486,681 research outputs found
A 16 x 16 CMOS amperometric microelectrode array for simultaneous electrochemical measurements
There is a requirement for an electrochemical sensor technology capable of making multivariate measurements in environmental, healthcare, and manufacturing applications. Here, we present a new device that is highly parallelized with an excellent bandwidth. For the first time, electrochemical cross-talk for a chip-based sensor is defined and characterized. The new CMOS electrochemical sensor chip is capable of simultaneously taking multiple, independent electroanalytical measurements. The chip is structured as an electrochemical cell microarray, comprised of a microelectrode array connected to embedded self-contained potentiostats. Speed and sensitivity are essential in dynamic variable electrochemical systems. Owing to the parallel function of the system, rapid data collection is possible while maintaining an appropriately low-scan rate. By performing multiple, simultaneous cyclic voltammetry scans in each of the electrochemical cells on the chip surface, we are able to show (with a cell-to-cell pitch of 456 ÎŒm) that the signal cross-talk is only 12% between nearest neighbors in a ferrocene rich solution. The system opens up the possibility to use multiple independently controlled electrochemical sensors on a single chip for applications in DNA sensing, medical diagnostics, environmental sensing, the food industry, neuronal sensing, and drug discovery
Local probing of ionic diffusion by electrochemical strain microscopy: spatial resolution and signal formation mechanisms
Electrochemical insertion-deintercalation reactions are typically associated
with significant change of molar volume of the host compound. This strong
coupling between ionic currents and strains underpins image formation
mechanisms in electrochemical strain microscopy (ESM), and allows exploring the
tip-induced electrochemical processes locally. Here we analyze the signal
formation mechanism in ESM, and develop the analytical description of operation
in frequency and time domains. The ESM spectroscopic modes are compared to
classical electrochemical methods including potentiostatic and galvanostatic
intermittent titration (PITT and GITT), and electrochemical impedance
spectroscopy (EIS). This analysis illustrates the feasibility of spatially
resolved studies of Li-ion dynamics on the sub-10 nanometer level using
electromechanical detection.Comment: 49 pages, 17 figures, 4 tables, 3 appendices, to be submitted to J.
Appl. Phys
Electromechanical Probing of Ionic Currents in Energy Storage Materials
The electrochemical processes in energy storage materials are generally
linked with changes of molar volume of the host compound. Here, the frequency
dependent strain response of 1D electrochemically active systems to periodic
electric bias is analyzed. The sensitivity and resolution of these
electrochemical strain measurements are compared to the current-based
electrochemical impedance spectroscopy. The resolution and detection limits of
interferometric and atomic force microscopy based systems for probing
electrochemical reactions on the nanoscale are analyzed.Comment: 12 pages, 4 figures, 2 tables, 2 appendices, submitted to Appl. Phys.
Let
Pseudo-single crystal electrochemistry on polycrystalline electrodes : visualizing activity at grains and grain boundaries on platinum for the Fe2+/Fe3+ redox reaction
The influence of electrode surface structure on electrochemical reaction rates and mechanisms is a major theme in electrochemical research, especially as electrodes with inherent structural heterogeneities are used ubiquitously. Yet, probing local electrochemistry and surface structure at complex surfaces is challenging. In this paper, high spatial resolution scanning electrochemical cell microscopy (SECCM) complemented with electron backscatter diffraction (EBSD) is demonstrated as a means of performing âpseudo-single-crystalâ electrochemical measurements at individual grains of a polycrystalline platinum electrode, while also allowing grain boundaries to be probed. Using the Fe2+/3+ couple as an illustrative case, a strong correlation is found between local surface structure and electrochemical activity. Variations in electrochemical activity for individual high index grains, visualized in a weakly adsorbing perchlorate medium, show that there is higher activity on grains with a significant (101) orientation contribution, compared to those with (001) and (111) contribution, consistent with findings on single-crystal electrodes. Interestingly, for Fe2+ oxidation in a sulfate medium a different pattern of activity emerges. Here, SECCM reveals only minor variations in activity between individual grains, again consistent with single-crystal studies, with a greatly enhanced activity at grain boundaries. This suggests that these sites may contribute significantly to the overall electrochemical behavior measured on the macroscale
A mean-field kinetic lattice gas model of electrochemical cells
We develop Electrochemical Mean-Field Kinetic Equations (EMFKE) to simulate
electrochemical cells. We start from a microscopic lattice-gas model with
charged particles, and build mean-field kinetic equations following the lines
of earlier work for neutral particles. We include the Poisson equation to
account for the influence of the electric field on ion migration, and
oxido-reduction processes on the electrode surfaces to allow for growth and
dissolution. We confirm the viability of our approach by simulating (i) the
electrochemical equilibrium at flat electrodes, which displays the correct
charged double-layer, (ii) the growth kinetics of one-dimensional
electrochemical cells during growth and dissolution, and (iii) electrochemical
dendrites in two dimensions.Comment: 14 pages twocolumn, 17 figure
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