Water-Gas Shift over Pt Nanoparticles Dispersed on CeO and Gadolinium-Doped Ceria (GDC) Supports with Specific Nano-Configurations.

The water-gas shift (WGS) reaction is one of the most significant reactions in hydrogen technology since it can be used directly to produce hydrogen from the reaction of CO and water; it is also a side reaction taking place in the hydrocarbon reforming processes, determining their selectivity towards H production. The development of highly active WGS catalysts, especially at temperatures below ~450 °C, where the reaction is thermodynamically favored but kinetically limited, remains a challenge. From a fundamental point of view, the reaction mechanism is still unclear.

Effect of Calcination Temperature on the Activity of Unsupported IrO Electrocatalysts for the Oxygen Evolution Reaction in Polymer Electrolyte Membrane Water Electrolyzers.

Polymer electrolyte membrane (PEM) water electrolyzers suffer mainly from slow kinetics regarding the oxygen evolution reaction (OER). Noble metal oxides, like IrO and RuO, are generally more active for OER than metal electrodes, exhibiting low anodic overpotentials and high catalytic activity. However, issues like electrocatalyst stability under continuous operation and cost minimization through a reduction in the catalyst loading are of great importance to the research community.

Effect of Steam to Carbon Dioxide Ratio on the Performance of a Solid Oxide Cell for HO/CO Co-Electrolysis.

The mixture of H and CO, the so-called syngas, is the value-added product of HO and CO co-electrolysis and the feedstock for the production of value-added chemicals (mainly through Fischer-Tropsch). The H/CO ratio determines the process in which syngas will be utilized and the type of chemicals it will produce. In the present work, we investigate the effect of HO/CO (steam/carbon dioxide, S/C) ratio of 0.

Insights into the Surface Reactivity of Cermet and Perovskite Electrodes in Oxidizing, Reducing, and Humid Environments.

Understanding the surface chemistry of electrode materials under gas environments is important in order to control their performance during electrochemical and catalytic applications. This work compares the surface reactivity of Ni/YSZ and LaSrCrFeO, which are commonly used types of electrodes in solid oxide electrochemical devices. In situ synchrotron-based near-ambient pressure photoemission and absorption spectroscopy experiments, assisted by theoretical spectral simulations and combined with microscopy and electrochemical measurements, are used to monitor the effect of the gas atmosphere on the chemical state, the morphology, and the electrical conductivity of the electrodes.

Ternary Pt-Ru-Ni catalytic layers for methanol electrooxidation prepared by electrodeposition and galvanic replacement.

Ternary Pt-Ru-Ni deposits on glassy carbon substrates, Pt-Ru(Ni)/GC, have been formed by initial electrodeposition of Ni layers onto glassy carbon electrodes, followed by their partial exchange for Pt and Ru, upon their immersion into equimolar solutions containing complex ions of the precious metals. The overall morphology and composition of the deposits has been studied by SEM microscopy and EDS spectroscopy. Continuous but nodular films have been confirmed, with a Pt ÷ Ru ÷ Ni % bulk atomic composition ratio of 37 ÷ 12 ÷ 51 (and for binary Pt-Ni control systems of 47 ÷ 53).