631 research outputs found
Resonant frequency measurements as an alternative to phase-selective A.C. polarography in tensammetry and pseudocapacitance determinations
Strongly nonlinear dynamics of electrolytes in large ac voltages
We study the response of a model micro-electrochemical cell to a large ac
voltage of frequency comparable to the inverse cell relaxation time. To bring
out the basic physics, we consider the simplest possible model of a symmetric
binary electrolyte confined between parallel-plate blocking electrodes,
ignoring any transverse instability or fluid flow. We analyze the resulting
one-dimensional problem by matched asymptotic expansions in the limit of thin
double layers and extend previous work into the strongly nonlinear regime,
which is characterized by two novel features - significant salt depletion in
the electrolyte near the electrodes and, at very large voltage, the breakdown
of the quasi-equilibrium structure of the double layers. The former leads to
the prediction of "ac capacitive desalination", since there is a time-averaged
transfer of salt from the bulk to the double layers, via oscillating diffusion
layers. The latter is associated with transient diffusion limitation, which
drives the formation and collapse of space-charge layers, even in the absence
of any net Faradaic current through the cell. We also predict that steric
effects of finite ion sizes (going beyond dilute solution theory) act to
suppress the strongly nonlinear regime in the limit of concentrated
electrolytes, ionic liquids and molten salts. Beyond the model problem, our
reduced equations for thin double layers, based on uniformly valid matched
asymptotic expansions, provide a useful mathematical framework to describe
additional nonlinear responses to large ac voltages, such as Faradaic
reactions, electro-osmotic instabilities, and induced-charge electrokinetic
phenomena.Comment: 30 pages, 17 eps-figures, RevTe
Impedance measurements of zinc and amalgamated zinc electrodes in alkaline electrolyte
Study of the electrochemical behaviour of a 300 W PEM fuel cell stack by Electrochemical Impedance Spectroscopy
Electrochemical Impedance Spectroscopy (EIS) is a suitable and powerful diagnostic testing method for fuel cells because it is non-destructive and provides useful information about fuel cell performance and its components. In this work, EIS measurements were carried out on a 300 W stack with 20 elementary cells. Electrochemical impedance spectra were recorded either on each cell or on the stack. Parameters of a Randles-like equivalent circuit were fitted to the experimental data. In order to improve the quality of the fit, the classical Randles cell was extended by changing the standard plane capacitor into a constant phase element (CPE). The effects of output current, cell position, operating temperature and humidification temperature on the impedance spectra were studied.This work was supported by Generalitat Valenciana (PROMETEO/2010/023).Pérez Page, M.; Pérez Herranz, V. (2014). Study of the electrochemical behaviour of a 300 W PEM fuel cell stack by Electrochemical Impedance Spectroscopy. International Journal of Hydrogen Energy. 39(8):4009-4015. https://doi.org/10.1016/j.ijhydene.2013.05.121S4009401539
Nonlinear electrochemical relaxation around conductors
We analyze the simplest problem of electrochemical relaxation in more than
one dimension - the response of an uncharged, ideally polarizable metallic
sphere (or cylinder) in a symmetric, binary electrolyte to a uniform electric
field. In order to go beyond the circuit approximation for thin double layers,
our analysis is based on the Poisson-Nernst-Planck (PNP) equations of dilute
solution theory. Unlike most previous studies, however, we focus on the
nonlinear regime, where the applied voltage across the conductor is larger than
the thermal voltage. In such strong electric fields, the classical model
predicts that the double layer adsorbs enough ions to produce bulk
concentration gradients and surface conduction. Our analysis begins with a
general derivation of surface conservation laws in the thin double-layer limit,
which provide effective boundary conditions on the quasi-neutral bulk. We solve
the resulting nonlinear partial differential equations numerically for strong
fields and also perform a time-dependent asymptotic analysis for weaker fields,
where bulk diffusion and surface conduction arise as first-order corrections.
We also derive various dimensionless parameters comparing surface to bulk
transport processes, which generalize the Bikerman-Dukhin number. Our results
have basic relevance for double-layer charging dynamics and nonlinear
electrokinetics in the ubiquitous PNP approximation.Comment: 25 pages, 17 figures, 4 table
Diffuse-Charge Dynamics in Electrochemical Systems
The response of a model micro-electrochemical system to a time-dependent
applied voltage is analyzed. The article begins with a fresh historical review
including electrochemistry, colloidal science, and microfluidics. The model
problem consists of a symmetric binary electrolyte between parallel-plate,
blocking electrodes which suddenly apply a voltage. Compact Stern layers on the
electrodes are also taken into account. The Nernst-Planck-Poisson equations are
first linearized and solved by Laplace transforms for small voltages, and
numerical solutions are obtained for large voltages. The ``weakly nonlinear''
limit of thin double layers is then analyzed by matched asymptotic expansions
in the small parameter , where is the
screening length and the electrode separation. At leading order, the system
initially behaves like an RC circuit with a response time of
(not ), where is the ionic diffusivity, but nonlinearity
violates this common picture and introduce multiple time scales. The charging
process slows down, and neutral-salt adsorption by the diffuse part of the
double layer couples to bulk diffusion at the time scale, . In the
``strongly nonlinear'' regime (controlled by a dimensionless parameter
resembling the Dukhin number), this effect produces bulk concentration
gradients, and, at very large voltages, transient space charge. The article
concludes with an overview of more general situations involving surface
conduction, multi-component electrolytes, and Faradaic processes.Comment: 10 figs, 26 pages (double-column), 141 reference
Electrochemical Study of Ion Transfer of Acetylcholine Across the Interface of Water and a Lipid-Modified 1,2-Dichloroethane
Characterizing archaeological bronze corrosion products intersecting electrochemical impedance measurements with voltammetry of immobilized particles
[EN] Application of electrochemical impedance measurements to microparticulate deposits of copper corrosion products attached to graphite electrodes in contact with 0.10 M aqueous HClO4 electrolyte is described. The impedance measurements were sensitive to the applied potential and the amount of solid sample and were modeled taking into account the contribution of the uncovered base electrode. Several pairs of circuit elements provide monotonic variations which are able to characterize different corrosion compounds regardless the amount of microparticulate solid on the electrode. Application to a set of archaeological samples from the archaeological Roman site of Gadara (Jordan, 4th century AD) permitted to establish a grouping of such samples suggesting different provenances/manufacturing techniques.Financial support from the MINECO ProjectsCTQ2014-53736-C3-1-P and CTQ2014-53736-C3-2-P which are also supported with ERDF funds and Grants ES-2012-052716 and EEBB-I-16-11558 is gratefully acknowledgedRedondo-Marugan, J.; Piquero-Cilla, J.; Domenech Carbo, MT.; Ramírez-Barat, B.; Al Sekhaneh, W.; Capelo, S.; Doménech Carbó, A. (2017). Characterizing archaeological bronze corrosion products intersecting electrochemical impedance measurements with voltammetry of immobilized particles. Electrochimica Acta. 246:269-279. https://doi.org/10.1016/j.electacta.2017.05.190S26927924
Reversible Metal-Insulator Transition in Ordered Metal Nanocrystal Monolayers Observed by Impedance Spectroscopy
On the impedance of galvanic cells: IX. The double layer capacity of the mercury-1 M HCIO4 solution interface at high d.c. potentials
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