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Electrocatalytic CO2 reduction reaction (CO2RR) conducted in a flow‐based device exhibits a substantial enhancement in Faradaic efficiency and catalytic current density compared to a conventional H‐type configuration. This highlights the distinct catalytic environment and behavior inherent in flow cells as opposed to H cells. To investigate the authentic properties of a catalyst within a flow‐based device, customized flow cells have been specifically devised for operando techniques during CO2RR and CORR, rather than resorting to an in‐situ three‐electrode H‐type configuration with its disparate catalytic environment and performance. This approach ensures a catalytic environment identical to that employed in electrochemical measurements. This review delineates the disparities between H‐type and flow‐based cells as well as the operando techniques tailored for flow‐based devices, including X‐ray absorption spectroscopy and Raman spectroscopy, preserving a consistent catalytic environment. It also compiles recent findings on copper‐based systems using operando flow‐based devices. The operando insights reveal a significant augmentation in catalytic current density, impacting both chemical properties and crystal structures. Furthermore, the observation of various catalytic intermediates enriches our comprehension. In essence, the application of operando techniques to flow‐based devices furnishes a comprehensive understanding of the catalytic behavior exhibited by diverse systems, propelling progress toward achieving Net Zero emissions. [ABSTRACT FROM AUTHOR]

Developing ruthenium‐based heterogeneous catalysts with an efficient and stable interface is essential for enhanced acidic oxygen evolution reaction (OER). Herein, we report a defect‐rich ultrathin boron nitride nanosheet support with relatively independent electron donor and acceptor sites, which serves as an electron reservoir and receiving station for RuO2, realizing the rapid supply and reception of electrons. Through precisely controlling the reaction interface, a low OER overpotential of only 180 mV (at 10 mA cm−2) and long‐term operational stability (350 h) are achieved, suggesting potential practical applications. In situ characterization and theoretical calculations have validated the existence of a localized electronic recycling between RuO2 and ultrathin BN nanosheets (BNNS). The electron‐rich Ru sites accelerate the adsorption of water molecules and the dissociation of intermediates, while the interconnection between the O‐terminal and B‐terminal edge establishes electronic back‐donation, effectively suppressing the over‐oxidation of lattice oxygen. This study provides a new perspective for constructing a stable and highly active catalytic interface. [ABSTRACT FROM AUTHOR]

Semihydrogenation is a crucial industrial process. Noble metals such as Pd have been extensively studied in semihydrogenation reactions, owing to their unique catalytic activity toward hydrogen activation. However, the overhydrogenation of alkenes to alkanes often happens due to the rather strong adsorption of alkenes on Pd active phases. Herein, we demonstrate that the incorporation of Pd active phases as single-atom sites in perovskite lattices such as SrTiO3 can greatly alternate the electronic structure and coordination environment of Pd active phases to facilitate the desorption of alkenes rather than further hydrogenation. Furthermore, the incorporated Pd sites can be well stabilized without sintering by a strong host-guest interaction with SrTiO3 during the activation of H species in hydrogenation reactions. As a result, the Pd incorporated SrTiO3 (Pd-SrTiO3) exhibits an excellent time-independent selectivity (> 99.9 %) and robust durability for the photocatalytic semihydrogenation of phenylacetylene to styrene. This strategy based on incorporation of active phases in perovskite lattices will have broad implications in the development of high-performance photocatalysts for selective hydrogenation reactions., (© 2024 Wiley‐VCH GmbH.)

Developing ruthenium-based heterogeneous catalysts with an efficient and stable interface is essential for enhanced acidic oxygen evolution reaction (OER). Herein, we report a defect-rich ultrathin boron nitride nanosheet support with relatively independent electron donor and acceptor sites, which serves as an electron reservoir and receiving station for RuO 2 , realizing the rapid supply and reception of electrons. Through precisely controlling the reaction interface, a low OER overpotential of only 180 mV (at 10 mA cm -2 ) and long-term operational stability (350 h) are achieved, suggesting potential practical applications. In situ characterization and theoretical calculations have validated the existence of a localized electronic recycling between RuO 2 and ultrathin BN nanosheets (BNNS). The electron-rich Ru sites accelerate the adsorption of water molecules and the dissociation of intermediates, while the interconnection between the O-terminal and B-terminal edge establishes electronic back-donation, effectively suppressing the over-oxidation of lattice oxygen. This study provides a new perspective for constructing a stable and highly active catalytic interface., (© 2024 Wiley‐VCH GmbH.)