Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain
the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in
Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles
and JavaScript.
Conventional gas diffusion electrodes improve transport of gaseous species, but they suffer from electrolyte penetration and flooding when used with non-aqueous solvents. Here, Manthiram and co-workers report a gas diffusion electrode architecture that is compatible with non-aqueous solvents to utilise sparingly soluble gases in electrochemical reactions. These electrodes are used to simultaneously reduce nitrogen and oxidise water-splitting-derived hydrogen to produce ammonia at ambient conditions.
A rapid and efficient electrochemical reaction requires active catalytic material, as well as proper electrode and cell design. Now, a gas diffusion electrode based on a stainless steel cloth successfully overcomes gas transport limitations for high-current ammonia electrosynthesis in non-aqueous solvents at ambient conditions.
Nonlinear effects in catalysis have been shown to allow for asymmetric amplification. Here the authors report a particularly intriguing case whereby a catalytic asymmetric reaction gives a significantly higher product e.e. when run with a non-enantiopure catalyst compared to the enantiopure version.
There has been a long-standing debate on whether heterogeneously catalysed Suzuki cross-couplings can occur homogeneously due to metal leaching. Here the authors show that while the palladium from the nanoparticle catalyst is mobile during the reaction, the active sites remain heterogeneous in nature.
Oxidative carbonylation using CO/O2 is an attractive strategy to construct carbonyl compounds, but the explosive limit of the gas mixture hampers its application. Now, this safety issue is overcome in the aminocarbonylation of alkynes by replacing the external oxidant O2 by electrochemistry facilitating a mild and safe reaction.
Reducible metal oxides selectively catalyse the hydrodeoxygenation of C–O bonds in bio-based aromatic molecules, although they show limited performance. Now, using TiO2 as an example, a method is reported to enhance the activity of the oxide by surface doping with an ultralow loading of Pt.
Efficient hydrogen oxidation catalysts must maintain an oxide-free metal surface in a relatively high potential range. Now, a catalyst consisting of Ru clusters partially confined in the lattice of urchin-like TiO2 crystals is shown to catalyse the reaction up to a potential of 0.9 VRHE with high mass activity and CO tolerance under both acidic and basic conditions.
Non-polar gaseous reactants such as N2 and H2 exhibit low solubility and slow transport in non-aqueous solvents and conventional gas diffusion electrodes cannot avoid non-aqueous electrolyte penetration. Here, transport limitations and catalyst flooding in tetrahydrofuran are overcome by using a stainless steel cloth-based support for lithium-mediated ammonia synthesis paired with H2 oxidation.