Abstract. Synthesis of different size of nano-and microparticles is important in designing nanostructured materials with various properties. Wet synthesis methods lack flexibility to create various sizes of particles (particle libraries) using fixed conditions without the repetition of the steps of the method with a new set of parameters. Here, we report a synthesis method based on nucleation and particle growth in the wake of a moving chemical front in a gel matrix. The process yields well-separated regions (bands) filled with nearly mono-disperse nano-and microparticles, with the size of particles varying from band to band in a predictable way. The origin of the effect is due to an interplay of a precipitation reaction of the reagents and their diffusion that are controlled in space and time by the moving chemical front. The method represents a new approach and a promising tool for fast and competitive synthesis of various sizes of colloidal particles.

Solar hydrogen generation by water splitting in photoelectrochemical cells (PEC) is an appealing technology for a future hydrogen economy. Hematite is a prospective photoanode material in this respect because of its visible light conjugated band gap, its corrosion stability, its environmentally benign nature and its low cost. Its bulk and surface electronic structure has been under scrutiny for many decades and is considered critical for improvement of efficiency. In the present study, hematite films of nominally 500 nm thickness were obtained by dip-coating on fluorine doped tin oxide (FTO) glass slides and then anodised in 1 molar KOH at 500, 600, and 700 mV for 1, 10, 120 and 1440 minutes under dark conditions. X-ray photoelectron spectra recorded at the Fe 3p resonant absorption threshold show that the e(g) transition before the Fermi energy, which is well developed in the pristine hematite film, becomes depleted upon anodisation. The spectral weight of the e(g) peak decreases with the square-root of the anodisation time, pointing to a diffusion controlled process. The speed of this process increases with the anodisation potential, pointing to Arrhenius behaviour. Concomitantly, the weakly developed t(2g) peak intensity becomes enhanced in the same manner. This suggests that the surface of the photoanode contains Fe(2+) species which become oxidized toward Fe(3+) during anodisation. The kinetic behaviour derived from the experimental data suggests that the anodisation forms an electron hole doped film on and below the hematite surface.

Experiments are performed in which a large number (approximately 10(4)) of relaxation oscillators are globally coupled through the concentration of chemicals in the surrounding solution. Each oscillator consists of a microscopic catalyst-loaded particle that displays oscillations in the concentrations of chemical species when suspended in catalyst-free Belousov-Zhabotinsky (BZ) reaction solution. In the absence of stirring, the uncoupled particles display a range of oscillatory frequencies. In the well-stirred system, oscillations appear in the surrounding solution for greater than a critical number density of particles (n(crit)). There is a growth in the amplitude of oscillations with increasing n, accompanied by a slight increase or no change in frequency. A model is proposed to account for the behavior, in which the transfer of activator and inhibitor to and from the bulk medium is considered for each particle. We demonstrate that the appearance and subsequent growth in the amplitude of oscillations may be associated with partial synchronization of the oscillators.

We experimentally investigate the transition to synchronization in a population of photochemical oscillators with weak global coupling. Above a critical coupling strength the oscillators join a one-phase group or two-phase clusters. The number of oscillators in each cluster depends on the initial phase distribution, and irregular switching of oscillators between clusters is observed. The fully synchronized state emerges above a second critical coupling strength. In agreement with earlier theory, the experiments demonstrate the importance of population heterogeneity in cluster multistability.

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A SEM picture of the microspheroids (tilted), scheme depicting the vesicle templated sol–gel process and squared normalized electric field intensity distribution inside the microspheroid calculated by finite-difference time-domain simulation.

We propose that the behavior of nonlinear media can be controlled dynamically through coevolutionary systems. In this study, a light-sensitive subexcitable Belousov–Zhabotinsky reaction is controlled using a heterogeneous cellular automaton. A checkerboard image comprising of varying light intensity cells is projected onto the surface of a catalyst-loaded gel resulting in rich spatiotemporal chemical wave behavior. The coevolved cellular automaton is shown to be able to either increase or decrease chemical activity through dynamic control of the light intensity within each cell in both simulated and real chemical systems. The approach is then extended to construct a number of simple logical functions.