Air‐Promoted Light‐Driven Hydrogen Production from Bioethanol over Core/Shell Cr2O3@GaN Nanoarchitecture

Air is explored as a promoter rather than quencher for light-driven hydrogen production from bioethanol over a core/shell Cr₂O₃@GaN nanoarchitecture, showing an impressive H₂ evolution rate by only feeding ethanol, air, and light without notable degradation over 180 hours operation. Value-added aldehyde compounds are simultaneously generated.

Abstract

Light-driven hydrogen production from biomass derivatives offers a path towards carbon neutrality. It is often however operated with the limitations of sluggish kinetics and severe coking. Herein, a disruptive air-promoted strategy is explored for efficient and durable light-driven hydrogen production from ethanol over a core/shell Cr₂O₃@GaN nanoarchitecture. The correlative computational and experimental investigations show ethanol is energetically favorable to be adsorbed on the Cr₂O₃@GaN interface, followed by dehydrogenation toward acetaldehyde and protons by photoexcited holes. The released protons are then consumed for H₂ evolution by photogenerated electrons. Afterward, O₂ can be evolved into active oxygen species and promote the deprotonation and C−C cleavage of the key C₂ intermediate, thus significantly lowering the reaction energy barrier of hydrogen evolution and removing the carbon residual with inhibited overoxidation. Consequently, hydrogen is produced at a high rate of 76.9 mole H₂ per gram Cr₂O₃@GaN per hour by only feeding ethanol, air, and light, leading to the achievement of a turnover number of 266,943,000 mole H₂ per mole Cr₂O₃ over a long-term operation of 180 hours. Notably, an unprecedented light-to-hydrogen efficiency of 17.6 % is achieved under concentrated light illumination. The simultaneous generation of aldehyde from ethanol dehydrogenation enables the process more economically promising.

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