A photocatalytic redox cycle over a polyimide catalyst drives efficient solar-to-H 2 O 2 conversion.
Wenwen ChiYuming DongBing LiuChengsi PanJiawei ZhangHui ZhaoYongfa ZhuZeyu LiuPublished in: Nature communications (2024)
Circumventing the conventional two-electron oxygen reduction pathway remains a great problem in enhancing the efficiency of H 2 O 2 photosynthesis. A promising approach to achieve outstanding photocatalytic activity involves the utilization of redox intermediates. Here, we engineer a polyimide aerogel photocatalyst with photoreductive carbonyl groups for non-sacrificial H 2 O 2 production. Under photoexcitation, carbonyl groups on the photocatalyst surface are reduced, forming an anion radical intermediate. The produced intermediate is oxidized by O 2 to produce H 2 O 2 and subsequently restores the carbonyl group. The high catalytic efficiency is ascribed to a photocatalytic redox cycle mediated by the radical anion, which not only promotes oxygen adsorption but also lowers the energy barrier of O 2 reduction reaction for H 2 O 2 generation. An apparent quantum yield of 14.28% at 420 ± 10 nm with a solar-to-chemical conversion efficiency of 0.92% is achieved. Moreover, we demonstrate that a mere 0.5 m 2 self-supported polyimide aerogel exposed to natural sunlight for 6 h yields significant H 2 O 2 production of 34.3 mmol m -2 .