Abstract
Graphene-like porous g-C3N4 nanosheets were synthesized via direct pyrolysis of thiourea followed by a thermal exfoliation. With increased exfoliation temperature, the color of the resulting samples gradually became shallow, and the thickness and size of the layers were decreased. A formation mechanism involving layer-by-layer exfoliation coupled with layer splitting was proposed. The band structure of the g-C3N4 nanosheets was continuously tuned because of quantum size effect. Time-resolved decay spectra indicated that the radiative lifetime of charge carriers (τ1 and τ2) increased from 4.13 and 26.23ns for bulk g-C3N4 to 5.36 and 36.57ns for graphene-like g-C3N4 nanosheets. The g-C3N4 nanosheet samples were applied for visible light photocatalytic removal of NOx in air. The performance of porous g-C3N4 nanosheets was significantly enhanced with increased exfoliation temperature from 450 to 550°C. Moreover, photochemical and structural stability was well maintained after multiple reaction cycles. By monitoring the reaction intermediate NO2, it was found that the generation of NO2 was inhibited. The activity enhancement of graphene-like g-C3N4 nanosheets can be predominantly ascribed to the prolonged lifetime and improved photo-oxidation ability of charge carriers arising from the unique electronic structure. As the synthesis method for graphene-like g-C3N4 nanosheets with high a performance is simple, the g-C3N4 nanosheets can be envisioned to be applicable in environmental remediation and solar energy conversion.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.