Light-Induced Hypoxia in Carbon Quantum Dots and Ultrahigh Photocatalytic Efficiency

Carbon quantum dots (CQDs) represent a class of carbon materials exhibiting photoresponse and many potential applications. Here, we present a unique property that dissolved CQDs capture large amounts of molecular oxygen from the air, the quantity of which can be controlled by light irradiation. The O-2 content can be varied between a remarkable 1 wt % of the CQDs in the dark to nearly half of it under illumination, in a reversible manner. Moreover, O-2 depletion enhances away from the air-solution interface as the nearby CQDs quickly regain them from the air, creating a pronounced concentration gradient in the solution. We elucidate the role of the CQD functional groups and show that excitons generated under light are responsible for their tunable adsorbed-oxygen content. Because of O-2 enrichment, the photocatalytic efficiency of the CQDs toward oxidation of benzylamines in the air is the same as under oxygen flow and far higher than the existing photocatalysts. The findings should encourage the development of a new class of oxygen-enricher materials and air as a sustainable oxidant in chemical transformations.

Automated summary

This article presents a unique property of carbon quantum dots (CQDs) that they can capture large amounts of molecular oxygen from the air and the quantity can be controlled by light irradiation. Research shows that the adsorption of oxygen by CQDs is tunable, and the oxygen enrichment enhances the photocatalytic efficiency of CQDs towards oxidation of benzylamines in the air compared to existing photocatalysts.