A photocatalytic redox cycle over a polyimide catalyst drives efficient solar-to-H<sub>2</sub>O<sub>2</sub> conversion.

Chi, Wenwen; Dong, Yuming; Liu, Bing; Pan, Chengsi; Zhang, Jiawei; Zhao, Hui; Zhu, Yongfa; Liu, Zeyu · Nat Commun · 2024

basic_science · Level V

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Abstract

Circumventing the conventional two-electron oxygen reduction pathway remains a great problem in enhancing the efficiency of H<sub>2</sub>O<sub>2</sub> 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<sub>2</sub>O<sub>2</sub> production. Under photoexcitation, carbonyl groups on the photocatalyst surface are reduced, forming an anion radical intermediate. The produced intermediate is oxidized by O<sub>2</sub> to produce H<sub>2</sub>O<sub>2</sub> 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<sub>2</sub> reduction reaction for H<sub>2</sub>O<sub>2</sub> 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<sup>2</sup> self-supported polyimide aerogel exposed to natural sunlight for 6 h yields significant H<sub>2</sub>O<sub>2</sub> production of 34.3 mmol m<sup>-2</sup>.