Abstract

Atomically thin 2D carbon nitride sheets (CNs) became one of the most promising solar energy conversion materials. However, the application of CNs is still limited due to two reasons: (i) the bandgap of CNs is wider than its counterpart due to the quantum size effect, which reduces its effective utilization of the entire solar spectrum, and (ii) the visible-light photocatalytic activity of CNs is still low due to its faster recombination of photogenerated carriers than photocatalytic reaction. Here, we achieve a strong visible-light absorption band in CNs through fluorination followed by thermal defluorination in Se vapor (Se-CNs). Experimental results and theoretical calculations confirm that the formation of cyano groups accompanied with in-situ Se doping expands the absorption edge of CNs from 416 to 584 nm. More importantly, a downward electron spin polarization in the CNs structure improves dramatically the efficiency of charge separation and surface catalysis reaction. The hydrogen generation rate of Se-CNs with 3 wt% Pt under visible-light irradiation (> 420 nm) reaches up to 5411.2 μmol h−1 g−1 that is 176.5 times of the hydrogen generation of CNs. Additionally, the visible-light photocatalytic oxygen evolution of Se-CNs acquires tremendous improvements. This work provides a new approach for improving electron structure of atomically thin 2D non-metal semiconductor materials.

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