dpbpy)][PF6] (Hppy = 2-phenylpyridine, dpbpy = 6,6'-diphenyl-2,2'-bipyridine) has been prepared and evaluated as an electroluminescent component for light-emitting electrochemical cells (LECs); the complex exhibits two intramolecular face-to-face π-stacking interactions and long-lived LECs have been constructed; the device characteristics are not significantly improved in comparison to analogous LECs with 6-phenyl-2,2'-bipyridine. Costa Riquelme, Ruben Dario, Ruben.Costa@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es ; Bolink, Henk, Henk.Bolink@uv.es

Electrochemistry of TiO2–iron hexacyanocobaltate composite electrodes

2014

Abstract In this paper we investigate the electrochemical behavior of iron hexacyanocobaltate (FeHCC) in comparison to the cobalt hexacyanoferrate (CoHCF). The best results were achieved on electrochemical synthesized film of FeHCC on the TiO2 modified electrodes. The chemical and physical characterizations confirm the formation of the FeHCC with the classical cubic crystal structure of the Prussian blue analogs, with cell parameter a very close to 10 A, as well as the formation of micro aggregates of TiO2 covered by FeHCC. The synthesis was performed on various substrates such as glassy carbon (GC), graphite foil (GF) and indium tin oxide (ITO) in order to develop new technological applica…