Electrolyte Effects on Electrochemical CO Reduction Reaction at Sn Metallic Electrode.

Understanding the electrolyte factors governing the electrochemical CO reduction reaction (CORR) is fundamental for selecting the optimized electrolyte conditions for practical applications. While noble metals are frequently studied, the electrolyte effects on the CORR on Sn catalysts are not well explored. Here, we studied the electrolyte effect on Sn metallic electrodes, investigating the impact of electrolyte concentration, cation identity, and anion properties, and how it shapes the CORR activity and selectivity.

Role of Structural and Compositional Changes of CuO Nanocubes in Nitrate Electroreduction to Ammonia.

Nitrate electroreduction reaction (NORR) to ammonia (NH) still faces fundamental and technological challenges. While Cu-based catalysts have been widely explored, their activity and stability relationship are still not fully understood. Here, we systematically monitored the dynamic alterations in the chemical and morphological characteristics of CuO nanocubes (NCs) during NORR in an alkaline electrolyte.

Finding influential nodes in networks using pinning control: Centrality measures confirmed with electrochemical oscillators.

The spatiotemporal organization of networks of dynamical units can break down resulting in diseases (e.g., in the brain) or large-scale malfunctions (e.

A numerical investigation of the effect of external resistance and applied potential on the distribution of periodicity and chaos in the anodic dissolution of nickel.

The oscillatory electrodissolution of nickel is one among several reactions utilized as a model-system to study the emergence of oscillations and pattern formation in electrochemical interfaces, in addition to frequently providing experimental proofs for theoretical predictions in synchronization engineering. The reaction was modeled in 1992 by Haim and co-workers [J. Phys.

Quasiperiodic behavior in the electrodeposition of Cu/Sn multilayers: extraction of activation energies and wavelet analysis.

Living systems are one of the many examples in which self-organizing systems yield more intricate structures than those that can be achieved using a "step-by-step" approach. This phenomenon can be observed in electrochemical organic synthesis, oscillating metal deposition and in chemical clocks. There is a plenitude of temporal instabilities during self-organization, from ordinary period-one oscillations, going through quasiperiodicity, to the onset of chaos.

Tuning Electrochemical Bistability by Surface Area Blocking in the Cathodic Deposition of Copper.

We report herein a precise control of the electrochemical bistability induced by surface area changes during the cathodic deposition of copper. Small additions of 1,10-phenanthroline (Phen) in the reaction media present an inhibiting effect on the global rate mainly due to the adsorption of protonated Phen. The increase of its concentration favors a shrinkage of the bifurcation (saddle-node) diagram and shifts it to less negative potentials.

Multivariate statistical analysis of chemical and electrochemical oscillators for an accurate frequency selection.

The effect of experimental parameters on the frequency of chemical oscillators has been systematically studied since the first observations of clock reactions. The approach is mainly based on univariate changes in one specific parameter while others are kept constant. The frequency is then monitored and the effect of each parameter is discussed separately.

Modulation of Turing Patterns in the CDIMA Reaction by Ultraviolet and Visible Light.

We have carried out the first systematic study of the effects of ultraviolet light, both alone and in combination with visible white light, on Turing patterns in the chlorine dioxide-iodine-malonic acid (CDIMA) reaction. The ultraviolet light used has a sharp peak at 368 nm and can perturb the system selectively. It primarily decomposes chlorine dioxide in a zeroth-order reaction, and when it is used to illuminate Turing patterns, shrunken spots are formed with an imperfect hexagonal arrangement.

Restoring oscillatory behavior from amplitude death with anti-phase synchronization patterns in networks of electrochemical oscillations.

The dynamical behavior of delay-coupled networks of electrochemical reactions is investigated to explore the formation of amplitude death (AD) and the synchronization states in a parameter region around the amplitude death region. It is shown that difference coupling with odd and even numbered ring and random networks can produce the AD phenomenon. Furthermore, this AD can be restored by changing the coupling type from difference to direct coupling.

Elucidation of Reaction Mechanisms Far from Thermodynamic Equilibrium.

Far from equilibrium: This thesis provides a deep mechanistic analysis of the electrooxidation of methanol when the system is kept far from the thermodynamic equilibrium. Under an oscillatory regime, interesting characteristics between the elementary reaction steps were observed. We were able to elucidate the effect of the intrinsic drift in a potential time-series responsible for spontaneous transition of temporal patterns and the carbon dioxide decoupling from direct and indirect pathways.

Phase-selective entrainment of nonlinear oscillator ensembles.

The ability to organize and finely manipulate the hierarchy and timing of dynamic processes is important for understanding and influencing brain functions, sleep and metabolic cycles, and many other natural phenomena. However, establishing spatiotemporal structures in biological oscillator ensembles is a challenging task that requires controlling large collections of complex nonlinear dynamical units. In this report, we present a method to design entrainment signals that create stable phase patterns in ensembles of heterogeneous nonlinear oscillators without using state feedback information.

Restoration of rhythmicity in diffusively coupled dynamical networks.

Oscillatory behaviour is essential for proper functioning of various physical and biological processes. However, diffusive coupling is capable of suppressing intrinsic oscillations due to the manifestation of the phenomena of amplitude and oscillation deaths. Here we present a scheme to revoke these quenching states in diffusively coupled dynamical networks, and demonstrate the approach in experiments with an oscillatory chemical reaction.

Coupled slow and fast surface dynamics in an electrocatalytic oscillator: model and simulations.

The co-existence of disparate time scales is pervasive in many systems. In particular for surface reactions, it has been shown that the long-term evolution of the core oscillator is decisively influenced by slow surface changes, such as progressing deactivation. Here we present an in-depth numerical investigation of the coupled slow and fast surface dynamics in an electrocatalytic oscillator.

Fronts and patterns in a spatially forced CDIMA reaction.

We use the CDIMA chemical reaction and the Lengyel-Epstein model of this reaction to study resonant responses of a pattern-forming system to time-independent spatial periodic forcing. We focus on the 2 : 1 resonance, where the wavenumber of a one-dimensional periodic forcing is about twice the wavenumber of the natural stripe pattern that the unforced system tends to form. Within this resonance, we study transverse fronts that shift the phase of resonant stripe patterns by π.

The electro-oxidation of ethylene glycol on platinum over a wide pH range: oscillations and temperature effects.

We report a comprehensive study of the electro-oxidation of ethylene glycol (EG) on platinum with emphasis on the effects exerted by the electrolyte pH, the EG concentration, and temperature, under both regular and oscillatory conditions. We extracted and discussed parameters such as voltammetric activity, reaction orders (with respect to [EG]), oscillation's amplitude, frequency and waveform, and the evolution of the mean electrode potential at six pH values from 0 to 14. In addition, we obtained the apparent activation energies under several different conditions.

Forcing of Turing patterns in the chlorine dioxide-iodine-malonic acid reaction with strong visible light.

We investigate the sensitivity of Turing patterns in the chlorine dioxide-iodine-malonic acid reaction to illumination by strong white light. Intense illumination results in an increase of [I(-)], in contrast to previous studies, which found only decreased [I(-)] for weak and intermediate intensities of illumination. We propose an expanded mechanism to explain the experimental observations.

Mechanistic aspects of the linear stabilization of non-stationary electrochemical oscillations.

The problem of non-stationarity in experimentally recorded time-series is common in many (electro)chemical systems. Underlying this non-stationarity is the slow drift in some uncontrollable parameter, and it occurs in spite of the fact that all controllable parameters are kept constant. Particularly for electrochemical systems, some of us have recently suggested [J.

Turing patterns in the chlorine dioxide-iodine-malonic acid reaction with square spatial periodic forcing.

We use the photosensitive chlorine dioxide-iodine-malonic acid reaction-diffusion system to study wavenumber locking of Turing patterns to two-dimensional "square" spatial forcing, implemented as orthogonal sets of bright bands projected onto the reaction medium. Various resonant structures emerge in a broad range of forcing wavelengths and amplitudes, including square lattices and superlattices, one-dimensional stripe patterns and oblique rectangular patterns. Numerical simulations using a model that incorporates additive two-dimensional spatially periodic forcing reproduce well the experimental observations.

The dual pathway in action: decoupling parallel routes for CO2 production during the oscillatory electro-oxidation of methanol.

As in the case of most small organic molecules, the electro-oxidation of methanol to CO(2) is believed to proceed through a so-called dual pathway mechanism. The direct pathway proceeds via reactive intermediates such as formaldehyde or formic acid, whereas the indirect pathway occurs in parallel, and proceeds via the formation of adsorbed carbon monoxide (CO(ad)). Despite the extensive literature on the electro-oxidation of methanol, no study to date distinguished the production of CO(2) from direct and indirect pathways.

Temperature effects on the oscillatory electro-oxidation of methanol on platinum.

We report in this paper the effect of temperature on the oscillatory electro-oxidation of methanol on polycrystalline platinum in aqueous sulfuric acid media. Potential oscillations were studied under galvanostatic control and at four temperatures ranging from 5 to 35 degrees C. For a given temperature, the departure from thermodynamic equilibrium does not affect the oscillation period and results in a slight increase of the oscillation amplitude.

Temperature (over)compensation in an oscillatory surface reaction.

Biological rhythms are regulated by homeostatic mechanisms that assure that physiological clocks function reliably independent of temperature changes in the environment. Temperature compensation, the independence of the oscillatory period on temperature, is known to play a central role in many biological rhythms, but it is rather rare in chemical oscillators. We study the influence of temperature on the oscillatory dynamics during the catalytic oxidation of formic acid on a polycrystalline platinum electrode.