Abstract
Carbon nitride photoactivity is limited by poor light utilization, rapid recombination of electron-hole (e--h+) pairs, and sluggish surface/interface reaction. Surface/interface modification is a promising strategy to get rid of these restrictions. Therefore, understanding surface/interface properties is highly worth in-depth consideration to improve carbon nitride photoactivity. Herein, the nitrogen-vacancy (Nv) and oxygen substitution (Os) co-modified carbon nitride coral-like array were rationally designed by a combination of thermal calcination and hydrothermal process. Results verified Nv extended the adsorption edge toward visible light and hampered the recombination of e--h+ pairs and Os accelerated surface/interface kinetics. In consequence, the optimized photocatalyst (Nv, Os)-CN-6 can degrade 80 % of tetracycline (TC) with the pseudo-first-order kinetic constant of 0.124 min−1, 13.8-fold higher than pristine carbon nitride. Furthermore, Nv and Os can well resist the toxic effect of interfering agents in simulated practical wastewater. Finally, Nv and Os endow (Nv, Os)-CN-6 mineralizing TC with low/non-ecology-risk intermediates evolution based on the HPLC-MS and T.E.S.T. software simulation. This study provides new insights into the rational design of carbon nitride for photodegrading TC.
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.