Balanced work function as a driver for facile hydrogen evolution reaction - comprehension and experimental assessment of interfacial catalytic descriptor.

A major step in the development of (electro)catalysis would be the possibility to estimate accurately the energetics of adsorption processes related to reaction intermediates. Computational chemistry (e.g.

Regenerative nano-hybrid coating tailored for autonomous corrosion protection.

A novel bilayer coating system for autonomous corrosion-triggered self-healing is demonstrated. The storage of the encapsulated monomer and the catalyst is separated in two different layers. The encapsulated catalyst is stored inside a metallic coating, which ensures its activity even for an extended exposure time.

Redox-responsive self-healing for corrosion protection.

Raspberry-shaped redox-responsive capsules for storing corrosion inhibitors are introduced, targeted to solve the drawbacks of conducting-polymer-based coating systems for corrosion protection. These capsules synthesized via the miniemulsion technique have a remarkable release property upon reduction (onset of corrosion) and cease release upon reoxidation (passivation of the defect). The self-healing capability is demonstrated by application of these capsules as part of a composite coating on zinc.

Redox responsive release of hydrophobic self-healing agents from polyaniline capsules.

Redox-responsive nanocapsules consisting of conductive polyaniline and polypyrrole shells were successfully synthesized by using the interface of miniemulsion droplets as a template for oxidative polymerizations. The redox properties of the capsules were investigated by optical spectroscopies, electron microscopy, and cyclic voltammetry. Self-healing (SH) chemicals such as diglycidyl ether or dicarboxylic acid terminated polydimethylsiloxane (PDMS-DE or PDMS-DC) were encapsulated into the nanocapsules during the miniemulsion process and their redox-responsive release was monitored by (1)H NMR spectroscopy.

Existence of a lower critical radius for incorporation of silica particles into zinc during electro-codeposition.

Recently, it was shown that the surface modification of silica particles with -SH functional groups enables their electro-codeposition with zinc. Here, however, we report that no incorporation into Zn can be observed for such modified particles with diameters of <100 nm, while incorporation is possible for particles with diameters of 225 nm and larger. Furthermore, when silica particles are functionalized with mixtures of -SH and -Cl functional groups, which affect the interface energy at the particle/metal interface differently but have similar interfacial energies for the particle/electrolyte interface, it is found that, for successful incorporation of the particles, a minimum amount of -SH functional groups is needed.