Intermetallic Cobalt Indium Nanoparticles as Oxygen Evolution Reaction Precatalyst: A Non-Leaching p-Block Element.

Merely all transition-metal-based materials reconstruct into similar oxyhydroxides during the electrocatalytic oxygen evolution reaction (OER), severely limiting the options for a tailored OER catalyst design. In such reconstructions, initial constituent p-block elements take a sacrificial role and leach into the electrolyte as oxyanions, thereby losing the ability to tune the catalyst's properties systematically. From a thermodynamic point of view, indium is expected to behave differently and should remain in the solid phase under alkaline OER conditions. However, the structural behavior of transition metal indium phases during the OER remains unexplored. Herein, are synthesized intermetallic cobalt indium (CoIn3 ) nanoparticles and revealed by in situ X-ray absorption spectroscopy and scanning transmission microscopy that they undergo phase segregation to cobalt oxyhydroxide and indium hydroxide. The obtained cobalt oxyhydroxide outperforms a metallic-cobalt-derived one due to more accessible active sites. The observed phase segregation shows that indium behaves distinctively differently from most p-block elements and remains at the electrode surface, where it can form lasting interfaces with the active metal oxo phases.

Challenges for Hybrid Water Electrolysis to Replace the Oxygen Evolution Reaction on an Industrial Scale.

To enable a future society based on sun and wind energy, transforming electricity into chemical energy in the form of fuels is crucial. This transformation can be achieved in an electrolyzer performing water splitting, where at the anode, water is oxidized to oxygen-oxygen evolution reaction (OER)-to produce protons and electrons that can be combined at the cathode to form hydrogen-hydrogen evolution reaction (HER). While hydrogen is a desired fuel, the obtained oxygen has no economic value. A techno-economically more suitable alternative is hybrid water electrolysis, where value-added oxidation reactions of abundant organic feedstocks replace the OER. However, tremendous challenges remain for the industrial-scale application of hybrid water electrolysis. Herein, these challenges, including the higher kinetic overpotentials of organic oxidation reactions compared to the OER, the small feedstock availably and product demand of these processes compared to the HER (and carbon dioxide reduction), additional purifications costs, and electrocatalytic challenges to meet the industrially required activities, selectivities, and especially long-term stabilities are critically discussed. It is anticipated that this perspective helps the academic research community to identify industrially relevant research questions concerning hybrid water electrolysis.

Nanophotonic light trapping in 3-dimensional thin-film silicon architectures.

Emerging low cost and large area periodic texturing methods promote the fabrication of complex absorber structures for thin film silicon solar cells. We present a comprehensive numerical analysis of a 2 µm square periodic polycrystalline silicon absorber architecture designed in our laboratories. Simulations are performed on the basis of a precise finite element reconstruction of the experimentally realized silicon structure. In contrast to many other publications, superstrate light trapping effects are included in our model. Excellent agreement to measured absorptance spectra is obtained. For the inclusion of the absorber into a standard single junction cell layout, we show that light trapping close to the Yablonovitch limit can be realized, but is usually strongly damped by parasitic absorption.