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Cobalt-based subsurface dopants induce a shift in the rate-determining step of electrochemical CO₂ reduction on copper to the chemical step: OCCO* + H* → OCCHO* + *. Electrochemical production of ethylene over the optimized catalyst is achieved at low voltage and high current in a membrane electrode assembly system.

The electro-oxidative synthesis of valued chemicals offers to enhance the overall efficiency and economic viability of renewable electrosynthesis systems. Here, the authors use dopant-tuned catalysts to promote the electrosynthesis of dimethyl carbonate from CO and methanol via oxidative carbonylation.

Large potentials required for C(sp³)-H bond activation and low water solubility make electrochemical functionalization of alkanes challenging. Here, the authors report that Pt/IrO_x enables selective generation of Cl free radicals for chlorination of cyclohexane at industrially relevant rates.

Copper-based catalysts, especially the so-called oxide-derived copper, are capable of producing multicarbon species from electrochemical CO₂ reduction. However, little is known about their active sites despite intensive research efforts. Now, Lum and Ager show that oxide-derived copper catalysts have three distinct product-specific sites for the formation of C₂₊ chemicals, unlike polycrystalline copper or (111)- and (100)-oriented copper films which show no evidence of product specific sites.

Electroreduction uses renewable energy to upgrade carbon dioxide to value-added chemicals and fuels. Here, the authors design a suite of ligand-stabilized metal oxide clusters to modulate the reduction pathways on a copper catalyst, enabling record activity for CO₂-to-methane conversion.

CO₂ electroreduction to higher-value carbons can occur through adsorbed hydrogen or through proton-coupled electron transfer from water. Understanding the impact of each route on product selectivity is challenging. Now H/D isotopic labelling reveals the contribution of each mechanism towards product formation and shows that adsorbed hydrogen dominates the reaction.

Ethylene glycol is a commodity chemical with an annual consumption of 20 million tonnes. Its production generates 1.6 tonnes of CO₂ per tonne of ethylene glycol. To reduce these CO₂ emissions, the authors report a one-step electrochemical route to selectively convert ethylene to ethylene glycol at ambient temperature and pressure in aqueous media.

The controlled functionalization of multihydrosilanes is challenging. Now, using a hydrogen-atom-transfer photocatalyst based on neutral eosin Y, a method for the diverse functionalization of hydrosilanes has been developed, enabling the stepwise on-demand decoration of silicon atoms. This approach is distinguished by its atom-, step-, redox- and catalyst-economy, metal-free nature, its versatility (>150 examples), modularity, selectivity and scalability.

Direct electroreduction of dilute CO₂ in flue gas streams is challenging due to the presence of O₂ impurities. Here the authors demonstrate that an acidic electrolyte can overcome this challenge, enabling the generation of multicarbon products from simulated flue gas at reasonable rates.

Modulating interfacial electric fields provides a means to control electrocatalyst activity for a broad range of reactions. Here the authors show that this can be achieved by tuning the nanocurvature of carbon supported single-atom catalysts.

Electrochemical conversion of CO₂ into liquid fuels, powered by renewable electricity, offers one means to address the need for the storage of intermittent renewable energy. Now, Sargent and co-workers present a cooperative catalyst design of molecule–metal interfaces to improve the electrosynthesis of ethanol from CO₂ by producing a reaction-intermediate-rich local environment.

A better understanding of the mechanism of electrochemical CO₂ reduction should enable development of electrocatalysts that are more active and selective. Now, through an isotopic labelling strategy, it has been discovered that there are at least two types of active sites on Cu electrocatalysts, one responsible for converting CO₂ to CO and another for further converting CO to useful C₂₊ products.

Producing ethanol from carbon dioxide, water, and renewable electricity offers a route to sustainable energy. Here, the authors enhance electrocatalytic activity for carbon dioxide reduction by tuning adsorbed hydrogen in a class of copper catalysts with oxide- and hydroxide-modified surfaces.

The electrocatalytic upgrading of CO to higher-value fuels provides a promising route to multi-carbon alcohol products. Here, the authors show that high alcohol selectivity and activity can be achieved by incorporating palladium in copper.

The electroreduction of CO₂ to ethanol could enable the clean production of fuels using renewable power. This study shows how confinement effects from nitrogen-doped carbon layers on copper catalysts enable selective ethanol production from CO₂ with a Faradaic efficiency of up to 52%.

Electrocatalytic reduction of CO₂ to multicarbon products is useful for producing high-value chemicals and fuels. Here the authors present a strategy that is based on the in situ electrodeposition of copper under CO₂ reduction conditions that preferentially expose and maintain Cu(100) facets, which favour the formation of C₂₊ products.

Machine learning is poised to accelerate the development of technologies for a renewable energy future. This Perspective highlights recent advances and in particular proposes Acc(X)eleration Performance Indicators (XPIs) to measure the effectiveness of platforms developed for accelerated energy materials discovery.