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aIn real catalyst systems, it is difficult to establish a correlation between catalytic properties and the shape (crystal planes, corners and steps) of the active catalytic particles. In this paper we present a clear shape dependence of the catalytic properties of a Vulcan-supported fuel cell catalyst having 4 nm cubo-octahedral platinum(0) nanocrystallites with (111) and (100) surfaces stabilized by sodium polyacrylate. The electrode materials were characterized by CO-stripping cyclic voltammetry and transmission electron microscopy (TEM), showing that no agglomeration had occurred among the nanoparticles on the catalyst surfaces.

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The title redox couple, in noncoordinating perchlorate medium, has been used to probe the electrochemical behavior of different IrO2-based electrodes; pure oxide electrodes, as well as IrO2-SnO2 mixtures, have been investigated. The obtained results show that the electrode material strongly affects the electrochemical response. A tentative explanation, based on the different point of zero charge of the considered oxides, is presented.

Oxygen-depolarized cathodes consisting of gas-diffusion electrodes (GDEs) for electrolysis in a chlor-alkali cell at 90°C were studied. The electrode design was based on a carbon-free catalyst and comprised of a mixture of micronized silver particles, a small amount of Hg and PTFE binder. The cathodes were investigated by electrochemical measurements, and surface and morphological analyses before and after different operation times in chlor-alkali cells. Electrode stability was investigated by life-time tests. The surface properties of gas diffusion electrodes were studied for both fresh and used cathodes by X-ray photoelectron spectroscopy (XPS). Transmission (TEM) and scanning electron microscopy (SEM-EDX) were used to investigate morphology. The bulk of gas diffusion electrodes was studied by X-ray diffraction (XRD) and thermogravimetric analysis (TG-DSC). At least two main degradation processes that occur on different time-scales were identified and attributed to segregation and loss of the second metal at the interface and a decrease in the hydrophilic properties with time. Furthermore, an increase in the precipitation of compounds from the reaction process also decreased performance by the occlusion of reaction pores.