A photocatalytic redox cycle over a polyimide catalyst drives efficient solar-to-H<sub>2</sub>O<sub>2</sub> conversion.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 38909037.
- Also identified by DOI 10.1038/s41467-024-49663-6 and PMC identifier 11535368.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
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>.