Abstract

Photocatalysis has been reported as a potential water purification technology for combating the pathogenic bacteria and degrading the hazardous chemicals. The photoactive organic semiconductors as the emerging class of an alternative to the traditional developed inorganic semiconductors are being widely pursued due to their tunable structures and low toxicity. Herein, the all-organic [6,6]-phenyl C71 butyric acid methyl ester (PC71BM)/g-C3N4 heterostructure have been created by introducing self-assembled n-type fullerene small molecule to the g-C3N4 surface in situ. The absorption edge of the heterostructures with PC71BM as the photosensitizer extend from 450 to 650 nm. Moreover, the charge separation and transfer efficiencies of the photocatalysts are greatly promoted even with 1.0% amount of PC71BM because of its low reorganization energy and high reduction potential. All of these superiorities endow the heterostructures with over 99.7% antibacterial rates toward E. coli and S. aureus and excellent performance against their biofilms after irradiation for 135 and 180 min, respectively. Additionally, the heterostructures achieve excellent photocatalytic degradation ability for Rhodamine B and tetracycline. Importantly, the in vitro experiments reveal that the as-prepared heterostructures possess satisfactory biocompatibility and their toxicity is negligible. This study provides a new perspective for designing ecofriendly all-organic heterostructures with high photocatalytic activity.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.