We report stationary, nonequilibrium potential and adsorbate patterns with an intrinsic wavelength that were observed in an electrochemical system with a specific type of current/electrode-potential (I-phi(DL)) characteristic. The patterns emerge owing to the interplay of a self-enhancing step in the reaction dynamics and a long-range inhibition by migration currents rather than by diffusion. Theoretical analysis revealed that this self-structuring of the electrode occurs in all electrochemical systems with an S-shaped I-phi(DL) characteristic in wide and well-accessible parameter ranges. This unusual pattern-forming instability in electrochemical systems has all the characteristics of the mechanism proposed by Turing in 1952 in the framework of an early theory of morphogenesis. Our finding might account for structure formation in certain biological systems that have gradients in the electric potential and may open new paths for fabricating patterned electrodes.
A new determination of the decay rate of the negative ion of positronium (Ps-), using a beam-foil method and a stripping-based detection technique, is reported. The measured result of gamma = 2.089(15) ns(-1) is a factor of 6 more precise than the previous experimental value of gamma = 2.09(9) ns(-1), and is in excellent agreement with the theoretical value of gamma = 2.086(6) ns(-1).
Spatio-temporal bifurcations and complex dynamics in globally coupled intrinsically bistable electrochemical systems with an S-shaped current-voltage characteristic under galvanostatic control are studied theoretically on a one-dimensional domain. The results are compared with the dynamics and the bifurcation scenarios occurring in a closely related model which describes pattern formation in semiconductors. Under galvanostatic control both systems are unstable with respect to the formation of stationary large amplitude current domains. The current domains as well as the homogeneous steady state exhibit oscillatory instabilities for slow dynamics of the potential drop across the double layer, or across the semiconductor device, respectively. The interplay of the different instabilities leads to complex spatio-temporal behavior. We find breathing current domains and chaotic spatio-temporal dynamics in the electrochemical system. Comparing these findings with the results obtained earlier for the semiconductor system, we outline bifurcation scenarios leading to complex dynamics in globally coupled bistable systems with subcritical spatial bifurcations.
A quantitative model of oscillations observed during hydrogen oxidation on platinum in the presence of electrosorbing metal ions and specifically adsorbing anions is presented and the model predictions are compared with experiments. Mass and charge balances of all reactants lead in a first step to a seven variable model which is governed by reaction steps that have been widely studied. We demonstrate that attractive interactions between metal and halide ions on the electrode surface, which were recently reported [1], are crucial for the observed dynamics. The model parameters were almost exclusively taken out of the literature. The model is then reduced to its minimal form without losing dynamic features arriving at a four variable system. Experimental time series of three of the four variables of the model and measured bifurcation diagrams are presented. It is shown that the integrated time evolution and the calculated bifurcation diagrams of the model agree almost quantitatively with the experiment.
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