Open Circuit Interaction Between Ethanol or 2-Propanol and Oxidized Platinum Surfaces.

The interaction between organic molecules and oxidized catalyst surfaces has frequently been used to study the fuel crossover from the anode to the cathode in direct liquid fuel cells. In such experiments, the oxidized surface is put in contact with the fuel under open circuit conditions, and the evolution of the potential is registered. The open circuit potential (OCP) vs. time features can then inform on the reactivity of the fuel with the oxidized surface and provide valuable information not only to applications in fuel cells but also to the electrochemical reform of those molecules to produce clean hydrogen. In this paper, we present an experimental investigation of the open circuit interaction between ethanol or 2-propanol with oxidized platinum surfaces. Besides the OCP time traces, we have also employed cyclic voltammetry and fast oxide reduction sweep in the presence of the alcohols. Comparable reaction currents are obtained in the cyclic voltammogram, but the electro-oxidation of 2-propanol sets in at considerably lower overpotentials than that of ethanol. At the high potential region, both the magnitude and the potential of the current peak are nearly identical in both cases. In contrast, under open circuit conditions, the interaction of ethanol with the oxidized platinum surface is more pronounced than that found for 2-propanol, and these results are corroborated by the facile reduction of the platinum oxides along the fast backward sweep for the case of the latter.

Role of Fast and Slow Inhibitors in Oscillatory Rhythm Design.

In biological or abiotic systems, rhythms occur, owing to the coupling between positive and negative feedback loops in a reaction network. Using the Semenov-Whitesides oscillatory network for thioester hydrolysis as a prototype, we experimentally and theoretically analyzed the role of fast and slow inhibitors in oscillatory reaction networks. In the presence of positive feedback, a single fast inhibitor generates a time delay, resulting in two saddle-node bifurcations and bistability in a continuously stirred tank reactor. A slow inhibitor produces a node-focus bifurcation, resulting in damped oscillations. With both fast and slow inhibitors present, the node-focus bifurcation repeatedly modulates the saddle-node bifurcations, producing stable periodic oscillations. These fast and slow inhibitions result in a pair of time delays between steeply ascending and descending dynamics, which originate from the positive and negative feedbacks, respectively. This pattern can be identified in many chemical relaxation oscillators and oscillatory models, e.g., the bromate-sulfite pH oscillatory system, the Belousov-Zhabotinsky reaction, the trypsin oscillatory system, and the Boissonade-De Kepper model. This study provides a novel understanding of chemical and biochemical rhythms and suggests an approach to designing such behavior.

Transitions of Collective Motions Driven by Phase Resetting.

The front cover artwork is provided by Prof. Gao's group. The image shows the motion patterns transition of the active gel group under the step light intensity, which describes the mechanism of a new collective emergence structure. Read the full text of the Research Article at 10.1002/cphc.202300054.

Transitions of Collective Motions Driven by Phase Resetting.

Abrupt (i. e. step) environmental changes, such as natural disasters or the intervention of predators, can alter the internal dynamics of groups with active units, leading to the rapid destruction and/or restructuring of the group, with the emergence of new collective structures that endow the system with adaptability. Few studies, to date, have considered the influence of abrupt environmental changes on emergent behavior. Here, we use a model of active matter, the Belousov-Zhabotinsky (BZ) self-oscillating gel, to study the mechanism of formation and transition between modes of collective locomotion caused by changes of illumination intensity in arrays of interacting photosensitive active units. New forms of collective motion can be generated by step changes of illumination intensity. These transformations arise from the phase resetting and wave-signal regeneration induced by the abrupt parameter variation, while gradual change results in different evolution of collective motion. Our results not only suggest a novel mechanism for emergence, but also imply that new collective behaviors could be accessible via discontinuous parameter changes.

Compatible Kinetic Model for Quantitative Description of Dual-Clock Behavior of the Complex Thiourea-Iodate Reaction.

The thiourea-iodate reaction has been investigated simultaneously by ultraviolet-visible spectroscopy and high-performance liquid chromatography (HPLC). Absorbance-time traces measured at the isosbestic point of the iodine-triiodide system have revealed a special dual-clock behavior. During the first kinetic stage of the title reaction, iodine suddenly appears only after a well-defined time lag when thiourea is totally consumed due to the rapid thiourea-iodine system giving rise to a substrate-depletive clock reaction. After this delay, iodine in the system starts to build up suddenly to a certain level, where the system remains for quite a while. During this period, hydrolysis of formamidine disulfide as well as the formamidine disulfide-iodine system along with the Dushman reaction and subsequent reactions of the intermediates governs the parallel formation and disappearance of iodine, resulting in a fairly constant absorbance. The kinetic phase mentioned above is then followed by a more slowly increasing sigmoidally shaped profile that is characteristic of autocatalysis-driven clock reactions. HPLC studies have clearly shown that the thiourea dioxide-iodate system is responsible mainly for the latter characteristics. Of course, depending on the initial concentration ratio of the reactants, the absorbance-time curve may level off or reach a maximum followed by a declining phase. With an excess of thiourea, iodine may completely disappear from the solution as a result of the thiourea dioxide-iodine reaction. In the opposite case, with an excess of iodate, the final absorbance reaches a finite value, and at the same time, iodide ion will disappear completely from the solution due to the well-known Dushman (iodide-iodate) reaction. In addition, we have also shown that in the case of the formamidine disulfide-iodine reaction, unexpectedly the triiodide ion is more reactive toward formamidine disulfide than iodine. This feature can readily be interpreted by the enhancement of the rate of formation of the transition complex containing oppositely charged reactants. A 25-step kinetic model is proposed with just 10 fitted parameters to fit the 68 kinetic traces measured in the thiourea-iodate system and the second, but slower, kinetic phase of the thiourea-iodine reaction. The comprehensive kinetic model is constituted in such a way as to remain coherent in quantitatively describing all of the most important characteristics of the formamidine disulfide-iodine, thiourea dioxide-iodine, and thiourea dioxide-iodate systems.

Multiple iodide autocatalysis paths of chemo-hydrodynamical patterns in the Briggs-Rauscher reaction.

Autocatalytic feedback is often regarded as the core step for the chemo-hydrodynamical patterns in the nonlinear reaction system. The Briggs-Rauscher (BR) reaction shows sequential chemo-hydrodynamical patterns with three states, i.e. labyrinth, high iodine state, and rotating dendritic patterns. The short-lived labyrinth patterns, depending on [Mn2+]0, the ratio of [CH2(COOH)2]0 and [KIO3]0 and light intensities, result from iodide autocatalytic loop, which has three paths (involving Mn2+-induced radical reactions, the oxidation of iodomalonic compounds, and light-induced radical reactions, respectively). The high iodine state appears in a high ratio of [CH2(COOH)2]0 and [KIO3]0, relating to the autocatalytic path involving the oxidation of iodomalonic compounds. The light-induced radical autocatalytic path can act as a convenient control parameter to modulate the patterns in the first stage by increasing the iodine radicals. The dendritic patterns in the third stage result from the Marangoni effect caused by the evaporation of the solutions and reactions between H2O2 and iodine-containing species, which is independent of [CH2(COOH)2]0 and [Mn2+]0. This work contributes to a better understanding of the complex spatiotemporal patterns in the chemo-hydrodynamical system.

Peptide-Modulated pH Rhythms.

Many drugs adjust and/or control the spatiotemporal dynamics of periodic processes such as heartbeat, neuronal signaling and metabolism, often by interacting with proteins or oligopeptides. Here we use a quasi-biocompatible, non-equilibrium pH oscillatory system as a biomimetic biological clock to study the effect of pH-responsive peptides on rhythm dynamics. The added peptides generate feedback that can lengthen or shorten the oscillatory period during which the peptides alternate between random coil and coiled-coil conformations. This modulation of a chemical clock supports the notion that short peptide reagents may have utility as drugs to regulate human body clocks.

In†Situ Corrosion Fabrication of NaNbO3 /Nb3 O7 F Heterojunctions with Optimized Band Realignment for Enhanced Photocatalytic Hydrogen Evolution.

Heterostructured photocatalysis is a significant issue owing to the unique band alignment, improved spectrum absorption, and enhanced photocatalytic activity. However, the construction of uniform, controllable, and effective heterojunctions is still a huge challenge. Herein, NaNbO3 /Nb3 O7 F heterojunctions are fabricated through an in situ corrosion technique for the first time. The influence of phase transformation on the hydrogen evolution reaction (HER) activity is investigated systematically in terms of photocatalytic water splitting for H2 production. Interestingly, the band realignment and good interfacial contact endow the NaNbO3 /Nb3 O7 F heterojunctions with a high HER activity (43.3 mmol g-1 h-1 ), which is about 2.4 times that of pure Nb3 O7 F and 1.36 times that of pure NaNbO3 . The results may provide some new insights into the corrosion technique and HER activity of novel heterostructured catalysts.

Boosted visible-light photocatalytic activity and retarded carrier recombination of Eu3+-doped Nb3O7F nanomaterials prepared by hydrothermal method.

Novel trivalent europium (Eu3+)-doped niobium oxyfluoride (Nb3O7F) nanomaterials with retarded carrier recombination and enhanced photocatalytic activity were successfully synthesized by a facile hydrothermal method. Through changing the doping ratio of Eu3+ ions, the phase, composition, morphology, absorption spectra and photocatalytic properties were investigated in detail. The results showed that Eu3+ ions were successfully incorporated into the interstitial sites of Nb3O7F crystal lattice. With the increase of Eu3+ amounts, the morphology gradually changed from nanowall to irregular nanoparticle. Meanwhile, incorporation of Eu3+ ions had a slight influence on the light absorption. However, Eu3+-doped samples exhibited excellent photodegradation activity towards Rhodamine B dyes. The improvement may be ascribed to higher specific surface area, and lower carrier recombination prohibited by forming Eu3+/Eu2+ self-redox centers. This work envisages that Eu3+-doped Nb3O7F nanomaterials may be a promising kind of photocatalysts.

Modulation Effects of Permanganate and Manganese(II) Ions on the Oscillatory Dynamics in a Bromate-Sulfite Reaction System.

It is important to study nonlinear dynamical systems showing pH and temperature oscillations simultaneously. Here, we systematically investigated the bromate-sulfite reaction in its coupled system. Large-amplitude temperature oscillations could be measured accompanied by the pH oscillations with or without permanganate and manganese(II) ions. The modulation effects on the oscillatory dynamics of the bromate-sulfite reaction system produced by permanganate and manganese(II) ions were investigated in detail. On the one hand, with permanganate, an additional negative pH feedback process between permanganate and bisulfite occurs, leading to weakening the pH positive feedback. The above opposite effects make the period length change unmonotonically when adjusting the permanganate concentration and flow rate. On the other hand, with Mn2+ as the feedback agent, the nonmonotonic change of period was not obvious because it only contained one feedback loop, which can only reinforce negative feedback without affecting positive feedback.

Capillarity-Induced Propagation Reversal of Chemical Waves in a Self-oscillating Gel.

In a self-oscillating gel, unidirectional chemical waves generated by the Belousov-Zhabotinsky reaction can drive locomotion, which results from the difference between the push and pull forces in the wavefront and waveback, respectively. In a narrow tube, such a gel is subject not only to the asymmetric force engendered by the propagation of the chemical waves but also to additional forces originating from the capillary effect in the polymer skeleton. The ends of a self-oscillating gel in a tube are squeezed unequally during unidirectional motion, causing new waves of higher frequency and ultimately giving rise to reversal of the direction of chemical wave propagation. This peculiar phenomenon of a self-oscillating gel in a narrow glass tube results in a nonmonotonic evolution of the gel locomotion velocity.

Autonomous reciprocating migration of an active material.

Periodic to-and-fro migration is a sophisticated mode of locomotion found in many forms of active matter in nature. Providing a general description of periodic migration is challenging, because many details of animal migration remain a mystery. We study periodic migration in a simpler system using a mechanistic model of a photosensitive, active material in which a stimulus-responsive polymer gel is propelled by chemical waves under the regulation of an illumination gradient sensed by the gel, which plays a role analogous to the environment in periodic animal migration. The reciprocating gel migration results from autonomous transitions between retrograde and direct wave locomotion modes arising from the gradient distribution of the illumination intensity. The local dynamics of the chemical waves modulates the asymmetry between push and pull forces to achieve repeated reorientation of the direction of locomotion. Materials that display similar intelligent, self-adaptive locomotion might be tailored for such functions as drug delivery or self-cleaning systems.

Programmed Locomotion of an Active Gel Driven by Spiral Waves.

Active media that host spiral waves can display complex modes of locomotion driven by the dynamics of those waves. We use a model of a photosensitive stimulus-responsive gel that supports the propagation of spiral chemical waves to study locomotive transition and programmed locomotion. The mode transition between circular and toroidal locomotion results from the onset of spiral tip meandering that arises via a secondary Hopf bifurcation as the level of illumination is increased. This dynamic instability of the system introduces a second circular locomotion with a small diameter caused by tip meandering. The original circular locomotion with large diameter is driven by the push-pull asymmetry of the wavefront and waveback of the simple spiral waves initiated at one corner of gel. By harnessing this mode transition of the gel locomotion via coded illumination, we design programmable pathways of nature-inspired angular locomotion of the gel.

Exact Concentration Dependence of the Landolt Time in the Thiourea Dioxide-Bromate Substrate-Depletive Clock Reaction.

The thiourea dioxide (TDO)-bromate reaction has been reinvestigated spectrophotometrically under acidic conditions using phosphoric acid-dihydrogen-phosphate buffer within the pH range of 1.1-1.8 at 1.0 M ionic strength adjusted by sodium perchlorate and at 25 °C. The title system shows a remarkable resemblance to the classical Landolt reaction, namely, the clock species (bromine) may only appear after the substrate TDO is completely consumed. Thus, the title system can be classified as substrate-depletive clock reaction. Despite the well-known slow rearrangement characteristic of TDO in acidic solution, it is surprisingly found that the Landolt time of the title reaction does not depend at all on the age of TDO solution applied. It is, however, shown experimentally that the inverse of Landolt time linearly depends on the initial bromate concentration as well as on the square of the hydrogen ion concentration. In addition to this, it is also noticed that dihydrogen phosphate markedly affects the Landolt time as well, and this feature may easily be taken into consideration by the H2PO4- dependence of the rate of bromate-bromide reaction quantitatively. Based on the experiments, a simple three-step kinetic model is proposed from which a complex formula is derived to indicate the exact concentration dependence of the Landolt time.

Autocatalysis-Driven Clock Reaction III: Clarifying the Kinetics and Mechanism of the Thiourea Dioxide-Iodate Reaction in an Acidic Medium.

The thiourea dioxide-iodate reaction has been reinvestigated spectrophotometrically under acidic conditions using phosphoric acid-dihydrogen phosphate buffer within the pH range of 1.1-1.8 at 1.0 M ionic strength adjusted by sodium perchlorate and at 25 °C. The system was found to exhibit clock behavior, having a well-defined and reproducible time lag called Landolt time, though elementary iodine may even be detected in substrate excess; hence, under these conditions, the reaction can be classified as an autocatalysis-driven clock reaction. It is clearly demonstrated that the previously proposed kinetic model suffers from serious drawbacks from both theoretical and experimental points of view. The reaction may be characterized by either sigmoidal-shaped or rise-and-fall kinetic traces, depending on the initial concentration ratio of the reactants. Iodide significantly accelerates the appearance of the clock species iodine acting therefore as an autocatalyst. The age of stock TDO solution also has a great, so far completely overlooked impact on the Landolt time. On the basis of evaluating simultaneously the kinetic curves, a 16 step kinetic model including 5 well-known rapidly established equilibria is proposed with 7 fitted rate coefficients in which the rate coefficients of both forms of TDO were determined.

Kinetics and Mechanism of the Concurrent Reactions of Hexathionate with S(IV) and Thiosulfate in a Slightly Acidic Medium.

Reactions of hexathionate with thiosulfate and sulfite have been investigated by high-performance liquid chromatography via monitoring the concentration-time series of tetrathionate, pentathionate, hexathionate, and thiosulfate simultaneously within the pH range of 4.0-5.0. In both reactions, elementary sulfur forms; more significant sulfur precipitation may be observed in the case of the hexathionate-thiosulfate reaction, but slight turbidity in the other system means that elementary sulfur also appears in a detectable amount in the hexathionate-sulfite reaction. Initial rate studies have revealed that the formal kinetic orders of both reactants in both systems are clearly unity but pH-dependence can only be observed in the case of the hexathionate-sulfite reaction. The proposed kinetic model appears to suggest that nucleophilic attack of sulfite and thiosulfate may also occur on the ß- or γ-sulfur of the polythionate chain and breakages of the α-ß, ß-γ, and γ-γ' bonds are all conceivable possibilities to drive the reactions. Consequently, the generally accepted sulfur-chain elongating effect of thiosulfate on longer polythionates is also proven to be accompanied by sulfur-chain shortening pathways, eventually leading to the formation of elementary sulfur.

On the Kinetics and Mechanism of the Thiourea Dioxide-Periodate Autocatalysis-Driven Iodine-Clock Reaction.

The thiourea dioxide-periodate reaction has been investigated under acidic conditions using phosphate buffer within the pH range of 1.1-2.0 at 1.0 M ionic strength adjusted by sodium perchlorate. Absorbance-time series are monitored as a function of time at 468 nm, the isosbestic point of the I2-I3- system. The profile of these kinetic runs follows either sigmoidal-shaped or rise-and-fall traces depending on the initial concentration ratio of the reactants. The clock species iodine appears after a well-defined but reproducible time lag even in substrate excess, meaning that the system may be classified as an autocatalysis-driven clock reaction. It is also demonstrated that the age of the thiourea dioxide solution markedly shortens the Landolt time, suggesting that the original form of thiourea dioxide (TDO) rearranges into a more reactive form and reacts faster than the original one. The behavior found is consistent with that recently observed in other oxidation reactions of TDO. To characterize the system quantitatively, a 22-step kinetic model is constructed from adapting the kinetic model of the TDO-iodate reaction published recently by supplementing it with six different reactions of periodate. By the help of seven fitted rate coefficients a sound agreement between the measured and calculated absorbance-time traces is obtained.

Effect of Reaction Parameters on the Wavelength of Pulse Waves in the Belousov-Zhabotinsky Reaction-Diffusion System.

The wavelength of Belousov-Zhabotinsky (BZ) traveling waves is the key factor that limits the scale of BZ self-oscillating gel motors. To achieve control of the wavelength, it is necessary to evaluate the wavelength dependence on species concentrations and temperature. In this work, the effect of reaction parameters on the wavelength of BZ pulse waves was studied. The most effective way to reduce the wavelength of pulse waves is to increase the concentration of organic species and/or the temperature. Decreasing the concentration of bromate, hydrogen ion, or metal catalyst also reduces the wavelength of pulse waves. This work provides a convenient and direct method to produce sub-millimeter BZ waves, which could be applied to designing BZ wave-driven small-scale gel motors as well as providing insight into other emergent behaviors of self-oscillating gels.

Solvent-Controlled Synthesis of Highly Luminescent Carbon Dots with a Wide Color Gamut and Narrowed Emission Peak Widths.

Carbon dots (CDs) have tremendous potential applications in bioimaging, biomedicine, and optoelectronics. By far, it is still difficult to produce photoluminescence (PL) tunable CDs with high quantum yield (QY) across the entire visible spectrum and narrow the emission peak widths of CDs close to those of typical quantum dots. In this work, a series of CDs with tunable emission from 443 to 745 nm, quantum yield within 13-54%, and narrowed full width at half maximum (FWHM) from 108 to 55 nm, are obtained by only adjusting the reaction solvents in a one-pot solvothermal route. The distinct optical features of these CDs are based on their differences in the particle size, and the content of graphitic nitrogen and oxygen-containing functional groups, which can be modulated by controlling the dehydration and carbonization processes during solvothermal reactions. Blue, green, yellow, red, and even pure white light emitting films (Commission Internationale de L'Eclairage (CIE)= 0.33, 0.33, QY = 39%) are prepared by dispersing one or three kinds of CDs into polyvinyl alcohol with appropriate ratios. The near-infrared emissive CDs are excellent fluorescent probes for both in vitro and in vivo bioimaging because of their high QY in water, long-term stability, and low cytotoxicity.

Kinetics of the Two-Stage Oxidation of Sulfide by Chlorine Dioxide.

The sulfide-chlorine dioxide reaction was found to have two distinct kinetic stages at alkaline conditions. The first stage proceeds so rapidly that it can only be measured by a stopped-flow technique at low temperature and leads to the parallel formation of polysulfide and sulfate as sulfur-containing products. At the same time, chlorite, chlorate, and chloride are produced from chlorine dioxide in detectable amounts, suggesting a complex stoichiometry. A nine-step kinetic model including short-lived intermediates like sulfide radical and •HSClO2- is proposed to describe the kinetic data in this rapid stage. In an excess of chlorine dioxide, the first stage is followed by a significantly slower one to be measured by conventional UV-vis spectroscopy at room temperature. Considering that tetrasulfide is formed during the first rapid course of the reaction, the subsequent slow kinetic stage can only be described by the direct oxidation of tetrasulfide by chlorine dioxide and, surprisingly, the tetrasulfide-catalyzed disproportionation of chlorine dioxide.