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Model thiophene-decorated nickel porphyrins are synthesized to examine how sulfur promotes CO₂-to-CO conversion and tandem CO₂-to-C₂ product conversion in electrocatalytic CO₂ reduction. Combined theoretical and experimental analyses show that thiophene substituents generate a ligand hole character that modulates the nickel-centred electronic structure, enhancing overall catalytic performance.

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.

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 proton shuttle plays a critical role in the proton transfer process during lithium-mediated ammonia synthesis. Here, the authors establish the structure-activity relationship and design principles for effective proton shuttles.

Metal borides/borates are promising candidates to become high-performance alkaline oxygen evolution reaction catalysts. This study reports an in-situ phase composition modulation approach to fabricate boride/borate-based catalysts.

Copper is unique among CO₂ electrocatalysts owing to its ability to produce multicarbon products at high rates; however, achieving selectivity for specific products remains challenging. Here, Cu surfaces decorated with alkaline earth metal oxides are found to strongly favour alcohols over hydrocarbons.

Converting CO2 and H2O into value-added chemical feedstocks and fuels offers a carbon neutral approach to tackling global energy and climate concerns. Here the authors report a metal supported single-atom catalytic site enabling the electrocatalytic reduction of CO2 to methane.

Electrochemical conversion of carbon dioxide to methane can store intermittent renewable electricity in a staple of global energy. Here, the authors develop a moderator strategy to maintain the catalyst in a low coordination state, thereby enabling stable and selective electrochemical methanation.

Use of a chain-ether-based solvent instead of tetrahydrofuran for lithium-mediated nitrogen reduction enables long-term continuous ammonia electrosynthesis with high efficiency and improved gas-phase ammonia distribution.

The electrochemical reduction of CO for sustainable fuel production has gained attention, but the reaction mechanism needs further clarification. Here the authors delve into the discussion regarding whether the rate-determining step for the generation of multi-carbon products is the C-C coupling or the hydrogenation of CO, and provide evidence for dimerization of two *CO as the pivotal step in this process.

The production of ammonia via the Haber–Bosch process is carbon-intensive and centralized, but electrochemical methods such as lithium-mediated processes in organic electrolytes could enable decentralized production using renewable energy. Calcium is now shown to mediate nitrogen reduction for ammonia synthesis.

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.

Catalysts for CO electroreduction have focused on Cu, and their main products have been C₂ chemicals. Here authors use the concept of asymmetric active sites to develop a class of doped Cu catalysts for C-C coupling, delivering record selectivity to n-propanol.

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%.