Dynamic in situ Formation of Cu2O Sub‐Nanoclusters through Photoinduced pseudo‐Fehling's Reaction for Selective and Efficient Nitrate‐to‐Ammonia Photosynthesis

Abstract Copper (Cu) is evidenced to be effective for constructing advanced catalysts. In particular, Cu 2 O is identified to be active for general catalytic reactions. However, conflicting results regarding the true structure‐activity correlations between Cu 2 O‐based active sites and efficiencies are usually reported. The structure of Cu 2 O undergoes dynamic evolution rather than remaining stable under working conditions, in which the actual reaction cannot proceed over the prefabricated Cu 2 O sites. Therefore, the dynamic construction of Cu 2 O active sites can be developed to promote catalytic efficiency and reveal the true structure‐activity correlations. Herein, by introducing the redox pairs of Cu 2+ and reducing sugar into a photocatalysis system, it is clarified that the Cu 2 O sub‐nanoclusters (NCs), working as novel active sites, are on‐site constructed on the substrate via a photoinduced pseudo ‐Fehling's route. The realistic interfacial charge separation and transformation capacities are remarkably promoted by the dynamic Cu 2 O NCs under the actual catalysis condition, which achieves a milestone efficiency for nitrate‐to‐ammonia photosynthesis, including the targets of production rate (1.98±0.04 mol g Cu −1 h −1 ), conversion ratio (94.2±0.91 %), and selectivity (98.6 %±0.55 %). The current work develops an effective strategy for integrating the active site construction into realistic reactions, providing new opportunities for Cu‐based chemistry and catalysis sciences research.