A series of microstructured, supported platinum (Pt) catalyst films (supported on single-crystal yttria-stabilized zirconia) and an appropriate Pt catalyst reference system (supported on single-crystal alumina) were fabricated using pulsed laser deposition and ion-beam etching. The thin films exhibit area-specific lengths of the three-phase boundary (length of three-phase boundary between the Pt, support, and gas phase divided by the superficial area of the sample) that vary over 4 orders of magnitude from 4.5 × 102 to 4.9 × 106 m m–2, equivalent to structural length scales of 0.2 μm to approximately 9000 μm. The catalyst films have been characterized using X-ray diffraction, atomic force microscopy, high-resolution scanning electron microscopy, and catalytic activity tests employing the carbon monoxide oxidation reaction. When Pt is supported on yttria-stabilized zirconia, the reaction rate clearly depends upon the area-specific length of the three-phase boundary, l(tpb). A similar relationship is not observed when Pt is supported on alumina. We suggest that the presence of the three-phase boundary provides an extra channel of oxygen supply to the Pt through diffusion in or on the yttria-stabilized zirconia support coupled with surface diffusion across the Pt.
To better understand the electrode kinetics of oxygen reduction and oxidation of gadolinia doped ceria (GDC), the electrochemical properties of platinum electrodes on GDC single crystals and polycrystalline samples were investigated with geometrically well-defined microelectrodes. For comparison measurements were also performed on polycrystalline samples using platinum interdigital electrodes in order to access the effect of the electrode geometry on the electrochemical properties. The transport properties were characterised using impedance spectroscopy, allowing to separate the transport processes of the electrode and the electrolyte. Evaluation of the temperature dependence shows activation energies of 0.77 eV for bulk transport and 1.03 eV for the electrode exchange. Oxygen partial pressure dependent measurements in a reducing atmosphere reveal a strong increase in activation energy due to electronic defect formation. A distinct chemical capacitance is observed in the electrode impedance for all sample types independent of the electrode geometry. While this chemical capacitance is only visible in the electrolyte contribution for the samples measured with interdigital electrodes, for the samples investigated with microelectrodes no chemical capacitance is observed in the electrolyte contribution of the impedance. As the chemical capacitance is related to stoichiometry changes in the electrolyte materials, the results confirm the non-uniform potential distribution occurring at a microelectrode, which results in a vanishing lateral potential gradient and therefore in a negligible stoichiometry gradient inside the electrolyte at a distance from the microelectrode.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.