Dynamical processes in many engineered and living systems take place on complex networks of discrete dynamical units. We present laboratory experiments with a networked chemical system of nickel electrodissolution in which synchronization patterns are recorded in systems with smooth periodic, relaxation periodic, and chaotic oscillators organized in networks composed of up to twenty dynamical units and 140 connections. The reaction system formed domains of synchronization patterns that are strongly affected by the architecture of the network. Spatially organized partial synchronization could be observed either due to densely connected network nodes or through the ‘chimera’ symmetry breaking mechanism. Relaxation periodic and chaotic oscillators formed structures by dynamical differentiation. We have identified effects of network structure on pattern selection (through permutation symmetry and coupling directness) and on formation of hierarchical and ‘fuzzy’ clusters. With chaotic oscillators we provide experimental evidence that critical coupling strengths at which transition to identical synchronization occurs can be interpreted by experiments with a pair of oscillators and analysis of the eigenvalues of the Laplacian connectivity matrix. The experiments thus provide an insight into the extent of the impact of the architecture of a network on self-organized synchronization patterns.
We propose a method to infer the coupling structure in networks of nonlinear oscillatory systems with multiple time scales. The method of partial phase synchronization allows us to infer the coupling structure for coupled nonlinear oscillators with one well-defined time scale. The case of oscillators with multiple time scales has remained a challenge until now. Here, we introduce partial recurrence based synchronization analysis to tackle this challenge. We successfully apply the proposed method to model systems and experimental data from coupled electrochemical oscillators. The statistical significance of the results is evaluated based on a surrogate hypothesis test.
Detailed experimental and numerical results are presented about the pattern formation mechanism of spatially organized partially synchronized states in a networked chemical system with oscillatory metal dissolution. Numerical simulations of the reaction system are used to identify experimental conditions (heterogeneity, network topology, and coupling time-scale) under which the chemical reactions, which take place in a network, are split into coexisting coherent and incoherent domains through the chimera mechanism. Experiments are carried out with a network of twenty electrodes arranged in a ring with seven nearest neighbor couplings in both directions along the ring. The patterns are characterized by analyzing the oscillation frequencies and entrainments to the mean field of the phases of oscillations. The chimera state forms from two domains of elements: the chimera core in which the elements have identical frequencies and are entrained to their corresponding mean field and the chimera shell where the elements exhibit desynchrony with each other and the mean field. The experiments point out the importance of low level of heterogeneities (e.g., surface conditions) and optimal level of coupling strength and time-scale as necessary components for the realization of the chimera state. For systems with large heterogeneities, a 'remnant' chimera state is identified where the pattern is strongly affected by the presence of frequency clusters. The exploration of dynamical features with networked reactions could open up ways for identification of novel types of patterns that cannot be observed with reaction diffusion systems (with localized interactions) or with reactions under global constraints, coupling, or feedback.
Experiments are presented to describe the effect of capacitive coupling of two electrochemical oscillators during Ni dissolution in sulfuric acid solution. Equivalent circuit analysis shows that the coupling between the oscillators occurs through the difference between the differentials of the electrode potentials. The differential nature of the coupling introduces strong negative nonisochronicity (i.e., phase shear, strong dependence of the period on the amplitude) in the coupling mechanism with smooth oscillators (under conditions just above a Hopf bifurcation point). Because of the negative nonisochronicity, asymmetrically coupled oscillators exhibit anomalous phase synchronization in the form of frequency difference enhancement. At strong coupling bistability is observed between in-phase and antiphase synchronized states. With relaxation oscillators, in contrast to the resistive coupling where antiphase synchronization can occur, the typical system response with weak coupling is out-of-phase synchronization. When the capacitance is applied on the individual resistors attached to the electrodes the oscillators exhibit weak positive nonisochronicity; this is in contrast with the strong negative nonisochronicity obtained with cross coupling. The proposed coupling configurations reveal the importance of the nonisochronicity level of oscillations for the experimentally observed synchronization patterns and also provide efficient ways of tuning the nonisochronicity level of the oscillations. This latter feature can be exploited to design synchronization features with a combination of resistive (difference) and capacitive (differential) coupling.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.