Taking carbon out of the ammonial recipe: The reaction used to make ammonia for synthetic fertilizer requires hydrogen. Nowadays, that hydrogen is stripped from methane, creating CO ₂ as a by-product. Licht et al. demonstrate a relatively efficient electrochemical process in which water and nitrogen react directly to form ammonia. The approach removes the need for an independent hydrogen generation step. The process takes place in molten hydroxide salt and requires a nanostructured iron oxide–derived catalyst. Although the catalyst suspension is currently only stable for a few hours, the protocol points to a way to produce ammonia from purely renewable resources. Science , this issue p. 637

Carbon nanofibers, CNFs, due to their superior strength, conductivity, flexibility, and durability have great potential as a material resource but still have limited use due to the cost intensive complexities of their synthesis. Herein, we report the high-yield and scalable electrolytic conversion of atmospheric CO₂ dissolved in molten carbonates into CNFs. It is demonstrated that the conversion of CO₂ → C_CNF + O₂ can be driven by efficient solar, as well as conventional, energy at inexpensive steel or nickel electrodes. The structure is tuned by controlling the electrolysis conditions, such as the addition of trace transition metals to act as CNF nucleation sites, the addition of zinc as an initiator and the control of current density. A less expensive source of CNFs will facilitate its adoption as a societal resource, and using carbon dioxide as a reactant to generate a value added product such as CNFs provides impetus to consume this greenhouse gas to mitigate climate change.

The electrocatalytic hydrogen evolution reaction (HER) is one of the most studied and promising processes for hydrogen fuel generation. Single-atom catalysts have been shown to exhibit ultra-high HER catalytic activity, but the harsh preparation conditions and the low single-atom loading hinder their practical applications. Furthermore, promoting hydrogen evolution reaction kinetics, especially in alkaline electrolytes, remains as an important challenge. Herein, Pt/C₆₀ catalysts with high-loading, high-dispersion single-atomic platinum anchored on C₆₀ are achieved through a room-temperature synthetic strategy. Pt/C₆₀-2 exhibits high HER catalytic performance with a low overpotential (η₁₀) of 25 mV at 10 mA cm⁻². Density functional theory calculations reveal that the Pt-C₆₀ polymeric structures in Pt/C₆₀-2 favors water adsorption, and the shell-like charge redistribution around the Pt-bonding region induced by the curved surfaces of two adjacent C₆₀ facilitates the desorption of hydrogen, thus favoring fast reaction kinetics for hydrogen evolution.