Air-Promoted Light-Driven Hydrogen Production from Bioethanol over Core/Shell Cr 2 O 3 @GaN Nanoarchitecture.
Zhouzhou WangYiqing ChenBowen ShengJinglin LiLin YaoYing YuJun SongTianqi YuYixin LiHu PanPing WangXinqiang WangLei ZhuBaowen ZhouPublished in: Angewandte Chemie (International ed. in English) (2024)
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 Cr 2 O 3 @GaN nanoarchitecture. The correlative computational and experimental investigations show ethanol is energetically favorable to be adsorbed on the Cr 2 O 3 @GaN interface, followed by dehydrogenation toward acetaldehyde and protons by photoexcited holes. The released protons are then consumed for H 2 evolution by photogenerated electrons. Afterward, O 2 can be evolved into active oxygen species and promote the deprotonation and C-C cleavage of the key C 2 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 H 2 per gram Cr 2 O 3 @GaN per hour by only feeding ethanol, air, and light, leading to the achievement of a turnover number of 266,943,000 mole H 2 per mole Cr 2 O 3 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.