Abstract
Adjusting the desired structure and heterojunction interface of photocatalytic materials using a facile and efficient strategy is still challenging. In this study, a novel two-dimensional/three-dimensional (2D/3D) oxygen-doped g-C3N4/BiOI heterostructure nano-sphere (O-g-C3N4/BiOI) was successfully prepared by a facile solvothermal method for the degradation of nondye organic contaminants.Its composition, morphological characteristics, chemical structure and electrochemical properties have been measured. The result shows the introduction of oxygen doping (O-doping) causes a new defect energy level, extends the light absorption range, and the formation of heterojunction enables the effective separation of photo-generated carriers. Under visible light irradiation, the optimum ratio of O-g-C3N4/BiOI (2:1) exhibited 100% removal efficiency of bisphenol A within 80 min, which was about 9.1, 2.33, 3.45, and 1.6 times that of pure g-C3N4, O-g-C3N4, BiOI, and O-doped-poor heterostructure, respectively. Based on the identified intermediates, the photocatalytic mechanism of O-doped O-g-C3N4/BiOI (2:1) was also revealed. This finding suggested that the synergistic effect between 2D/3D heterojunction and O-doped greatly promoted visible light photoabsorption and photoinduced carrier separation efficiency with a prolonged lifetime, which was confirmed by multiple optical and electrochemical analyses. This study could bring new opportunities for the rational design of highly efficient photocatalysts by combining 2D/3D heterojunctions with O-doped in environmental remediation.
Sign-in/Register to access full text options 
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 callDisclaimer: 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.
