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Free keywords:
hydrogen neutral atoms; pattern formation; spatiotemporal phenomena; surface chemistry; oxidation; electrochemistry; harmonic oscillators; CO oxidation; spatial bifurcations; cluster patterns; ring-electrode; surface; Pt(110); synchronization; feedback; systems; model
Abstract:
The impact of the strength of negative (desynchronizing) global coupling (NGC) on the spatiotemporal dynamics of an electrochemical relaxation oscillator is studied numerically with a prototypical model, the electro-oxidation of hydrogen in the presence of poisons. The results are compared with recent experiments. The NGC has a destabilizing effect on the homogeneous oscillations. Both, in theory and in experiments, the basic patterns found with increasing global coupling strength are modulated oscillations, target patterns (including an asymmetric variant), and modulated pulses, the average spatial inhomogeneity during an oscillation increasing with the intensity of the NGC. It is suggested that this scenario is typical for strong relaxation oscillations, and a comparison with an electrochemical oscillator exhibiting harmonic oscillations points to the fact that the critical coupling strength, upon which the complete synchronization is destroyed, is larger for relaxation oscillations than for harmonic oscillations. In addition, the numerical simulations predicted two- and three-phase cluster patterns at high coupling strength. Also in experiments cluster patterns were observed, however only in parameter regions of the local dynamics which were different from the one investigated in this study.
