Z-scheme junction Bi2O2(NO3)(OH)/g-C3N4 for promoting CO2 photoreduction

Photocatalytic CO2 reduction is believed to be an emerging strategy to address fossil fuels consumption and global warming problems. However, the rapid recombination of photogenerated carriers restricts the application of photocatalytic technology severely. Constructing heterojunction structure is one of the most effective pathways to facilitate the charge separation and photocatalytic performance. In this work, a series of direct Z-scheme heterojunction Bi2O2(NO3)(OH)/g-C3N4 (BON/CN) was developed by an electrostatic self-assembly method. The optimal BON/CN-2 photocatalyst exhibits a conspicuous photocatalytic CO2 reduction activity with a high CO evolution rate of 14.84 mu mol g-1h-1 under the stimulated solar light irradiation, which is about 15 and 3.5 times higher than that of pure BON and g-C3N4, respectively. The significantly promoted photocatalytic performance is attributed to the tightly-contact interface and formation of Z-scheme between BON and g-C3N4, which favor for the separation and transfer of photogenerated electrons and holes, as confirmed by high resolution transmission electron microscope (HRTEM), electron spin resonance (ESR), photoelectrochemical measurement and photoluminescence (PL) results. This work may provide a new reference for developing rational tactics to fabricate efficient Z-scheme heterojunction photocatalysts for CO2 conversion.

Automated summary

Constructing a direct Z-scheme heterojunction Bi2O2(NO3)(OH)/g-C3N4 significantly enhances the separation and transfer of photogenerated carriers, resulting in improved photocatalytic CO2 reduction performance.